Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 730 |
| ensemblid | ENSG00000112936.21 |
| hgncid | 1346 |
| symbol | C7 |
| name | complement C7 |
| refseq_nuc | NM_000587.4 |
| refseq_prot | NP_000578.2 |
| ensembl_nuc | ENST00000313164.10 |
| ensembl_prot | ENSP00000322061.9 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 40909497 |
| end | 40984643 |
| strand | + |
| ver | v1.2 |
| region | chr5:40909497-40984643 |
| region5000 | chr5:40904497-40989643 |
| regionname0 | C7_chr5_40909497_40984643 |
| regionname5000 | C7_chr5_40904497_40989643 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 843 | 137 | 59 | 23 | 46 | 3 | 5 | 44 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0002 | 0/0 | 843 | 116 | 17 | 20 | 66 | 2 | 11 | 50 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0003 | 0/1 | 843 | 41 | 1 | 2 | 28 | 2 | 7 | 24 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0004 | 0/0 | 843 | 23 | 0 | 1 | 22 | 0 | 0 | 14 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0005 | 0/0 | 843 | 19 | 3 | 7 | 5 | 1 | 3 | 4 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0006 | 0/0 | 843 | 9 | 1 | 3 | 0 | 2 | 3 | 0 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0007 | 0/0 | 843 | 8 | 1 | 5 | 0 | 2 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0008 | 0/0 | 843 | 7 | 0 | 2 | 5 | 0 | 0 | 5 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0009 | 0/0 | 843 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0010 | 0/0 | 843 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0011 | 0/0 | 843 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0012 | 0/0 | 843 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0013 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0014 | 0/0 | 843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0015 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0016 | 0/0 | 401 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | MKVIS others(396): Show |
chr5 | 40904497 | 40989643 |
| a0017 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0018 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0019 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0020 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0021 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| a0022 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | MKVIS others(838): Show |
chr5 | 40904497 | 40989643 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2529 | 135 | 58 | 23 | 45 | 3 | 5 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0001c0022 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0001c0025 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0002c0002 | 0/0 | 2529 | 116 | 17 | 20 | 66 | 2 | 11 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0003c0003 | 0/1 | 2529 | 40 | 1 | 2 | 27 | 2 | 7 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0003c0023 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0004c0004 | 0/0 | 2529 | 22 | 0 | 1 | 21 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0004c0014 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0005c0005 | 0/0 | 2529 | 18 | 3 | 7 | 5 | 1 | 2 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0005c0013 | 0/0 | 2529 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0006c0006 | 0/0 | 2529 | 8 | 1 | 3 | 0 | 2 | 2 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0006c0016 | 0/0 | 2529 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0007c0007 | 0/0 | 2529 | 8 | 1 | 5 | 0 | 2 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0008c0008 | 0/0 | 2529 | 7 | 0 | 2 | 5 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0009c0009 | 0/0 | 2529 | 3 | 0 | 0 | 2 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0010c0010 | 0/0 | 2529 | 3 | 0 | 0 | 3 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0011c0011 | 0/0 | 2529 | 2 | 0 | 1 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0012c0012 | 0/0 | 2529 | 2 | 0 | 0 | 2 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0013c0028 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0014c0021 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0015c0015 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0016c0019 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0017c0027 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0018c0018 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0019c0024 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0020c0017 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0021c0020 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 | ||
| a0022c0026 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | ATGAA others(2524): Show |
chr5 | 40904497 | 40989643 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5716 | 39 | 7 | 11 | 18 | 1 | 1 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0001c0001t0002 | 0/0 | 5713 | 51 | 24 | 5 | 17 | 2 | 3 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0001c0001t0003 | 0/0 | 5716 | 6 | 5 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0001c0001t0004 | 0/0 | 5716 | 33 | 17 | 5 | 10 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0001c0001t0005 | 0/0 | 5716 | 3 | 3 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0001c0001t0007 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0001c0001t0008 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0001c0001t0012 | 0/0 | 5713 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0001c0022t0001 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0001c0025t0011 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0002c0002t0001 | 0/0 | 5716 | 60 | 6 | 15 | 34 | 1 | 4 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0002c0002t0002 | 0/0 | 5713 | 35 | 4 | 2 | 25 | 1 | 3 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0002c0002t0003 | 0/0 | 5716 | 9 | 6 | 0 | 0 | 0 | 3 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0002c0002t0004 | 0/0 | 5716 | 11 | 1 | 3 | 6 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0002c0002t0010 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(3108): Show |
chr5 | 40904497 | 40989643 |
| a0003c0003t0003 | 0/0 | 5716 | 39 | 1 | 2 | 27 | 2 | 7 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0003c0003t0009 | 0/1 | 5716 | 1 | 0 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0003c0023t0003 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0004c0004t0001 | 0/0 | 5716 | 19 | 0 | 1 | 18 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0004c0004t0002 | 0/0 | 5713 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0004c0004t0004 | 0/0 | 5716 | 2 | 0 | 0 | 2 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0004c0014t0001 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0005c0005t0002 | 0/0 | 5713 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0005c0005t0003 | 0/0 | 5716 | 17 | 3 | 6 | 5 | 1 | 2 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0005c0013t0003 | 0/0 | 5716 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0006c0006t0002 | 0/0 | 5713 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0006c0006t0004 | 0/0 | 5716 | 6 | 0 | 2 | 0 | 2 | 2 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0006c0006t0006 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0006c0016t0004 | 0/0 | 5716 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0007c0007t0004 | 0/0 | 5716 | 7 | 1 | 4 | 0 | 2 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0007c0007t0006 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0008c0008t0001 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0008c0008t0003 | 0/0 | 5716 | 6 | 0 | 2 | 4 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0009c0009t0001 | 0/0 | 5716 | 2 | 0 | 0 | 2 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0009c0009t0002 | 0/0 | 5713 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0010c0010t0001 | 0/0 | 5716 | 3 | 0 | 0 | 3 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0011c0011t0002 | 0/0 | 5713 | 2 | 0 | 1 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0012c0012t0003 | 0/0 | 5716 | 2 | 0 | 0 | 2 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0013c0028t0002 | 0/0 | 5713 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0014c0021t0001 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0015c0015t0003 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0016c0019t0001 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0017c0027t0002 | 0/0 | 5713 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0018c0018t0002 | 0/0 | 5713 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5708): Show |
chr5 | 40904497 | 40989643 |
| a0019c0024t0001 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0020c0017t0001 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0021c0020t0001 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| a0022c0026t0004 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | AGGGA others(5711): Show |
chr5 | 40904497 | 40989643 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0004g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0005g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0005g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0005g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0001t0012g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0022t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0001c0025t0011g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0002c0002t0010g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0003g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0003t0009g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0003c0023t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0004t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0004c0014t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0005t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0005c0013t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0006c0006t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0006c0006t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0006c0006t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0006c0006t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0006c0006t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0006c0006t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0006c0006t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0006c0006t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0006c0016t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0007c0007t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0007c0007t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0007c0007t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0007c0007t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0007c0007t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0007c0007t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0007c0007t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0007c0007t0006g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0008c0008t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0008c0008t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0008c0008t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0008c0008t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0008c0008t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0008c0008t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0008c0008t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0009c0009t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0009c0009t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0009c0009t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0010c0010t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0010c0010t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0010c0010t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0011c0011t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0011c0011t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0012c0012t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0012c0012t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0013c0028t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0014c0021t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0015c0015t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0016c0019t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0017c0027t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0018c0018t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0019c0024t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0020c0017t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0021c0020t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| a0022c0026t0004g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00099 | hp2 | a0003 | c0003 | t0003 | g0092 | EUR | GBR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00140 | hp1 | a0005 | c0005 | t0003 | g0088 | EUR | GBR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00140 | hp2 | a0003 | c0003 | t0003 | g0328 | EUR | GBR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0261 | EUR | FIN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0071 | EUR | FIN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00408 | hp1 | a0004 | c0004 | t0001 | g0026 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00408 | hp2 | a0003 | c0003 | t0003 | g0262 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00423 | hp1 | a0002 | c0002 | t0004 | g0182 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00423 | hp2 | a0003 | c0003 | t0003 | g0350 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00544 | hp2 | a0004 | c0004 | t0001 | g0303 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00558 | hp2 | a0002 | c0002 | t0004 | g0111 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00597 | hp2 | a0004 | c0004 | t0001 | g0025 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00621 | hp1 | a0013 | c0028 | t0002 | g0170 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00642 | hp1 | a0014 | c0021 | t0001 | g0271 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00642 | hp2 | a0007 | c0007 | t0004 | g0264 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00673 | hp1 | a0015 | c0015 | t0003 | g0308 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | CHS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00735 | hp2 | a0007 | c0007 | t0006 | g0360 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00741 | hp1 | a0006 | c0006 | t0004 | g0091 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG00741 | hp2 | a0005 | c0005 | t0003 | g0135 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01069 | hp1 | a0003 | c0003 | t0003 | g0250 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01070 | hp1 | a0005 | c0005 | t0003 | g0085 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0030 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01167 | hp2 | a0002 | c0002 | t0004 | g0146 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01168 | hp1 | a0007 | c0007 | t0004 | g0265 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01169 | hp2 | a0002 | c0002 | t0004 | g0017 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01175 | hp1 | a0007 | c0007 | t0004 | g0266 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01192 | hp1 | a0005 | c0005 | t0003 | g0280 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01255 | hp1 | a0007 | c0007 | t0004 | g0268 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0162 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01261 | hp2 | a0016 | c0019 | t0001 | g0089 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01358 | hp1 | a0003 | c0003 | t0003 | g0029 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0371 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01361 | hp1 | a0006 | c0006 | t0006 | g0106 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01433 | hp1 | a0005 | c0005 | t0003 | g0103 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01496 | hp2 | a0002 | c0002 | t0004 | g0134 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0097 | EUR | IBS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0154 | EUR | IBS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01516 | hp1 | a0006 | c0006 | t0004 | g0096 | EUR | IBS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01516 | hp2 | a0006 | c0006 | t0004 | g0094 | EUR | IBS | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0263 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01928 | hp1 | a0011 | c0011 | t0002 | g0305 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0272 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01934 | hp2 | a0004 | c0004 | t0001 | g0310 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01975 | hp1 | a0005 | c0005 | t0003 | g0131 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01981 | hp1 | a0008 | c0008 | t0003 | g0314 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01981 | hp2 | a0005 | c0005 | t0002 | g0133 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02004 | hp1 | a0008 | c0008 | t0003 | g0313 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0237 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02027 | hp1 | a0004 | c0004 | t0001 | g0297 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02040 | hp1 | a0004 | c0004 | t0001 | g0021 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0273 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02056 | hp1 | a0004 | c0004 | t0001 | g0024 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02080 | hp1 | a0005 | c0005 | t0003 | g0173 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02080 | hp2 | a0004 | c0014 | t0001 | g0023 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0138 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02145 | hp2 | a0017 | c0027 | t0002 | g0148 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0373 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0075 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | CDX | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02155 | hp2 | a0003 | c0003 | t0003 | g0338 | EAS | CDX | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | CDX | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02165 | hp2 | a0009 | c0009 | t0001 | g0318 | EAS | CDX | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0200 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02280 | hp1 | a0002 | c0002 | t0003 | g0199 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0317 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02300 | hp1 | a0005 | c0005 | t0003 | g0082 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | PEL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02451 | hp1 | a0002 | c0002 | t0003 | g0198 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0087 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02523 | hp2 | a0003 | c0003 | t0003 | g0230 | EAS | KHV | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0189 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02615 | hp2 | a0018 | c0018 | t0002 | g0193 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0368 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0285 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02698 | hp1 | a0005 | c0013 | t0003 | g0183 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0140 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02818 | hp2 | a0002 | c0002 | t0004 | g0145 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02886 | hp1 | a0001 | c0025 | t0011 | g0366 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02886 | hp2 | a0019 | c0024 | t0001 | g0059 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0141 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02965 | hp1 | a0005 | c0005 | t0003 | g0281 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02965 | hp2 | a0001 | c0001 | t0012 | g0365 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02976 | hp2 | a0007 | c0007 | t0004 | g0039 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03017 | hp1 | a0009 | c0009 | t0002 | g0315 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03017 | hp2 | a0006 | c0016 | t0004 | g0108 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0206 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03139 | hp1 | a0002 | c0002 | t0003 | g0139 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0093 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03239 | hp2 | a0006 | c0006 | t0004 | g0073 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03486 | hp1 | a0002 | c0002 | t0003 | g0149 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03490 | hp1 | a0002 | c0002 | t0003 | g0004 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03490 | hp2 | a0003 | c0003 | t0003 | g0364 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0004 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03492 | hp2 | a0003 | c0003 | t0003 | g0363 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0142 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03654 | hp2 | a0003 | c0003 | t0003 | g0323 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03669 | hp1 | a0002 | c0002 | t0003 | g0107 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03704 | hp1 | a0003 | c0003 | t0003 | g0212 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03704 | hp2 | a0002 | c0002 | t0004 | g0129 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03710 | hp1 | a0006 | c0006 | t0004 | g0095 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0333 | SAS | BEB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03927 | hp2 | a0005 | c0005 | t0003 | g0179 | SAS | BEB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0161 | SAS | STU | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG04115 | hp2 | a0003 | c0003 | t0003 | g0337 | SAS | STU | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0090 | SAS | STU | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0102 | SAS | STU | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG04204 | hp1 | a0003 | c0003 | t0003 | g0361 | SAS | STU | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0060 | SAS | STU | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0178 | SAS | STU | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG04228 | hp2 | a0005 | c0005 | t0003 | g0232 | SAS | STU | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0369 | AFR | YRI | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18522 | hp2 | a0006 | c0006 | t0002 | g0147 | AFR | YRI | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | CHB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18612 | hp2 | a0004 | c0004 | t0001 | g0290 | EAS | CHB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | YRI | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18939 | hp1 | a0004 | c0004 | t0001 | g0302 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18940 | hp2 | a0004 | c0004 | t0004 | g0301 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18941 | hp2 | a0004 | c0004 | t0001 | g0300 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0344 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18944 | hp2 | a0003 | c0003 | t0003 | g0339 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18945 | hp1 | a0003 | c0003 | t0003 | g0215 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18947 | hp1 | a0009 | c0009 | t0001 | g0304 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18947 | hp2 | a0003 | c0003 | t0003 | g0234 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18951 | hp1 | a0003 | c0003 | t0003 | g0358 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18953 | hp1 | a0003 | c0003 | t0003 | g0246 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18954 | hp2 | a0004 | c0004 | t0001 | g0306 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18956 | hp1 | a0020 | c0017 | t0001 | g0112 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18956 | hp2 | a0012 | c0012 | t0003 | g0164 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18957 | hp1 | a0010 | c0010 | t0001 | g0113 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18959 | hp2 | a0003 | c0003 | t0003 | g0334 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18961 | hp1 | a0003 | c0003 | t0003 | g0220 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18962 | hp1 | a0003 | c0003 | t0003 | g0231 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18964 | hp1 | a0004 | c0004 | t0001 | g0027 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18964 | hp2 | a0003 | c0003 | t0003 | g0226 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18965 | hp2 | a0003 | c0003 | t0003 | g0287 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18967 | hp2 | a0003 | c0003 | t0003 | g0355 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18973 | hp2 | a0003 | c0003 | t0003 | g0340 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18977 | hp2 | a0004 | c0004 | t0001 | g0028 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18979 | hp1 | a0008 | c0008 | t0003 | g0316 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18979 | hp2 | a0005 | c0005 | t0003 | g0119 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18981 | hp2 | a0003 | c0023 | t0003 | g0335 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18982 | hp1 | a0002 | c0002 | t0004 | g0289 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18983 | hp1 | a0002 | c0002 | t0004 | g0167 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18983 | hp2 | a0003 | c0003 | t0003 | g0245 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18985 | hp2 | a0008 | c0008 | t0001 | g0359 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18989 | hp1 | a0003 | c0003 | t0003 | g0342 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18990 | hp1 | a0004 | c0004 | t0001 | g0288 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18991 | hp1 | a0004 | c0004 | t0001 | g0207 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18991 | hp2 | a0010 | c0010 | t0001 | g0067 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18993 | hp2 | a0003 | c0003 | t0003 | g0362 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA18997 | hp2 | a0002 | c0002 | t0004 | g0274 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19002 | hp1 | a0004 | c0004 | t0001 | g0311 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19006 | hp2 | a0011 | c0011 | t0002 | g0354 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19009 | hp1 | a0002 | c0002 | t0010 | g0356 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19009 | hp2 | a0005 | c0005 | t0003 | g0166 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19011 | hp1 | a0008 | c0008 | t0003 | g0351 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | LWK | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | LWK | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | LWK | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | LWK | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19055 | hp1 | a0003 | c0003 | t0003 | g0357 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19055 | hp2 | a0001 | c0022 | t0001 | g0343 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19059 | hp1 | a0004 | c0004 | t0001 | g0298 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19062 | hp1 | a0008 | c0008 | t0003 | g0352 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19062 | hp2 | a0012 | c0012 | t0003 | g0105 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19063 | hp2 | a0008 | c0008 | t0003 | g0353 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19064 | hp2 | a0004 | c0004 | t0002 | g0319 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19065 | hp2 | a0003 | c0003 | t0003 | g0223 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19066 | hp1 | a0003 | c0003 | t0003 | g0235 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19066 | hp2 | a0003 | c0003 | t0003 | g0341 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19068 | hp1 | a0003 | c0003 | t0003 | g0349 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19074 | hp1 | a0021 | c0020 | t0001 | g0209 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19074 | hp2 | a0003 | c0003 | t0003 | g0346 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19076 | hp2 | a0004 | c0004 | t0001 | g0299 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19077 | hp1 | a0005 | c0005 | t0003 | g0124 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19077 | hp2 | a0003 | c0003 | t0003 | g0239 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19080 | hp1 | a0004 | c0004 | t0004 | g0022 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19082 | hp1 | a0005 | c0005 | t0003 | g0084 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19084 | hp1 | a0003 | c0003 | t0003 | g0253 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19088 | hp2 | a0004 | c0004 | t0001 | g0309 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19090 | hp1 | a0010 | c0010 | t0001 | g0114 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19090 | hp2 | a0002 | c0002 | t0004 | g0312 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA20129 | hp1 | a0005 | c0005 | t0003 | g0282 | AFR | ASW | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA20129 | hp2 | a0022 | c0026 | t0004 | g0372 | AFR | ASW | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA20805 | hp1 | a0007 | c0007 | t0004 | g0267 | EUR | TSI | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA20805 | hp2 | a0007 | c0007 | t0004 | g0243 | EUR | TSI | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0163 | SAS | GIH | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA20905 | hp2 | a0003 | c0003 | t0003 | g0045 | SAS | GIH | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01123 | hp1 | a0006 | c0006 | t0004 | g0100 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0203 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | MSL | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | USA | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| HG06807 | hp2 | a0005 | c0005 | t0003 | g0074 | AFR | USA | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA20300 | hp1 | a0003 | c0003 | t0003 | g0330 | AFR | USA | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0367 | AFR | USA | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0009 | g0219 | REF | REF | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0128 | REF | REF | C7_chr5_40904497_40989643 | C7 | chr5 | 40904497 | 40989643 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:40934334 | C | T | 1 | a0013 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.148C>T | p.Arg50Trp | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/18 | 262/5716 | 148/2532 | 50/843 | chr5 | 40934334 | |||
| chr5:40936439 | T | C | 3 | a0008 a0009 a0011 |
12 | HG01928.hp1 HG01981.hp1 HG02004.hp1 others(9): Show |
missense_variant | MODERATE | c.382T>C | p.Cys128Arg | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/18 | 496/5716 | 382/2532 | 128/843 | chr5 | 40936439 | |||
| chr5:40945295 | G | A | 2 | a0004 a0015 |
24 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(21): Show |
missense_variant | MODERATE | c.665G>A | p.Arg222His | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/18 | 779/5716 | 665/2532 | 222/843 | chr5 | 40945295 | |||
| chr5:40945322 | C | G | 1 | a0017 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.692C>G | p.Ser231Cys | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/18 | 806/5716 | 692/2532 | 231/843 | chr5 | 40945322 | |||
| chr5:40955459 | G | C | 11 | a0002 a0005 a0006 others(8): Show |
156 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(153): Show |
missense_variant | MODERATE | c.1166G>C | p.Ser389Thr | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/18 | 1280/5716 | 1166/2532 | 389/843 | chr5 | 40955459 | |||
| chr5:40955497 | C | T | 1 | a0016 | 1 | HG01261.hp2 | stop_gained | HIGH | c.1204C>T | p.Arg402* | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/18 | 1318/5716 | 1204/2532 | 402/843 | chr5 | 40955497 | |||
| chr5:40955551 | A | C | 2 | a0010 a0012 |
5 | NA18956.hp2 NA18957.hp1 NA18991.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.1258A>C | p.Lys420Gln | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/18 | 1372/5716 | 1258/2532 | 420/843 | chr5 | 40955551 | |||
| chr5:40958187 | A | G | 1 | a0022 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1415A>G | p.His472Arg | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/18 | 1529/5716 | 1415/2532 | 472/843 | chr5 | 40958187 | |||
| chr5:40959521 | G | A | 2 | a0020 a0021 |
2 | NA18956.hp1 NA19074.hp1 |
missense_variant | MODERATE | c.1562G>A | p.Arg521His | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/18 | 1676/5716 | 1562/2532 | 521/843 | chr5 | 40959521 | |||
| chr5:40962099 | A | G | 1 | a0019 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1676A>G | p.His559Arg | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/18 | 1790/5716 | 1676/2532 | 559/843 | chr5 | 40962099 | |||
| chr5:40964750 | A | C | 5 | a0003 a0005 a0008 others(2): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
missense_variant | MODERATE | c.1759A>C | p.Thr587Pro | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/18 | 1873/5716 | 1759/2532 | 587/843 | chr5 | 40964750 | |||
| chr5:40964783 | A | T | 3 | a0006 a0007 a0017 |
18 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(15): Show |
missense_variant | MODERATE | c.1792A>T | p.Thr598Ser | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/18 | 1906/5716 | 1792/2532 | 598/843 | chr5 | 40964783 | |||
| chr5:40972432 | G | A | 1 | a0018 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1912G>A | p.Asp638Asn | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/18 | 2026/5716 | 1912/2532 | 638/843 | chr5 | 40972432 | |||
| chr5:40972528 | G | A | 1 | a0014 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.2008G>A | p.Ala670Thr | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/18 | 2122/5716 | 2008/2532 | 670/843 | chr5 | 40972528 | |||
| chr5:40982040 | AAGAGGAC others(3395): Show |
A | 1 | a0002 | 1 | NA19009.hp1 | splice_region_variant | LOW | c.*471_*3872del | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 40982040 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:40934369 | G | A | 1 | a0005c0013 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.183G>A | p.Gln61Gln | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/18 | 297/5716 | 183/2532 | 61/843 | chr5 | 40934369 | |||
| chr5:40958113 | G | A | 1 | a0006c0016 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1341G>A | p.Glu447Glu | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/18 | 1455/5716 | 1341/2532 | 447/843 | chr5 | 40958113 | |||
| chr5:40959564 | C | T | 1 | a0001c0025 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.1605C>T | p.Cys535Cys | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/18 | 1719/5716 | 1605/2532 | 535/843 | chr5 | 40959564 | |||
| chr5:40972470 | A | C | 1 | a0003c0023 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.1950A>C | p.Thr650Thr | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/18 | 2064/5716 | 1950/2532 | 650/843 | chr5 | 40972470 | |||
| chr5:40976832 | C | T | 1 | a0004c0014 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.2157C>T | p.Tyr719Tyr | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/18 | 2271/5716 | 2157/2532 | 719/843 | chr5 | 40976832 | |||
| chr5:40979827 | C | G | 1 | a0001c0022 | 1 | NA19055.hp2 | synonymous_variant | LOW | c.2268C>G | p.Thr756Thr | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/18 | 2382/5716 | 2268/2532 | 756/843 | chr5 | 40979827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:40909531 | T | A | 1 | a0001c0001t0007 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-80T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/18 | 80 | chr5 | 40909531 | ||||||
| chr5:40909532 | C | T | 1 | a0001c0001t0007 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/18 | 79 | chr5 | 40909532 | ||||||
| chr5:40909592 | C | T | 3 | a0001c0001t0005 a0001c0001t0012 a0001c0025t0011 |
5 | HG02630.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-19C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/18 | 19 | chr5 | 40909592 | ||||||
| chr5:40981587 | C | A | 21 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(18): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*14C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 14 | chr5 | 40981587 | ||||||
| chr5:40981666 | CCTT | C | 11 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(8): Show |
96 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*99_*101delTCT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 99 | INFO_REALIGN_3_PRIME | chr5 | 40981666 | |||||
| chr5:40981825 | A | G | 2 | a0006c0006t0006 a0007c0007t0006 |
2 | HG00735.hp2 HG01361.hp1 |
3_prime_UTR_variant | MODIFIER | c.*252A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 252 | chr5 | 40981825 | ||||||
| chr5:40981929 | T | C | 11 | a0001c0001t0004 a0001c0001t0008 a0001c0025t0011 others(8): Show |
65 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*356T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 356 | chr5 | 40981929 | ||||||
| chr5:40981945 | T | C | 1 | a0001c0001t0008 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 372 | chr5 | 40981945 | ||||||
| chr5:40982073 | T | C | 12 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0012 others(9): Show |
97 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*500T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 500 | chr5 | 40982073 | ||||||
| chr5:40982097 | C | T | 1 | a0001c0001t0002 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*524C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 524 | chr5 | 40982097 | ||||||
| chr5:40982126 | C | T | 1 | a0001c0001t0002 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 553 | chr5 | 40982126 | ||||||
| chr5:40982197 | G | A | 1 | a0006c0006t0004 | 2 | HG01123.hp1 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*624G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 624 | chr5 | 40982197 | ||||||
| chr5:40982317 | C | CATTTTTT others(181): Show |
1 | a0003c0003t0003 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*750_*751insTTTTTT others(182): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 751 | INFO_REALIGN_3_PRIME | chr5 | 40982317 | |||||
| chr5:40982332 | T | C | 1 | a0003c0003t0003 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*759T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 759 | chr5 | 40982332 | ||||||
| chr5:40982354 | C | T | 9 | a0001c0001t0003 a0002c0002t0003 a0003c0003t0003 others(6): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*781C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 781 | chr5 | 40982354 | ||||||
