Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4126 |
| ensemblid | ENSG00000109323.11 |
| hgncid | 6831 |
| symbol | MANBA |
| name | mannosidase beta |
| refseq_nuc | NM_005908.4 |
| refseq_prot | NP_005899.3 |
| ensembl_nuc | ENST00000647097.2 |
| ensembl_prot | ENSP00000495247.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 102630770 |
| end | 102760968 |
| strand | - |
| ver | v1.2 |
| region | chr4:102630770-102760968 |
| region5000 | chr4:102625770-102765968 |
| regionname0 | MANBA_chr4_102630770_102760968 |
| regionname5000 | MANBA_chr4_102625770_102765968 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 879 | 146 | 46 | 35 | 46 | 5 | 14 | 32 | MANBA_chr4_102625770_102765968 | MANBA | MRLHL others(874): Show |
chr4 | 102625770 | 102765968 |
| a0002 | 0/1 | 879 | 78 | 11 | 18 | 29 | 5 | 14 | 19 | MANBA_chr4_102625770_102765968 | MANBA | MRLHL others(874): Show |
chr4 | 102625770 | 102765968 |
| a0003 | 1/0 | 879 | 33 | 18 | 3 | 8 | 1 | 2 | 4 | MANBA_chr4_102625770_102765968 | MANBA | MRLHL others(874): Show |
chr4 | 102625770 | 102765968 |
| a0004 | 0/0 | 879 | 13 | 0 | 3 | 8 | 1 | 1 | 8 | MANBA_chr4_102625770_102765968 | MANBA | MRLHL others(874): Show |
chr4 | 102625770 | 102765968 |
| a0005 | 0/0 | 879 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | MRLHL others(874): Show |
chr4 | 102625770 | 102765968 |
| a0006 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | MRLHL others(874): Show |
chr4 | 102625770 | 102765968 |
| a0007 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | MRLHL others(874): Show |
chr4 | 102625770 | 102765968 |
| a0008 | 0/0 | 879 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | MRLHL others(874): Show |
chr4 | 102625770 | 102765968 |
| a0009 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | MRLHL others(874): Show |
chr4 | 102625770 | 102765968 |
| a0010 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | MRLHL others(874): Show |
chr4 | 102625770 | 102765968 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2637 | 124 | 27 | 34 | 45 | 4 | 14 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0001c0004 | 0/0 | 2637 | 17 | 15 | 1 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0001c0009 | 0/0 | 2637 | 3 | 3 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0001c0015 | 0/0 | 2637 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0001c0017 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0002c0002 | 0/1 | 2637 | 72 | 5 | 18 | 29 | 5 | 14 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0002c0007 | 0/0 | 2637 | 6 | 6 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0003c0003 | 1/0 | 2637 | 18 | 4 | 2 | 8 | 1 | 2 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0003c0005 | 0/0 | 2637 | 13 | 12 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0003c0010 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0004c0006 | 0/0 | 2637 | 13 | 0 | 3 | 8 | 1 | 1 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0005c0008 | 0/0 | 2637 | 5 | 5 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0006c0016 | 0/0 | 2637 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0007c0014 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0008c0013 | 0/0 | 2637 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0009c0011 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 | ||
| a0010c0012 | 0/0 | 2637 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | ATGCG others(2632): Show |
chr4 | 102625770 | 102765968 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 3989 | 48 | 1 | 14 | 26 | 1 | 6 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3984): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0003 | 0/0 | 3999 | 29 | 12 | 10 | 5 | 1 | 1 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3994): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0004 | 0/0 | 3991 | 11 | 0 | 3 | 6 | 0 | 2 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3986): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0005 | 0/0 | 4001 | 11 | 5 | 3 | 1 | 0 | 2 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0006 | 0/0 | 3995 | 5 | 1 | 1 | 2 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3990): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0008 | 0/0 | 3997 | 5 | 1 | 2 | 0 | 2 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3992): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0009 | 0/0 | 3987 | 3 | 0 | 0 | 2 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3982): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0010 | 0/0 | 3995 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3990): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0011 | 0/0 | 4003 | 3 | 1 | 0 | 1 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3998): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0012 | 0/0 | 3983 | 3 | 3 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3978): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0016 | 0/0 | 3997 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3992): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0017 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3985): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0018 | 0/0 | 3997 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3992): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0019 | 0/0 | 3985 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3980): Show |
chr4 | 102625770 | 102765968 |
| a0001c0001t0021 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0001c0004t0002 | 0/0 | 3989 | 2 | 1 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3984): Show |
chr4 | 102625770 | 102765968 |
| a0001c0004t0005 | 0/0 | 4001 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0001c0004t0006 | 0/0 | 3995 | 6 | 6 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3990): Show |
chr4 | 102625770 | 102765968 |
| a0001c0004t0008 | 0/0 | 3997 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3992): Show |
chr4 | 102625770 | 102765968 |
| a0001c0004t0009 | 0/0 | 3987 | 3 | 3 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3982): Show |
chr4 | 102625770 | 102765968 |
| a0001c0004t0010 | 0/0 | 3995 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3990): Show |
chr4 | 102625770 | 102765968 |
| a0001c0004t0014 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3982): Show |
chr4 | 102625770 | 102765968 |
| a0001c0009t0010 | 0/0 | 3995 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3990): Show |
chr4 | 102625770 | 102765968 |
| a0001c0009t0015 | 0/0 | 3989 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3984): Show |
chr4 | 102625770 | 102765968 |
| a0001c0009t0022 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3994): Show |
chr4 | 102625770 | 102765968 |
| a0001c0015t0009 | 0/0 | 3987 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3982): Show |
chr4 | 102625770 | 102765968 |
| a0001c0017t0006 | 0/0 | 3995 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3990): Show |
chr4 | 102625770 | 102765968 |
| a0002c0002t0001 | 0/1 | 4001 | 69 | 4 | 16 | 29 | 5 | 14 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0002c0002t0007 | 0/0 | 4001 | 3 | 1 | 2 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0002c0007t0001 | 0/0 | 4001 | 6 | 6 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0003c0003t0001 | 1/0 | 4001 | 9 | 2 | 1 | 3 | 1 | 1 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0003c0003t0007 | 0/0 | 4001 | 9 | 2 | 1 | 5 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0003c0005t0001 | 0/0 | 4001 | 10 | 9 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0003c0005t0010 | 0/0 | 3995 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3990): Show |
chr4 | 102625770 | 102765968 |
| a0003c0005t0013 | 0/0 | 4001 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0003c0010t0001 | 0/0 | 4001 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0004c0006t0002 | 0/0 | 3989 | 6 | 0 | 2 | 3 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3984): Show |
chr4 | 102625770 | 102765968 |
| a0004c0006t0003 | 0/0 | 3999 | 3 | 0 | 0 | 3 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3994): Show |
chr4 | 102625770 | 102765968 |
| a0004c0006t0004 | 0/0 | 3991 | 2 | 0 | 0 | 1 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3986): Show |
chr4 | 102625770 | 102765968 |
| a0004c0006t0006 | 0/0 | 3995 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3990): Show |
chr4 | 102625770 | 102765968 |
| a0004c0006t0008 | 0/0 | 3997 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3992): Show |
chr4 | 102625770 | 102765968 |
| a0005c0008t0003 | 0/0 | 3999 | 5 | 5 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3994): Show |
chr4 | 102625770 | 102765968 |
| a0006c0016t0004 | 0/0 | 3991 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3986): Show |
chr4 | 102625770 | 102765968 |
| a0007c0014t0002 | 0/0 | 3989 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3984): Show |
chr4 | 102625770 | 102765968 |
| a0008c0013t0001 | 0/0 | 4001 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| a0009c0011t0020 | 0/0 | 3989 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3984): Show |
chr4 | 102625770 | 102765968 |
| a0010c0012t0001 | 0/0 | 4001 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | GAGTG others(3996): Show |
chr4 | 102625770 | 102765968 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0008g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0009g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0011g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0011g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0012g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0012g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0016g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0017g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0018g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0019g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0021g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0008g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0010g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0014g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0009t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0009t0015g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0009t0022g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0015t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0017t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0007g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0001g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0013g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0010t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0010t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0008g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0005c0008t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0005c0008t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0005c0008t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0005c0008t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0005c0008t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0006c0016t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0007c0014t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0008c0013t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0009c0011t0020g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0010c0012t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0002 | g0026 | EUR | GBR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0079 | EUR | GBR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0123 | EUR | GBR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0246 | EUR | GBR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0030 | EUR | FIN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0151 | EUR | FIN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0242 | EUR | FIN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0029 | EUR | FIN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00438 | hp2 | a0003 | c0003 | t0007 | g0257 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00558 | hp1 | a0001 | c0001 | t0009 | g0176 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00609 | hp1 | a0001 | c0001 | t0006 | g0162 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00639 | hp1 | a0006 | c0016 | t0004 | g0214 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00735 | hp1 | a0004 | c0006 | t0002 | g0061 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00735 | hp2 | a0001 | c0004 | t0008 | g0014 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01070 | hp1 | a0003 | c0003 | t0007 | g0238 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0239 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0200 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0215 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01081 | hp2 | a0004 | c0006 | t0002 | g0115 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01099 | hp1 | a0002 | c0002 | t0007 | g0064 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0077 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0216 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01192 | hp2 | a0003 | c0005 | t0001 | g0009 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01243 | hp2 | a0004 | c0006 | t0008 | g0112 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0158 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0080 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0082 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0081 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0211 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01515 | hp1 | a0001 | c0001 | t0008 | g0240 | EUR | IBS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0085 | EUR | IBS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01884 | hp1 | a0003 | c0005 | t0001 | g0013 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01891 | hp2 | a0001 | c0004 | t0006 | g0263 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01978 | hp1 | a0001 | c0001 | t0017 | g0145 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0088 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0228 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0205 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0258 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02135 | hp2 | a0003 | c0003 | t0007 | g0117 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02145 | hp1 | a0003 | c0005 | t0001 | g0006 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02145 | hp2 | a0001 | c0004 | t0006 | g0267 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02148 | hp2 | a0002 | c0002 | t0007 | g0116 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02257 | hp1 | a0002 | c0007 | t0001 | g0107 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02257 | hp2 | a0007 | c0014 | t0002 | g0031 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02280 | hp1 | a0002 | c0002 | t0007 | g0033 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0152 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02451 | hp1 | a0002 | c0007 | t0001 | g0106 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0130 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02615 | hp1 | a0001 | c0009 | t0022 | g0016 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02622 | hp1 | a0002 | c0007 | t0001 | g0109 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02622 | hp2 | a0001 | c0001 | t0018 | g0202 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02630 | hp1 | a0001 | c0004 | t0006 | g0266 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0198 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02647 | hp1 | a0005 | c0008 | t0003 | g0219 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02647 | hp2 | a0001 | c0004 | t0009 | g0024 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02698 | hp1 | a0008 | c0013 | t0001 | g0272 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02717 | hp2 | a0003 | c0005 | t0001 | g0012 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02723 | hp1 | a0001 | c0017 | t0006 | g0237 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0021 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0136 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02738 | hp2 | a0001 | c0001 | t0009 | g0159 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02809 | hp2 | a0005 | c0008 | t0003 | g0138 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02818 | hp2 | a0001 | c0004 | t0002 | g0243 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02886 | hp1 | a0003 | c0005 | t0010 | g0015 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02886 | hp2 | a0001 | c0004 | t0005 | g0141 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02896 | hp1 | a0001 | c0004 | t0006 | g0264 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02896 | hp2 | a0005 | c0008 | t0003 | g0222 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02897 | hp2 | a0005 | c0008 | t0003 | g0218 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0199 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02922 | hp2 | a0001 | c0004 | t0009 | g0140 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02965 | hp1 | a0009 | c0011 | t0020 | g0018 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02965 | hp2 | a0001 | c0009 | t0010 | g0034 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02970 | hp1 | a0002 | c0007 | t0001 | g0110 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02970 | hp2 | a0003 | c0010 | t0001 | g0271 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03041 | hp1 | a0003 | c0005 | t0001 | g0008 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03098 | hp2 | a0003 | c0003 | t0007 | g0220 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03130 | hp2 | a0003 | c0005 | t0001 | g0001 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03195 | hp1 | a0003 | c0005 | t0001 | g0017 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0023 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03209 | hp1 | a0001 | c0004 | t0006 | g0265 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03209 | hp2 | a0001 | c0004 | t0010 | g0275 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0250 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03225 | hp2 | a0001 | c0009 | t0015 | g0005 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03486 | hp1 | a0003 | c0005 | t0013 | g0252 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0132 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03516 | hp1 | a0003 | c0005 | t0013 | g0251 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0168 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03540 | hp1 | a0005 | c0008 | t0003 | g0221 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03540 | hp2 | a0001 | c0001 | t0021 | g0174 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03579 | hp1 | a0001 | c0004 | t0009 | g0011 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03579 | hp2 | a0001 | c0004 | t0014 | g0004 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0124 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0127 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0277 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0247 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0052 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0209 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0099 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04184 | hp2 | a0003 | c0003 | t0007 | g0160 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0059 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04204 | hp1 | a0004 | c0006 | t0002 | g0154 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18522 | hp1 | a0003 | c0005 | t0001 | g0010 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18522 | hp2 | a0001 | c0004 | t0005 | g0269 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18906 | hp1 | a0002 | c0007 | t0001 | g0118 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0232 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18949 | hp2 | a0004 | c0006 | t0002 | g0045 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18957 | hp2 | a0003 | c0003 | t0007 | g0255 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18960 | hp2 | a0001 | c0001 | t0011 | g0051 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18968 | hp1 | a0001 | c0001 | t0019 | g0194 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18969 | hp2 | a0004 | c0006 | t0003 | g0072 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18988 | hp2 | a0004 | c0006 | t0003 | g0068 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18990 | hp1 | a0004 | c0006 | t0002 | g0035 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18990 | hp2 | a0001 | c0001 | t0009 | g0184 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18995 | hp2 | a0003 | c0003 | t0001 | g0244 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18999 | hp1 | a0001 | c0001 | t0016 | g0157 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19000 | hp2 | a0004 | c0006 | t0003 | g0053 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19030 | hp1 | a0001 | c0004 | t0006 | g0268 | AFR | LWK | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19030 | hp2 | a0003 | c0003 | t0007 | g0256 | AFR | LWK | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | LWK | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | LWK | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19054 | hp2 | a0003 | c0003 | t0007 | g0143 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19055 | hp1 | a0010 | c0012 | t0001 | g0103 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19055 | hp2 | a0004 | c0006 | t0006 | g0129 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19063 | hp1 | a0001 | c0015 | t0009 | g0173 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19063 | hp2 | a0003 | c0003 | t0007 | g0248 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19077 | hp2 | a0004 | c0006 | t0004 | g0042 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19091 | hp1 | a0004 | c0006 | t0002 | g0204 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19240 | hp1 | a0003 | c0005 | t0001 | g0027 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19240 | hp2 | a0003 | c0005 | t0001 | g0001 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | ASW | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ASW | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0076 | EUR | TSI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20752 | hp2 | a0004 | c0006 | t0004 | g0025 | EUR | TSI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | GIH | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20905 | hp2 | a0001 | c0001 | t0011 | g0210 | SAS | GIH | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02109 | hp2 | a0003 | c0010 | t0001 | g0274 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02486 | hp1 | a0002 | c0007 | t0001 | g0108 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03471 | hp1 | a0001 | c0004 | t0010 | g0253 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0083 | AFR | USA | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20300 | hp2 | a0001 | c0001 | t0012 | g0153 | AFR | USA | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0262 | REF | REF | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0125 | REF | REF | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102632215 | C | T | 1 | a0006 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2482G>A | p.Val828Ile | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 2556/4001 | 2482/2640 | 828/879 | chr4 | 102632215 | |||
| chr4:102634852 | G | C | 1 | a0005 | 5 | HG02647.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
missense_variant | MODERATE | c.2351C>G | p.Pro784Arg | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/17 | 2425/4001 | 2351/2640 | 784/879 | chr4 | 102634852 | |||
| chr4:102634957 | A | T | 1 | a0010 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.2246T>A | p.Leu749His | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/17 | 2320/4001 | 2246/2640 | 749/879 | chr4 | 102634957 | |||
| chr4:102635023 | G | A | 1 | a0009 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.2180C>T | p.Ser727Phe | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/17 | 2254/4001 | 2180/2640 | 727/879 | chr4 | 102635023 | |||
| chr4:102635920 | G | A | 6 | a0001 a0004 a0005 others(3): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
missense_variant | MODERATE | c.2102C>T | p.Thr701Met | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/17 | 2176/4001 | 2102/2640 | 701/879 | chr4 | 102635920 | |||
| chr4:102650568 | C | A | 1 | a0008 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.1838G>T | p.Arg613Leu | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/17 | 1912/4001 | 1838/2640 | 613/879 | chr4 | 102650568 | |||
| chr4:102664693 | C | T | 1 | a0007 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.1477G>A | p.Val493Ile | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/17 | 1551/4001 | 1477/2640 | 493/879 | chr4 | 102664693 | |||
| chr4:102690688 | C | T | 5 | a0002 a0004 a0008 others(2): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
missense_variant | MODERATE | c.757G>A | p.Val253Ile | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/17 | 831/4001 | 757/2640 | 253/879 | chr4 | 102690688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102634835 | A | G | 10 | a0001c0001 a0001c0004 a0001c0009 others(7): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
synonymous_variant | LOW | c.2368T>C | p.Leu790Leu | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/17 | 2442/4001 | 2368/2640 | 790/879 | chr4 | 102634835 | |||
| chr4:102635907 | A | G | 1 | a0001c0015 | 1 | NA19063.hp1 | synonymous_variant | LOW | c.2115T>C | p.Tyr705Tyr | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/17 | 2189/4001 | 2115/2640 | 705/879 | chr4 | 102635907 | |||
| chr4:102664688 | C | A | 1 | a0002c0007 | 6 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.1482G>T | p.Leu494Leu | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/17 | 1556/4001 | 1482/2640 | 494/879 | chr4 | 102664688 | |||
| chr4:102690614 | T | C | 3 | a0001c0009 a0001c0017 a0003c0005 |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
synonymous_variant | LOW | c.831A>G | p.Leu277Leu | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/17 | 905/4001 | 831/2640 | 277/879 | chr4 | 102690614 | |||
| chr4:102723925 | C | T | 5 | a0001c0004 a0001c0009 a0003c0005 others(2): Show |
36 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(33): Show |
synonymous_variant | LOW | c.315G>A | p.Thr105Thr | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 3/17 | 389/4001 | 315/2640 | 105/879 | chr4 | 102723925 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102630911 | T | C | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1146A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 1146 | chr4 | 102630911 | ||||||
| chr4:102630998 | C | T | 6 | a0001c0001t0010 a0001c0004t0010 a0001c0004t0014 others(3): Show |
7 | HG02886.hp1 HG02965.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1059G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 1059 | chr4 | 102630998 | ||||||
| chr4:102631091 | C | T | 1 | a0001c0001t0018 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*966G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 966 | chr4 | 102631091 | ||||||
| chr4:102631096 | T | C | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*961A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 961 | chr4 | 102631096 | ||||||
| chr4:102631104 | C | CTG | 1 | a0001c0001t0011 | 3 | HG02723.hp2 NA18960.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*952_*953insCA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 952 | chr4 | 102631104 | ||||||
| chr4:102631104 | CTT | C | 4 | a0001c0001t0003 a0001c0009t0022 a0004c0006t0003 others(1): Show |
38 | HG00140.hp2 HG00544.hp1 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*951_*952delAA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 951 | chr4 | 102631104 | ||||||
| chr4:102631104 | CTTTG | C | 5 | a0001c0001t0008 a0001c0001t0016 a0001c0001t0018 others(2): Show |
9 | HG00735.hp2 HG01081.hp1 HG01175.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*949_*952delCAAA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 949 | chr4 | 102631104 | ||||||
| chr4:102631104 | CTTTGTG | C | 8 | a0001c0001t0006 a0001c0001t0010 a0001c0004t0006 others(5): Show |
18 | HG00609.hp1 HG01346.hp1 HG01884.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*947_*952delCACAAA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 947 | chr4 | 102631104 | ||||||
| chr4:102631104 | CTTTGTGT others(3): Show |
C | 3 | a0001c0001t0004 a0004c0006t0004 a0006c0016t0004 |
14 | HG00639.hp1 HG01074.hp1 HG01257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*943_*952delCACACA others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 943 | chr4 | 102631104 | ||||||
| chr4:102631104 | CTTTGTGT others(5): Show |
C | 6 | a0001c0001t0002 a0001c0004t0002 a0001c0009t0015 others(3): Show |
59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*941_*952delCACACA others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 941 | chr4 | 102631104 | ||||||
| chr4:102631104 | CTTTGTGT others(7): Show |
C | 4 | a0001c0001t0009 a0001c0004t0009 a0001c0004t0014 others(1): Show |
8 | HG00558.hp1 HG02647.hp2 HG02738.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*939_*952delCACACA others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 939 | chr4 | 102631104 | ||||||
| chr4:102631104 | CTTTGTGT others(9): Show |
C | 1 | a0001c0001t0019 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937_*952delCACACA others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 937 | chr4 | 102631104 | ||||||
| chr4:102631104 | CTTTGTGT others(11): Show |
C | 1 | a0001c0001t0012 | 3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*935_*952delCACACA others(12): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 935 | chr4 | 102631104 | ||||||
| chr4:102631106 | T | G | 5 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0017 others(2): Show |
16 | HG01106.hp2 HG01358.hp2 HG01978.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*951A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 951 | chr4 | 102631106 | ||||||
| chr4:102631106 | T | TTG | 1 | a0002c0002t0001 | 6 | HG01168.hp2 HG01258.hp2 HG03688.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*949_*950dupCA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 950 | chr4 | 102631106 | ||||||
| chr4:102631106 | T | TTGTG | 3 | a0002c0002t0001 a0002c0007t0001 a0003c0003t0001 |
11 | HG02083.hp2 HG02135.hp1 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*947_*950dupCACA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 950 | chr4 | 102631106 | ||||||
| chr4:102631106 | T | TTGTGTG | 3 | a0002c0002t0001 a0002c0007t0001 a0003c0003t0007 |
5 | HG01070.hp1 HG02257.hp1 HG03492.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*945_*950dupCACACA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 950 | chr4 | 102631106 | ||||||
| chr4:102631106 | TTGTG | T | 5 | a0002c0002t0001 a0002c0002t0007 a0003c0003t0001 others(2): Show |
9 | HG01496.hp2 HG02148.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*947_*950delCACA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 947 | chr4 | 102631106 | ||||||
| chr4:102631106 | TTGTGTG | T | 5 | a0002c0002t0001 a0002c0002t0007 a0003c0003t0001 others(2): Show |
10 | HG00438.hp2 HG01099.hp1 HG02080.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*945_*950delCACACA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 945 | chr4 | 102631106 | ||||||
| chr4:102631106 | TTGTGTGT others(3): Show |
T | 1 | a0003c0005t0001 | 10 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*941_*950delCACACA others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 941 | chr4 | 102631106 | ||||||
| chr4:102631106 | TTGTGTGT others(5): Show |
T | 1 | a0003c0003t0007 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*939_*950delCACACA others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 939 | chr4 | 102631106 | ||||||
| chr4:102631106 | TTGTGTGT others(7): Show |
T | 1 | a0002c0002t0001 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*937_*950delCACACA others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 937 | chr4 | 102631106 | ||||||
| chr4:102631106 | TTGTGTGT others(9): Show |
T | 1 | a0002c0002t0001 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*935_*950delCACACA others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 935 | chr4 | 102631106 | ||||||
| chr4:102631141 | TGTGTGTG others(4): Show |
T | 1 | a0001c0001t0017 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*905_*915delCACACA others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 905 | chr4 | 102631141 | ||||||
| chr4:102631273 | A | G | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*784T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 784 | chr4 | 102631273 | ||||||
| chr4:102631376 | C | T | 1 | a0003c0005t0013 | 2 | HG03486.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*681G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 681 | chr4 | 102631376 | ||||||
| chr4:102631536 | C | T | 1 | a0009c0011t0020 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 521 | chr4 | 102631536 | ||||||
| chr4:102631541 | A | G | 1 | a0001c0001t0016 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 516 | chr4 | 102631541 | ||||||
| chr4:102631552 | C | T | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*505G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 505 | chr4 | 102631552 | ||||||
| chr4:102631611 | G | A | 1 | a0001c0001t0012 | 3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*446C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 446 | chr4 | 102631611 | ||||||
| chr4:102631656 | C | T | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*401G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 401 | chr4 | 102631656 | ||||||
| chr4:102631673 | G | A | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*384C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 384 | chr4 | 102631673 | ||||||
| chr4:102631701 | C | T | 2 | a0002c0002t0007 a0003c0003t0007 |
12 | HG00438.hp2 HG01070.hp1 HG01099.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*356G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 356 | chr4 | 102631701 | ||||||
| chr4:102631740 | T | C | 6 | a0001c0001t0010 a0001c0004t0010 a0001c0004t0014 others(3): Show |
7 | HG02886.hp1 HG02965.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*317A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 317 | chr4 | 102631740 | ||||||
| chr4:102631896 | G | A | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*161C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 161 | chr4 | 102631896 | ||||||
| chr4:102631933 | A | G | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(34): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*124T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 124 | chr4 | 102631933 | ||||||
| chr4:102631979 | T | C | 2 | a0001c0001t0021 a0001c0009t0022 |
2 | HG02615.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*78A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 78 | chr4 | 102631979 | ||||||
| chr4:102760941 | C | T | 1 | a0001c0009t0015 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-47G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/17 | 47 | chr4 | 102760941 | ||||||
| chr4:102760952 | C | T | 1 | a0001c0004t0014 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-58G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/17 | 58 | chr4 | 102760952 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102632290 | GA | G | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2416-10delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632290 | |||||||
| chr4:102632346 | A | C | 1 | a0004c0006t0002g0035 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2416-65T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632346 | |||||||
| chr4:102632386 | C | T | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-105G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632386 | |||||||
| chr4:102632417 | A | G | 1 | a0009c0011t0020g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2416-136T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632417 | |||||||
| chr4:102632470 | C | T | 3 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 |
3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2416-189G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632470 | |||||||
| chr4:102632508 | G | A | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-227C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632508 | |||||||
| chr4:102632759 | A | C | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-478T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632759 | |||||||
| chr4:102632769 | C | T | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-488G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632769 | |||||||
| chr4:102632803 | T | C | 15 | a0002c0002t0007g0033 a0002c0002t0007g0064 a0002c0002t0007g0116 others(12): Show |
15 | HG00438.hp2 HG01070.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2416-522A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632803 | |||||||
| chr4:102632862 | G | A | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-581C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632862 | |||||||
| chr4:102632951 | C | G | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-670G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632951 | |||||||
| chr4:102632956 | T | A | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-675A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632956 | |||||||
| chr4:102633104 | T | G | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-823A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633104 | |||||||
| chr4:102633116 | A | G | 4 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02886.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2416-835T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633116 | |||||||
| chr4:102633173 | C | CT | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-893dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633173 | |||||||
| chr4:102633178 | T | A | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-897A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633178 | |||||||
| chr4:102633183 | C | T | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-902G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633183 | |||||||
| chr4:102633193 | T | A | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-912A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633193 | |||||||
| chr4:102633196 | T | C | 3 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 |
3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2416-915A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633196 | |||||||
| chr4:102633214 | CA | C | 5 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 others(2): Show |
5 | HG02886.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2416-934delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633214 | |||||||
| chr4:102633216 | G | T | 5 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 others(2): Show |
5 | HG02886.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2416-935C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633216 | |||||||
