Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 130560 |
| ensemblid | ENSG00000173699.17 |
| hgncid | 17884 |
| symbol | SPATA3 |
| name | spermatogenesis associated 3 |
| refseq_nuc | NM_139073.5 |
| refseq_prot | NP_620712.2 |
| ensembl_nuc | ENST00000433428.7 |
| ensembl_prot | ENSP00000403804.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 230996121 |
| end | 231008040 |
| strand | + |
| ver | v1.2 |
| region | chr2:230996121-231008040 |
| region5000 | chr2:230991121-231013040 |
| regionname0 | SPATA3_chr2_230996121_231008040 |
| regionname5000 | SPATA3_chr2_230991121_231013040 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 183 | 167 | 17 | 24 | 101 | 8 | 17 | 85 | SPATA3_chr2_230991121_231013040 | SPATA3 | MKKVK others(178): Show |
chr2 | 230991121 | 231013040 |
| a0002 | 1/1 | 192 | 105 | 21 | 19 | 51 | 1 | 11 | 39 | SPATA3_chr2_230991121_231013040 | SPATA3 | MKKVK others(187): Show |
chr2 | 230991121 | 231013040 |
| a0003 | 0/0 | 192 | 79 | 26 | 15 | 25 | 4 | 9 | 18 | SPATA3_chr2_230991121_231013040 | SPATA3 | MKKVK others(187): Show |
chr2 | 230991121 | 231013040 |
| a0004 | 0/0 | 183 | 58 | 9 | 11 | 29 | 3 | 6 | 20 | SPATA3_chr2_230991121_231013040 | SPATA3 | MKKVK others(178): Show |
chr2 | 230991121 | 231013040 |
| a0005 | 0/0 | 192 | 24 | 10 | 7 | 4 | 0 | 3 | 4 | SPATA3_chr2_230991121_231013040 | SPATA3 | MKKVK others(187): Show |
chr2 | 230991121 | 231013040 |
| a0006 | 0/0 | 192 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | MKKVK others(187): Show |
chr2 | 230991121 | 231013040 |
| a0007 | 0/0 | 192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | MKKVK others(187): Show |
chr2 | 230991121 | 231013040 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 549 | 107 | 11 | 18 | 59 | 7 | 12 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(544): Show |
chr2 | 230991121 | 231013040 | ||
| a0001c0005 | 0/0 | 549 | 57 | 5 | 5 | 41 | 1 | 5 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(544): Show |
chr2 | 230991121 | 231013040 | ||
| a0001c0013 | 0/0 | 549 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(544): Show |
chr2 | 230991121 | 231013040 | ||
| a0001c0014 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(544): Show |
chr2 | 230991121 | 231013040 | ||
| a0001c0016 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(544): Show |
chr2 | 230991121 | 231013040 | ||
| a0002c0002 | 1/1 | 576 | 100 | 18 | 19 | 51 | 1 | 9 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(571): Show |
chr2 | 230991121 | 231013040 | ||
| a0002c0009 | 0/0 | 576 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(571): Show |
chr2 | 230991121 | 231013040 | ||
| a0002c0010 | 0/0 | 576 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(571): Show |
chr2 | 230991121 | 231013040 | ||
| a0002c0012 | 0/0 | 576 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(571): Show |
chr2 | 230991121 | 231013040 | ||
| a0003c0003 | 0/0 | 576 | 76 | 25 | 15 | 24 | 4 | 8 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(571): Show |
chr2 | 230991121 | 231013040 | ||
| a0003c0007 | 0/0 | 576 | 3 | 1 | 0 | 1 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(571): Show |
chr2 | 230991121 | 231013040 | ||
| a0004c0004 | 0/0 | 549 | 57 | 9 | 11 | 28 | 3 | 6 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(544): Show |
chr2 | 230991121 | 231013040 | ||
| a0004c0015 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(544): Show |
chr2 | 230991121 | 231013040 | ||
| a0005c0006 | 0/0 | 576 | 24 | 10 | 7 | 4 | 0 | 3 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(571): Show |
chr2 | 230991121 | 231013040 | ||
| a0006c0008 | 0/0 | 576 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(571): Show |
chr2 | 230991121 | 231013040 | ||
| a0007c0011 | 0/0 | 576 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | ATGAA others(571): Show |
chr2 | 230991121 | 231013040 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1602 | 95 | 4 | 17 | 57 | 7 | 10 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0001c0001t0002 | 0/0 | 1602 | 7 | 4 | 1 | 1 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0001c0001t0010 | 0/0 | 1602 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0001c0001t0013 | 0/0 | 1667 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1662): Show |
chr2 | 230991121 | 231013040 |
| a0001c0001t0014 | 0/0 | 1602 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0001c0001t0015 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0001c0005t0002 | 0/0 | 1602 | 57 | 5 | 5 | 41 | 1 | 5 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0001c0013t0001 | 0/0 | 1602 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0001c0014t0001 | 0/0 | 1602 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0001c0016t0002 | 0/0 | 1602 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0002c0002t0001 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0002c0002t0002 | 0/0 | 1629 | 3 | 1 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0002c0002t0003 | 0/1 | 1629 | 73 | 1 | 16 | 49 | 1 | 5 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGCTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0002c0002t0004 | 0/0 | 1629 | 13 | 12 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0002c0002t0006 | 1/0 | 1629 | 7 | 0 | 2 | 0 | 0 | 4 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGCTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0002c0002t0008 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0002c0009t0003 | 0/0 | 1629 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGCTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0002c0010t0001 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0002c0012t0002 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0003c0003t0001 | 0/0 | 1629 | 52 | 14 | 9 | 21 | 3 | 5 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0003c0003t0002 | 0/0 | 1629 | 12 | 8 | 2 | 0 | 1 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0003c0003t0005 | 0/0 | 1629 | 9 | 1 | 4 | 3 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGCTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0003c0003t0011 | 0/0 | 1629 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0003c0003t0012 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0003c0003t0016 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0003c0007t0001 | 0/0 | 1629 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0003c0007t0017 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0004c0004t0002 | 0/0 | 1602 | 54 | 6 | 11 | 28 | 3 | 6 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0004c0004t0007 | 0/0 | 1602 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0004c0015t0002 | 0/0 | 1602 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1597): Show |
chr2 | 230991121 | 231013040 |
| a0005c0006t0002 | 0/0 | 1629 | 9 | 9 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0005c0006t0003 | 0/0 | 1629 | 15 | 1 | 7 | 4 | 0 | 3 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGCTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0006c0008t0009 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| a0007c0011t0002 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | AGTTG others(1624): Show |
chr2 | 230991121 | 231013040 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 31 | 1 | 10 | 10 | 3 | 7 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0004 | 0/0 | 25 | 2 | 2 | 21 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0002g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0010g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0013g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0014g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0001t0015g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0005 | 0/0 | 14 | 1 | 0 | 12 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0015 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0027 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0042 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0005t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0013t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0014t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0001c0016t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0002 | 0/0 | 28 | 1 | 8 | 14 | 1 | 4 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0011 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0023 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0004g0008 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0006g0002 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0006g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0006g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0002t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0009t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0009t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0010t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0002c0012t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0006 | 0/0 | 14 | 1 | 0 | 8 | 0 | 5 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0024 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0002g0007 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0005g0010 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0011g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0003t0016g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0007t0001g0052 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0003c0007t0017g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0001 | 0/0 | 32 | 2 | 7 | 15 | 3 | 5 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0004t0007g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0004c0015t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0005c0006t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0005c0006t0002g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0005c0006t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0005c0006t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0005c0006t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0005c0006t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0005c0006t0003g0001 | 0/0 | 9 | 1 | 4 | 1 | 0 | 3 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0005c0006t0003g0016 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0005c0006t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0006c0008t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0006c0008t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| a0007c0011t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00140 | hp2 | a0004 | c0004 | t0002 | g0001 | EUR | GBR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0024 | EUR | FIN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00280 | hp2 | a0001 | c0005 | t0002 | g0027 | EUR | FIN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00323 | hp1 | a0004 | c0004 | t0002 | g0001 | EUR | FIN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0017 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00438 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00544 | hp1 | a0001 | c0005 | t0002 | g0009 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00544 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00609 | hp1 | a0002 | c0002 | t0003 | g0133 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00609 | hp2 | a0002 | c0002 | t0003 | g0141 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00621 | hp1 | a0004 | c0004 | t0002 | g0087 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00639 | hp1 | a0004 | c0004 | t0002 | g0039 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00639 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00642 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00673 | hp2 | a0001 | c0005 | t0002 | g0009 | EAS | CHS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0138 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00733 | hp2 | a0005 | c0006 | t0003 | g0001 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00735 | hp1 | a0002 | c0002 | t0003 | g0053 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00735 | hp2 | a0004 | c0004 | t0002 | g0001 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00738 | hp2 | a0003 | c0003 | t0002 | g0100 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00741 | hp1 | a0004 | c0004 | t0002 | g0101 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG00741 | hp2 | a0005 | c0006 | t0003 | g0001 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01069 | hp1 | a0001 | c0005 | t0002 | g0027 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0013 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0013 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01074 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0044 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01081 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01099 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01106 | hp1 | a0004 | c0004 | t0002 | g0039 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01109 | hp1 | a0002 | c0002 | t0004 | g0008 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0013 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01168 | hp1 | a0002 | c0002 | t0003 | g0134 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01169 | hp1 | a0004 | c0004 | t0002 | g0001 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01175 | hp1 | a0002 | c0002 | t0003 | g0053 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01175 | hp2 | a0005 | c0006 | t0003 | g0001 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01243 | hp1 | a0003 | c0003 | t0002 | g0007 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01243 | hp2 | a0001 | c0005 | t0002 | g0015 | AMR | PUR | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01256 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01256 | hp2 | a0005 | c0006 | t0003 | g0016 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01257 | hp2 | a0001 | c0005 | t0002 | g0082 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01258 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0153 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01261 | hp2 | a0005 | c0006 | t0003 | g0001 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01346 | hp1 | a0004 | c0004 | t0002 | g0001 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01358 | hp1 | a0001 | c0013 | t0001 | g0003 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01361 | hp1 | a0001 | c0005 | t0002 | g0037 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01361 | hp2 | a0004 | c0004 | t0002 | g0001 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01515 | hp2 | a0004 | c0004 | t0002 | g0001 | EUR | IBS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01884 | hp1 | a0001 | c0014 | t0001 | g0111 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01891 | hp1 | a0001 | c0005 | t0002 | g0042 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01891 | hp2 | a0004 | c0004 | t0002 | g0088 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01928 | hp1 | a0003 | c0003 | t0005 | g0010 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0011 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01934 | hp1 | a0003 | c0003 | t0005 | g0010 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01934 | hp2 | a0004 | c0004 | t0002 | g0072 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0010 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01952 | hp1 | a0004 | c0004 | t0002 | g0001 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01952 | hp2 | a0002 | c0002 | t0003 | g0011 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01975 | hp1 | a0005 | c0006 | t0003 | g0016 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01978 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0024 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01993 | hp1 | a0001 | c0005 | t0002 | g0027 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01993 | hp2 | a0003 | c0003 | t0005 | g0010 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02015 | hp1 | a0001 | c0001 | t0014 | g0102 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02015 | hp2 | a0001 | c0005 | t0002 | g0005 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02027 | hp1 | a0004 | c0004 | t0002 | g0001 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02040 | hp1 | a0004 | c0004 | t0002 | g0001 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02055 | hp2 | a0005 | c0006 | t0002 | g0128 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02056 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02056 | hp2 | a0001 | c0005 | t0002 | g0009 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02074 | hp2 | a0004 | c0004 | t0002 | g0001 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02080 | hp1 | a0003 | c0003 | t0005 | g0149 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0146 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02083 | hp2 | a0001 | c0005 | t0002 | g0005 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02129 | hp2 | a0004 | c0004 | t0002 | g0001 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02135 | hp1 | a0004 | c0015 | t0002 | g0001 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0029 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02145 | hp1 | a0003 | c0003 | t0002 | g0007 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0143 | EAS | CDX | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | CDX | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0047 | EAS | CDX | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02257 | hp1 | a0003 | c0003 | t0012 | g0007 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02257 | hp2 | a0003 | c0003 | t0016 | g0154 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0070 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02280 | hp1 | a0002 | c0002 | t0004 | g0008 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02280 | hp2 | a0001 | c0005 | t0002 | g0064 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02293 | hp1 | a0005 | c0006 | t0003 | g0016 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02293 | hp2 | a0004 | c0004 | t0002 | g0001 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0011 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02300 | hp2 | a0003 | c0003 | t0005 | g0010 | AMR | PEL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02451 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02523 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02523 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | KHV | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02572 | hp1 | a0005 | c0006 | t0003 | g0001 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02572 | hp2 | a0003 | c0003 | t0005 | g0150 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02602 | hp1 | a0002 | c0002 | t0006 | g0002 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02615 | hp1 | a0007 | c0011 | t0002 | g0022 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02615 | hp2 | a0002 | c0010 | t0001 | g0035 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02622 | hp1 | a0005 | c0006 | t0002 | g0041 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02622 | hp2 | a0002 | c0002 | t0004 | g0008 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02630 | hp1 | a0004 | c0004 | t0002 | g0001 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02630 | hp2 | a0004 | c0004 | t0007 | g0028 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0130 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02647 | hp2 | a0002 | c0002 | t0004 | g0022 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02698 | hp2 | a0002 | c0002 | t0006 | g0031 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02717 | hp1 | a0002 | c0002 | t0004 | g0008 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02717 | hp2 | a0002 | c0002 | t0004 | g0147 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0021 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02723 | hp2 | a0004 | c0004 | t0002 | g0085 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02735 | hp1 | a0005 | c0006 | t0003 | g0001 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02735 | hp2 | a0004 | c0004 | t0002 | g0001 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02738 | hp2 | a0002 | c0002 | t0003 | g0002 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02895 | hp1 | a0002 | c0002 | t0004 | g0022 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02895 | hp2 | a0002 | c0002 | t0004 | g0008 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02896 | hp1 | a0003 | c0003 | t0002 | g0007 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02896 | hp2 | a0006 | c0008 | t0009 | g0127 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02897 | hp1 | a0003 | c0003 | t0002 | g0007 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02897 | hp2 | a0002 | c0002 | t0004 | g0022 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02922 | hp1 | a0005 | c0006 | t0002 | g0030 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02922 | hp2 | a0005 | c0006 | t0002 | g0001 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02965 | hp1 | a0002 | c0002 | t0004 | g0008 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0021 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02976 | hp2 | a0004 | c0004 | t0002 | g0093 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03017 | hp1 | a0002 | c0009 | t0003 | g0002 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03017 | hp2 | a0001 | c0005 | t0002 | g0096 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0021 | AFR | GWD | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03098 | hp1 | a0001 | c0005 | t0002 | g0005 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0155 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03130 | hp1 | a0002 | c0002 | t0008 | g0032 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0034 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03139 | hp1 | a0002 | c0012 | t0002 | g0065 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0060 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03195 | hp1 | a0005 | c0006 | t0002 | g0030 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03195 | hp2 | a0004 | c0004 | t0007 | g0028 | AFR | ESN | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0068 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03225 | hp2 | a0005 | c0006 | t0002 | g0041 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0006 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0151 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03453 | hp2 | a0001 | c0005 | t0002 | g0103 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03486 | hp1 | a0004 | c0004 | t0007 | g0028 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0034 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03490 | hp1 | a0004 | c0004 | t0002 | g0091 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03490 | hp2 | a0002 | c0002 | t0006 | g0002 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03492 | hp1 | a0002 | c0002 | t0006 | g0002 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0006 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0069 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03579 | hp2 | a0002 | c0002 | t0004 | g0008 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03654 | hp1 | a0003 | c0007 | t0001 | g0052 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03669 | hp1 | a0004 | c0004 | t0002 | g0001 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0002 | SAS | STU | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | STU | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03704 | hp1 | a0004 | c0004 | t0002 | g0001 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03704 | hp2 | a0003 | c0003 | t0001 | g0006 | SAS | PJL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03831 | hp1 | a0001 | c0005 | t0002 | g0097 | SAS | BEB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03831 | hp2 | a0001 | c0001 | t0013 | g0105 | SAS | BEB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03834 | hp1 | a0003 | c0003 | t0005 | g0075 | SAS | BEB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03834 | hp2 | a0001 | c0005 | t0002 | g0005 | SAS | BEB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03927 | hp1 | a0002 | c0002 | t0003 | g0031 | SAS | BEB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03927 | hp2 | a0005 | c0006 | t0003 | g0001 | SAS | BEB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03942 | hp1 | a0003 | c0003 | t0011 | g0051 | SAS | BEB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0006 | SAS | BEB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG04115 | hp1 | a0005 | c0006 | t0003 | g0001 | SAS | STU | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG04115 | hp2 | a0002 | c0009 | t0003 | g0140 | SAS | STU | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG04184 | hp1 | a0004 | c0004 | t0002 | g0001 | SAS | BEB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG04184 | hp2 | a0001 | c0005 | t0002 | g0037 | SAS | BEB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0051 | SAS | STU | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG04204 | hp1 | a0001 | c0005 | t0002 | g0042 | SAS | STU | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG04204 | hp2 | a0004 | c0004 | t0002 | g0001 | SAS | STU | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG04228 | hp2 | a0002 | c0002 | t0003 | g0002 | SAS | STU | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0061 | AFR | YRI | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0109 | AFR | YRI | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18612 | hp1 | a0004 | c0004 | t0002 | g0001 | EAS | CHB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18612 | hp2 | a0001 | c0005 | t0002 | g0038 | EAS | CHB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18747 | hp1 | a0004 | c0004 | t0002 | g0084 | EAS | CHB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18747 | hp2 | a0004 | c0004 | t0002 | g0077 | EAS | CHB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18939 | hp1 | a0002 | c0002 | t0003 | g0056 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18939 | hp2 | a0002 | c0002 | t0003 | g0136 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18940 | hp1 | a0001 | c0005 | t0002 | g0014 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18940 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18941 | hp1 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18941 | hp2 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18942 | hp1 | a0004 | c0004 | t0002 | g0040 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18945 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18945 | hp2 | a0001 | c0005 | t0002 | g0015 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18946 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18947 | hp1 | a0002 | c0002 | t0003 | g0055 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18947 | hp2 | a0001 | c0005 | t0002 | g0078 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18948 | hp2 | a0001 | c0005 | t0002 | g0015 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18949 | hp1 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18949 | hp2 | a0001 | c0005 | t0002 | g0063 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18952 | hp2 | a0004 | c0004 | t0002 | g0073 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18954 | hp2 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18956 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18956 | hp2 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18957 | hp1 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18957 | hp2 | a0003 | c0003 | t0005 | g0148 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18959 | hp2 | a0002 | c0002 | t0003 | g0145 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18963 | hp2 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18964 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18965 | hp2 | a0004 | c0004 | t0002 | g0092 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18966 | hp2 | a0005 | c0006 | t0003 | g0135 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18967 | hp2 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18968 | hp2 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18970 | hp2 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18971 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18973 | hp2 | a0001 | c0005 | t0002 | g0014 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18974 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18974 | hp2 | a0004 | c0004 | t0002 | g0036 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18978 | hp1 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18978 | hp2 | a0001 | c0005 | t0002 | g0014 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18979 | hp1 | a0001 | c0005 | t0002 | g0009 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18979 | hp2 | a0002 | c0002 | t0003 | g0144 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18981 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18981 | hp2 | a0004 | c0004 | t0002 | g0043 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18982 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18983 | hp1 | a0002 | c0002 | t0003 | g0056 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18983 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18984 | hp1 | a0005 | c0006 | t0003 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18984 | hp2 | a0001 | c0005 | t0002 | g0015 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18985 | hp1 | a0002 | c0002 | t0003 | g0129 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18986 | hp1 | a0004 | c0004 | t0002 | g0040 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18986 | hp2 | a0003 | c0003 | t0005 | g0010 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18988 | hp1 | a0001 | c0005 | t0002 | g0038 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18988 | hp2 | a0004 | c0004 | t0002 | g0086 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18989 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18989 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18990 | hp1 | a0005 | c0006 | t0003 | g0016 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18991 