| chr5:40982358 | C | T | 9 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(6): Show |
67 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*785C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 785 | chr5 | 40982358 | ||||||
| chr5:40982386 | C | T | 1 | a0001c0001t0002 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*813C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 813 | chr5 | 40982386 | ||||||
| chr5:40982387 | G | A | 3 | a0001c0022t0001 a0002c0002t0001 a0009c0009t0001 |
4 | NA18947.hp1 NA18966.hp1 NA19055.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*814G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 814 | chr5 | 40982387 | ||||||
| chr5:40982388 | C | T | 9 | a0001c0001t0003 a0002c0002t0003 a0003c0003t0003 others(6): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*815C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 815 | chr5 | 40982388 | ||||||
| chr5:40982518 | G | T | 9 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(6): Show |
67 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*945G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 945 | chr5 | 40982518 | ||||||
| chr5:40982520 | G | T | 8 | a0001c0001t0002 a0002c0002t0002 a0004c0004t0002 others(5): Show |
65 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*947G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 947 | chr5 | 40982520 | ||||||
| chr5:40982678 | A | G | 11 | a0001c0001t0004 a0001c0001t0008 a0001c0025t0011 others(8): Show |
65 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1105A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 1105 | chr5 | 40982678 | ||||||
| chr5:40982796 | G | T | 1 | a0002c0002t0001 | 7 | HG00597.hp1 HG02027.hp2 HG02056.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1223G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 1223 | chr5 | 40982796 | ||||||
| chr5:40982875 | A | G | 8 | a0001c0001t0002 a0002c0002t0002 a0004c0004t0002 others(5): Show |
65 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1302A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 1302 | chr5 | 40982875 | ||||||
| chr5:40982955 | G | T | 5 | a0006c0006t0004 a0006c0006t0006 a0006c0016t0004 others(2): Show |
16 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1382G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 1382 | chr5 | 40982955 | ||||||
| chr5:40982989 | T | G | 12 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(9): Show |
85 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1416T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 1416 | chr5 | 40982989 | ||||||
| chr5:40983196 | A | T | 1 | a0001c0001t0001 | 2 | HG02723.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1623A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 1623 | chr5 | 40983196 | ||||||
| chr5:40983334 | G | A | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(9): Show |
64 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1761G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 1761 | chr5 | 40983334 | ||||||
| chr5:40983425 | G | C | 11 | a0001c0001t0004 a0001c0001t0008 a0001c0025t0011 others(8): Show |
64 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1852G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 1852 | chr5 | 40983425 | ||||||
| chr5:40983460 | G | T | 1 | a0002c0002t0004 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1887G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 1887 | chr5 | 40983460 | ||||||
| chr5:40983546 | A | T | 1 | a0001c0001t0002 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1973A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 1973 | chr5 | 40983546 | ||||||
| chr5:40983685 | A | G | 1 | a0001c0001t0002 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2112A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2112 | chr5 | 40983685 | ||||||
| chr5:40983698 | A | AAAAATGT others(12): Show |
1 | a0001c0001t0004 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2131_*2149dupGTTT others(15): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2150 | INFO_REALIGN_3_PRIME | chr5 | 40983698 | |||||
| chr5:40983707 | T | G | 1 | a0001c0001t0004 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2134T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2134 | chr5 | 40983707 | ||||||
| chr5:40983806 | A | C | 21 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0012 others(18): Show |
150 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*2233A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2233 | chr5 | 40983806 | ||||||
| chr5:40983808 | A | G | 21 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0012 others(18): Show |
150 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*2235A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2235 | chr5 | 40983808 | ||||||
| chr5:40984005 | T | C | 2 | a0006c0006t0002 a0017c0027t0002 |
2 | HG02145.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2432T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2432 | chr5 | 40984005 | ||||||
| chr5:40984040 | C | T | 2 | a0006c0006t0002 a0017c0027t0002 |
2 | HG02145.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2467C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2467 | chr5 | 40984040 | ||||||
| chr5:40984184 | G | T | 3 | a0001c0001t0003 a0001c0001t0005 a0002c0002t0003 |
9 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2611G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2611 | chr5 | 40984184 | ||||||
| chr5:40984199 | A | G | 1 | a0001c0001t0001 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2626A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2626 | chr5 | 40984199 | ||||||
| chr5:40984413 | C | T | 2 | a0001c0001t0002 a0002c0002t0002 |
4 | HG03927.hp1 HG04115.hp1 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2840C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2840 | chr5 | 40984413 | ||||||
| chr5:40984485 | C | A | 1 | a0001c0001t0002 | 5 | HG01346.hp1 HG02055.hp2 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2912C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 18/18 | 2912 | chr5 | 40984485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:40909647 | T | A | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6+31T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40909647 | |||||||
| chr5:40909648 | G | T | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6+32G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40909648 | |||||||
| chr5:40909695 | C | T | 3 | a0001c0001t0004g0371 a0001c0001t0004g0373 a0022c0026t0004g0372 |
3 | HG01358.hp2 HG02148.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.6+79C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40909695 | |||||||
| chr5:40909717 | G | C | 6 | a0001c0001t0001g0011 a0001c0001t0002g0008 a0001c0001t0004g0002 others(3): Show |
7 | NA18971.hp2 NA18992.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+101G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40909717 | |||||||
| chr5:40909728 | A | C | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.6+112A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40909728 | |||||||
| chr5:40909911 | TAA | T | 5 | a0001c0001t0005g0367 a0001c0001t0005g0368 a0001c0001t0005g0369 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+297_6+298delAA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40909911 | ||||||
| chr5:40909912 | A | C | 2 | a0003c0003t0003g0361 a0003c0003t0003g0363 |
2 | HG03492.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.6+296A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40909912 | |||||||
| chr5:40909919 | TAAAG | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(76): Show |
80 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.6+307_6+310delGAAA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40909919 | ||||||
| chr5:40909974 | A | AT | 149 | a0001c0001t0001g0006 a0001c0001t0001g0210 a0001c0001t0001g0211 others(146): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.6+376dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40909974 | ||||||
| chr5:40909974 | A | ATT | 11 | a0001c0001t0001g0011 a0001c0001t0002g0277 a0001c0001t0002g0278 others(8): Show |
11 | HG00735.hp2 HG01175.hp2 HG03490.hp2 others(8): Show |
intron_variant | MODIFIER | c.6+375_6+376dupTT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40909974 | ||||||
| chr5:40909974 | A | ATTT | 12 | a0001c0001t0002g0284 a0001c0001t0003g0283 a0001c0001t0003g0285 others(9): Show |
12 | HG01192.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+374_6+376dupTTT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40909974 | ||||||
| chr5:40909974 | AT | A | 8 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0003g0020 others(5): Show |
8 | HG01169.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+376delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40909974 | ||||||
| chr5:40910006 | A | C | 17 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(14): Show |
17 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+390A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910006 | |||||||
| chr5:40910263 | G | A | 26 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(23): Show |
26 | HG00408.hp1 HG00597.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.6+647G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910263 | |||||||
| chr5:40910277 | A | T | 1 | a0003c0003t0003g0358 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.6+661A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910277 | |||||||
| chr5:40910311 | A | G | 1 | a0001c0001t0003g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6+695A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910311 | |||||||
| chr5:40910392 | T | C | 108 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(105): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.6+776T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910392 | |||||||
| chr5:40910435 | T | C | 88 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(85): Show |
89 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.6+819T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910435 | |||||||
| chr5:40910490 | T | C | 1 | a0004c0004t0001g0021 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6+874T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910490 | |||||||
| chr5:40910515 | T | C | 1 | a0003c0003t0003g0029 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6+899T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910515 | |||||||
| chr5:40910523 | T | G | 78 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(75): Show |
79 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.6+907T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910523 | |||||||
| chr5:40910603 | A | T | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+987A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910603 | |||||||
| chr5:40910666 | C | T | 1 | a0002c0002t0010g0356 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6+1050C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910666 | |||||||
| chr5:40910693 | AT | A | 26 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(23): Show |
26 | HG00408.hp1 HG00597.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.6+1082delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40910693 | ||||||
| chr5:40910791 | C | CA | 91 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(88): Show |
92 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.6+1189dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40910791 | ||||||
| chr5:40910804 | AAC | A | 14 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(11): Show |
14 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.6+1190_6+1191delCA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40910804 | ||||||
| chr5:40910805 | AC | A | 8 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(5): Show |
8 | HG01361.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+1190delC | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910805 | |||||||
| chr5:40910806 | C | A | 1 | a0011c0011t0002g0354 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.6+1190C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910806 | |||||||
| chr5:40910807 | A | C | 14 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(11): Show |
14 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.6+1191A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910807 | |||||||
| chr5:40910808 | A | C | 8 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(5): Show |
8 | HG01361.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+1192A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910808 | |||||||
| chr5:40910869 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+1253C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40910869 | |||||||
| chr5:40911000 | C | G | 1 | a0003c0003t0003g0262 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.6+1384C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911000 | |||||||
| chr5:40911019 | C | T | 1 | a0018c0018t0002g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6+1403C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911019 | |||||||
| chr5:40911194 | T | C | 17 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(14): Show |
17 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+1578T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911194 | |||||||
| chr5:40911490 | C | T | 306 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(303): Show |
312 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.6+1874C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911490 | |||||||
| chr5:40911495 | C | A | 26 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(23): Show |
26 | HG00408.hp1 HG00597.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.6+1879C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911495 | |||||||
| chr5:40911632 | T | G | 1 | a0001c0001t0002g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6+2016T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911632 | |||||||
| chr5:40911740 | C | CT | 105 | a0001c0001t0001g0006 a0001c0001t0001g0066 a0001c0001t0001g0322 others(102): Show |
106 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.6+2140dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40911740 | ||||||
| chr5:40911740 | CT | C | 10 | a0001c0001t0001g0370 a0001c0001t0002g0032 a0002c0002t0001g0068 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.6+2140delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40911740 | ||||||
| chr5:40911777 | T | C | 370 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(367): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.6+2161T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911777 | |||||||
| chr5:40911802 | G | C | 2 | a0002c0002t0001g0136 a0002c0002t0001g0137 |
2 | HG00621.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.6+2186G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911802 | |||||||
| chr5:40911837 | C | T | 3 | a0008c0008t0003g0351 a0008c0008t0003g0352 a0008c0008t0003g0353 |
3 | NA19011.hp1 NA19062.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.6+2221C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911837 | |||||||
| chr5:40911884 | G | A | 7 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0004g0202 others(4): Show |
7 | HG01361.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+2268G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911884 | |||||||
| chr5:40911887 | C | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0322 others(89): Show |
93 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.6+2271C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911887 | |||||||
| chr5:40911888 | G | A | 7 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0004g0202 others(4): Show |
7 | HG01361.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+2272G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911888 | |||||||
| chr5:40911913 | A | AT | 8 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(5): Show |
8 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+2313dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40911913 | ||||||
| chr5:40911994 | T | C | 344 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(341): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.6+2378T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911994 | |||||||
| chr5:40911995 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+2379G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911995 | |||||||
| chr5:40911999 | T | C | 26 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(23): Show |
26 | HG00408.hp1 HG00597.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.6+2383T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40911999 | |||||||
| chr5:40912051 | C | T | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+2435C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912051 | |||||||
| chr5:40912099 | T | C | 1 | a0004c0004t0004g0022 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.6+2483T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912099 | |||||||
| chr5:40912503 | T | C | 17 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(14): Show |
17 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+2887T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912503 | |||||||
| chr5:40912513 | G | A | 10 | a0001c0001t0002g0205 a0001c0001t0002g0284 a0001c0001t0003g0283 others(7): Show |
10 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+2897G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912513 | |||||||
| chr5:40912527 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+2911C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912527 | |||||||
| chr5:40912565 | A | G | 26 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(23): Show |
26 | HG00408.hp1 HG00597.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.6+2949A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912565 | |||||||
| chr5:40912566 | A | ACAAGGTC others(13): Show |
17 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(14): Show |
17 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+2952_6+2953insAG others(18): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40912566 | ||||||
| chr5:40912608 | T | C | 17 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(14): Show |
17 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+2992T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912608 | |||||||
| chr5:40912709 | T | G | 309 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(306): Show |
315 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.6+3093T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912709 | |||||||
| chr5:40912713 | C | T | 1 | a0001c0001t0005g0369 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6+3097C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912713 | |||||||
| chr5:40912874 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.6+3258G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912874 | |||||||
| chr5:40912889 | G | T | 1 | a0001c0001t0002g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6+3273G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912889 | |||||||
| chr5:40912964 | T | G | 1 | a0001c0001t0002g0063 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6+3348T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912964 | |||||||
| chr5:40912976 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+3360C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40912976 | |||||||
| chr5:40913099 | T | C | 17 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(14): Show |
17 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+3483T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913099 | |||||||
| chr5:40913172 | A | G | 17 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(14): Show |
17 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+3556A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913172 | |||||||
| chr5:40913359 | G | C | 1 | a0001c0025t0011g0366 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6+3743G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913359 | |||||||
| chr5:40913508 | A | G | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | NA19056.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.6+3892A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913508 | |||||||
| chr5:40913520 | T | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(119): Show |
123 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.6+3904T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913520 | |||||||
| chr5:40913620 | G | T | 17 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(14): Show |
17 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+4004G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913620 | |||||||
| chr5:40913644 | G | A | 1 | a0001c0001t0004g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6+4028G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913644 | |||||||
| chr5:40913659 | A | AAT | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+4054_6+4055dupAT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40913659 | ||||||
| chr5:40913698 | A | G | 17 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(14): Show |
17 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+4082A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913698 | |||||||
| chr5:40913710 | T | C | 17 | a0001c0001t0002g0007 a0001c0001t0002g0205 a0001c0001t0002g0275 others(14): Show |
17 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.6+4094T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913710 | |||||||
| chr5:40913743 | G | T | 112 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(109): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.6+4127G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913743 | |||||||
| chr5:40913773 | G | A | 3 | a0002c0002t0003g0198 a0002c0002t0003g0199 a0002c0002t0003g0200 |
3 | HG02257.hp2 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.6+4157G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913773 | |||||||
| chr5:40913824 | T | A | 1 | a0004c0004t0001g0288 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.6+4208T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913824 | |||||||
| chr5:40913840 | T | C | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+4224T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913840 | |||||||
| chr5:40913926 | G | A | 10 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0002g0140 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+4310G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913926 | |||||||
| chr5:40913974 | C | T | 1 | a0002c0002t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6+4358C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40913974 | |||||||
| chr5:40914037 | T | C | 1 | a0002c0002t0004g0289 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6+4421T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914037 | |||||||
| chr5:40914043 | G | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+4427G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914043 | |||||||
| chr5:40914094 | G | A | 1 | a0012c0012t0003g0105 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.6+4478G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914094 | |||||||
| chr5:40914224 | C | A | 36 | a0001c0001t0001g0370 a0002c0002t0001g0015 a0002c0002t0001g0075 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.6+4608C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914224 | |||||||
| chr5:40914254 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+4638A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914254 | |||||||
| chr5:40914289 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+4673C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914289 | |||||||
| chr5:40914328 | T | C | 109 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(106): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.6+4712T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914328 | |||||||
| chr5:40914537 | T | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(119): Show |
123 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.6+4921T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914537 | |||||||
| chr5:40914542 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0014 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6+4926C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914542 | |||||||
| chr5:40914622 | T | C | 1 | a0002c0002t0003g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6+5006T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914622 | |||||||
| chr5:40914651 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+5035G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914651 | |||||||
| chr5:40914752 | T | C | 248 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(245): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.6+5136T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914752 | |||||||
| chr5:40914890 | A | G | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+5274A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914890 | |||||||
| chr5:40914937 | A | G | 8 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0007c0007t0004g0264 others(5): Show |
8 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+5321A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40914937 | |||||||
| chr5:40915063 | G | A | 53 | a0001c0001t0002g0154 a0002c0002t0001g0018 a0002c0002t0001g0019 others(50): Show |
54 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.6+5447G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915063 | |||||||
| chr5:40915221 | C | T | 1 | a0002c0002t0003g0149 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6+5605C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915221 | |||||||
| chr5:40915226 | A | G | 3 | a0005c0005t0003g0280 a0005c0005t0003g0281 a0005c0005t0003g0282 |
3 | HG01192.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.6+5610A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915226 | |||||||
| chr5:40915339 | G | A | 1 | a0001c0001t0007g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.6+5723G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915339 | |||||||
| chr5:40915340 | C | T | 1 | a0001c0001t0007g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.6+5724C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915340 | |||||||
| chr5:40915354 | A | AC | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+5741dupC | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40915354 | ||||||
| chr5:40915397 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+5781G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915397 | |||||||
| chr5:40915435 | G | A | 4 | a0002c0002t0001g0150 a0002c0002t0001g0151 a0002c0002t0001g0152 others(1): Show |
4 | HG02155.hp1 NA18944.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+5819G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915435 | |||||||
| chr5:40915520 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+5904C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915520 | |||||||
| chr5:40915545 | AC | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+5930delC | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915545 | |||||||
| chr5:40915552 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+5936G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915552 | |||||||
| chr5:40915588 | C | T | 8 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(5): Show |
8 | HG01361.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+5972C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915588 | |||||||
| chr5:40915612 | C | T | 13 | a0001c0001t0002g0205 a0001c0001t0002g0284 a0001c0001t0003g0283 others(10): Show |
13 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.6+5996C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915612 | |||||||
| chr5:40915619 | G | A | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+6003G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915619 | |||||||
| chr5:40915629 | C | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6013C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915629 | |||||||
| chr5:40915673 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6057G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915673 | |||||||
| chr5:40915753 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6137A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915753 | |||||||
| chr5:40915766 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6150G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915766 | |||||||
| chr5:40915845 | G | T | 1 | a0001c0001t0002g0061 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.6+6229G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915845 | |||||||
| chr5:40915850 | G | A | 3 | a0005c0005t0003g0280 a0005c0005t0003g0281 a0005c0005t0003g0282 |
3 | HG01192.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.6+6234G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40915850 | |||||||
| chr5:40916015 | G | T | 1 | a0001c0001t0004g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6+6399G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916015 | |||||||
| chr5:40916016 | G | A | 1 | a0001c0001t0004g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6+6400G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916016 | |||||||
| chr5:40916021 | ATTTGATA others(3): Show |
A | 1 | a0001c0001t0005g0367 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6+6408_6+6417delTG others(8): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40916021 | ||||||
| chr5:40916026 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6410A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916026 | |||||||
| chr5:40916084 | C | CAGTTAAA others(16): Show |
10 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0002g0140 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+6490_6+6491insGA others(21): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40916084 | ||||||
| chr5:40916122 | A | C | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6506A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916122 | |||||||
| chr5:40916212 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6596A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916212 | |||||||
| chr5:40916279 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6663G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916279 | |||||||
| chr5:40916326 | C | T | 8 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(5): Show |
8 | HG01361.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+6710C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916326 | |||||||
| chr5:40916342 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6726A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916342 | |||||||
| chr5:40916350 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6+6734C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916350 | |||||||
| chr5:40916462 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+6846A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916462 | |||||||
| chr5:40916511 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6+6895G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916511 | |||||||
| chr5:40916534 | C | T | 5 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0004g0017 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+6918C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916534 | |||||||
| chr5:40916563 | G | C | 221 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(218): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.6+6947G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916563 | |||||||
| chr5:40916583 | G | A | 87 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(84): Show |
88 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.6+6967G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916583 | |||||||
| chr5:40916642 | T | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(76): Show |
80 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.6+7026T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916642 | |||||||
| chr5:40916713 | T | A | 1 | a0003c0003t0003g0212 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6+7097T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916713 | |||||||
| chr5:40916714 | T | A | 88 | a0001c0001t0001g0011 a0001c0001t0001g0066 a0001c0001t0001g0194 others(85): Show |
92 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.6+7098T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916714 | |||||||
| chr5:40916715 | T | A | 180 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(177): Show |
184 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.6+7099T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916715 | |||||||
| chr5:40916817 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+7201A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916817 | |||||||
| chr5:40916866 | T | C | 1 | a0004c0004t0001g0290 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.6+7250T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40916866 | |||||||
| chr5:40916998 | G | GTTGGC | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+7383_6+7387dupTT others(3): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40916998 | ||||||
| chr5:40917004 | G | T | 7 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(4): Show |
7 | HG01978.hp1 NA18960.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+7388G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917004 | |||||||
| chr5:40917109 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6+7493T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917109 | |||||||
| chr5:40917121 | C | T | 1 | a0001c0001t0003g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6+7505C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917121 | |||||||
| chr5:40917128 | C | A | 4 | a0002c0002t0001g0049 a0005c0005t0003g0280 a0005c0005t0003g0281 others(1): Show |
4 | HG01192.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+7512C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917128 | |||||||
| chr5:40917134 | C | CAAA | 87 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(84): Show |
88 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.6+7530_6+7532dupAA others(1): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40917134 | ||||||
| chr5:40917142 | A | G | 1 | a0002c0002t0002g0188 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.6+7526A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917142 | |||||||
| chr5:40917176 | A | C | 1 | a0001c0001t0002g0269 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.6+7560A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917176 | |||||||
| chr5:40917223 | A | G | 22 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0002g0205 others(19): Show |
22 | HG01192.hp1 HG01361.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.6+7607A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917223 | |||||||
| chr5:40917266 | A | C | 1 | a0004c0004t0002g0319 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.6+7650A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917266 | |||||||
| chr5:40917307 | TCTTTA | T | 6 | a0002c0002t0001g0291 a0002c0002t0001g0292 a0002c0002t0001g0293 others(3): Show |
6 | HG00597.hp1 HG02027.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+7695_6+7699delTA others(3): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40917307 | ||||||
| chr5:40917346 | A | G | 22 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0002g0205 others(19): Show |
22 | HG01192.hp1 HG01361.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.6+7730A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917346 | |||||||
| chr5:40917447 | G | A | 1 | a0001c0001t0003g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6+7831G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917447 | |||||||
| chr5:40917648 | G | A | 1 | a0001c0001t0012g0365 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.6+8032G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917648 | |||||||
| chr5:40917844 | T | G | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0050 others(7): Show |
10 | HG01109.hp1 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+8228T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917844 | |||||||
| chr5:40917896 | C | T | 4 | a0002c0002t0002g0016 a0002c0002t0002g0125 a0002c0002t0002g0126 others(1): Show |
4 | NA18959.hp1 NA18982.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+8280C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917896 | |||||||
| chr5:40917933 | T | A | 1 | a0002c0002t0002g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6+8317T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917933 | |||||||
| chr5:40917940 | C | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.6+8324C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40917940 | |||||||
| chr5:40918112 | C | A | 7 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0004g0202 others(4): Show |
7 | HG01361.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+8496C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918112 | |||||||
| chr5:40918113 | G | A | 1 | a0007c0007t0004g0265 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.6+8497G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918113 | |||||||
| chr5:40918163 | C | T | 4 | a0002c0002t0001g0049 a0005c0005t0003g0280 a0005c0005t0003g0281 others(1): Show |
4 | HG01192.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+8547C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918163 | |||||||
| chr5:40918230 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6+8614G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918230 | |||||||
| chr5:40918275 | A | T | 1 | a0001c0001t0012g0365 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.6+8659A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918275 | |||||||
| chr5:40918311 | G | T | 1 | a0005c0005t0003g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6+8695G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918311 | |||||||
| chr5:40918350 | T | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.6+8734T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918350 | |||||||
| chr5:40918379 | CACAACAA others(17): Show |
C | 1 | a0003c0003t0003g0350 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.6+8776_6+8799delAC others(22): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918379 | ||||||