| chr4:102633365 | C | T | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-1084G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633365 | |||||||
| chr4:102633395 | T | C | 27 | a0001c0001t0003g0002 a0001c0001t0003g0038 a0001c0001t0003g0089 others(24): Show |
28 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.2416-1114A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633395 | |||||||
| chr4:102633418 | T | G | 3 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 |
3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2416-1137A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633418 | |||||||
| chr4:102633556 | G | A | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1232C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633556 | |||||||
| chr4:102633565 | A | G | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1223T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633565 | |||||||
| chr4:102633576 | G | A | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1212C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633576 | |||||||
| chr4:102633616 | C | G | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1172G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633616 | |||||||
| chr4:102633618 | C | T | 1 | a0002c0002t0001g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2415+1170G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633618 | |||||||
| chr4:102633636 | A | G | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1152T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633636 | |||||||
| chr4:102633653 | C | A | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1135G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633653 | |||||||
| chr4:102633664 | T | C | 185 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(182): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.2415+1124A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633664 | |||||||
| chr4:102633665 | C | T | 16 | a0001c0001t0003g0002 a0001c0001t0003g0089 a0001c0001t0003g0090 others(13): Show |
17 | HG00544.hp1 HG01167.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.2415+1123G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633665 | |||||||
| chr4:102633753 | A | C | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1035T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633753 | |||||||
| chr4:102633773 | TG | T | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1014delC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633773 | |||||||
| chr4:102633818 | A | G | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+970T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633818 | |||||||
| chr4:102633835 | A | G | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+953T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633835 | |||||||
| chr4:102633904 | G | GC | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+883dupG | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633904 | |||||||
| chr4:102634076 | T | C | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+712A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634076 | |||||||
| chr4:102634095 | G | A | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+693C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634095 | |||||||
| chr4:102634096 | T | C | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+692A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634096 | |||||||
| chr4:102634260 | A | C | 166 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(163): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+528T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634260 | |||||||
| chr4:102634454 | A | C | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+334T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634454 | |||||||
| chr4:102634455 | G | A | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+333C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634455 | |||||||
| chr4:102634462 | C | G | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+326G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634462 | |||||||
| chr4:102634485 | T | C | 1 | a0002c0002t0001g0249 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2415+303A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634485 | |||||||
| chr4:102634488 | TG | T | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+299delC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634488 | |||||||
| chr4:102634519 | T | C | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+269A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634519 | |||||||
| chr4:102634646 | G | C | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+142C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634646 | |||||||
| chr4:102634664 | G | A | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+124C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634664 | |||||||
| chr4:102634769 | C | T | 1 | a0001c0001t0016g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2415+19G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634769 | |||||||
| chr4:102634770 | G | A | 1 | a0002c0007t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2415+18C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634770 | |||||||
| chr4:102635159 | T | C | 163 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(160): Show |
165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2158-114A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635159 | |||||||
| chr4:102635210 | G | GT | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2158-166dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635210 | |||||||
| chr4:102635305 | G | C | 160 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(157): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2158-260C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635305 | |||||||
| chr4:102635318 | G | A | 1 | a0003c0005t0001g0006 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2158-273C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635318 | |||||||
| chr4:102635370 | C | T | 1 | a0001c0001t0009g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2158-325G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635370 | |||||||
| chr4:102635653 | C | T | 1 | a0002c0002t0001g0277 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2157+212G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635653 | |||||||
| chr4:102635704 | T | C | 158 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(155): Show |
160 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.2157+161A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635704 | |||||||
| chr4:102635790 | A | G | 1 | a0001c0001t0016g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2157+75T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635790 | |||||||
| chr4:102636035 | C | T | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-28G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636035 | |||||||
| chr4:102636047 | G | A | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2015-40C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636047 | |||||||
| chr4:102636062 | C | T | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-55G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636062 | |||||||
| chr4:102636093 | C | CA | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2015-87_2015-86ins others(1): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636093 | |||||||
| chr4:102636094 | G | A | 163 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(160): Show |
165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2015-87C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636094 | |||||||
| chr4:102636097 | G | T | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2015-90C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636097 | |||||||
| chr4:102636131 | C | G | 1 | a0001c0001t0002g0164 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2015-124G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636131 | |||||||
| chr4:102636154 | G | C | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-147C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636154 | |||||||
| chr4:102636303 | G | T | 1 | a0003c0010t0001g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2015-296C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636303 | |||||||
| chr4:102636306 | A | T | 41 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0022 others(38): Show |
41 | HG00735.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.2015-299T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636306 | |||||||
| chr4:102636372 | T | G | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-365A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636372 | |||||||
| chr4:102636386 | A | G | 2 | a0001c0001t0005g0225 a0001c0009t0010g0034 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2015-379T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636386 | |||||||
| chr4:102636504 | T | C | 1 | a0001c0004t0006g0263 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2015-497A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636504 | |||||||
| chr4:102636507 | A | G | 163 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(160): Show |
165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2015-500T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636507 | |||||||
| chr4:102636527 | T | C | 1 | a0001c0001t0002g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2015-520A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636527 | |||||||
| chr4:102636596 | T | C | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-589A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636596 | |||||||
| chr4:102636960 | G | C | 1 | a0003c0003t0001g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2015-953C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636960 | |||||||
| chr4:102637001 | C | A | 1 | a0001c0001t0002g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2015-994G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637001 | |||||||
| chr4:102637012 | C | G | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-1005G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637012 | |||||||
| chr4:102637357 | T | A | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-1350A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637357 | |||||||
| chr4:102637549 | G | C | 1 | a0002c0002t0001g0046 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2015-1542C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637549 | |||||||
| chr4:102637574 | C | T | 39 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0022 others(36): Show |
39 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.2015-1567G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637574 | |||||||
| chr4:102637648 | T | C | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-1641A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637648 | |||||||
| chr4:102637676 | C | A | 69 | a0001c0001t0003g0002 a0001c0001t0003g0019 a0001c0001t0003g0020 others(66): Show |
70 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.2015-1669G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637676 | |||||||
| chr4:102637696 | A | G | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-1689T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637696 | |||||||
| chr4:102637794 | T | C | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-1787A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637794 | |||||||
| chr4:102637908 | G | A | 1 | a0003c0003t0001g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2014+1805C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637908 | |||||||
| chr4:102637972 | C | A | 1 | a0002c0002t0001g0134 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2014+1741G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637972 | |||||||
| chr4:102638172 | C | T | 11 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0022 others(8): Show |
11 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2014+1541G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638172 | |||||||
| chr4:102638183 | G | T | 1 | a0004c0006t0002g0035 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2014+1530C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638183 | |||||||
| chr4:102638193 | G | C | 4 | a0003c0005t0001g0001 a0003c0005t0001g0006 a0003c0005t0001g0008 others(1): Show |
5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2014+1520C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638193 | |||||||
| chr4:102638316 | C | G | 1 | a0003c0005t0001g0001 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2014+1397G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638316 | |||||||
| chr4:102638398 | C | A | 2 | a0001c0004t0009g0011 a0001c0004t0009g0024 |
2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2014+1315G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638398 | |||||||
| chr4:102638471 | G | GT | 160 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(157): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2014+1241dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638471 | |||||||
| chr4:102638471 | G | GTT | 3 | a0001c0001t0004g0156 a0001c0001t0009g0159 a0004c0006t0003g0053 |
3 | HG02602.hp1 HG02738.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2014+1241_2014+124 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638471 | |||||||
| chr4:102638473 | C | T | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2014+1240G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638473 | |||||||
| chr4:102638476 | G | T | 165 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(162): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2014+1237C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638476 | |||||||
| chr4:102638705 | C | T | 2 | a0002c0002t0001g0063 a0002c0002t0001g0101 |
2 | HG00438.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.2014+1008G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638705 | |||||||
| chr4:102638719 | A | G | 153 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(150): Show |
155 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2014+994T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638719 | |||||||
| chr4:102639011 | T | C | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2014+702A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639011 | |||||||
| chr4:102639102 | T | G | 3 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 |
3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2014+611A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639102 | |||||||
| chr4:102639161 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2014+552T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639161 | |||||||
| chr4:102639544 | C | T | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2014+169G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639544 | |||||||
| chr4:102639588 | A | T | 69 | a0001c0001t0003g0002 a0001c0001t0003g0019 a0001c0001t0003g0020 others(66): Show |
70 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.2014+125T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639588 | |||||||
| chr4:102639644 | T | C | 3 | a0001c0001t0003g0246 a0001c0001t0006g0082 a0001c0001t0006g0247 |
3 | HG00140.hp2 HG01346.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2014+69A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639644 | |||||||
| chr4:102639949 | T | C | 20 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(17): Show |
21 | HG00639.hp1 HG00673.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1870-92A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102639949 | |||||||
| chr4:102640181 | A | G | 1 | a0002c0002t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1870-324T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640181 | |||||||
| chr4:102640323 | A | T | 3 | a0003c0003t0001g0198 a0003c0003t0001g0199 a0003c0010t0001g0274 |
3 | HG02109.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1870-466T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640323 | |||||||
| chr4:102640384 | T | C | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1870-527A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640384 | |||||||
| chr4:102640552 | G | A | 93 | a0001c0001t0002g0254 a0002c0002t0001g0028 a0002c0002t0001g0029 others(90): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1870-695C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640552 | |||||||
| chr4:102640748 | G | A | 11 | a0001c0004t0005g0141 a0001c0004t0006g0263 a0001c0004t0006g0264 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1870-891C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640748 | |||||||
| chr4:102640773 | A | C | 1 | a0001c0001t0005g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1870-916T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640773 | |||||||
| chr4:102641091 | T | A | 5 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 others(2): Show |
5 | HG01071.hp2 HG01109.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1870-1234A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102641091 | |||||||
| chr4:102641165 | A | C | 1 | a0001c0004t0002g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1870-1308T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102641165 | |||||||
| chr4:102641197 | A | G | 1 | a0001c0001t0005g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1870-1340T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102641197 | |||||||
| chr4:102641841 | A | G | 1 | a0001c0004t0005g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1870-1984T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102641841 | |||||||
| chr4:102642002 | C | T | 2 | a0001c0001t0002g0195 a0004c0006t0004g0042 |
2 | HG02080.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1870-2145G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642002 | |||||||
| chr4:102642067 | C | T | 1 | a0001c0001t0006g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1870-2210G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642067 | |||||||
| chr4:102642092 | GGCTATT | G | 25 | a0001c0001t0003g0002 a0001c0001t0003g0089 a0001c0001t0003g0090 others(22): Show |
26 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1870-2241_1870-223 others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642092 | |||||||
| chr4:102642408 | T | C | 2 | a0001c0015t0009g0173 a0003c0003t0007g0256 |
2 | NA19030.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1870-2551A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642408 | |||||||
| chr4:102642534 | G | A | 2 | a0001c0001t0002g0270 a0001c0001t0016g0157 |
2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2677C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642534 | |||||||
| chr4:102642535 | A | G | 2 | a0001c0001t0002g0270 a0001c0001t0016g0157 |
2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2678T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642535 | |||||||
| chr4:102642536 | G | T | 2 | a0001c0001t0002g0270 a0001c0001t0016g0157 |
2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2679C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642536 | |||||||
| chr4:102642540 | G | GTGAGCCG others(9): Show |
2 | a0001c0001t0002g0270 a0001c0001t0016g0157 |
2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2684_1870-268 others(20): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642540 | |||||||
| chr4:102642543 | G | C | 2 | a0001c0001t0002g0270 a0001c0001t0016g0157 |
2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2686C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642543 | |||||||
| chr4:102642544 | T | TTGGAG | 2 | a0001c0001t0002g0270 a0001c0001t0016g0157 |
2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2688_1870-268 others(9): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642544 | |||||||
| chr4:102642593 | C | CG | 12 | a0001c0001t0003g0223 a0001c0001t0003g0231 a0001c0001t0005g0261 others(9): Show |
12 | HG01070.hp1 HG01175.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1870-2737dupC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642593 | |||||||
| chr4:102642756 | T | C | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1870-2899A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642756 | |||||||
| chr4:102642809 | T | C | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1870-2952A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642809 | |||||||
| chr4:102642868 | T | C | 13 | a0001c0009t0015g0005 a0003c0005t0001g0001 a0003c0005t0001g0006 others(10): Show |
14 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1870-3011A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642868 | |||||||
| chr4:102643056 | T | C | 2 | a0001c0001t0003g0231 a0001c0001t0008g0216 |
2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1870-3199A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643056 | |||||||
| chr4:102643105 | G | C | 1 | a0003c0003t0007g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1870-3248C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643105 | |||||||
| chr4:102643183 | C | T | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1870-3326G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643183 | |||||||
| chr4:102643266 | A | T | 1 | a0001c0001t0012g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1870-3409T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643266 | |||||||
| chr4:102643275 | C | T | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1870-3418G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643275 | |||||||
| chr4:102643310 | T | G | 1 | a0001c0004t0005g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1870-3453A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643310 | |||||||
| chr4:102643382 | T | C | 1 | a0001c0001t0021g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1870-3525A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643382 | |||||||
| chr4:102643556 | T | C | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1870-3699A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643556 | |||||||
| chr4:102643655 | T | C | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1870-3798A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643655 | |||||||
| chr4:102643859 | T | G | 1 | a0001c0001t0009g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1870-4002A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643859 | |||||||
| chr4:102643863 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1870-4006C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643863 | |||||||
| chr4:102643995 | A | G | 6 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0004t0005g0141 others(3): Show |
6 | HG02280.hp2 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870-4138T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643995 | |||||||
| chr4:102644052 | C | A | 1 | a0001c0004t0008g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1870-4195G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644052 | |||||||
| chr4:102644215 | A | T | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1870-4358T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644215 | |||||||
| chr4:102644352 | A | T | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1870-4495T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644352 | |||||||
| chr4:102644429 | C | T | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1870-4572G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644429 | |||||||
| chr4:102644780 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1870-4923T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644780 | |||||||
| chr4:102644810 | C | T | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1870-4953G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644810 | |||||||
| chr4:102644921 | A | T | 6 | a0001c0001t0002g0178 a0001c0001t0002g0182 a0001c0001t0002g0185 others(3): Show |
6 | HG00621.hp2 HG02071.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870-5064T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644921 | |||||||
| chr4:102645206 | T | C | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1869+5331A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645206 | |||||||
| chr4:102645297 | A | G | 1 | a0002c0002t0001g0128 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1869+5240T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645297 | |||||||
| chr4:102645637 | T | A | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1869+4900A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645637 | |||||||
| chr4:102645805 | T | C | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1869+4732A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645805 | |||||||
| chr4:102645908 | T | C | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1869+4629A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645908 | |||||||
| chr4:102645966 | T | C | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1869+4571A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645966 | |||||||
| chr4:102646191 | G | T | 122 | a0001c0001t0002g0254 a0001c0001t0012g0152 a0001c0001t0012g0153 others(119): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1869+4346C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646191 | |||||||
| chr4:102646325 | C | A | 1 | a0005c0008t0003g0219 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1869+4212G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646325 | |||||||
| chr4:102646406 | C | T | 1 | a0001c0004t0009g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1869+4131G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646406 | |||||||
| chr4:102646892 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1869+3645G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646892 | |||||||
| chr4:102646919 | T | G | 1 | a0001c0004t0005g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1869+3618A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646919 | |||||||
| chr4:102646928 | G | A | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1869+3609C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646928 | |||||||
| chr4:102647327 | G | A | 1 | a0001c0001t0002g0177 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1869+3210C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647327 | |||||||
| chr4:102647332 | T | C | 1 | a0001c0001t0002g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1869+3205A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647332 | |||||||
| chr4:102647565 | C | T | 1 | a0003c0003t0001g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1869+2972G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647565 | |||||||
| chr4:102647638 | T | C | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1869+2899A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647638 | |||||||
| chr4:102647850 | A | T | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1869+2687T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647850 | |||||||
| chr4:102647852 | G | A | 6 | a0001c0001t0002g0254 a0003c0003t0007g0117 a0003c0003t0007g0248 others(3): Show |
6 | HG00438.hp2 HG02056.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869+2685C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647852 | |||||||
| chr4:102648051 | A | C | 1 | a0001c0001t0002g0196 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1869+2486T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648051 | |||||||
| chr4:102648059 | C | A | 4 | a0002c0002t0001g0050 a0002c0002t0001g0054 a0002c0002t0001g0059 others(1): Show |
4 | HG02735.hp2 HG02738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+2478G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648059 | |||||||
| chr4:102648126 | A | G | 130 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(127): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1869+2411T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648126 | |||||||
| chr4:102648133 | A | T | 6 | a0001c0001t0012g0023 a0005c0008t0003g0138 a0005c0008t0003g0218 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869+2404T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648133 | |||||||
| chr4:102648543 | A | G | 2 | a0002c0002t0001g0043 a0002c0002t0001g0057 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1869+1994T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648543 | |||||||
| chr4:102648895 | T | A | 8 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0004t0009g0011 others(5): Show |
8 | HG02280.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1869+1642A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648895 | |||||||
| chr4:102648987 | A | G | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1869+1550T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648987 | |||||||
| chr4:102649069 | C | G | 1 | a0002c0002t0001g0128 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1869+1468G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649069 | |||||||
| chr4:102649118 | G | A | 1 | a0003c0003t0007g0143 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1869+1419C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649118 | |||||||
| chr4:102649130 | T | C | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1869+1407A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649130 | |||||||
| chr4:102649526 | G | T | 8 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0004t0009g0011 others(5): Show |
8 | HG02280.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1869+1011C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649526 | |||||||
| chr4:102649679 | T | C | 1 | a0001c0001t0002g0270 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1869+858A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649679 | |||||||
| chr4:102649698 | C | G | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1869+839G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649698 | |||||||
| chr4:102649760 | A | C | 1 | a0002c0007t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1869+777T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649760 | |||||||
| chr4:102650103 | C | T | 1 | a0001c0004t0006g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1869+434G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102650103 | |||||||
| chr4:102650356 | T | C | 5 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 others(2): Show |
5 | HG01071.hp2 HG01109.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1869+181A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102650356 | |||||||
| chr4:102650714 | G | A | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1705-13C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102650714 | |||||||
| chr4:102650714 | G | T | 6 | a0001c0001t0003g0190 a0001c0001t0003g0230 a0001c0001t0003g0273 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1705-13C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102650714 | |||||||
| chr4:102650770 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0179 |
2 | HG01074.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1705-69C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102650770 | |||||||
| chr4:102651163 | G | A | 123 | a0001c0001t0002g0254 a0001c0001t0012g0152 a0001c0001t0012g0153 others(120): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1705-462C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651163 | |||||||
| chr4:102651283 | G | A | 123 | a0001c0001t0002g0254 a0001c0001t0012g0152 a0001c0001t0012g0153 others(120): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1705-582C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651283 | |||||||
| chr4:102651298 | TA | T | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1705-598delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651298 | |||||||
| chr4:102651460 | A | G | 1 | a0004c0006t0006g0129 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1705-759T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651460 | |||||||
| chr4:102651537 | T | C | 3 | a0001c0004t0009g0011 a0001c0004t0009g0024 a0001c0004t0009g0140 |
3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1705-836A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651537 | |||||||
| chr4:102651594 | G | T | 109 | a0001c0001t0002g0254 a0001c0004t0009g0011 a0001c0004t0009g0024 others(106): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1705-893C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651594 | |||||||
| chr4:102651789 | C | T | 115 | a0001c0001t0002g0254 a0001c0001t0012g0152 a0001c0001t0012g0153 others(112): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1705-1088G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651789 | |||||||
| chr4:102651925 | C | T | 106 | a0001c0001t0002g0254 a0001c0009t0015g0005 a0001c0017t0006g0237 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1705-1224G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651925 | |||||||
| chr4:102651965 | TTTAA | T | 106 | a0001c0001t0002g0254 a0001c0009t0015g0005 a0001c0017t0006g0237 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1705-1268_1705-126 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651965 | |||||||
| chr4:102651989 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1705-1288G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651989 | |||||||
| chr4:102652098 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1705-1397C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652098 | |||||||
| chr4:102652166 | C | T | 108 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(105): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1705-1465G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652166 | |||||||
| chr4:102652220 | G | C | 107 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(104): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1705-1519C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652220 | |||||||
| chr4:102652283 | T | C | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1705-1582A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652283 | |||||||
| chr4:102652334 | C | A | 1 | a0002c0002t0007g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1705-1633G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652334 | |||||||
| chr4:102652469 | G | A | 1 | a0001c0004t0002g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1705-1768C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652469 | |||||||
| chr4:102652568 | TA | T | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1705-1868delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652568 | |||||||
| chr4:102652569 | A | T | 18 | a0001c0001t0010g0232 a0001c0001t0012g0152 a0001c0001t0012g0153 others(15): Show |
18 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1705-1868T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652569 | |||||||
| chr4:102652592 | G | A | 120 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(117): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1705-1891C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652592 | |||||||
| chr4:102652670 | T | C | 2 | a0001c0001t0021g0174 a0001c0009t0022g0016 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1705-1969A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652670 | |||||||
| chr4:102652706 | C | T | 86 | a0001c0001t0005g0077 a0001c0001t0005g0081 a0002c0002t0001g0028 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1705-2005G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652706 | |||||||
| chr4:102652718 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1705-2017G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652718 | |||||||
| chr4:102652747 | C | T | 125 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(122): Show |
126 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1705-2046G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652747 | |||||||
| chr4:102652761 | G | A | 13 | a0001c0009t0015g0005 a0003c0005t0001g0001 a0003c0005t0001g0006 others(10): Show |
14 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1705-2060C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652761 | |||||||
| chr4:102653046 | G | T | 1 | a0001c0001t0009g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1705-2345C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653046 | |||||||
| chr4:102653197 | C | T | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1705-2496G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653197 | |||||||
| chr4:102653220 | GCA | G | 23 | a0001c0001t0002g0146 a0001c0001t0002g0175 a0001c0001t0002g0179 others(20): Show |
23 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1705-2521_1705-252 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653220 | GCACA | G | 48 | a0001c0001t0002g0003 a0001c0001t0002g0105 a0001c0001t0002g0133 others(45): Show |
49 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.1705-2523_1705-252 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653220 | GCACACA | G | 35 | a0001c0001t0002g0270 a0001c0001t0003g0002 a0001c0001t0003g0038 others(32): Show |
36 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.1705-2525_1705-252 others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653220 | GCACACAC others(1): Show |
G | 10 | a0001c0001t0002g0093 a0001c0001t0002g0193 a0001c0001t0003g0190 others(7): Show |
10 | HG01243.hp2 HG01358.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1705-2527_1705-252 others(12): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653220 | GCACACAC others(5): Show |
G | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1705-2531_1705-252 others(16): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653220 | GCACACAC others(7): Show |
G | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(1): Show |
4 | HG02886.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1705-2533_1705-252 others(18): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653220 | GCACACAC others(9): Show |
G | 3 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 |
3 | HG02280.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1705-2535_1705-252 others(20): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653220 | GCACACAC others(11): Show |
G | 2 | a0001c0004t0009g0024 a0003c0003t0001g0198 |
2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1705-2537_1705-252 others(22): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653220 | GCACACAC others(13): Show |
G | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1705-2539_1705-252 others(24): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653220 | GCACACAC others(15): Show |
G | 107 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(104): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1705-2541_1705-252 others(26): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653220 | GCACACAC others(17): Show |
G | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1705-2543_1705-252 others(28): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | |||||||
| chr4:102653350 | G | A | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1705-2649C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653350 | |||||||
| chr4:102653418 | G | A | 5 | a0001c0001t0003g0038 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG00621.hp1 HG02083.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1705-2717C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653418 | |||||||
