Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 116988 |
| ensemblid | ENSG00000133612.20 |
| hgncid | 16923 |
| symbol | AGAP3 |
| name | ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 |
| refseq_nuc | NM_031946.7 |
| refseq_prot | NP_114152.3 |
| ensembl_nuc | ENST00000397238.7 |
| ensembl_prot | ENSP00000380413.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 151086475 |
| end | 151144434 |
| strand | + |
| ver | v1.2 |
| region | chr7:151086475-151144434 |
| region5000 | chr7:151081475-151149434 |
| regionname0 | AGAP3_chr7_151086475_151144434 |
| regionname5000 | AGAP3_chr7_151081475_151149434 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 911 | 338 | 84 | 64 | 137 | 15 | 37 | 98 | AGAP3_chr7_151081475_151149434 | AGAP3 | MNFQA others(906): Show |
chr7 | 151081475 | 151149434 |
| a0002 | 0/0 | 128 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | MNFQA others(123): Show |
chr7 | 151081475 | 151149434 |
| a0003 | 0/0 | 911 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | MNFQA others(906): Show |
chr7 | 151081475 | 151149434 |
| a0004 | 0/0 | 911 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | MNFQA others(906): Show |
chr7 | 151081475 | 151149434 |
| a0005 | 0/0 | 265 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | MNFQA others(260): Show |
chr7 | 151081475 | 151149434 |
| a0006 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | MNFQA others(906): Show |
chr7 | 151081475 | 151149434 |
| a0007 | 0/0 | 911 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | MNFQA others(906): Show |
chr7 | 151081475 | 151149434 |
| a0008 | 0/0 | 911 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | MNFQA others(906): Show |
chr7 | 151081475 | 151149434 |
| a0009 | 0/1 | 912 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | MNFQA others(907): Show |
chr7 | 151081475 | 151149434 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2733 | 316 | 68 | 61 | 135 | 15 | 36 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0001c0003 | 0/0 | 2733 | 6 | 6 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0001c0004 | 0/0 | 2733 | 4 | 4 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0001c0005 | 0/0 | 2733 | 3 | 3 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0001c0006 | 0/0 | 2733 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0001c0007 | 0/0 | 2733 | 2 | 2 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0001c0008 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0001c0010 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0001c0012 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0001c0016 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0001c0017 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0002c0002 | 0/0 | 2734 | 8 | 8 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2729): Show |
chr7 | 151081475 | 151149434 | ||
| a0002c0020 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2729): Show |
chr7 | 151081475 | 151149434 | ||
| a0003c0014 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0004c0013 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0005c0018 | 0/0 | 2756 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2751): Show |
chr7 | 151081475 | 151149434 | ||
| a0006c0011 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0007c0009 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0008c0015 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2728): Show |
chr7 | 151081475 | 151149434 | ||
| a0009c0019 | 0/1 | 2736 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | ATGAA others(2731): Show |
chr7 | 151081475 | 151149434 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3491 | 215 | 35 | 46 | 97 | 11 | 26 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0001t0002 | 0/0 | 3488 | 66 | 19 | 13 | 22 | 2 | 10 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3483): Show |
chr7 | 151081475 | 151149434 |
| a0001c0001t0003 | 0/0 | 3491 | 12 | 12 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0001t0004 | 1/0 | 3494 | 8 | 0 | 2 | 3 | 2 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3489): Show |
chr7 | 151081475 | 151149434 |
| a0001c0001t0005 | 0/0 | 3488 | 8 | 0 | 0 | 8 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3483): Show |
chr7 | 151081475 | 151149434 |
| a0001c0001t0006 | 0/0 | 3494 | 2 | 2 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3489): Show |
chr7 | 151081475 | 151149434 |
| a0001c0001t0007 | 0/0 | 3488 | 3 | 0 | 0 | 3 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3483): Show |
chr7 | 151081475 | 151149434 |
| a0001c0001t0008 | 0/0 | 3491 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0001t0009 | 0/0 | 3491 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0003t0001 | 0/0 | 3491 | 5 | 5 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0003t0006 | 0/0 | 3494 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3489): Show |
chr7 | 151081475 | 151149434 |
| a0001c0004t0001 | 0/0 | 3491 | 4 | 4 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0005t0006 | 0/0 | 3494 | 3 | 3 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3489): Show |
chr7 | 151081475 | 151149434 |
| a0001c0006t0001 | 0/0 | 3491 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0007t0002 | 0/0 | 3488 | 2 | 2 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3483): Show |
chr7 | 151081475 | 151149434 |
| a0001c0008t0001 | 0/0 | 3491 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0010t0001 | 0/0 | 3491 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0012t0001 | 0/0 | 3491 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0016t0001 | 0/0 | 3491 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0001c0017t0001 | 0/0 | 3491 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0002c0002t0002 | 0/0 | 3489 | 8 | 8 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3484): Show |
chr7 | 151081475 | 151149434 |
| a0002c0020t0002 | 0/0 | 3489 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3484): Show |
chr7 | 151081475 | 151149434 |
| a0003c0014t0001 | 0/0 | 3491 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0004c0013t0001 | 0/0 | 3491 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0005c0018t0004 | 0/0 | 3517 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3512): Show |
chr7 | 151081475 | 151149434 |
| a0006c0011t0002 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3483): Show |
chr7 | 151081475 | 151149434 |
| a0007c0009t0001 | 0/0 | 3491 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0008c0015t0001 | 0/0 | 3491 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| a0009c0019t0002 | 0/1 | 3491 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | GTTGT others(3486): Show |
chr7 | 151081475 | 151149434 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0006g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0006g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0001t0009g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0003t0006g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0004t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0005t0006g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0005t0006g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0005t0006g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0006t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0006t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0007t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0007t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0008t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0010t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0012t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0016t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0001c0017t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0002c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0002c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0002c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0002c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0002c0002t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0002c0002t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0002c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0002c0002t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0002c0020t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0003c0014t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0004c0013t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0005c0018t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0006c0011t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0007c0009t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0008c0015t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| a0009c0019t0002g0322 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0341 | EUR | GBR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00140 | hp1 | a0003 | c0014 | t0001 | g0123 | EUR | GBR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | FIN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0295 | EUR | FIN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01081 | hp1 | a0001 | c0006 | t0001 | g0019 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01109 | hp2 | a0001 | c0006 | t0001 | g0042 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01255 | hp2 | a0001 | c0008 | t0001 | g0066 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0252 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0272 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0343 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0342 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0310 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01891 | hp1 | a0002 | c0020 | t0002 | g0318 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0340 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02056 | hp1 | a0001 | c0012 | t0001 | g0211 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02071 | hp2 | a0004 | c0013 | t0001 | g0033 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02257 | hp2 | a0001 | c0005 | t0006 | g0338 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0317 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02280 | hp2 | a0001 | c0017 | t0001 | g0107 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0336 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02572 | hp1 | a0001 | c0005 | t0006 | g0337 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0331 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02723 | hp1 | a0001 | c0007 | t0002 | g0315 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0316 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0320 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02922 | hp1 | a0001 | c0003 | t0006 | g0339 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0312 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02976 | hp2 | a0001 | c0005 | t0006 | g0335 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0311 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0329 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0309 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0131 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0319 | AFR | GWD | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0133 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03831 | hp2 | a0005 | c0018 | t0004 | g0291 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03834 | hp1 | a0001 | c0016 | t0001 | g0220 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0324 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0304 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18522 | hp1 | a0006 | c0011 | t0002 | g0333 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19011 | hp2 | a0007 | c0009 | t0001 | g0243 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0017 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0154 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19065 | hp2 | a0008 | c0015 | t0001 | g0052 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0171 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19083 | hp2 | a0001 | c0010 | t0001 | g0217 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19090 | hp1 | a0001 | c0001 | t0009 | g0203 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | YRI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | ASW | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | TSI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0270 | EUR | TSI | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | GIH | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0306 | SAS | GIH | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG06807 | hp1 | a0001 | c0007 | t0002 | g0314 | AFR | USA | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | USA | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| homoSapiens | chm13v2 | a0009 | c0019 | t0002 | g0322 | REF | REF | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0271 | REF | REF | AGAP3_chr7_151081475_151149434 | AGAP3 | chr7 | 151081475 | 151149434 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151086812 | G | GT | 1 | a0002 | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
frameshift_variant | HIGH | c.71_72insT | p.Ala25fs | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 339/3494 | 72/2736 | 24/911 | chr7 | 151086812 | |||
| chr7:151117643 | C | CTGGGCGT others(6): Show |
1 | a0005 | 1 | HG03831.hp2 | frameshift_variant | HIGH | c.572_573insTGGGCGTG others(5): Show |
p.Trp192fs | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 840/3494 | 573/2736 | 191/911 | chr7 | 151117643 | |||
| chr7:151117645 | T | TTGTTGGT others(3): Show |
1 | a0005 | 1 | HG03831.hp2 | frameshift_variant | HIGH | c.574_575insTGTTGGTT others(2): Show |
p.Trp192fs | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 842/3494 | 575/2736 | 192/911 | chr7 | 151117645 | |||
| chr7:151117652 | A | C | 1 | a0005 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.581A>C | p.Asp194Ala | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 848/3494 | 581/2736 | 194/911 | chr7 | 151117652 | |||
| chr7:151117661 | T | A | 1 | a0005 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.590T>A | p.Val197Glu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 857/3494 | 590/2736 | 197/911 | chr7 | 151117661 | |||
| chr7:151117669 | T | G | 1 | a0005 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.598T>G | p.Phe200Val | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 865/3494 | 598/2736 | 200/911 | chr7 | 151117669 | |||
| chr7:151117686 | A | C | 1 | a0005 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.615A>C | p.Glu205Asp | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 882/3494 | 615/2736 | 205/911 | chr7 | 151117686 | |||
| chr7:151118624 | A | T | 1 | a0008 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.961A>T | p.Ile321Phe | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/18 | 1228/3494 | 961/2736 | 321/911 | chr7 | 151118624 | |||
| chr7:151119999 | G | A | 1 | a0007 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.982G>A | p.Gly328Ser | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/18 | 1249/3494 | 982/2736 | 328/911 | chr7 | 151119999 | |||
| chr7:151138250 | G | A | 1 | a0006 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.1603G>A | p.Val535Ile | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/18 | 1870/3494 | 1603/2736 | 535/911 | chr7 | 151138250 | |||
| chr7:151143353 | A | T | 1 | a0003 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.2286A>T | p.Glu762Asp | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 17/18 | 2553/3494 | 2286/2736 | 762/911 | chr7 | 151143353 | |||
| chr7:151143924 | G | A | 1 | a0004 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2717G>A | p.Arg906His | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 18/18 | 2984/3494 | 2717/2736 | 906/911 | chr7 | 151143924 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151086813 | C | G | 2 | a0002c0002 a0002c0020 |
9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
synonymous_variant | LOW | c.72C>G | p.Gly24Gly | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 339/3494 | 72/2736 | 24/911 | chr7 | 151086813 | |||
| chr7:151117656 | A | T | 1 | a0005c0018 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.585A>T | p.Ala195Ala | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 852/3494 | 585/2736 | 195/911 | chr7 | 151117656 | |||
| chr7:151117717 | C | T | 1 | a0001c0007 | 2 | HG02723.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.646C>T | p.Leu216Leu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/18 | 913/3494 | 646/2736 | 216/911 | chr7 | 151117717 | |||
| chr7:151118259 | C | T | 2 | a0001c0004 a0002c0002 |
12 | HG01884.hp2 HG02280.hp1 HG02886.hp1 others(9): Show |
synonymous_variant | LOW | c.756C>T | p.Arg252Arg | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 6/18 | 1023/3494 | 756/2736 | 252/911 | chr7 | 151118259 | |||
| chr7:151118543 | C | T | 2 | a0001c0003 a0001c0017 |
7 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
synonymous_variant | LOW | c.880C>T | p.Leu294Leu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/18 | 1147/3494 | 880/2736 | 294/911 | chr7 | 151118543 | |||
| chr7:151118593 | C | T | 1 | a0001c0016 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.930C>T | p.Ala310Ala | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/18 | 1197/3494 | 930/2736 | 310/911 | chr7 | 151118593 | |||
| chr7:151118614 | G | A | 1 | a0001c0008 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.951G>A | p.Pro317Pro | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/18 | 1218/3494 | 951/2736 | 317/911 | chr7 | 151118614 | |||
| chr7:151123838 | G | A | 1 | a0001c0010 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.1173G>A | p.Glu391Glu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/18 | 1440/3494 | 1173/2736 | 391/911 | chr7 | 151123838 | |||
| chr7:151123850 | C | T | 1 | a0001c0006 | 2 | HG01081.hp1 HG01109.hp2 |
synonymous_variant | LOW | c.1185C>T | p.Asp395Asp | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/18 | 1452/3494 | 1185/2736 | 395/911 | chr7 | 151123850 | |||
| chr7:151134553 | C | T | 2 | a0001c0005 a0001c0017 |
4 | HG02257.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
synonymous_variant | LOW | c.1480C>T | p.Leu494Leu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/18 | 1747/3494 | 1480/2736 | 494/911 | chr7 | 151134553 | |||
| chr7:151141911 | G | A | 1 | a0006c0011 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1818G>A | p.Ser606Ser | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 14/18 | 2085/3494 | 1818/2736 | 606/911 | chr7 | 151141911 | |||
| chr7:151142437 | G | C | 1 | a0001c0012 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.2076G>C | p.Leu692Leu | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/18 | 2343/3494 | 2076/2736 | 692/911 | chr7 | 151142437 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151086523 | G | T | 1 | a0001c0001t0009 | 1 | NA19090.hp1 | 5_prime_UTR_variant | MODIFIER | c.-219G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 219 | chr7 | 151086523 | ||||||
| chr7:151086669 | TGCC | T | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(13): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
5_prime_UTR_variant | MODIFIER | c.-51_-49delGCC | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 49 | INFO_REALIGN_3_PRIME | chr7 | 151086669 | |||||
| chr7:151086669 | TGCCGCC | T | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(4): Show |
89 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(86): Show |
5_prime_UTR_variant | MODIFIER | c.-54_-49delGCCGCC | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | 49 | INFO_REALIGN_3_PRIME | chr7 | 151086669 | |||||
| chr7:151086675 | C | T | 3 | a0001c0001t0006 a0001c0003t0006 a0001c0005t0006 |
6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-67C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/18 | chr7 | 151086675 | |||||||
| chr7:151144095 | C | T | 1 | a0001c0001t0007 | 3 | NA18967.hp2 NA19065.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*152C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 18/18 | 152 | chr7 | 151144095 | ||||||
| chr7:151144231 | A | G | 1 | a0001c0001t0003 | 12 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*288A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 18/18 | 288 | chr7 | 151144231 | ||||||
| chr7:151144291 | G | A | 3 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 |
12 | NA18941.hp1 NA18942.hp2 NA18961.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*348G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 18/18 | 348 | chr7 | 151144291 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151087173 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0010 |
3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.331+101G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087173 | |||||||
| chr7:151087175 | T | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0010 |
3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.331+103T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087175 | |||||||
| chr7:151087176 | C | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0010 |
