Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 735 |
| ensemblid | ENSG00000113600.12 |
| hgncid | 1358 |
| symbol | C9 |
| name | complement C9 |
| refseq_nuc | NM_001737.5 |
| refseq_prot | NP_001728.1 |
| ensembl_nuc | ENST00000263408.5 |
| ensembl_prot | ENSP00000263408.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 39284140 |
| end | 39364495 |
| strand | - |
| ver | v1.2 |
| region | chr5:39284140-39364495 |
| region5000 | chr5:39279140-39369495 |
| regionname0 | C9_chr5_39284140_39364495 |
| regionname5000 | C9_chr5_39279140_39369495 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 559 | 276 | 53 | 53 | 136 | 9 | 24 | 108 | C9_chr5_39279140_39369495 | C9 | MSACR others(554): Show |
chr5 | 39279140 | 39369495 |
| a0002 | 0/1 | 559 | 86 | 23 | 24 | 20 | 3 | 15 | 18 | C9_chr5_39279140_39369495 | C9 | MSACW others(554): Show |
chr5 | 39279140 | 39369495 |
| a0003 | 0/0 | 559 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | MSACR others(554): Show |
chr5 | 39279140 | 39369495 |
| a0004 | 0/0 | 559 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | MSACR others(554): Show |
chr5 | 39279140 | 39369495 |
| a0005 | 0/0 | 115 | 5 | 1 | 0 | 4 | 0 | 0 | 3 | C9_chr5_39279140_39369495 | C9 | MSACR others(110): Show |
chr5 | 39279140 | 39369495 |
| a0006 | 0/0 | 559 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | MSACR others(554): Show |
chr5 | 39279140 | 39369495 |
| a0007 | 0/0 | 559 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | MSACR others(554): Show |
chr5 | 39279140 | 39369495 |
| a0008 | 0/0 | 559 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | MSACW others(554): Show |
chr5 | 39279140 | 39369495 |
| a0009 | 0/0 | 559 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | MSACR others(554): Show |
chr5 | 39279140 | 39369495 |
| a0010 | 0/0 | 559 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | MSACW others(554): Show |
chr5 | 39279140 | 39369495 |
| a0011 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | MSACR others(554): Show |
chr5 | 39279140 | 39369495 |
| a0012 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | MSACW others(554): Show |
chr5 | 39279140 | 39369495 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1677 | 264 | 48 | 50 | 133 | 9 | 23 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0001c0005 | 0/0 | 1677 | 4 | 3 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0001c0009 | 0/0 | 1677 | 3 | 1 | 2 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0001c0010 | 0/0 | 1677 | 2 | 0 | 0 | 2 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0001c0013 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0001c0015 | 0/0 | 1677 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0001c0016 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0002c0002 | 0/1 | 1677 | 84 | 21 | 24 | 20 | 3 | 15 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0002c0018 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0002c0021 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0003c0004 | 0/0 | 1677 | 7 | 7 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0004c0003 | 0/0 | 1677 | 7 | 7 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0005c0007 | 0/0 | 1677 | 4 | 0 | 0 | 4 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0005c0017 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0006c0006 | 0/0 | 1677 | 4 | 4 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0007c0008 | 0/0 | 1677 | 3 | 2 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0008c0011 | 0/0 | 1677 | 2 | 2 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0009c0012 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0010c0020 | 0/0 | 1677 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0011c0014 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 | ||
| a0012c0019 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ATGTC others(1672): Show |
chr5 | 39279140 | 39369495 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2770 | 185 | 20 | 37 | 103 | 7 | 18 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0001t0002 | 1/0 | 2770 | 46 | 21 | 11 | 10 | 1 | 2 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0001t0003 | 0/0 | 2770 | 18 | 2 | 2 | 10 | 1 | 3 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0001t0004 | 0/0 | 2770 | 9 | 0 | 0 | 9 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0001t0006 | 0/0 | 2770 | 5 | 5 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0001t0010 | 0/0 | 2770 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0005t0002 | 0/0 | 2770 | 4 | 3 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0009t0002 | 0/0 | 2770 | 3 | 1 | 2 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0010t0001 | 0/0 | 2770 | 2 | 0 | 0 | 2 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0013t0002 | 0/0 | 2770 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0015t0008 | 0/0 | 2770 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0001c0016t0001 | 0/0 | 2770 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0002c0002t0001 | 0/0 | 2770 | 66 | 16 | 21 | 15 | 3 | 11 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0002c0002t0002 | 0/0 | 2770 | 11 | 4 | 2 | 5 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0002c0002t0003 | 0/1 | 2770 | 7 | 1 | 1 | 0 | 0 | 4 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0002c0018t0009 | 0/0 | 2770 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0002c0021t0002 | 0/0 | 2770 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0003c0004t0001 | 0/0 | 2770 | 7 | 7 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0004c0003t0005 | 0/0 | 2770 | 7 | 7 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0005c0007t0001 | 0/0 | 2770 | 4 | 0 | 0 | 4 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0005c0017t0002 | 0/0 | 2770 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0006c0006t0001 | 0/0 | 2770 | 4 | 4 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0007c0008t0007 | 0/0 | 2770 | 3 | 2 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0008c0011t0001 | 0/0 | 2770 | 2 | 2 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0009c0012t0002 | 0/0 | 2770 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0010c0020t0001 | 0/0 | 2770 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0011c0014t0001 | 0/0 | 2770 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| a0012c0019t0001 | 0/0 | 2770 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | ACCCC others(2765): Show |