| chr5:40918384 | C | A | 22 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0002g0205 others(19): Show |
22 | HG01192.hp1 HG01361.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.6+8768C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918384 | |||||||
| chr5:40918527 | G | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.6+8911G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918527 | |||||||
| chr5:40918537 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+8921C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918537 | |||||||
| chr5:40918613 | C | T | 1 | a0003c0003t0003g0364 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.6+8997C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918613 | |||||||
| chr5:40918686 | G | T | 1 | a0009c0009t0001g0318 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.6+9070G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918686 | |||||||
| chr5:40918687 | T | TA | 23 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0002g0205 others(20): Show |
23 | HG01192.hp1 HG01361.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.6+9082dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918687 | ||||||
| chr5:40918687 | TA | T | 121 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(118): Show |
125 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.6+9082delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918687 | ||||||
| chr5:40918700 | T | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.6+9084T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918700 | |||||||
| chr5:40918819 | G | C | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+9203G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918819 | |||||||
| chr5:40918830 | T | C | 22 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0002g0205 others(19): Show |
22 | HG01192.hp1 HG01361.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.6+9214T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918830 | |||||||
| chr5:40918851 | G | GTATTGCA others(17): Show |
1 | a0001c0001t0002g0213 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.6+9239_6+9240insGC others(22): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918851 | ||||||
| chr5:40918918 | G | A | 2 | a0001c0001t0004g0202 a0001c0001t0004g0203 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.6+9302G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918918 | |||||||
| chr5:40918925 | G | T | 3 | a0003c0003t0003g0287 a0003c0003t0003g0349 a0003c0003t0003g0355 |
3 | NA18965.hp2 NA18967.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.6+9309G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40918925 | |||||||
| chr5:40918949 | G | GAC | 71 | a0001c0001t0001g0011 a0001c0001t0001g0227 a0001c0001t0001g0233 others(68): Show |
72 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.6+9375_6+9376dupCA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | G | GACAC | 68 | a0001c0001t0001g0064 a0001c0001t0001g0194 a0001c0001t0001g0195 others(65): Show |
68 | HG00280.hp1 HG00544.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.6+9373_6+9376dupCA others(2): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | G | GACACAC | 37 | a0001c0001t0001g0066 a0001c0001t0001g0252 a0001c0001t0001g0254 others(34): Show |
41 | HG00280.hp2 HG01346.hp2 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.6+9371_6+9376dupCA others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | G | GACACACA others(1): Show |
13 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0251 others(10): Show |
13 | HG01074.hp2 HG01496.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.6+9369_6+9376dupCA others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | G | GACACACA others(3): Show |
5 | a0001c0001t0002g0154 a0001c0001t0004g0033 a0001c0001t0004g0038 others(2): Show |
5 | HG01515.hp2 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+9367_6+9376dupCA others(8): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | G | GACACACA others(5): Show |
3 | a0001c0001t0004g0037 a0001c0001t0004g0203 a0005c0005t0003g0135 |
3 | HG00741.hp2 HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6+9365_6+9376dupCA others(10): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | G | GACACACA others(7): Show |
5 | a0001c0001t0004g0034 a0001c0001t0004g0035 a0001c0001t0004g0036 others(2): Show |
5 | HG02572.hp2 HG03471.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+9363_6+9376dupCA others(12): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | GAC | G | 24 | a0001c0001t0002g0055 a0001c0001t0003g0285 a0001c0001t0003g0286 others(21): Show |
24 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.6+9375_6+9376delCA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | GACAC | G | 20 | a0002c0002t0001g0110 a0002c0002t0001g0118 a0002c0002t0001g0120 others(17): Show |
20 | HG00558.hp2 HG00673.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.6+9373_6+9376delCA others(2): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | GACACACA others(1): Show |
G | 10 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(7): Show |
10 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+9369_6+9376delCA others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | GACACACA others(3): Show |
G | 6 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(3): Show |
6 | HG01069.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+9367_6+9376delCA others(8): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | GACACACA others(5): Show |
G | 37 | a0002c0002t0001g0291 a0002c0002t0001g0292 a0002c0002t0001g0293 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.6+9365_6+9376delCA others(10): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40918949 | GACACACA others(7): Show |
G | 50 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(47): Show |
51 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.6+9363_6+9376delCA others(12): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40918949 | ||||||
| chr5:40919126 | CTT | C | 111 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(108): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.7-9440_7-9439delTT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40919126 | ||||||
| chr5:40919129 | T | TG | 6 | a0002c0002t0001g0190 a0002c0002t0001g0191 a0002c0002t0002g0159 others(3): Show |
6 | HG02040.hp2 NA19000.hp1 NA19006.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-9451_7-9450insG | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40919129 | |||||||
| chr5:40919270 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-9310G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40919270 | |||||||
| chr5:40919313 | C | T | 1 | a0005c0005t0003g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7-9267C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40919313 | |||||||
| chr5:40919580 | T | A | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7-9000T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40919580 | |||||||
| chr5:40919584 | C | T | 108 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(105): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.7-8996C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40919584 | |||||||
| chr5:40919820 | C | T | 1 | a0005c0005t0003g0084 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.7-8760C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40919820 | |||||||
| chr5:40919873 | T | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-8707T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40919873 | |||||||
| chr5:40920005 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-8575G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920005 | |||||||
| chr5:40920069 | C | A | 5 | a0001c0001t0005g0367 a0001c0001t0005g0368 a0001c0001t0005g0369 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-8511C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920069 | |||||||
| chr5:40920156 | A | G | 2 | a0002c0002t0001g0102 a0005c0005t0003g0103 |
2 | HG01433.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.7-8424A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920156 | |||||||
| chr5:40920232 | CT | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(76): Show |
80 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.7-8347delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920232 | |||||||
| chr5:40920318 | T | C | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-8262T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920318 | |||||||
| chr5:40920329 | C | T | 233 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(230): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.7-8251C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920329 | |||||||
| chr5:40920350 | G | A | 1 | a0002c0002t0002g0181 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.7-8230G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920350 | |||||||
| chr5:40920365 | G | C | 1 | a0004c0004t0001g0297 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.7-8215G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920365 | |||||||
| chr5:40920431 | G | T | 120 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(117): Show |
124 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.7-8149G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920431 | |||||||
| chr5:40920498 | G | A | 1 | a0007c0007t0004g0266 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.7-8082G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920498 | |||||||
| chr5:40920510 | T | C | 1 | a0001c0001t0003g0285 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7-8070T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920510 | |||||||
| chr5:40920536 | T | TA | 34 | a0001c0001t0001g0218 a0001c0001t0001g0227 a0001c0001t0002g0201 others(31): Show |
34 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.7-8026dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40920536 | ||||||
| chr5:40920536 | TA | T | 15 | a0001c0001t0001g0249 a0001c0001t0001g0348 a0001c0001t0002g0054 others(12): Show |
15 | HG00140.hp1 HG01070.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.7-8026delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40920536 | ||||||
| chr5:40920571 | C | T | 1 | a0006c0006t0004g0073 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.7-8009C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920571 | |||||||
| chr5:40920729 | T | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-7851T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920729 | |||||||
| chr5:40920910 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.7-7670G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920910 | |||||||
| chr5:40920970 | A | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-7610A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40920970 | |||||||
| chr5:40921013 | C | T | 1 | a0018c0018t0002g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.7-7567C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921013 | |||||||
| chr5:40921027 | C | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-7553C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921027 | |||||||
| chr5:40921034 | G | C | 87 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(84): Show |
88 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.7-7546G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921034 | |||||||
| chr5:40921049 | C | CA | 12 | a0001c0001t0001g0218 a0001c0001t0001g0224 a0001c0001t0001g0241 others(9): Show |
12 | HG00099.hp1 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.7-7516dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40921049 | ||||||
| chr5:40921049 | C | CAA | 94 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(91): Show |
98 | HG00280.hp1 HG00408.hp2 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.7-7517_7-7516dupAA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40921049 | ||||||
| chr5:40921049 | CA | C | 11 | a0002c0002t0001g0075 a0002c0002t0001g0076 a0002c0002t0001g0077 others(8): Show |
11 | HG01257.hp2 HG01496.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.7-7516delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40921049 | ||||||
| chr5:40921063 | A | T | 109 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(106): Show |
110 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.7-7517A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921063 | |||||||
| chr5:40921064 | A | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(107): Show |
111 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.7-7516A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921064 | |||||||
| chr5:40921064 | A | T | 2 | a0001c0001t0002g0270 a0003c0003t0003g0355 |
2 | NA18967.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7-7516A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921064 | |||||||
| chr5:40921065 | T | G | 2 | a0001c0001t0002g0270 a0003c0003t0003g0355 |
2 | NA18967.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7-7515T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921065 | |||||||
| chr5:40921065 | TG | T | 109 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(106): Show |
110 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.7-7514delG | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921065 | |||||||
| chr5:40921066 | G | A | 1 | a0004c0004t0001g0298 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.7-7514G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921066 | |||||||
| chr5:40921066 | G | T | 2 | a0001c0001t0002g0270 a0003c0003t0003g0355 |
2 | NA18967.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7-7514G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921066 | |||||||
| chr5:40921069 | A | G | 1 | a0004c0004t0001g0298 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.7-7511A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921069 | |||||||
| chr5:40921126 | C | A | 2 | a0001c0001t0004g0038 a0001c0001t0004g0040 |
2 | HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.7-7454C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921126 | |||||||
| chr5:40921168 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-7412C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921168 | |||||||
| chr5:40921361 | C | A | 87 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(84): Show |
88 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.7-7219C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921361 | |||||||
| chr5:40921373 | C | A | 120 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(117): Show |
124 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.7-7207C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921373 | |||||||
| chr5:40921595 | G | A | 234 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(231): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.7-6985G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921595 | |||||||
| chr5:40921599 | T | C | 87 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(84): Show |
88 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.7-6981T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921599 | |||||||
| chr5:40921605 | CA | C | 224 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(221): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.7-6964delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40921605 | ||||||
| chr5:40921605 | CAA | C | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-6965_7-6964delAA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40921605 | ||||||
| chr5:40921637 | G | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-6943G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921637 | |||||||
| chr5:40921642 | C | A | 1 | a0003c0003t0003g0226 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.7-6938C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921642 | |||||||
| chr5:40921689 | C | T | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-6891C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921689 | |||||||
| chr5:40921705 | C | T | 87 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(84): Show |
88 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.7-6875C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921705 | |||||||
| chr5:40921761 | G | T | 22 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0002g0205 others(19): Show |
22 | HG01192.hp1 HG01361.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.7-6819G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921761 | |||||||
| chr5:40921764 | T | C | 87 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(84): Show |
88 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.7-6816T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921764 | |||||||
| chr5:40921773 | A | C | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-6807A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921773 | |||||||
| chr5:40921956 | T | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-6624T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921956 | |||||||
| chr5:40921980 | G | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-6600G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40921980 | |||||||
| chr5:40922006 | C | T | 2 | a0001c0001t0004g0202 a0001c0001t0004g0203 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.7-6574C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922006 | |||||||
| chr5:40922007 | C | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-6573C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922007 | |||||||
| chr5:40922039 | A | AAAAC | 89 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(86): Show |
90 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.7-6513_7-6510dupCA others(2): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922039 | ||||||
| chr5:40922039 | AAAAC | A | 10 | a0001c0001t0002g0007 a0001c0001t0002g0270 a0001c0001t0002g0275 others(7): Show |
10 | HG01257.hp2 HG02148.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.7-6513_7-6510delCA others(2): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922039 | ||||||
| chr5:40922074 | A | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-6506A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922074 | |||||||
| chr5:40922102 | T | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(107): Show |
111 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.7-6478T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922102 | |||||||
| chr5:40922165 | A | C | 1 | a0002c0002t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-6415A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922165 | |||||||
| chr5:40922221 | G | A | 1 | a0002c0002t0001g0291 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.7-6359G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922221 | |||||||
| chr5:40922285 | G | A | 14 | a0002c0002t0001g0075 a0002c0002t0001g0076 a0002c0002t0001g0077 others(11): Show |
14 | HG01070.hp1 HG01257.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-6295G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922285 | |||||||
| chr5:40922296 | A | G | 111 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(108): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.7-6284A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922296 | |||||||
| chr5:40922368 | C | G | 111 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(108): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.7-6212C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922368 | |||||||
| chr5:40922374 | C | CA | 23 | a0001c0001t0001g0348 a0001c0001t0002g0201 a0001c0001t0002g0204 others(20): Show |
23 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.7-6179dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922374 | ||||||
| chr5:40922374 | C | CAA | 47 | a0001c0001t0001g0006 a0001c0001t0001g0324 a0001c0001t0001g0325 others(44): Show |
48 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.7-6180_7-6179dupAA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922374 | ||||||
| chr5:40922374 | C | CAAA | 9 | a0001c0001t0001g0322 a0001c0001t0002g0321 a0001c0001t0008g0206 others(6): Show |
9 | HG02056.hp1 HG02080.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-6181_7-6179dupAA others(1): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922374 | ||||||
| chr5:40922374 | C | CAAAA | 24 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(21): Show |
24 | HG00597.hp1 HG00673.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-6182_7-6179dupAA others(2): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922374 | ||||||
| chr5:40922374 | C | CAAAAA | 15 | a0001c0001t0002g0320 a0001c0001t0004g0317 a0002c0002t0001g0291 others(12): Show |
15 | HG00544.hp2 HG01928.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.7-6183_7-6179dupAA others(3): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922374 | ||||||
| chr5:40922374 | CA | C | 13 | a0001c0001t0001g0224 a0001c0001t0002g0061 a0001c0001t0002g0258 others(10): Show |
13 | HG01069.hp2 HG01175.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.7-6179delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922374 | ||||||
| chr5:40922374 | CAA | C | 101 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(98): Show |
103 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.7-6180_7-6179delAA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922374 | ||||||
| chr5:40922374 | CAAAAAA | C | 9 | a0001c0001t0002g0284 a0001c0001t0003g0283 a0001c0001t0003g0285 others(6): Show |
9 | HG02630.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-6184_7-6179delAA others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922374 | ||||||
| chr5:40922416 | C | T | 1 | a0018c0018t0002g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.7-6164C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922416 | |||||||
| chr5:40922491 | G | A | 1 | a0001c0001t0004g0058 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.7-6089G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922491 | |||||||
| chr5:40922558 | G | C | 8 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0007c0007t0004g0264 others(5): Show |
8 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-6022G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922558 | |||||||
| chr5:40922566 | T | C | 1 | a0002c0002t0001g0185 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.7-6014T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922566 | |||||||
| chr5:40922588 | C | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0031 |
4 | HG02109.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-5992C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922588 | |||||||
| chr5:40922625 | C | G | 1 | a0017c0027t0002g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.7-5955C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922625 | |||||||
| chr5:40922625 | C | T | 4 | a0002c0002t0001g0049 a0005c0005t0003g0280 a0005c0005t0003g0281 others(1): Show |
4 | HG01192.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-5955C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922625 | |||||||
| chr5:40922634 | G | C | 1 | a0001c0001t0003g0283 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7-5946G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922634 | |||||||
| chr5:40922642 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-5938A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922642 | |||||||
| chr5:40922652 | G | T | 1 | a0001c0025t0011g0366 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7-5928G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922652 | |||||||
| chr5:40922666 | A | T | 1 | a0001c0001t0002g0240 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.7-5914A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922666 | |||||||
| chr5:40922696 | C | CA | 15 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(12): Show |
15 | HG01257.hp2 HG01496.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.7-5871dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922696 | ||||||
| chr5:40922696 | C | CAAAAAAA others(3): Show |
27 | a0001c0001t0002g0007 a0001c0001t0002g0204 a0001c0001t0002g0205 others(24): Show |
27 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.7-5880_7-5871dupAA others(8): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922696 | ||||||
| chr5:40922696 | C | CAAAAAAA others(4): Show |
75 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0325 others(72): Show |
76 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7-5881_7-5871dupAA others(9): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922696 | ||||||
| chr5:40922696 | C | CAAAAAAA others(5): Show |
8 | a0001c0001t0001g0324 a0001c0001t0002g0275 a0001c0001t0004g0276 others(5): Show |
8 | HG01192.hp1 HG02293.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-5882_7-5871dupAA others(10): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922696 | ||||||
| chr5:40922696 | C | CAAAAAAA others(7): Show |
1 | a0002c0002t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-5871_7-5870insAA others(12): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40922696 | ||||||
| chr5:40922843 | T | C | 3 | a0003c0003t0003g0287 a0003c0003t0003g0349 a0003c0003t0003g0355 |
3 | NA18965.hp2 NA18967.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.7-5737T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922843 | |||||||
| chr5:40922857 | T | C | 4 | a0001c0001t0004g0003 a0001c0001t0004g0038 a0001c0001t0004g0040 others(1): Show |
5 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-5723T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922857 | |||||||
| chr5:40922880 | A | G | 3 | a0003c0003t0003g0287 a0003c0003t0003g0349 a0003c0003t0003g0355 |
3 | NA18965.hp2 NA18967.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.7-5700A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922880 | |||||||
| chr5:40922893 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-5687A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922893 | |||||||
| chr5:40922983 | A | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-5597A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40922983 | |||||||
| chr5:40923138 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-5442A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923138 | |||||||
| chr5:40923145 | T | A | 1 | a0004c0004t0001g0207 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.7-5435T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923145 | |||||||
| chr5:40923218 | A | C | 1 | a0018c0018t0002g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.7-5362A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923218 | |||||||
| chr5:40923230 | A | G | 19 | a0001c0001t0001g0064 a0001c0001t0001g0211 a0001c0001t0002g0013 others(16): Show |
19 | HG01109.hp1 HG01346.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.7-5350A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923230 | |||||||
| chr5:40923436 | C | T | 5 | a0001c0001t0001g0066 a0001c0001t0004g0034 a0001c0001t0004g0037 others(2): Show |
5 | HG02486.hp2 HG02976.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-5144C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923436 | |||||||
| chr5:40923652 | A | G | 14 | a0001c0001t0002g0205 a0001c0001t0002g0284 a0001c0001t0003g0283 others(11): Show |
14 | HG01192.hp1 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-4928A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923652 | |||||||
| chr5:40923694 | C | G | 2 | a0002c0002t0002g0161 a0005c0005t0003g0179 |
2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.7-4886C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923694 | |||||||
| chr5:40923701 | G | T | 22 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0002g0205 others(19): Show |
22 | HG01192.hp1 HG01361.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.7-4879G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923701 | |||||||
| chr5:40923725 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-4855G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923725 | |||||||
| chr5:40923745 | T | TA | 10 | a0002c0002t0001g0150 a0004c0004t0001g0021 a0004c0004t0001g0024 others(7): Show |
10 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.7-4821dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40923745 | ||||||
| chr5:40923745 | TA | T | 172 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0066 others(169): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.7-4821delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40923745 | ||||||
| chr5:40923930 | A | AGTT | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-4650_7-4649insGT others(1): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923930 | |||||||
| chr5:40923931 | A | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-4649A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923931 | |||||||
| chr5:40923934 | G | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-4646G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923934 | |||||||
| chr5:40923999 | A | G | 1 | a0004c0004t0001g0207 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.7-4581A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40923999 | |||||||
| chr5:40924108 | A | G | 120 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(117): Show |
124 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.7-4472A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924108 | |||||||
| chr5:40924157 | T | C | 2 | a0001c0001t0004g0229 a0003c0003t0003g0245 |
2 | NA18983.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.7-4423T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924157 | |||||||
| chr5:40924217 | G | C | 4 | a0002c0002t0001g0049 a0005c0005t0003g0280 a0005c0005t0003g0281 others(1): Show |
4 | HG01192.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-4363G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924217 | |||||||
| chr5:40924297 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.7-4283C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924297 | |||||||
| chr5:40924303 | G | A | 2 | a0002c0002t0001g0132 a0005c0005t0003g0131 |
2 | HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.7-4277G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924303 | |||||||
| chr5:40924320 | T | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-4260T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924320 | |||||||
| chr5:40924381 | A | G | 112 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(109): Show |
113 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.7-4199A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924381 | |||||||
| chr5:40924488 | G | C | 1 | a0002c0002t0002g0162 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.7-4092G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924488 | |||||||
| chr5:40924499 | C | T | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-4081C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924499 | |||||||
| chr5:40924541 | G | A | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7-4039G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924541 | |||||||
| chr5:40924652 | A | ATCC | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-3926_7-3925insCT others(1): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40924652 | ||||||
| chr5:40924754 | C | T | 1 | a0005c0005t0003g0085 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7-3826C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924754 | |||||||
| chr5:40924755 | C | T | 233 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(230): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.7-3825C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924755 | |||||||
| chr5:40924756 | T | C | 248 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(245): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.7-3824T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924756 | |||||||
| chr5:40924757 | G | A | 2 | a0001c0001t0003g0263 a0004c0004t0001g0306 |
2 | HG01884.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.7-3823G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924757 | |||||||
| chr5:40924928 | G | T | 1 | a0002c0002t0002g0178 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.7-3652G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924928 | |||||||
| chr5:40924964 | C | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-3616C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924964 | |||||||
| chr5:40924991 | T | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-3589T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40924991 | |||||||
| chr5:40925085 | C | A | 1 | a0003c0003t0003g0362 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.7-3495C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925085 | |||||||
| chr5:40925088 | C | T | 2 | a0002c0002t0001g0121 a0002c0002t0001g0122 |
2 | HG00673.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.7-3492C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925088 | |||||||
| chr5:40925422 | A | G | 1 | a0001c0001t0004g0058 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.7-3158A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925422 | |||||||
| chr5:40925578 | T | A | 7 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0038 others(4): Show |
8 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-3002T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925578 | |||||||
| chr5:40925605 | G | A | 120 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(117): Show |
124 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.7-2975G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925605 | |||||||
| chr5:40925652 | G | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-2928G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925652 | |||||||
| chr5:40925678 | T | C | 1 | a0002c0002t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7-2902T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925678 | |||||||
| chr5:40925685 | T | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-2895T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925685 | |||||||
| chr5:40925765 | C | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-2815C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925765 | |||||||
| chr5:40925766 | G | A | 120 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(117): Show |
124 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.7-2814G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925766 | |||||||
| chr5:40925776 | C | G | 233 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(230): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.7-2804C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925776 | |||||||
| chr5:40925794 | C | T | 1 | a0002c0002t0001g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.7-2786C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925794 | |||||||
| chr5:40925856 | T | C | 233 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(230): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.7-2724T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925856 | |||||||
| chr5:40925912 | G | A | 2 | a0002c0002t0001g0185 a0002c0002t0001g0186 |
2 | NA18966.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.7-2668G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40925912 | |||||||
| chr5:40926065 | C | T | 1 | a0002c0002t0004g0274 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.7-2515C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926065 | |||||||
| chr5:40926099 | T | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-2481T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926099 | |||||||
| chr5:40926171 | T | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-2409T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926171 | |||||||
| chr5:40926286 | C | T | 55 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(52): Show |
56 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.7-2294C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926286 | |||||||
| chr5:40926360 | CCCACTTT others(2): Show |
C | 232 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(229): Show |
237 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.7-2202_7-2194delGC others(7): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40926360 | ||||||
| chr5:40926385 | T | G | 1 | a0001c0001t0004g0057 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.7-2195T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926385 | |||||||
| chr5:40926473 | A | G | 8 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(5): Show |
8 | HG01361.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-2107A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926473 | |||||||
| chr5:40926521 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7-2059C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926521 | |||||||
| chr5:40926529 | A | C | 7 | a0001c0001t0001g0222 a0001c0001t0002g0208 a0001c0001t0002g0216 others(4): Show |
7 | NA18939.hp2 NA18957.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-2051A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926529 | |||||||
| chr5:40926731 | A | C | 1 | a0001c0001t0004g0057 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.7-1849A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926731 | |||||||
| chr5:40926848 | C | T | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0050 others(7): Show |
10 | HG01109.hp1 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.7-1732C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926848 | |||||||
| chr5:40926850 | A | G | 1 | a0002c0002t0001g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.7-1730A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926850 | |||||||
| chr5:40926865 | C | A | 1 | a0003c0003t0003g0230 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.7-1715C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926865 | |||||||
| chr5:40926919 | CA | C | 10 | a0002c0002t0001g0118 a0002c0002t0001g0120 a0002c0002t0001g0121 others(7): Show |
10 | HG00558.hp2 HG00673.hp2 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.7-1654delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40926919 | ||||||
| chr5:40926947 | A | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7-1633A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40926947 | |||||||
| chr5:40926953 | A | AAAAAGAA others(26): Show |
5 | a0001c0001t0005g0367 a0001c0001t0005g0368 a0001c0001t0005g0369 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-1625_7-1593dupAA others(31): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40926953 | ||||||