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18992 | hp2 | a0001 | c0005 | t0002 | g0009 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18995 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18998 | hp1 | a0001 | c0005 | t0002 | g0014 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18998 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18999 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18999 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19000 | hp1 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19000 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19002 | hp2 | a0001 | c0005 | t0002 | g0080 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19003 | hp1 | a0001 | c0005 | t0002 | g0025 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19003 | hp2 | a0001 | c0005 | t0002 | g0014 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19004 | hp1 | a0001 | c0005 | t0002 | g0033 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19005 | hp1 | a0003 | c0003 | t0001 | g0029 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19006 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19009 | hp1 | a0001 | c0005 | t0002 | g0025 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19011 | hp1 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0029 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19012 | hp2 | a0001 | c0005 | t0002 | g0015 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19030 | hp1 | a0003 | c0003 | t0002 | g0079 | AFR | LWK | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19030 | hp2 | a0002 | c0002 | t0004 | g0008 | AFR | LWK | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19043 | hp1 | a0003 | c0003 | t0002 | g0007 | AFR | LWK | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19043 | hp2 | a0005 | c0006 | t0002 | g0089 | AFR | LWK | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19054 | hp1 | a0001 | c0005 | t0002 | g0009 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19054 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19055 | hp1 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19057 | hp2 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19058 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19060 | hp1 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19062 | hp1 | a0001 | c0005 | t0002 | g0033 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19063 | hp1 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19064 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19065 | hp1 | a0001 | c0005 | t0002 | g0062 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19066 | hp1 | a0003 | c0007 | t0001 | g0052 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19066 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19067 | hp1 | a0004 | c0004 | t0002 | g0043 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19067 | hp2 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19070 | hp1 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19070 | hp2 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19072 | hp1 | a0002 | c0002 | t0003 | g0055 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19072 | hp2 | a0001 | c0005 | t0002 | g0081 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19074 | hp1 | a0001 | c0005 | t0002 | g0009 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19074 | hp2 | a0001 | c0016 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19077 | hp1 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19078 | hp1 | a0004 | c0004 | t0002 | g0001 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19078 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19079 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19079 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19081 | hp2 | a0004 | c0004 | t0002 | g0036 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0126 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19082 | hp2 | a0005 | c0006 | t0003 | g0016 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19084 | hp1 | a0001 | c0005 | t0002 | g0025 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19085 | hp1 | a0001 | c0005 | t0002 | g0067 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19088 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19091 | hp1 | a0003 | c0003 | t0001 | g0110 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19240 | hp1 | a0003 | c0003 | t0001 | g0021 | AFR | YRI | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0156 | AFR | YRI | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA20752 | hp1 | a0002 | c0002 | t0003 | g0002 | EUR | TSI | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA20752 | hp2 | a0003 | c0003 | t0002 | g0132 | EUR | TSI | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0114 | EUR | TSI | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA20805 | hp2 | a0003 | c0003 | t0001 | g0013 | EUR | TSI | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0006 | SAS | GIH | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0002 | SAS | GIH | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01123 | hp1 | a0002 | c0002 | t0003 | g0139 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG01123 | hp2 | a0004 | c0004 | t0002 | g0001 | AMR | CLM | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02109 | hp1 | a0002 | c0010 | t0001 | g0035 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02109 | hp2 | a0004 | c0004 | t0002 | g0001 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02486 | hp1 | a0002 | c0002 | t0004 | g0008 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02486 | hp2 | a0006 | c0008 | t0009 | g0057 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02559 | hp1 | a0003 | c0007 | t0017 | g0058 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG02559 | hp2 | a0005 | c0006 | t0002 | g0030 | AFR | ACB | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03471 | hp1 | a0005 | c0006 | t0002 | g0090 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0007 | AFR | MSL | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG06807 | hp1 | a0004 | c0004 | t0002 | g0095 | AFR | USA | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| HG06807 | hp2 | a0002 | c0002 | t0008 | g0032 | AFR | USA | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18955 | hp1 | a0004 | c0004 | t0002 | g0094 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA18955 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA20300 | hp1 | a0003 | c0003 | t0002 | g0131 | AFR | USA | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA20300 | hp2 | a0001 | c0005 | t0002 | g0083 | AFR | USA | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA21309 | hp1 | a0003 | c0003 | t0002 | g0007 | AFR | LWK | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0152 | AFR | LWK | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0137 | REF | REF | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0006 | g0142 | REF | REF | SPATA3_chr2_230991121_231013040 | SPATA3 | chr2 | 230991121 | 231013040 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:230996317 | TCAGCAGC others(20): Show |
T | 2 | a0001 a0004 |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
disruptive_inframe_deletion | MODERATE | c.96_122delCCCTGAATC others(18): Show |
p.Pro33_Ser41del | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/5 | 209/1629 | 96/579 | 32/192 | INFO_REALIGN_3_PRIME | chr2 | 230996317 | ||
| chr2:230996435 | G | A | 1 | a0007 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.202G>A | p.Ala68Thr | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/5 | 315/1629 | 202/579 | 68/192 | chr2 | 230996435 | |||
| chr2:231000375 | T | C | 3 | a0001 a0003 a0006 |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
missense_variant | MODERATE | c.311T>C | p.Ile104Thr | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/5 | 424/1629 | 311/579 | 104/192 | chr2 | 231000375 | |||
| chr2:231000429 | G | C | 2 | a0004 a0005 |
82 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(79): Show |
missense_variant | MODERATE | c.365G>C | p.Cys122Ser | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/5 | 478/1629 | 365/579 | 122/192 | chr2 | 231000429 | |||
| chr2:231000435 | G | A | 1 | a0006 | 2 | HG02486.hp2 HG02896.hp2 |
missense_variant | MODERATE | c.371G>A | p.Arg124His | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/5 | 484/1629 | 371/579 | 124/192 | chr2 | 231000435 | |||
| chr2:231000443 | G | T | 1 | a0001 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.379G>T | p.Gly127Trp | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/5 | 492/1629 | 379/579 | 127/192 | chr2 | 231000443 | |||
| chr2:231000490 | G | T | 1 | a0001 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.426G>T | p.Trp142Cys | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/5 | 539/1629 | 426/579 | 142/192 | chr2 | 231000490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:231000388 | G | A | 1 | a0001c0013 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.324G>A | p.Pro108Pro | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/5 | 437/1629 | 324/579 | 108/192 | chr2 | 231000388 | |||
| chr2:231000472 | C | T | 1 | a0002c0012 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.408C>T | p.Val136Val | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/5 | 521/1629 | 408/579 | 136/192 | chr2 | 231000472 | |||
| chr2:231000487 | C | T | 1 | a0002c0010 | 2 | HG02109.hp1 HG02615.hp2 |
synonymous_variant | LOW | c.423C>T | p.Asp141Asp | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/5 | 536/1629 | 423/579 | 141/192 | chr2 | 231000487 | |||
| chr2:231000511 | A | G | 1 | a0004c0015 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.447A>G | p.Gly149Gly | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/5 | 560/1629 | 447/579 | 149/192 | chr2 | 231000511 | |||
| chr2:231002687 | A | G | 1 | a0003c0007 | 3 | HG02559.hp1 HG03654.hp1 NA19066.hp1 |
synonymous_variant | LOW | c.477A>G | p.Lys159Lys | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/5 | 590/1629 | 477/579 | 159/192 | chr2 | 231002687 | |||
| chr2:231002768 | G | A | 1 | a0002c0009 | 2 | HG03017.hp1 HG04115.hp2 |
synonymous_variant | LOW | c.558G>A | p.Arg186Arg | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/5 | 671/1629 | 558/579 | 186/192 | chr2 | 231002768 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:230996123 | C | T | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0010 others(26): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-111C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/5 | chr2 | 230996123 | |||||||
| chr2:230996133 | A | G | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0010 others(30): Show |
428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
5_prime_UTR_variant | MODIFIER | c.-101A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/5 | 101 | chr2 | 230996133 | ||||||
| chr2:230996212 | G | A | 1 | a0002c0002t0004 | 13 | HG01109.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/5 | 22 | chr2 | 230996212 | ||||||
| chr2:230996212 | G | T | 1 | a0003c0007t0017 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/5 | 22 | chr2 | 230996212 | ||||||
| chr2:231004069 | A | G | 1 | a0003c0003t0016 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*69A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/5 | 1280 | chr2 | 231004069 | ||||||
| chr2:231007368 | G | A | 1 | a0002c0002t0008 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*265G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4579 | chr2 | 231007368 | ||||||
| chr2:231007500 | A | G | 1 | a0001c0001t0015 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4711 | chr2 | 231007500 | ||||||
| chr2:231007536 | C | T | 12 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0014 others(9): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*433C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4747 | chr2 | 231007536 | ||||||
| chr2:231007554 | C | A | 1 | a0001c0001t0013 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*451C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4765 | chr2 | 231007554 | ||||||
| chr2:231007555 | C | A | 1 | a0001c0001t0013 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*452C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4766 | chr2 | 231007555 | ||||||
| chr2:231007556 | T | TTACATGC others(58): Show |
1 | a0001c0001t0013 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*453_*454insTACATG others(59): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4768 | chr2 | 231007556 | ||||||
| chr2:231007558 | T | A | 1 | a0001c0001t0013 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*455T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4769 | chr2 | 231007558 | ||||||
| chr2:231007560 | T | A | 1 | a0001c0001t0013 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*457T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4771 | chr2 | 231007560 | ||||||
| chr2:231007580 | C | G | 12 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0014 others(9): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*477C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4791 | chr2 | 231007580 | ||||||
| chr2:231007596 | T | C | 1 | a0004c0004t0007 | 3 | HG02630.hp2 HG03195.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*493T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4807 | chr2 | 231007596 | ||||||
| chr2:231007600 | C | A | 1 | a0001c0001t0014 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*497C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4811 | chr2 | 231007600 | ||||||
| chr2:231007668 | C | T | 12 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0014 others(9): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*565C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4879 | chr2 | 231007668 | ||||||
| chr2:231007764 | C | T | 1 | a0003c0003t0012 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*661C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 4975 | chr2 | 231007764 | ||||||
| chr2:231007810 | A | G | 14 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0013 others(11): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*707A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 5021 | chr2 | 231007810 | ||||||
| chr2:231007935 | A | G | 1 | a0003c0003t0011 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*832A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 5146 | chr2 | 231007935 | ||||||
| chr2:231007968 | C | A | 1 | a0006c0008t0009 | 2 | HG02486.hp2 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*865C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 5/5 | 5179 | chr2 | 231007968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:230996541 | T | A | 1 | a0006c0008t0009g0057 | 1 | HG02486.hp2 | splice_region_variant&intron_variant | LOW | c.301+7T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230996541 | |||||||
| chr2:230996635 | G | A | 2 | a0002c0002t0008g0032 a0003c0007t0017g0058 |
3 | HG02559.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.301+101G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230996635 | |||||||