chr5 | 39279140 | 39369495 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0004g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0004g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0001t0010g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0005t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0005t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0005t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0009t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0009t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0009t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0010t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0010t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0013t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0015t0008g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0001c0016t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0002g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0003g0284 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0002t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0018t0009g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0002c0021t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0003c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0003c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0003c0004t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0003c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0003c0004t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0003c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0003c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0004c0003t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0004c0003t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0004c0003t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0004c0003t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0004c0003t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0004c0003t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0005c0007t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0005c0007t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0005c0007t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0005c0017t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0006c0006t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0006c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0006c0006t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0006c0006t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0007c0008t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0007c0008t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0007c0008t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0008c0011t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0008c0011t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0009c0012t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0010c0020t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0011c0014t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| a0012c0019t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0074 | EUR | FIN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0368 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0345 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0338 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0295 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0332 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0316 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0331 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0350 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0355 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0361 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0291 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01167 | hp1 | a0001 | c0009 | t0002 | g0227 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01167 | hp2 | a0007 | c0008 | t0007 | g0137 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01169 | hp1 | a0001 | c0009 | t0002 | g0228 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01243 | hp1 | a0001 | c0005 | t0002 | g0272 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0344 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0356 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0358 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01496 | hp1 | a0002 | c0002 | t0003 | g0297 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0347 | EUR | IBS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0335 | EUR | IBS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0016 | EUR | IBS | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01884 | hp2 | a0001 | c0009 | t0002 | g0231 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0302 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0359 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0353 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0300 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0369 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02056 | hp2 | a0005 | c0007 | t0001 | g0168 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0315 | EAS | CDX | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CDX | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0287 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02258 | hp1 | a0003 | c0004 | t0001 | g0193 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02258 | hp2 | a0005 | c0017 | t0002 | g0229 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0343 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0360 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02572 | hp1 | a0006 | c0006 | t0001 | g0053 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0349 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0224 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0330 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0354 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02630 | hp2 | a0004 | c0003 | t0005 | g0005 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02647 | hp1 | a0003 | c0004 | t0001 | g0192 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0305 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0307 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02717 | hp1 | a0001 | c0013 | t0002 | g0119 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02723 | hp1 | a0004 | c0003 | t0005 | g0204 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02723 | hp2 | a0009 | c0012 | t0002 | g0276 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0323 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0325 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02818 | hp1 | a0006 | c0006 | t0001 | g0120 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0220 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02886 | hp2 | a0003 | c0004 | t0001 | g0268 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0319 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02895 | hp2 | a0004 | c0003 | t0005 | g0041 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02896 | hp2 | a0003 | c0004 | t0001 | g0270 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02897 | hp1 | a0003 | c0004 | t0001 | g0269 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0318 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0326 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02965 | hp1 | a0001 | c0005 | t0002 | g0012 