| chr5:40927011 | T | C | 22 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0002g0205 others(19): Show |
22 | HG01192.hp1 HG01361.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.7-1569T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40927011 | |||||||
| chr5:40927124 | G | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-1456G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40927124 | |||||||
| chr5:40927236 | A | G | 1 | a0002c0002t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-1344A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40927236 | |||||||
| chr5:40927325 | T | A | 79 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(76): Show |
80 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.7-1255T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40927325 | |||||||
| chr5:40927327 | T | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-1253T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40927327 | |||||||
| chr5:40927426 | G | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-1154G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40927426 | |||||||
| chr5:40927674 | T | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-906T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40927674 | |||||||
| chr5:40927686 | A | G | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.7-894A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40927686 | |||||||
| chr5:40927765 | G | A | 1 | a0001c0001t0004g0317 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7-815G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40927765 | |||||||
| chr5:40927818 | AG | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0125 a0005c0005t0003g0124 |
3 | NA18959.hp1 NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.7-759delG | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 40927818 | ||||||
| chr5:40927942 | T | C | 1 | a0003c0003t0003g0364 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.7-638T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40927942 | |||||||
| chr5:40928079 | T | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-501T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40928079 | |||||||
| chr5:40928085 | G | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-495G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40928085 | |||||||
| chr5:40928086 | G | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.7-494G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40928086 | |||||||
| chr5:40928242 | G | C | 2 | a0001c0001t0004g0002 a0001c0001t0004g0012 |
3 | NA18971.hp2 NA18992.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.7-338G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40928242 | |||||||
| chr5:40928335 | G | A | 1 | a0002c0002t0002g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.7-245G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40928335 | |||||||
| chr5:40928364 | T | C | 1 | a0001c0001t0004g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7-216T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40928364 | |||||||
| chr5:40928472 | A | C | 233 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(230): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.7-108A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 1/17 | chr5 | 40928472 | |||||||
| chr5:40928690 | T | A | 233 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(230): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.62+55T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40928690 | |||||||
| chr5:40928980 | C | A | 26 | a0001c0001t0002g0007 a0001c0001t0002g0201 a0001c0001t0002g0204 others(23): Show |
26 | HG01192.hp1 HG01361.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.62+345C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40928980 | |||||||
| chr5:40929067 | T | C | 1 | a0001c0001t0004g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.62+432T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929067 | |||||||
| chr5:40929105 | G | A | 2 | a0002c0002t0003g0138 a0002c0002t0003g0139 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.62+470G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929105 | |||||||
| chr5:40929294 | G | C | 56 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(53): Show |
57 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.62+659G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929294 | |||||||
| chr5:40929301 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0004g0002 a0001c0001t0004g0012 |
4 | NA18971.hp2 NA18992.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+666G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929301 | |||||||
| chr5:40929316 | A | G | 55 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0194 others(52): Show |
58 | HG00735.hp1 HG01106.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.62+681A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929316 | |||||||
| chr5:40929411 | G | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.62+776G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929411 | |||||||
| chr5:40929433 | T | A | 2 | a0001c0001t0002g0320 a0001c0001t0004g0317 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.62+798T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929433 | |||||||
| chr5:40929441 | G | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(110): Show |
114 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.62+806G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929441 | |||||||
| chr5:40929492 | A | G | 233 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(230): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.62+857A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929492 | |||||||
| chr5:40929527 | A | G | 10 | a0001c0001t0002g0205 a0001c0001t0002g0284 a0001c0001t0003g0283 others(7): Show |
10 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.62+892A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929527 | |||||||
| chr5:40929616 | G | A | 56 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(53): Show |
57 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.62+981G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929616 | |||||||
| chr5:40929700 | T | G | 1 | a0002c0002t0004g0182 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.62+1065T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929700 | |||||||
| chr5:40929713 | G | A | 142 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(139): Show |
146 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.62+1078G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929713 | |||||||
| chr5:40929730 | T | G | 233 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(230): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.62+1095T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929730 | |||||||
| chr5:40929761 | A | G | 2 | a0001c0001t0002g0205 a0001c0001t0002g0284 |
2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.62+1126A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929761 | |||||||
| chr5:40929917 | G | T | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.63-1147G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40929917 | |||||||
| chr5:40930197 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-867C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930197 | |||||||
| chr5:40930204 | C | CT | 14 | a0001c0001t0001g0222 a0001c0001t0002g0208 a0001c0001t0002g0216 others(11): Show |
14 | HG02647.hp2 NA18939.hp2 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.63-841dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 40930204 | ||||||
| chr5:40930204 | CT | C | 46 | a0001c0001t0001g0248 a0001c0001t0002g0007 a0001c0001t0002g0201 others(43): Show |
46 | HG00408.hp1 HG00597.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.63-841delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 40930204 | ||||||
| chr5:40930204 | CTT | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0066 others(133): Show |
140 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.63-842_63-841delTT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 40930204 | ||||||
| chr5:40930204 | CTTT | C | 9 | a0001c0001t0001g0325 a0001c0001t0004g0058 a0002c0002t0001g0049 others(6): Show |
9 | HG01192.hp1 HG01975.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.63-843_63-841delTT others(1): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 40930204 | ||||||
| chr5:40930270 | A | G | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63-794A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930270 | |||||||
| chr5:40930282 | T | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.63-782T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930282 | |||||||
| chr5:40930338 | C | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(85): Show |
89 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.63-726C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930338 | |||||||
| chr5:40930339 | G | A | 4 | a0002c0002t0001g0049 a0005c0005t0003g0280 a0005c0005t0003g0281 others(1): Show |
4 | HG01192.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.63-725G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930339 | |||||||
| chr5:40930394 | C | T | 1 | a0017c0027t0002g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.63-670C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930394 | |||||||
| chr5:40930412 | G | A | 91 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(88): Show |
92 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.63-652G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930412 | |||||||
| chr5:40930498 | A | G | 244 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(241): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.63-566A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930498 | |||||||
| chr5:40930499 | C | A | 5 | a0001c0001t0005g0367 a0001c0001t0005g0368 a0001c0001t0005g0369 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.63-565C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930499 | |||||||
| chr5:40930502 | G | A | 1 | a0018c0018t0002g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.63-562G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930502 | |||||||
| chr5:40930664 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.63-400G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930664 | |||||||
| chr5:40930688 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-376G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930688 | |||||||
| chr5:40930709 | C | T | 4 | a0001c0001t0002g0279 a0003c0003t0003g0220 a0003c0003t0003g0230 others(1): Show |
4 | HG02523.hp2 NA18961.hp1 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-355C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930709 | |||||||
| chr5:40930711 | C | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(88): Show |
92 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.63-353C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930711 | |||||||
| chr5:40930717 | C | A | 1 | a0001c0001t0002g0240 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.63-347C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930717 | |||||||
| chr5:40930719 | T | G | 1 | a0001c0001t0002g0240 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.63-345T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930719 | |||||||
| chr5:40930725 | G | A | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.63-339G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930725 | |||||||
| chr5:40930813 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63-251G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930813 | |||||||
| chr5:40930950 | C | T | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.63-114C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 2/17 | chr5 | 40930950 | |||||||
| chr5:40931178 | C | T | 1 | a0001c0001t0012g0365 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.138+39C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931178 | |||||||
| chr5:40931255 | A | G | 111 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(108): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.138+116A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931255 | |||||||
| chr5:40931305 | T | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0125 a0005c0005t0003g0124 |
3 | NA18959.hp1 NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.138+166T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931305 | |||||||
| chr5:40931388 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0244 |
2 | NA18981.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.138+249T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931388 | |||||||
| chr5:40931427 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+288C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931427 | |||||||
| chr5:40931431 | G | C | 7 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0004g0202 others(4): Show |
7 | HG01361.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+292G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931431 | |||||||
| chr5:40931451 | A | G | 1 | a0003c0003t0003g0349 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.138+312A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931451 | |||||||
| chr5:40931521 | A | G | 1 | a0007c0007t0004g0243 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.138+382A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931521 | |||||||
| chr5:40931538 | A | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.138+399A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931538 | |||||||
| chr5:40931581 | G | GA | 128 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(125): Show |
132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.138+449dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 40931581 | ||||||
| chr5:40931587 | A | AG | 87 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(84): Show |
88 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.138+448_138+449ins others(1): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931587 | |||||||
| chr5:40931601 | T | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(11): Show |
15 | HG00140.hp2 HG01975.hp2 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+462T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931601 | |||||||
| chr5:40931712 | G | A | 91 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(88): Show |
92 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.138+573G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931712 | |||||||
| chr5:40931844 | C | T | 10 | a0001c0001t0002g0205 a0001c0001t0002g0284 a0001c0001t0003g0283 others(7): Show |
10 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+705C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931844 | |||||||
| chr5:40931845 | G | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+706G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931845 | |||||||
| chr5:40931883 | C | T | 22 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0002g0205 others(19): Show |
22 | HG01192.hp1 HG01361.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.138+744C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931883 | |||||||
| chr5:40931944 | G | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+805G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40931944 | |||||||
| chr5:40932009 | C | T | 87 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(84): Show |
88 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.138+870C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932009 | |||||||
| chr5:40932393 | C | G | 1 | a0005c0005t0003g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.138+1254C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932393 | |||||||
| chr5:40932481 | A | T | 1 | a0006c0006t0004g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.138+1342A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932481 | |||||||
| chr5:40932493 | T | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(88): Show |
92 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.138+1354T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932493 | |||||||
| chr5:40932517 | A | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(88): Show |
92 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.138+1378A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932517 | |||||||
| chr5:40932521 | T | C | 10 | a0001c0001t0003g0263 a0004c0004t0001g0021 a0004c0004t0001g0024 others(7): Show |
10 | HG00408.hp1 HG00597.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+1382T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932521 | |||||||
| chr5:40932641 | A | C | 1 | a0006c0006t0004g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.138+1502A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932641 | |||||||
| chr5:40932736 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(89): Show |
93 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.139-1589G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932736 | |||||||
| chr5:40932774 | G | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(88): Show |
92 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.139-1551G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932774 | |||||||
| chr5:40932879 | A | G | 9 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-1446A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932879 | |||||||
| chr5:40932958 | TG | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(5): Show |
9 | HG01975.hp2 HG02273.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-1365delG | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 40932958 | ||||||
| chr5:40932981 | C | T | 1 | a0001c0001t0003g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.139-1344C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40932981 | |||||||
| chr5:40933051 | C | T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(79): Show |
83 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.139-1274C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40933051 | |||||||
| chr5:40933138 | C | A | 60 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(57): Show |
61 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.139-1187C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40933138 | |||||||
| chr5:40933396 | G | A | 1 | a0001c0001t0012g0365 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.139-929G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40933396 | |||||||
| chr5:40933477 | T | C | 1 | a0001c0001t0002g0333 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.139-848T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40933477 | |||||||
| chr5:40933846 | G | C | 1 | a0001c0001t0002g0320 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.139-479G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40933846 | |||||||
| chr5:40933940 | C | CT | 180 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(177): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.139-372dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 40933940 | ||||||
| chr5:40933959 | G | A | 3 | a0001c0001t0003g0283 a0001c0001t0003g0285 a0001c0001t0003g0286 |
3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.139-366G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40933959 | |||||||
| chr5:40934049 | A | AT | 29 | a0001c0001t0001g0345 a0001c0001t0002g0007 a0001c0001t0002g0261 others(26): Show |
29 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.139-263dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 40934049 | ||||||
| chr5:40934049 | AT | A | 41 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(38): Show |
44 | HG00735.hp1 HG01106.hp1 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.139-263delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 40934049 | ||||||
| chr5:40934050 | T | G | 1 | a0006c0006t0004g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.139-275T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40934050 | |||||||
| chr5:40934052 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.139-273T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40934052 | |||||||
| chr5:40934064 | C | A | 8 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0007c0007t0004g0264 others(5): Show |
8 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-261C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40934064 | |||||||
| chr5:40934316 | T | C | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-9T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 3/17 | chr5 | 40934316 | |||||||
| chr5:40934532 | C | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+66C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40934532 | |||||||
| chr5:40934730 | A | C | 56 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(53): Show |
57 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.280+264A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40934730 | |||||||
| chr5:40934878 | C | T | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.280+412C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40934878 | |||||||
| chr5:40935065 | T | A | 1 | a0003c0003t0003g0245 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.280+599T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40935065 | |||||||
| chr5:40935137 | A | G | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+671A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40935137 | |||||||
| chr5:40935418 | G | C | 10 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0002g0140 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-920G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40935418 | |||||||
| chr5:40935500 | A | T | 1 | a0001c0001t0004g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-838A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40935500 | |||||||
| chr5:40935610 | T | C | 4 | a0002c0002t0001g0049 a0005c0005t0003g0280 a0005c0005t0003g0281 others(1): Show |
4 | HG01192.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-728T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40935610 | |||||||
| chr5:40935665 | G | A | 1 | a0002c0002t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-673G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40935665 | |||||||
| chr5:40935717 | C | A | 1 | a0010c0010t0001g0114 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.281-621C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40935717 | |||||||
| chr5:40935875 | G | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-463G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40935875 | |||||||
| chr5:40935929 | G | T | 1 | a0021c0020t0001g0209 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.281-409G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40935929 | |||||||
| chr5:40935980 | CT | C | 8 | a0002c0002t0001g0109 a0002c0002t0001g0132 a0002c0002t0002g0071 others(5): Show |
8 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-356delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 40935980 | ||||||
| chr5:40936080 | TG | T | 3 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0260 |
3 | HG01346.hp1 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.281-255delG | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 40936080 | ||||||
| chr5:40936180 | C | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-158C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40936180 | |||||||
| chr5:40936316 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.281-22C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 4/17 | chr5 | 40936316 | |||||||
| chr5:40936531 | T | C | 1 | a0005c0005t0003g0131 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.428+46T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40936531 | |||||||
| chr5:40936567 | C | T | 66 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(63): Show |
67 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.428+82C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40936567 | |||||||
| chr5:40936689 | C | T | 75 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(72): Show |
76 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.428+204C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40936689 | |||||||
| chr5:40936741 | C | T | 178 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(175): Show |
183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.428+256C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40936741 | |||||||
| chr5:40936743 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.428+258C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40936743 | |||||||
| chr5:40936759 | C | T | 41 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(38): Show |
44 | HG00735.hp1 HG01106.hp1 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.428+274C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40936759 | |||||||
| chr5:40936806 | G | C | 66 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(63): Show |
67 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.428+321G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40936806 | |||||||
| chr5:40936996 | G | C | 33 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(30): Show |
33 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.428+511G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40936996 | |||||||
| chr5:40937030 | G | C | 1 | a0006c0006t0004g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.429-522G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40937030 | |||||||
| chr5:40937257 | G | A | 1 | a0002c0002t0001g0153 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.429-295G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40937257 | |||||||
| chr5:40937362 | G | A | 1 | a0003c0003t0003g0092 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.429-190G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40937362 | |||||||
| chr5:40937374 | T | C | 5 | a0002c0002t0002g0161 a0002c0002t0002g0163 a0002c0002t0002g0178 others(2): Show |
5 | HG03927.hp2 HG04115.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-178T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 5/17 | chr5 | 40937374 | |||||||
| chr5:40937898 | T | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(58): Show |
62 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.567+208T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40937898 | |||||||
| chr5:40938162 | A | G | 33 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(30): Show |
33 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.567+472A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40938162 | |||||||
| chr5:40938240 | T | C | 219 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(216): Show |
224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.567+550T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40938240 | |||||||
| chr5:40938343 | C | T | 179 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(176): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.567+653C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40938343 | |||||||
| chr5:40938465 | T | C | 1 | a0007c0007t0004g0243 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.567+775T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40938465 | |||||||
| chr5:40938603 | G | A | 7 | a0001c0001t0001g0222 a0001c0001t0002g0208 a0001c0001t0002g0216 others(4): Show |
7 | NA18939.hp2 NA18957.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.567+913G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40938603 | |||||||
| chr5:40938820 | T | C | 180 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(177): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.567+1130T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40938820 | |||||||
| chr5:40938874 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.567+1184T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40938874 | |||||||
| chr5:40938894 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.567+1204G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40938894 | |||||||
| chr5:40938953 | C | T | 42 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(39): Show |
45 | HG00735.hp1 HG01106.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.567+1263C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40938953 | |||||||
| chr5:40939131 | C | CT | 4 | a0001c0001t0005g0367 a0001c0001t0005g0368 a0001c0001t0012g0365 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+1445dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 40939131 | ||||||
| chr5:40939152 | C | G | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+1462C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939152 | |||||||
| chr5:40939164 | G | A | 1 | a0001c0001t0004g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.567+1474G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939164 | |||||||
| chr5:40939189 | A | G | 180 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(177): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.567+1499A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939189 | |||||||
| chr5:40939192 | C | A | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.567+1502C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939192 | |||||||
| chr5:40939238 | G | T | 4 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0004g0202 others(1): Show |
4 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+1548G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939238 | |||||||
| chr5:40939265 | C | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+1575C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939265 | |||||||
| chr5:40939313 | G | A | 1 | a0002c0002t0002g0069 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.567+1623G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939313 | |||||||
| chr5:40939455 | A | G | 185 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(182): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.567+1765A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939455 | |||||||
| chr5:40939538 | C | T | 186 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(183): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.567+1848C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939538 | |||||||
| chr5:40939578 | T | C | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+1888T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939578 | |||||||
| chr5:40939653 | A | G | 10 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0002g0140 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.567+1963A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939653 | |||||||
| chr5:40939769 | G | A | 2 | a0001c0001t0001g0233 a0003c0003t0003g0262 |
2 | HG00408.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.567+2079G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939769 | |||||||
| chr5:40939892 | A | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.567+2202A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40939892 | |||||||
| chr5:40940108 | G | A | 1 | a0003c0003t0003g0364 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.567+2418G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940108 | |||||||
| chr5:40940198 | C | T | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.567+2508C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940198 | |||||||
| chr5:40940226 | C | T | 4 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0004g0202 others(1): Show |
4 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+2536C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940226 | |||||||
| chr5:40940305 | T | C | 2 | a0001c0001t0002g0050 a0001c0001t0002g0054 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.567+2615T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940305 | |||||||
| chr5:40940406 | G | A | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.567+2716G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940406 | |||||||
| chr5:40940426 | A | G | 1 | a0001c0001t0001g0370 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.567+2736A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940426 | |||||||
| chr5:40940452 | G | A | 2 | a0001c0001t0002g0336 a0003c0023t0003g0335 |
2 | NA18951.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.567+2762G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940452 | |||||||
| chr5:40940588 | T | C | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+2898T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940588 | |||||||
| chr5:40940707 | C | T | 1 | a0001c0001t0004g0373 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.567+3017C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940707 | |||||||
| chr5:40940713 | G | A | 185 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(182): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.567+3023G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940713 | |||||||
| chr5:40940969 | T | C | 184 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(181): Show |
189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.567+3279T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40940969 | |||||||
| chr5:40941062 | C | CT | 142 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0210 others(139): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.567+3387dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 40941062 | ||||||
| chr5:40941119 | A | C | 68 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(65): Show |
69 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.567+3429A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941119 | |||||||
| chr5:40941209 | G | A | 3 | a0003c0003t0003g0337 a0003c0003t0003g0361 a0003c0003t0003g0363 |
3 | HG03492.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.567+3519G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941209 | |||||||
| chr5:40941211 | G | A | 53 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(50): Show |
54 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.567+3521G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941211 | |||||||
| chr5:40941290 | C | T | 68 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(65): Show |
69 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.567+3600C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941290 | |||||||
| chr5:40941389 | T | A | 1 | a0001c0001t0001g0252 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.567+3699T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941389 | |||||||
| chr5:40941454 | G | A | 1 | a0003c0003t0003g0092 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.568-3744G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941454 | |||||||
| chr5:40941473 | A | G | 1 | a0001c0001t0005g0369 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.568-3725A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941473 | |||||||
| chr5:40941584 | C | G | 1 | a0002c0002t0001g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.568-3614C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941584 | |||||||
| chr5:40941639 | G | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-3559G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941639 | |||||||
| chr5:40941674 | C | T | 9 | a0008c0008t0001g0359 a0008c0008t0003g0351 a0008c0008t0003g0352 others(6): Show |
9 | HG01928.hp1 HG02165.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.568-3524C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941674 | |||||||
| chr5:40941815 | A | G | 8 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG02723.hp1 HG02809.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.568-3383A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941815 | |||||||
| chr5:40941863 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.568-3335G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941863 | |||||||
| chr5:40941878 | A | G | 6 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(3): Show |
6 | HG01361.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.568-3320A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40941878 | |||||||
| chr5:40942253 | T | G | 4 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0004g0202 others(1): Show |
4 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.568-2945T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942253 | |||||||
| chr5:40942318 | A | G | 53 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(50): Show |
54 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.568-2880A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942318 | |||||||
| chr5:40942438 | T | C | 1 | a0001c0001t0003g0283 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.568-2760T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942438 | |||||||
| chr5:40942465 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.568-2733A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942465 | |||||||
| chr5:40942500 | G | C | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.568-2698G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942500 | |||||||
| chr5:40942513 | G | A | 10 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0002g0140 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.568-2685G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942513 | |||||||
| chr5:40942583 | T | C | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.568-2615T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942583 | |||||||
| chr5:40942620 | A | G | 8 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG02723.hp1 HG02809.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.568-2578A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942620 | |||||||
| chr5:40942638 | G | A | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-2560G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942638 | |||||||
| chr5:40942715 | C | T | 6 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(3): Show |
6 | HG01361.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.568-2483C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942715 | |||||||
| chr5:40942741 | C | T | 6 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(3): Show |
6 | HG01361.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.568-2457C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942741 | |||||||
| chr5:40942753 | C | T | 8 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG02723.hp1 HG02809.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.568-2445C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942753 | |||||||