| chr4:102653493 | T | G | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1705-2792A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653493 | |||||||
| chr4:102653910 | C | T | 121 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(118): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1705-3209G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653910 | |||||||
| chr4:102653996 | A | G | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1705-3295T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653996 | |||||||
| chr4:102654083 | C | T | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1705-3382G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654083 | |||||||
| chr4:102654123 | T | C | 116 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(113): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1705-3422A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654123 | |||||||
| chr4:102654129 | C | T | 2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1705-3428G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654129 | |||||||
| chr4:102654228 | C | A | 116 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(113): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1704+3454G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654228 | |||||||
| chr4:102654656 | A | G | 1 | a0001c0001t0004g0180 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1704+3026T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654656 | |||||||
| chr4:102654816 | T | C | 1 | a0001c0001t0002g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1704+2866A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654816 | |||||||
| chr4:102654853 | G | A | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1704+2829C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654853 | |||||||
| chr4:102655011 | A | G | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1704+2671T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655011 | |||||||
| chr4:102655328 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1704+2354A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655328 | |||||||
| chr4:102655603 | G | C | 1 | a0002c0002t0001g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1704+2079C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655603 | |||||||
| chr4:102655635 | T | C | 1 | a0001c0001t0006g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1704+2047A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655635 | |||||||
| chr4:102655686 | C | G | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1704+1996G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655686 | |||||||
| chr4:102655710 | C | T | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1704+1972G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655710 | |||||||
| chr4:102655903 | T | C | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1704+1779A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655903 | |||||||
| chr4:102656308 | T | C | 123 | a0001c0001t0002g0254 a0001c0001t0012g0152 a0001c0001t0012g0153 others(120): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1704+1374A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102656308 | |||||||
| chr4:102656723 | T | A | 1 | a0002c0002t0001g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1704+959A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102656723 | |||||||
| chr4:102656835 | T | C | 28 | a0001c0001t0002g0270 a0001c0001t0003g0002 a0001c0001t0003g0038 others(25): Show |
29 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.1704+847A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102656835 | |||||||
| chr4:102656872 | G | GA | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1704+809dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102656872 | |||||||
| chr4:102656898 | C | T | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1704+784G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102656898 | |||||||
| chr4:102657108 | A | C | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1704+574T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657108 | |||||||
| chr4:102657118 | C | A | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1704+564G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657118 | |||||||
| chr4:102657172 | A | T | 1 | a0002c0002t0001g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1704+510T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657172 | |||||||
| chr4:102657221 | G | GT | 6 | a0001c0001t0002g0254 a0001c0004t0009g0024 a0003c0003t0001g0211 others(3): Show |
6 | HG01496.hp2 HG02056.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1704+460dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657221 | |||||||
| chr4:102657222 | T | TG | 77 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0104 others(74): Show |
78 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1704+459dupC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657222 | |||||||
| chr4:102657222 | T | TTG | 19 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0001c0009t0015g0005 others(16): Show |
19 | HG00438.hp2 HG01884.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1704+459_1704+460i others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657222 | |||||||
| chr4:102657222 | T | TTGG | 45 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(42): Show |
46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1704+459_1704+460i others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657222 | |||||||
| chr4:102657222 | T | TTGGG | 43 | a0001c0004t0014g0004 a0002c0002t0001g0032 a0002c0002t0001g0039 others(40): Show |
43 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1704+459_1704+460i others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657222 | |||||||
| chr4:102657222 | T | TTGGGG | 4 | a0002c0002t0001g0114 a0002c0002t0001g0233 a0002c0002t0001g0235 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1704+459_1704+460i others(7): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657222 | |||||||
| chr4:102657227 | G | A | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1704+455C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657227 | |||||||
| chr4:102657230 | G | C | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1704+452C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657230 | |||||||
| chr4:102657238 | G | A | 114 | a0001c0001t0002g0254 a0001c0004t0005g0269 a0001c0004t0006g0263 others(111): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1704+444C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657238 | |||||||
| chr4:102657436 | A | G | 1 | a0006c0016t0004g0214 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1704+246T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657436 | |||||||
| chr4:102657480 | G | A | 127 | a0001c0001t0002g0254 a0001c0001t0010g0232 a0001c0001t0012g0152 others(124): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1704+202C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657480 | |||||||
| chr4:102658075 | C | T | 2 | a0003c0003t0007g0220 a0003c0003t0007g0238 |
2 | HG01070.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1486-175G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658075 | |||||||
| chr4:102658303 | A | C | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-403T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658303 | |||||||
| chr4:102658303 | A | T | 114 | a0001c0001t0002g0254 a0001c0004t0005g0269 a0001c0004t0006g0263 others(111): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1486-403T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658303 | |||||||
| chr4:102658450 | G | A | 1 | a0001c0004t0006g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1486-550C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658450 | |||||||
| chr4:102658463 | G | A | 2 | a0002c0002t0001g0043 a0002c0002t0001g0057 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1486-563C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658463 | |||||||
| chr4:102658534 | G | A | 123 | a0001c0001t0002g0254 a0001c0001t0012g0152 a0001c0001t0012g0153 others(120): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1486-634C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658534 | |||||||
| chr4:102658568 | T | C | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1486-668A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658568 | |||||||
| chr4:102658569 | T | C | 1 | a0002c0002t0001g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1486-669A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658569 | |||||||
| chr4:102658608 | G | A | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1486-708C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658608 | |||||||
| chr4:102658737 | A | T | 1 | a0002c0002t0001g0055 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1486-837T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658737 | |||||||
| chr4:102658897 | C | A | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1486-997G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658897 | |||||||
| chr4:102658907 | T | C | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-1007A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658907 | |||||||
| chr4:102658921 | A | G | 4 | a0003c0005t0001g0001 a0003c0005t0001g0006 a0003c0005t0001g0008 others(1): Show |
5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-1021T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658921 | |||||||
| chr4:102658997 | G | A | 9 | a0001c0009t0015g0005 a0003c0005t0001g0010 a0003c0005t0001g0012 others(6): Show |
9 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1486-1097C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658997 | |||||||
| chr4:102659139 | C | T | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-1239G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102659139 | |||||||
| chr4:102659160 | T | C | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1486-1260A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102659160 | |||||||
| chr4:102659220 | G | C | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1486-1320C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102659220 | |||||||
| chr4:102659454 | C | A | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1486-1554G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102659454 | |||||||
| chr4:102659631 | T | C | 125 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(122): Show |
126 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1486-1731A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102659631 | |||||||
| chr4:102660105 | C | T | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-2205G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660105 | |||||||
| chr4:102660219 | T | G | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-2319A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660219 | |||||||
| chr4:102660245 | C | G | 3 | a0002c0002t0001g0123 a0002c0002t0001g0124 a0002c0002t0001g0126 |
3 | HG00140.hp1 HG01433.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1486-2345G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660245 | |||||||
| chr4:102660247 | G | T | 2 | a0001c0001t0003g0169 a0001c0001t0005g0168 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1486-2347C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660247 | |||||||
| chr4:102660259 | C | T | 1 | a0002c0002t0001g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1486-2359G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660259 | |||||||
| chr4:102660335 | T | A | 7 | a0001c0009t0015g0005 a0003c0005t0001g0010 a0003c0005t0001g0012 others(4): Show |
7 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1486-2435A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660335 | |||||||
| chr4:102660933 | C | T | 1 | a0004c0006t0002g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1486-3033G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660933 | |||||||
| chr4:102661055 | G | A | 1 | a0002c0002t0001g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1486-3155C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661055 | |||||||
| chr4:102661092 | T | C | 1 | a0002c0002t0001g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1486-3192A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661092 | |||||||
| chr4:102661119 | T | A | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-3219A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661119 | |||||||
| chr4:102661446 | A | G | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+3239T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661446 | |||||||
| chr4:102661641 | C | T | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485+3044G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661641 | |||||||
| chr4:102661643 | C | T | 1 | a0002c0002t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1485+3042G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661643 | |||||||
| chr4:102661689 | C | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+2996G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661689 | |||||||
| chr4:102661776 | A | G | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1485+2909T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661776 | |||||||
| chr4:102661930 | T | G | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+2755A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661930 | |||||||
| chr4:102661980 | G | A | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485+2705C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661980 | |||||||
| chr4:102661985 | T | TAATACTA others(811): Show |
2 | a0001c0001t0003g0038 a0001c0001t0003g0207 |
2 | NA18949.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1485+2699_1485+270 others(822): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661985 | |||||||
| chr4:102661985 | T | TAATACTA others(810): Show |
1 | a0001c0001t0003g0208 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1485+2699_1485+270 others(821): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661985 | |||||||
| chr4:102662032 | A | C | 107 | a0001c0001t0002g0254 a0001c0004t0014g0004 a0001c0009t0015g0005 others(104): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1485+2653T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662032 | |||||||
| chr4:102662039 | G | A | 106 | a0001c0001t0002g0254 a0001c0009t0015g0005 a0001c0017t0006g0237 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1485+2646C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662039 | |||||||
| chr4:102662051 | A | G | 106 | a0001c0001t0002g0254 a0001c0009t0015g0005 a0001c0017t0006g0237 others(103): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1485+2634T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662051 | |||||||
| chr4:102662262 | C | A | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+2423G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662262 | |||||||
| chr4:102662300 | C | T | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1485+2385G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662300 | |||||||
| chr4:102662368 | TG | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+2316delC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662368 | |||||||
| chr4:102662504 | T | C | 12 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0004t0005g0269 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1485+2181A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662504 | |||||||
| chr4:102662538 | T | C | 1 | a0002c0002t0001g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1485+2147A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662538 | |||||||
| chr4:102662551 | CA | C | 112 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(109): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.1485+2133delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662551 | |||||||
| chr4:102662551 | CAA | C | 9 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1485+2132_1485+213 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662551 | |||||||
| chr4:102662612 | G | A | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+2073C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662612 | |||||||
| chr4:102662619 | C | T | 3 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 |
3 | HG02280.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1485+2066G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662619 | |||||||
| chr4:102663101 | C | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+1584G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663101 | |||||||
| chr4:102663150 | C | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+1535G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663150 | |||||||
| chr4:102663153 | G | A | 16 | a0001c0001t0003g0002 a0001c0001t0003g0089 a0001c0001t0003g0090 others(13): Show |
17 | HG00544.hp1 HG01167.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1485+1532C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663153 | |||||||
| chr4:102663176 | T | TA | 12 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0004t0005g0269 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1485+1508dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663176 | |||||||
| chr4:102663294 | T | C | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485+1391A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663294 | |||||||
| chr4:102663380 | A | G | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+1305T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663380 | |||||||
| chr4:102663438 | A | C | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1485+1247T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663438 | |||||||
| chr4:102663461 | G | C | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1485+1224C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663461 | |||||||
| chr4:102663710 | C | T | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+975G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663710 | |||||||
| chr4:102663770 | A | C | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485+915T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663770 | |||||||
| chr4:102663819 | A | G | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+866T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663819 | |||||||
| chr4:102663901 | G | A | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+784C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663901 | |||||||
| chr4:102663922 | T | A | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1485+763A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663922 | |||||||
| chr4:102664037 | C | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+648G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664037 | |||||||
| chr4:102664041 | C | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+644G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664041 | |||||||
| chr4:102664042 | G | T | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+643C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664042 | |||||||
| chr4:102664171 | T | C | 2 | a0001c0001t0012g0152 a0001c0001t0012g0153 |
2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1485+514A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664171 | |||||||
| chr4:102664352 | C | CT | 112 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1485+332dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664352 | |||||||
| chr4:102664352 | CT | C | 5 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1485+332delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664352 | |||||||
| chr4:102664380 | G | A | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1485+305C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664380 | |||||||
| chr4:102664400 | G | C | 1 | a0002c0002t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1485+285C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664400 | |||||||
| chr4:102664418 | G | A | 1 | a0002c0002t0007g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1485+267C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664418 | |||||||
| chr4:102664473 | C | G | 6 | a0001c0001t0002g0122 a0001c0001t0002g0131 a0001c0001t0002g0167 others(3): Show |
6 | HG01074.hp2 HG02257.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1485+212G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664473 | |||||||
| chr4:102664515 | AT | A | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+169delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664515 | |||||||
| chr4:102664557 | C | A | 1 | a0003c0003t0007g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1485+128G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664557 | |||||||
| chr4:102664662 | C | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+23G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664662 | |||||||
| chr4:102665183 | C | G | 1 | a0003c0003t0001g0211 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1318-331G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665183 | |||||||
| chr4:102665491 | G | A | 1 | a0003c0010t0001g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1318-639C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665491 | |||||||
| chr4:102665573 | G | A | 1 | a0002c0002t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1318-721C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665573 | |||||||
| chr4:102665618 | T | C | 1 | a0002c0002t0001g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1318-766A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665618 | |||||||
| chr4:102665628 | C | CA | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1318-777dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665628 | |||||||
| chr4:102665685 | C | T | 5 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1318-833G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665685 | |||||||
| chr4:102665820 | C | T | 127 | a0001c0001t0002g0254 a0001c0001t0010g0232 a0001c0001t0012g0152 others(124): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1318-968G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665820 | |||||||
| chr4:102665850 | C | T | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1318-998G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665850 | |||||||
| chr4:102665957 | A | T | 2 | a0001c0001t0003g0172 a0005c0008t0003g0218 |
2 | HG02897.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1318-1105T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665957 | |||||||
| chr4:102666046 | T | C | 1 | a0002c0002t0001g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1318-1194A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666046 | |||||||
| chr4:102666158 | T | TA | 3 | a0001c0001t0004g0069 a0001c0001t0004g0156 a0003c0003t0001g0130 |
3 | HG02602.hp1 HG02602.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1318-1307dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666158 | |||||||
| chr4:102666174 | G | A | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1318-1322C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666174 | |||||||
| chr4:102666330 | C | T | 13 | a0001c0004t0005g0141 a0001c0004t0005g0269 a0001c0004t0006g0263 others(10): Show |
13 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1318-1478G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666330 | |||||||
| chr4:102666421 | T | C | 1 | a0003c0003t0007g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1318-1569A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666421 | |||||||
| chr4:102666488 | G | C | 1 | a0001c0004t0006g0263 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1318-1636C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666488 | |||||||
| chr4:102666610 | T | C | 9 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1318-1758A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666610 | |||||||
| chr4:102666649 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1318-1797C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666649 | |||||||
| chr4:102666658 | C | T | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1318-1806G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666658 | |||||||
| chr4:102666659 | AT | A | 9 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1318-1808delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666659 | |||||||
| chr4:102666738 | T | C | 1 | a0001c0001t0002g0270 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1318-1886A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666738 | |||||||
| chr4:102666800 | C | T | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1318-1948G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666800 | |||||||
| chr4:102666816 | A | T | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1318-1964T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666816 | |||||||
| chr4:102666989 | A | T | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317+1974T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666989 | |||||||
| chr4:102667015 | A | C | 13 | a0001c0004t0005g0141 a0001c0004t0005g0269 a0001c0004t0006g0263 others(10): Show |
13 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1317+1948T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667015 | |||||||
| chr4:102667057 | T | C | 13 | a0001c0004t0005g0141 a0001c0004t0005g0269 a0001c0004t0006g0263 others(10): Show |
13 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1317+1906A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667057 | |||||||
| chr4:102667115 | T | C | 2 | a0001c0001t0021g0174 a0001c0009t0022g0016 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1317+1848A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667115 | |||||||
| chr4:102667356 | A | G | 11 | a0001c0004t0005g0141 a0001c0004t0005g0269 a0001c0004t0006g0263 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1317+1607T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667356 | |||||||
| chr4:102667367 | TAACATTG others(8): Show |
T | 6 | a0001c0001t0002g0122 a0001c0001t0002g0131 a0001c0001t0002g0167 others(3): Show |
6 | HG01074.hp2 HG02257.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1317+1581_1317+159 others(19): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667367 | |||||||
| chr4:102667419 | G | A | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317+1544C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667419 | |||||||
| chr4:102667473 | C | A | 10 | a0001c0001t0010g0232 a0001c0004t0005g0269 a0001c0004t0006g0263 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1317+1490G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667473 | |||||||
| chr4:102667510 | C | T | 1 | a0001c0001t0005g0007 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1317+1453G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667510 | |||||||
| chr4:102667521 | C | T | 14 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(11): Show |
14 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1317+1442G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667521 | |||||||
| chr4:102667766 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1317+1197A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667766 | |||||||
| chr4:102667796 | T | C | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317+1167A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667796 | |||||||
| chr4:102667892 | C | T | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317+1071G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667892 | |||||||
| chr4:102667977 | G | T | 17 | a0001c0001t0002g0201 a0001c0001t0003g0139 a0001c0001t0003g0223 others(14): Show |
17 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1317+986C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667977 | |||||||
| chr4:102668012 | C | T | 1 | a0001c0004t0002g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1317+951G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668012 | |||||||
| chr4:102668054 | A | G | 27 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(24): Show |
28 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1317+909T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668054 | |||||||
| chr4:102668102 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1317+861C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668102 | |||||||
| chr4:102668148 | T | C | 1 | a0001c0009t0022g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1317+815A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668148 | |||||||
| chr4:102668323 | T | G | 27 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(24): Show |
28 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1317+640A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668323 | |||||||
| chr4:102668356 | TAAG | T | 92 | a0001c0001t0002g0254 a0002c0002t0001g0028 a0002c0002t0001g0029 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1317+604_1317+606d others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668356 | |||||||
| chr4:102668453 | G | A | 1 | a0001c0001t0009g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1317+510C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668453 | |||||||
| chr4:102668564 | C | T | 1 | a0001c0004t0005g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1317+399G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668564 | |||||||
| chr4:102668628 | T | C | 3 | a0001c0001t0005g0136 a0001c0001t0005g0209 a0001c0001t0011g0210 |
3 | HG02735.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1317+335A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668628 | |||||||
| chr4:102668642 | C | A | 4 | a0003c0005t0001g0001 a0003c0005t0001g0006 a0003c0005t0001g0008 others(1): Show |
5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317+321G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668642 | |||||||
| chr4:102668768 | C | G | 2 | a0002c0002t0007g0033 a0002c0002t0007g0116 |
2 | HG02148.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1317+195G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668768 | |||||||
| chr4:102668856 | C | A | 23 | a0001c0001t0010g0232 a0001c0004t0005g0269 a0001c0004t0006g0263 others(20): Show |
24 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1317+107G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668856 | |||||||
| chr4:102668857 | A | T | 23 | a0001c0001t0010g0232 a0001c0004t0005g0269 a0001c0004t0006g0263 others(20): Show |
24 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1317+106T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668857 | |||||||
| chr4:102668892 | C | G | 27 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(24): Show |
28 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1317+71G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668892 | |||||||
| chr4:102669107 | A | G | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-58T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669107 | |||||||
| chr4:102669188 | G | A | 1 | a0001c0001t0002g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1231-139C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669188 | |||||||
| chr4:102669313 | A | G | 1 | a0001c0004t0005g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1231-264T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669313 | |||||||
| chr4:102669333 | G | A | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(1): Show |
4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-284C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669333 | |||||||
| chr4:102669343 | A | G | 1 | a0001c0004t0009g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1231-294T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669343 | |||||||
| chr4:102669705 | G | T | 10 | a0001c0001t0010g0232 a0001c0004t0005g0269 a0001c0004t0006g0263 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-656C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669705 | |||||||
| chr4:102669707 | A | G | 182 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(179): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1231-658T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669707 | |||||||
| chr4:102669775 | T | C | 1 | a0009c0011t0020g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1231-726A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669775 | |||||||
| chr4:102669781 | C | A | 1 | a0003c0005t0013g0251 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1231-732G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669781 | |||||||
| chr4:102669821 | G | A | 1 | a0004c0006t0002g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1231-772C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669821 | |||||||
| chr4:102669896 | C | T | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1231-847G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669896 | |||||||
| chr4:102669897 | G | A | 10 | a0001c0001t0010g0232 a0001c0004t0005g0269 a0001c0004t0006g0263 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-848C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669897 | |||||||
| chr4:102669905 | A | G | 5 | a0001c0001t0003g0038 a0001c0001t0003g0206 a0001c0001t0003g0207 others(2): Show |
5 | HG00621.hp1 HG02083.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-856T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669905 | |||||||
| chr4:102669936 | T | C | 27 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(24): Show |
28 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1231-887A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669936 | |||||||
| chr4:102670070 | G | A | 4 | a0002c0002t0001g0050 a0002c0002t0001g0054 a0002c0002t0001g0059 others(1): Show |
4 | HG02735.hp2 HG02738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1021C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670070 | |||||||
| chr4:102670127 | C | T | 2 | a0002c0002t0001g0048 a0002c0002t0001g0055 |
2 | NA18957.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1231-1078G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670127 | |||||||
| chr4:102670154 | C | CA | 10 | a0001c0001t0002g0182 a0001c0001t0002g0226 a0001c0001t0002g0276 others(7): Show |
10 | HG00621.hp2 HG01175.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-1106dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | |||||||
| chr4:102670154 | C | CAAAA | 9 | a0001c0009t0015g0005 a0003c0005t0001g0001 a0003c0005t0001g0006 others(6): Show |
10 | HG01192.hp2 HG02145.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.1231-1109_1231-110 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | |||||||
| chr4:102670154 | C | CAAAAAA | 8 | a0001c0001t0010g0232 a0001c0004t0005g0269 a0001c0004t0006g0264 others(5): Show |
8 | HG02145.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-1111_1231-110 others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | |||||||
| chr4:102670154 | CA | C | 13 | a0001c0001t0002g0234 a0001c0001t0003g0038 a0001c0001t0003g0094 others(10): Show |
13 | HG00621.hp1 HG01070.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1231-1106delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | |||||||
| chr4:102670154 | CAAAAAAA others(3): Show |
C | 1 | a0004c0006t0002g0035 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1231-1115_1231-110 others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | |||||||
| chr4:102670154 | CAAAAAAA others(4): Show |
C | 91 | a0001c0001t0002g0254 a0002c0002t0001g0028 a0002c0002t0001g0029 others(88): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1230+1116_1231-110 others(15): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | |||||||
| chr4:102670169 | A | T | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1230+1112T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670169 | |||||||
| chr4:102670481 | A | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1230+800T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670481 | |||||||
| chr4:102670609 | A | C | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1230+672T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670609 | |||||||
| chr4:102670949 | C | G | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1230+332G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670949 | |||||||
| chr4:102671116 | G | GCT | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1230+164_1230+165i others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102671116 | |||||||
| chr4:102671128 | C | T | 5 | a0002c0002t0001g0120 a0002c0002t0001g0121 a0002c0002t0001g0123 others(2): Show |
5 | HG00140.hp1 HG01168.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+153G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102671128 | |||||||
| chr4:102671137 | T | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1230+144A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102671137 | |||||||
| chr4:102671473 | A | ATC | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113-77_1113-76dup others(2): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671473 | |||||||
| chr4:102671495 | A | G | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113-97T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671495 | |||||||
| chr4:102671513 | T | C | 1 | a0001c0001t0005g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1113-115A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671513 | |||||||
| chr4:102671712 | C | A | 4 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113-314G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671712 | |||||||
| chr4:102671889 | T | C | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1113-491A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671889 | |||||||
| chr4:102671923 | A | C | 1 | a0001c0001t0002g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1113-525T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671923 | |||||||
| chr4:102671933 | C | G | 2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1113-535G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671933 | |||||||
| chr4:102672021 | T | C | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113-623A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672021 | |||||||
| chr4:102672185 | C | T | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113-787G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672185 | |||||||
| chr4:102672289 | A | C | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113-891T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672289 | |||||||
| chr4:102672323 | A | G | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1113-925T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672323 | |||||||
| chr4:102672438 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1113-1040T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672438 | |||||||
| chr4:102672639 | G | C | 1 | a0001c0001t0002g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1113-1241C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672639 | |||||||
| chr4:102672672 | T | C | 23 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(20): Show |
24 | HG00639.hp1 HG00673.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1112+1247A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672672 | |||||||
| chr4:102672699 | A | G | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+1220T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672699 | |||||||
| chr4:102672709 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1112+1210G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672709 | |||||||