| chr2:230996849 | G | C | 1 | a0002c0002t0003g0011 | 6 | HG00423.hp1 HG01928.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+315G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230996849 | |||||||
| chr2:230996913 | C | G | 2 | a0003c0003t0001g0155 a0003c0003t0001g0156 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.301+379C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230996913 | |||||||
| chr2:230996947 | C | A | 1 | a0001c0001t0001g0059 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.301+413C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230996947 | |||||||
| chr2:230996959 | A | G | 1 | a0003c0003t0016g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.301+425A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230996959 | |||||||
| chr2:230996978 | A | G | 2 | a0003c0003t0001g0024 a0003c0003t0001g0153 |
5 | HG00280.hp1 HG00738.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+444A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230996978 | |||||||
| chr2:230996986 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(104): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.301+452T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230996986 | |||||||
| chr2:230996996 | C | T | 1 | a0002c0002t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.301+462C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230996996 | |||||||
| chr2:230997214 | G | A | 5 | a0002c0002t0001g0049 a0003c0007t0017g0058 a0005c0006t0002g0128 others(2): Show |
6 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+680G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997214 | |||||||
| chr2:230997283 | C | A | 16 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0066 others(13): Show |
51 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.301+749C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997283 | |||||||
| chr2:230997300 | T | C | 3 | a0001c0005t0002g0067 a0002c0002t0003g0050 a0002c0002t0003g0129 |
4 | NA18956.hp1 NA18985.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+766T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997300 | |||||||
| chr2:230997305 | C | T | 1 | a0002c0002t0001g0049 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.301+771C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997305 | |||||||
| chr2:230997311 | G | A | 14 | a0001c0001t0001g0071 a0001c0001t0010g0034 a0001c0001t0015g0060 others(11): Show |
20 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.301+777G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997311 | |||||||
| chr2:230997380 | C | A | 1 | a0004c0004t0002g0072 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.301+846C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997380 | |||||||
| chr2:230997687 | G | A | 5 | a0001c0001t0010g0034 a0001c0001t0015g0060 a0002c0002t0002g0152 others(2): Show |
7 | HG02109.hp1 HG02615.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.301+1153G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997687 | |||||||
| chr2:230997776 | G | T | 6 | a0001c0001t0010g0034 a0001c0001t0015g0060 a0002c0002t0002g0152 others(3): Show |
7 | HG02486.hp2 HG02896.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.301+1242G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997776 | |||||||
| chr2:230997976 | C | G | 1 | a0002c0002t0004g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.301+1442C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997976 | |||||||
| chr2:230997976 | C | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(60): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.301+1442C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997976 | |||||||
| chr2:230997991 | G | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(60): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.301+1457G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230997991 | |||||||
| chr2:230998070 | G | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(63): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.301+1536G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998070 | |||||||
| chr2:230998139 | G | A | 1 | a0001c0001t0014g0102 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.301+1605G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998139 | |||||||
| chr2:230998380 | A | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(61): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.301+1846A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998380 | |||||||
| chr2:230998394 | C | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(60): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.301+1860C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998394 | |||||||
| chr2:230998468 | A | G | 1 | a0002c0002t0003g0146 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.302-1898A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998468 | |||||||
| chr2:230998525 | G | A | 1 | a0003c0007t0017g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.302-1841G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998525 | |||||||
| chr2:230998561 | A | G | 1 | a0002c0002t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.302-1805A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998561 | |||||||
| chr2:230998575 | G | A | 1 | a0002c0002t0008g0032 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.302-1791G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998575 | |||||||
| chr2:230998594 | A | T | 1 | a0003c0003t0016g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.302-1772A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998594 | |||||||
| chr2:230998673 | A | G | 1 | a0001c0001t0001g0048 | 2 | HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.302-1693A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998673 | |||||||
| chr2:230998785 | A | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(59): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.302-1581A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998785 | |||||||
| chr2:230998934 | C | T | 6 | a0001c0001t0001g0044 a0002c0002t0008g0032 a0003c0003t0001g0024 others(3): Show |
10 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.302-1432C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998934 | |||||||
| chr2:230998951 | G | C | 9 | a0001c0001t0002g0007 a0001c0001t0002g0019 a0001c0001t0002g0076 others(6): Show |
18 | HG01243.hp1 HG01975.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.302-1415G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998951 | |||||||
| chr2:230998954 | G | C | 2 | a0004c0004t0002g0036 a0004c0004t0002g0073 |
3 | NA18952.hp2 NA18974.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.302-1412G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230998954 | |||||||
| chr2:230999021 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.302-1345T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999021 | |||||||
| chr2:230999038 | C | T | 1 | a0002c0010t0001g0035 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.302-1328C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999038 | |||||||
| chr2:230999060 | T | C | 1 | a0004c0004t0002g0077 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.302-1306T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999060 | |||||||
| chr2:230999170 | C | T | 2 | a0001c0001t0010g0034 a0001c0001t0015g0060 |
3 | HG03130.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.302-1196C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999170 | |||||||
| chr2:230999171 | G | T | 2 | a0001c0001t0010g0034 a0001c0001t0015g0060 |
3 | HG03130.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.302-1195G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999171 | |||||||
| chr2:230999205 | G | A | 1 | a0001c0005t0002g0078 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.302-1161G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999205 | |||||||
| chr2:230999212 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.302-1154T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999212 | |||||||
| chr2:230999237 | G | A | 1 | a0001c0001t0013g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.302-1129G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999237 | |||||||
| chr2:230999279 | G | A | 16 | a0001c0005t0002g0005 a0001c0005t0002g0009 a0001c0005t0002g0014 others(13): Show |
44 | HG00280.hp2 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.302-1087G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999279 | |||||||
| chr2:230999292 | C | T | 1 | a0003c0003t0001g0047 | 2 | HG02074.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.302-1074C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999292 | |||||||
| chr2:230999404 | T | A | 1 | a0002c0002t0003g0134 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.302-962T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999404 | |||||||
| chr2:230999452 | T | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.302-914T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999452 | |||||||
| chr2:230999471 | C | T | 1 | a0003c0003t0016g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.302-895C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999471 | |||||||
| chr2:230999472 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(62): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.302-894G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999472 | |||||||
| chr2:230999486 | T | A | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.302-880T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999486 | |||||||
| chr2:230999574 | A | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.302-792A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999574 | |||||||
| chr2:230999575 | C | T | 1 | a0002c0002t0001g0049 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.302-791C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999575 | |||||||
| chr2:230999630 | C | T | 1 | a0002c0012t0002g0065 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.302-736C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999630 | |||||||
| chr2:230999659 | G | T | 1 | a0003c0003t0001g0126 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.302-707G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999659 | |||||||
| chr2:230999731 | T | C | 1 | a0002c0002t0008g0032 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.302-635T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999731 | |||||||
| chr2:230999775 | T | C | 15 | a0001c0005t0002g0005 a0001c0005t0002g0009 a0001c0005t0002g0014 others(12): Show |
43 | HG00280.hp2 HG00544.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.302-591T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999775 | |||||||
| chr2:230999814 | A | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.302-552A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999814 | |||||||
| chr2:230999850 | C | T | 1 | a0001c0005t0002g0033 | 2 | NA19004.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.302-516C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999850 | |||||||
| chr2:230999851 | G | A | 1 | a0002c0010t0001g0035 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.302-515G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999851 | |||||||
| chr2:230999885 | T | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.302-481T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999885 | |||||||
| chr2:230999928 | C | T | 1 | a0002c0010t0001g0035 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.302-438C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999928 | |||||||
| chr2:230999931 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0046 others(16): Show |
54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.302-435A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 230999931 | |||||||
| chr2:231000090 | T | G | 3 | a0001c0001t0001g0010 a0003c0003t0001g0010 a0003c0003t0005g0010 |
7 | HG01928.hp1 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.302-276T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 231000090 | |||||||
| chr2:231000102 | G | A | 35 | a0001c0005t0002g0042 a0001c0005t0002g0096 a0001c0005t0002g0103 others(32): Show |
95 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.302-264G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 231000102 | |||||||
| chr2:231000241 | G | A | 1 | a0002c0002t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.302-125G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 231000241 | |||||||
| chr2:231000303 | A | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.302-63A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 231000303 | |||||||
| chr2:231000310 | C | T | 1 | a0005c0006t0002g0030 | 3 | HG02559.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.302-56C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 231000310 | |||||||
| chr2:231000332 | T | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(77): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.302-34T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 231000332 | |||||||
| chr2:231000350 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.302-16C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 1/4 | chr2 | 231000350 | |||||||
| chr2:231000548 | C | T | 1 | a0002c0002t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.473+11C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231000548 | |||||||
| chr2:231000554 | G | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(68): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.473+17G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231000554 | |||||||
| chr2:231000654 | A | G | 1 | a0001c0005t0002g0014 | 5 | NA18940.hp1 NA18973.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+117A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231000654 | |||||||
| chr2:231000680 | C | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(66): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.473+143C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231000680 | |||||||
| chr2:231000720 | G | A | 2 | a0002c0002t0001g0049 a0002c0002t0002g0152 |
3 | HG02809.hp1 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.473+183G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231000720 | |||||||
| chr2:231000740 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.473+203C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231000740 | |||||||
| chr2:231000911 | C | T | 4 | a0002c0002t0003g0012 a0002c0002t0003g0023 a0002c0002t0003g0145 others(1): Show |
12 | HG00423.hp2 HG00544.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.473+374C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231000911 | |||||||
| chr2:231000915 | G | A | 2 | a0002c0002t0003g0017 a0002c0002t0003g0136 |
6 | HG00408.hp1 NA18939.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+378G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231000915 | |||||||
| chr2:231000979 | G | A | 1 | a0001c0001t0001g0020 | 4 | HG00438.hp1 HG02040.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+442G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231000979 | |||||||