| chr5:40942768 | CT | C | 7 | a0001c0001t0002g0213 a0001c0001t0004g0056 a0002c0002t0003g0198 others(4): Show |
7 | HG01361.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.568-2415delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 40942768 | ||||||
| chr5:40942806 | C | T | 47 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(44): Show |
50 | HG00544.hp2 HG00735.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.568-2392C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40942806 | |||||||
| chr5:40943048 | C | T | 3 | a0005c0005t0003g0280 a0005c0005t0003g0281 a0005c0005t0003g0282 |
3 | HG01192.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.568-2150C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943048 | |||||||
| chr5:40943116 | T | C | 47 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(44): Show |
50 | HG00544.hp2 HG00735.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.568-2082T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943116 | |||||||
| chr5:40943153 | A | G | 218 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(215): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.568-2045A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943153 | |||||||
| chr5:40943173 | A | G | 5 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0004g0017 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.568-2025A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943173 | |||||||
| chr5:40943285 | T | A | 1 | a0007c0007t0004g0266 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.568-1913T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943285 | |||||||
| chr5:40943340 | T | C | 77 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(74): Show |
78 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.568-1858T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943340 | |||||||
| chr5:40943392 | AG | A | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-1805delG | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943392 | |||||||
| chr5:40943416 | A | C | 24 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(21): Show |
24 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.568-1782A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943416 | |||||||
| chr5:40943561 | A | AT | 7 | a0001c0001t0003g0283 a0001c0001t0003g0285 a0001c0001t0003g0286 others(4): Show |
7 | HG02647.hp1 HG02818.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.568-1623dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 40943561 | ||||||
| chr5:40943561 | AT | A | 73 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(70): Show |
74 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.568-1623delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 40943561 | ||||||
| chr5:40943638 | A | G | 19 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(16): Show |
19 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.568-1560A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943638 | |||||||
| chr5:40943691 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.568-1507G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943691 | |||||||
| chr5:40943697 | G | GTA | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-1490_568-1489d others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 40943697 | ||||||
| chr5:40943718 | C | CAT | 47 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(44): Show |
50 | HG00544.hp2 HG00735.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.568-1471_568-1470d others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 40943718 | ||||||
| chr5:40943807 | T | A | 8 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG02723.hp1 HG02809.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.568-1391T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943807 | |||||||
| chr5:40943818 | T | C | 3 | a0002c0002t0003g0198 a0002c0002t0003g0199 a0002c0002t0003g0200 |
3 | HG02257.hp2 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.568-1380T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943818 | |||||||
| chr5:40943830 | TTCTTA | T | 77 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(74): Show |
78 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.568-1363_568-1359d others(7): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 40943830 | ||||||
| chr5:40943947 | G | A | 1 | a0005c0005t0002g0133 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.568-1251G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40943947 | |||||||
| chr5:40944055 | CTG | C | 53 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(50): Show |
54 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.568-1139_568-1138d others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 40944055 | ||||||
| chr5:40944199 | G | A | 1 | a0002c0002t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.568-999G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40944199 | |||||||
| chr5:40944211 | T | C | 8 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG02723.hp1 HG02809.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.568-987T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40944211 | |||||||
| chr5:40944348 | C | T | 1 | a0002c0002t0001g0075 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.568-850C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40944348 | |||||||
| chr5:40944461 | T | G | 3 | a0002c0002t0003g0149 a0006c0006t0002g0147 a0017c0027t0002g0148 |
3 | HG02145.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.568-737T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40944461 | |||||||
| chr5:40944791 | A | G | 8 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG02723.hp1 HG02809.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.568-407A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40944791 | |||||||
| chr5:40944844 | G | A | 3 | a0002c0002t0003g0149 a0006c0006t0002g0147 a0017c0027t0002g0148 |
3 | HG02145.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.568-354G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40944844 | |||||||
| chr5:40944904 | C | T | 5 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0002c0002t0003g0198 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.568-294C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40944904 | |||||||
| chr5:40945026 | C | T | 2 | a0001c0001t0002g0336 a0003c0023t0003g0335 |
2 | NA18951.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.568-172C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40945026 | |||||||
| chr5:40945096 | A | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.568-102A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 6/17 | chr5 | 40945096 | |||||||
| chr5:40945424 | A | C | 4 | a0002c0002t0001g0049 a0005c0005t0003g0280 a0005c0005t0003g0281 others(1): Show |
4 | HG01192.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.738+56A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40945424 | |||||||
| chr5:40945435 | C | A | 1 | a0003c0003t0003g0245 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.738+67C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40945435 | |||||||
| chr5:40945463 | A | G | 4 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.738+95A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40945463 | |||||||
| chr5:40945511 | A | G | 32 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(29): Show |
32 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.738+143A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40945511 | |||||||
| chr5:40945584 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.738+216C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40945584 | |||||||
| chr5:40945754 | C | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.738+386C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40945754 | |||||||
| chr5:40945875 | C | CAT | 4 | a0005c0005t0003g0282 a0007c0007t0004g0265 a0009c0009t0001g0318 others(1): Show |
4 | HG00642.hp1 HG01168.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.738+540_738+541dup others(2): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | C | CATAT | 4 | a0001c0001t0001g0329 a0001c0001t0002g0270 a0005c0005t0003g0280 others(1): Show |
4 | HG01192.hp1 HG02965.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.738+538_738+541dup others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | C | CATATATA others(3): Show |
1 | a0002c0002t0002g0159 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.738+532_738+541dup others(10): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | C | CATATATA others(5): Show |
1 | a0008c0008t0003g0316 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.738+530_738+541dup others(12): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | CAT | C | 86 | a0001c0001t0001g0006 a0001c0001t0001g0214 a0001c0001t0001g0222 others(83): Show |
88 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.738+540_738+541del others(2): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | CATAT | C | 72 | a0001c0001t0001g0210 a0001c0001t0001g0218 a0001c0001t0001g0224 others(69): Show |
73 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.738+538_738+541del others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | CATATAT | C | 71 | a0001c0001t0004g0317 a0001c0001t0004g0344 a0001c0001t0012g0365 others(68): Show |
72 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.738+536_738+541del others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | CATATATA others(1): Show |
C | 8 | a0001c0001t0002g0205 a0001c0001t0002g0284 a0001c0001t0002g0320 others(5): Show |
8 | HG01123.hp1 HG02258.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.738+534_738+541del others(8): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | CATATATA others(3): Show |
C | 5 | a0001c0001t0003g0283 a0001c0001t0004g0033 a0001c0025t0011g0366 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.738+532_738+541del others(10): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | CATATATA others(5): Show |
C | 2 | a0001c0001t0005g0367 a0001c0001t0005g0368 |
2 | HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.738+530_738+541del others(12): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | CATATATA others(7): Show |
C | 32 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(29): Show |
32 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.738+528_738+541del others(14): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | CATATATA others(9): Show |
C | 12 | a0001c0001t0001g0064 a0001c0001t0001g0211 a0001c0001t0001g0370 others(9): Show |
14 | HG01167.hp1 HG01346.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.738+526_738+541del others(16): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945875 | CATATATA others(11): Show |
C | 36 | a0001c0001t0001g0066 a0001c0001t0001g0251 a0001c0001t0001g0252 others(33): Show |
37 | HG00735.hp1 HG01106.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.738+524_738+541del others(18): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40945875 | ||||||
| chr5:40945906 | A | G | 32 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(29): Show |
32 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.738+538A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40945906 | |||||||
| chr5:40945908 | A | G | 32 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(29): Show |
32 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.738+540A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40945908 | |||||||
| chr5:40945953 | T | C | 1 | a0004c0004t0001g0025 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.738+585T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40945953 | |||||||
| chr5:40945963 | A | G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0031 |
4 | HG02109.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.738+595A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40945963 | |||||||
| chr5:40946156 | TAAAAACA others(49): Show |
T | 1 | a0002c0002t0004g0274 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.738+789_738+844del others(56): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946156 | |||||||
| chr5:40946274 | T | A | 1 | a0002c0002t0004g0289 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.738+906T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946274 | |||||||
| chr5:40946326 | G | T | 1 | a0002c0002t0004g0274 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.738+958G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946326 | |||||||
| chr5:40946343 | A | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0050 others(7): Show |
10 | HG01109.hp1 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.738+975A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946343 | |||||||
| chr5:40946363 | T | TC | 6 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(3): Show |
6 | HG01361.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+996dupC | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40946363 | ||||||
| chr5:40946374 | G | A | 1 | a0002c0002t0002g0178 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.738+1006G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946374 | |||||||
| chr5:40946473 | A | G | 8 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0007c0007t0004g0264 others(5): Show |
8 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.738+1105A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946473 | |||||||
| chr5:40946503 | A | T | 77 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(74): Show |
78 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.739-1099A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946503 | |||||||
| chr5:40946546 | A | G | 239 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(236): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.739-1056A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946546 | |||||||
| chr5:40946642 | G | A | 212 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(209): Show |
217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.739-960G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946642 | |||||||
| chr5:40946772 | A | C | 1 | a0002c0002t0004g0274 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.739-830A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946772 | |||||||
| chr5:40946773 | A | G | 61 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(58): Show |
62 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.739-829A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40946773 | |||||||
| chr5:40947016 | G | C | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.739-586G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40947016 | |||||||
| chr5:40947097 | A | AT | 21 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(18): Show |
22 | HG00544.hp2 HG01168.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.739-485dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40947097 | ||||||
| chr5:40947097 | AT | A | 178 | a0001c0001t0001g0011 a0001c0001t0001g0233 a0001c0001t0002g0008 others(175): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.739-485delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 40947097 | ||||||
| chr5:40947110 | T | G | 1 | a0002c0002t0001g0144 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.739-492T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40947110 | |||||||
| chr5:40947244 | T | C | 369 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(366): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.739-358T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40947244 | |||||||
| chr5:40947245 | G | A | 1 | a0003c0003t0003g0338 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.739-357G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40947245 | |||||||
| chr5:40947290 | G | C | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.739-312G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40947290 | |||||||
| chr5:40947486 | C | T | 3 | a0004c0004t0001g0288 a0004c0004t0001g0298 a0004c0004t0001g0299 |
3 | NA18990.hp1 NA19059.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.739-116C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40947486 | |||||||
| chr5:40947507 | A | G | 10 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0002g0140 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.739-95A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40947507 | |||||||
| chr5:40947588 | T | C | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.739-14T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 7/17 | chr5 | 40947588 | |||||||
| chr5:40947999 | A | G | 4 | a0001c0001t0001g0322 a0001c0001t0001g0329 a0001c0001t0001g0331 others(1): Show |
4 | NA18950.hp2 NA18953.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.982+154A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40947999 | |||||||
| chr5:40948005 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.982+160A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948005 | |||||||
| chr5:40948037 | T | A | 185 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(182): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.982+192T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948037 | |||||||
| chr5:40948038 | G | C | 6 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(3): Show |
6 | HG01361.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+193G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948038 | |||||||
| chr5:40948252 | T | TA | 231 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0194 others(228): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.982+414dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 40948252 | ||||||
| chr5:40948324 | G | T | 3 | a0001c0001t0001g0222 a0001c0001t0002g0208 a0001c0001t0002g0217 |
3 | NA18939.hp2 NA19065.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.982+479G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948324 | |||||||
| chr5:40948388 | A | T | 195 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(192): Show |
200 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.982+543A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948388 | |||||||
| chr5:40948464 | G | A | 1 | a0002c0002t0004g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.982+619G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948464 | |||||||
| chr5:40948465 | A | T | 149 | a0002c0002t0001g0015 a0002c0002t0001g0018 a0002c0002t0001g0019 others(146): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.982+620A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948465 | |||||||
| chr5:40948517 | G | T | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.982+672G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948517 | |||||||
| chr5:40948522 | T | G | 67 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(64): Show |
68 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.982+677T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948522 | |||||||
| chr5:40948529 | T | C | 1 | a0002c0002t0001g0123 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.982+684T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948529 | |||||||
| chr5:40948710 | C | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.982+865C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948710 | |||||||
| chr5:40948713 | A | G | 6 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(3): Show |
6 | HG01361.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+868A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948713 | |||||||
| chr5:40948991 | A | T | 3 | a0002c0002t0001g0087 a0002c0002t0001g0099 a0002c0002t0001g0273 |
3 | HG02055.hp1 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.983-913A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40948991 | |||||||
| chr5:40949023 | C | T | 1 | a0002c0002t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.983-881C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949023 | |||||||
| chr5:40949101 | A | T | 1 | a0002c0002t0004g0274 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.983-803A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949101 | |||||||
| chr5:40949173 | C | T | 2 | a0001c0001t0003g0047 a0003c0003t0003g0045 |
2 | HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.983-731C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949173 | |||||||
| chr5:40949272 | T | C | 1 | a0003c0003t0003g0234 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.983-632T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949272 | |||||||
| chr5:40949311 | A | G | 1 | a0001c0001t0004g0048 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.983-593A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949311 | |||||||
| chr5:40949360 | C | CA | 59 | a0001c0001t0001g0331 a0001c0001t0002g0007 a0001c0001t0002g0013 others(56): Show |
59 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.983-531dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 40949360 | ||||||
| chr5:40949360 | C | CAA | 54 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(51): Show |
55 | HG00099.hp1 HG00280.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.983-532_983-531dup others(2): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 40949360 | ||||||
| chr5:40949360 | C | CAAA | 8 | a0001c0001t0001g0218 a0001c0001t0001g0241 a0001c0001t0002g0216 others(5): Show |
8 | HG00408.hp2 HG01243.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.983-533_983-531dup others(3): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 40949360 | ||||||
| chr5:40949360 | CA | C | 22 | a0001c0001t0012g0365 a0002c0002t0001g0049 a0002c0002t0001g0143 others(19): Show |
22 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.983-531delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 40949360 | ||||||
| chr5:40949383 | C | A | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.983-521C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949383 | |||||||
| chr5:40949674 | T | G | 227 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0194 others(224): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.983-230T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949674 | |||||||
| chr5:40949702 | T | G | 67 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(64): Show |
68 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.983-202T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949702 | |||||||
| chr5:40949765 | C | T | 2 | a0001c0001t0003g0285 a0001c0001t0003g0286 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.983-139C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949765 | |||||||
| chr5:40949782 | C | A | 3 | a0002c0002t0003g0149 a0006c0006t0002g0147 a0017c0027t0002g0148 |
3 | HG02145.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.983-122C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949782 | |||||||
| chr5:40949833 | C | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.983-71C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949833 | |||||||
| chr5:40949895 | C | T | 233 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0194 others(230): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.983-9C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 8/17 | chr5 | 40949895 | |||||||
| chr5:40950055 | C | CT | 68 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(65): Show |
69 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.1093+51dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40950055 | ||||||
| chr5:40950224 | C | T | 1 | a0002c0002t0001g0098 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1093+210C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950224 | |||||||
| chr5:40950242 | CTCTG | C | 149 | a0002c0002t0001g0015 a0002c0002t0001g0018 a0002c0002t0001g0019 others(146): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1093+232_1093+235d others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40950242 | ||||||
| chr5:40950328 | T | A | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1093+314T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950328 | |||||||
| chr5:40950369 | C | A | 27 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(24): Show |
27 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1093+355C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950369 | |||||||
| chr5:40950373 | G | A | 153 | a0002c0002t0001g0015 a0002c0002t0001g0018 a0002c0002t0001g0019 others(150): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1093+359G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950373 | |||||||
| chr5:40950420 | T | C | 1 | a0002c0002t0004g0289 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1093+406T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950420 | |||||||
| chr5:40950433 | C | G | 1 | a0007c0007t0004g0264 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1093+419C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950433 | |||||||
| chr5:40950473 | C | T | 1 | a0001c0022t0001g0343 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1093+459C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950473 | |||||||
| chr5:40950474 | G | A | 233 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0194 others(230): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1093+460G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950474 | |||||||
| chr5:40950494 | AATT | A | 27 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(24): Show |
27 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1093+482_1093+484d others(5): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40950494 | ||||||
| chr5:40950519 | G | C | 6 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(3): Show |
6 | HG01361.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1093+505G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950519 | |||||||
| chr5:40950570 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1093+556G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950570 | |||||||
| chr5:40950595 | C | A | 19 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(16): Show |
19 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1093+581C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950595 | |||||||
| chr5:40950706 | A | G | 57 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(54): Show |
58 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1093+692A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950706 | |||||||
| chr5:40950739 | G | T | 1 | a0001c0001t0002g0336 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1093+725G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950739 | |||||||
| chr5:40950818 | G | A | 1 | a0018c0018t0002g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1093+804G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950818 | |||||||
| chr5:40950894 | T | C | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1093+880T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950894 | |||||||
| chr5:40950902 | T | A | 1 | a0002c0002t0004g0274 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1093+888T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950902 | |||||||
| chr5:40950964 | T | G | 1 | a0018c0018t0002g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1093+950T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950964 | |||||||
| chr5:40950979 | G | T | 3 | a0001c0001t0003g0283 a0001c0001t0003g0285 a0001c0001t0003g0286 |
3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1093+965G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40950979 | |||||||
| chr5:40951009 | T | A | 300 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(297): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1093+995T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951009 | |||||||
| chr5:40951097 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0031 |
4 | HG02109.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093+1083G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951097 | |||||||
| chr5:40951186 | C | T | 2 | a0010c0010t0001g0113 a0012c0012t0003g0164 |
2 | NA18956.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1093+1172C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951186 | |||||||
| chr5:40951233 | TGTTAA | T | 3 | a0001c0001t0002g0055 a0001c0001t0007g0030 a0002c0002t0002g0162 |
3 | HG01109.hp1 HG01257.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1093+1228_1093+123 others(9): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40951233 | ||||||
| chr5:40951248 | C | T | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1093+1234C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951248 | |||||||
| chr5:40951266 | T | A | 67 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(64): Show |
68 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1093+1252T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951266 | |||||||
| chr5:40951302 | T | G | 1 | a0003c0003t0003g0223 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1093+1288T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951302 | |||||||
| chr5:40951505 | A | G | 2 | a0002c0002t0004g0289 a0002c0002t0004g0312 |
2 | NA18982.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1093+1491A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951505 | |||||||
| chr5:40951506 | T | C | 1 | a0005c0005t0003g0085 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1093+1492T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951506 | |||||||
| chr5:40951536 | G | A | 4 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0004g0202 others(1): Show |
4 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093+1522G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951536 | |||||||
| chr5:40951561 | G | A | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1093+1547G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951561 | |||||||
| chr5:40951592 | G | C | 1 | a0001c0001t0004g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1093+1578G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951592 | |||||||
| chr5:40951621 | C | T | 75 | a0001c0001t0001g0011 a0001c0001t0001g0194 a0001c0001t0001g0195 others(72): Show |
76 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1093+1607C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951621 | |||||||
| chr5:40951673 | T | C | 4 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093+1659T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951673 | |||||||
| chr5:40951835 | G | A | 1 | a0004c0014t0001g0023 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1093+1821G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951835 | |||||||
| chr5:40951842 | A | G | 300 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(297): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1093+1828A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951842 | |||||||
| chr5:40951885 | C | A | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1093+1871C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951885 | |||||||
| chr5:40951937 | C | T | 153 | a0002c0002t0001g0015 a0002c0002t0001g0018 a0002c0002t0001g0019 others(150): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1093+1923C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40951937 | |||||||
| chr5:40952007 | G | T | 1 | a0001c0001t0004g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1093+1993G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952007 | |||||||
| chr5:40952010 | T | G | 1 | a0003c0003t0003g0230 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1093+1996T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952010 | |||||||
| chr5:40952143 | C | T | 1 | a0009c0009t0001g0304 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1093+2129C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952143 | |||||||
| chr5:40952246 | A | G | 99 | a0001c0001t0001g0011 a0001c0001t0001g0194 a0001c0001t0001g0195 others(96): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1093+2232A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952246 | |||||||
| chr5:40952295 | G | A | 1 | a0003c0003t0003g0334 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1093+2281G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952295 | |||||||
| chr5:40952346 | T | C | 3 | a0002c0002t0003g0198 a0002c0002t0003g0199 a0002c0002t0003g0200 |
3 | HG02257.hp2 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1093+2332T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952346 | |||||||
| chr5:40952454 | C | A | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1093+2440C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952454 | |||||||
| chr5:40952469 | T | C | 94 | a0001c0001t0001g0011 a0001c0001t0001g0194 a0001c0001t0001g0195 others(91): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1093+2455T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952469 | |||||||
| chr5:40952478 | T | TTTTA | 28 | a0001c0001t0003g0263 a0001c0001t0004g0033 a0001c0001t0012g0365 others(25): Show |
28 | HG00597.hp1 HG01070.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.1093+2488_1093+249 others(8): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40952478 | ||||||
| chr5:40952478 | T | TTTTATTT others(1): Show |
6 | a0001c0001t0002g0007 a0002c0002t0002g0071 a0002c0002t0002g0072 others(3): Show |
6 | HG00280.hp2 HG00741.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1093+2484_1093+249 others(12): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40952478 | ||||||
| chr5:40952478 | T | TTTTATTT others(5): Show |
6 | a0001c0001t0002g0201 a0001c0001t0002g0275 a0001c0001t0004g0276 others(3): Show |
6 | HG01070.hp2 HG01361.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1093+2480_1093+249 others(16): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40952478 | ||||||
| chr5:40952478 | T | TTTTATTT others(9): Show |
10 | a0001c0001t0001g0214 a0001c0001t0002g0154 a0001c0001t0002g0247 others(7): Show |
10 | HG00280.hp1 HG01074.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1093+2476_1093+249 others(20): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40952478 | ||||||
| chr5:40952478 | T | TTTTATTT others(13): Show |
70 | a0001c0001t0001g0011 a0001c0001t0001g0197 a0001c0001t0001g0224 others(67): Show |
71 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1093+2472_1093+249 others(24): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40952478 | ||||||
| chr5:40952478 | T | TTTTATTT others(17): Show |
13 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(10): Show |
13 | HG01123.hp2 HG01243.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1093+2468_1093+249 others(28): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40952478 | ||||||
| chr5:40952537 | C | T | 3 | a0002c0002t0003g0198 a0002c0002t0003g0199 a0002c0002t0003g0200 |
3 | HG02257.hp2 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1093+2523C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952537 | |||||||
| chr5:40952588 | A | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1093+2574A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952588 | |||||||
| chr5:40952642 | C | A | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1093+2628C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952642 | |||||||
| chr5:40952668 | C | T | 1 | a0018c0018t0002g0193 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1093+2654C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952668 | |||||||
| chr5:40952763 | C | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1094-2624C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952763 | |||||||
| chr5:40952790 | T | A | 76 | a0001c0001t0001g0011 a0001c0001t0001g0194 a0001c0001t0001g0195 others(73): Show |
77 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1094-2597T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952790 | |||||||
| chr5:40952801 | A | G | 361 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(358): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1094-2586A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952801 | |||||||
| chr5:40952950 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1094-2437C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40952950 | |||||||
| chr5:40953089 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(48): Show |
52 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1094-2298C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40953089 | |||||||
| chr5:40953123 | T | C | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1094-2264T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40953123 | |||||||
| chr5:40953133 | A | G | 2 | a0002c0002t0001g0120 a0002c0002t0001g0175 |
2 | NA18968.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1094-2254A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40953133 | |||||||
| chr5:40953185 | G | C | 201 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1094-2202G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40953185 | |||||||
| chr5:40953619 | A | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1094-1768A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40953619 | |||||||
| chr5:40953639 | C | CA | 28 | a0001c0001t0001g0227 a0001c0001t0001g0244 a0001c0001t0002g0001 others(25): Show |
30 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1094-1730dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40953639 | ||||||
| chr5:40953639 | C | CAA | 63 | a0001c0001t0001g0066 a0001c0001t0001g0251 a0001c0001t0001g0252 others(60): Show |
64 | HG00544.hp2 HG00735.hp1 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.1094-1731_1094-173 others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40953639 | ||||||
| chr5:40953639 | C | CAAA | 138 | a0001c0001t0001g0064 a0001c0001t0001g0211 a0001c0001t0001g0370 others(135): Show |
140 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1094-1732_1094-173 others(7): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40953639 | ||||||
| chr5:40953639 | C | CAAAA | 61 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(58): Show |
62 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1094-1733_1094-173 others(8): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40953639 | ||||||
| chr5:40953639 | C | CAAAAA | 7 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0007c0007t0004g0264 others(4): Show |
7 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1094-1734_1094-173 others(9): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40953639 | ||||||
| chr5:40953835 | A | G | 3 | a0001c0001t0005g0367 a0001c0001t0005g0368 a0001c0001t0012g0365 |
3 | HG02630.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1094-1552A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40953835 | |||||||