| chr4:102672710 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1112+1209C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672710 | |||||||
| chr4:102672741 | A | C | 133 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(130): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1112+1178T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672741 | |||||||
| chr4:102672930 | G | A | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+989C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672930 | |||||||
| chr4:102672931 | T | G | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+988A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672931 | |||||||
| chr4:102673014 | A | AT | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+904dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673014 | |||||||
| chr4:102673131 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1112+788G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673131 | |||||||
| chr4:102673132 | G | A | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+787C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673132 | |||||||
| chr4:102673149 | G | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1112+770C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673149 | |||||||
| chr4:102673168 | T | C | 23 | a0001c0001t0010g0232 a0001c0004t0005g0269 a0001c0004t0006g0263 others(20): Show |
24 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1112+751A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673168 | |||||||
| chr4:102673435 | G | A | 1 | a0003c0005t0001g0013 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1112+484C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673435 | |||||||
| chr4:102673439 | C | T | 23 | a0001c0001t0010g0232 a0001c0004t0005g0269 a0001c0004t0006g0263 others(20): Show |
24 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1112+480G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673439 | |||||||
| chr4:102673466 | C | G | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+453G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673466 | |||||||
| chr4:102673761 | T | C | 98 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(95): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1112+158A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673761 | |||||||
| chr4:102673781 | G | A | 126 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(123): Show |
127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1112+138C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673781 | |||||||
| chr4:102673793 | G | A | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+126C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673793 | |||||||
| chr4:102673805 | A | G | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1112+114T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673805 | |||||||
| chr4:102674120 | A | G | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-50T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674120 | |||||||
| chr4:102674132 | A | T | 27 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(24): Show |
28 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.961-62T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674132 | |||||||
| chr4:102674226 | A | G | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.961-156T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674226 | |||||||
| chr4:102674241 | T | C | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-171A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674241 | |||||||
| chr4:102674326 | T | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-256A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674326 | |||||||
| chr4:102674371 | C | T | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.961-301G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674371 | |||||||
| chr4:102674449 | G | A | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.961-379C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674449 | |||||||
| chr4:102674464 | A | T | 1 | a0001c0001t0002g0270 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.961-394T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674464 | |||||||
| chr4:102674494 | A | G | 100 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(97): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.961-424T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674494 | |||||||
| chr4:102674557 | A | G | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.961-487T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674557 | |||||||
| chr4:102674585 | A | G | 23 | a0001c0001t0010g0232 a0001c0004t0005g0269 a0001c0004t0006g0263 others(20): Show |
24 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.961-515T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674585 | |||||||
| chr4:102674923 | T | A | 1 | a0001c0001t0002g0229 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.961-853A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674923 | |||||||
| chr4:102674992 | C | T | 26 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0005g0269 others(23): Show |
27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.961-922G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674992 | |||||||
| chr4:102675052 | C | T | 10 | a0001c0001t0010g0232 a0001c0004t0005g0269 a0001c0004t0006g0263 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.961-982G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675052 | |||||||
| chr4:102675250 | C | G | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.961-1180G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675250 | |||||||
| chr4:102675726 | C | T | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-1656G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675726 | |||||||
| chr4:102675768 | C | G | 16 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-1698G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675768 | |||||||
| chr4:102675802 | A | C | 1 | a0005c0008t0003g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.961-1732T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675802 | |||||||
| chr4:102675823 | T | C | 16 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-1753A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675823 | |||||||
| chr4:102675875 | A | G | 130 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(127): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.961-1805T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675875 | |||||||
| chr4:102675905 | AG | A | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-1836delC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675905 | |||||||
| chr4:102675907 | T | A | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-1837A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675907 | |||||||
| chr4:102675934 | G | T | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-1864C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675934 | |||||||
| chr4:102676195 | G | A | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-2125C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676195 | |||||||
| chr4:102676273 | A | G | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-2203T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676273 | |||||||
| chr4:102676369 | A | G | 1 | a0002c0002t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.961-2299T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676369 | |||||||
| chr4:102676423 | C | T | 16 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-2353G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676423 | |||||||
| chr4:102676491 | C | T | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-2421G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676491 | |||||||
| chr4:102676632 | T | C | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-2562A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676632 | |||||||
| chr4:102676692 | ACTT | A | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-2625_961-2623d others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676692 | |||||||
| chr4:102676711 | T | C | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-2641A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676711 | |||||||
| chr4:102676878 | G | C | 7 | a0001c0001t0012g0023 a0003c0003t0007g0160 a0005c0008t0003g0138 others(4): Show |
7 | HG02647.hp1 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-2808C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676878 | |||||||
| chr4:102676923 | GA | G | 130 | a0001c0001t0002g0254 a0001c0001t0005g0077 a0001c0001t0005g0081 others(127): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.961-2854delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676923 | |||||||
| chr4:102677150 | TAGAA | T | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-3084_961-3081d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677150 | |||||||
| chr4:102677188 | A | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-3118T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677188 | |||||||
| chr4:102677191 | T | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-3121A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677191 | |||||||
| chr4:102677207 | A | G | 20 | a0002c0002t0001g0036 a0002c0002t0001g0037 a0002c0002t0001g0040 others(17): Show |
20 | HG00408.hp1 HG00609.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-3137T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677207 | |||||||
| chr4:102677228 | G | A | 6 | a0001c0001t0002g0122 a0001c0001t0002g0131 a0001c0001t0002g0167 others(3): Show |
6 | HG01074.hp2 HG02257.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.961-3158C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677228 | |||||||
| chr4:102677261 | G | A | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-3191C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677261 | |||||||
| chr4:102677510 | G | T | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-3440C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677510 | |||||||
| chr4:102677566 | C | T | 1 | a0002c0002t0001g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.961-3496G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677566 | |||||||
| chr4:102677637 | T | G | 1 | a0001c0001t0002g0270 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.961-3567A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677637 | |||||||
| chr4:102677682 | C | T | 1 | a0004c0006t0002g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.961-3612G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677682 | |||||||
| chr4:102677820 | C | T | 16 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-3750G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677820 | |||||||
| chr4:102677897 | G | T | 2 | a0001c0001t0003g0166 a0001c0001t0003g0172 |
2 | HG02572.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.961-3827C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677897 | |||||||
| chr4:102678026 | G | A | 1 | a0002c0002t0001g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.961-3956C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678026 | |||||||
| chr4:102678107 | AT | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-4038delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678107 | |||||||
| chr4:102678113 | T | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-4043A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678113 | |||||||
| chr4:102678364 | G | A | 4 | a0001c0001t0012g0152 a0001c0001t0012g0153 a0001c0009t0010g0034 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-4294C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678364 | |||||||
| chr4:102678439 | A | G | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.961-4369T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678439 | |||||||
| chr4:102678447 | T | TGAAAAGA others(2068): Show |
1 | a0001c0004t0009g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.961-4378_961-4377i others(2077): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678447 | |||||||
| chr4:102678447 | T | TGAAAAGA others(2068): Show |
2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.961-4378_961-4377i others(2077): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678447 | |||||||
| chr4:102678469 | A | G | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.961-4399T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678469 | |||||||
| chr4:102678805 | G | A | 16 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-4735C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678805 | |||||||
| chr4:102678948 | C | G | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-4878G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678948 | |||||||
| chr4:102679265 | G | A | 2 | a0001c0001t0002g0182 a0001c0001t0004g0183 |
2 | HG00621.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.961-5195C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102679265 | |||||||
| chr4:102679318 | A | T | 2 | a0001c0001t0002g0195 a0001c0001t0019g0194 |
2 | HG02080.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.961-5248T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102679318 | |||||||
| chr4:102679440 | C | T | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-5370G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102679440 | |||||||
| chr4:102679905 | T | C | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-5835A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102679905 | |||||||
| chr4:102679926 | TA | T | 10 | a0001c0001t0002g0178 a0001c0001t0002g0182 a0001c0001t0002g0185 others(7): Show |
10 | HG00621.hp2 HG02071.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.961-5857delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102679926 | |||||||
| chr4:102680057 | T | C | 16 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-5987A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680057 | |||||||
| chr4:102680097 | T | C | 17 | a0001c0001t0002g0201 a0001c0001t0003g0139 a0001c0001t0003g0223 others(14): Show |
17 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-6027A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680097 | |||||||
| chr4:102680184 | A | G | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-6114T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680184 | |||||||
| chr4:102680189 | G | T | 19 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-6119C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680189 | |||||||
| chr4:102680273 | C | T | 1 | a0002c0002t0007g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.961-6203G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680273 | |||||||
| chr4:102680582 | T | TA | 20 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(17): Show |
21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.961-6513dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680582 | |||||||
| chr4:102680696 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.961-6626A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680696 | |||||||
| chr4:102680739 | C | T | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-6669G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680739 | |||||||
| chr4:102680886 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-6816G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680886 | |||||||
| chr4:102680943 | C | T | 3 | a0001c0004t0009g0024 a0003c0003t0001g0198 a0003c0003t0001g0199 |
3 | HG02630.hp2 HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-6873G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680943 | |||||||
| chr4:102680949 | T | C | 1 | a0001c0001t0005g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.961-6879A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680949 | |||||||
| chr4:102680970 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-6900G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680970 | |||||||
| chr4:102681072 | C | T | 1 | a0001c0001t0008g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.961-7002G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681072 | |||||||
| chr4:102681080 | T | C | 97 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0104 others(94): Show |
99 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.961-7010A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681080 | |||||||
| chr4:102681392 | A | G | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-7322T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681392 | |||||||
| chr4:102681443 | C | T | 21 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(18): Show |
22 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.961-7373G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681443 | |||||||
| chr4:102681462 | A | G | 21 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(18): Show |
22 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.961-7392T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681462 | |||||||
| chr4:102681538 | C | T | 4 | a0001c0004t0009g0024 a0003c0003t0001g0198 a0003c0003t0001g0199 others(1): Show |
4 | HG02630.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-7468G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681538 | |||||||
| chr4:102681740 | A | G | 18 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(15): Show |
19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.961-7670T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681740 | |||||||
| chr4:102681880 | T | C | 1 | a0003c0005t0013g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.960+7694A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681880 | |||||||
| chr4:102681927 | C | T | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.960+7647G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681927 | |||||||
| chr4:102682039 | C | T | 2 | a0001c0001t0005g0225 a0003c0005t0013g0251 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.960+7535G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682039 | |||||||
| chr4:102682096 | G | GAGATCAC others(26): Show |
1 | a0002c0002t0001g0040 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.960+7445_960+7477d others(35): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682096 | |||||||
| chr4:102682125 | T | C | 1 | a0003c0005t0001g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.960+7449A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682125 | |||||||
| chr4:102682146 | C | CA | 23 | a0001c0001t0002g0201 a0001c0001t0002g0227 a0001c0001t0003g0169 others(20): Show |
24 | HG00438.hp2 HG01192.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.960+7427dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682146 | |||||||
| chr4:102682186 | T | G | 15 | a0001c0009t0010g0034 a0001c0009t0015g0005 a0001c0009t0022g0016 others(12): Show |
16 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.960+7388A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682186 | |||||||
| chr4:102682322 | G | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+7252C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682322 | |||||||
| chr4:102682468 | T | C | 18 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(15): Show |
19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+7106A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682468 | |||||||
| chr4:102682676 | G | C | 1 | a0002c0002t0001g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.960+6898C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682676 | |||||||
| chr4:102682792 | A | G | 182 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(179): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.960+6782T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682792 | |||||||
| chr4:102682831 | G | A | 1 | a0001c0001t0008g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.960+6743C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682831 | |||||||
| chr4:102682904 | G | C | 1 | a0002c0002t0001g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.960+6670C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682904 | |||||||
| chr4:102682952 | CAGA | C | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+6619_960+6621d others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682952 | |||||||
| chr4:102683176 | GA | G | 13 | a0001c0001t0002g0161 a0001c0001t0002g0234 a0001c0001t0003g0038 others(10): Show |
13 | HG00609.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.960+6397delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683176 | |||||||
| chr4:102683276 | C | T | 18 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(15): Show |
19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+6298G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683276 | |||||||
| chr4:102683426 | A | G | 18 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(15): Show |
19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+6148T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683426 | |||||||
| chr4:102683550 | T | C | 18 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(15): Show |
19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+6024A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683550 | |||||||
| chr4:102683554 | C | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+6020G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683554 | |||||||
| chr4:102683568 | C | T | 1 | a0001c0001t0003g0273 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.960+6006G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683568 | |||||||
| chr4:102683747 | C | T | 12 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0003c0005t0001g0001 others(9): Show |
13 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.960+5827G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683747 | |||||||
| chr4:102683794 | T | C | 1 | a0009c0011t0020g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960+5780A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683794 | |||||||
| chr4:102683877 | C | G | 2 | a0001c0001t0004g0163 a0001c0001t0004g0180 |
2 | NA18979.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.960+5697G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683877 | |||||||
| chr4:102683966 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.960+5608G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683966 | |||||||
| chr4:102684099 | A | G | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+5475T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684099 | |||||||
| chr4:102684108 | T | TA | 18 | a0001c0004t0009g0024 a0001c0009t0010g0034 a0001c0009t0022g0016 others(15): Show |
19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+5465dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684108 | |||||||
| chr4:102684133 | G | A | 7 | a0002c0002t0001g0050 a0002c0002t0001g0052 a0002c0002t0001g0054 others(4): Show |
7 | HG02735.hp2 HG02738.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+5441C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684133 | |||||||
| chr4:102684586 | T | A | 34 | a0002c0002t0001g0036 a0002c0002t0001g0037 a0002c0002t0001g0039 others(31): Show |
34 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.960+4988A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684586 | |||||||
| chr4:102684660 | C | T | 15 | a0001c0009t0010g0034 a0001c0009t0015g0005 a0001c0009t0022g0016 others(12): Show |
16 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.960+4914G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684660 | |||||||
| chr4:102684756 | A | G | 1 | a0001c0001t0002g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.960+4818T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684756 | |||||||
| chr4:102684759 | G | A | 158 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(155): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.960+4815C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684759 | |||||||
| chr4:102684988 | A | G | 18 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(15): Show |
19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+4586T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684988 | |||||||
| chr4:102685116 | C | T | 18 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(15): Show |
19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+4458G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685116 | |||||||
| chr4:102685237 | A | G | 1 | a0002c0002t0001g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.960+4337T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685237 | |||||||
| chr4:102685279 | A | G | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+4295T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685279 | |||||||
| chr4:102685292 | T | C | 18 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(15): Show |
19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+4282A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685292 | |||||||
| chr4:102685499 | T | A | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+4075A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685499 | |||||||
| chr4:102685501 | C | T | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+4073G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685501 | |||||||
| chr4:102685503 | C | CTATGAAA others(5): Show |
3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+4070_960+4071i others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685503 | |||||||
| chr4:102685511 | A | T | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+4063T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685511 | |||||||
| chr4:102685515 | C | T | 164 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.960+4059G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685515 | |||||||
| chr4:102685697 | T | A | 1 | a0001c0001t0003g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.960+3877A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685697 | |||||||
| chr4:102685715 | C | T | 164 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.960+3859G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685715 | |||||||
| chr4:102685729 | C | A | 182 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(179): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.960+3845G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685729 | |||||||
| chr4:102685974 | A | G | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.960+3600T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685974 | |||||||
| chr4:102686096 | C | G | 183 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.960+3478G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686096 | |||||||
| chr4:102686190 | A | ATG | 150 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(147): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.960+3382_960+3383d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686190 | |||||||
| chr4:102686190 | A | ATGTG | 14 | a0001c0001t0010g0232 a0001c0004t0005g0141 a0001c0004t0009g0011 others(11): Show |
14 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.960+3380_960+3383d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686190 | |||||||
| chr4:102686190 | A | ATGTGTG | 17 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0002c0002t0001g0048 others(14): Show |
18 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.960+3378_960+3383d others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686190 | |||||||
| chr4:102686190 | A | ATGTGTGT others(5): Show |
1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.960+3372_960+3383d others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686190 | |||||||
| chr4:102686249 | T | C | 16 | a0001c0009t0010g0034 a0001c0009t0015g0005 a0001c0009t0022g0016 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.960+3325A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686249 | |||||||
| chr4:102686267 | C | T | 2 | a0002c0002t0001g0040 a0002c0002t0001g0041 |
2 | HG02129.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.960+3307G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686267 | |||||||
| chr4:102686478 | G | A | 164 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.960+3096C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686478 | |||||||
| chr4:102686649 | C | T | 165 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.960+2925G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686649 | |||||||
| chr4:102687039 | T | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+2535A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687039 | |||||||
| chr4:102687151 | C | T | 165 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.960+2423G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687151 | |||||||
| chr4:102687182 | A | T | 1 | a0001c0001t0002g0170 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.960+2392T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687182 | |||||||
| chr4:102687241 | G | A | 1 | a0001c0001t0005g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.960+2333C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687241 | |||||||
| chr4:102687470 | A | G | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+2104T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687470 | |||||||
| chr4:102687573 | C | T | 3 | a0002c0002t0001g0049 a0002c0002t0001g0056 a0002c0002t0001g0096 |
3 | NA18960.hp1 NA18970.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.960+2001G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687573 | |||||||
| chr4:102688096 | C | T | 2 | a0001c0004t0009g0024 a0003c0010t0001g0271 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.960+1478G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688096 | |||||||
| chr4:102688138 | T | C | 7 | a0001c0001t0002g0104 a0001c0001t0002g0179 a0001c0001t0002g0186 others(4): Show |
7 | HG01071.hp2 HG01074.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+1436A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688138 | |||||||
| chr4:102688173 | T | C | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.960+1401A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688173 | |||||||
| chr4:102688212 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.960+1362G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688212 | |||||||
| chr4:102688290 | C | T | 1 | a0005c0008t0003g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.960+1284G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688290 | |||||||
| chr4:102688292 | C | T | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.960+1282G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688292 | |||||||
| chr4:102688293 | G | A | 1 | a0001c0004t0002g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.960+1281C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688293 | |||||||
| chr4:102688295 | G | GCA | 6 | a0001c0001t0003g0139 a0001c0001t0021g0174 a0001c0004t0005g0141 others(3): Show |
6 | HG01109.hp2 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+1277_960+1278d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688295 | |||||||
| chr4:102688295 | GCA | G | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+1277_960+1278d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688295 | |||||||
| chr4:102688295 | GCACA | G | 6 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(3): Show |
6 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+1275_960+1278d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688295 | |||||||
| chr4:102688297 | A | G | 5 | a0005c0008t0003g0138 a0005c0008t0003g0218 a0005c0008t0003g0219 others(2): Show |
5 | HG02647.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+1277T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688297 | |||||||
| chr4:102688322 | CACAT | C | 6 | a0002c0007t0001g0106 a0002c0007t0001g0107 a0002c0007t0001g0108 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+1248_960+1251d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688322 | |||||||
| chr4:102688353 | A | G | 1 | a0001c0001t0004g0183 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.960+1221T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688353 | |||||||
| chr4:102688364 | TTC | T | 5 | a0001c0001t0003g0230 a0001c0001t0003g0273 a0001c0001t0005g0136 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+1208_960+1209d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688364 | |||||||
| chr4:102688386 | T | TAC | 5 | a0001c0001t0002g0201 a0001c0001t0003g0206 a0001c0001t0004g0183 others(2): Show |
5 | HG00621.hp1 HG02738.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+1186_960+1187d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | |||||||
| chr4:102688386 | T | TACAC | 14 | a0001c0001t0002g0161 a0001c0001t0004g0069 a0001c0001t0010g0232 others(11): Show |
14 | HG01496.hp2 HG02145.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.960+1184_960+1187d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | |||||||
| chr4:102688386 | T | TACACAC | 20 | a0001c0001t0002g0093 a0001c0001t0002g0105 a0001c0001t0002g0133 others(17): Show |
20 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.960+1182_960+1187d others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | |||||||
| chr4:102688386 | T | TACACACA others(1): Show |
83 | a0001c0001t0002g0003 a0001c0001t0002g0146 a0001c0001t0002g0148 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.960+1180_960+1187d others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | |||||||
| chr4:102688386 | T | TACACACA others(3): Show |
29 | a0001c0001t0003g0095 a0001c0001t0003g0246 a0001c0001t0004g0155 others(26): Show |
29 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.960+1178_960+1187d others(12): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | |||||||
| chr4:102688386 | T | TACACACA others(5): Show |
14 | a0001c0001t0003g0089 a0001c0001t0003g0090 a0001c0001t0003g0091 others(11): Show |
14 | HG00438.hp1 HG00609.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.960+1176_960+1187d others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | |||||||
| chr4:102688386 | T | TACACACA others(7): Show |
2 | a0002c0002t0001g0098 a0002c0002t0001g0102 |
2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.960+1174_960+1187d others(16): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | |||||||
| chr4:102688386 | TAC | T | 46 | a0001c0001t0002g0104 a0001c0001t0002g0179 a0001c0001t0002g0186 others(43): Show |
47 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.960+1186_960+1187d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | |||||||
| chr4:102688386 | TACACACA others(5): Show |
T | 1 | a0001c0001t0011g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.960+1176_960+1187d others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | |||||||
| chr4:102688636 | T | A | 165 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.960+938A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688636 | |||||||
| chr4:102688672 | G | A | 1 | a0002c0002t0001g0050 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.960+902C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688672 | |||||||
| chr4:102689075 | C | T | 1 | a0003c0003t0007g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.960+499G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689075 | |||||||
| chr4:102689091 | C | T | 164 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.960+483G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689091 | |||||||
| chr4:102689104 | C | T | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.960+470G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689104 | |||||||
| chr4:102689153 | T | A | 183 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.960+421A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689153 | |||||||
| chr4:102689348 | CA | C | 107 | a0001c0001t0002g0254 a0001c0001t0003g0089 a0001c0001t0003g0090 others(104): Show |
107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.960+225delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689348 | |||||||
| chr4:102689348 | CAAA | C | 6 | a0001c0004t0005g0141 a0003c0005t0001g0001 a0003c0005t0001g0006 others(3): Show |
7 | HG01192.hp2 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.960+223_960+225del others(3): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689348 | |||||||
| chr4:102689352 | A | G | 9 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0003c0005t0001g0010 others(6): Show |
9 | HG01884.hp1 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.960+222T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689352 | |||||||
| chr4:102689353 | A | G | 1 | a0003c0005t0001g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.960+221T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689353 | |||||||
| chr4:102689355 | A | G | 4 | a0003c0005t0001g0001 a0003c0005t0001g0006 a0003c0005t0001g0008 others(1): Show |
5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+219T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689355 | |||||||
| chr4:102689358 | AAAT | A | 18 | a0001c0001t0005g0225 a0001c0004t0006g0264 a0001c0004t0009g0140 others(15): Show |
18 | HG01496.hp2 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.960+213_960+215del others(3): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689358 | |||||||
| chr4:102689359 | A | T | 2 | a0001c0001t0002g0175 a0001c0017t0006g0237 |
2 | HG01993.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.960+215T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689359 | |||||||
| chr4:102689360 | AT | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(34): Show |
38 | HG00323.hp2 HG00408.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.960+213delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689360 | |||||||
| chr4:102689361 | T | A | 6 | a0001c0001t0002g0276 a0001c0001t0003g0169 a0001c0001t0005g0168 others(3): Show |
6 | HG00639.hp1 HG02970.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+213A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689361 | |||||||
| chr4:102689363 | T | A | 2 | a0001c0001t0002g0148 a0003c0010t0001g0271 |
2 | HG02970.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.960+211A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689363 | |||||||
| chr4:102689365 | T | A | 2 | a0001c0001t0010g0232 a0001c0004t0010g0275 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.960+209A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689365 | |||||||
| chr4:102689378 | ATGTG | A | 148 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(145): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.960+192_960+195del others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689378 | |||||||
| chr4:102689380 | G | A | 31 | a0001c0001t0005g0225 a0001c0001t0010g0232 a0001c0004t0005g0141 others(28): Show |
32 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.960+194C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689380 | |||||||
| chr4:102689382 | G | A | 15 | a0001c0001t0010g0232 a0001c0004t0006g0267 a0001c0004t0009g0024 others(12): Show |
15 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.960+192C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689382 | |||||||
| chr4:102689439 | C | A | 3 | a0001c0001t0003g0095 a0001c0001t0005g0092 a0001c0001t0011g0051 |
3 | HG00544.hp1 NA18960.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.960+135G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689439 | |||||||
| chr4:102689466 | T | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+108A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689466 | |||||||