| chr2:231001031 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.473+494C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001031 | |||||||
| chr2:231001042 | C | T | 1 | a0002c0002t0008g0032 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.473+505C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001042 | |||||||
| chr2:231001124 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(63): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.473+587C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001124 | |||||||
| chr2:231001226 | A | G | 3 | a0002c0002t0002g0099 a0002c0002t0003g0056 a0002c0002t0003g0144 |
4 | NA18939.hp1 NA18979.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+689A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001226 | |||||||
| chr2:231001260 | G | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(67): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.473+723G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001260 | |||||||
| chr2:231001268 | G | A | 1 | a0003c0007t0017g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.473+731G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001268 | |||||||
| chr2:231001305 | C | T | 2 | a0002c0002t0004g0022 a0007c0011t0002g0022 |
4 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+768C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001305 | |||||||
| chr2:231001362 | C | T | 1 | a0002c0002t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.473+825C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001362 | |||||||
| chr2:231001571 | C | T | 2 | a0006c0008t0009g0057 a0006c0008t0009g0127 |
2 | HG02486.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.473+1034C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001571 | |||||||
| chr2:231001651 | G | A | 2 | a0006c0008t0009g0057 a0006c0008t0009g0127 |
2 | HG02486.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.474-1033G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001651 | |||||||
| chr2:231001916 | C | CCTGTCAA others(92): Show |
1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.474-767_474-669dup others(99): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 231001916 | ||||||
| chr2:231001936 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.474-748C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001936 | |||||||
| chr2:231001944 | G | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(66): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.474-740G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001944 | |||||||
| chr2:231001983 | G | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(66): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.474-701G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231001983 | |||||||
| chr2:231002095 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(66): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.474-589C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002095 | |||||||
| chr2:231002159 | C | T | 1 | a0002c0012t0002g0065 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.474-525C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002159 | |||||||
| chr2:231002226 | G | T | 1 | a0003c0003t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.474-458G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002226 | |||||||
| chr2:231002347 | GTTGTTGT others(65): Show |
G | 1 | a0001c0005t0002g0062 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.474-336_474-265del others(72): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002347 | |||||||
| chr2:231002384 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.474-300T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002384 | |||||||
| chr2:231002462 | A | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.474-222A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002462 | |||||||
| chr2:231002505 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(137): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.474-179A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002505 | |||||||
| chr2:231002528 | G | A | 1 | a0004c0004t0002g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.474-156G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002528 | |||||||
| chr2:231002542 | C | T | 1 | a0002c0002t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.474-142C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002542 | |||||||
| chr2:231002634 | G | A | 1 | a0002c0002t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.474-50G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002634 | |||||||
| chr2:231002663 | C | T | 2 | a0002c0002t0004g0022 a0007c0011t0002g0022 |
4 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-21C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002663 | |||||||
| chr2:231002670 | G | A | 2 | a0006c0008t0009g0057 a0006c0008t0009g0127 |
2 | HG02486.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.474-14G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 2/4 | chr2 | 231002670 | |||||||
| chr2:231002839 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.*38+12G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231002839 | |||||||
| chr2:231002840 | C | T | 3 | a0002c0002t0003g0012 a0002c0002t0003g0145 a0002c0002t0003g0146 |
8 | HG00423.hp2 HG00544.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.*38+13C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231002840 | |||||||
| chr2:231002863 | G | C | 16 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0003c0003t0001g0006 others(13): Show |
39 | HG00408.hp2 HG00673.hp1 HG01928.hp1 others(36): Show |
intron_variant | MODIFIER | c.*38+36G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231002863 | |||||||
| chr2:231002943 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(64): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.*38+116C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231002943 | |||||||
| chr2:231002944 | G | A | 1 | a0002c0002t0008g0032 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.*38+117G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231002944 | |||||||
| chr2:231002965 | C | T | 6 | a0001c0005t0002g0042 a0001c0005t0002g0096 a0001c0005t0002g0103 others(3): Show |
15 | HG01109.hp1 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.*38+138C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231002965 | |||||||
| chr2:231002983 | C | T | 1 | a0003c0003t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.*38+156C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231002983 | |||||||
| chr2:231003033 | C | T | 1 | a0004c0004t0007g0028 | 3 | HG02630.hp2 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.*38+206C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231003033 | |||||||
| chr2:231003057 | G | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(64): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.*38+230G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231003057 | |||||||
| chr2:231003214 | A | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.*38+387A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231003214 | |||||||
| chr2:231003261 | C | T | 2 | a0002c0002t0004g0022 a0007c0011t0002g0022 |
4 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.*38+434C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231003261 | |||||||
| chr2:231003417 | A | AG | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(67): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.*38+592dupG | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 231003417 | ||||||
| chr2:231003441 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.*39-598G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231003441 | |||||||
| chr2:231003486 | T | C | 1 | a0001c0005t0002g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.*39-553T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231003486 | |||||||
| chr2:231003576 | A | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.*39-463A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231003576 | |||||||
| chr2:231003577 | C | G | 1 | a0002c0002t0003g0144 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.*39-462C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231003577 | |||||||
| chr2:231003801 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.*39-238C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231003801 | |||||||
| chr2:231003939 | C | T | 1 | a0003c0003t0001g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.*39-100C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231003939 | |||||||
| chr2:231004029 | C | G | 1 | a0002c0010t0001g0035 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.*39-10C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 3/4 | chr2 | 231004029 | |||||||
| chr2:231004214 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.*118+96G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004214 | |||||||
| chr2:231004229 | G | A | 2 | a0002c0002t0004g0022 a0007c0011t0002g0022 |
4 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.*118+111G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004229 | |||||||
| chr2:231004229 | G | GTTTCCTG others(55): Show |
1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+112_*118+173d others(64): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231004229 | ||||||
| chr2:231004326 | T | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.*118+208T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004326 | |||||||
| chr2:231004417 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.*118+299G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004417 | |||||||
| chr2:231004500 | G | A | 1 | a0003c0003t0002g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*118+382G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004500 | |||||||
| chr2:231004546 | GAGGGGAT others(64): Show |
G | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+429_*118+499d others(73): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004546 | |||||||
| chr2:231004580 | A | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(67): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.*118+462A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004580 | |||||||
| chr2:231004621 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(72): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.*118+503A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004621 | |||||||
| chr2:231004679 | T | C | 1 | a0002c0002t0003g0053 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.*118+561T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004679 | |||||||
| chr2:231004710 | T | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+592T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004710 | |||||||
| chr2:231004712 | G | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+594G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004712 | |||||||
| chr2:231004714 | G | A | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+596G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004714 | |||||||
| chr2:231004715 | G | A | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+597G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004715 | |||||||
| chr2:231004721 | G | T | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+603G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004721 | |||||||
| chr2:231004722 | G | T | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+604G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004722 | |||||||
| chr2:231004725 | T | A | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+607T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004725 | |||||||
| chr2:231004726 | C | G | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+608C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004726 | |||||||
| chr2:231004727 | T | A | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+609T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004727 | |||||||
| chr2:231004730 | A | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+612A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004730 | |||||||
| chr2:231004731 | A | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+613A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004731 | |||||||
| chr2:231004735 | C | A | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+617C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004735 | |||||||
| chr2:231004738 | G | T | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+620G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004738 | |||||||
| chr2:231004739 | T | G | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+621T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004739 | |||||||
| chr2:231004741 | T | A | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+623T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004741 | |||||||
| chr2:231004744 | C | T | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+626C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004744 | |||||||
| chr2:231004746 | G | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+628G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004746 | |||||||
| chr2:231004748 | G | T | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+630G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004748 | |||||||
| chr2:231004749 | G | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+631G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004749 | |||||||
| chr2:231004750 | C | T | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+632C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004750 | |||||||
| chr2:231004751 | C | A | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+633C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004751 | |||||||
| chr2:231004756 | G | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+638G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004756 | |||||||
| chr2:231004758 | A | T | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+640A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004758 | |||||||
| chr2:231004759 | G | A | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+641G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004759 | |||||||
| chr2:231004785 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+667T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004785 | |||||||
| chr2:231004789 | T | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+671T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004789 | |||||||
| chr2:231004789 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+671T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004789 | |||||||
| chr2:231004797 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+679A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004797 | |||||||
| chr2:231004817 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+699A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004817 | |||||||
| chr2:231004820 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+702T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004820 | |||||||