| chr5:40953854 | T | TAACATAA others(43): Show |
1 | a0002c0002t0002g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1094-1531_1094-153 others(54): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40953854 | ||||||
| chr5:40953855 | A | AACATAAA others(55): Show |
1 | a0006c0006t0004g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1094-1531_1094-153 others(66): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40953855 | ||||||
| chr5:40953855 | A | AACATAAA others(55): Show |
150 | a0001c0001t0001g0370 a0002c0002t0001g0015 a0002c0002t0001g0018 others(147): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1094-1531_1094-153 others(66): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40953855 | ||||||
| chr5:40953997 | C | G | 47 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(44): Show |
50 | HG00544.hp2 HG00735.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.1094-1390C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40953997 | |||||||
| chr5:40954053 | A | G | 48 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(45): Show |
51 | HG00544.hp2 HG00735.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.1094-1334A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954053 | |||||||
| chr5:40954077 | A | G | 19 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(16): Show |
19 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1094-1310A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954077 | |||||||
| chr5:40954123 | C | G | 1 | a0003c0003t0003g0334 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1094-1264C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954123 | |||||||
| chr5:40954139 | C | T | 369 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(366): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1094-1248C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954139 | |||||||
| chr5:40954200 | G | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(37): Show |
41 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1094-1187G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954200 | |||||||
| chr5:40954316 | T | C | 1 | a0002c0002t0004g0274 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1094-1071T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954316 | |||||||
| chr5:40954324 | A | T | 1 | a0002c0002t0001g0120 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1094-1063A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954324 | |||||||
| chr5:40954525 | A | C | 62 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(59): Show |
63 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1094-862A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954525 | |||||||
| chr5:40954582 | A | G | 2 | a0001c0001t0002g0336 a0003c0023t0003g0335 |
2 | NA18951.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1094-805A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954582 | |||||||
| chr5:40954743 | G | T | 9 | a0001c0001t0002g0007 a0001c0001t0002g0201 a0001c0001t0002g0204 others(6): Show |
9 | HG01361.hp2 HG02486.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1094-644G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954743 | |||||||
| chr5:40954752 | C | T | 46 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(43): Show |
49 | HG00544.hp2 HG00735.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.1094-635C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954752 | |||||||
| chr5:40954753 | G | A | 8 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0007c0007t0004g0264 others(5): Show |
8 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1094-634G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954753 | |||||||
| chr5:40954777 | A | G | 50 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0211 others(47): Show |
53 | HG00544.hp2 HG00735.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.1094-610A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954777 | |||||||
| chr5:40954826 | T | C | 3 | a0001c0001t0005g0367 a0001c0001t0005g0368 a0001c0001t0012g0365 |
3 | HG02630.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1094-561T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954826 | |||||||
| chr5:40954877 | C | CA | 160 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0066 others(157): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1094-482dupA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40954877 | ||||||
| chr5:40954877 | C | CAA | 34 | a0001c0001t0001g0194 a0001c0001t0001g0218 a0001c0001t0002g0061 others(31): Show |
34 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.1094-483_1094-482d others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40954877 | ||||||
| chr5:40954877 | C | CAAA | 18 | a0002c0002t0001g0099 a0002c0002t0002g0142 a0002c0002t0003g0138 others(15): Show |
18 | HG00673.hp1 HG01934.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1094-484_1094-482d others(5): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40954877 | ||||||
| chr5:40954877 | C | CAAAA | 8 | a0002c0002t0003g0199 a0004c0004t0001g0025 a0004c0004t0001g0026 others(5): Show |
8 | HG00408.hp1 HG00597.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1094-485_1094-482d others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40954877 | ||||||
| chr5:40954877 | CA | C | 34 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(31): Show |
35 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1094-482delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40954877 | ||||||
| chr5:40954877 | CAA | C | 23 | a0001c0001t0001g0326 a0001c0001t0002g0007 a0001c0001t0002g0269 others(20): Show |
23 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1094-483_1094-482d others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40954877 | ||||||
| chr5:40954890 | A | AAAAG | 54 | a0002c0002t0001g0019 a0002c0002t0001g0068 a0002c0002t0001g0081 others(51): Show |
55 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1094-494_1094-493i others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 40954890 | ||||||
| chr5:40954960 | T | C | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1094-427T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40954960 | |||||||
| chr5:40955142 | T | C | 1 | a0005c0005t0003g0084 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1094-245T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40955142 | |||||||
| chr5:40955254 | T | C | 1 | a0001c0001t0002g0333 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1094-133T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40955254 | |||||||
| chr5:40955265 | T | C | 1 | a0003c0003t0003g0029 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1094-122T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40955265 | |||||||
| chr5:40955288 | G | A | 2 | a0001c0001t0004g0033 a0001c0025t0011g0366 |
2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1094-99G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 9/17 | chr5 | 40955288 | |||||||
| chr5:40955615 | A | G | 1 | a0001c0001t0002g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1260+62A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40955615 | |||||||
| chr5:40955726 | A | T | 2 | a0001c0001t0002g0001 a0001c0001t0002g0031 |
4 | HG02109.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+173A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40955726 | |||||||
| chr5:40956177 | A | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+624A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40956177 | |||||||
| chr5:40956178 | C | G | 369 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(366): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1260+625C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40956178 | |||||||
| chr5:40956237 | G | A | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+684G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40956237 | |||||||
| chr5:40956316 | A | G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0031 |
4 | HG02109.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+763A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40956316 | |||||||
| chr5:40956317 | G | C | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+764G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40956317 | |||||||
| chr5:40956320 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1260+767C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40956320 | |||||||
| chr5:40956451 | A | G | 2 | a0001c0001t0002g0154 a0001c0001t0002g0261 |
2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1260+898A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40956451 | |||||||
| chr5:40956509 | C | T | 7 | a0001c0001t0001g0222 a0001c0001t0002g0208 a0001c0001t0002g0216 others(4): Show |
7 | NA18939.hp2 NA18957.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+956C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40956509 | |||||||
| chr5:40956586 | A | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1260+1033A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40956586 | |||||||
| chr5:40957070 | A | G | 2 | a0002c0002t0001g0136 a0002c0002t0001g0137 |
2 | HG00621.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1261-963A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957070 | |||||||
| chr5:40957106 | T | C | 5 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0003g0020 others(2): Show |
5 | HG01361.hp2 HG02486.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-927T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957106 | |||||||
| chr5:40957446 | CTATTTTA others(8): Show |
C | 14 | a0001c0001t0001g0222 a0001c0001t0001g0227 a0001c0001t0001g0244 others(11): Show |
14 | NA18939.hp2 NA18947.hp2 NA18953.hp1 others(11): Show |
intron_variant | MODIFIER | c.1261-575_1261-561d others(17): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 40957446 | ||||||
| chr5:40957450 | T | A | 3 | a0005c0005t0003g0280 a0005c0005t0003g0281 a0005c0005t0003g0282 |
3 | HG01192.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1261-583T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957450 | |||||||
| chr5:40957549 | A | G | 369 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(366): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1261-484A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957549 | |||||||
| chr5:40957617 | T | G | 257 | a0001c0001t0001g0011 a0001c0001t0001g0194 a0001c0001t0001g0195 others(254): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1261-416T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957617 | |||||||
| chr5:40957701 | C | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1261-332C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957701 | |||||||
| chr5:40957705 | C | T | 1 | a0017c0027t0002g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1261-328C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957705 | |||||||
| chr5:40957727 | G | A | 147 | a0001c0001t0002g0201 a0001c0001t0002g0204 a0001c0001t0002g0269 others(144): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1261-306G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957727 | |||||||
| chr5:40957735 | C | T | 4 | a0004c0004t0001g0297 a0004c0004t0001g0300 a0004c0004t0001g0306 others(1): Show |
4 | HG00673.hp1 HG02027.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-298C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957735 | |||||||
| chr5:40957736 | G | A | 4 | a0001c0001t0002g0204 a0001c0001t0004g0202 a0001c0001t0004g0203 others(1): Show |
4 | HG02486.hp1 HG03471.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-297G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957736 | |||||||
| chr5:40957758 | G | GT | 8 | a0001c0001t0002g0240 a0001c0001t0002g0270 a0002c0002t0001g0018 others(5): Show |
8 | HG00673.hp2 NA18612.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.1261-266dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 40957758 | ||||||
| chr5:40957768 | G | GT | 108 | a0001c0001t0001g0006 a0001c0001t0001g0066 a0001c0001t0001g0194 others(105): Show |
112 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1261-251dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 40957768 | ||||||
| chr5:40957768 | G | T | 3 | a0001c0001t0001g0233 a0001c0001t0002g0270 a0003c0003t0003g0262 |
3 | HG00408.hp2 NA18974.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1261-265G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957768 | |||||||
| chr5:40957773 | T | TG | 131 | a0001c0001t0002g0333 a0002c0002t0001g0015 a0002c0002t0001g0019 others(128): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1261-260_1261-259i others(3): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957773 | |||||||
| chr5:40957774 | T | G | 20 | a0004c0004t0001g0021 a0004c0004t0001g0024 a0004c0004t0001g0025 others(17): Show |
20 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1261-259T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957774 | |||||||
| chr5:40957790 | A | T | 1 | a0006c0006t0002g0147 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1261-243A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957790 | |||||||
| chr5:40957901 | A | G | 6 | a0001c0001t0002g0007 a0001c0001t0002g0275 a0001c0001t0004g0035 others(3): Show |
6 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1261-132A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957901 | |||||||
| chr5:40957925 | G | A | 369 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(366): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1261-108G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957925 | |||||||
| chr5:40957929 | G | A | 19 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(16): Show |
19 | HG00544.hp2 HG00735.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.1261-104G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 10/17 | chr5 | 40957929 | |||||||
| chr5:40958299 | A | G | 1 | a0002c0002t0001g0099 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1489+38A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40958299 | |||||||
| chr5:40958400 | C | T | 4 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0260 others(1): Show |
4 | HG01346.hp1 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489+139C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40958400 | |||||||
| chr5:40958472 | C | T | 3 | a0005c0005t0003g0280 a0005c0005t0003g0281 a0005c0005t0003g0282 |
3 | HG01192.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1489+211C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40958472 | |||||||
| chr5:40958537 | G | C | 3 | a0001c0001t0002g0007 a0001c0001t0002g0055 a0001c0001t0005g0368 |
3 | HG02630.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1489+276G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40958537 | |||||||
| chr5:40958547 | C | T | 1 | a0001c0001t0005g0367 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1489+286C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40958547 | |||||||
| chr5:40958591 | T | C | 2 | a0001c0001t0002g0240 a0001c0001t0002g0279 |
2 | NA18994.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.1489+330T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40958591 | |||||||
| chr5:40958832 | C | T | 1 | a0003c0003t0003g0245 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1489+571C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40958832 | |||||||
| chr5:40958833 | G | A | 1 | a0005c0005t0003g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1489+572G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40958833 | |||||||
| chr5:40959045 | T | C | 1 | a0003c0003t0003g0212 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1490-404T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40959045 | |||||||
| chr5:40959052 | C | T | 2 | a0001c0001t0002g0270 a0001c0001t0012g0365 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1490-397C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40959052 | |||||||
| chr5:40959185 | G | A | 1 | a0002c0002t0001g0272 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1490-264G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 11/17 | chr5 | 40959185 | |||||||
| chr5:40959638 | C | A | 2 | a0001c0001t0001g0326 a0001c0001t0001g0348 |
2 | NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1661+18C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40959638 | |||||||
| chr5:40959857 | T | C | 18 | a0006c0006t0002g0147 a0006c0006t0004g0073 a0006c0006t0004g0091 others(15): Show |
18 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1661+237T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40959857 | |||||||
| chr5:40959874 | G | A | 1 | a0002c0002t0003g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1661+254G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40959874 | |||||||
| chr5:40959920 | A | G | 5 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0005g0367 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1661+300A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40959920 | |||||||
| chr5:40959966 | A | C | 26 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(23): Show |
28 | HG01346.hp1 HG01361.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1661+346A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40959966 | |||||||
| chr5:40960029 | A | G | 1 | a0001c0001t0004g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1661+409A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960029 | |||||||
| chr5:40960059 | A | G | 18 | a0006c0006t0002g0147 a0006c0006t0004g0073 a0006c0006t0004g0091 others(15): Show |
18 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1661+439A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960059 | |||||||
| chr5:40960064 | A | T | 69 | a0003c0003t0003g0029 a0003c0003t0003g0045 a0003c0003t0003g0092 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.1661+444A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960064 | |||||||
| chr5:40960176 | C | T | 22 | a0001c0001t0001g0218 a0001c0001t0001g0227 a0001c0001t0001g0241 others(19): Show |
23 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1661+556C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960176 | |||||||
| chr5:40960224 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1661+604G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960224 | |||||||
| chr5:40960521 | A | T | 76 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(73): Show |
77 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1661+901A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960521 | |||||||
| chr5:40960591 | A | G | 5 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0005g0367 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1661+971A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960591 | |||||||
| chr5:40960678 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1661+1058C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960678 | |||||||
| chr5:40960746 | A | G | 5 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0005g0367 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1661+1126A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960746 | |||||||
| chr5:40960825 | G | A | 2 | a0002c0002t0001g0165 a0002c0002t0001g0176 |
2 | NA18940.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1661+1205G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960825 | |||||||
| chr5:40960860 | A | T | 16 | a0006c0006t0004g0073 a0006c0006t0004g0091 a0006c0006t0004g0094 others(13): Show |
16 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1662-1225A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960860 | |||||||
| chr5:40960874 | G | T | 101 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(98): Show |
104 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1662-1211G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960874 | |||||||
| chr5:40960889 | A | T | 69 | a0003c0003t0003g0029 a0003c0003t0003g0045 a0003c0003t0003g0092 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.1662-1196A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960889 | |||||||
| chr5:40960905 | G | C | 1 | a0003c0003t0003g0250 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1662-1180G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40960905 | |||||||
| chr5:40961022 | T | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1662-1063T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961022 | |||||||
| chr5:40961024 | A | G | 5 | a0001c0001t0002g0236 a0002c0002t0002g0005 a0002c0002t0002g0157 others(2): Show |
6 | HG02071.hp1 NA18960.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1662-1061A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961024 | |||||||
| chr5:40961062 | A | G | 107 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0013 others(104): Show |
110 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1662-1023A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961062 | |||||||
| chr5:40961315 | G | C | 1 | a0007c0007t0004g0268 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1662-770G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961315 | |||||||
| chr5:40961390 | C | CT | 71 | a0001c0001t0002g0216 a0001c0022t0001g0343 a0003c0003t0003g0029 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.1662-683dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr5 | 40961390 | ||||||
| chr5:40961390 | CT | C | 25 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(22): Show |
27 | HG01346.hp1 HG01361.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1662-683delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr5 | 40961390 | ||||||
| chr5:40961424 | A | T | 2 | a0001c0001t0002g0270 a0001c0001t0012g0365 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1662-661A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961424 | |||||||
| chr5:40961471 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1662-614G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961471 | |||||||
| chr5:40961549 | T | A | 22 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(19): Show |
23 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1662-536T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961549 | |||||||
| chr5:40961678 | A | G | 322 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1662-407A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961678 | |||||||
| chr5:40961682 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(5): Show |
9 | HG01975.hp2 HG02273.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1662-403C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961682 | |||||||
| chr5:40961718 | G | T | 1 | a0001c0001t0012g0365 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1662-367G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961718 | |||||||
| chr5:40961745 | G | A | 6 | a0001c0001t0001g0210 a0001c0001t0001g0224 a0002c0002t0001g0093 others(3): Show |
6 | HG00642.hp1 HG01123.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662-340G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961745 | |||||||
| chr5:40961750 | A | G | 18 | a0006c0006t0002g0147 a0006c0006t0004g0073 a0006c0006t0004g0091 others(15): Show |
18 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1662-335A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961750 | |||||||
| chr5:40961771 | A | G | 106 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0013 others(103): Show |
109 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1662-314A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961771 | |||||||
| chr5:40961792 | C | A | 322 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1662-293C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 12/17 | chr5 | 40961792 | |||||||
| chr5:40962266 | C | T | 10 | a0001c0001t0002g0007 a0001c0001t0003g0283 a0001c0001t0003g0285 others(7): Show |
10 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1749+94C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962266 | |||||||
| chr5:40962311 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1749+139G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962311 | |||||||
| chr5:40962344 | A | G | 1 | a0001c0001t0002g0336 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1749+172A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962344 | |||||||
| chr5:40962445 | G | A | 322 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1749+273G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962445 | |||||||
| chr5:40962528 | CT | C | 11 | a0001c0001t0002g0007 a0001c0001t0002g0053 a0001c0001t0003g0283 others(8): Show |
11 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1749+366delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 40962528 | ||||||
| chr5:40962538 | T | C | 9 | a0001c0001t0003g0283 a0001c0001t0003g0285 a0001c0001t0003g0286 others(6): Show |
9 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1749+366T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962538 | |||||||
| chr5:40962568 | A | G | 30 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(27): Show |
32 | HG01346.hp1 HG01361.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1749+396A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962568 | |||||||
| chr5:40962750 | A | G | 1 | a0005c0005t0003g0074 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1749+578A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962750 | |||||||
| chr5:40962761 | C | T | 65 | a0003c0003t0003g0029 a0003c0003t0003g0045 a0003c0003t0003g0092 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.1749+589C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962761 | |||||||
| chr5:40962848 | T | G | 1 | a0002c0002t0001g0075 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1749+676T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962848 | |||||||
| chr5:40962884 | A | C | 1 | a0002c0002t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1749+712A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962884 | |||||||
| chr5:40962885 | G | A | 53 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(50): Show |
54 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1749+713G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962885 | |||||||
| chr5:40962892 | G | C | 1 | a0002c0002t0002g0155 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1749+720G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962892 | |||||||
| chr5:40962965 | C | T | 1 | a0001c0001t0012g0365 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1749+793C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962965 | |||||||
| chr5:40962966 | G | A | 1 | a0005c0005t0003g0074 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1749+794G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40962966 | |||||||
| chr5:40963029 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1749+857C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40963029 | |||||||
| chr5:40963293 | G | A | 2 | a0002c0002t0001g0185 a0002c0002t0001g0186 |
2 | NA18966.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1749+1121G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40963293 | |||||||
| chr5:40963334 | A | T | 18 | a0006c0006t0002g0147 a0006c0006t0004g0073 a0006c0006t0004g0091 others(15): Show |
18 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1749+1162A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40963334 | |||||||
| chr5:40963342 | C | T | 2 | a0002c0002t0002g0162 a0009c0009t0002g0315 |
2 | HG01257.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1749+1170C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40963342 | |||||||
| chr5:40963346 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1749+1174C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40963346 | |||||||
| chr5:40963414 | T | G | 48 | a0001c0001t0003g0047 a0001c0001t0004g0002 a0001c0001t0004g0003 others(45): Show |
50 | HG00423.hp1 HG00558.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1749+1242T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40963414 | |||||||
| chr5:40963493 | C | G | 1 | a0001c0001t0004g0203 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1750-1248C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40963493 | |||||||
| chr5:40963728 | T | C | 322 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1750-1013T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40963728 | |||||||
| chr5:40963762 | C | G | 2 | a0001c0001t0002g0270 a0001c0001t0012g0365 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1750-979C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40963762 | |||||||
| chr5:40964020 | C | CTTTT | 27 | a0001c0001t0002g0008 a0001c0001t0002g0228 a0001c0001t0002g0236 others(24): Show |
28 | HG00544.hp1 HG01257.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.1750-693_1750-690d others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 40964020 | ||||||
| chr5:40964020 | C | CTTTTT | 40 | a0001c0001t0002g0032 a0001c0001t0002g0061 a0001c0001t0002g0154 others(37): Show |
40 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1750-694_1750-690d others(7): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 40964020 | ||||||
| chr5:40964020 | C | CTTTTTT | 8 | a0001c0001t0002g0238 a0001c0001t0002g0278 a0001c0001t0003g0263 others(5): Show |
8 | HG00597.hp1 HG01070.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1750-695_1750-690d others(8): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 40964020 | ||||||
| chr5:40964020 | CT | C | 60 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(57): Show |
62 | HG00558.hp1 HG00735.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1750-690delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 40964020 | ||||||
| chr5:40964020 | CTT | C | 25 | a0001c0001t0001g0064 a0001c0001t0002g0007 a0001c0001t0003g0047 others(22): Show |
25 | HG00642.hp2 HG00735.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1750-691_1750-690d others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 40964020 | ||||||
| chr5:40964020 | CTTT | C | 108 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0002g0270 others(105): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.1750-692_1750-690d others(5): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 40964020 | ||||||
| chr5:40964020 | CTTTT | C | 75 | a0001c0001t0001g0006 a0001c0001t0001g0211 a0001c0001t0001g0218 others(72): Show |
77 | HG00099.hp1 HG00408.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.1750-693_1750-690d others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 40964020 | ||||||
| chr5:40964020 | CTTTTTTT others(11): Show |
C | 2 | a0002c0002t0002g0163 a0002c0002t0002g0178 |
2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1750-707_1750-690d others(20): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 40964020 | ||||||
| chr5:40964029 | T | G | 5 | a0001c0001t0002g0065 a0001c0001t0002g0258 a0001c0001t0002g0259 others(2): Show |
5 | HG01346.hp1 HG02055.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1750-712T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964029 | |||||||
| chr5:40964030 | T | G | 21 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(18): Show |
23 | HG01361.hp2 HG02109.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1750-711T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964030 | |||||||
| chr5:40964033 | T | G | 5 | a0001c0001t0002g0065 a0001c0001t0002g0258 a0001c0001t0002g0259 others(2): Show |
5 | HG01346.hp1 HG02055.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1750-708T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964033 | |||||||
| chr5:40964034 | T | G | 21 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(18): Show |
23 | HG01361.hp2 HG02109.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1750-707T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964034 | |||||||
| chr5:40964263 | G | A | 1 | a0005c0005t0003g0124 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1750-478G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964263 | |||||||
| chr5:40964331 | C | T | 66 | a0003c0003t0003g0029 a0003c0003t0003g0045 a0003c0003t0003g0092 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.1750-410C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964331 | |||||||
| chr5:40964338 | C | T | 2 | a0001c0001t0002g0238 a0002c0002t0003g0107 |
2 | HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1750-403C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964338 | |||||||
| chr5:40964365 | G | A | 4 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0260 others(1): Show |
4 | HG01346.hp1 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1750-376G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964365 | |||||||
| chr5:40964366 | T | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(19): Show |
23 | HG00408.hp1 HG00544.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1750-375T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964366 | |||||||
| chr5:40964439 | T | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0322 a0001c0001t0001g0324 others(4): Show |
8 | HG01975.hp2 HG02273.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1750-302T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964439 | |||||||
| chr5:40964453 | AATAATTT others(117): Show |
A | 5 | a0002c0002t0001g0081 a0002c0002t0001g0109 a0002c0002t0002g0071 others(2): Show |
5 | HG00280.hp2 HG01070.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1750-287_1750-164d others(2): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964453 | |||||||
| chr5:40964455 | T | C | 53 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(50): Show |
54 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1750-286T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964455 | |||||||
| chr5:40964493 | A | G | 98 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0013 others(95): Show |
101 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1750-248A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964493 | |||||||
| chr5:40964580 | C | T | 322 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1750-161C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964580 | |||||||
| chr5:40964582 | A | G | 322 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1750-159A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964582 | |||||||
| chr5:40964714 | C | A | 102 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0013 others(99): Show |
105 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1750-27C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 13/17 | chr5 | 40964714 | |||||||
| chr5:40964883 | G | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(19): Show |
23 | HG00408.hp1 HG00544.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1882+10G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40964883 | |||||||
| chr5:40964973 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1882+100T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40964973 | |||||||
| chr5:40965019 | G | T | 1 | a0007c0007t0004g0268 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1882+146G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965019 | |||||||
| chr5:40965216 | C | T | 67 | a0001c0001t0003g0047 a0003c0003t0003g0029 a0003c0003t0003g0045 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.1882+343C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965216 | |||||||
| chr5:40965244 | G | T | 1 | a0001c0001t0004g0048 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1882+371G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965244 | |||||||
| chr5:40965335 | G | A | 1 | a0009c0009t0002g0315 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1882+462G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965335 | |||||||
| chr5:40965412 | T | C | 72 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(69): Show |
73 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1882+539T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965412 | |||||||
| chr5:40965450 | A | G | 69 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(66): Show |
72 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1882+577A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965450 | |||||||
| chr5:40965511 | T | C | 31 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(28): Show |
33 | HG01346.hp1 HG01361.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1882+638T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965511 | |||||||
| chr5:40965619 | T | C | 322 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1882+746T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965619 | |||||||
| chr5:40965627 | G | GATATATA others(3): Show |
1 | a0022c0026t0004g0372 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1882+767_1882+776d others(12): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965627 | ||||||
| chr5:40965627 | GAT | G | 56 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0204 others(53): Show |
57 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1882+775_1882+776d others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965627 | ||||||
| chr5:40965641 | TA | T | 7 | a0001c0001t0002g0061 a0001c0001t0002g0154 a0001c0001t0002g0238 others(4): Show |
7 | HG00280.hp1 HG01175.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1882+769delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965641 | |||||||
| chr5:40965642 | A | T | 59 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0208 others(56): Show |
60 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1882+769A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965642 | |||||||
| chr5:40965643 | TA | T | 7 | a0001c0001t0001g0064 a0001c0001t0001g0194 a0001c0001t0001g0195 others(4): Show |
7 | HG01109.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1882+771delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965643 | |||||||
| chr5:40965644 | A | T | 71 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(68): Show |
72 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1882+771A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965644 | |||||||
| chr5:40965646 | A | ATTT | 2 | a0002c0002t0003g0004 a0004c0004t0001g0303 |
3 | HG00544.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1882+774_1882+775i others(5): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965646 | ||||||
| chr5:40965646 | A | T | 79 | a0001c0001t0001g0064 a0001c0001t0001g0194 a0001c0001t0001g0195 others(76): Show |
80 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1882+773A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965646 | |||||||
| chr5:40965647 | TA | T | 25 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(22): Show |