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0351 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0186 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03017 | hp1 | a0002 | c0002 | t0003 | g0322 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0327 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0304 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0288 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03098 | hp2 | a0003 | c0004 | t0001 | g0267 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03130 | hp2 | a0006 | c0006 | t0001 | g0121 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03139 | hp1 | a0002 | c0021 | t0002 | g0289 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0286 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03195 | hp2 | a0007 | c0008 | t0007 | g0230 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03209 | hp1 | a0001 | c0005 | t0002 | g0023 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03225 | hp1 | a0004 | c0003 | t0005 | g0005 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03225 | hp2 | a0006 | c0006 | t0001 | g0183 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03486 | hp2 | a0007 | c0008 | t0007 | g0063 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0292 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0293 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0310 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0185 | AFR | GWD | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03579 | hp1 | a0004 | c0003 | t0005 | g0044 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03579 | hp2 | a0001 | c0005 | t0002 | g0012 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03710 | hp1 | a0002 | c0002 | t0003 | g0357 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03834 | hp1 | a0001 | c0015 | t0008 | g0138 | SAS | BEB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0329 | SAS | BEB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0283 | SAS | BEB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG04115 | hp1 | a0010 | c0020 | t0001 | g0309 | SAS | STU | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0321 | SAS | STU | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0311 | SAS | STU | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | STU | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | STU | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0282 | SAS | STU | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0320 | AFR | YRI | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18612 | hp2 | a0011 | c0014 | t0001 | g0178 | EAS | CHB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0352 | AFR | YRI | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18906 | hp2 | a0008 | c0011 | t0001 | g0324 | AFR | YRI | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18949 | hp1 | a0001 | c0010 | t0001 | g0077 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0362 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0365 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18966 | hp2 | a0005 | c0007 | t0001 | g0013 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18968 | hp2 | a0005 | c0007 | t0001 | g0233 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0339 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0363 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18993 | hp1 | a0005 | c0007 | t0001 | g0013 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0366 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18995 | hp2 | a0012 | c0019 | t0001 | g0306 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0337 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19006 | hp2 | a0001 | c0016 | t0001 | g0158 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19030 | hp2 | a0008 | c0011 | t0001 | g0285 | AFR | LWK | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | LWK | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0336 | AFR | LWK | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19062 | hp2 | a0001 | c0010 | t0001 | g0132 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0341 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19080 | hp2 | a0001 | c0001 | t0010 | g0364 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0367 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0348 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA19240 | hp2 | a0004 | c0003 | t0005 | g0219 | AFR | YRI | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ASW | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0314 | AFR | ASW | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0070 | EUR | TSI | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02559 | hp1 | a0002 | c0002 | t0003 | g0290 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG02559 | hp2 | a0004 | c0003 | t0005 | g0218 | AFR | ACB | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03471 | hp1 | a0003 | c0004 | t0001 | g0266 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | MSL | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG06807 | hp1 | a0002 | c0018 | t0009 | g0346 | AFR | USA | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0221 | AFR | USA | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | USA | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0333 | AFR | USA | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0284 | REF | REF | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0146 | REF | REF | C9_chr5_39279140_39369495 | C9 | chr5 | 39279140 | 39369495 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:39288800 | T | G | 1 | a0010 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1568A>C | p.Asp523Ala | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/11 | 1599/2770 | 1568/1680 | 523/559 | chr5 | 39288800 | |||
| chr5:39306754 | A | T | 1 | a0004 | 7 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
missense_variant | MODERATE | c.1279T>A | p.Ser427Thr | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/11 | 1310/2770 | 1279/1680 | 427/559 | chr5 | 39306754 | |||
| chr5:39308247 | C | T | 1 | a0011 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.1223G>A | p.Arg408Lys | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/11 | 1254/2770 | 1223/1680 | 408/559 | chr5 | 39308247 | |||
| chr5:39311269 | G | T | 1 | a0012 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.979C>A | p.Pro327Thr | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/11 | 1010/2770 | 979/1680 | 327/559 | chr5 | 39311269 | |||
| chr5:39315809 | G | C | 1 | a0007 | 3 | HG01167.hp2 HG03195.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.836C>G | p.Thr279Ser | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/11 | 867/2770 | 836/1680 | 279/559 | chr5 | 39315809 | |||
| chr5:39331684 | T | C | 2 | a0006 a0008 |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
missense_variant | MODERATE | c.607A>G | p.Ile203Val | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/11 | 638/2770 | 607/1680 | 203/559 | chr5 | 39331684 | |||