| chr4:102689715 | A | G | 165 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.850-31T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102689715 | |||||||
| chr4:102689823 | G | T | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.850-139C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102689823 | |||||||
| chr4:102690006 | T | A | 1 | a0003c0003t0007g0248 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.850-322A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102690006 | |||||||
| chr4:102690067 | A | T | 1 | a0003c0003t0007g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.850-383T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102690067 | |||||||
| chr4:102690207 | G | A | 164 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.849+389C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102690207 | |||||||
| chr4:102690376 | A | T | 157 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(154): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.849+220T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102690376 | |||||||
| chr4:102690583 | T | G | 3 | a0002c0002t0001g0049 a0002c0002t0001g0056 a0002c0002t0001g0096 |
3 | NA18960.hp1 NA18970.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.849+13A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102690583 | |||||||
| chr4:102690794 | A | AAT | 4 | a0001c0001t0008g0250 a0001c0004t0008g0014 a0001c0004t0009g0011 others(1): Show |
4 | HG00735.hp2 HG02280.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-25_674-24dupAT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690794 | |||||||
| chr4:102690794 | AATATAT | A | 16 | a0001c0009t0010g0034 a0001c0009t0015g0005 a0001c0009t0022g0016 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.674-29_674-24delAT others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690794 | |||||||
| chr4:102690861 | G | T | 165 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.674-90C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690861 | |||||||
| chr4:102690886 | T | C | 184 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(181): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.674-115A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690886 | |||||||
| chr4:102690924 | A | G | 2 | a0001c0001t0010g0232 a0001c0004t0010g0275 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.674-153T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690924 | |||||||
| chr4:102690980 | G | A | 165 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.674-209C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690980 | |||||||
| chr4:102690999 | C | T | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.674-228G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690999 | |||||||
| chr4:102691014 | T | A | 1 | a0002c0002t0001g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.674-243A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691014 | |||||||
| chr4:102691059 | G | A | 1 | a0006c0016t0004g0214 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.674-288C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691059 | |||||||
| chr4:102691382 | T | C | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-611A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691382 | |||||||
| chr4:102691493 | G | C | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-722C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691493 | |||||||
| chr4:102691514 | CT | C | 6 | a0001c0001t0010g0232 a0001c0001t0018g0202 a0001c0004t0010g0253 others(3): Show |
6 | HG01070.hp1 HG02622.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.674-744delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691514 | |||||||
| chr4:102691557 | C | T | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-786G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691557 | |||||||
| chr4:102691634 | C | A | 16 | a0001c0009t0010g0034 a0001c0009t0015g0005 a0001c0009t0022g0016 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.674-863G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691634 | |||||||
| chr4:102691635 | A | G | 16 | a0001c0009t0010g0034 a0001c0009t0015g0005 a0001c0009t0022g0016 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.674-864T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691635 | |||||||
| chr4:102691760 | T | C | 181 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(178): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.674-989A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691760 | |||||||
| chr4:102691785 | G | A | 2 | a0001c0001t0003g0169 a0001c0001t0005g0168 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.674-1014C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691785 | |||||||
| chr4:102692109 | A | G | 184 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(181): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.674-1338T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692109 | |||||||
| chr4:102692142 | A | G | 165 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(162): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.674-1371T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692142 | |||||||
| chr4:102692242 | G | C | 1 | a0001c0001t0002g0093 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.674-1471C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692242 | |||||||
| chr4:102692409 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.674-1638C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692409 | |||||||
| chr4:102692410 | C | T | 5 | a0001c0001t0010g0232 a0001c0004t0009g0024 a0001c0004t0010g0253 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-1639G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692410 | |||||||
| chr4:102692421 | T | C | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-1650A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692421 | |||||||
| chr4:102692448 | T | C | 5 | a0001c0001t0010g0232 a0001c0004t0009g0024 a0001c0004t0010g0253 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-1677A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692448 | |||||||
| chr4:102692468 | C | T | 5 | a0001c0001t0010g0232 a0001c0004t0009g0024 a0001c0004t0010g0253 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-1697G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692468 | |||||||
| chr4:102692615 | CA | C | 3 | a0001c0001t0010g0232 a0001c0004t0010g0253 a0001c0004t0010g0275 |
3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.674-1845delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692615 | |||||||
| chr4:102692746 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-1975C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692746 | |||||||
| chr4:102692747 | T | G | 14 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0003c0005t0001g0001 others(11): Show |
15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.674-1976A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692747 | |||||||
| chr4:102692793 | C | T | 1 | a0002c0002t0001g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.674-2022G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692793 | |||||||
| chr4:102692850 | G | A | 16 | a0001c0001t0003g0139 a0001c0001t0003g0223 a0001c0001t0003g0231 others(13): Show |
16 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.674-2079C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692850 | |||||||
| chr4:102692881 | G | A | 2 | a0001c0009t0010g0034 a0001c0017t0006g0237 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.674-2110C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692881 | |||||||
| chr4:102693201 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-2430C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693201 | |||||||
| chr4:102693302 | T | C | 2 | a0002c0002t0001g0052 a0002c0002t0001g0111 |
2 | HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.674-2531A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693302 | |||||||
| chr4:102693454 | G | A | 1 | a0003c0010t0001g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674-2683C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693454 | |||||||
| chr4:102693659 | A | C | 1 | a0001c0001t0002g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.674-2888T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693659 | |||||||
| chr4:102693717 | G | A | 1 | a0001c0001t0002g0270 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.674-2946C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693717 | |||||||
| chr4:102693844 | CA | C | 20 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(17): Show |
21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.674-3074delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693844 | |||||||
| chr4:102694001 | C | T | 1 | a0001c0009t0022g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.674-3230G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694001 | |||||||
| chr4:102694101 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-3330C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694101 | |||||||
| chr4:102694145 | C | T | 1 | a0003c0003t0007g0143 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.674-3374G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694145 | |||||||
| chr4:102694267 | A | G | 2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.674-3496T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694267 | |||||||
| chr4:102694352 | G | C | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.674-3581C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694352 | |||||||
| chr4:102694521 | C | T | 1 | a0005c0008t0003g0219 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.674-3750G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694521 | |||||||
| chr4:102694577 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.674-3806A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694577 | |||||||
| chr4:102694803 | C | T | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-4032G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694803 | |||||||
| chr4:102694827 | CT | C | 5 | a0002c0002t0001g0098 a0002c0002t0001g0099 a0002c0002t0001g0100 others(2): Show |
5 | HG00438.hp1 HG00609.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-4057delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694827 | |||||||
| chr4:102694847 | G | T | 1 | a0003c0005t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.674-4076C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694847 | |||||||
| chr4:102694866 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-4095G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694866 | |||||||
| chr4:102695017 | C | A | 2 | a0001c0001t0006g0162 a0001c0001t0016g0157 |
2 | HG00609.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.674-4246G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695017 | |||||||
| chr4:102695237 | A | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-4466T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695237 | |||||||
| chr4:102695369 | C | T | 1 | a0001c0001t0005g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.674-4598G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695369 | |||||||
| chr4:102695421 | C | T | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-4650G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695421 | |||||||
| chr4:102695659 | G | A | 5 | a0001c0001t0002g0254 a0003c0003t0007g0117 a0003c0003t0007g0248 others(2): Show |
5 | HG00438.hp2 HG02056.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-4888C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695659 | |||||||
| chr4:102695818 | C | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(10): Show |
14 | HG00673.hp1 HG01081.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.674-5047G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695818 | |||||||
| chr4:102696019 | G | A | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-5248C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696019 | |||||||
| chr4:102696064 | A | G | 4 | a0003c0005t0001g0001 a0003c0005t0001g0006 a0003c0005t0001g0008 others(1): Show |
5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-5293T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696064 | |||||||
| chr4:102696334 | C | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-5563G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696334 | |||||||
| chr4:102696364 | G | GA | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-5594_674-5593i others(3): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696364 | |||||||
| chr4:102696447 | G | A | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.674-5676C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696447 | |||||||
| chr4:102696459 | A | G | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.674-5688T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696459 | |||||||
| chr4:102696493 | T | C | 1 | a0001c0001t0008g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.674-5722A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696493 | |||||||
| chr4:102696530 | C | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.674-5759G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696530 | |||||||
| chr4:102696545 | A | G | 2 | a0003c0003t0001g0198 a0003c0003t0001g0199 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.674-5774T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696545 | |||||||
| chr4:102696546 | G | A | 1 | a0001c0001t0004g0156 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.674-5775C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696546 | |||||||
| chr4:102696563 | A | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-5792T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696563 | |||||||
| chr4:102696688 | T | C | 2 | a0001c0004t0010g0253 a0001c0004t0010g0275 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.674-5917A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696688 | |||||||
| chr4:102696762 | T | C | 1 | a0001c0001t0011g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.674-5991A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696762 | |||||||
| chr4:102696866 | T | C | 96 | a0001c0001t0005g0077 a0001c0001t0005g0081 a0001c0001t0006g0082 others(93): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.674-6095A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696866 | |||||||
| chr4:102696967 | G | A | 1 | a0005c0008t0003g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.674-6196C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696967 | |||||||
| chr4:102697119 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6348A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697119 | |||||||
| chr4:102697341 | CTTTAT | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6575_674-6571d others(7): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697341 | |||||||
| chr4:102697442 | G | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6671C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697442 | |||||||
| chr4:102697463 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6692A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697463 | |||||||
| chr4:102697502 | C | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6731G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697502 | |||||||
| chr4:102697523 | A | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6752T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697523 | |||||||
| chr4:102697551 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6780G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697551 | |||||||
| chr4:102697603 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.674-6832G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697603 | |||||||
| chr4:102697665 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6894A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697665 | |||||||
| chr4:102697776 | G | A | 1 | a0003c0003t0007g0255 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.674-7005C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697776 | |||||||
| chr4:102697776 | G | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7005C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697776 | |||||||
| chr4:102697820 | C | G | 1 | a0003c0010t0001g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674-7049G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697820 | |||||||
| chr4:102697904 | C | A | 183 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.674-7133G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697904 | |||||||
| chr4:102698075 | T | C | 1 | a0003c0003t0001g0228 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.674-7304A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698075 | |||||||
| chr4:102698114 | A | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7343T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698114 | |||||||
| chr4:102698128 | A | ATG | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7359_674-7358d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698128 | |||||||
| chr4:102698179 | C | T | 158 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(155): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.674-7408G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698179 | |||||||
| chr4:102698208 | T | A | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.674-7437A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698208 | |||||||
| chr4:102698209 | C | T | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.674-7438G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698209 | |||||||
| chr4:102698389 | T | G | 1 | a0001c0001t0002g0170 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.674-7618A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698389 | |||||||
| chr4:102698450 | G | C | 2 | a0001c0004t0009g0024 a0003c0010t0001g0271 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.674-7679C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698450 | |||||||
| chr4:102698494 | A | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7723T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698494 | |||||||
| chr4:102698497 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7726C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698497 | |||||||
| chr4:102698572 | T | C | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.674-7801A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698572 | |||||||
| chr4:102698596 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7825G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698596 | |||||||
| chr4:102698605 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7834C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698605 | |||||||
| chr4:102698606 | A | T | 1 | a0001c0004t0009g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.674-7835T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698606 | |||||||
| chr4:102698615 | T | A | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-7844A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698615 | |||||||
| chr4:102698628 | G | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7857C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698628 | |||||||
| chr4:102698638 | C | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7867G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698638 | |||||||
| chr4:102698657 | A | C | 2 | a0001c0004t0009g0024 a0003c0010t0001g0271 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.674-7886T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698657 | |||||||
| chr4:102698678 | G | A | 1 | a0001c0001t0003g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.674-7907C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698678 | |||||||
| chr4:102698706 | C | A | 20 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(17): Show |
21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.674-7935G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698706 | |||||||
| chr4:102698758 | A | T | 1 | a0001c0001t0003g0095 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.674-7987T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698758 | |||||||
| chr4:102698765 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7994A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698765 | |||||||
| chr4:102698767 | G | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7996C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698767 | |||||||
| chr4:102698783 | G | A | 1 | a0009c0011t0020g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.674-8012C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698783 | |||||||
| chr4:102698804 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8033A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698804 | |||||||
| chr4:102699097 | G | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8326C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699097 | |||||||
| chr4:102699102 | T | G | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-8331A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699102 | |||||||
| chr4:102699170 | G | T | 16 | a0001c0009t0010g0034 a0001c0009t0015g0005 a0001c0009t0022g0016 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.674-8399C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699170 | |||||||
| chr4:102699183 | C | T | 1 | a0001c0001t0017g0145 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.674-8412G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699183 | |||||||
| chr4:102699193 | A | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8422T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699193 | |||||||
| chr4:102699228 | C | A | 185 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(182): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.674-8457G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699228 | |||||||
| chr4:102699243 | T | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8472A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699243 | |||||||
| chr4:102699295 | G | A | 14 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0003c0005t0001g0001 others(11): Show |
15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.674-8524C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699295 | |||||||
| chr4:102699338 | A | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8567T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699338 | |||||||
| chr4:102699399 | A | C | 1 | a0001c0001t0011g0021 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.674-8628T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699399 | |||||||
| chr4:102699477 | T | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8706A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699477 | |||||||
| chr4:102699526 | C | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.674-8755G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699526 | |||||||
| chr4:102699607 | A | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8836T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699607 | |||||||
| chr4:102699608 | G | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.674-8837C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699608 | |||||||
| chr4:102699636 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8865A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699636 | |||||||
| chr4:102699652 | T | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8881A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699652 | |||||||
| chr4:102699661 | G | T | 184 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(181): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.674-8890C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699661 | |||||||
| chr4:102699672 | A | G | 179 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(176): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.674-8901T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699672 | |||||||
| chr4:102699702 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8931A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699702 | |||||||
| chr4:102699749 | A | T | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-8978T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699749 | |||||||
| chr4:102699751 | C | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8980G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699751 | |||||||
| chr4:102699752 | C | T | 5 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(2): Show |
5 | HG02647.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-8981G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699752 | |||||||
| chr4:102699796 | G | C | 160 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(157): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.674-9025C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699796 | |||||||
| chr4:102699867 | C | A | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.674-9096G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699867 | |||||||
| chr4:102700092 | T | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.674-9321A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700092 | |||||||
| chr4:102700101 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9330G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700101 | |||||||
| chr4:102700102 | G | C | 7 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0024 others(4): Show |
7 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.674-9331C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700102 | |||||||
| chr4:102700144 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9373C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700144 | |||||||
| chr4:102700161 | A | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9390T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700161 | |||||||
| chr4:102700284 | T | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9513A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700284 | |||||||
| chr4:102700303 | A | C | 1 | a0002c0002t0001g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.674-9532T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700303 | |||||||
| chr4:102700559 | T | C | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-9788A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700559 | |||||||
| chr4:102700665 | G | A | 1 | a0003c0005t0001g0006 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.674-9894C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700665 | |||||||
| chr4:102700708 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9937C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700708 | |||||||
| chr4:102700740 | A | C | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.674-9969T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700740 | |||||||
| chr4:102700748 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9977G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700748 | |||||||
| chr4:102700790 | A | C | 1 | a0003c0003t0001g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.674-10019T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700790 | |||||||
| chr4:102700807 | A | G | 6 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(3): Show |
6 | HG02630.hp2 HG02647.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.674-10036T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700807 | |||||||
| chr4:102700847 | T | A | 2 | a0001c0004t0010g0253 a0001c0004t0010g0275 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.674-10076A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700847 | |||||||
| chr4:102700936 | T | C | 1 | a0001c0001t0016g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.674-10165A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700936 | |||||||
| chr4:102701017 | G | A | 160 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(157): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.674-10246C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701017 | |||||||
| chr4:102701065 | T | G | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-10294A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701065 | |||||||
| chr4:102701178 | C | G | 1 | a0001c0001t0002g0187 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.674-10407G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701178 | |||||||
| chr4:102701293 | T | C | 13 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0022 others(10): Show |
13 | HG02572.hp1 HG02622.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.674-10522A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701293 | |||||||
| chr4:102701306 | T | G | 1 | a0002c0002t0001g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-10535A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701306 | |||||||
| chr4:102701400 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-10629A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701400 | |||||||
| chr4:102701411 | G | A | 94 | a0001c0001t0003g0038 a0002c0002t0001g0028 a0002c0002t0001g0029 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.674-10640C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701411 | |||||||
| chr4:102701412 | C | T | 94 | a0001c0001t0003g0038 a0002c0002t0001g0028 a0002c0002t0001g0029 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.674-10641G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701412 | |||||||
| chr4:102701456 | C | G | 1 | a0003c0003t0001g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.674-10685G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701456 | |||||||
| chr4:102701468 | A | G | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-10697T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701468 | |||||||
| chr4:102701518 | G | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-10747C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701518 | |||||||
| chr4:102701541 | T | G | 1 | a0003c0003t0007g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.674-10770A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701541 | |||||||
| chr4:102701544 | G | A | 1 | a0003c0003t0007g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.674-10773C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701544 | |||||||
| chr4:102701551 | C | T | 2 | a0001c0004t0009g0024 a0003c0010t0001g0271 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.674-10780G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701551 | |||||||
| chr4:102701594 | G | T | 183 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.674-10823C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701594 | |||||||
| chr4:102701644 | T | C | 4 | a0002c0002t0007g0033 a0002c0002t0007g0116 a0004c0006t0002g0115 others(1): Show |
4 | HG01081.hp2 HG01243.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-10873A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701644 | |||||||
| chr4:102701663 | T | C | 1 | a0001c0004t0010g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.674-10892A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701663 | |||||||
| chr4:102701728 | C | T | 1 | a0001c0001t0006g0162 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.674-10957G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701728 | |||||||
| chr4:102701746 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-10975G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701746 | |||||||
| chr4:102701843 | G | A | 1 | a0002c0002t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.674-11072C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701843 | |||||||
| chr4:102701922 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11151G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701922 | |||||||
| chr4:102701923 | A | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11152T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701923 | |||||||
| chr4:102702005 | C | T | 1 | a0001c0001t0009g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.674-11234G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702005 | |||||||
| chr4:102702042 | G | A | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0003c0003t0001g0151 |
3 | HG00280.hp2 HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.674-11271C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702042 | |||||||
| chr4:102702063 | T | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11292A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702063 | |||||||
| chr4:102702093 | G | A | 16 | a0001c0001t0003g0139 a0001c0001t0003g0223 a0001c0001t0003g0231 others(13): Show |
16 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.674-11322C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702093 | |||||||
| chr4:102702107 | A | G | 1 | a0002c0007t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.674-11336T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702107 | |||||||
| chr4:102702198 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11427A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702198 | |||||||
| chr4:102702259 | G | A | 2 | a0001c0001t0003g0231 a0001c0001t0008g0216 |
2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.674-11488C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702259 | |||||||
| chr4:102702268 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11497G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702268 | |||||||
| chr4:102702334 | C | T | 183 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.674-11563G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702334 | |||||||
| chr4:102702341 | C | A | 2 | a0001c0001t0002g0192 a0001c0015t0009g0173 |
2 | NA18953.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.674-11570G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702341 | |||||||
| chr4:102702357 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11586A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702357 | |||||||
| chr4:102702360 | C | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11589G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702360 | |||||||
| chr4:102702407 | C | T | 3 | a0002c0002t0001g0070 a0002c0002t0001g0075 a0002c0002t0007g0064 |
3 | HG01099.hp1 HG01106.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.674-11636G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702407 | |||||||
| chr4:102702476 | A | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11705T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702476 | |||||||
| chr4:102702483 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11712G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702483 | |||||||
| chr4:102702484 | G | A | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.674-11713C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702484 | |||||||
| chr4:102702499 | T | G | 2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.674-11728A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702499 | |||||||
| chr4:102702564 | T | G | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.674-11793A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702564 | |||||||
| chr4:102702670 | A | G | 1 | a0002c0002t0001g0249 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.673+11768T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702670 | |||||||
| chr4:102702690 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.673+11748A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702690 | |||||||
| chr4:102702765 | C | CAATT | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11672_673+1167 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702765 | |||||||
| chr4:102702808 | A | C | 1 | a0004c0006t0002g0154 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.673+11630T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702808 | |||||||
| chr4:102702951 | G | A | 1 | a0003c0005t0001g0001 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.673+11487C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702951 | |||||||
| chr4:102703022 | T | C | 20 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(17): Show |
21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.673+11416A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703022 | |||||||
| chr4:102703023 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11415C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703023 | |||||||
| chr4:102703081 | T | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11357A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703081 | |||||||
| chr4:102703112 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.673+11326G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703112 | |||||||
| chr4:102703132 | C | CTTGT | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11302_673+1130 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703132 | |||||||
| chr4:102703197 | C | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11241G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703197 | |||||||
| chr4:102703278 | A | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11160T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703278 | |||||||
| chr4:102703356 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.673+11082A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703356 | |||||||
| chr4:102703430 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11008G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703430 | |||||||
| chr4:102703622 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10816C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703622 | |||||||
| chr4:102703628 | G | C | 6 | a0002c0002t0001g0036 a0002c0002t0001g0037 a0002c0002t0001g0040 others(3): Show |
6 | HG01496.hp1 HG02129.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.673+10810C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703628 | |||||||
| chr4:102703713 | C | T | 2 | a0001c0004t0010g0253 a0001c0004t0010g0275 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.673+10725G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703713 | |||||||
| chr4:102703814 | C | T | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673+10624G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703814 | |||||||
| chr4:102703867 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10571C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703867 | |||||||
| chr4:102704005 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10433C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704005 | |||||||
| chr4:102704026 | T | C | 111 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(108): Show |
113 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.673+10412A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704026 | |||||||
| chr4:102704073 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10365A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704073 | |||||||
| chr4:102704090 | A | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10348T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704090 | |||||||
| chr4:102704107 | C | A | 20 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(17): Show |
21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.673+10331G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704107 | |||||||
| chr4:102704108 | C | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10330G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704108 | |||||||
| chr4:102704134 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10304G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704134 | |||||||