27 | HG01346.hp1 HG01361.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1882+775delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965647 | |||||||
| chr5:40965648 | A | ATATATAT others(2): Show |
17 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
18 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1882+776_1882+777i others(11): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965648 | ||||||
| chr5:40965648 | A | ATATATAT others(4): Show |
21 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0010 others(18): Show |
22 | HG00423.hp1 HG00558.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.1882+776_1882+777i others(13): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965648 | ||||||
| chr5:40965648 | A | ATATATAT others(6): Show |
1 | a0001c0001t0004g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1882+776_1882+777i others(15): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965648 | ||||||
| chr5:40965648 | A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0048 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1882+776_1882+777i others(17): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965648 | ||||||
| chr5:40965648 | A | ATATATAT others(4): Show |
3 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0004c0004t0004g0022 |
3 | NA18948.hp1 NA18997.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1882+776_1882+777i others(13): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965648 | ||||||
| chr5:40965648 | A | ATATTT | 22 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0002c0002t0001g0086 others(19): Show |
22 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1882+776_1882+777i others(7): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965648 | ||||||
| chr5:40965648 | A | ATTT | 86 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.1882+783_1882+785d others(5): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965648 | ||||||
| chr5:40965648 | A | ATTTTT | 44 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(41): Show |
44 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1882+781_1882+785d others(7): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40965648 | ||||||
| chr5:40965648 | A | T | 119 | a0001c0001t0001g0064 a0001c0001t0001g0194 a0001c0001t0001g0195 others(116): Show |
121 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1882+775A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965648 | |||||||
| chr5:40965651 | T | A | 4 | a0001c0001t0003g0020 a0001c0001t0005g0367 a0002c0002t0003g0138 others(1): Show |
4 | HG02145.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882+778T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965651 | |||||||
| chr5:40965902 | T | C | 321 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(318): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1882+1029T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965902 | |||||||
| chr5:40965935 | G | T | 5 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0005g0367 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1882+1062G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965935 | |||||||
| chr5:40965969 | A | G | 1 | a0001c0001t0002g0336 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1882+1096A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965969 | |||||||
| chr5:40965996 | C | T | 70 | a0001c0001t0003g0047 a0003c0003t0003g0029 a0003c0003t0003g0045 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.1882+1123C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965996 | |||||||
| chr5:40965998 | T | C | 72 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(69): Show |
73 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1882+1125T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40965998 | |||||||
| chr5:40966062 | G | A | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1882+1189G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966062 | |||||||
| chr5:40966118 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1882+1245T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966118 | |||||||
| chr5:40966156 | C | T | 225 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(222): Show |
230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1882+1283C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966156 | |||||||
| chr5:40966256 | AC | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(19): Show |
23 | HG00408.hp1 HG00544.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1882+1388delC | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40966256 | ||||||
| chr5:40966258 | C | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(19): Show |
23 | HG00408.hp1 HG00544.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1882+1385C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966258 | |||||||
| chr5:40966260 | C | G | 1 | a0001c0001t0002g0261 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1882+1387C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966260 | |||||||
| chr5:40966376 | C | CT | 11 | a0001c0001t0002g0270 a0001c0001t0003g0020 a0001c0001t0003g0263 others(8): Show |
11 | HG01192.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1882+1516dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40966376 | ||||||
| chr5:40966392 | G | A | 2 | a0002c0002t0002g0116 a0002c0002t0002g0117 |
2 | NA18986.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1882+1519G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966392 | |||||||
| chr5:40966532 | C | T | 1 | a0001c0001t0005g0368 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1882+1659C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966532 | |||||||
| chr5:40966568 | G | A | 10 | a0001c0001t0002g0007 a0001c0001t0003g0283 a0001c0001t0003g0285 others(7): Show |
10 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1882+1695G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966568 | |||||||
| chr5:40966574 | T | C | 75 | a0001c0001t0003g0020 a0001c0001t0003g0047 a0001c0001t0003g0263 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.1882+1701T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966574 | |||||||
| chr5:40966626 | A | C | 210 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(207): Show |
216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1882+1753A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966626 | |||||||
| chr5:40966671 | C | T | 73 | a0001c0001t0001g0211 a0001c0001t0002g0008 a0001c0001t0002g0032 others(70): Show |
74 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1882+1798C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966671 | |||||||
| chr5:40966838 | A | G | 16 | a0006c0006t0004g0073 a0006c0006t0004g0091 a0006c0006t0004g0094 others(13): Show |
16 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1882+1965A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966838 | |||||||
| chr5:40966880 | C | T | 16 | a0006c0006t0004g0073 a0006c0006t0004g0091 a0006c0006t0004g0094 others(13): Show |
16 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1882+2007C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40966880 | |||||||
| chr5:40967040 | GTC | G | 7 | a0002c0002t0001g0130 a0002c0002t0001g0291 a0002c0002t0001g0292 others(4): Show |
7 | HG00597.hp1 HG02027.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1882+2169_1882+217 others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40967040 | ||||||
| chr5:40967069 | A | AT | 109 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0065 others(106): Show |
112 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1882+2208dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40967069 | ||||||
| chr5:40967069 | A | ATT | 12 | a0001c0001t0001g0211 a0001c0001t0002g0216 a0001c0001t0002g0258 others(9): Show |
12 | HG02055.hp2 HG02486.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.1882+2207_1882+220 others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40967069 | ||||||
| chr5:40967080 | TTC | T | 69 | a0001c0001t0003g0047 a0003c0003t0003g0029 a0003c0003t0003g0045 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.1882+2209_1882+221 others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40967080 | ||||||
| chr5:40967081 | TC | T | 68 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(65): Show |
69 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1882+2209delC | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967081 | |||||||
| chr5:40967082 | C | T | 162 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0008 others(159): Show |
167 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1882+2209C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967082 | |||||||
| chr5:40967091 | G | A | 2 | a0001c0001t0002g0270 a0001c0001t0012g0365 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1882+2218G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967091 | |||||||
| chr5:40967179 | T | C | 321 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(318): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1882+2306T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967179 | |||||||
| chr5:40967211 | G | A | 6 | a0001c0001t0003g0283 a0001c0001t0003g0286 a0001c0001t0005g0369 others(3): Show |
6 | HG02145.hp2 HG02818.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1882+2338G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967211 | |||||||
| chr5:40967300 | A | G | 88 | a0001c0001t0002g0007 a0001c0001t0002g0270 a0001c0001t0003g0020 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1882+2427A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967300 | |||||||
| chr5:40967310 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1882+2437C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967310 | |||||||
| chr5:40967342 | G | A | 88 | a0001c0001t0002g0007 a0001c0001t0002g0270 a0001c0001t0003g0020 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1882+2469G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967342 | |||||||
| chr5:40967353 | C | T | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1882+2480C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967353 | |||||||
| chr5:40967405 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1882+2532T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967405 | |||||||
| chr5:40967565 | T | A | 299 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(296): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1882+2692T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967565 | |||||||
| chr5:40967578 | A | G | 1 | a0002c0002t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1882+2705A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967578 | |||||||
| chr5:40967634 | A | G | 1 | a0001c0001t0012g0365 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1882+2761A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967634 | |||||||
| chr5:40967679 | C | T | 3 | a0002c0002t0001g0079 a0002c0002t0001g0118 a0002c0002t0001g0177 |
3 | NA18954.hp1 NA18968.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1882+2806C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967679 | |||||||
| chr5:40967770 | G | A | 4 | a0001c0001t0003g0020 a0001c0001t0005g0367 a0002c0002t0003g0138 others(1): Show |
4 | HG02145.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882+2897G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967770 | |||||||
| chr5:40967784 | G | A | 162 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0008 others(159): Show |
167 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1882+2911G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967784 | |||||||
| chr5:40967804 | C | T | 4 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1882+2931C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967804 | |||||||
| chr5:40967928 | T | C | 86 | a0001c0001t0002g0007 a0001c0001t0003g0020 a0001c0001t0003g0047 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1882+3055T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967928 | |||||||
| chr5:40967938 | G | T | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1882+3065G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967938 | |||||||
| chr5:40967992 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1882+3119A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967992 | |||||||
| chr5:40967994 | T | C | 321 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(318): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1882+3121T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40967994 | |||||||
| chr5:40968074 | A | C | 299 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(296): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1882+3201A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968074 | |||||||
| chr5:40968203 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1882+3330G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968203 | |||||||
| chr5:40968268 | T | G | 321 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(318): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1882+3395T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968268 | |||||||
| chr5:40968280 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1882+3407T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968280 | |||||||
| chr5:40968416 | G | A | 7 | a0004c0004t0001g0288 a0004c0004t0001g0298 a0004c0004t0001g0299 others(4): Show |
7 | HG01934.hp2 NA18956.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.1882+3543G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968416 | |||||||
| chr5:40968449 | C | T | 2 | a0001c0001t0002g0270 a0001c0001t0012g0365 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1882+3576C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968449 | |||||||
| chr5:40968520 | T | C | 1 | a0003c0003t0003g0323 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1882+3647T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968520 | |||||||
| chr5:40968556 | ATTATATA others(4): Show |
A | 3 | a0001c0001t0003g0020 a0001c0001t0012g0365 a0003c0003t0003g0323 |
3 | HG02965.hp2 HG03516.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1882+3694_1882+370 others(15): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968556 | ||||||
| chr5:40968557 | TTATATAT others(6): Show |
T | 2 | a0001c0001t0003g0263 a0006c0006t0002g0147 |
2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1882+3694_1882+370 others(17): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968557 | ||||||
| chr5:40968557 | TTATATAT others(8): Show |
T | 3 | a0001c0001t0002g0270 a0004c0004t0001g0299 a0016c0019t0001g0089 |
3 | HG01261.hp2 NA19043.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1882+3694_1882+370 others(19): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968557 | ||||||
| chr5:40968557 | TTATATAT others(10): Show |
T | 40 | a0001c0001t0001g0222 a0001c0001t0001g0241 a0001c0001t0001g0242 others(37): Show |
41 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1882+3694_1882+371 others(21): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968557 | ||||||
| chr5:40968557 | TTATATAT others(12): Show |
T | 8 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0227 others(5): Show |
8 | HG01074.hp2 HG01243.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.1882+3694_1882+371 others(23): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968557 | ||||||
| chr5:40968557 | TTATATAT others(14): Show |
T | 1 | a0017c0027t0002g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1882+3694_1882+371 others(25): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968557 | ||||||
| chr5:40968559 | ATATATAT others(2): Show |
A | 4 | a0001c0001t0003g0283 a0002c0002t0003g0139 a0003c0003t0003g0212 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1882+3694_1882+370 others(13): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968559 | ||||||
| chr5:40968560 | T | G | 1 | a0002c0002t0001g0292 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1882+3687T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968560 | |||||||
| chr5:40968561 | ATATATTT | A | 3 | a0003c0003t0003g0253 a0005c0005t0003g0084 a0008c0008t0003g0316 |
3 | NA18979.hp1 NA19082.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1882+3694_1882+370 others(11): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968561 | ||||||
| chr5:40968563 | ATATTT | A | 5 | a0003c0003t0003g0246 a0003c0003t0003g0364 a0005c0005t0003g0103 others(2): Show |
5 | HG01433.hp1 HG03490.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1882+3694_1882+369 others(9): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968563 | ||||||
| chr5:40968565 | ATTT | A | 68 | a0001c0001t0003g0047 a0001c0001t0003g0285 a0001c0001t0003g0286 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.1882+3694_1882+369 others(7): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968565 | ||||||
| chr5:40968567 | T | A | 74 | a0001c0001t0001g0211 a0001c0001t0002g0008 a0001c0001t0002g0032 others(71): Show |
75 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1882+3694T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968567 | |||||||
| chr5:40968568 | T | TTA | 3 | a0002c0002t0001g0120 a0002c0002t0001g0165 a0002c0002t0001g0176 |
3 | NA18940.hp1 NA18967.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1882+3727_1882+372 others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968568 | ||||||
| chr5:40968568 | T | TTATA | 9 | a0001c0001t0001g0252 a0002c0002t0001g0075 a0002c0002t0001g0080 others(6): Show |
9 | HG00642.hp1 HG01928.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.1882+3725_1882+372 others(8): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968568 | ||||||
| chr5:40968568 | T | TTATATA | 5 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0077 others(2): Show |
5 | HG01978.hp2 NA18974.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1882+3723_1882+372 others(10): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968568 | ||||||
| chr5:40968568 | T | TTATATAT others(3): Show |
4 | a0001c0001t0001g0064 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG03139.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1882+3719_1882+372 others(14): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968568 | ||||||
| chr5:40968568 | TTATATAT others(7): Show |
T | 3 | a0001c0001t0002g0277 a0002c0002t0002g0072 a0002c0002t0002g0117 |
3 | HG01175.hp2 HG01346.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1882+3715_1882+372 others(18): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968568 | ||||||
| chr5:40968568 | TTATATAT others(9): Show |
T | 2 | a0001c0001t0002g0154 a0001c0001t0002g0247 |
2 | HG01109.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1882+3713_1882+372 others(20): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968568 | ||||||
| chr5:40968582 | ATATATAT others(27): Show |
A | 8 | a0003c0003t0003g0235 a0003c0003t0003g0262 a0003c0003t0003g0338 others(5): Show |
8 | HG00408.hp2 HG00673.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1882+3711_1882+374 others(38): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968582 | ||||||
| chr5:40968584 | ATATATAT others(20): Show |
A | 1 | a0006c0016t0004g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1882+3713_1882+373 others(31): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968584 | ||||||
| chr5:40968586 | ATATATAT others(8): Show |
A | 3 | a0001c0001t0002g0238 a0002c0002t0001g0109 a0002c0002t0002g0071 |
3 | HG00280.hp2 HG01070.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1882+3715_1882+372 others(19): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968586 | ||||||
| chr5:40968586 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0261 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1882+3715_1882+373 others(21): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968586 | ||||||
| chr5:40968586 | ATATATAT others(11): Show |
A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(15): Show |
19 | HG00408.hp1 HG00544.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.1882+3715_1882+373 others(22): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968586 | ||||||
| chr5:40968586 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0332 a0004c0004t0001g0302 |
2 | NA18939.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1882+3715_1882+373 others(23): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968586 | ||||||
| chr5:40968586 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0005g0368 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1882+3715_1882+373 others(25): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968586 | ||||||
| chr5:40968586 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0002g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1882+3715_1882+373 others(27): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968586 | ||||||
| chr5:40968586 | ATATATAT others(19): Show |
A | 2 | a0001c0001t0002g0065 a0001c0001t0004g0229 |
2 | HG03540.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1882+3715_1882+374 others(30): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968586 | ||||||
| chr5:40968586 | ATATATAT others(20): Show |
A | 48 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0009 others(45): Show |
50 | HG00558.hp2 HG00642.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.1882+3715_1882+374 others(31): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968586 | ||||||
| chr5:40968586 | ATATATAT others(21): Show |
A | 4 | a0001c0001t0004g0046 a0001c0001t0008g0206 a0002c0002t0004g0146 others(1): Show |
4 | HG01106.hp1 HG01167.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882+3715_1882+374 others(32): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968586 | ||||||
| chr5:40968587 | TATATATA others(6): Show |
T | 2 | a0002c0002t0002g0116 a0002c0002t0003g0107 |
2 | HG03669.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1882+3715_1882+372 others(17): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968587 | |||||||
| chr5:40968588 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0002g0333 a0002c0002t0002g0156 |
2 | HG03927.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1882+3717_1882+372 others(17): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(7): Show |
A | 10 | a0001c0001t0002g0061 a0002c0002t0001g0081 a0002c0002t0002g0005 others(7): Show |
10 | HG00544.hp1 HG01496.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1882+3717_1882+373 others(18): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(8): Show |
A | 4 | a0001c0001t0002g0213 a0002c0002t0002g0159 a0002c0002t0002g0181 others(1): Show |
4 | NA18945.hp2 NA19006.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882+3717_1882+373 others(19): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(9): Show |
A | 1 | a0002c0002t0002g0184 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1882+3717_1882+373 others(20): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(11): Show |
A | 1 | a0004c0004t0001g0311 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1882+3717_1882+373 others(22): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(12): Show |
A | 1 | a0004c0004t0001g0306 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1882+3717_1882+373 others(23): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(14): Show |
A | 4 | a0001c0001t0003g0285 a0002c0002t0003g0198 a0002c0002t0003g0199 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1882+3717_1882+373 others(25): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(16): Show |
A | 4 | a0001c0001t0002g0050 a0001c0001t0002g0053 a0001c0001t0002g0062 others(1): Show |
4 | HG02258.hp1 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882+3717_1882+373 others(27): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(17): Show |
A | 2 | a0001c0001t0002g0051 a0002c0002t0002g0141 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1882+3717_1882+374 others(28): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0004g0048 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1882+3717_1882+374 others(29): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(19): Show |
A | 6 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0260 others(3): Show |
6 | HG00735.hp2 HG01346.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1882+3717_1882+374 others(30): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968588 | ATATATAT others(20): Show |
A | 8 | a0001c0001t0004g0037 a0001c0001t0004g0057 a0002c0002t0004g0182 others(5): Show |
8 | HG00423.hp1 HG03492.hp2 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.1882+3717_1882+374 others(31): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968588 | ||||||
| chr5:40968590 | ATATATAT others(6): Show |
A | 9 | a0002c0002t0001g0291 a0002c0002t0001g0292 a0002c0002t0001g0293 others(6): Show |
9 | HG00597.hp1 HG02027.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1882+3719_1882+373 others(17): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968590 | ||||||
| chr5:40968590 | ATATATAT others(7): Show |
A | 23 | a0001c0001t0001g0211 a0001c0001t0002g0008 a0001c0001t0002g0208 others(20): Show |
23 | HG00621.hp1 HG02040.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1882+3719_1882+373 others(18): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968590 | ||||||
| chr5:40968590 | ATATATAT others(8): Show |
A | 6 | a0001c0001t0002g0269 a0001c0001t0002g0279 a0001c0001t0002g0327 others(3): Show |
6 | HG01192.hp2 HG01257.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1882+3719_1882+373 others(19): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968590 | ||||||
| chr5:40968590 | ATATATAT others(14): Show |
A | 1 | a0002c0002t0003g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1882+3719_1882+373 others(25): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968590 | ||||||
| chr5:40968590 | ATATATAT others(16): Show |
A | 16 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(13): Show |
18 | HG01361.hp2 HG01981.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1882+3719_1882+374 others(27): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968590 | ||||||
| chr5:40968590 | ATATATAT others(17): Show |
A | 5 | a0003c0003t0003g0328 a0003c0003t0003g0340 a0003c0003t0003g0362 others(2): Show |
5 | HG00140.hp1 HG00140.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1882+3719_1882+374 others(28): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968590 | ||||||
| chr5:40968590 | ATATATAT others(18): Show |
A | 1 | a0012c0012t0003g0164 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1882+3719_1882+374 others(29): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968590 | ||||||
| chr5:40968592 | ATATATAT others(4): Show |
A | 1 | a0002c0002t0001g0130 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1882+3721_1882+373 others(15): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968592 | ||||||
| chr5:40968592 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0002g0278 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1882+3721_1882+373 others(16): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968592 | ||||||
| chr5:40968592 | ATATATAT others(7): Show |
A | 3 | a0001c0001t0002g0032 a0002c0002t0002g0125 a0004c0004t0002g0319 |
3 | NA18942.hp2 NA19002.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1882+3721_1882+373 others(18): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968592 | ||||||
| chr5:40968592 | ATATATAT others(8): Show |
A | 4 | a0002c0002t0002g0016 a0002c0002t0002g0069 a0002c0002t0002g0070 others(1): Show |
4 | NA18959.hp1 NA18963.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882+3721_1882+373 others(19): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968592 | ||||||
| chr5:40968592 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0002g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1882+3721_1882+374 others(24): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968592 | ||||||
| chr5:40968592 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0003g0286 a0002c0002t0003g0149 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1882+3721_1882+374 others(25): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968592 | ||||||
| chr5:40968592 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0005g0369 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1882+3721_1882+374 others(26): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968592 | ||||||
| chr5:40968592 | ATATATAT others(16): Show |
A | 20 | a0001c0001t0002g0284 a0001c0001t0003g0047 a0003c0003t0003g0029 others(17): Show |
20 | HG00099.hp2 HG00735.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1882+3721_1882+374 others(27): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968592 | ||||||
| chr5:40968592 | ATATATAT others(17): Show |
A | 7 | a0003c0003t0003g0287 a0003c0003t0003g0346 a0003c0003t0003g0349 others(4): Show |
7 | HG00423.hp2 HG01192.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1882+3721_1882+374 others(28): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968592 | ||||||
| chr5:40968594 | ATATATAT others(14): Show |
A | 2 | a0003c0003t0003g0223 a0003c0003t0003g0250 |
2 | HG01069.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1882+3723_1882+374 others(25): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968594 | ||||||
| chr5:40968594 | ATATATAT others(15): Show |
A | 2 | a0003c0003t0003g0355 a0005c0005t0003g0281 |
2 | HG02965.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1882+3723_1882+374 others(26): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968594 | ||||||
| chr5:40968594 | ATATATAT others(16): Show |
A | 2 | a0003c0003t0003g0045 a0005c0005t0003g0074 |
2 | HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1882+3723_1882+374 others(27): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968594 | ||||||
| chr5:40968594 | ATATATAT others(17): Show |
A | 4 | a0003c0003t0003g0215 a0008c0008t0003g0351 a0008c0008t0003g0352 others(1): Show |
4 | NA18945.hp1 NA19011.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1882+3723_1882+374 others(28): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968594 | ||||||
| chr5:40968596 | ATATATTT others(14): Show |
A | 1 | a0005c0005t0003g0119 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1882+3725_1882+374 others(25): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968596 | ||||||
| chr5:40968596 | ATATATTT others(17): Show |
A | 1 | a0005c0005t0003g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1882+3725_1882+374 others(28): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968596 | ||||||
| chr5:40968597 | TA | T | 4 | a0002c0002t0001g0015 a0002c0002t0001g0137 a0002c0002t0001g0273 others(1): Show |
4 | HG00621.hp2 HG02055.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882+3725delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968597 | |||||||
| chr5:40968598 | A | T | 2 | a0001c0001t0012g0365 a0004c0004t0001g0298 |
2 | HG02965.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.1882+3725A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968598 | |||||||
| chr5:40968599 | TA | T | 28 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(25): Show |
28 | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1882+3727delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968599 | |||||||
| chr5:40968600 | A | T | 18 | a0001c0001t0001g0218 a0001c0001t0001g0248 a0001c0001t0001g0249 others(15): Show |
18 | HG00621.hp2 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.1882+3727A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968600 | |||||||
| chr5:40968600 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0003g0283 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1882+3746_1882+375 others(15): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968600 | ||||||
| chr5:40968600 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0003g0020 a0003c0003t0003g0323 |
2 | HG03516.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1882+3745_1882+375 others(16): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968600 | ||||||
| chr5:40968600 | ATTTTTTT others(6): Show |
A | 3 | a0002c0002t0003g0139 a0003c0003t0003g0234 a0003c0003t0003g0253 |
3 | HG03139.hp1 NA18947.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1882+3744_1882+375 others(17): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968600 | ||||||
| chr5:40968600 | ATTTTTTT others(7): Show |
A | 1 | a0003c0003t0003g0212 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1882+3743_1882+375 others(18): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968600 | ||||||
| chr5:40968600 | ATTTTTTT others(8): Show |
A | 5 | a0003c0003t0003g0246 a0003c0003t0003g0364 a0005c0005t0003g0084 others(2): Show |
5 | HG01433.hp1 HG03490.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1882+3742_1882+375 others(19): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968600 | ||||||
| chr5:40968600 | ATTTTTTT others(9): Show |
A | 2 | a0005c0005t0003g0282 a0008c0008t0003g0316 |
2 | NA18979.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1882+3741_1882+375 others(20): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40968600 | ||||||
| chr5:40968601 | T | TATA | 3 | a0002c0002t0001g0076 a0002c0002t0001g0175 a0002c0002t0001g0187 |
3 | HG01257.hp2 NA18971.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1882+3728_1882+372 others(7): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968601 | |||||||
| chr5:40968601 | T | TATATATA others(4): Show |
1 | a0002c0002t0001g0078 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1882+3728_1882+372 others(15): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968601 | |||||||
| chr5:40968602 | T | A | 12 | a0001c0001t0001g0064 a0001c0001t0001g0195 a0001c0001t0001g0197 others(9): Show |
12 | HG01928.hp2 HG01978.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1882+3729T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968602 | |||||||
| chr5:40968603 | T | A | 6 | a0001c0001t0001g0196 a0001c0001t0001g0345 a0002c0002t0001g0076 others(3): Show |
6 | HG00558.hp1 HG01257.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1882+3730T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968603 | |||||||
| chr5:40968604 | T | A | 5 | a0001c0001t0001g0064 a0002c0002t0001g0075 a0002c0002t0001g0077 others(2): Show |
5 | HG01928.hp2 HG01978.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1882+3731T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968604 | |||||||
| chr5:40968605 | T | A | 1 | a0002c0002t0001g0076 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1882+3732T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968605 | |||||||
| chr5:40968606 | T | A | 1 | a0002c0002t0001g0083 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1882+3733T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968606 | |||||||
| chr5:40968607 | T | A | 1 | a0002c0002t0001g0076 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1882+3734T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968607 | |||||||
| chr5:40968668 | G | C | 1 | a0003c0003t0003g0342 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1883-3735G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968668 | |||||||
| chr5:40968675 | A | G | 299 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(296): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1883-3728A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968675 | |||||||
| chr5:40968757 | G | A | 74 | a0001c0001t0001g0211 a0001c0001t0002g0008 a0001c0001t0002g0032 others(71): Show |
75 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1883-3646G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968757 | |||||||
| chr5:40968956 | T | A | 69 | a0001c0001t0003g0047 a0003c0003t0003g0029 a0003c0003t0003g0045 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.1883-3447T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40968956 | |||||||
| chr5:40969014 | G | A | 2 | a0006c0006t0004g0094 a0006c0006t0004g0100 |
2 | HG01123.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1883-3389G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969014 | |||||||
| chr5:40969082 | C | T | 88 | a0001c0001t0002g0007 a0001c0001t0002g0270 a0001c0001t0003g0020 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1883-3321C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969082 | |||||||
| chr5:40969187 | C | T | 3 | a0002c0002t0001g0104 a0002c0002t0001g0143 a0002c0002t0001g0144 |
3 | HG01243.hp1 HG01261.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1883-3216C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969187 | |||||||
| chr5:40969220 | A | T | 2 | a0001c0001t0002g0270 a0001c0001t0012g0365 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1883-3183A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969220 | |||||||
| chr5:40969231 | G | A | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1883-3172G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969231 | |||||||
| chr5:40969258 | TTA | T | 162 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0008 others(159): Show |
167 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1883-3143_1883-314 others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40969258 | ||||||
| chr5:40969366 | A | G | 2 | a0006c0006t0002g0147 a0017c0027t0002g0148 |
2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1883-3037A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969366 | |||||||
| chr5:40969406 | G | GT | 6 | a0001c0001t0002g0216 a0002c0002t0002g0016 a0002c0002t0002g0069 others(3): Show |
6 | NA18959.hp1 NA18963.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1883-2989dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40969406 | ||||||
| chr5:40969414 | TG | T | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1883-2987delG | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40969414 | ||||||
| chr5:40969434 | C | G | 162 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0008 others(159): Show |
167 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1883-2969C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969434 | |||||||
| chr5:40969445 | G | C | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1883-2958G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969445 | |||||||
| chr5:40969519 | T | C | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1883-2884T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969519 | |||||||
| chr5:40969821 | G | T | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1883-2582G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969821 | |||||||