3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.331+104C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087176 | |||||||
| chr7:151087178 | T | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0010 |
3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.331+106T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087178 | |||||||
| chr7:151087180 | GC | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0010 |
3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.331+109delC | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087180 | |||||||
| chr7:151087320 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
177 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.331+248T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087320 | |||||||
| chr7:151087321 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.331+249T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087321 | |||||||
| chr7:151087367 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331+295G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087367 | |||||||
| chr7:151087426 | C | T | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
180 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.331+354C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087426 | |||||||
| chr7:151087428 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.331+356G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087428 | |||||||
| chr7:151087459 | G | A | 4 | a0001c0001t0001g0016 a0001c0004t0001g0014 a0001c0004t0001g0015 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+387G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087459 | |||||||
| chr7:151087474 | C | T | 1 | a0001c0001t0004g0341 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.331+402C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087474 | |||||||
| chr7:151087593 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.331+521G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087593 | |||||||
| chr7:151087594 | G | T | 1 | a0001c0001t0002g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.331+522G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087594 | |||||||
| chr7:151087650 | C | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(87): Show |
92 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.331+578C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087650 | |||||||
| chr7:151087737 | G | T | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.331+665G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087737 | |||||||
| chr7:151087748 | CGCACCCG others(7): Show |
C | 9 | a0001c0001t0002g0332 a0001c0001t0002g0334 a0001c0001t0006g0336 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.331+678_331+691del others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151087748 | ||||||
| chr7:151087774 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.331+702C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087774 | |||||||
| chr7:151087843 | G | T | 1 | a0001c0001t0002g0331 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.331+771G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087843 | |||||||
| chr7:151087925 | G | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.331+853G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087925 | |||||||
| chr7:151087967 | C | G | 1 | a0001c0001t0001g0330 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.331+895C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151087967 | |||||||
| chr7:151088061 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.331+989G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088061 | |||||||
| chr7:151088234 | C | T | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.331+1162C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088234 | |||||||
| chr7:151088393 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0106 a0001c0004t0001g0014 others(3): Show |
6 | HG02280.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+1321G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088393 | |||||||
| chr7:151088530 | C | G | 1 | a0001c0017t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.331+1458C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088530 | |||||||
| chr7:151088666 | C | T | 50 | a0001c0001t0002g0177 a0001c0001t0002g0292 a0001c0001t0002g0293 others(47): Show |
50 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.331+1594C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088666 | |||||||
| chr7:151088697 | G | A | 1 | a0001c0001t0002g0108 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.331+1625G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088697 | |||||||
| chr7:151088825 | T | A | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.331+1753T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088825 | |||||||
| chr7:151088964 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.331+1892C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088964 | |||||||
| chr7:151088974 | C | T | 126 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(123): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.331+1902C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088974 | |||||||
| chr7:151088996 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.331+1924G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151088996 | |||||||
| chr7:151089064 | G | C | 2 | a0001c0004t0001g0014 a0001c0004t0001g0015 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331+1992G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089064 | |||||||
| chr7:151089163 | A | G | 6 | a0001c0001t0006g0336 a0001c0001t0006g0340 a0001c0003t0006g0339 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+2091A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089163 | |||||||
| chr7:151089164 | G | GA | 10 | a0001c0001t0001g0005 a0001c0001t0001g0115 a0001c0001t0001g0116 others(7): Show |
11 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.331+2102dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151089164 | ||||||
| chr7:151089296 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.331+2224A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089296 | |||||||
| chr7:151089315 | G | T | 1 | a0001c0001t0002g0329 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.331+2243G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089315 | |||||||
| chr7:151089341 | C | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01496.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.331+2269C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089341 | |||||||
| chr7:151089474 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.331+2402G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089474 | |||||||
| chr7:151089549 | G | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+2477G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089549 | |||||||
| chr7:151089802 | CA | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(97): Show |
102 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.331+2731delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089802 | |||||||
| chr7:151089959 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(97): Show |
102 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.331+2887G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151089959 | |||||||
| chr7:151090154 | C | T | 1 | a0001c0001t0002g0328 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.331+3082C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090154 | |||||||
| chr7:151090236 | T | TG | 18 | a0001c0001t0001g0178 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
18 | HG00597.hp2 HG01099.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.331+3176dupG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151090236 | ||||||
| chr7:151090236 | TG | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.331+3176delG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151090236 | ||||||
| chr7:151090239 | G | C | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01167.hp1 HG01169.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.331+3167G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090239 | |||||||
| chr7:151090240 | G | C | 1 | a0001c0001t0003g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.331+3168G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090240 | |||||||
| chr7:151090240 | G | T | 1 | a0001c0004t0001g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.331+3168G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090240 | |||||||
| chr7:151090310 | A | G | 14 | a0001c0001t0002g0177 a0001c0001t0002g0313 a0001c0001t0002g0321 others(11): Show |
14 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.331+3238A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090310 | |||||||
| chr7:151090363 | T | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
180 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.331+3291T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090363 | |||||||
| chr7:151090380 | CT | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
115 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.331+3333delT | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151090380 | ||||||
| chr7:151090380 | CTT | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.331+3332_331+3333d others(4): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151090380 | ||||||
| chr7:151090380 | CTTT | C | 94 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(91): Show |
98 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.331+3331_331+3333d others(5): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151090380 | ||||||
| chr7:151090402 | T | A | 3 | a0002c0002t0002g0309 a0002c0002t0002g0310 a0002c0002t0002g0311 |
3 | HG01884.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.331+3330T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090402 | |||||||
| chr7:151090405 | T | A | 1 | a0001c0001t0001g0004 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.331+3333T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090405 | |||||||
| chr7:151090418 | C | T | 6 | a0001c0001t0006g0336 a0001c0001t0006g0340 a0001c0003t0006g0339 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+3346C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090418 | |||||||
| chr7:151090503 | G | C | 1 | a0001c0001t0005g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.331+3431G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090503 | |||||||
| chr7:151090652 | C | T | 4 | a0001c0001t0002g0321 a0001c0004t0001g0014 a0001c0004t0001g0015 others(1): Show |
4 | HG01081.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+3580C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090652 | |||||||
| chr7:151090714 | C | T | 3 | a0001c0001t0002g0332 a0001c0001t0002g0334 a0006c0011t0002g0333 |
3 | HG03209.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.331+3642C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090714 | |||||||
| chr7:151090718 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.331+3646C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090718 | |||||||
| chr7:151090743 | A | G | 304 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(301): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.331+3671A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090743 | |||||||
| chr7:151090801 | G | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.331+3729G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090801 | |||||||
| chr7:151090804 | C | T | 6 | a0001c0001t0006g0336 a0001c0001t0006g0340 a0001c0003t0006g0339 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+3732C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090804 | |||||||
| chr7:151090812 | C | A | 1 | a0001c0001t0002g0324 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.331+3740C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090812 | |||||||
| chr7:151090878 | A | G | 2 | a0001c0001t0004g0023 a0001c0001t0004g0089 |
2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.331+3806A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151090878 | |||||||
| chr7:151091114 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.331+4042C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091114 | |||||||
| chr7:151091173 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.331+4101G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091173 | |||||||
| chr7:151091217 | T | C | 311 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.331+4145T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091217 | |||||||
| chr7:151091335 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0269 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.331+4263C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091335 | |||||||
| chr7:151091348 | G | A | 3 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0323 |
3 | HG01109.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.331+4276G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091348 | |||||||
| chr7:151091506 | C | A | 6 | a0001c0001t0006g0336 a0001c0001t0006g0340 a0001c0003t0006g0339 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+4434C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091506 | |||||||
| chr7:151091590 | A | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(96): Show |
101 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.331+4518A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091590 | |||||||
| chr7:151091697 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331+4625C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091697 | |||||||
| chr7:151091812 | T | C | 3 | a0001c0005t0006g0335 a0001c0005t0006g0337 a0001c0005t0006g0338 |
3 | HG02257.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.331+4740T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151091812 | |||||||
| chr7:151092021 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.331+4949G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092021 | |||||||
| chr7:151092469 | G | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.331+5397G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092469 | |||||||
| chr7:151092505 | G | T | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.331+5433G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092505 | |||||||
| chr7:151092516 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.331+5444C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092516 | |||||||
| chr7:151092564 | C | T | 4 | a0001c0001t0002g0308 a0001c0001t0006g0336 a0001c0001t0006g0340 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+5492C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092564 | |||||||
| chr7:151092565 | G | A | 1 | a0001c0003t0001g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.331+5493G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092565 | |||||||
| chr7:151092674 | C | G | 41 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(38): Show |
44 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.331+5602C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092674 | |||||||
| chr7:151092704 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331+5632C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092704 | |||||||
| chr7:151092704 | C | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0115 others(69): Show |
76 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.331+5632C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092704 | |||||||
| chr7:151092912 | A | G | 2 | a0001c0001t0002g0299 a0001c0001t0002g0323 |
2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.331+5840A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092912 | |||||||
| chr7:151092951 | G | T | 1 | a0001c0001t0001g0016 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331+5879G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151092951 | |||||||
| chr7:151093001 | G | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG00735.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.331+5929G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093001 | |||||||
| chr7:151093032 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.331+5960C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093032 | |||||||
| chr7:151093107 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.331+6035T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093107 | |||||||
| chr7:151093265 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0290 |
3 | NA18975.hp1 NA18980.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.331+6193C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093265 | |||||||
| chr7:151093563 | G | T | 1 | a0001c0001t0001g0266 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.331+6491G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093563 | |||||||
| chr7:151093620 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.331+6548G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093620 | |||||||
| chr7:151093622 | C | CTCTTTGC others(5): Show |
1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+6552_331+6563d others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151093622 | ||||||
| chr7:151093654 | G | A | 6 | a0001c0001t0006g0336 a0001c0001t0006g0340 a0001c0003t0006g0339 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+6582G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093654 | |||||||
| chr7:151093843 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331+6771G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093843 | |||||||
| chr7:151093932 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0174 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.331+6860C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093932 | |||||||
| chr7:151093949 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.331+6877A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151093949 | |||||||
| chr7:151094165 | C | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.331+7093C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151094165 | |||||||
| chr7:151094228 | T | TGAAA | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
176 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.331+7158_331+7161d others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151094228 | ||||||
| chr7:151094346 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0135 a0001c0003t0001g0133 others(2): Show |
5 | HG01952.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+7274C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151094346 | |||||||
| chr7:151094479 | GA | G | 6 | a0001c0001t0001g0176 a0001c0001t0002g0303 a0001c0001t0002g0332 others(3): Show |
6 | HG01515.hp1 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+7421delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151094479 | ||||||
| chr7:151094543 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331+7471G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151094543 | |||||||
| chr7:151094592 | T | C | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.331+7520T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151094592 | |||||||
| chr7:151094873 | C | CCCTT | 3 | a0001c0001t0002g0332 a0001c0001t0002g0334 a0006c0011t0002g0333 |
3 | HG03209.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.331+7821_331+7824d others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151094873 | ||||||
| chr7:151094942 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.331+7870G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151094942 | |||||||
| chr7:151095184 | G | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.331+8112G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095184 | |||||||
| chr7:151095212 | T | C | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331+8140T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095212 | |||||||
| chr7:151095345 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.331+8273G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095345 | |||||||
| chr7:151095450 | C | T | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.331+8378C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095450 | |||||||
| chr7:151095537 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0106 a0001c0017t0001g0107 |
3 | HG02280.hp2 HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.331+8465G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095537 | |||||||
| chr7:151095701 | CA | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(52): Show |
56 | HG00544.hp1 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.331+8655delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151095701 | ||||||
| chr7:151095701 | CAA | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.331+8654_331+8655d others(4): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151095701 | ||||||
| chr7:151095701 | CAAA | C | 53 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0096 others(50): Show |
56 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.331+8653_331+8655d others(5): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151095701 | ||||||
| chr7:151095702 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331+8630A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095702 | |||||||