| chr4:102704191 | C | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10247G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704191 | |||||||
| chr4:102704258 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10180C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704258 | |||||||
| chr4:102704276 | G | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10162C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704276 | |||||||
| chr4:102704303 | G | C | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+10135C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704303 | |||||||
| chr4:102704374 | T | A | 58 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(55): Show |
59 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.673+10064A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704374 | |||||||
| chr4:102704433 | C | T | 114 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(111): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.673+10005G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704433 | |||||||
| chr4:102704445 | C | G | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673+9993G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704445 | |||||||
| chr4:102704469 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+9969G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704469 | |||||||
| chr4:102704552 | CT | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+9885delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704552 | |||||||
| chr4:102704579 | T | A | 20 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(17): Show |
21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.673+9859A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704579 | |||||||
| chr4:102704610 | C | T | 1 | a0001c0001t0002g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.673+9828G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704610 | |||||||
| chr4:102704760 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.673+9678G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704760 | |||||||
| chr4:102704778 | T | G | 1 | a0001c0001t0003g0097 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.673+9660A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704778 | |||||||
| chr4:102705112 | G | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+9326C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705112 | |||||||
| chr4:102705356 | C | A | 1 | a0003c0010t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.673+9082G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705356 | |||||||
| chr4:102705366 | A | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+9072T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705366 | |||||||
| chr4:102705567 | G | A | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+8871C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705567 | |||||||
| chr4:102705570 | C | T | 2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.673+8868G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705570 | |||||||
| chr4:102705637 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+8801G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705637 | |||||||
| chr4:102705676 | T | C | 2 | a0001c0004t0010g0253 a0001c0004t0010g0275 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.673+8762A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705676 | |||||||
| chr4:102705702 | T | C | 117 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(114): Show |
119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.673+8736A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705702 | |||||||
| chr4:102705833 | C | A | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+8605G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705833 | |||||||
| chr4:102706040 | C | T | 16 | a0001c0009t0010g0034 a0001c0009t0015g0005 a0001c0009t0022g0016 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.673+8398G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706040 | |||||||
| chr4:102706060 | G | A | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673+8378C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706060 | |||||||
| chr4:102706062 | G | T | 2 | a0001c0004t0009g0024 a0003c0010t0001g0271 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.673+8376C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706062 | |||||||
| chr4:102706331 | T | C | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673+8107A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706331 | |||||||
| chr4:102706408 | G | C | 4 | a0003c0005t0001g0001 a0003c0005t0001g0006 a0003c0005t0001g0008 others(1): Show |
5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+8030C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706408 | |||||||
| chr4:102706517 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+7921C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706517 | |||||||
| chr4:102706530 | T | C | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+7908A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706530 | |||||||
| chr4:102706538 | C | G | 1 | a0002c0002t0001g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.673+7900G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706538 | |||||||
| chr4:102706717 | A | G | 117 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(114): Show |
119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.673+7721T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706717 | |||||||
| chr4:102706803 | A | C | 1 | a0001c0001t0002g0135 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.673+7635T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706803 | |||||||
| chr4:102706811 | T | C | 115 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(112): Show |
117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.673+7627A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706811 | |||||||
| chr4:102707128 | A | T | 8 | a0001c0001t0002g0175 a0001c0001t0002g0177 a0001c0001t0002g0197 others(5): Show |
8 | HG00558.hp1 HG01993.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.673+7310T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102707128 | |||||||
| chr4:102707417 | C | G | 1 | a0001c0001t0002g0175 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.673+7021G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102707417 | |||||||
| chr4:102707525 | T | C | 14 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0003c0005t0001g0001 others(11): Show |
15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+6913A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102707525 | |||||||
| chr4:102707883 | G | A | 1 | a0001c0004t0005g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.673+6555C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102707883 | |||||||
| chr4:102707978 | T | C | 1 | a0002c0002t0007g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.673+6460A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102707978 | |||||||
| chr4:102708186 | A | G | 1 | a0001c0001t0003g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.673+6252T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708186 | |||||||
| chr4:102708319 | G | A | 16 | a0001c0009t0010g0034 a0001c0009t0015g0005 a0001c0009t0022g0016 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.673+6119C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708319 | |||||||
| chr4:102708608 | A | G | 2 | a0002c0002t0001g0059 a0002c0002t0001g0060 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.673+5830T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708608 | |||||||
| chr4:102708646 | T | A | 2 | a0001c0001t0012g0152 a0001c0001t0012g0153 |
2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.673+5792A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708646 | |||||||
| chr4:102708648 | A | G | 2 | a0001c0001t0012g0152 a0001c0001t0012g0153 |
2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.673+5790T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708648 | |||||||
| chr4:102708939 | A | G | 2 | a0001c0004t0009g0024 a0003c0010t0001g0271 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.673+5499T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708939 | |||||||
| chr4:102708980 | A | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+5458T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708980 | |||||||
| chr4:102708983 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.673+5455T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708983 | |||||||
| chr4:102709145 | C | T | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+5293G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709145 | |||||||
| chr4:102709234 | A | C | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+5204T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709234 | |||||||
| chr4:102709278 | GAAAGAAA others(41): Show |
G | 2 | a0001c0004t0010g0253 a0001c0004t0010g0275 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.673+5112_673+5159d others(50): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709278 | |||||||
| chr4:102709283 | AAAGG | A | 146 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(143): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.673+5151_673+5154d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709283 | |||||||
| chr4:102709283 | AAAGGAAG others(1): Show |
A | 15 | a0001c0001t0002g0122 a0001c0001t0002g0131 a0001c0001t0002g0182 others(12): Show |
15 | HG00621.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.673+5147_673+5154d others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709283 | |||||||
| chr4:102709283 | AAAGGAAG others(5): Show |
A | 14 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0003c0005t0001g0001 others(11): Show |
15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+5143_673+5154d others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709283 | |||||||
| chr4:102709291 | GAAGGAAG others(33): Show |
G | 2 | a0001c0004t0009g0024 a0003c0010t0001g0271 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.673+5107_673+5146d others(42): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709291 | |||||||
| chr4:102709303 | G | A | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+5135C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709303 | |||||||
| chr4:102709304 | AAGGAAGG | A | 4 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+5127_673+5133d others(9): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709304 | |||||||
| chr4:102709307 | G | A | 87 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0135 others(84): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.673+5131C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709307 | |||||||
| chr4:102709308 | AAGG | A | 87 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0135 others(84): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.673+5127_673+5129d others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709308 | |||||||
| chr4:102709323 | AG | A | 91 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0135 others(88): Show |
92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.673+5114delC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709323 | |||||||
| chr4:102709326 | A | G | 91 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0135 others(88): Show |
92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.673+5112T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709326 | |||||||
| chr4:102709331 | A | G | 91 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0135 others(88): Show |
92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.673+5107T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709331 | |||||||
| chr4:102709383 | GAAGAAAG others(14): Show |
G | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+5034_673+5054d others(23): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709383 | |||||||
| chr4:102709390 | GAAAGAAA others(6): Show |
G | 14 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0030 others(11): Show |
14 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.673+5035_673+5047d others(15): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709390 | |||||||
| chr4:102709398 | GA | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG00544.hp2 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+5039delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709398 | |||||||
| chr4:102709433 | G | A | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+5005C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709433 | |||||||
| chr4:102709436 | A | AAAGG | 110 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(107): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.673+4998_673+5001d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709436 | |||||||
| chr4:102709436 | A | G | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+5002T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709436 | |||||||
| chr4:102709643 | C | T | 270 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(267): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.673+4795G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709643 | |||||||
| chr4:102709969 | T | C | 14 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0003c0005t0001g0001 others(11): Show |
15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+4469A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709969 | |||||||
| chr4:102710117 | C | T | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+4321G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710117 | |||||||
| chr4:102710159 | A | G | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673+4279T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710159 | |||||||
| chr4:102710282 | T | C | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+4156A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710282 | |||||||
| chr4:102710549 | T | G | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+3889A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710549 | |||||||
| chr4:102710594 | C | T | 14 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0003c0005t0001g0001 others(11): Show |
15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+3844G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710594 | |||||||
| chr4:102710645 | C | T | 1 | a0001c0001t0003g0002 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.673+3793G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710645 | |||||||
| chr4:102710653 | G | A | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.673+3785C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710653 | |||||||
| chr4:102711002 | C | T | 1 | a0001c0004t0009g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.673+3436G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711002 | |||||||
| chr4:102711003 | G | A | 4 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+3435C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711003 | |||||||
| chr4:102711029 | G | T | 1 | a0003c0003t0007g0257 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.673+3409C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711029 | |||||||
| chr4:102711063 | T | G | 1 | a0002c0002t0001g0113 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.673+3375A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711063 | |||||||
| chr4:102711391 | C | A | 5 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(2): Show |
5 | HG02647.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+3047G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711391 | |||||||
| chr4:102711573 | T | C | 5 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(2): Show |
5 | HG02647.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+2865A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711573 | |||||||
| chr4:102711709 | G | A | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+2729C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711709 | |||||||
| chr4:102711714 | C | T | 8 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0003c0005t0001g0010 others(5): Show |
8 | HG01884.hp1 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.673+2724G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711714 | |||||||
| chr4:102711738 | A | C | 1 | a0009c0011t0020g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.673+2700T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711738 | |||||||
| chr4:102711806 | C | T | 73 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(70): Show |
74 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.673+2632G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711806 | |||||||
| chr4:102711852 | A | G | 20 | a0001c0004t0009g0024 a0001c0004t0010g0253 a0001c0004t0010g0275 others(17): Show |
21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.673+2586T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711852 | |||||||
| chr4:102712118 | G | A | 2 | a0002c0002t0001g0120 a0002c0002t0001g0121 |
2 | HG01168.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.673+2320C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712118 | |||||||
| chr4:102712235 | T | A | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.673+2203A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712235 | |||||||
| chr4:102712402 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.673+2036G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712402 | |||||||
| chr4:102712403 | A | T | 1 | a0001c0001t0002g0165 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.673+2035T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712403 | |||||||
| chr4:102712524 | C | CT | 7 | a0001c0001t0005g0224 a0001c0004t0005g0141 a0001c0004t0009g0011 others(4): Show |
7 | HG02451.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.673+1913dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712524 | |||||||
| chr4:102712524 | C | CTT | 89 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(86): Show |
90 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.673+1912_673+1913d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712524 | |||||||
| chr4:102712539 | A | T | 98 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(95): Show |
99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.673+1899T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712539 | |||||||
| chr4:102712658 | G | A | 94 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(91): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.673+1780C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712658 | |||||||
| chr4:102712680 | G | A | 14 | a0001c0009t0015g0005 a0001c0009t0022g0016 a0003c0005t0001g0001 others(11): Show |
15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+1758C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712680 | |||||||
| chr4:102712737 | T | C | 114 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(111): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.673+1701A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712737 | |||||||
| chr4:102712887 | G | A | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+1551C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712887 | |||||||
| chr4:102712890 | T | G | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+1548A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712890 | |||||||
| chr4:102712923 | T | C | 1 | a0001c0004t0006g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.673+1515A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712923 | |||||||
| chr4:102713043 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.673+1395G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713043 | |||||||
| chr4:102713063 | C | T | 90 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(87): Show |
91 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.673+1375G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713063 | |||||||
| chr4:102713084 | C | A | 2 | a0001c0004t0009g0024 a0003c0010t0001g0271 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.673+1354G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713084 | |||||||
| chr4:102713174 | G | A | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.673+1264C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713174 | |||||||
| chr4:102713271 | C | T | 1 | a0002c0002t0001g0036 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.673+1167G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713271 | |||||||
| chr4:102713277 | C | T | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.673+1161G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713277 | |||||||
| chr4:102713468 | G | A | 1 | a0001c0001t0009g0184 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.673+970C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713468 | |||||||
| chr4:102713571 | T | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.673+867A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713571 | |||||||
| chr4:102713694 | G | A | 4 | a0002c0002t0007g0033 a0002c0002t0007g0116 a0004c0006t0002g0115 others(1): Show |
4 | HG01081.hp2 HG01243.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+744C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713694 | |||||||
| chr4:102713815 | G | A | 4 | a0001c0001t0002g0105 a0001c0001t0002g0133 a0001c0001t0002g0147 others(1): Show |
4 | HG00673.hp1 HG02129.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+623C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713815 | |||||||
| chr4:102713835 | G | A | 1 | a0001c0009t0022g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.673+603C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713835 | |||||||
| chr4:102713865 | C | T | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+573G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713865 | |||||||
| chr4:102713896 | CA | C | 22 | a0001c0001t0002g0135 a0001c0001t0002g0226 a0001c0001t0002g0242 others(19): Show |
23 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.673+541delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713896 | |||||||
| chr4:102713896 | CAA | C | 14 | a0001c0009t0010g0034 a0001c0009t0015g0005 a0001c0009t0022g0016 others(11): Show |
14 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.673+540_673+541del others(2): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713896 | |||||||
| chr4:102713912 | A | G | 1 | a0001c0015t0009g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.673+526T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713912 | |||||||
| chr4:102714026 | T | C | 114 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(111): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.673+412A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102714026 | |||||||
| chr4:102714183 | C | A | 19 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 others(16): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.673+255G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102714183 | |||||||
| chr4:102714263 | C | T | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+175G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102714263 | |||||||
| chr4:102714713 | T | C | 1 | a0003c0003t0007g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.550-152A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102714713 | |||||||
| chr4:102714743 | A | G | 1 | a0001c0001t0004g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.550-182T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102714743 | |||||||
| chr4:102714771 | T | A | 1 | a0003c0010t0001g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.550-210A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102714771 | |||||||
| chr4:102714850 | C | T | 1 | a0002c0002t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.550-289G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102714850 | |||||||
| chr4:102715135 | A | G | 33 | a0001c0004t0002g0243 a0001c0004t0005g0141 a0001c0004t0005g0269 others(30): Show |
34 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.550-574T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102715135 | |||||||
| chr4:102715279 | G | T | 14 | a0001c0001t0003g0139 a0001c0001t0003g0223 a0001c0001t0003g0231 others(11): Show |
14 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.550-718C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102715279 | |||||||
| chr4:102715432 | T | C | 20 | a0001c0004t0005g0141 a0001c0004t0008g0014 a0001c0004t0009g0011 others(17): Show |
21 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.550-871A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102715432 | |||||||
| chr4:102715503 | T | G | 6 | a0001c0009t0010g0034 a0003c0005t0001g0001 a0003c0005t0001g0006 others(3): Show |
7 | HG01192.hp2 HG02145.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.550-942A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102715503 | |||||||
| chr4:102715655 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.550-1094G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102715655 | |||||||
| chr4:102716060 | A | C | 4 | a0002c0002t0001g0065 a0002c0002t0001g0066 a0002c0002t0001g0067 others(1): Show |
4 | HG00558.hp2 HG02071.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-1499T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716060 | |||||||
| chr4:102716075 | C | T | 1 | a0003c0005t0001g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.550-1514G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716075 | |||||||
| chr4:102716080 | C | T | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.550-1519G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716080 | |||||||
| chr4:102716155 | C | T | 5 | a0001c0009t0010g0034 a0003c0005t0001g0001 a0003c0005t0001g0006 others(2): Show |
6 | HG01192.hp2 HG02145.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-1594G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716155 | |||||||
| chr4:102716177 | T | C | 34 | a0001c0004t0002g0026 a0001c0004t0002g0243 a0001c0004t0005g0141 others(31): Show |
35 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.550-1616A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716177 | |||||||
| chr4:102716178 | A | G | 21 | a0001c0004t0005g0141 a0001c0004t0008g0014 a0001c0004t0009g0011 others(18): Show |
22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.550-1617T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716178 | |||||||
| chr4:102716309 | C | CA | 39 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(36): Show |
40 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.550-1749dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716309 | |||||||
| chr4:102716309 | CA | C | 99 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(96): Show |
101 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.550-1749delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716309 | |||||||
| chr4:102716309 | CAA | C | 6 | a0001c0001t0002g0241 a0001c0001t0003g0019 a0003c0003t0001g0198 others(3): Show |
6 | HG01099.hp2 HG02630.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-1750_550-1749d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716309 | |||||||
| chr4:102716649 | T | C | 4 | a0001c0004t0002g0026 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG00099.hp1 HG02109.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-2088A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716649 | |||||||
| chr4:102716753 | G | A | 21 | a0001c0004t0005g0141 a0001c0004t0008g0014 a0001c0004t0009g0011 others(18): Show |
22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.550-2192C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716753 | |||||||
| chr4:102716979 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.550-2418C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716979 | |||||||
| chr4:102717046 | A | AT | 3 | a0001c0001t0003g0246 a0001c0001t0006g0247 a0002c0002t0001g0277 |
3 | HG00140.hp2 HG03831.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.550-2486dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717046 | |||||||
| chr4:102717112 | T | C | 1 | a0001c0001t0002g0185 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.550-2551A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717112 | |||||||
| chr4:102717263 | T | C | 3 | a0001c0001t0005g0077 a0001c0001t0005g0081 a0001c0001t0006g0082 |
3 | HG01106.hp2 HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.550-2702A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717263 | |||||||
| chr4:102717382 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.550-2821G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717382 | |||||||
| chr4:102717424 | C | CT | 7 | a0001c0001t0002g0165 a0002c0007t0001g0106 a0002c0007t0001g0107 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-2864dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717424 | |||||||
| chr4:102717424 | CT | C | 7 | a0001c0009t0010g0034 a0002c0002t0001g0120 a0002c0002t0001g0121 others(4): Show |
8 | HG01168.hp2 HG01192.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.550-2864delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717424 | |||||||
| chr4:102717444 | G | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.550-2883C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717444 | |||||||
| chr4:102718113 | A | C | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-3552T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718113 | |||||||
| chr4:102718167 | C | A | 1 | a0001c0001t0008g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.550-3606G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718167 | |||||||
| chr4:102718246 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.550-3685G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718246 | |||||||
| chr4:102718281 | A | G | 2 | a0001c0001t0004g0155 a0001c0001t0004g0158 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.550-3720T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718281 | |||||||
| chr4:102718490 | T | G | 3 | a0002c0002t0001g0044 a0002c0002t0001g0058 a0002c0002t0001g0113 |
3 | HG00544.hp2 HG02080.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.550-3929A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718490 | |||||||
| chr4:102718515 | C | T | 5 | a0001c0004t0002g0026 a0001c0004t0009g0024 a0001c0004t0010g0253 others(2): Show |
5 | HG00099.hp1 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-3954G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718515 | |||||||
| chr4:102718527 | T | A | 1 | a0001c0001t0002g0193 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.550-3966A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718527 | |||||||
| chr4:102718614 | G | T | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.550-4053C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718614 | |||||||
| chr4:102718683 | A | G | 21 | a0001c0004t0005g0141 a0001c0004t0008g0014 a0001c0004t0009g0011 others(18): Show |
22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.550-4122T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718683 | |||||||
| chr4:102718703 | C | G | 4 | a0001c0004t0002g0026 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG00099.hp1 HG02109.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-4142G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718703 | |||||||
| chr4:102718715 | A | G | 12 | a0001c0004t0008g0014 a0001c0009t0015g0005 a0001c0009t0022g0016 others(9): Show |
12 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.550-4154T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718715 | |||||||
| chr4:102718780 | A | G | 1 | a0002c0002t0001g0120 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.549+4091T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718780 | |||||||
| chr4:102718833 | G | A | 18 | a0001c0004t0008g0014 a0001c0009t0010g0034 a0001c0009t0015g0005 others(15): Show |
19 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+4038C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718833 | |||||||
| chr4:102718978 | C | T | 1 | a0002c0002t0001g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.549+3893G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718978 | |||||||
| chr4:102718986 | A | G | 118 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(115): Show |
120 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.549+3885T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718986 | |||||||
| chr4:102719016 | T | C | 18 | a0001c0004t0008g0014 a0001c0009t0010g0034 a0001c0009t0015g0005 others(15): Show |
19 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+3855A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719016 | |||||||
| chr4:102719156 | G | A | 1 | a0001c0004t0002g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.549+3715C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719156 | |||||||
| chr4:102719158 | A | C | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.549+3713T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719158 | |||||||
| chr4:102719183 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+3688G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719183 | |||||||
| chr4:102719184 | G | A | 1 | a0003c0010t0001g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.549+3687C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719184 | |||||||
| chr4:102719253 | G | A | 2 | a0001c0001t0005g0224 a0001c0001t0005g0261 |
2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.549+3618C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719253 | |||||||
| chr4:102719276 | C | T | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.549+3595G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719276 | |||||||
| chr4:102719379 | G | A | 1 | a0002c0002t0001g0067 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.549+3492C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719379 | |||||||
| chr4:102719403 | C | T | 4 | a0001c0004t0002g0026 a0001c0004t0010g0253 a0001c0004t0010g0275 others(1): Show |
4 | HG00099.hp1 HG02109.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+3468G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719403 | |||||||
| chr4:102719574 | C | T | 1 | a0004c0006t0002g0035 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.549+3297G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719574 | |||||||
| chr4:102719601 | T | C | 86 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(83): Show |
87 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.549+3270A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719601 | |||||||
| chr4:102719745 | C | T | 21 | a0001c0004t0005g0141 a0001c0004t0008g0014 a0001c0004t0009g0011 others(18): Show |
22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+3126G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719745 | |||||||
| chr4:102719746 | G | A | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.549+3125C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719746 | |||||||
| chr4:102719763 | T | C | 8 | a0001c0001t0002g0104 a0001c0001t0002g0186 a0001c0001t0002g0187 others(5): Show |
8 | HG01071.hp2 HG01074.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.549+3108A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719763 | |||||||
| chr4:102719816 | A | G | 1 | a0004c0006t0004g0042 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.549+3055T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719816 | |||||||
| chr4:102719865 | G | A | 1 | a0001c0001t0002g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.549+3006C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719865 | |||||||
| chr4:102719935 | T | C | 1 | a0001c0001t0004g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.549+2936A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719935 | |||||||
| chr4:102720028 | G | A | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.549+2843C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720028 | |||||||
| chr4:102720029 | A | G | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.549+2842T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720029 | |||||||
| chr4:102720043 | T | C | 1 | a0003c0003t0007g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.549+2828A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720043 | |||||||
| chr4:102720263 | C | T | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.549+2608G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720263 | |||||||
| chr4:102720292 | G | A | 2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.549+2579C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720292 | |||||||
| chr4:102720307 | C | T | 1 | a0002c0002t0001g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.549+2564G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720307 | |||||||
| chr4:102720434 | C | CA | 9 | a0001c0001t0002g0104 a0001c0001t0002g0186 a0001c0001t0002g0187 others(6): Show |
9 | HG01071.hp2 HG01074.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+2436dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720434 | |||||||
| chr4:102720434 | CA | C | 11 | a0001c0004t0002g0026 a0001c0004t0002g0243 a0001c0004t0005g0269 others(8): Show |
11 | HG00099.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.549+2436delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720434 | |||||||
| chr4:102720447 | A | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+2424T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720447 | |||||||
| chr4:102720498 | G | A | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.549+2373C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720498 | |||||||
| chr4:102720530 | G | A | 21 | a0001c0004t0005g0141 a0001c0004t0008g0014 a0001c0004t0009g0011 others(18): Show |
22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+2341C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720530 | |||||||
| chr4:102720668 | T | C | 2 | a0001c0001t0012g0152 a0001c0001t0012g0153 |
2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.549+2203A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720668 | |||||||
| chr4:102720680 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.549+2191C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720680 | |||||||
| chr4:102720933 | T | C | 21 | a0001c0004t0005g0141 a0001c0004t0008g0014 a0001c0004t0009g0011 others(18): Show |
22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+1938A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720933 | |||||||
| chr4:102720948 | A | G | 3 | a0001c0004t0010g0253 a0001c0004t0010g0275 a0003c0010t0001g0274 |
3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.549+1923T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720948 | |||||||
| chr4:102721061 | C | T | 1 | a0001c0001t0006g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.549+1810G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721061 | |||||||
| chr4:102721062 | G | C | 1 | a0003c0003t0007g0248 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.549+1809C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721062 | |||||||
| chr4:102721090 | G | A | 21 | a0001c0004t0005g0141 a0001c0004t0008g0014 a0001c0004t0009g0011 others(18): Show |
22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+1781C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721090 | |||||||
| chr4:102721145 | G | A | 12 | a0001c0004t0008g0014 a0001c0009t0015g0005 a0001c0009t0022g0016 others(9): Show |
12 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.549+1726C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721145 | |||||||