| chr5:40969978 | G | C | 321 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(318): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1883-2425G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969978 | |||||||
| chr5:40969990 | C | T | 9 | a0001c0001t0003g0283 a0001c0001t0003g0285 a0001c0001t0003g0286 others(6): Show |
9 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1883-2413C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969990 | |||||||
| chr5:40969991 | G | A | 1 | a0003c0003t0003g0346 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1883-2412G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40969991 | |||||||
| chr5:40970239 | A | C | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1883-2164A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40970239 | |||||||
| chr5:40970602 | T | A | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1883-1801T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40970602 | |||||||
| chr5:40970920 | G | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(19): Show |
23 | HG00408.hp1 HG00544.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1883-1483G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40970920 | |||||||
| chr5:40970959 | C | T | 1 | a0001c0001t0002g0278 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1883-1444C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40970959 | |||||||
| chr5:40971070 | G | T | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1883-1333G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971070 | |||||||
| chr5:40971147 | T | C | 88 | a0001c0001t0002g0007 a0001c0001t0002g0270 a0001c0001t0003g0020 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1883-1256T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971147 | |||||||
| chr5:40971231 | A | G | 73 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(70): Show |
74 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1883-1172A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971231 | |||||||
| chr5:40971337 | T | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(19): Show |
23 | HG00408.hp1 HG00544.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1883-1066T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971337 | |||||||
| chr5:40971363 | T | C | 13 | a0001c0001t0003g0020 a0001c0001t0003g0283 a0001c0001t0003g0285 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1883-1040T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971363 | |||||||
| chr5:40971418 | C | CT | 3 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0317 |
3 | HG02280.hp2 HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1883-980dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 40971418 | ||||||
| chr5:40971480 | A | G | 73 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(70): Show |
74 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1883-923A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971480 | |||||||
| chr5:40971556 | A | G | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1883-847A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971556 | |||||||
| chr5:40971595 | A | G | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1883-808A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971595 | |||||||
| chr5:40971608 | A | G | 73 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(70): Show |
74 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1883-795A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971608 | |||||||
| chr5:40971655 | T | C | 1 | a0007c0007t0004g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1883-748T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971655 | |||||||
| chr5:40971771 | T | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(19): Show |
23 | HG00408.hp1 HG00544.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1883-632T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971771 | |||||||
| chr5:40971813 | G | A | 1 | a0005c0005t0003g0124 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1883-590G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971813 | |||||||
| chr5:40971828 | A | G | 1 | a0002c0002t0001g0098 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1883-575A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971828 | |||||||
| chr5:40971915 | A | G | 226 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(223): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1883-488A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971915 | |||||||
| chr5:40971939 | C | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(19): Show |
23 | HG00408.hp1 HG00544.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1883-464C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971939 | |||||||
| chr5:40971977 | A | G | 1 | a0010c0010t0001g0113 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1883-426A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40971977 | |||||||
| chr5:40972009 | C | T | 365 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(362): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1883-394C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40972009 | |||||||
| chr5:40972109 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1883-294A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40972109 | |||||||
| chr5:40972118 | G | C | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1883-285G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40972118 | |||||||
| chr5:40972182 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1883-221G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40972182 | |||||||
| chr5:40972269 | A | G | 88 | a0001c0001t0002g0007 a0001c0001t0002g0270 a0001c0001t0003g0020 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1883-134A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 14/17 | chr5 | 40972269 | |||||||
| chr5:40972667 | G | A | 73 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(70): Show |
74 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.2074+73G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40972667 | |||||||
| chr5:40972708 | G | A | 1 | a0001c0001t0002g0336 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2074+114G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40972708 | |||||||
| chr5:40972735 | A | G | 3 | a0004c0004t0001g0288 a0004c0004t0001g0298 a0004c0004t0001g0299 |
3 | NA18990.hp1 NA19059.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.2074+141A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40972735 | |||||||
| chr5:40972736 | CTGAG | C | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.2074+144_2074+147d others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 40972736 | ||||||
| chr5:40972804 | G | A | 49 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(46): Show |
50 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.2074+210G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40972804 | |||||||
| chr5:40972873 | G | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(19): Show |
23 | HG00408.hp1 HG00544.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.2074+279G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40972873 | |||||||
| chr5:40972875 | C | T | 1 | a0002c0002t0001g0123 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2074+281C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40972875 | |||||||
| chr5:40973012 | A | T | 2 | a0006c0006t0002g0147 a0017c0027t0002g0148 |
2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2074+418A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973012 | |||||||
| chr5:40973084 | T | C | 1 | a0005c0005t0003g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2074+490T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973084 | |||||||
| chr5:40973106 | C | T | 2 | a0001c0001t0002g0270 a0001c0001t0012g0365 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2074+512C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973106 | |||||||
| chr5:40973107 | A | G | 328 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(325): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.2074+513A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973107 | |||||||
| chr5:40973203 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2074+609G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973203 | |||||||
| chr5:40973320 | A | G | 25 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0010 others(22): Show |
26 | HG00423.hp1 HG00558.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.2074+726A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973320 | |||||||
| chr5:40973424 | T | G | 1 | a0017c0027t0002g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2074+830T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973424 | |||||||
| chr5:40973501 | G | A | 82 | a0001c0001t0003g0020 a0001c0001t0003g0047 a0001c0001t0003g0263 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.2074+907G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973501 | |||||||
| chr5:40973816 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2074+1222T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973816 | |||||||
| chr5:40973903 | A | G | 51 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(48): Show |
52 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.2074+1309A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973903 | |||||||
| chr5:40973906 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2074+1312T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973906 | |||||||
| chr5:40973955 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2074+1361T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973955 | |||||||
| chr5:40973959 | A | G | 88 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(85): Show |
92 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.2074+1365A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40973959 | |||||||
| chr5:40974057 | A | G | 227 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2074+1463A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40974057 | |||||||
| chr5:40974107 | T | TG | 227 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2074+1514dupG | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 40974107 | ||||||
| chr5:40974220 | C | T | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2074+1626C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40974220 | |||||||
| chr5:40974387 | G | GT | 80 | a0001c0001t0002g0007 a0001c0001t0003g0047 a0001c0001t0003g0263 others(77): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.2074+1806dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 40974387 | ||||||
| chr5:40974388 | T | TG | 3 | a0003c0003t0003g0330 a0008c0008t0003g0313 a0008c0008t0003g0314 |
3 | HG01981.hp1 HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2074+1794_2074+179 others(5): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40974388 | |||||||
| chr5:40974408 | G | A | 89 | a0001c0001t0002g0007 a0001c0001t0002g0270 a0001c0001t0003g0020 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2074+1814G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40974408 | |||||||
| chr5:40974421 | AT | A | 134 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.2074+1839delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 40974421 | ||||||
| chr5:40974421 | ATT | A | 90 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0007 others(87): Show |
94 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.2074+1838_2074+183 others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 40974421 | ||||||
| chr5:40974447 | G | T | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2074+1853G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40974447 | |||||||
| chr5:40974460 | G | T | 1 | a0010c0010t0001g0114 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2074+1866G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40974460 | |||||||
| chr5:40974473 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2074+1879C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40974473 | |||||||
| chr5:40974577 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2074+1983G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40974577 | |||||||
| chr5:40974578 | G | A | 89 | a0001c0001t0002g0007 a0001c0001t0002g0270 a0001c0001t0003g0020 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2074+1984G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40974578 | |||||||
| chr5:40974661 | G | A | 51 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(48): Show |
52 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.2074+2067G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40974661 | |||||||
| chr5:40975031 | A | G | 1 | a0002c0002t0001g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2075-1719A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975031 | |||||||
| chr5:40975066 | A | T | 1 | a0001c0001t0003g0285 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2075-1684A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975066 | |||||||
| chr5:40975171 | T | G | 4 | a0001c0001t0003g0283 a0001c0001t0003g0286 a0001c0001t0005g0369 others(1): Show |
4 | HG02818.hp1 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2075-1579T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975171 | |||||||
| chr5:40975183 | A | G | 1 | a0004c0004t0001g0024 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2075-1567A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975183 | |||||||
| chr5:40975199 | C | T | 14 | a0001c0001t0003g0020 a0001c0001t0003g0263 a0001c0001t0003g0283 others(11): Show |
14 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2075-1551C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975199 | |||||||
| chr5:40975214 | TA | T | 8 | a0001c0001t0004g0034 a0001c0001t0004g0035 a0001c0001t0004g0036 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2075-1530delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 40975214 | ||||||
| chr5:40975238 | C | T | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2075-1512C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975238 | |||||||
| chr5:40975328 | G | A | 1 | a0005c0005t0003g0124 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2075-1422G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975328 | |||||||
| chr5:40975363 | G | GT | 80 | a0001c0001t0002g0007 a0001c0001t0002g0270 a0001c0001t0003g0020 others(77): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.2075-1386dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 40975363 | ||||||
| chr5:40975363 | G | GTT | 7 | a0001c0001t0003g0285 a0002c0002t0003g0138 a0003c0003t0003g0234 others(4): Show |
7 | HG01981.hp1 HG02145.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2075-1386_2075-138 others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 40975363 | ||||||
| chr5:40975364 | TG | T | 69 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(66): Show |
72 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.2075-1385delG | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975364 | |||||||
| chr5:40975365 | G | T | 157 | a0001c0001t0002g0007 a0001c0001t0002g0258 a0001c0001t0002g0259 others(154): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.2075-1385G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975365 | |||||||
| chr5:40975366 | C | T | 226 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(223): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2075-1384C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975366 | |||||||
| chr5:40975395 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2075-1355G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975395 | |||||||
| chr5:40975457 | G | A | 68 | a0001c0001t0003g0047 a0003c0003t0003g0029 a0003c0003t0003g0045 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.2075-1293G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975457 | |||||||
| chr5:40975499 | G | A | 1 | a0002c0002t0002g0159 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2075-1251G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975499 | |||||||
| chr5:40975510 | T | C | 227 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2075-1240T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975510 | |||||||
| chr5:40975640 | G | A | 227 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0218 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2075-1110G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975640 | |||||||
| chr5:40975655 | C | A | 89 | a0001c0001t0002g0007 a0001c0001t0002g0270 a0001c0001t0003g0020 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2075-1095C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975655 | |||||||
| chr5:40975906 | G | T | 1 | a0001c0001t0001g0252 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2075-844G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975906 | |||||||
| chr5:40975936 | G | A | 64 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(61): Show |
65 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2075-814G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40975936 | |||||||
| chr5:40976015 | A | T | 51 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(48): Show |
52 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.2075-735A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976015 | |||||||
| chr5:40976078 | T | G | 21 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(18): Show |
23 | HG01361.hp2 HG02109.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.2075-672T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976078 | |||||||
| chr5:40976111 | G | T | 4 | a0001c0001t0003g0285 a0002c0002t0003g0198 a0002c0002t0003g0199 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2075-639G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976111 | |||||||
| chr5:40976112 | A | G | 2 | a0004c0004t0001g0027 a0004c0004t0001g0028 |
2 | NA18964.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.2075-638A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976112 | |||||||
| chr5:40976205 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2075-545G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976205 | |||||||
| chr5:40976212 | C | G | 1 | a0002c0002t0002g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2075-538C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976212 | |||||||
| chr5:40976233 | G | T | 51 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(48): Show |
52 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.2075-517G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976233 | |||||||
| chr5:40976370 | T | G | 4 | a0001c0001t0002g0061 a0001c0001t0002g0238 a0001c0001t0002g0277 others(1): Show |
4 | HG01175.hp2 HG02071.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.2075-380T>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976370 | |||||||
| chr5:40976425 | T | C | 4 | a0001c0001t0003g0283 a0001c0001t0003g0286 a0001c0001t0005g0369 others(1): Show |
4 | HG02818.hp1 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2075-325T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976425 | |||||||
| chr5:40976567 | A | G | 321 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0211 others(318): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.2075-183A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976567 | |||||||
| chr5:40976730 | T | A | 1 | a0001c0001t0005g0368 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2075-20T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 15/17 | chr5 | 40976730 | |||||||
| chr5:40976845 | G | A | 1 | a0014c0021t0001g0271 | 1 | HG00642.hp1 | splice_region_variant&intron_variant | LOW | c.2165+5G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40976845 | |||||||
| chr5:40976967 | C | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0194 a0001c0001t0001g0195 others(3): Show |
6 | HG02886.hp2 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2165+127C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40976967 | |||||||
| chr5:40977029 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2165+189A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977029 | |||||||
| chr5:40977034 | G | C | 1 | a0001c0001t0002g0277 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2165+194G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977034 | |||||||
| chr5:40977471 | C | T | 1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2165+631C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977471 | |||||||
| chr5:40977478 | G | T | 1 | a0001c0001t0002g0258 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2165+638G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977478 | |||||||
| chr5:40977601 | G | A | 271 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(268): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2165+761G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977601 | |||||||
| chr5:40977607 | C | T | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2165+767C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977607 | |||||||
| chr5:40977616 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0211 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2165+776G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977616 | |||||||
| chr5:40977658 | C | T | 147 | a0001c0001t0001g0064 a0001c0001t0001g0211 a0001c0001t0003g0020 others(144): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2165+818C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977658 | |||||||
| chr5:40977677 | T | C | 1 | a0002c0002t0001g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2165+837T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977677 | |||||||
| chr5:40977740 | A | G | 2 | a0001c0001t0004g0202 a0001c0001t0004g0203 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2165+900A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977740 | |||||||
| chr5:40977767 | G | A | 16 | a0006c0006t0004g0073 a0006c0006t0004g0091 a0006c0006t0004g0094 others(13): Show |
16 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.2165+927G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977767 | |||||||
| chr5:40977809 | C | T | 16 | a0003c0003t0003g0262 a0003c0003t0003g0287 a0003c0003t0003g0338 others(13): Show |
16 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.2165+969C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977809 | |||||||
| chr5:40977840 | A | G | 322 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.2165+1000A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977840 | |||||||
| chr5:40977917 | C | T | 123 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(120): Show |
127 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.2165+1077C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977917 | |||||||
| chr5:40977951 | T | A | 94 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(91): Show |
97 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2165+1111T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977951 | |||||||
| chr5:40977976 | A | G | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2165+1136A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977976 | |||||||
| chr5:40977977 | T | A | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2165+1137T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40977977 | |||||||
| chr5:40978016 | C | T | 1 | a0002c0002t0001g0086 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2165+1176C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978016 | |||||||
| chr5:40978140 | GA | G | 217 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0214 others(214): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2165+1320delA | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978140 | ||||||
| chr5:40978140 | GAA | G | 7 | a0001c0001t0001g0064 a0001c0001t0001g0211 a0001c0001t0004g0010 others(4): Show |
7 | HG02723.hp2 HG02965.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.2165+1319_2165+132 others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978140 | ||||||
| chr5:40978144 | A | AG | 63 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(60): Show |
64 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.2165+1304_2165+130 others(5): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978144 | |||||||
| chr5:40978145 | A | G | 1 | a0001c0001t0002g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2165+1305A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978145 | |||||||
| chr5:40978160 | A | AG | 23 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(20): Show |
25 | HG01361.hp2 HG02109.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.2165+1321dupG | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978160 | ||||||
| chr5:40978160 | A | G | 69 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0032 others(66): Show |
70 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2165+1320A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978160 | |||||||
| chr5:40978211 | G | A | 4 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2165+1371G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978211 | |||||||
| chr5:40978412 | C | A | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2166-1313C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978412 | |||||||
| chr5:40978435 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2166-1290C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978435 | |||||||
| chr5:40978568 | A | C | 1 | a0001c0001t0002g0061 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2166-1157A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978568 | |||||||
| chr5:40978568 | A | G | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2166-1157A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978568 | |||||||
| chr5:40978589 | A | G | 26 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(23): Show |
28 | HG01346.hp1 HG01361.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.2166-1136A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978589 | |||||||
| chr5:40978619 | A | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0211 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2166-1106A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978619 | |||||||
| chr5:40978762 | C | T | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2166-963C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978762 | |||||||
| chr5:40978781 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2166-944T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978781 | |||||||
| chr5:40978824 | C | T | 63 | a0001c0001t0002g0008 a0001c0001t0002g0032 a0001c0001t0002g0061 others(60): Show |
64 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.2166-901C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978824 | |||||||
| chr5:40978854 | G | A | 2 | a0003c0003t0003g0226 a0003c0023t0003g0335 |
2 | NA18964.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.2166-871G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40978854 | |||||||
| chr5:40978873 | A | AT | 14 | a0001c0001t0001g0210 a0001c0001t0001g0222 a0001c0001t0001g0233 others(11): Show |
14 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.2166-828dupT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTT | 32 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0033 others(29): Show |
34 | HG00558.hp2 HG01106.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.2166-831_2166-828d others(6): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTT | 13 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0012 others(10): Show |
13 | HG00423.hp1 HG01433.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2166-832_2166-828d others(7): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT | 12 | a0003c0003t0003g0349 a0003c0003t0003g0355 a0006c0006t0004g0073 others(9): Show |
12 | HG00642.hp2 HG01168.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.2166-834_2166-828d others(9): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(4): Show |
1 | a0005c0005t0003g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2166-838_2166-828d others(13): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(5): Show |
5 | a0001c0001t0001g0064 a0001c0001t0003g0283 a0005c0005t0003g0282 others(2): Show |
5 | HG00741.hp1 HG01516.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2166-839_2166-828d others(14): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(6): Show |
4 | a0001c0001t0003g0286 a0001c0001t0005g0368 a0001c0001t0005g0369 others(1): Show |
4 | HG01192.hp1 HG02630.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2166-840_2166-828d others(15): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(7): Show |
1 | a0002c0002t0003g0149 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2166-841_2166-828d others(16): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0003g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2166-842_2166-828d others(17): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(9): Show |
1 | a0001c0001t0003g0047 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2166-843_2166-828d others(18): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(10): Show |
1 | a0003c0003t0003g0334 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2166-844_2166-828d others(19): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(17): Show |
1 | a0007c0007t0004g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2166-851_2166-828d others(26): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(18): Show |
14 | a0003c0003t0003g0212 a0003c0003t0003g0231 a0003c0003t0003g0239 others(11): Show |
14 | HG00140.hp1 HG00140.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.2166-828_2166-827i others(27): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(19): Show |
28 | a0003c0003t0003g0215 a0003c0003t0003g0220 a0003c0003t0003g0223 others(25): Show |
28 | HG00408.hp2 HG00673.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2166-828_2166-827i others(28): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(20): Show |
7 | a0003c0003t0003g0235 a0003c0003t0003g0330 a0003c0003t0003g0337 others(4): Show |
7 | HG00741.hp2 HG01981.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.2166-828_2166-827i others(29): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(21): Show |
1 | a0005c0013t0003g0183 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2166-828_2166-827i others(30): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(22): Show |
5 | a0002c0002t0003g0107 a0003c0003t0003g0323 a0003c0003t0003g0350 others(2): Show |
5 | HG00423.hp2 HG03654.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.2166-828_2166-827i others(31): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(23): Show |
1 | a0003c0003t0003g0226 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2166-828_2166-827i others(32): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(24): Show |
1 | a0003c0003t0003g0234 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2166-828_2166-827i others(33): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | A | ATTTTTTT others(25): Show |
1 | a0003c0003t0003g0364 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2166-828_2166-827i others(34): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | AT | A | 25 | a0001c0001t0001g0242 a0001c0001t0002g0007 a0001c0001t0002g0013 others(22): Show |
25 | HG00099.hp1 HG01070.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.2166-828delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | ATT | A | 74 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0031 others(71): Show |
77 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.2166-829_2166-828d others(4): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40978873 | ATTT | A | 8 | a0001c0001t0002g0065 a0001c0001t0002g0236 a0001c0001t0002g0258 others(5): Show |
8 | HG01346.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2166-830_2166-828d others(5): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40978873 | ||||||
| chr5:40979004 | T | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2166-721T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979004 | |||||||
| chr5:40979022 | G | A | 60 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0009 others(57): Show |
62 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.2166-703G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979022 | |||||||
| chr5:40979029 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2166-696G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979029 | |||||||
| chr5:40979036 | C | T | 1 | a0005c0005t0003g0124 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2166-689C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979036 | |||||||
| chr5:40979129 | G | A | 5 | a0001c0001t0002g0065 a0001c0001t0002g0258 a0001c0001t0002g0259 others(2): Show |
5 | HG01346.hp1 HG02055.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2166-596G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979129 | |||||||
| chr5:40979368 | T | A | 2 | a0005c0005t0003g0280 a0005c0005t0003g0281 |
2 | HG01192.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2166-357T>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979368 | |||||||
| chr5:40979368 | T | C | 2 | a0001c0001t0001g0210 a0002c0002t0001g0102 |
2 | HG01123.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2166-357T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979368 | |||||||
| chr5:40979491 | C | A | 10 | a0006c0006t0004g0073 a0006c0006t0004g0094 a0006c0006t0004g0095 others(7): Show |
10 | HG00642.hp2 HG01123.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.2166-234C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979491 | |||||||
| chr5:40979502 | A | T | 64 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0032 others(61): Show |
65 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2166-223A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979502 | |||||||
| chr5:40979560 | G | T | 147 | a0001c0001t0001g0064 a0001c0001t0001g0211 a0001c0001t0003g0020 others(144): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2166-165G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979560 | |||||||
| chr5:40979596 | CT | C | 198 | a0001c0001t0001g0064 a0001c0001t0001g0211 a0001c0001t0001g0214 others(195): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2166-115delT | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 40979596 | ||||||
| chr5:40979688 | A | T | 64 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0032 others(61): Show |
65 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2166-37A>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 16/17 | chr5 | 40979688 | |||||||
| chr5:40979918 | C | A | 1 | a0001c0001t0002g0270 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2350+9C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40979918 | |||||||
| chr5:40979984 | T | C | 148 | a0001c0001t0001g0064 a0001c0001t0001g0211 a0001c0001t0003g0020 others(145): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.2350+75T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40979984 | |||||||
| chr5:40980000 | C | T | 91 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(88): Show |
94 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2350+91C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40980000 | |||||||
| chr5:40980064 | C | A | 51 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0222 others(48): Show |
52 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.2350+155C>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40980064 | |||||||
| chr5:40980156 | C | T | 2 | a0001c0001t0001g0326 a0001c0001t0001g0348 |
2 | NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2350+247C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40980156 | |||||||
| chr5:40980391 | G | GAGTTTAG others(45): Show |
1 | a0004c0004t0001g0298 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2350+483_2350+534d others(54): Show |
C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 40980391 | ||||||
| chr5:40980483 | A | G | 271 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(268): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2350+574A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40980483 | |||||||
| chr5:40980510 | G | A | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2350+601G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40980510 | |||||||
| chr5:40980567 | C | G | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2350+658C>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40980567 | |||||||
| chr5:40980577 | A | G | 320 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(317): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.2350+668A>G | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40980577 | |||||||
| chr5:40980596 | G | C | 1 | a0012c0012t0003g0105 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2350+687G>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40980596 | |||||||
| chr5:40980685 | A | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0233 others(27): Show |
31 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2351-707A>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40980685 | |||||||
| chr5:40980705 | C | T | 147 | a0001c0001t0001g0064 a0001c0001t0001g0211 a0001c0001t0003g0020 others(144): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2351-687C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40980705 | |||||||
| chr5:40981001 | G | T | 93 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(90): Show |
96 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.2351-391G>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40981001 | |||||||
| chr5:40981273 | G | A | 271 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0064 others(268): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2351-119G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40981273 | |||||||
| chr5:40981278 | T | C | 146 | a0001c0001t0003g0020 a0001c0001t0003g0047 a0001c0001t0003g0263 others(143): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.2351-114T>C | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40981278 | |||||||
| chr5:40981289 | G | A | 25 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(22): Show |
27 | HG01346.hp1 HG01361.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.2351-103G>A | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40981289 | |||||||
| chr5:40981296 | C | T | 93 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(90): Show |
96 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.2351-96C>T | C7 | ENSG00000112936.21 | transcript | ENST00000313164.10 | protein_coding | 17/17 | chr5 | 40981296 |