| chr7:151095962 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0173 others(1): Show |
4 | HG03098.hp1 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+8890A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151095962 | |||||||
| chr7:151096005 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0003g0280 |
3 | HG02896.hp2 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.331+8933G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096005 | |||||||
| chr7:151096254 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0180 a0001c0001t0001g0265 others(1): Show |
4 | HG00735.hp1 HG02015.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+9182C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096254 | |||||||
| chr7:151096338 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.331+9266G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096338 | |||||||
| chr7:151096369 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.331+9297G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096369 | |||||||
| chr7:151096383 | TC | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(94): Show |
99 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.331+9312delC | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096383 | |||||||
| chr7:151096445 | C | T | 1 | a0001c0003t0001g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.331+9373C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096445 | |||||||
| chr7:151096504 | G | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+9432G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096504 | |||||||
| chr7:151096523 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.331+9451A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096523 | |||||||
| chr7:151096541 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.331+9469C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096541 | |||||||
| chr7:151096597 | C | T | 9 | a0001c0001t0002g0011 a0001c0001t0002g0157 a0001c0001t0002g0158 others(6): Show |
9 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.331+9525C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096597 | |||||||
| chr7:151096629 | C | T | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.331+9557C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096629 | |||||||
| chr7:151096633 | C | T | 1 | a0001c0004t0001g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.331+9561C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096633 | |||||||
| chr7:151096686 | G | A | 1 | a0001c0001t0002g0329 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.331+9614G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096686 | |||||||
| chr7:151096717 | C | G | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+9645C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096717 | |||||||
| chr7:151096719 | G | C | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+9647G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096719 | |||||||
| chr7:151096811 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.331+9739C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096811 | |||||||
| chr7:151096839 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.331+9767T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096839 | |||||||
| chr7:151096872 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(94): Show |
99 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.331+9800G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096872 | |||||||
| chr7:151096957 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0009g0203 |
2 | NA18944.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.331+9885G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096957 | |||||||
| chr7:151096982 | A | T | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+9910A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096982 | |||||||
| chr7:151096983 | C | A | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+9911C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151096983 | |||||||
| chr7:151097058 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.331+9986G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097058 | |||||||
| chr7:151097294 | G | C | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10222G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097294 | |||||||
| chr7:151097295 | C | G | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10223C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097295 | |||||||
| chr7:151097297 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.331+10225G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097297 | |||||||
| chr7:151097391 | C | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.331+10319C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097391 | |||||||
| chr7:151097424 | C | G | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01167.hp1 HG01169.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.331+10352C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097424 | |||||||
| chr7:151097424 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.331+10352C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097424 | |||||||
| chr7:151097517 | C | CA | 6 | a0001c0001t0001g0281 a0001c0001t0002g0296 a0001c0001t0002g0297 others(3): Show |
6 | HG01081.hp2 HG01109.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+10463dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151097517 | ||||||
| chr7:151097517 | CA | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.331+10463delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151097517 | ||||||
| chr7:151097614 | G | T | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10542G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097614 | |||||||
| chr7:151097639 | G | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.331+10567G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097639 | |||||||
| chr7:151097773 | C | A | 1 | a0001c0001t0001g0024 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.331+10701C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097773 | |||||||
| chr7:151097887 | T | C | 1 | a0001c0001t0002g0303 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.331+10815T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097887 | |||||||
| chr7:151097967 | G | T | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10895G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151097967 | |||||||
| chr7:151098002 | C | G | 1 | a0001c0001t0002g0011 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331+10930C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098002 | |||||||
| chr7:151098044 | G | C | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10972G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098044 | |||||||
| chr7:151098045 | C | G | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+10973C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098045 | |||||||
| chr7:151098084 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.331+11012C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098084 | |||||||
| chr7:151098455 | A | C | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+11383A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098455 | |||||||
| chr7:151098456 | C | A | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.331+11384C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098456 | |||||||
| chr7:151098498 | A | T | 1 | a0001c0001t0002g0329 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.331+11426A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098498 | |||||||
| chr7:151098522 | G | A | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(288): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.331+11450G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098522 | |||||||
| chr7:151098529 | T | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.331+11457T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098529 | |||||||
| chr7:151098630 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.331+11558G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098630 | |||||||
| chr7:151098733 | C | CT | 75 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0026 others(72): Show |
79 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.331+11680dupT | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151098733 | ||||||
| chr7:151098733 | CT | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.331+11680delT | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151098733 | ||||||
| chr7:151098733 | CTT | C | 7 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0194 others(4): Show |
7 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.331+11679_331+1168 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151098733 | ||||||
| chr7:151098738 | T | C | 2 | a0001c0001t0002g0300 a0001c0001t0002g0304 |
2 | HG02735.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.331+11666T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098738 | |||||||
| chr7:151098854 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0289 |
3 | HG03017.hp1 HG03688.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.331+11782C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098854 | |||||||
| chr7:151098894 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0135 a0001c0003t0001g0133 others(2): Show |
5 | HG01952.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+11822C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098894 | |||||||
| chr7:151098982 | C | T | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(288): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.331+11910C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098982 | |||||||
| chr7:151098983 | A | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.331+11911A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151098983 | |||||||
| chr7:151099021 | C | A | 1 | a0001c0001t0002g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.331+11949C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099021 | |||||||
| chr7:151099113 | G | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
183 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.331+12041G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099113 | |||||||
| chr7:151099160 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331+12088A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099160 | |||||||
| chr7:151099334 | C | A | 14 | a0001c0001t0002g0177 a0001c0001t0002g0313 a0001c0003t0001g0167 others(11): Show |
14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.331+12262C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099334 | |||||||
| chr7:151099339 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(94): Show |
99 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.331+12267T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099339 | |||||||
| chr7:151099342 | C | CA | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(91): Show |
96 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.331+12287dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151099342 | ||||||
| chr7:151099342 | CA | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(185): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.331+12287delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151099342 | ||||||
| chr7:151099365 | A | C | 3 | a0001c0001t0002g0332 a0001c0001t0002g0334 a0006c0011t0002g0333 |
3 | HG03209.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.331+12293A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099365 | |||||||
| chr7:151099432 | TG | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.331+12361delG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099432 | |||||||
| chr7:151099581 | T | G | 1 | a0001c0001t0003g0208 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.331+12509T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099581 | |||||||
| chr7:151099674 | C | T | 13 | a0001c0001t0002g0177 a0001c0001t0002g0313 a0001c0007t0002g0314 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.331+12602C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099674 | |||||||
| chr7:151099692 | A | T | 3 | a0001c0005t0006g0335 a0001c0005t0006g0337 a0001c0005t0006g0338 |
3 | HG02257.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.331+12620A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099692 | |||||||
| chr7:151099724 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.331+12652G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099724 | |||||||
| chr7:151099819 | T | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(73): Show |
80 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.331+12747T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099819 | |||||||
| chr7:151099840 | T | A | 76 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(73): Show |
80 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.331+12768T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099840 | |||||||
| chr7:151099859 | T | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.331+12787T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099859 | |||||||
| chr7:151099967 | C | A | 3 | a0001c0001t0006g0336 a0001c0001t0006g0340 a0001c0003t0006g0339 |
3 | HG01891.hp2 HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.331+12895C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151099967 | |||||||
| chr7:151100002 | T | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.331+12930T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100002 | |||||||
| chr7:151100052 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.331+12980C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100052 | |||||||
| chr7:151100147 | G | A | 30 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0108 others(27): Show |
33 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.331+13075G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100147 | |||||||
| chr7:151100165 | T | C | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.331+13093T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100165 | |||||||
| chr7:151100209 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.331+13137C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100209 | |||||||
| chr7:151100319 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.331+13247C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100319 | |||||||
| chr7:151100332 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0180 a0001c0001t0001g0196 others(5): Show |
9 | HG00438.hp2 HG02015.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.331+13260G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100332 | |||||||
| chr7:151100478 | T | C | 1 | a0001c0001t0002g0139 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.331+13406T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100478 | |||||||
| chr7:151100494 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.331+13422G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100494 | |||||||
| chr7:151100494 | G | T | 4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+13422G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100494 | |||||||
| chr7:151100611 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331+13539C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100611 | |||||||
| chr7:151100899 | C | T | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.331+13827C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151100899 | |||||||
| chr7:151101040 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.331+13968C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101040 | |||||||
| chr7:151101063 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.331+13991G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101063 | |||||||
| chr7:151101564 | C | T | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.331+14492C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101564 | |||||||
| chr7:151101639 | T | C | 294 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(291): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.331+14567T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101639 | |||||||
| chr7:151101893 | G | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
176 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.331+14821G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101893 | |||||||
| chr7:151101962 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.332-14831G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101962 | |||||||
| chr7:151101986 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.332-14807G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151101986 | |||||||
| chr7:151102072 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.332-14721C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102072 | |||||||
| chr7:151102104 | C | T | 3 | a0001c0001t0006g0336 a0001c0001t0006g0340 a0001c0003t0006g0339 |
3 | HG01891.hp2 HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.332-14689C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102104 | |||||||
| chr7:151102212 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.332-14581C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102212 | |||||||
| chr7:151102230 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0174 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.332-14563C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102230 | |||||||
| chr7:151102291 | G | A | 1 | a0001c0001t0002g0303 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.332-14502G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102291 | |||||||
| chr7:151102292 | T | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.332-14501T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102292 | |||||||
| chr7:151102345 | C | T | 3 | a0001c0001t0002g0332 a0001c0001t0002g0334 a0006c0011t0002g0333 |
3 | HG03209.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.332-14448C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102345 | |||||||
| chr7:151102385 | A | G | 1 | a0001c0001t0002g0303 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.332-14408A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102385 | |||||||
| chr7:151102598 | C | CA | 120 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.332-14178dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151102598 | ||||||
| chr7:151102598 | C | CAA | 8 | a0001c0001t0001g0210 a0001c0001t0001g0266 a0001c0001t0001g0267 others(5): Show |
8 | HG01192.hp1 HG02056.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-14179_332-1417 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151102598 | ||||||
| chr7:151102598 | CA | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(67): Show |
74 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.332-14178delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151102598 | ||||||
| chr7:151102609 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.332-14184A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102609 | |||||||
| chr7:151102616 | T | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0225 |
2 | NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.332-14177T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102616 | |||||||
| chr7:151102663 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.332-14130C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102663 | |||||||
| chr7:151102774 | C | G | 1 | a0001c0001t0002g0329 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.332-14019C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102774 | |||||||
| chr7:151102781 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.332-14012A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102781 | |||||||
| chr7:151102831 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.332-13962G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102831 | |||||||
| chr7:151102887 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0081 |
2 | HG01257.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.332-13906C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102887 | |||||||
| chr7:151102969 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG02717.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.332-13824C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151102969 | |||||||
| chr7:151103148 | C | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0119 |
2 | HG00639.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.332-13645C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103148 | |||||||
| chr7:151103154 | T | G | 1 | a0001c0001t0005g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-13639T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103154 | |||||||
| chr7:151103173 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332-13620T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103173 | |||||||
| chr7:151103317 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.332-13476A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103317 | |||||||
| chr7:151103398 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.332-13395G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103398 | |||||||