| chr2:231004850 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+732A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004850 | |||||||
| chr2:231004852 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+734A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004852 | |||||||
| chr2:231004854 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+736A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004854 | |||||||
| chr2:231004862 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+744T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004862 | |||||||
| chr2:231004863 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+745A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004863 | |||||||
| chr2:231004868 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+750A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004868 | |||||||
| chr2:231004870 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+752T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004870 | |||||||
| chr2:231004890 | G | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+772G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004890 | |||||||
| chr2:231004895 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+777A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004895 | |||||||
| chr2:231004895 | A | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+777A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004895 | |||||||
| chr2:231004896 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+778G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004896 | |||||||
| chr2:231004897 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+779C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004897 | |||||||
| chr2:231004898 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+780A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004898 | |||||||
| chr2:231004902 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+784A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004902 | |||||||
| chr2:231004904 | C | A | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+786C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004904 | |||||||
| chr2:231004904 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+786C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004904 | |||||||
| chr2:231004905 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+787A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004905 | |||||||
| chr2:231004906 | T | C | 2 | a0001c0001t0001g0120 a0004c0004t0002g0084 |
2 | HG01071.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.*118+788T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004906 | |||||||
| chr2:231004907 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+789A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004907 | |||||||
| chr2:231004909 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+791C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004909 | |||||||
| chr2:231004910 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+792T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004910 | |||||||
| chr2:231004911 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+793A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004911 | |||||||
| chr2:231004916 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+798A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004916 | |||||||
| chr2:231004919 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+801A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004919 | |||||||
| chr2:231004921 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+803T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004921 | |||||||
| chr2:231004937 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+819A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004937 | |||||||
| chr2:231004940 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+822A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004940 | |||||||
| chr2:231004945 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+827C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004945 | |||||||
| chr2:231004946 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+828A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004946 | |||||||
| chr2:231004948 | C | A | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+830C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004948 | |||||||
| chr2:231004948 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+830C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004948 | |||||||
| chr2:231004949 | A | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+831A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004949 | |||||||
| chr2:231004950 | T | G | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+832T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004950 | |||||||
| chr2:231004951 | T | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+833T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004951 | |||||||
| chr2:231004951 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+833T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004951 | |||||||
| chr2:231004953 | T | A | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+835T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004953 | |||||||
| chr2:231004956 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+838C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004956 | |||||||
| chr2:231004956 | C | G | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+838C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004956 | |||||||
| chr2:231004958 | A | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+840A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004958 | |||||||
| chr2:231004959 | T | G | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+841T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004959 | |||||||
| chr2:231004961 | A | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+843A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004961 | |||||||
| chr2:231004962 | T | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+844T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004962 | |||||||
| chr2:231004964 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+846C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004964 | |||||||
| chr2:231004965 | T | A | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+847T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004965 | |||||||
| chr2:231004965 | T | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+847T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004965 | |||||||
| chr2:231004965 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+847T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004965 | |||||||
| chr2:231004967 | A | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+849A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004967 | |||||||
| chr2:231004973 | A | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+855A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004973 | |||||||
| chr2:231004974 | T | C | 1 | a0004c0004t0002g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*118+856T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004974 | |||||||
| chr2:231004974 | T | TCACCACA others(436): Show |
1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+861_*118+862i others(445): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231004974 | ||||||
| chr2:231004976 | A | C | 2 | a0004c0004t0002g0084 a0005c0006t0003g0135 |
2 | NA18747.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.*118+858A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004976 | |||||||
| chr2:231004977 | C | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+859C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004977 | |||||||
| chr2:231004980 | T | C | 1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+862T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004980 | |||||||
| chr2:231004981 | C | A | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+863C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004981 | |||||||
| chr2:231004982 | C | A | 1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+864C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004982 | |||||||
| chr2:231004983 | T | C | 1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+865T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004983 | |||||||
| chr2:231004984 | C | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+866C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004984 | |||||||
| chr2:231004985 | A | C | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+867A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004985 | |||||||
| chr2:231004990 | C | A | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+872C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004990 | |||||||
| chr2:231004991 | A | G | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+873A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004991 | |||||||
| chr2:231004992 | T | C | 1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+874T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004992 | |||||||
| chr2:231004994 | C | A | 2 | a0002c0002t0003g0133 a0005c0006t0003g0135 |
2 | HG00609.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.*118+876C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004994 | |||||||
| chr2:231004994 | C | CTCACCA | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(64): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.*118+880_*118+885d others(8): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231004994 | ||||||
| chr2:231004998 | C | T | 1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+880C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231004998 | |||||||
| chr2:231005001 | T | C | 1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+883T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005001 | |||||||
| chr2:231005004 | T | C | 1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+886T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005004 | |||||||
| chr2:231005004 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+886T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005004 | |||||||
| chr2:231005007 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+889C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005007 | |||||||
| chr2:231005007 | C | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+889C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005007 | |||||||
| chr2:231005010 | C | CCAT | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(132): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.*118+898_*118+900d others(5): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005010 | ||||||
| chr2:231005010 | C | G | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+892C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005010 | |||||||
| chr2:231005010 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+892C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005010 | |||||||
| chr2:231005016 | T | C | 1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+898T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005016 | |||||||
| chr2:231005018 | A | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+900A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005018 | |||||||
| chr2:231005019 | C | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+901C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005019 | |||||||
| chr2:231005021 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+903A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005021 | |||||||
| chr2:231005022 | T | C | 2 | a0001c0001t0001g0120 a0002c0002t0003g0133 |
2 | HG00609.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.*118+904T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005022 | |||||||
| chr2:231005022 | T | TCACCATC others(497): Show |
1 | a0002c0002t0003g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.*118+917_*118+918i others(506): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005022 | ||||||
| chr2:231005025 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+907C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005025 | |||||||
| chr2:231005028 | T | C | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+910T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005028 | |||||||
| chr2:231005031 | T | C | 1 | a0001c0014t0001g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*118+913T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005031 | |||||||
| chr2:231005031 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+913T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005031 | |||||||
| chr2:231005033 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+915A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005033 | |||||||
| chr2:231005037 | T | C | 3 | a0002c0002t0003g0133 a0002c0002t0003g0143 a0005c0006t0003g0135 |
3 | HG00609.hp1 HG02155.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.*118+919T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005037 | |||||||
| chr2:231005043 | T | TCACCAC | 1 | a0004c0004t0007g0028 | 3 | HG02630.hp2 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.*118+934_*118+939d others(8): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005043 | ||||||
| chr2:231005058 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+940T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005058 | |||||||
| chr2:231005064 | T | C | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+946T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005064 | |||||||
| chr2:231005067 | T | TCATCACC others(5): Show |
2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+951_*118+952i others(14): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005067 | ||||||
| chr2:231005073 | C | T | 1 | a0005c0006t0003g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*118+955C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005073 | |||||||
| chr2:231005087 | A | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.*118+969A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005087 | |||||||
| chr2:231005088 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+970T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005088 | |||||||
| chr2:231005088 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+970T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005088 | |||||||
| chr2:231005090 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+972A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005090 | |||||||
| chr2:231005094 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.*118+976T>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005094 | |||||||
| chr2:231005096 | C | A | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+978C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005096 | |||||||
| chr2:231005106 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+988T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005106 | |||||||