| chr4:102721198 | C | T | 1 | a0002c0002t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.549+1673G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721198 | |||||||
| chr4:102721199 | G | A | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.549+1672C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721199 | |||||||
| chr4:102721222 | G | A | 18 | a0001c0004t0008g0014 a0001c0009t0010g0034 a0001c0009t0015g0005 others(15): Show |
19 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+1649C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721222 | |||||||
| chr4:102721255 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+1616G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721255 | |||||||
| chr4:102721309 | G | C | 2 | a0001c0004t0002g0243 a0001c0004t0014g0004 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.549+1562C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721309 | |||||||
| chr4:102721329 | C | CATAA | 17 | a0001c0001t0002g0105 a0001c0001t0002g0161 a0001c0001t0003g0137 others(14): Show |
17 | HG01891.hp2 HG01993.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.549+1538_549+1541d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721329 | |||||||
| chr4:102721329 | C | CATAAATA others(5): Show |
8 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0001c0009t0010g0034 others(5): Show |
9 | HG01192.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.549+1530_549+1541d others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721329 | |||||||
| chr4:102721329 | CATAA | C | 3 | a0002c0002t0001g0127 a0002c0002t0001g0277 a0008c0013t0001g0272 |
3 | HG02698.hp1 HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.549+1538_549+1541d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721329 | |||||||
| chr4:102721382 | A | G | 21 | a0001c0004t0005g0141 a0001c0004t0008g0014 a0001c0004t0009g0011 others(18): Show |
22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+1489T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721382 | |||||||
| chr4:102721508 | T | C | 1 | a0001c0001t0003g0095 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.549+1363A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721508 | |||||||
| chr4:102721532 | A | T | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.549+1339T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721532 | |||||||
| chr4:102721647 | T | C | 1 | a0002c0002t0007g0033 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.549+1224A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721647 | |||||||
| chr4:102721806 | T | C | 1 | a0002c0002t0001g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.549+1065A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721806 | |||||||
| chr4:102721864 | C | T | 2 | a0001c0001t0003g0246 a0001c0001t0006g0247 |
2 | HG00140.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.549+1007G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721864 | |||||||
| chr4:102721960 | G | T | 21 | a0001c0004t0005g0141 a0001c0004t0008g0014 a0001c0004t0009g0011 others(18): Show |
22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+911C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721960 | |||||||
| chr4:102721971 | G | A | 82 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(79): Show |
83 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.549+900C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721971 | |||||||
| chr4:102721972 | G | A | 12 | a0001c0004t0008g0014 a0001c0009t0015g0005 a0001c0009t0022g0016 others(9): Show |
12 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.549+899C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721972 | |||||||
| chr4:102722029 | CA | C | 125 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0105 others(122): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.549+841delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722029 | |||||||
| chr4:102722029 | CAA | C | 115 | a0001c0001t0002g0047 a0001c0001t0002g0104 a0001c0001t0002g0122 others(112): Show |
117 | HG00323.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.549+840_549+841del others(2): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722029 | |||||||
| chr4:102722094 | G | A | 18 | a0001c0004t0008g0014 a0001c0009t0010g0034 a0001c0009t0015g0005 others(15): Show |
19 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+777C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722094 | |||||||
| chr4:102722179 | A | C | 5 | a0001c0009t0010g0034 a0003c0005t0001g0001 a0003c0005t0001g0006 others(2): Show |
6 | HG01192.hp2 HG02145.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.549+692T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722179 | |||||||
| chr4:102722211 | A | G | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+660T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722211 | |||||||
| chr4:102722271 | C | T | 1 | a0002c0002t0001g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.549+600G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722271 | |||||||
| chr4:102722278 | T | G | 1 | a0002c0002t0001g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.549+593A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722278 | |||||||
| chr4:102722429 | C | T | 2 | a0001c0001t0003g0166 a0001c0001t0003g0172 |
2 | HG02572.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.549+442G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722429 | |||||||
| chr4:102722526 | C | T | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.549+345G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722526 | |||||||
| chr4:102722631 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0011 a0001c0004t0009g0140 |
3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+240G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722631 | |||||||
| chr4:102722687 | A | G | 1 | a0001c0001t0005g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.549+184T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722687 | |||||||
| chr4:102723420 | C | T | 9 | a0001c0004t0002g0243 a0001c0004t0005g0269 a0001c0004t0006g0263 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-379G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 3/16 | chr4 | 102723420 | |||||||
| chr4:102723492 | A | C | 1 | a0002c0002t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.378+370T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 3/16 | chr4 | 102723492 | |||||||
| chr4:102723656 | T | C | 1 | a0001c0001t0002g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.378+206A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 3/16 | chr4 | 102723656 | |||||||
| chr4:102723829 | AT | A | 9 | a0001c0001t0002g0003 a0001c0001t0002g0105 a0001c0001t0002g0133 others(6): Show |
10 | HG00673.hp1 HG01978.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+32delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 3/16 | chr4 | 102723829 | |||||||
| chr4:102724029 | T | C | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.273-62A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724029 | |||||||
| chr4:102724403 | C | T | 1 | a0001c0001t0005g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.273-436G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724403 | |||||||
| chr4:102724525 | C | T | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.273-558G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724525 | |||||||
| chr4:102724542 | C | CA | 8 | a0002c0002t0001g0032 a0002c0002t0001g0065 a0002c0002t0001g0066 others(5): Show |
8 | HG00558.hp2 HG01106.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.273-576dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724542 | |||||||
| chr4:102724542 | CA | C | 169 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(166): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.273-576delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724542 | |||||||
| chr4:102724542 | CAA | C | 10 | a0001c0001t0002g0270 a0001c0004t0005g0269 a0001c0004t0006g0263 others(7): Show |
10 | HG00408.hp1 HG00408.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.273-577_273-576del others(2): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724542 | |||||||
| chr4:102724721 | G | A | 1 | a0004c0006t0003g0068 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.273-754C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724721 | |||||||
| chr4:102724748 | G | A | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.273-781C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724748 | |||||||
| chr4:102724787 | C | CA | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.273-821dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724787 | |||||||
| chr4:102725070 | G | A | 3 | a0001c0004t0010g0253 a0001c0004t0010g0275 a0003c0010t0001g0274 |
3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.273-1103C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725070 | |||||||
| chr4:102725072 | GT | G | 3 | a0001c0004t0010g0253 a0001c0004t0010g0275 a0003c0010t0001g0274 |
3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.273-1106delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725072 | |||||||
| chr4:102725277 | A | T | 10 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0010g0253 others(7): Show |
11 | HG00099.hp1 HG01192.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.273-1310T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725277 | |||||||
| chr4:102725295 | C | G | 9 | a0001c0004t0008g0014 a0001c0009t0015g0005 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+1294G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725295 | |||||||
| chr4:102725408 | G | T | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.272+1181C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725408 | |||||||
| chr4:102725414 | C | T | 7 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0001c0004t0010g0253 others(4): Show |
7 | HG02109.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.272+1175G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725414 | |||||||
| chr4:102725487 | C | T | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.272+1102G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725487 | |||||||
| chr4:102725657 | T | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0003c0005t0001g0027 |
3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.272+932A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725657 | |||||||
| chr4:102725751 | G | A | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.272+838C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725751 | |||||||
| chr4:102725784 | C | A | 13 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0004t0010g0253 others(10): Show |
13 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.272+805G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725784 | |||||||
| chr4:102725890 | C | T | 115 | a0001c0001t0002g0131 a0001c0001t0002g0135 a0001c0001t0002g0164 others(112): Show |
117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.272+699G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725890 | |||||||
| chr4:102725985 | A | G | 10 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0015g0005 others(7): Show |
10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.272+604T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725985 | |||||||
| chr4:102726074 | C | G | 1 | a0001c0004t0006g0264 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.272+515G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726074 | |||||||
| chr4:102726100 | C | CA | 10 | a0001c0001t0004g0069 a0001c0001t0004g0191 a0001c0001t0008g0076 others(7): Show |
10 | HG00099.hp1 HG02015.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.272+488dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726100 | |||||||
| chr4:102726101 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.272+488T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726101 | |||||||
| chr4:102726178 | A | G | 81 | a0001c0001t0002g0131 a0001c0001t0002g0135 a0001c0001t0002g0164 others(78): Show |
82 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.272+411T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726178 | |||||||
| chr4:102726242 | T | C | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.272+347A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726242 | |||||||
| chr4:102726398 | T | C | 1 | a0001c0001t0006g0162 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.272+191A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726398 | |||||||
| chr4:102726404 | A | G | 15 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0004t0010g0253 others(12): Show |
15 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.272+185T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726404 | |||||||
| chr4:102726466 | C | CAAACA | 25 | a0001c0004t0002g0243 a0001c0004t0005g0269 a0001c0004t0006g0263 others(22): Show |
25 | HG00735.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.272+118_272+122dup others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726466 | |||||||
| chr4:102726528 | C | A | 10 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0015g0005 others(7): Show |
10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.272+61G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726528 | |||||||
| chr4:102726795 | C | T | 1 | a0001c0001t0008g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.178-112G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102726795 | |||||||
| chr4:102726890 | C | T | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-207G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102726890 | |||||||
| chr4:102727072 | C | T | 1 | a0001c0001t0005g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.178-389G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727072 | |||||||
| chr4:102727131 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.178-448C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727131 | |||||||
| chr4:102727143 | G | A | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-460C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727143 | |||||||
| chr4:102727221 | C | G | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-538G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727221 | |||||||
| chr4:102727507 | T | C | 1 | a0003c0010t0001g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.178-824A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727507 | |||||||
| chr4:102727569 | C | T | 1 | a0001c0001t0004g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.178-886G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727569 | |||||||
| chr4:102727645 | TCACAGTC others(3): Show |
T | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-972_178-963del others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727645 | |||||||
| chr4:102727672 | T | C | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-989A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727672 | |||||||
| chr4:102727706 | G | C | 1 | a0001c0004t0005g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.178-1023C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727706 | |||||||
| chr4:102727782 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.178-1099C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727782 | |||||||
| chr4:102727828 | A | G | 1 | a0001c0001t0008g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.178-1145T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727828 | |||||||
| chr4:102727860 | A | T | 1 | a0002c0002t0001g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-1177T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727860 | |||||||
| chr4:102727886 | T | C | 10 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0015g0005 others(7): Show |
10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-1203A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727886 | |||||||
| chr4:102727977 | T | A | 2 | a0001c0001t0002g0241 a0001c0001t0002g0242 |
2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.178-1294A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727977 | |||||||
| chr4:102728057 | G | C | 5 | a0001c0001t0005g0007 a0003c0005t0001g0001 a0003c0005t0001g0006 others(2): Show |
6 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-1374C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728057 | |||||||
| chr4:102728367 | C | T | 5 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0170 others(2): Show |
6 | HG01168.hp1 HG01169.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-1684G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728367 | |||||||
| chr4:102728499 | A | AG | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-1817_178-1816i others(3): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728499 | |||||||
| chr4:102728708 | C | T | 16 | a0001c0001t0003g0139 a0001c0001t0003g0223 a0001c0001t0003g0231 others(13): Show |
16 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-2025G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728708 | |||||||
| chr4:102728709 | G | A | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-2026C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728709 | |||||||
| chr4:102728792 | T | C | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-2109A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728792 | |||||||
| chr4:102729099 | C | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-2416G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729099 | |||||||
| chr4:102729100 | G | A | 1 | a0001c0001t0005g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.178-2417C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729100 | |||||||
| chr4:102729124 | G | A | 1 | a0002c0002t0001g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.178-2441C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729124 | |||||||
| chr4:102729145 | C | T | 2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.178-2462G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729145 | |||||||
| chr4:102729173 | T | C | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-2490A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729173 | |||||||
| chr4:102729175 | C | G | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-2492G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729175 | |||||||
| chr4:102729410 | C | T | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-2727G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729410 | |||||||
| chr4:102729418 | C | T | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-2735G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729418 | |||||||
| chr4:102729497 | G | C | 1 | a0003c0003t0001g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.178-2814C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729497 | |||||||
| chr4:102729642 | T | C | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-2959A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729642 | |||||||
| chr4:102729664 | C | T | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.178-2981G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729664 | |||||||
| chr4:102729829 | A | G | 34 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0141 others(31): Show |
35 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.178-3146T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729829 | |||||||
| chr4:102729835 | C | G | 1 | a0001c0001t0002g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178-3152G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729835 | |||||||
| chr4:102729852 | T | C | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-3169A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729852 | |||||||
| chr4:102729910 | G | A | 1 | a0002c0002t0001g0087 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.178-3227C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729910 | |||||||
| chr4:102729942 | T | G | 1 | a0002c0002t0001g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.178-3259A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729942 | |||||||
| chr4:102729997 | T | C | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-3314A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729997 | |||||||
| chr4:102730011 | T | C | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-3328A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730011 | |||||||
| chr4:102730019 | G | A | 2 | a0001c0001t0002g0193 a0002c0002t0001g0121 |
2 | HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.178-3336C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730019 | |||||||
| chr4:102730094 | T | C | 3 | a0001c0004t0009g0024 a0003c0005t0013g0251 a0003c0005t0013g0252 |
3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-3411A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730094 | |||||||
| chr4:102730298 | A | G | 1 | a0001c0001t0002g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178-3615T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730298 | |||||||
| chr4:102730389 | C | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-3706G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730389 | |||||||
| chr4:102730468 | C | T | 4 | a0001c0004t0010g0253 a0001c0004t0010g0275 a0001c0004t0014g0004 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-3785G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730468 | |||||||
| chr4:102730475 | G | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0003c0005t0001g0027 |
3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178-3792C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730475 | |||||||
| chr4:102730569 | G | A | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-3886C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730569 | |||||||
| chr4:102730592 | T | G | 1 | a0002c0002t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.178-3909A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730592 | |||||||
| chr4:102730593 | C | T | 1 | a0002c0002t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.178-3910G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730593 | |||||||
| chr4:102730611 | G | C | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-3928C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730611 | |||||||
| chr4:102730622 | T | C | 1 | a0001c0001t0003g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.178-3939A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730622 | |||||||
| chr4:102730689 | C | T | 3 | a0001c0004t0010g0253 a0001c0004t0010g0275 a0003c0010t0001g0274 |
3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.178-4006G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730689 | |||||||
| chr4:102730720 | G | C | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-4037C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730720 | |||||||
| chr4:102730754 | A | G | 10 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0015g0005 others(7): Show |
10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-4071T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730754 | |||||||
| chr4:102730761 | T | C | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-4078A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730761 | |||||||
| chr4:102730778 | T | C | 1 | a0008c0013t0001g0272 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.178-4095A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730778 | |||||||
| chr4:102730805 | A | C | 182 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0104 others(179): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.178-4122T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730805 | |||||||
| chr4:102730944 | A | T | 1 | a0001c0001t0002g0226 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.178-4261T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730944 | |||||||
| chr4:102730987 | T | A | 14 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0004t0010g0253 others(11): Show |
14 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.178-4304A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730987 | |||||||
| chr4:102731011 | A | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0148 a0001c0001t0002g0149 others(1): Show |
5 | NA18953.hp1 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-4328T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731011 | |||||||
| chr4:102731389 | T | C | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-4706A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731389 | |||||||
| chr4:102731656 | T | G | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-4973A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731656 | |||||||
| chr4:102731691 | T | C | 4 | a0001c0001t0002g0135 a0001c0001t0002g0195 a0001c0001t0002g0196 others(1): Show |
4 | HG02080.hp1 NA18968.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-5008A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731691 | |||||||
| chr4:102731773 | G | T | 14 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0004t0010g0253 others(11): Show |
14 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.178-5090C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731773 | |||||||
| chr4:102731789 | G | T | 1 | a0002c0002t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.178-5106C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731789 | |||||||
| chr4:102731894 | C | A | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-5211G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731894 | |||||||
| chr4:102731898 | TC | T | 19 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(16): Show |
19 | HG00735.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-5216delG | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731898 | |||||||
| chr4:102732221 | C | G | 4 | a0001c0004t0010g0253 a0001c0004t0010g0275 a0001c0004t0014g0004 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-5538G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102732221 | |||||||
| chr4:102732433 | A | T | 4 | a0001c0004t0010g0253 a0001c0004t0010g0275 a0001c0004t0014g0004 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-5750T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102732433 | |||||||
| chr4:102732450 | G | A | 1 | a0002c0002t0001g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-5767C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102732450 | |||||||
| chr4:102732761 | A | G | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-6078T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102732761 | |||||||
| chr4:102732819 | T | C | 168 | a0001c0001t0002g0003 a0001c0001t0002g0131 a0001c0001t0002g0133 others(165): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.178-6136A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102732819 | |||||||
| chr4:102733219 | A | C | 1 | a0002c0002t0001g0121 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.178-6536T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733219 | |||||||
| chr4:102733282 | A | G | 114 | a0001c0001t0002g0131 a0001c0001t0002g0135 a0001c0001t0002g0164 others(111): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.178-6599T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733282 | |||||||
| chr4:102733349 | A | AT | 31 | a0001c0001t0003g0169 a0001c0001t0005g0007 a0001c0001t0005g0168 others(28): Show |
32 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.178-6667dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733349 | |||||||
| chr4:102733349 | AT | A | 19 | a0001c0001t0002g0212 a0001c0001t0002g0254 a0001c0001t0002g0276 others(16): Show |
19 | HG00438.hp2 HG00639.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-6667delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733349 | |||||||
| chr4:102733413 | G | A | 6 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0003c0005t0001g0001 others(3): Show |
7 | HG00099.hp1 HG01192.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-6730C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733413 | |||||||
| chr4:102733446 | G | A | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-6763C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733446 | |||||||
| chr4:102733567 | C | T | 2 | a0001c0001t0002g0254 a0003c0003t0007g0255 |
2 | HG02056.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.178-6884G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733567 | |||||||
| chr4:102734105 | T | C | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.178-7422A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734105 | |||||||
| chr4:102734276 | G | A | 4 | a0001c0004t0010g0253 a0001c0004t0010g0275 a0001c0004t0014g0004 others(1): Show |
4 | HG02109.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-7593C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734276 | |||||||
| chr4:102734318 | G | A | 25 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0269 others(22): Show |
26 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.178-7635C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734318 | |||||||
| chr4:102734400 | C | T | 1 | a0004c0006t0002g0045 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.178-7717G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734400 | |||||||
| chr4:102734465 | T | C | 1 | a0001c0004t0005g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178-7782A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734465 | |||||||
| chr4:102734966 | A | G | 3 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0003c0005t0001g0027 |
3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178-8283T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734966 | |||||||
| chr4:102735220 | A | G | 80 | a0001c0001t0002g0131 a0001c0001t0002g0135 a0001c0001t0002g0164 others(77): Show |
81 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.178-8537T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735220 | |||||||
| chr4:102735324 | AC | A | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-8642delG | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735324 | |||||||
| chr4:102735350 | A | G | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.178-8667T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735350 | |||||||
| chr4:102735457 | G | A | 5 | a0001c0004t0002g0026 a0001c0004t0010g0253 a0001c0004t0010g0275 others(2): Show |
5 | HG00099.hp1 HG02109.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-8774C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735457 | |||||||
| chr4:102735470 | A | G | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-8787T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735470 | |||||||
| chr4:102735471 | A | G | 1 | a0001c0001t0008g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.178-8788T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735471 | |||||||
| chr4:102735521 | CA | C | 101 | a0001c0001t0002g0131 a0001c0001t0002g0135 a0001c0001t0002g0164 others(98): Show |
102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.178-8839delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735521 | |||||||
| chr4:102735521 | CAA | C | 6 | a0001c0004t0005g0269 a0001c0004t0006g0264 a0001c0004t0006g0265 others(3): Show |
6 | HG02145.hp2 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-8840_178-8839d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735521 | |||||||
| chr4:102735847 | T | C | 1 | a0001c0009t0022g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178-9164A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735847 | |||||||
| chr4:102736347 | C | T | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-9664G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102736347 | |||||||
| chr4:102736383 | A | G | 1 | a0002c0002t0001g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.178-9700T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102736383 | |||||||
| chr4:102736436 | C | A | 1 | a0001c0001t0002g0197 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.178-9753G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102736436 | |||||||
| chr4:102737287 | G | A | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-10604C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737287 | |||||||
| chr4:102737385 | A | G | 10 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0015g0005 others(7): Show |
10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-10702T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737385 | |||||||
| chr4:102737478 | T | G | 1 | a0002c0002t0001g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-10795A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737478 | |||||||
| chr4:102737494 | T | G | 90 | a0001c0001t0002g0003 a0001c0001t0002g0133 a0001c0001t0002g0146 others(87): Show |
92 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.178-10811A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737494 | |||||||
| chr4:102737605 | C | A | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.178-10922G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737605 | |||||||
| chr4:102737695 | G | A | 1 | a0001c0001t0004g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.178-11012C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737695 | |||||||
| chr4:102737848 | C | A | 3 | a0003c0005t0001g0012 a0003c0005t0001g0013 a0003c0005t0010g0015 |
3 | HG01884.hp1 HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.178-11165G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737848 | |||||||
| chr4:102737967 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.178-11284T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737967 | |||||||
| chr4:102738016 | T | C | 33 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0141 others(30): Show |
34 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.178-11333A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738016 | |||||||
| chr4:102738077 | C | G | 2 | a0001c0001t0012g0152 a0001c0001t0012g0153 |
2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.178-11394G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738077 | |||||||
| chr4:102738158 | G | A | 1 | a0010c0012t0001g0103 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.178-11475C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738158 | |||||||
| chr4:102738211 | A | C | 10 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0015g0005 others(7): Show |
10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-11528T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738211 | |||||||
| chr4:102738553 | A | G | 1 | a0002c0002t0001g0046 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.178-11870T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738553 | |||||||
| chr4:102738726 | C | T | 1 | a0004c0006t0002g0045 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.178-12043G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738726 | |||||||
| chr4:102739449 | T | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0148 a0001c0001t0002g0149 others(1): Show |
5 | NA18953.hp1 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-12766A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102739449 | |||||||
| chr4:102739866 | C | A | 15 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0004t0010g0253 others(12): Show |
15 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-13183G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102739866 | |||||||
| chr4:102739868 | C | T | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178-13185G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102739868 | |||||||
| chr4:102739924 | G | A | 1 | a0001c0001t0003g0208 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.178-13241C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102739924 | |||||||
| chr4:102740114 | G | A | 3 | a0001c0001t0018g0202 a0001c0017t0006g0237 a0002c0002t0001g0235 |
3 | HG02622.hp2 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.178-13431C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740114 | |||||||
| chr4:102740228 | T | C | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-13545A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740228 | |||||||
| chr4:102740309 | T | C | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-13626A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740309 | |||||||
| chr4:102740383 | C | T | 14 | a0001c0001t0003g0139 a0001c0001t0003g0223 a0001c0001t0003g0231 others(11): Show |
14 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.178-13700G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740383 | |||||||
| chr4:102740404 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.178-13721G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740404 | |||||||
| chr4:102740530 | A | C | 4 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0030 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-13847T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740530 | |||||||
| chr4:102740601 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178-13918A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740601 | |||||||
| chr4:102740705 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.178-14022G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740705 | |||||||
| chr4:102740885 | G | A | 12 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0015g0005 others(9): Show |
12 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.178-14202C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740885 | |||||||
| chr4:102740933 | C | A | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-14250G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740933 | |||||||
| chr4:102740934 | G | A | 1 | a0001c0001t0008g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.178-14251C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740934 | |||||||
| chr4:102741400 | C | G | 2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.178-14717G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102741400 | |||||||
| chr4:102741619 | G | A | 15 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0004t0010g0253 others(12): Show |
15 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-14936C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102741619 | |||||||
| chr4:102741674 | T | A | 1 | a0002c0002t0001g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.178-14991A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102741674 | |||||||
| chr4:102741867 | C | T | 3 | a0001c0004t0010g0253 a0001c0004t0010g0275 a0003c0010t0001g0274 |
3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.178-15184G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102741867 | |||||||
| chr4:102742165 | A | G | 33 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0141 others(30): Show |
34 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.178-15482T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742165 | |||||||
| chr4:102742176 | C | T | 1 | a0005c0008t0003g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.178-15493G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742176 | |||||||
| chr4:102742184 | G | A | 1 | a0002c0002t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.178-15501C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742184 | |||||||
| chr4:102742189 | C | T | 1 | a0003c0010t0001g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.178-15506G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742189 | |||||||
| chr4:102742307 | A | G | 1 | a0003c0003t0001g0244 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.178-15624T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742307 | |||||||
| chr4:102742338 | C | T | 15 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0004t0010g0253 others(12): Show |