| chr7:151103422 | A | C | 1 | a0001c0001t0005g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-13371A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103422 | |||||||
| chr7:151103449 | A | C | 1 | a0001c0001t0005g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-13344A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103449 | |||||||
| chr7:151103450 | C | A | 1 | a0001c0001t0005g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-13343C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103450 | |||||||
| chr7:151103491 | G | A | 1 | a0001c0017t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.332-13302G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103491 | |||||||
| chr7:151103514 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0212 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-13279G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103514 | |||||||
| chr7:151103534 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0174 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.332-13259A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103534 | |||||||
| chr7:151103652 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.332-13141A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103652 | |||||||
| chr7:151103736 | G | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.332-13057G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103736 | |||||||
| chr7:151103867 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.332-12926C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151103867 | |||||||
| chr7:151104001 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.332-12792G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104001 | |||||||
| chr7:151104002 | T | TG | 5 | a0001c0001t0001g0041 a0001c0001t0001g0078 a0001c0001t0002g0108 others(2): Show |
5 | HG00642.hp1 HG02056.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-12789dupG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151104002 | ||||||
| chr7:151104005 | C | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.332-12788C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104005 | |||||||
| chr7:151104009 | G | A | 2 | a0001c0001t0001g0106 a0001c0017t0001g0107 |
2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.332-12784G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104009 | |||||||
| chr7:151104079 | G | T | 1 | a0001c0001t0002g0329 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.332-12714G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104079 | |||||||
| chr7:151104151 | A | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(70): Show |
77 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.332-12642A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104151 | |||||||
| chr7:151104242 | G | C | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.332-12551G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104242 | |||||||
| chr7:151104253 | T | C | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.332-12540T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104253 | |||||||
| chr7:151104256 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0106 a0001c0017t0001g0107 |
3 | HG02280.hp2 HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.332-12537C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104256 | |||||||
| chr7:151104333 | C | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.332-12460C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104333 | |||||||
| chr7:151104406 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.332-12387G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104406 | |||||||
| chr7:151104430 | G | T | 1 | a0001c0001t0001g0260 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.332-12363G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104430 | |||||||
| chr7:151104478 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.332-12315A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104478 | |||||||
| chr7:151104562 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | NA18951.hp1 NA18986.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.332-12231G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104562 | |||||||
| chr7:151104563 | C | A | 2 | a0001c0001t0001g0106 a0001c0017t0001g0107 |
2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.332-12230C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104563 | |||||||
| chr7:151104584 | G | C | 14 | a0001c0001t0002g0177 a0001c0001t0002g0313 a0001c0003t0001g0027 others(11): Show |
14 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.332-12209G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104584 | |||||||
| chr7:151104585 | C | T | 11 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0001g0129 others(8): Show |
11 | HG01952.hp2 HG02027.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.332-12208C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104585 | |||||||
| chr7:151104720 | A | T | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.332-12073A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104720 | |||||||
| chr7:151104764 | G | A | 1 | a0001c0001t0005g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-12029G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104764 | |||||||
| chr7:151104765 | A | G | 1 | a0001c0001t0005g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-12028A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104765 | |||||||
| chr7:151104862 | AAGAACGG others(2): Show |
A | 3 | a0001c0004t0001g0014 a0001c0004t0001g0015 a0001c0004t0001g0017 |
3 | HG02970.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.332-11925_332-1191 others(13): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151104862 | ||||||
| chr7:151104970 | C | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.332-11823C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104970 | |||||||
| chr7:151104981 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.332-11812G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104981 | |||||||
| chr7:151104982 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.332-11811A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151104982 | |||||||
| chr7:151105314 | T | A | 1 | a0001c0001t0002g0303 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.332-11479T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105314 | |||||||
| chr7:151105365 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0173 |
3 | HG03098.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.332-11428C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105365 | |||||||
| chr7:151105421 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0119 a0003c0014t0001g0123 |
3 | HG00140.hp1 HG00639.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.332-11372A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105421 | |||||||
| chr7:151105592 | C | CA | 6 | a0001c0001t0001g0078 a0001c0001t0001g0097 a0001c0001t0001g0266 others(3): Show |
6 | HG00642.hp1 HG02738.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-11187dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105592 | ||||||
| chr7:151105606 | A | G | 1 | a0001c0001t0005g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.332-11187A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105606 | |||||||
| chr7:151105607 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0005g0140 |
2 | NA18961.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.332-11186G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105607 | |||||||
| chr7:151105736 | C | T | 23 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0108 others(20): Show |
26 | HG00408.hp1 HG00597.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.332-11057C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105736 | |||||||
| chr7:151105776 | G | GC | 64 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0070 others(61): Show |
68 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.332-11006dupC | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | ||||||
| chr7:151105776 | G | GCC | 16 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0120 others(13): Show |
16 | HG00408.hp1 HG00558.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.332-11007_332-1100 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | ||||||
| chr7:151105776 | G | GCCCCC | 15 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0029 others(12): Show |
15 | HG00741.hp2 HG01952.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-11010_332-1100 others(9): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | ||||||
| chr7:151105776 | G | GCCCCCC | 24 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 others(21): Show |
24 | HG00673.hp2 HG00733.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.332-11011_332-1100 others(10): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | ||||||
| chr7:151105776 | G | GCCCCCCC | 22 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0036 others(19): Show |
23 | HG00544.hp1 HG00609.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.332-11012_332-1100 others(11): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | ||||||
| chr7:151105776 | G | GCCCCCCC others(1): Show |
14 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0030 others(11): Show |
15 | HG00099.hp2 HG00438.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-11013_332-1100 others(12): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | ||||||
| chr7:151105776 | G | GCCCCCCC others(3): Show |
1 | a0001c0001t0001g0092 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.332-11015_332-1100 others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | ||||||
| chr7:151105776 | G | GCCCCCCC others(4): Show |
1 | a0001c0001t0001g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.332-11016_332-1100 others(15): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105776 | ||||||
| chr7:151105787 | CGA | C | 4 | a0001c0001t0007g0154 a0001c0007t0002g0314 a0002c0002t0002g0317 others(1): Show |
4 | HG02280.hp1 HG03540.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-11005_332-1100 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105787 | |||||||
| chr7:151105788 | G | C | 13 | a0001c0001t0001g0028 a0001c0001t0001g0075 a0001c0001t0001g0096 others(10): Show |
13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-11005G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105788 | |||||||
| chr7:151105789 | A | C | 15 | a0001c0001t0001g0028 a0001c0001t0001g0075 a0001c0001t0001g0076 others(12): Show |
15 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-11004A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105789 | |||||||
| chr7:151105791 | A | C | 17 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0075 others(14): Show |
17 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.332-11002A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105791 | |||||||
| chr7:151105791 | A | G | 3 | a0001c0001t0002g0153 a0001c0001t0005g0168 a0001c0001t0007g0154 |
3 | HG02523.hp2 NA18986.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.332-11002A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105791 | |||||||
| chr7:151105792 | C | A | 3 | a0001c0001t0002g0153 a0001c0001t0005g0168 a0001c0001t0007g0154 |
3 | HG02523.hp2 NA18986.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.332-11001C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105792 | |||||||
| chr7:151105792 | C | CCA | 23 | a0001c0001t0001g0036 a0001c0001t0001g0054 a0001c0001t0001g0069 others(20): Show |
23 | HG00642.hp2 HG00735.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.332-10962_332-1096 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACA | 95 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(92): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-10964_332-1096 others(8): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACAACA others(8): Show |
1 | a0001c0001t0001g0266 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.332-10997_332-1099 others(19): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(38): Show |
44 | HG00140.hp2 HG00673.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.332-10966_332-1096 others(10): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(1): Show |
30 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0030 others(27): Show |
31 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.332-10968_332-1096 others(12): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(3): Show |
20 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0071 others(17): Show |
20 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.332-10970_332-1096 others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(5): Show |
12 | a0001c0001t0001g0077 a0001c0001t0001g0182 a0001c0001t0001g0186 others(9): Show |
12 | HG00423.hp1 HG02056.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.332-10972_332-1096 others(16): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(7): Show |
4 | a0001c0001t0001g0185 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | NA18970.hp2 NA19056.hp1 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-10974_332-1096 others(18): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(9): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0106 a0001c0005t0006g0337 |
4 | HG01257.hp1 HG01258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-10976_332-1096 others(20): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(11): Show |
1 | a0001c0001t0001g0117 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.332-10978_332-1096 others(22): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(13): Show |
5 | a0001c0001t0001g0118 a0001c0001t0001g0180 a0001c0001t0001g0214 others(2): Show |
5 | HG02015.hp1 HG02129.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-10980_332-1096 others(24): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(15): Show |
4 | a0001c0001t0001g0082 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG00140.hp1 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-10982_332-1096 others(26): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(17): Show |
2 | a0001c0001t0001g0119 a0001c0004t0001g0131 |
2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.332-10984_332-1096 others(28): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(19): Show |
1 | a0001c0001t0001g0121 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.332-10986_332-1096 others(30): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(21): Show |
1 | a0001c0001t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.332-10988_332-1096 others(32): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | C | CCACACAC others(23): Show |
4 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0128 others(1): Show |
4 | HG02109.hp2 HG02257.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-10990_332-1096 others(34): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | CCA | C | 15 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0001g0209 others(12): Show |
15 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-10962_332-1096 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105792 | CCACA | C | 25 | a0001c0001t0001g0070 a0001c0001t0001g0126 a0001c0001t0001g0174 others(22): Show |
28 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.332-10964_332-1096 others(8): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105792 | ||||||
| chr7:151105793 | C | G | 10 | a0001c0007t0002g0314 a0001c0007t0002g0315 a0002c0002t0002g0309 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-11000C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105793 | |||||||
| chr7:151105794 | A | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0076 |
2 | HG04115.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.332-10999A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105794 | |||||||
| chr7:151105796 | A | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0076 |
2 | HG04115.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.332-10997A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105796 | |||||||
| chr7:151105797 | C | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0076 |
2 | HG04115.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.332-10996C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105797 | |||||||
| chr7:151105797 | CA | C | 12 | a0001c0001t0001g0028 a0001c0001t0002g0177 a0001c0007t0002g0314 others(9): Show |
12 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.332-10995delA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105797 | |||||||
| chr7:151105869 | C | CT | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(147): Show |
155 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.332-10910dupT | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105869 | ||||||
| chr7:151105869 | C | CTT | 110 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
114 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.332-10911_332-1091 others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105869 | ||||||
| chr7:151105869 | CT | C | 6 | a0001c0001t0001g0020 a0001c0001t0002g0303 a0001c0003t0006g0339 others(3): Show |
6 | HG01515.hp1 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-10910delT | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151105869 | ||||||
| chr7:151105884 | A | T | 6 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0001g0267 others(3): Show |
6 | NA18975.hp1 NA18980.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-10909A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151105884 | |||||||
| chr7:151106009 | A | T | 1 | a0001c0001t0001g0262 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.332-10784A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106009 | |||||||
| chr7:151106138 | T | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0225 |
2 | NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.332-10655T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106138 | |||||||
| chr7:151106275 | TCTTTC | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0077 others(12): Show |
16 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-10513_332-1050 others(9): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151106275 | ||||||
| chr7:151106462 | A | G | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
294 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.332-10331A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106462 | |||||||
| chr7:151106678 | C | T | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.332-10115C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106678 | |||||||
| chr7:151106719 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0214 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.332-10074C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106719 | |||||||
| chr7:151106720 | G | A | 2 | a0001c0007t0002g0314 a0001c0007t0002g0315 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.332-10073G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106720 | |||||||
| chr7:151106784 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.332-10009C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106784 | |||||||
| chr7:151106785 | G | A | 2 | a0001c0004t0001g0014 a0001c0004t0001g0015 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-10008G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106785 | |||||||
| chr7:151106813 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.332-9980C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151106813 | |||||||
| chr7:151107183 | A | G | 33 | a0001c0001t0001g0126 a0001c0001t0002g0001 a0001c0001t0002g0006 others(30): Show |
36 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.332-9610A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107183 | |||||||
| chr7:151107235 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.332-9558G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107235 | |||||||
| chr7:151107310 | C | CA | 23 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0056 others(20): Show |
24 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.332-9466dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151107310 | ||||||
| chr7:151107317 | A | AG | 47 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(44): Show |
50 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.332-9476_332-9475i others(3): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107317 | |||||||
| chr7:151107317 | A | G | 1 | a0001c0001t0002g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.332-9476A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107317 | |||||||
| chr7:151107352 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332-9441G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107352 | |||||||
| chr7:151107486 | C | T | 7 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0160 others(4): Show |
7 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-9307C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107486 | |||||||
| chr7:151107512 | T | C | 3 | a0001c0005t0006g0335 a0001c0005t0006g0337 a0001c0005t0006g0338 |
3 | HG02257.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.332-9281T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107512 | |||||||