| chr2:231005109 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+991C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005109 | |||||||
| chr2:231005115 | TCACCACC others(14): Show |
T | 1 | a0002c0002t0003g0002 | 2 | HG02451.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.*118+1012_*118+103 others(25): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005115 | ||||||
| chr2:231005121 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1003C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005121 | |||||||
| chr2:231005130 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1012T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005130 | |||||||
| chr2:231005133 | TCAC | T | 26 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0044 others(23): Show |
56 | HG00280.hp1 HG00408.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.*118+1027_*118+102 others(7): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005133 | ||||||
| chr2:231005136 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1018C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005136 | |||||||
| chr2:231005139 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1021C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005139 | |||||||
| chr2:231005139 | CCACCACC others(2): Show |
C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(39): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.*118+1027_*118+103 others(13): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005139 | ||||||
| chr2:231005145 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1027C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005145 | |||||||
| chr2:231005151 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1033C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005151 | |||||||
| chr2:231005157 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1039C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005157 | |||||||
| chr2:231005163 | CCAT | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(39): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.*118+1051_*118+105 others(7): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005163 | ||||||
| chr2:231005163 | CCATCATC others(5): Show |
C | 2 | a0002c0002t0004g0022 a0007c0011t0002g0022 |
4 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.*118+1060_*118+107 others(16): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005163 | ||||||
| chr2:231005166 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1048T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005166 | |||||||
| chr2:231005169 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1051T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005169 | |||||||
| chr2:231005175 | T | C | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1057T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005175 | |||||||
| chr2:231005177 | A | G | 2 | a0002c0002t0004g0022 a0007c0011t0002g0022 |
4 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.*118+1059A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005177 | |||||||
| chr2:231005181 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1063T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005181 | |||||||
| chr2:231005187 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1069T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005187 | |||||||
| chr2:231005195 | T | A | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1077T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005195 | |||||||
| chr2:231005197 | C | A | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1079C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005197 | |||||||
| chr2:231005206 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1088C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005206 | |||||||
| chr2:231005211 | T | C | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1093T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005211 | |||||||
| chr2:231005214 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1096C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005214 | |||||||
| chr2:231005220 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1102T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005220 | |||||||
| chr2:231005222 | A | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1104A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005222 | |||||||
| chr2:231005232 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1114C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005232 | |||||||
| chr2:231005241 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1123C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005241 | |||||||
| chr2:231005244 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1126C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005244 | |||||||
| chr2:231005250 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1132C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005250 | |||||||
| chr2:231005253 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1135C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005253 | |||||||
| chr2:231005256 | T | C | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1138T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005256 | |||||||
| chr2:231005259 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1141T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005259 | |||||||
| chr2:231005262 | T | C | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1144T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005262 | |||||||
| chr2:231005263 | T | C | 3 | a0002c0002t0003g0133 a0002c0002t0003g0143 a0003c0003t0001g0151 |
3 | HG00609.hp1 HG02155.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.*118+1145T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005263 | |||||||
| chr2:231005268 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1150T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005268 | |||||||
| chr2:231005271 | T | C | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1153T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005271 | |||||||
| chr2:231005274 | C | A | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1156C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005274 | |||||||
| chr2:231005280 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1162C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005280 | |||||||
| chr2:231005282 | A | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(64): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.*118+1164A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005282 | |||||||
| chr2:231005291 | A | G | 1 | a0002c0010t0001g0035 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.*118+1173A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005291 | |||||||
| chr2:231005294 | A | C | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1176A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005294 | |||||||
| chr2:231005298 | C | T | 3 | a0002c0002t0003g0133 a0002c0002t0003g0143 a0003c0003t0001g0151 |
3 | HG00609.hp1 HG02155.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.*118+1180C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005298 | |||||||
| chr2:231005301 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*118+1183C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005301 | |||||||
| chr2:231005310 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1192C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005310 | |||||||
| chr2:231005319 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1201T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005319 | |||||||
| chr2:231005328 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1210T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005328 | |||||||
| chr2:231005334 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1216C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005334 | |||||||
| chr2:231005337 | T | TCATCAC | 20 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0010g0034 others(17): Show |
44 | HG00408.hp2 HG00673.hp1 HG01928.hp1 others(41): Show |
intron_variant | MODIFIER | c.*118+1221_*118+122 others(10): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005337 | ||||||
| chr2:231005337 | TCAC | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(44): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.*118+1222_*118+122 others(7): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005337 | ||||||
| chr2:231005340 | C | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0010g0034 others(17): Show |
44 | HG00408.hp2 HG00673.hp1 HG01928.hp1 others(41): Show |
intron_variant | MODIFIER | c.*118+1222C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005340 | |||||||
| chr2:231005346 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1228T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005346 | |||||||
| chr2:231005349 | C | T | 3 | a0002c0002t0003g0133 a0002c0002t0003g0143 a0003c0007t0017g0058 |
3 | HG00609.hp1 HG02155.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.*118+1231C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005349 | |||||||
| chr2:231005352 | T | C | 1 | a0003c0007t0017g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*118+1234T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005352 | |||||||
| chr2:231005355 | C | T | 3 | a0002c0002t0003g0133 a0002c0002t0003g0143 a0003c0007t0017g0058 |
3 | HG00609.hp1 HG02155.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.*118+1237C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005355 | |||||||
| chr2:231005358 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1240C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005358 | |||||||
| chr2:231005367 | T | C | 1 | a0003c0007t0017g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*118+1249T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005367 | |||||||
| chr2:231005380 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1262C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005380 | |||||||
| chr2:231005385 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1267C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005385 | |||||||
| chr2:231005388 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1270C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005388 | |||||||
| chr2:231005394 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1276T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005394 | |||||||
| chr2:231005395 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1277C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005395 | |||||||
| chr2:231005397 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1279C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005397 | |||||||
| chr2:231005409 | G | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(73): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.*118+1291G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005409 | |||||||
| chr2:231005410 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1292T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005410 | |||||||
| chr2:231005421 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1303T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005421 | |||||||
| chr2:231005427 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1309C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005427 | |||||||
| chr2:231005433 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1315C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005433 | |||||||
| chr2:231005437 | A | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1319A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005437 | |||||||
| chr2:231005439 | T | C | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1321T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005439 | |||||||
| chr2:231005448 | T | TCAC | 72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(69): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.*118+1351_*118+135 others(7): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005448 | ||||||
| chr2:231005448 | TCAC | T | 6 | a0001c0005t0002g0009 a0001c0005t0002g0025 a0001c0005t0002g0038 others(3): Show |
16 | HG00544.hp1 HG00673.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.*118+1351_*118+135 others(7): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005448 | ||||||
| chr2:231005463 | C | T | 1 | a0002c0002t0004g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*118+1345C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005463 | |||||||
| chr2:231005466 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1348C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005466 | |||||||
| chr2:231005482 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.*118+1364C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005482 | |||||||
| chr2:231005496 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1378C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005496 | |||||||
| chr2:231005499 | T | C | 4 | a0002c0002t0003g0133 a0002c0002t0003g0143 a0002c0002t0004g0147 others(1): Show |
4 | HG00609.hp1 HG02155.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.*118+1381T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005499 | |||||||
| chr2:231005502 | T | C | 4 | a0002c0002t0003g0133 a0002c0002t0003g0143 a0002c0002t0004g0147 others(1): Show |
4 | HG00609.hp1 HG02155.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.*118+1384T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005502 | |||||||
| chr2:231005508 | C | T | 1 | a0003c0003t0016g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*118+1390C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005508 | |||||||
| chr2:231005514 | C | T | 2 | a0002c0002t0003g0133 a0002c0002t0003g0143 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*118+1396C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005514 | |||||||
| chr2:231005520 | C | T | 2 | a0002c0002t0004g0147 a0003c0003t0016g0154 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.*118+1402C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005520 | |||||||
| chr2:231005526 | C | T | 2 | a0002c0002t0004g0022 a0007c0011t0002g0022 |
4 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.*118+1408C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005526 | |||||||
| chr2:231005528 | A | ATCACCAC others(1201): Show |
2 | a0002c0002t0004g0022 a0007c0011t0002g0022 |
4 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.*118+1410_*118+141 others(1212): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005528 | |||||||
| chr2:231005529 | C | CCACCATC others(978): Show |
1 | a0003c0003t0016g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*118+1413_*118+141 others(989): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005529 | ||||||
| chr2:231005530 | C | CACCATCA others(1204): Show |
1 | a0002c0002t0004g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*118+1413_*118+141 others(1215): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005530 | ||||||
| chr2:231005530 | C | G | 2 | a0002c0002t0004g0022 a0007c0011t0002g0022 |