15 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-15655G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742338 | |||||||
| chr4:102742352 | GAGTGGTA others(14): Show |
G | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-15690_178-1567 others(25): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742352 | |||||||
| chr4:102742394 | A | G | 1 | a0002c0002t0007g0033 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.178-15711T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742394 | |||||||
| chr4:102742605 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0003c0005t0001g0027 |
3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178-15922G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742605 | |||||||
| chr4:102742919 | C | T | 2 | a0001c0001t0012g0152 a0001c0001t0012g0153 |
2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.178-16236G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742919 | |||||||
| chr4:102742964 | T | C | 15 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0004t0010g0253 others(12): Show |
15 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-16281A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742964 | |||||||
| chr4:102743000 | C | T | 3 | a0001c0004t0010g0253 a0001c0004t0010g0275 a0003c0010t0001g0274 |
3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.178-16317G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743000 | |||||||
| chr4:102743334 | A | T | 1 | a0003c0003t0007g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.178-16651T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743334 | |||||||
| chr4:102743450 | G | A | 1 | a0001c0004t0006g0267 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.178-16767C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743450 | |||||||
| chr4:102743483 | T | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0003c0005t0001g0027 |
3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178-16800A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743483 | |||||||
| chr4:102743576 | T | C | 1 | a0002c0002t0001g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.178-16893A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743576 | |||||||
| chr4:102743724 | G | A | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.177+16994C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743724 | |||||||
| chr4:102743747 | T | C | 3 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0003c0005t0001g0027 |
3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.177+16971A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743747 | |||||||
| chr4:102743783 | T | C | 1 | a0002c0002t0001g0041 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.177+16935A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743783 | |||||||
| chr4:102743896 | C | T | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+16822G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743896 | |||||||
| chr4:102744006 | C | A | 1 | a0001c0004t0010g0253 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.177+16712G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744006 | |||||||
| chr4:102744138 | C | T | 3 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0003c0005t0001g0027 |
3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.177+16580G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744138 | |||||||
| chr4:102744167 | G | A | 3 | a0001c0004t0005g0141 a0001c0004t0009g0140 a0003c0005t0001g0027 |
3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.177+16551C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744167 | |||||||
| chr4:102744260 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.177+16458G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744260 | |||||||
| chr4:102744315 | T | A | 1 | a0003c0003t0001g0211 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.177+16403A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744315 | |||||||
| chr4:102744500 | T | C | 14 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0269 others(11): Show |
15 | HG00099.hp1 HG01192.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.177+16218A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744500 | |||||||
| chr4:102744529 | G | T | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.177+16189C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744529 | |||||||
| chr4:102744869 | T | C | 30 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0269 others(27): Show |
31 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.177+15849A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744869 | |||||||
| chr4:102745267 | T | C | 1 | a0003c0003t0007g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.177+15451A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745267 | |||||||
| chr4:102745369 | G | T | 1 | a0001c0001t0002g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.177+15349C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745369 | |||||||
| chr4:102745441 | C | T | 1 | a0001c0001t0002g0164 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.177+15277G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745441 | |||||||
| chr4:102745577 | C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15141G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745577 | |||||||
| chr4:102745584 | C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15134G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745584 | |||||||
| chr4:102745586 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15132C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745586 | |||||||
| chr4:102745588 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15130C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745588 | |||||||
| chr4:102745592 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15126C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745592 | |||||||
| chr4:102745593 | ATCAGGCA others(50): Show |
A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15068_177+1512 others(61): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745593 | |||||||
| chr4:102745653 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15065C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745653 | |||||||
| chr4:102745654 | C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15064G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745654 | |||||||
| chr4:102745658 | T | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15060A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745658 | |||||||
| chr4:102745662 | C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15056G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745662 | |||||||
| chr4:102745663 | T | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15055A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745663 | |||||||
| chr4:102745665 | T | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15053A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745665 | |||||||
| chr4:102745668 | G | GAAAAAAA others(54): Show |
1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15049_177+1505 others(65): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745668 | |||||||
| chr4:102745671 | C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15047G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745671 | |||||||
| chr4:102745672 | C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15046G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745672 | |||||||
| chr4:102745674 | T | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15044A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745674 | |||||||
| chr4:102745689 | A | C | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15029T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745689 | |||||||
| chr4:102745808 | C | T | 60 | a0001c0001t0002g0131 a0001c0001t0002g0135 a0001c0001t0002g0164 others(57): Show |
61 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.177+14910G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745808 | |||||||
| chr4:102745982 | G | A | 4 | a0002c0007t0001g0106 a0002c0007t0001g0107 a0002c0007t0001g0108 others(1): Show |
4 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+14736C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745982 | |||||||
| chr4:102746044 | C | T | 2 | a0002c0002t0001g0044 a0002c0002t0001g0113 |
2 | HG00544.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.177+14674G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746044 | |||||||
| chr4:102746136 | C | T | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+14582G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746136 | |||||||
| chr4:102746423 | A | C | 1 | a0001c0004t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.177+14295T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746423 | |||||||
| chr4:102746483 | C | T | 5 | a0001c0001t0005g0007 a0003c0005t0001g0001 a0003c0005t0001g0006 others(2): Show |
6 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+14235G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746483 | |||||||
| chr4:102746555 | T | C | 1 | a0009c0011t0020g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.177+14163A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746555 | |||||||
| chr4:102746624 | T | G | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+14094A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746624 | |||||||
| chr4:102746658 | G | C | 12 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0004t0010g0253 others(9): Show |
12 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+14060C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746658 | |||||||
| chr4:102746710 | C | T | 1 | a0002c0002t0001g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.177+14008G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746710 | |||||||
| chr4:102746712 | A | T | 1 | a0001c0004t0009g0140 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.177+14006T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746712 | |||||||
| chr4:102746840 | C | T | 1 | a0001c0001t0005g0261 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.177+13878G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746840 | |||||||
| chr4:102746966 | C | T | 2 | a0001c0004t0006g0263 a0001c0004t0006g0267 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.177+13752G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746966 | |||||||
| chr4:102746971 | C | CAA | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+13745_177+1374 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746971 | |||||||
| chr4:102747001 | C | T | 12 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0004t0010g0253 others(9): Show |
12 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+13717G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747001 | |||||||
| chr4:102747158 | G | GAT | 10 | a0001c0004t0005g0141 a0001c0004t0005g0269 a0001c0004t0006g0263 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.177+13558_177+1355 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | |||||||
| chr4:102747158 | G | GATAT | 5 | a0001c0001t0005g0007 a0003c0005t0001g0001 a0003c0005t0001g0006 others(2): Show |
6 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+13556_177+1355 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | |||||||
| chr4:102747158 | G | GATATATA others(23): Show |
3 | a0001c0004t0010g0253 a0001c0009t0022g0016 a0009c0011t0020g0018 |
3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.177+13559_177+1356 others(34): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | |||||||
| chr4:102747158 | G | GATATATA others(25): Show |
2 | a0001c0004t0008g0014 a0003c0005t0010g0015 |
2 | HG00735.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.177+13559_177+1356 others(36): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | |||||||
| chr4:102747158 | G | GATATATA others(29): Show |
5 | a0001c0004t0009g0011 a0003c0005t0001g0010 a0003c0005t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+13559_177+1356 others(40): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | |||||||
| chr4:102747158 | G | GATATATA others(37): Show |
1 | a0001c0004t0010g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.177+13559_177+1356 others(48): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | |||||||
| chr4:102747187 | T | G | 80 | a0001c0001t0002g0131 a0001c0001t0002g0135 a0001c0001t0002g0164 others(77): Show |
81 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.177+13531A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747187 | |||||||
| chr4:102747240 | C | G | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.177+13478G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747240 | |||||||
| chr4:102747313 | T | A | 1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.177+13405A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747313 | |||||||
| chr4:102747479 | C | T | 1 | a0003c0003t0001g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.177+13239G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747479 | |||||||
| chr4:102747742 | G | A | 6 | a0001c0001t0003g0230 a0001c0001t0003g0273 a0001c0001t0005g0136 others(3): Show |
6 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+12976C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747742 | |||||||
| chr4:102747749 | T | C | 1 | a0001c0001t0005g0261 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.177+12969A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747749 | |||||||
| chr4:102747816 | C | T | 1 | a0003c0010t0001g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.177+12902G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747816 | |||||||
| chr4:102748330 | T | C | 2 | a0001c0001t0005g0224 a0001c0001t0005g0261 |
2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.177+12388A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748330 | |||||||
| chr4:102748333 | T | A | 2 | a0001c0004t0009g0024 a0001c0009t0015g0005 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.177+12385A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748333 | |||||||
| chr4:102748430 | C | CTA | 9 | a0001c0001t0003g0038 a0001c0001t0003g0206 a0001c0001t0003g0207 others(6): Show |
9 | HG00099.hp1 HG00621.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+12286_177+1228 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748430 | |||||||
| chr4:102748447 | A | C | 1 | a0001c0009t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.177+12271T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748447 | |||||||
| chr4:102748806 | G | A | 16 | a0001c0001t0005g0007 a0001c0004t0005g0141 a0001c0004t0005g0269 others(13): Show |
17 | HG01192.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+11912C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748806 | |||||||
| chr4:102748842 | A | G | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+11876T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748842 | |||||||
| chr4:102748877 | C | T | 12 | a0001c0001t0002g0003 a0001c0001t0002g0133 a0001c0001t0002g0146 others(9): Show |
13 | HG00673.hp1 HG01081.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.177+11841G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748877 | |||||||
| chr4:102748885 | C | A | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+11833G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748885 | |||||||
| chr4:102748994 | T | A | 9 | a0001c0004t0005g0141 a0001c0004t0005g0269 a0001c0004t0006g0263 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+11724A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748994 | |||||||
| chr4:102749027 | C | T | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+11691G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749027 | |||||||
| chr4:102749387 | G | A | 19 | a0001c0001t0005g0077 a0001c0001t0005g0081 a0001c0001t0006g0082 others(16): Show |
19 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.177+11331C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749387 | |||||||
| chr4:102749590 | G | A | 1 | a0002c0007t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.177+11128C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749590 | |||||||
| chr4:102749615 | G | T | 17 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0141 others(14): Show |
18 | HG00099.hp1 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+11103C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749615 | |||||||
| chr4:102749673 | A | G | 1 | a0001c0001t0008g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.177+11045T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749673 | |||||||
| chr4:102749842 | C | T | 1 | a0001c0009t0015g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.177+10876G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749842 | |||||||
| chr4:102750122 | G | T | 1 | a0004c0006t0004g0042 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.177+10596C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750122 | |||||||
| chr4:102750184 | A | G | 2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.177+10534T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750184 | |||||||
| chr4:102750522 | T | A | 26 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0141 others(23): Show |
27 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.177+10196A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750522 | |||||||
| chr4:102750553 | C | T | 2 | a0001c0004t0005g0141 a0001c0004t0009g0140 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.177+10165G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750553 | |||||||
| chr4:102750661 | C | A | 1 | a0001c0001t0008g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.177+10057G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750661 | |||||||
| chr4:102750692 | C | T | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+10026G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750692 | |||||||
| chr4:102750806 | G | C | 2 | a0002c0002t0001g0259 a0003c0003t0007g0257 |
2 | HG00438.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.177+9912C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750806 | |||||||
| chr4:102751023 | A | G | 1 | a0001c0001t0003g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.177+9695T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751023 | |||||||
| chr4:102751212 | G | A | 6 | a0001c0001t0003g0230 a0001c0001t0003g0273 a0001c0001t0005g0136 others(3): Show |
6 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+9506C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751212 | |||||||
| chr4:102751479 | G | A | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+9239C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751479 | |||||||
| chr4:102751527 | G | A | 20 | a0001c0001t0002g0093 a0001c0001t0002g0104 a0001c0001t0003g0089 others(17): Show |
20 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.177+9191C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751527 | |||||||
| chr4:102751552 | T | C | 1 | a0001c0001t0002g0212 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.177+9166A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751552 | |||||||
| chr4:102751567 | T | C | 1 | a0002c0002t0001g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.177+9151A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751567 | |||||||
| chr4:102752155 | A | T | 1 | a0003c0003t0007g0143 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.177+8563T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752155 | |||||||
| chr4:102752224 | G | A | 1 | a0002c0002t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.177+8494C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752224 | |||||||
| chr4:102752272 | A | G | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+8446T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752272 | |||||||
| chr4:102752347 | C | T | 2 | a0002c0002t0001g0040 a0002c0002t0001g0041 |
2 | HG02129.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.177+8371G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752347 | |||||||
| chr4:102752449 | CA | C | 5 | a0001c0001t0005g0007 a0003c0005t0001g0001 a0003c0005t0001g0006 others(2): Show |
6 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+8268delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752449 | |||||||
| chr4:102752462 | G | T | 1 | a0001c0001t0005g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.177+8256C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752462 | |||||||
| chr4:102752577 | G | T | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+8141C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752577 | |||||||
| chr4:102752676 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.177+8042A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752676 | |||||||
| chr4:102752750 | A | C | 1 | a0002c0002t0001g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.177+7968T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752750 | |||||||
| chr4:102753172 | T | C | 1 | a0006c0016t0004g0214 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.177+7546A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753172 | |||||||
| chr4:102753278 | T | TAGTA | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+7439_177+7440i others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753278 | |||||||
| chr4:102753279 | T | A | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+7439A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753279 | |||||||
| chr4:102753375 | C | T | 15 | a0001c0001t0005g0007 a0001c0004t0005g0141 a0001c0004t0005g0269 others(12): Show |
16 | HG01192.hp2 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+7343G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753375 | |||||||
| chr4:102753381 | T | C | 17 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0141 others(14): Show |
18 | HG00099.hp1 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+7337A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753381 | |||||||
| chr4:102753397 | A | G | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+7321T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753397 | |||||||
| chr4:102753898 | C | T | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+6820G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753898 | |||||||
| chr4:102753901 | G | T | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.177+6817C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753901 | |||||||
| chr4:102753951 | G | C | 122 | a0001c0001t0002g0003 a0001c0001t0002g0131 a0001c0001t0002g0133 others(119): Show |
124 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.177+6767C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753951 | |||||||
| chr4:102754002 | CA | C | 148 | a0001c0001t0002g0003 a0001c0001t0002g0131 a0001c0001t0002g0133 others(145): Show |
151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.177+6715delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754002 | |||||||
| chr4:102754018 | G | A | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+6700C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754018 | |||||||
| chr4:102754019 | A | G | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+6699T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754019 | |||||||
| chr4:102754286 | C | T | 1 | a0003c0005t0001g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.177+6432G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754286 | |||||||
| chr4:102754338 | A | T | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+6380T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754338 | |||||||
| chr4:102754429 | C | G | 28 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0141 others(25): Show |
29 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.177+6289G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754429 | |||||||
| chr4:102754474 | A | G | 9 | a0001c0004t0005g0141 a0001c0004t0005g0269 a0001c0004t0006g0263 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+6244T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754474 | |||||||
| chr4:102754479 | T | C | 2 | a0001c0004t0009g0024 a0001c0009t0015g0005 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.177+6239A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754479 | |||||||
| chr4:102754563 | A | T | 4 | a0001c0001t0003g0142 a0001c0001t0008g0216 a0002c0002t0001g0120 others(1): Show |
4 | HG01175.hp1 HG01361.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+6155T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754563 | |||||||
| chr4:102754566 | T | C | 1 | a0001c0001t0008g0215 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.177+6152A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754566 | |||||||
| chr4:102754567 | T | A | 1 | a0001c0004t0006g0267 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.177+6151A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754567 | |||||||
| chr4:102754650 | G | A | 3 | a0003c0005t0001g0006 a0003c0005t0001g0008 a0003c0005t0001g0009 |
3 | HG01192.hp2 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.177+6068C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754650 | |||||||
| chr4:102754714 | G | T | 1 | a0001c0001t0003g0002 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.177+6004C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754714 | |||||||
| chr4:102754758 | G | A | 2 | a0003c0003t0001g0130 a0003c0005t0001g0027 |
2 | HG02602.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.177+5960C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754758 | |||||||
| chr4:102754801 | C | T | 7 | a0001c0001t0005g0007 a0001c0004t0009g0024 a0001c0009t0015g0005 others(4): Show |
8 | HG01192.hp2 HG02145.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+5917G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754801 | |||||||
| chr4:102754910 | T | G | 6 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0022 others(3): Show |
6 | HG02723.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+5808A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754910 | |||||||
| chr4:102755000 | G | C | 2 | a0001c0004t0010g0275 a0003c0010t0001g0274 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.177+5718C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755000 | |||||||
| chr4:102755068 | G | C | 1 | a0001c0004t0009g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+5650C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755068 | |||||||
| chr4:102755077 | A | C | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+5641T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755077 | |||||||
| chr4:102755098 | T | C | 1 | a0001c0004t0006g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.177+5620A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755098 | |||||||
| chr4:102755192 | G | A | 1 | a0003c0003t0001g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.177+5526C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755192 | |||||||
| chr4:102755513 | A | C | 1 | a0004c0006t0006g0129 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.177+5205T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755513 | |||||||
| chr4:102755696 | A | G | 26 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0141 others(23): Show |
27 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.177+5022T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755696 | |||||||
| chr4:102755738 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.177+4980A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755738 | |||||||
| chr4:102755904 | C | A | 6 | a0002c0007t0001g0106 a0002c0007t0001g0107 a0002c0007t0001g0108 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+4814G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755904 | |||||||
| chr4:102755968 | T | G | 1 | a0002c0002t0001g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.177+4750A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755968 | |||||||
| chr4:102756129 | T | C | 16 | a0001c0001t0003g0139 a0001c0001t0003g0223 a0001c0001t0003g0231 others(13): Show |
16 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+4589A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756129 | |||||||
| chr4:102756207 | A | G | 1 | a0001c0001t0002g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.177+4511T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756207 | |||||||
| chr4:102756215 | T | G | 1 | a0001c0004t0014g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.177+4503A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756215 | |||||||
| chr4:102756286 | T | A | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+4432A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756286 | |||||||
| chr4:102756288 | G | A | 17 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0141 others(14): Show |
18 | HG00099.hp1 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+4430C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756288 | |||||||
| chr4:102756302 | G | T | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+4416C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756302 | |||||||
| chr4:102756358 | G | A | 17 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0141 others(14): Show |
18 | HG00099.hp1 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+4360C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756358 | |||||||
| chr4:102756542 | C | T | 1 | a0004c0006t0008g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.177+4176G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756542 | |||||||
| chr4:102756657 | A | G | 2 | a0003c0005t0013g0251 a0003c0005t0013g0252 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.177+4061T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756657 | |||||||
| chr4:102756797 | T | TA | 119 | a0001c0001t0002g0003 a0001c0001t0002g0131 a0001c0001t0002g0146 others(116): Show |
121 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.177+3920dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756797 | |||||||
| chr4:102756797 | T | TAA | 14 | a0001c0001t0002g0133 a0001c0001t0002g0226 a0001c0001t0002g0227 others(11): Show |
15 | HG00673.hp1 HG00673.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.177+3919_177+3920d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756797 | |||||||
| chr4:102756797 | TA | T | 13 | a0001c0001t0002g0270 a0001c0001t0003g0246 a0001c0001t0006g0247 others(10): Show |
13 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+3920delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756797 | |||||||
| chr4:102756797 | TAAA | T | 8 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(5): Show |
8 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+3918_177+3920d others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756797 | |||||||
| chr4:102756830 | TGCTTCAA others(48): Show |
T | 1 | a0001c0001t0002g0133 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.177+3833_177+3887d others(57): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756830 | |||||||
| chr4:102756891 | G | GTCCTTTT others(49): Show |
1 | a0001c0001t0002g0133 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.177+3826_177+3827i others(58): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756891 | |||||||
| chr4:102757110 | G | A | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+3608C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757110 | |||||||
| chr4:102757150 | A | T | 7 | a0001c0004t0005g0269 a0001c0004t0006g0263 a0001c0004t0006g0264 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+3568T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757150 | |||||||
| chr4:102757181 | T | C | 26 | a0001c0001t0005g0007 a0001c0004t0002g0026 a0001c0004t0005g0269 others(23): Show |
27 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.177+3537A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757181 | |||||||
| chr4:102757270 | G | A | 2 | a0001c0004t0009g0024 a0001c0009t0015g0005 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.177+3448C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757270 | |||||||
| chr4:102757289 | A | G | 1 | a0002c0002t0001g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.177+3429T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757289 | |||||||
| chr4:102757383 | G | A | 1 | a0002c0002t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.177+3335C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757383 | |||||||
| chr4:102757403 | G | A | 9 | a0001c0004t0008g0014 a0001c0004t0009g0011 a0001c0009t0022g0016 others(6): Show |
9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+3315C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757403 | |||||||
| chr4:102757537 | C | G | 2 | a0001c0001t0002g0241 a0001c0001t0002g0242 |
2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.177+3181G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757537 | |||||||
| chr4:102757601 | C | T | 269 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0093 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.177+3117G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757601 | |||||||
| chr4:102757888 | C | A | 1 | a0001c0001t0012g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.177+2830G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757888 | |||||||
| chr4:102757960 | G | T | 154 | a0001c0001t0002g0003 a0001c0001t0002g0131 a0001c0001t0002g0133 others(151): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.177+2758C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757960 | |||||||
| chr4:102758142 | T | C | 1 | a0002c0002t0001g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.177+2576A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758142 | |||||||
| chr4:102758204 | GTA | G | 15 | a0001c0001t0005g0007 a0001c0004t0008g0014 a0001c0004t0009g0011 others(12): Show |
16 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+2512_177+2513d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758204 | |||||||
| chr4:102758301 | A | T | 1 | a0001c0001t0002g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.177+2417T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758301 | |||||||
| chr4:102758302 | T | A | 1 | a0001c0001t0008g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.177+2416A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758302 | |||||||
| chr4:102758311 | C | T | 6 | a0001c0001t0005g0007 a0001c0004t0014g0004 a0003c0005t0001g0001 others(3): Show |
7 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+2407G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758311 | |||||||
| chr4:102758347 | T | G | 1 | a0001c0001t0002g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.177+2371A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758347 | |||||||
| chr4:102758510 | G | A | 2 | a0001c0001t0002g0241 a0001c0001t0002g0242 |
2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.177+2208C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758510 | |||||||
| chr4:102758549 | T | C | 1 | a0002c0002t0001g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.177+2169A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758549 | |||||||
| chr4:102758686 | G | A | 1 | a0002c0002t0001g0128 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.177+2032C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758686 | |||||||
| chr4:102758692 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.177+2026C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758692 | |||||||
| chr4:102758693 | C | T | 1 | a0001c0009t0015g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.177+2025G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758693 | |||||||
| chr4:102758863 | C | T | 1 | a0003c0005t0001g0001 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.177+1855G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758863 | |||||||
| chr4:102758917 | T | C | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+1801A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758917 | |||||||
| chr4:102759031 | T | G | 1 | a0003c0003t0001g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.177+1687A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759031 | |||||||
| chr4:102759118 | T | C | 1 | a0001c0017t0006g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177+1600A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759118 | |||||||
| chr4:102759126 | ATTCT | A | 2 | a0001c0004t0002g0026 a0004c0006t0004g0025 |
2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.177+1588_177+1591d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759126 | |||||||
| chr4:102759137 | C | CT | 124 | a0001c0001t0002g0003 a0001c0001t0002g0131 a0001c0001t0002g0133 others(121): Show |
126 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.177+1580dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759137 | |||||||
| chr4:102759137 | C | CTT | 20 | a0001c0001t0002g0254 a0001c0001t0003g0246 a0001c0001t0006g0247 others(17): Show |
20 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.177+1579_177+1580d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759137 | |||||||
| chr4:102759141 | T | C | 1 | a0003c0005t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+1577A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759141 | |||||||
| chr4:102759342 | G | C | 1 | a0004c0006t0006g0129 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.177+1376C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759342 | |||||||
| chr4:102759442 | A | C | 5 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0030 others(2): Show |
5 | HG00280.hp1 HG00323.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+1276T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759442 | |||||||
| chr4:102759566 | GA | G | 168 | a0001c0001t0002g0003 a0001c0001t0002g0131 a0001c0001t0002g0133 others(165): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.177+1151delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759566 | |||||||
| chr4:102759784 | C | T | 2 | a0001c0001t0003g0019 a0001c0001t0003g0020 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.177+934G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759784 | |||||||
| chr4:102759827 | A | G | 122 | a0001c0001t0002g0003 a0001c0001t0002g0131 a0001c0001t0002g0133 others(119): Show |
124 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.177+891T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759827 | |||||||
| chr4:102760089 | T | TAC | 145 | a0001c0001t0002g0003 a0001c0001t0002g0131 a0001c0001t0002g0133 others(142): Show |
147 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.177+627_177+628dup others(2): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102760089 | |||||||
| chr4:102760089 | T | TACAC | 3 | a0001c0001t0003g0273 a0001c0004t0010g0275 a0003c0010t0001g0274 |
3 | HG01891.hp1 HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.177+625_177+628dup others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102760089 | |||||||
| chr4:102760215 | T | C | 1 | a0001c0001t0002g0276 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.177+503A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102760215 | |||||||
| chr4:102760244 | G | C | 1 | a0002c0002t0001g0277 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.177+474C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102760244 | |||||||
| chr4:102760535 | C | T | 15 | a0001c0001t0005g0007 a0001c0004t0008g0014 a0001c0004t0009g0011 others(12): Show |
16 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+183G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102760535 |