| chr7:151107580 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.332-9213C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107580 | |||||||
| chr7:151107581 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.332-9212G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107581 | |||||||
| chr7:151107628 | A | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(48): Show |
55 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.332-9165A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107628 | |||||||
| chr7:151107686 | T | C | 1 | a0001c0001t0009g0203 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.332-9107T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107686 | |||||||
| chr7:151107811 | C | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0121 |
3 | HG01257.hp1 HG01258.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.332-8982C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107811 | |||||||
| chr7:151107995 | C | T | 33 | a0001c0001t0001g0126 a0001c0001t0002g0001 a0001c0001t0002g0006 others(30): Show |
36 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.332-8798C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151107995 | |||||||
| chr7:151108050 | A | G | 47 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(44): Show |
50 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.332-8743A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108050 | |||||||
| chr7:151108111 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0003g0280 a0001c0017t0001g0107 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.332-8682C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108111 | |||||||
| chr7:151108172 | T | C | 1 | a0001c0001t0002g0308 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.332-8621T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108172 | |||||||
| chr7:151108185 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
291 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.332-8608A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108185 | |||||||
| chr7:151108315 | C | T | 7 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0160 others(4): Show |
7 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-8478C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108315 | |||||||
| chr7:151108392 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.332-8401C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108392 | |||||||
| chr7:151108424 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.332-8369C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108424 | |||||||
| chr7:151108455 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.332-8338C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108455 | |||||||
| chr7:151108545 | T | A | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.332-8248T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151108545 | |||||||
| chr7:151109037 | T | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0077 others(12): Show |
16 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-7756T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109037 | |||||||
| chr7:151109055 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.332-7738C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109055 | |||||||
| chr7:151109069 | T | C | 1 | a0001c0001t0003g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.332-7724T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109069 | |||||||
| chr7:151109165 | T | TA | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.332-7613dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151109165 | ||||||
| chr7:151109165 | T | TAA | 21 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0029 others(18): Show |
22 | HG00544.hp1 HG00741.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.332-7614_332-7613d others(4): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151109165 | ||||||
| chr7:151109168 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0002g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.332-7618_332-7606d others(15): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151109168 | ||||||
| chr7:151109174 | A | AC | 38 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0126 others(35): Show |
41 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-7619_332-7618i others(3): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109174 | |||||||
| chr7:151109174 | A | C | 6 | a0001c0001t0002g0332 a0001c0001t0002g0334 a0001c0004t0001g0014 others(3): Show |
6 | HG02970.hp1 HG03209.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-7619A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109174 | |||||||
| chr7:151109181 | C | A | 5 | a0001c0001t0001g0062 a0001c0001t0002g0127 a0001c0001t0004g0023 others(2): Show |
5 | HG01167.hp2 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-7612C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109181 | |||||||
| chr7:151109235 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.332-7558T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109235 | |||||||
| chr7:151109239 | T | TA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
71 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.332-7551dupA | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151109239 | ||||||
| chr7:151109240 | A | C | 3 | a0001c0004t0001g0014 a0001c0004t0001g0015 a0001c0004t0001g0017 |
3 | HG02970.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.332-7553A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109240 | |||||||
| chr7:151109263 | C | T | 11 | a0001c0001t0002g0177 a0001c0001t0002g0313 a0002c0002t0002g0309 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.332-7530C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109263 | |||||||
| chr7:151109289 | G | C | 3 | a0001c0001t0001g0106 a0001c0001t0003g0280 a0001c0017t0001g0107 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.332-7504G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109289 | |||||||
| chr7:151109533 | G | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0214 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.332-7260G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109533 | |||||||
| chr7:151109916 | C | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
71 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.332-6877C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109916 | |||||||
| chr7:151109939 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.332-6854G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151109939 | |||||||
| chr7:151110151 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.332-6642C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110151 | |||||||
| chr7:151110394 | C | A | 3 | a0001c0004t0001g0014 a0001c0004t0001g0015 a0001c0004t0001g0017 |
3 | HG02970.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.332-6399C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110394 | |||||||
| chr7:151110417 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02258.hp2 HG02717.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-6376G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110417 | |||||||
| chr7:151110558 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.332-6235G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110558 | |||||||
| chr7:151110608 | C | G | 37 | a0001c0001t0001g0126 a0001c0001t0001g0174 a0001c0001t0002g0001 others(34): Show |
40 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-6185C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110608 | |||||||
| chr7:151110688 | G | C | 2 | a0002c0002t0002g0309 a0002c0002t0002g0310 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.332-6105G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110688 | |||||||
| chr7:151110789 | C | T | 1 | a0001c0016t0001g0220 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.332-6004C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110789 | |||||||
| chr7:151110856 | G | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0180 others(35): Show |
39 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.332-5937G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110856 | |||||||
| chr7:151110885 | A | G | 305 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.332-5908A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110885 | |||||||
| chr7:151110889 | G | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG02027.hp1 NA18747.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-5904G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110889 | |||||||
| chr7:151110992 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.332-5801C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151110992 | |||||||
| chr7:151111021 | C | T | 3 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0323 |
3 | HG01109.hp1 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.332-5772C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111021 | |||||||
| chr7:151111022 | G | A | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(156): Show |
162 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.332-5771G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111022 | |||||||
| chr7:151111087 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.332-5706C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111087 | |||||||
| chr7:151111124 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.332-5669G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111124 | |||||||
| chr7:151111191 | A | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.332-5602A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111191 | |||||||
| chr7:151111208 | C | T | 1 | a0001c0001t0004g0252 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.332-5585C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111208 | |||||||
| chr7:151111374 | C | T | 3 | a0001c0004t0001g0014 a0001c0004t0001g0015 a0001c0004t0001g0017 |
3 | HG02970.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.332-5419C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111374 | |||||||
| chr7:151111485 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.332-5308T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111485 | |||||||
| chr7:151111488 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.332-5305C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111488 | |||||||
| chr7:151111564 | G | A | 10 | a0001c0001t0001g0174 a0001c0001t0006g0336 a0001c0001t0006g0340 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.332-5229G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111564 | |||||||
| chr7:151111601 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0240 a0001c0001t0002g0127 |
3 | HG00741.hp1 HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.332-5192C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111601 | |||||||
| chr7:151111649 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.332-5144C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111649 | |||||||
| chr7:151111662 | C | T | 336 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(333): Show |
346 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.332-5131C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111662 | |||||||
| chr7:151111791 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.332-5002C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151111791 | |||||||
| chr7:151112077 | C | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.332-4716C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112077 | |||||||
| chr7:151112130 | T | C | 1 | a0001c0001t0002g0329 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.332-4663T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112130 | |||||||
| chr7:151112193 | C | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
76 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.332-4600C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112193 | |||||||
| chr7:151112245 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0121 |
3 | HG01257.hp1 HG01258.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.332-4548G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112245 | |||||||
| chr7:151112292 | A | G | 1 | a0001c0001t0005g0141 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.332-4501A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112292 | |||||||
| chr7:151112396 | C | CGT | 46 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0032 others(43): Show |
47 | HG00323.hp1 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.332-4358_332-4357d others(4): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | C | CGTGT | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(53): Show |
58 | HG00099.hp2 HG00558.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.332-4360_332-4357d others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | C | CGTGTGT | 12 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0046 others(9): Show |
12 | HG00323.hp2 HG01071.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.332-4362_332-4357d others(8): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0090 others(5): Show |
8 | HG01123.hp1 HG01243.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-4364_332-4357d others(10): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0078 a0001c0001t0003g0251 |
2 | HG00642.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.332-4366_332-4357d others(12): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | C | CGTGTGTG others(9): Show |
1 | a0001c0001t0001g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.332-4372_332-4357d others(18): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.332-4397C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112396 | |||||||
| chr7:151112396 | CGT | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0083 others(28): Show |
32 | HG00280.hp2 HG00597.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.332-4358_332-4357d others(4): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | CGTGT | C | 8 | a0001c0001t0001g0109 a0001c0001t0001g0225 a0001c0001t0001g0228 others(5): Show |
8 | HG00099.hp1 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-4360_332-4357d others(6): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | CGTGTGT | C | 8 | a0001c0001t0001g0080 a0001c0001t0002g0158 a0001c0001t0002g0159 others(5): Show |
8 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-4362_332-4357d others(8): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | CGTGTGTG others(3): Show |
C | 42 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(39): Show |
45 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.332-4366_332-4357d others(12): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | CGTGTGTG others(5): Show |
C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0020 others(28): Show |
32 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.332-4368_332-4357d others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112396 | CGTGTGTG others(21): Show |
C | 2 | a0001c0001t0004g0023 a0001c0001t0004g0089 |
2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.332-4384_332-4357d others(30): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151112396 | ||||||
| chr7:151112672 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.332-4121C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112672 | |||||||
| chr7:151112675 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.332-4118G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112675 | |||||||
| chr7:151112794 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.332-3999G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112794 | |||||||
| chr7:151112883 | C | T | 1 | a0001c0001t0002g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.332-3910C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112883 | |||||||
| chr7:151112986 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
78 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.332-3807A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112986 | |||||||
| chr7:151112997 | G | A | 4 | a0001c0001t0001g0106 a0001c0001t0006g0336 a0001c0001t0006g0340 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-3796G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151112997 | |||||||
| chr7:151113076 | T | C | 38 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(35): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-3717T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113076 | |||||||
| chr7:151113139 | C | G | 1 | a0001c0001t0001g0282 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.332-3654C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113139 | |||||||
| chr7:151113167 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.332-3626G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113167 | |||||||
| chr7:151113207 | T | C | 2 | a0001c0001t0002g0334 a0006c0011t0002g0333 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.332-3586T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113207 | |||||||
| chr7:151113278 | T | C | 1 | a0001c0005t0006g0337 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.332-3515T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113278 | |||||||
| chr7:151113366 | GGGCCTCT others(3): Show |
G | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332-3421_332-3412d others(12): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151113366 | ||||||
| chr7:151113368 | G | A | 2 | a0001c0001t0003g0280 a0001c0017t0001g0107 |
2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.332-3425G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113368 | |||||||
| chr7:151113574 | T | G | 4 | a0001c0001t0001g0106 a0001c0001t0006g0336 a0001c0001t0006g0340 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-3219T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113574 | |||||||
| chr7:151113676 | T | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.332-3117T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113676 | |||||||
| chr7:151113768 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0002g0011 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.332-3025C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151113768 | |||||||
| chr7:151114030 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.332-2763G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114030 | |||||||
| chr7:151114094 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.332-2699G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114094 | |||||||
| chr7:151114303 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.332-2490G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114303 | |||||||
| chr7:151114361 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.332-2432T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114361 | |||||||
| chr7:151114643 | G | C | 1 | a0001c0001t0001g0190 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.332-2150G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114643 | |||||||
| chr7:151114697 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.332-2096C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114697 | |||||||
| chr7:151114757 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.332-2036C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114757 | |||||||
| chr7:151114779 | G | C | 1 | a0001c0001t0002g0304 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.332-2014G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114779 | |||||||
| chr7:151114983 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.332-1810C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151114983 | |||||||
| chr7:151115176 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.332-1617G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115176 | |||||||
| chr7:151115399 | G | A | 2 | a0001c0001t0003g0280 a0001c0017t0001g0107 |
2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.332-1394G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115399 | |||||||
| chr7:151115406 | G | C | 302 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.332-1387G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115406 | |||||||
| chr7:151115478 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0077 others(12): Show |
16 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-1315C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115478 | |||||||
| chr7:151115489 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.332-1304C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115489 | |||||||
| chr7:151115565 | G | A | 29 | a0001c0001t0001g0026 a0001c0001t0001g0111 a0001c0001t0001g0112 others(26): Show |
32 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.332-1228G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115565 | |||||||
| chr7:151115596 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(84): Show |
90 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.332-1197G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115596 | |||||||
| chr7:151115652 | G | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(148): Show |
158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.332-1141G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115652 | |||||||