4 | HG02615.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.*118+1412C>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005530 | |||||||
| chr2:231005532 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(68): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.*118+1414T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005532 | |||||||
| chr2:231005538 | C | T | 3 | a0002c0002t0004g0022 a0002c0002t0004g0147 a0007c0011t0002g0022 |
5 | HG02615.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.*118+1420C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005538 | |||||||
| chr2:231005541 | C | T | 1 | a0003c0003t0016g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*118+1423C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005541 | |||||||
| chr2:231005542 | C | CACCACCA others(1017): Show |
1 | a0003c0003t0001g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.*118+1425_*118+142 others(1028): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005542 | ||||||
| chr2:231005542 | C | T | 1 | a0003c0003t0016g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*118+1424C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005542 | |||||||
| chr2:231005545 | C | CATCACCA others(1216): Show |
1 | a0002c0002t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(1227): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1228): Show |
1 | a0001c0005t0002g0080 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(1239): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1217): Show |
1 | a0004c0004t0002g0086 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(1228): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1231): Show |
3 | a0002c0002t0002g0099 a0002c0002t0003g0056 a0002c0002t0003g0144 |
4 | NA18939.hp1 NA18979.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.*118+1440_*118+144 others(1242): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1222): Show |
1 | a0004c0004t0002g0087 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(1233): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1228): Show |
1 | a0002c0002t0003g0138 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(1239): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1228): Show |
12 | a0001c0005t0002g0005 a0001c0005t0002g0009 a0001c0005t0002g0014 others(9): Show |
40 | HG00280.hp2 HG00544.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.*118+1440_*118+144 others(1239): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1231): Show |
40 | a0001c0001t0002g0007 a0001c0001t0002g0019 a0001c0001t0002g0076 others(37): Show |
116 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.*118+1440_*118+144 others(1242): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1231): Show |
1 | a0002c0002t0003g0145 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(1242): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1228): Show |
1 | a0002c0002t0003g0054 | 2 | NA19006.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.*118+1440_*118+144 others(1239): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1225): Show |
1 | a0004c0004t0002g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(1236): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1225): Show |
28 | a0001c0001t0002g0107 a0001c0005t0002g0082 a0004c0004t0002g0001 others(25): Show |
80 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.*118+1440_*118+144 others(1236): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1231): Show |
1 | a0002c0002t0003g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(1242): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1222): Show |
2 | a0006c0008t0009g0057 a0006c0008t0009g0127 |
2 | HG02486.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.*118+1440_*118+144 others(1233): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1213): Show |
1 | a0004c0004t0002g0072 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(1224): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1300): Show |
1 | a0001c0005t0002g0062 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(1311): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(2771): Show |
1 | a0001c0001t0015g0060 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*118+1440_*118+144 others(2782): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(2762): Show |
1 | a0001c0001t0010g0034 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.*118+1440_*118+144 others(2773): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(1228): Show |
1 | a0002c0010t0001g0035 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.*118+1464_*118+146 others(1239): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(701): Show |
1 | a0002c0002t0003g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*118+1437_*118+143 others(712): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | CATCACCA others(704): Show |
1 | a0002c0002t0003g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.*118+1437_*118+143 others(715): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005545 | ||||||
| chr2:231005545 | C | T | 3 | a0002c0002t0004g0022 a0002c0002t0004g0147 a0007c0011t0002g0022 |
5 | HG02615.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.*118+1427C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005545 | |||||||
| chr2:231005559 | T | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(62): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.*118+1441T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005559 | |||||||
| chr2:231005568 | T | TCATCATC others(1216): Show |
1 | a0002c0002t0008g0032 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.*118+1464_*118+146 others(1227): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005568 | ||||||
| chr2:231005580 | T | TCATCACC others(1023): Show |
1 | a0001c0001t0001g0003 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.*118+1467_*118+146 others(1034): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005580 | T | TCATCACC others(1026): Show |
1 | a0001c0001t0001g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.*118+1467_*118+146 others(1037): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005580 | T | TCATCACC others(1026): Show |
1 | a0003c0007t0001g0052 | 2 | HG03654.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.*118+1467_*118+146 others(1037): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005580 | T | TCATCACC others(1020): Show |
2 | a0003c0003t0001g0024 a0003c0003t0001g0044 |
2 | HG01081.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.*118+1467_*118+146 others(1031): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005580 | T | TCATCACC others(1026): Show |
16 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0003c0003t0001g0006 others(13): Show |
38 | HG00408.hp2 HG00673.hp1 HG01928.hp1 others(35): Show |
intron_variant | MODIFIER | c.*118+1467_*118+146 others(1037): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005580 | T | TCATCACC others(1014): Show |
1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.*118+1467_*118+146 others(1025): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005580 | T | TCATCACC others(1026): Show |
43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(40): Show |
111 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.*118+1467_*118+146 others(1037): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005580 | T | TCATCACC others(1026): Show |
1 | a0001c0001t0001g0003 | 5 | HG00099.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.*118+1467_*118+146 others(1037): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005580 | T | TCATCACC others(1080): Show |
1 | a0001c0001t0001g0004 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.*118+1467_*118+146 others(1091): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005580 | T | TCATCACC others(1012): Show |
1 | a0003c0003t0001g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*118+1467_*118+146 others(1023): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005580 | T | TCATCACC others(1023): Show |
1 | a0001c0001t0001g0115 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.*118+1467_*118+146 others(1034): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231005580 | ||||||
| chr2:231005586 | T | C | 2 | a0006c0008t0009g0057 a0006c0008t0009g0127 |
2 | HG02486.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.*118+1468T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005586 | |||||||
| chr2:231005588 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.*118+1470C>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005588 | |||||||
| chr2:231005598 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.*118+1480C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005598 | |||||||
| chr2:231005600 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.*118+1482A>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005600 | |||||||
| chr2:231005604 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.*118+1486T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005604 | |||||||
| chr2:231005904 | C | T | 1 | a0003c0003t0001g0130 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.*119-1318C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005904 | |||||||
| chr2:231005968 | A | G | 1 | a0004c0004t0002g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*119-1254A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231005968 | |||||||
| chr2:231006000 | C | CA | 52 | a0001c0001t0002g0107 a0001c0005t0002g0005 a0001c0005t0002g0009 others(49): Show |
139 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.*119-1207dupA | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231006000 | ||||||
| chr2:231006000 | CA | C | 7 | a0002c0002t0002g0152 a0002c0002t0004g0022 a0002c0002t0008g0032 others(4): Show |
11 | HG02109.hp1 HG02486.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.*119-1207delA | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231006000 | ||||||
| chr2:231006000 | CAA | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(62): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.*119-1208_*119-120 others(6): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231006000 | ||||||
| chr2:231006014 | A | AG | 3 | a0001c0001t0010g0034 a0001c0001t0015g0060 a0001c0005t0002g0083 |
4 | HG03130.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.*119-1208_*119-120 others(5): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006014 | |||||||
| chr2:231006063 | T | A | 1 | a0001c0001t0002g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.*119-1159T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006063 | |||||||
| chr2:231006201 | GA | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(143): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.*119-1003delA | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231006201 | ||||||
| chr2:231006201 | GAA | G | 6 | a0001c0005t0002g0081 a0003c0003t0001g0069 a0003c0003t0001g0109 others(3): Show |
7 | HG02976.hp2 HG03579.hp1 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.*119-1004_*119-100 others(6): Show |
SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231006201 | ||||||
| chr2:231006345 | C | CA | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(60): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.*119-868dupA | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231006345 | ||||||
| chr2:231006356 | A | G | 1 | a0002c0010t0001g0035 | 2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.*119-866A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006356 | |||||||
| chr2:231006372 | G | A | 1 | a0001c0001t0010g0034 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.*119-850G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006372 | |||||||
| chr2:231006430 | G | T | 1 | a0004c0004t0002g0092 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.*119-792G>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006430 | |||||||
| chr2:231006451 | C | T | 2 | a0006c0008t0009g0057 a0006c0008t0009g0127 |
2 | HG02486.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.*119-771C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006451 | |||||||
| chr2:231006490 | C | T | 1 | a0003c0003t0016g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*119-732C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006490 | |||||||
| chr2:231006503 | C | CA | 7 | a0002c0010t0001g0035 a0004c0004t0002g0093 a0005c0006t0002g0030 others(4): Show |
11 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.*119-707dupA | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231006503 | ||||||
| chr2:231006503 | CA | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(60): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.*119-707delA | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 231006503 | ||||||
| chr2:231006553 | T | C | 1 | a0004c0004t0002g0039 | 2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.*119-669T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006553 | |||||||
| chr2:231006627 | G | A | 1 | a0001c0001t0010g0034 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.*119-595G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006627 | |||||||
| chr2:231006640 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(64): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.*119-582C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006640 | |||||||
| chr2:231006649 | A | T | 10 | a0001c0001t0002g0007 a0001c0001t0002g0019 a0001c0001t0002g0076 others(7): Show |
19 | HG00738.hp2 HG01243.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.*119-573A>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006649 | |||||||
| chr2:231006659 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.*119-563G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006659 | |||||||
| chr2:231006708 | T | A | 1 | a0004c0004t0002g0092 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.*119-514T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006708 | |||||||
| chr2:231006709 | T | A | 1 | a0004c0004t0002g0092 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.*119-513T>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006709 | |||||||
| chr2:231006739 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.*119-483C>T | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006739 | |||||||
| chr2:231006740 | G | C | 1 | a0001c0005t0002g0033 | 2 | NA19004.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.*119-482G>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006740 | |||||||
| chr2:231006875 | T | C | 1 | a0003c0003t0002g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.*119-347T>C | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006875 | |||||||
| chr2:231006961 | G | A | 1 | a0004c0004t0002g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.*119-261G>A | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231006961 | |||||||
| chr2:231007092 | A | G | 1 | a0002c0002t0003g0017 | 5 | HG00408.hp1 NA18941.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.*119-130A>G | SPATA3 | ENSG00000173699.17 | transcript | ENST00000433428.7 | protein_coding | 4/4 | chr2 | 231007092 |