| chr7:151115700 | A | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(151): Show |
161 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.332-1093A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115700 | |||||||
| chr7:151115708 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0002g0011 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.332-1085A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115708 | |||||||
| chr7:151115773 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0240 a0001c0001t0002g0127 |
3 | HG00741.hp1 HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.332-1020C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115773 | |||||||
| chr7:151115928 | C | T | 3 | a0001c0005t0006g0335 a0001c0005t0006g0337 a0001c0005t0006g0338 |
3 | HG02257.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.332-865C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115928 | |||||||
| chr7:151115967 | TGCTGTGG others(12): Show |
T | 1 | a0005c0018t0004g0291 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.332-825_332-807del others(19): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151115967 | |||||||
| chr7:151116271 | C | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(133): Show |
143 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.332-522C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116271 | |||||||
| chr7:151116282 | GGGCCA | G | 3 | a0001c0001t0001g0246 a0001c0001t0002g0296 a0001c0001t0002g0297 |
3 | HG00735.hp2 HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.332-497_332-493del others(5): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 151116282 | ||||||
| chr7:151116307 | C | T | 1 | a0001c0001t0003g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.332-486C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116307 | |||||||
| chr7:151116314 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.332-479C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116314 | |||||||
| chr7:151116339 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0274 |
2 | NA18940.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.332-454C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116339 | |||||||
| chr7:151116348 | G | T | 4 | a0001c0003t0001g0027 a0001c0003t0001g0133 a0001c0003t0001g0134 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-445G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116348 | |||||||
| chr7:151116451 | G | A | 1 | a0001c0001t0006g0336 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.332-342G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116451 | |||||||
| chr7:151116494 | G | A | 2 | a0001c0007t0002g0314 a0001c0007t0002g0315 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.332-299G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116494 | |||||||
| chr7:151116508 | C | T | 1 | a0001c0004t0001g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.332-285C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 1/17 | chr7 | 151116508 | |||||||
| chr7:151116890 | T | TG | 74 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(71): Show |
78 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.390+46dupG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 151116890 | ||||||
| chr7:151117047 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0086 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.391-48C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 2/17 | chr7 | 151117047 | |||||||
| chr7:151117051 | G | A | 20 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0278 others(17): Show |
20 | HG01978.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.391-44G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 2/17 | chr7 | 151117051 | |||||||
| chr7:151117253 | T | TG | 7 | a0001c0001t0002g0295 a0001c0001t0002g0305 a0001c0001t0002g0307 others(4): Show |
7 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+77dupG | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 151117253 | ||||||
| chr7:151117476 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.564+20T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 4/17 | chr7 | 151117476 | |||||||
| chr7:151117485 | A | G | 1 | a0002c0002t0002g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.564+29A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 4/17 | chr7 | 151117485 | |||||||
| chr7:151117487 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.564+31C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 4/17 | chr7 | 151117487 | |||||||
| chr7:151117522 | T | G | 1 | a0001c0001t0008g0022 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.564+66T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 4/17 | chr7 | 151117522 | |||||||
| chr7:151117917 | C | T | 2 | a0001c0007t0002g0314 a0001c0007t0002g0315 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.706+140C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/17 | chr7 | 151117917 | |||||||
| chr7:151117926 | C | T | 1 | a0001c0001t0008g0022 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.706+149C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/17 | chr7 | 151117926 | |||||||
| chr7:151117952 | G | A | 11 | a0001c0001t0002g0157 a0001c0003t0001g0027 a0001c0003t0001g0133 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.706+175G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/17 | chr7 | 151117952 | |||||||
| chr7:151117975 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.706+198G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/17 | chr7 | 151117975 | |||||||
| chr7:151118190 | C | T | 2 | a0001c0007t0002g0314 a0001c0007t0002g0315 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.707-20C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 5/17 | chr7 | 151118190 | |||||||
| chr7:151118483 | T | C | 1 | a0001c0003t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.842-22T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 6/17 | chr7 | 151118483 | |||||||
| chr7:151118693 | G | A | 1 | a0001c0017t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.969+61G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151118693 | |||||||
| chr7:151118702 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.969+70C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151118702 | |||||||
| chr7:151118795 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0077 others(26): Show |
30 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.969+163C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151118795 | |||||||
| chr7:151118868 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.969+236G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151118868 | |||||||
| chr7:151119070 | G | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0053 a0001c0001t0001g0059 others(3): Show |
6 | HG00735.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.969+438G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119070 | |||||||
| chr7:151119089 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.969+457G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119089 | |||||||
| chr7:151119138 | T | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(81): Show |
86 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.969+506T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119138 | |||||||
| chr7:151119217 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.969+585G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119217 | |||||||
| chr7:151119341 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0077 others(87): Show |
94 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.970-646C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119341 | |||||||
| chr7:151119346 | C | T | 87 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0077 others(84): Show |
91 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.970-641C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119346 | |||||||
| chr7:151119405 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.970-582T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119405 | |||||||
| chr7:151119426 | C | T | 62 | a0001c0001t0001g0051 a0001c0001t0001g0096 a0001c0001t0001g0111 others(59): Show |
65 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.970-561C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119426 | |||||||
| chr7:151119468 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.970-519C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119468 | |||||||
| chr7:151119528 | G | A | 1 | a0001c0003t0006g0339 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.970-459G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119528 | |||||||
| chr7:151119540 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.970-447G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119540 | |||||||
| chr7:151119548 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.970-439C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119548 | |||||||
| chr7:151119555 | C | T | 34 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(31): Show |
37 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.970-432C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119555 | |||||||
| chr7:151119639 | C | T | 29 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0185 others(26): Show |
29 | HG00423.hp1 HG00544.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.970-348C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119639 | |||||||
| chr7:151119760 | C | T | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.970-227C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 7/17 | chr7 | 151119760 | |||||||
| chr7:151120228 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1128+83G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120228 | |||||||
| chr7:151120273 | C | T | 5 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128+128C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120273 | |||||||
| chr7:151120310 | C | T | 1 | a0001c0001t0001g0007 | 2 | NA18947.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1128+165C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120310 | |||||||
| chr7:151120374 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1128+229C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120374 | |||||||
| chr7:151120722 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1128+577C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120722 | |||||||
| chr7:151120917 | C | T | 1 | a0001c0017t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1128+772C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120917 | |||||||
| chr7:151120994 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1128+849C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151120994 | |||||||
| chr7:151121119 | A | G | 81 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0082 others(78): Show |
85 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1128+974A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121119 | |||||||
| chr7:151121162 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1128+1017C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121162 | |||||||
| chr7:151121215 | C | T | 1 | a0001c0005t0006g0335 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1128+1070C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121215 | |||||||
| chr7:151121352 | G | A | 2 | a0001c0001t0003g0208 a0001c0001t0003g0275 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1128+1207G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121352 | |||||||
| chr7:151121369 | C | CCTG | 23 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0082 others(20): Show |
24 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1128+1241_1128+124 others(7): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 151121369 | ||||||
| chr7:151121433 | T | C | 1 | a0001c0001t0001g0263 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1128+1288T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121433 | |||||||
| chr7:151121459 | C | T | 1 | a0002c0002t0002g0320 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1128+1314C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121459 | |||||||
| chr7:151121462 | C | T | 1 | a0002c0002t0002g0320 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1128+1317C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121462 | |||||||
| chr7:151121579 | C | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0082 others(33): Show |
37 | HG00140.hp1 HG00639.hp2 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.1128+1434C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121579 | |||||||
| chr7:151121699 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1128+1554C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121699 | |||||||
| chr7:151121826 | C | T | 38 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(35): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1128+1681C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121826 | |||||||
| chr7:151121921 | G | A | 30 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(27): Show |
33 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1128+1776G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151121921 | |||||||
| chr7:151122082 | C | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
76 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1129-1712C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122082 | |||||||
| chr7:151122230 | C | T | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1129-1564C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122230 | |||||||
| chr7:151122298 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1129-1496G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122298 | |||||||
| chr7:151122311 | G | A | 5 | a0001c0001t0002g0300 a0001c0001t0002g0302 a0001c0001t0002g0304 others(2): Show |
5 | HG02735.hp1 HG03017.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129-1483G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122311 | |||||||
| chr7:151122369 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1129-1425C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122369 | |||||||
| chr7:151122453 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1129-1341C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122453 | |||||||
| chr7:151122496 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1129-1298C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122496 | |||||||
| chr7:151122497 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | NA18970.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1129-1297G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122497 | |||||||
| chr7:151122504 | C | CCCG | 38 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0100 others(35): Show |
39 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.1129-1275_1129-127 others(7): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 151122504 | ||||||
| chr7:151122568 | TCTC | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0238 a0001c0001t0001g0246 |
3 | HG00735.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1129-1222_1129-122 others(7): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 151122568 | ||||||
| chr7:151122610 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1129-1184C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151122610 | |||||||
| chr7:151123236 | C | T | 1 | a0002c0002t0002g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1129-558C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 8/17 | chr7 | 151123236 | |||||||
| chr7:151123926 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1221+40G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151123926 | |||||||
| chr7:151124074 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1221+188C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124074 | |||||||
| chr7:151124114 | C | T | 2 | a0001c0001t0006g0336 a0001c0001t0006g0340 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1221+228C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124114 | |||||||
| chr7:151124160 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1221+274G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124160 | |||||||
| chr7:151124257 | A | C | 2 | a0001c0001t0006g0336 a0001c0001t0006g0340 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1221+371A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124257 | |||||||
| chr7:151124398 | C | T | 35 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(32): Show |
38 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1221+512C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124398 | |||||||
| chr7:151124407 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1221+521C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124407 | |||||||
| chr7:151124408 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(71): Show |
76 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1221+522G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124408 | |||||||
| chr7:151124426 | T | C | 1 | a0001c0001t0002g0139 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1221+540T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124426 | |||||||
| chr7:151124466 | G | A | 15 | a0001c0001t0001g0083 a0001c0001t0001g0109 a0001c0001t0001g0110 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1221+580G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124466 | |||||||
| chr7:151124538 | G | A | 2 | a0001c0001t0001g0080 a0001c0004t0001g0015 |
2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+652G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124538 | |||||||
| chr7:151124669 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1221+783C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124669 | |||||||
| chr7:151124720 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1221+834T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124720 | |||||||
| chr7:151124920 | G | A | 52 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0054 others(49): Show |
55 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1221+1034G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124920 | |||||||
| chr7:151124998 | G | A | 4 | a0001c0001t0001g0174 a0001c0001t0002g0011 a0001c0007t0002g0314 others(1): Show |
4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221+1112G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151124998 | |||||||
| chr7:151125105 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
109 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1221+1219C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125105 | |||||||
| chr7:151125239 | C | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(132): Show |
142 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1221+1353C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125239 | |||||||
| chr7:151125240 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1221+1354G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125240 | |||||||
| chr7:151125358 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
136 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1221+1472A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125358 | |||||||
| chr7:151125364 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0119 others(26): Show |
30 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1221+1478G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125364 | |||||||
| chr7:151125412 | CTTAGAG | C | 5 | a0001c0001t0001g0230 a0001c0001t0001g0258 a0001c0001t0001g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1221+1531_1221+153 others(10): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151125412 | ||||||
| chr7:151125451 | A | C | 1 | a0001c0001t0002g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1221+1565A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125451 | |||||||
| chr7:151125512 | T | A | 1 | a0006c0011t0002g0333 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1221+1626T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125512 | |||||||
| chr7:151125572 | G | C | 338 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(335): Show |
348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.1221+1686G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125572 | |||||||
| chr7:151125604 | G | A | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1221+1718G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125604 | |||||||
| chr7:151125620 | CTCT | C | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01167.hp1 HG01169.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1221+1740_1221+174 others(7): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151125620 | ||||||
| chr7:151125657 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1221+1771C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125657 | |||||||
| chr7:151125667 | C | G | 1 | a0001c0016t0001g0220 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1221+1781C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125667 | |||||||
| chr7:151125670 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1221+1784T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125670 | |||||||
| chr7:151125678 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
112 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1221+1792C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125678 | |||||||
| chr7:151125952 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1221+2066G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151125952 | |||||||
| chr7:151126047 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0269 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1221+2161C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126047 | |||||||
| chr7:151126052 | G | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1221+2166G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126052 | |||||||
| chr7:151126055 | TGGGTG | T | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.1221+2178_1221+218 others(9): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126055 | ||||||
| chr7:151126068 | G | C | 1 | a0001c0001t0002g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1221+2182G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126068 | |||||||
| chr7:151126087 | TCGTTCCG others(21): Show |
T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0119 others(25): Show |
29 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1221+2205_1221+223 others(32): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126087 | ||||||
| chr7:151126140 | TCCG | T | 35 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(32): Show |
38 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1221+2257_1221+225 others(7): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126140 | ||||||
| chr7:151126202 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(107): Show |
112 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1221+2316C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126202 | |||||||
| chr7:151126274 | CGCCCTGA others(8): Show |
C | 40 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0112 others(37): Show |
44 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1222-2304_1222-229 others(19): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126274 | ||||||
| chr7:151126291 | A | T | 40 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0112 others(37): Show |
44 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1222-2289A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126291 | |||||||
| chr7:151126356 | GGAGCA | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1222-2214_1222-221 others(9): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126356 | ||||||
| chr7:151126366 | A | G | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1222-2214A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126366 | |||||||
| chr7:151126381 | G | A | 3 | a0001c0005t0006g0335 a0001c0005t0006g0337 a0001c0005t0006g0338 |
3 | HG02257.hp2 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1222-2199G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126381 | |||||||
| chr7:151126391 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1222-2189C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126391 | |||||||
| chr7:151126411 | G | GAAGGCTG others(3): Show |
1 | a0001c0001t0001g0262 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1222-2168_1222-215 others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126411 | ||||||
| chr7:151126412 | A | AAGGCTGG others(13): Show |
3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1222-2159_1222-215 others(24): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126412 | ||||||
| chr7:151126412 | AAGGCTGG others(3): Show |
A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
143 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1222-2124_1222-211 others(14): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126412 | ||||||
| chr7:151126412 | AAGGCTGG others(13): Show |
A | 1 | a0001c0001t0001g0110 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1222-2134_1222-211 others(24): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 151126412 | ||||||
| chr7:151126422 | G | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1222-2158G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126422 | |||||||
| chr7:151126432 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(135): Show |
142 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1222-2148G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126432 | |||||||
| chr7:151126442 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1222-2138G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126442 | |||||||
| chr7:151126444 | G | A | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1222-2136G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126444 | |||||||
| chr7:151126483 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1222-2097G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126483 | |||||||
| chr7:151126535 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
143 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1222-2045T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126535 | |||||||
| chr7:151126625 | C | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0119 others(25): Show |
29 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1222-1955C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126625 | |||||||
| chr7:151126633 | C | A | 1 | a0001c0001t0002g0329 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1222-1947C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126633 | |||||||
| chr7:151126675 | T | C | 4 | a0001c0001t0001g0174 a0001c0001t0002g0011 a0001c0007t0002g0314 others(1): Show |
4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222-1905T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126675 | |||||||
| chr7:151126794 | C | T | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01167.hp1 HG01169.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1222-1786C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126794 | |||||||
| chr7:151126897 | C | T | 4 | a0001c0001t0001g0174 a0001c0001t0002g0011 a0001c0007t0002g0314 others(1): Show |
4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222-1683C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126897 | |||||||
| chr7:151126926 | C | T | 4 | a0001c0001t0001g0174 a0001c0001t0002g0011 a0001c0007t0002g0314 others(1): Show |
4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222-1654C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126926 | |||||||
| chr7:151126934 | C | T | 40 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0112 others(37): Show |
44 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1222-1646C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126934 | |||||||
| chr7:151126988 | A | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0079 others(2): Show |
5 | HG02717.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222-1592A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126988 | |||||||
| chr7:151126997 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1222-1583C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151126997 | |||||||
| chr7:151127066 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1222-1514C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127066 | |||||||
| chr7:151127138 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1222-1442G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127138 | |||||||
| chr7:151127247 | G | A | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0144 |
3 | HG00544.hp2 HG02083.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1222-1333G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127247 | |||||||
| chr7:151127257 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(137): Show |
144 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1222-1323G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127257 | |||||||
| chr7:151127383 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0051 others(35): Show |
39 | HG00140.hp1 HG01109.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1222-1197G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127383 | |||||||
| chr7:151127421 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1222-1159C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127421 | |||||||
| chr7:151127426 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0200 a0001c0001t0001g0237 others(2): Show |
6 | HG02015.hp2 HG02080.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222-1154T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127426 | |||||||
| chr7:151127648 | C | T | 40 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0112 others(37): Show |
44 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1222-932C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127648 | |||||||
| chr7:151127784 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(113): Show |
118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1222-796C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127784 | |||||||
| chr7:151127826 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1222-754G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127826 | |||||||
| chr7:151127944 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1222-636C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127944 | |||||||
| chr7:151127945 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1222-635G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127945 | |||||||
| chr7:151127950 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1222-630T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151127950 | |||||||
| chr7:151128000 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1222-580G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128000 | |||||||
| chr7:151128009 | G | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(65): Show |
70 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1222-571G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128009 | |||||||
| chr7:151128228 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(108): Show |
113 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1222-352G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128228 | |||||||
| chr7:151128263 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1222-317T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128263 | |||||||
| chr7:151128272 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1222-308C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128272 | |||||||
| chr7:151128307 | T | A | 1 | a0001c0001t0002g0108 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1222-273T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128307 | |||||||
| chr7:151128405 | A | G | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(117): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1222-175A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128405 | |||||||
| chr7:151128480 | C | G | 1 | a0001c0001t0001g0222 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1222-100C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128480 | |||||||
| chr7:151128480 | C | T | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1222-100C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 9/17 | chr7 | 151128480 | |||||||
| chr7:151128719 | T | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0054 |
3 | HG03098.hp1 HG03579.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1326+35T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128719 | |||||||
| chr7:151128752 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(101): Show |
106 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1326+68G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128752 | |||||||
| chr7:151128778 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1326+94C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128778 | |||||||
| chr7:151128846 | G | T | 1 | a0001c0017t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1326+162G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128846 | |||||||
| chr7:151128852 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0002g0156 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1326+168C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128852 | |||||||
| chr7:151128948 | A | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0051 others(34): Show |
38 | HG00140.hp1 HG01109.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.1326+264A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128948 | |||||||
| chr7:151128957 | G | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.1326+273G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151128957 | |||||||
| chr7:151129132 | C | G | 40 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0051 others(37): Show |
41 | HG00140.hp1 HG01109.hp1 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.1326+448C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129132 | |||||||
| chr7:151129231 | C | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(96): Show |
102 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1326+547C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129231 | |||||||
| chr7:151129258 | C | T | 2 | a0001c0001t0006g0336 a0001c0001t0006g0340 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1326+574C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129258 | |||||||
| chr7:151129298 | A | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(116): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1326+614A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129298 | |||||||
| chr7:151129319 | C | G | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(115): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1326+635C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129319 | |||||||
| chr7:151129330 | G | A | 1 | a0001c0001t0006g0336 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1326+646G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129330 | |||||||
| chr7:151129458 | C | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1326+774C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129458 | |||||||
| chr7:151129462 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1326+778G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129462 | |||||||
| chr7:151129468 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
111 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1326+784A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129468 | |||||||
| chr7:151129474 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0246 a0001c0001t0002g0158 others(1): Show |
4 | HG00735.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326+790C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129474 | |||||||
| chr7:151129710 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1326+1026G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129710 | |||||||
| chr7:151129731 | CTCGCGAG | C | 35 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(32): Show |
38 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1326+1050_1326+105 others(11): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 151129731 | ||||||
| chr7:151129825 | G | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1326+1141G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129825 | |||||||
| chr7:151129910 | C | T | 1 | a0001c0001t0002g0306 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1326+1226C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151129910 | |||||||
| chr7:151130017 | G | A | 13 | a0001c0001t0001g0083 a0001c0001t0001g0109 a0001c0001t0001g0110 others(10): Show |
13 | HG00280.hp1 HG00323.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1326+1333G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130017 | |||||||
| chr7:151130050 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1326+1366G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130050 | |||||||
| chr7:151130120 | A | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.1326+1436A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130120 | |||||||
| chr7:151130246 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0002g0166 |
2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1326+1562G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130246 | |||||||
| chr7:151130249 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0002g0156 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1326+1565G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130249 | |||||||
| chr7:151130587 | C | T | 4 | a0001c0001t0001g0187 a0001c0001t0001g0204 a0001c0001t0001g0225 others(1): Show |
4 | HG02132.hp1 NA18962.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326+1903C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130587 | |||||||
| chr7:151130715 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0002g0156 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1326+2031G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130715 | |||||||
| chr7:151130773 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1326+2089C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130773 | |||||||
| chr7:151130839 | T | A | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1326+2155T>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130839 | |||||||
| chr7:151130864 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1326+2180C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130864 | |||||||
| chr7:151130972 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1326+2288T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151130972 | |||||||
| chr7:151131017 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1326+2333G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131017 | |||||||
| chr7:151131082 | G | A | 4 | a0001c0001t0001g0259 a0001c0004t0001g0014 a0001c0004t0001g0017 others(1): Show |
4 | HG02055.hp1 HG02886.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326+2398G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131082 | |||||||
| chr7:151131132 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1326+2448C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131132 | |||||||
| chr7:151131229 | A | G | 58 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0111 others(55): Show |
62 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1326+2545A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131229 | |||||||
| chr7:151131385 | C | T | 1 | a0001c0001t0004g0252 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1326+2701C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131385 | |||||||
| chr7:151131432 | A | T | 1 | a0001c0001t0007g0171 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1326+2748A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131432 | |||||||
| chr7:151131437 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1326+2753C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131437 | |||||||
| chr7:151131494 | A | G | 10 | a0001c0001t0001g0106 a0001c0001t0001g0132 a0001c0004t0001g0131 others(7): Show |
10 | HG01884.hp2 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1326+2810A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131494 | |||||||
| chr7:151131559 | C | T | 4 | a0001c0003t0001g0133 a0001c0003t0001g0134 a0001c0003t0001g0136 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-2841C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131559 | |||||||
| chr7:151131589 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1327-2811T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131589 | |||||||
| chr7:151131605 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1327-2795G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131605 | |||||||
| chr7:151131995 | G | A | 1 | a0001c0001t0002g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1327-2405G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151131995 | |||||||
| chr7:151132014 | G | T | 2 | a0001c0001t0003g0103 a0001c0001t0003g0280 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1327-2386G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132014 | |||||||
| chr7:151132134 | G | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.1327-2266G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132134 | |||||||
| chr7:151132135 | G | A | 17 | a0001c0001t0001g0007 a0001c0001t0001g0176 a0001c0001t0001g0198 others(14): Show |
18 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.1327-2265G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132135 | |||||||
| chr7:151132371 | A | G | 311 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1327-2029A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132371 | |||||||
| chr7:151132374 | C | G | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1327-2026C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132374 | |||||||
| chr7:151132407 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1327-1993G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132407 | |||||||
| chr7:151132428 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1327-1972T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132428 | |||||||
| chr7:151132549 | G | A | 4 | a0001c0001t0001g0174 a0001c0001t0002g0011 a0001c0007t0002g0314 others(1): Show |
4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-1851G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132549 | |||||||
| chr7:151132570 | A | G | 2 | a0001c0004t0001g0014 a0002c0002t0002g0316 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1327-1830A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132570 | |||||||
| chr7:151132595 | G | A | 1 | a0001c0001t0002g0326 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1327-1805G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132595 | |||||||
| chr7:151132602 | C | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0238 |
3 | HG02896.hp2 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1327-1798C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132602 | |||||||
| chr7:151132622 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1327-1778G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132622 | |||||||
| chr7:151132741 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1327-1659G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132741 | |||||||
| chr7:151132849 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1327-1551C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132849 | |||||||
| chr7:151132928 | A | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
161 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1327-1472A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132928 | |||||||
| chr7:151132934 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1327-1466C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132934 | |||||||
| chr7:151132947 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-1453G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151132947 | |||||||
| chr7:151133037 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1327-1363C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133037 | |||||||
| chr7:151133064 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1327-1336C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133064 | |||||||
| chr7:151133134 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1327-1266A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133134 | |||||||
| chr7:151133204 | A | C | 10 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0004t0001g0131 others(7): Show |
10 | HG01884.hp2 HG01978.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1327-1196A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133204 | |||||||
| chr7:151133254 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0262 |
2 | HG01255.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1327-1146G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133254 | |||||||
| chr7:151133476 | G | A | 2 | a0001c0001t0003g0103 a0001c0001t0003g0280 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1327-924G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133476 | |||||||
| chr7:151133507 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0119 a0001c0001t0001g0124 |
3 | HG00639.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1327-893G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133507 | |||||||
| chr7:151133719 | C | T | 10 | a0001c0001t0001g0045 a0001c0001t0001g0178 a0001c0001t0001g0196 others(7): Show |
10 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.1327-681C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133719 | |||||||
| chr7:151133798 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1327-602C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133798 | |||||||
| chr7:151133801 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1327-599C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133801 | |||||||
| chr7:151133912 | G | A | 1 | a0001c0001t0004g0270 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1327-488G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133912 | |||||||
| chr7:151133945 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0135 a0001c0001t0002g0313 others(1): Show |
4 | HG01891.hp1 HG01952.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327-455G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151133945 | |||||||
| chr7:151134013 | C | A | 36 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(33): Show |
39 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1327-387C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134013 | |||||||
| chr7:151134025 | C | T | 1 | a0002c0002t0002g0311 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1327-375C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134025 | |||||||
| chr7:151134135 | T | C | 40 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0106 others(37): Show |
41 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1327-265T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134135 | |||||||
| chr7:151134142 | C | T | 1 | a0001c0001t0002g0332 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1327-258C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134142 | |||||||
| chr7:151134202 | C | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0115 others(20): Show |
24 | HG00140.hp1 HG01109.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1327-198C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134202 | |||||||
| chr7:151134231 | C | T | 7 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0001g0256 others(4): Show |
7 | NA18959.hp1 NA18975.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1327-169C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134231 | |||||||
| chr7:151134256 | A | G | 45 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0112 others(42): Show |
49 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1327-144A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134256 | |||||||
| chr7:151134276 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0218 a0001c0001t0001g0239 |
3 | HG03490.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1327-124G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134276 | |||||||
| chr7:151134344 | C | T | 8 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0188 others(5): Show |
8 | HG00280.hp1 HG00323.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1327-56C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 10/17 | chr7 | 151134344 | |||||||
| chr7:151134575 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0230 |
2 | HG03486.hp1 NA19010.hp1 |
splice_region_variant&intron_variant | LOW | c.1495+7C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134575 | |||||||
| chr7:151134677 | G | A | 10 | a0001c0001t0001g0106 a0001c0001t0001g0132 a0001c0004t0001g0131 others(7): Show |
10 | HG01884.hp2 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1495+109G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134677 | |||||||
| chr7:151134685 | C | T | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0331 |
3 | HG02109.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1495+117C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134685 | |||||||
| chr7:151134721 | C | G | 1 | a0001c0007t0002g0314 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1495+153C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134721 | |||||||
| chr7:151134721 | C | T | 48 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0112 others(45): Show |
52 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1495+153C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134721 | |||||||
| chr7:151134793 | G | T | 4 | a0001c0001t0001g0174 a0001c0001t0002g0011 a0001c0007t0002g0314 others(1): Show |
4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+225G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134793 | |||||||
| chr7:151134901 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0269 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1495+333G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134901 | |||||||
| chr7:151134950 | C | T | 4 | a0001c0001t0001g0174 a0001c0001t0002g0011 a0001c0007t0002g0314 others(1): Show |
4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+382C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134950 | |||||||
| chr7:151134965 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1495+397T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151134965 | |||||||
| chr7:151135130 | A | T | 2 | a0001c0001t0006g0336 a0001c0001t0006g0340 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1495+562A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135130 | |||||||
| chr7:151135195 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1495+627G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135195 | |||||||
| chr7:151135699 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0119 others(26): Show |
30 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1495+1131G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135699 | |||||||
| chr7:151135826 | A | G | 306 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.1495+1258A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135826 | |||||||
| chr7:151135836 | A | G | 45 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0112 others(42): Show |
49 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1495+1268A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135836 | |||||||
| chr7:151135872 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1495+1304A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135872 | |||||||
| chr7:151135906 | A | C | 66 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0025 others(63): Show |
70 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1495+1338A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151135906 | |||||||
| chr7:151136083 | T | G | 1 | a0001c0001t0001g0050 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1495+1515T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136083 | |||||||
| chr7:151136256 | C | A | 1 | a0001c0001t0002g0156 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1495+1688C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136256 | |||||||
| chr7:151136380 | C | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0253 |
2 | HG00280.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1496-1763C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136380 | |||||||
| chr7:151136384 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1496-1759C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136384 | |||||||
| chr7:151136418 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1496-1725C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136418 | |||||||
| chr7:151136440 | G | A | 1 | a0001c0001t0006g0340 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1496-1703G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136440 | |||||||
| chr7:151136711 | C | T | 9 | a0001c0001t0001g0249 a0001c0004t0001g0131 a0002c0002t0002g0309 others(6): Show |
9 | HG01884.hp2 HG02132.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1496-1432C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136711 | |||||||
| chr7:151136853 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1496-1290A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136853 | |||||||
| chr7:151136921 | G | GGGCAGCG others(27): Show |
1 | a0001c0001t0001g0098 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1221_1496-122 others(38): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 151136921 | ||||||
| chr7:151136933 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1210A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136933 | |||||||
| chr7:151136950 | G | T | 1 | a0001c0001t0001g0098 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1193G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136950 | |||||||
| chr7:151136983 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1160C>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136983 | |||||||
| chr7:151136984 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1159A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136984 | |||||||
| chr7:151136997 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1146A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136997 | |||||||
| chr7:151136998 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1145G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151136998 | |||||||
| chr7:151137001 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1142C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137001 | |||||||
| chr7:151137002 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1496-1141T>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137002 | |||||||
| chr7:151137079 | G | A | 1 | a0001c0001t0002g0328 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1496-1064G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137079 | |||||||
| chr7:151137261 | C | T | 1 | a0002c0002t0002g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1496-882C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137261 | |||||||
| chr7:151137360 | G | A | 5 | a0001c0001t0002g0300 a0001c0003t0001g0133 a0001c0003t0001g0134 others(2): Show |
5 | HG02055.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1496-783G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137360 | |||||||
| chr7:151137429 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0228 a0001c0001t0001g0289 |
4 | HG03017.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1496-714G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137429 | |||||||
| chr7:151137452 | C | T | 74 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0082 others(71): Show |
75 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1496-691C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137452 | |||||||
| chr7:151137536 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
42 | HG00140.hp2 HG01081.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1496-607G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137536 | |||||||
| chr7:151137600 | T | C | 16 | a0001c0001t0001g0054 a0001c0001t0001g0097 a0001c0001t0001g0113 others(13): Show |
16 | HG00438.hp1 HG01884.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1496-543T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137600 | |||||||
| chr7:151137640 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1496-503C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137640 | |||||||
| chr7:151137750 | G | A | 2 | a0001c0001t0001g0124 a0001c0003t0006g0339 |
2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1496-393G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137750 | |||||||
| chr7:151137825 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1496-318C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151137825 | |||||||
| chr7:151138123 | C | T | 1 | a0001c0017t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1496-20C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 11/17 | chr7 | 151138123 | |||||||
| chr7:151138724 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0096 a0001c0001t0001g0129 |
3 | NA18951.hp1 NA18989.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1666+411C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138724 | |||||||
| chr7:151138761 | T | C | 6 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
6 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1666+448T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138761 | |||||||
| chr7:151138782 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1666+469C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138782 | |||||||
| chr7:151138783 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1666+470G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138783 | |||||||
| chr7:151138860 | T | C | 1 | a0001c0001t0002g0308 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1666+547T>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138860 | |||||||
| chr7:151138875 | A | C | 2 | a0001c0001t0003g0103 a0001c0001t0003g0280 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1666+562A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138875 | |||||||
| chr7:151138898 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1666+585G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151138898 | |||||||
| chr7:151139005 | CCCTACTT others(6): Show |
C | 1 | a0001c0001t0001g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1666+693_1666+705d others(15): Show |
AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139005 | |||||||
| chr7:151139153 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
95 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1667-826A>G | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139153 | |||||||
| chr7:151139270 | C | T | 1 | a0004c0013t0001g0033 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1667-709C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139270 | |||||||
| chr7:151139520 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1667-459G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139520 | |||||||
| chr7:151139522 | C | A | 1 | a0004c0013t0001g0033 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1667-457C>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139522 | |||||||
| chr7:151139522 | C | T | 1 | a0001c0001t0006g0340 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1667-457C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139522 | |||||||
| chr7:151139540 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1667-439C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139540 | |||||||
| chr7:151139640 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1667-339A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139640 | |||||||
| chr7:151139833 | G | A | 3 | a0001c0001t0001g0174 a0001c0001t0002g0011 a0001c0007t0002g0314 |
3 | HG01884.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1667-146G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139833 | |||||||
| chr7:151139840 | G | C | 1 | a0001c0001t0002g0156 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1667-139G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139840 | |||||||
| chr7:151139921 | G | A | 4 | a0001c0001t0001g0259 a0001c0004t0001g0017 a0001c0005t0006g0335 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667-58G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139921 | |||||||
| chr7:151139963 | A | C | 1 | a0001c0001t0001g0091 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1667-16A>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 12/17 | chr7 | 151139963 | |||||||
| chr7:151140139 | C | T | 1 | a0001c0001t0006g0340 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1804+23C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151140139 | |||||||
| chr7:151140428 | C | T | 18 | a0001c0001t0001g0045 a0001c0001t0001g0122 a0001c0001t0001g0130 others(15): Show |
18 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.1804+312C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151140428 | |||||||
| chr7:151140442 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(108): Show |
113 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1804+326C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151140442 | |||||||
| chr7:151140951 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0278 |
2 | HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1804+835C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151140951 | |||||||
| chr7:151141079 | C | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0238 |
3 | HG02896.hp2 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1805-819C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151141079 | |||||||
| chr7:151141136 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1805-762C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151141136 | |||||||
| chr7:151141607 | A | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0174 a0001c0001t0002g0011 others(1): Show |
4 | HG01884.hp1 HG03195.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1805-291A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 13/17 | chr7 | 151141607 | |||||||
| chr7:151142269 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2050+16G>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 15/17 | chr7 | 151142269 | |||||||
| chr7:151142655 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2273+21A>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151142655 | |||||||
| chr7:151142677 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0054 others(2): Show |
5 | HG02717.hp1 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2273+43C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151142677 | |||||||
| chr7:151142706 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2273+72G>A | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151142706 | |||||||
| chr7:151142837 | C | T | 1 | a0003c0014t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2273+203C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151142837 | |||||||
| chr7:151143176 | G | C | 3 | a0001c0001t0001g0012 a0001c0001t0002g0158 a0001c0001t0006g0336 |
3 | HG02451.hp1 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2274-165G>C | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151143176 | |||||||
| chr7:151143200 | C | T | 4 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2274-141C>T | AGAP3 | ENSG00000133612.20 | transcript | ENST00000397238.7 | protein_coding | 16/17 | chr7 | 151143200 |