| chr5:39331711 | G | A | 1 | a0005 | 1 | HG02258.hp2 | stop_gained | HIGH | c.580C>T | p.Arg194* | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/11 | 611/2770 | 580/1680 | 194/559 | chr5 | 39331711 | |||
| chr5:39341206 | C | T | 1 | a0009 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.416G>A | p.Arg139His | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/11 | 447/2770 | 416/1680 | 139/559 | chr5 | 39341206 | |||
| chr5:39341243 | C | A | 1 | a0003 | 7 | HG02258.hp1 HG02647.hp1 HG02886.hp2 others(4): Show |
missense_variant | MODERATE | c.379G>T | p.Asp127Tyr | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/11 | 410/2770 | 379/1680 | 127/559 | chr5 | 39341243 | |||
| chr5:39341276 | G | A | 1 | a0005 | 4 | HG02056.hp2 NA18966.hp2 NA18968.hp2 others(1): Show |
stop_gained | HIGH | c.346C>T | p.Arg116* | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/11 | 377/2770 | 346/1680 | 116/559 | chr5 | 39341276 | |||
| chr5:39364452 | G | A | 4 | a0002 a0008 a0010 others(1): Show |
89 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(86): Show |
missense_variant | MODERATE | c.13C>T | p.Arg5Trp | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/11 | 44/2770 | 13/1680 | 5/559 | chr5 | 39364452 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:39288796 | T | C | 1 | a0001c0016 | 1 | NA19006.hp2 | synonymous_variant | LOW | c.1572A>G | p.Gly524Gly | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/11 | 1603/2770 | 1572/1680 | 524/559 | chr5 | 39288796 | |||
| chr5:39306632 | A | C | 1 | a0001c0015 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1401T>G | p.Val467Val | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/11 | 1432/2770 | 1401/1680 | 467/559 | chr5 | 39306632 | |||
| chr5:39311183 | G | C | 3 | a0001c0005 a0002c0021 a0009c0012 |
6 | HG01243.hp1 HG02723.hp2 HG02965.hp1 others(3): Show |
synonymous_variant | LOW | c.1065C>G | p.Leu355Leu | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/11 | 1096/2770 | 1065/1680 | 355/559 | chr5 | 39311183 | |||
| chr5:39316009 | G | A | 1 | a0001c0009 | 3 | HG01167.hp1 HG01169.hp1 HG01884.hp2 |
synonymous_variant | LOW | c.636C>T | p.Phe212Phe | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/11 | 667/2770 | 636/1680 | 212/559 | chr5 | 39316009 | |||
| chr5:39316021 | G | T | 1 | a0001c0013 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.624C>A | p.Gly208Gly | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/11 | 655/2770 | 624/1680 | 208/559 | chr5 | 39316021 | |||
| chr5:39331757 | A | G | 1 | a0002c0018 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.534T>C | p.Asn178Asn | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/11 | 565/2770 | 534/1680 | 178/559 | chr5 | 39331757 | |||
| chr5:39341205 | A | G | 1 | a0001c0010 | 2 | NA18949.hp1 NA19062.hp2 |
synonymous_variant | LOW | c.417T>C | p.Arg139Arg | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/11 | 448/2770 | 417/1680 | 139/559 | chr5 | 39341205 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:39284224 | C | A | 1 | a0004c0003t0005 | 7 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*975G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 11/11 | 975 | chr5 | 39284224 | ||||||
| chr5:39284313 | T | A | 2 | a0001c0001t0003 a0002c0002t0003 |
24 | HG00323.hp2 HG00558.hp2 HG01256.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*886A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 11/11 | 886 | chr5 | 39284313 | ||||||
| chr5:39284359 | C | T | 1 | a0004c0003t0005 | 7 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*840G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 11/11 | 840 | chr5 | 39284359 | ||||||
| chr5:39284363 | T | C | 1 | a0001c0015t0008 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 11/11 | 836 | chr5 | 39284363 | ||||||
| chr5:39284394 | C | A | 1 | a0002c0018t0009 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 11/11 | 805 | chr5 | 39284394 | ||||||
| chr5:39284619 | A | G | 1 | a0001c0001t0006 | 5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*580T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 11/11 | 580 | chr5 | 39284619 | ||||||
| chr5:39284858 | C | T | 1 | a0007c0008t0007 | 3 | HG01167.hp2 HG03195.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*341G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 11/11 | 341 | chr5 | 39284858 | ||||||
| chr5:39284885 | A | T | 1 | a0007c0008t0007 | 3 | HG01167.hp2 HG03195.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*314T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 11/11 | 314 | chr5 | 39284885 | ||||||
| chr5:39285037 | T | A | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 11/11 | 162 | chr5 | 39285037 | ||||||
| chr5:39364479 | G | A | 2 | a0001c0001t0004 a0001c0001t0010 |
10 | HG00438.hp1 HG02056.hp1 NA18952.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-15C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/11 | 15 | chr5 | 39364479 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:39285236 | A | G | 2 | a0007c0008t0007g0137 a0007c0008t0007g0230 |
2 | HG01167.hp2 HG03195.hp2 |
splice_region_variant&intron_variant | LOW | c.1646-3T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39285236 | |||||||
| chr5:39285508 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1646-275A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39285508 | |||||||
| chr5:39285700 | C | CT | 67 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(64): Show |
69 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1646-468dupA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39285700 | |||||||
| chr5:39285784 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(186): Show |
204 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1646-551G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39285784 | |||||||
| chr5:39285890 | C | T | 5 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1646-657G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39285890 | |||||||
| chr5:39285960 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG00280.hp1 HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1646-727A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39285960 | |||||||
| chr5:39286005 | C | CT | 5 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1646-773dupA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39286005 | |||||||
| chr5:39286200 | C | A | 1 | a0001c0001t0003g0240 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1646-967G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39286200 | |||||||
| chr5:39286318 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1646-1085C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39286318 | |||||||
| chr5:39286345 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1646-1112A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39286345 | |||||||
| chr5:39286579 | A | C | 1 | a0009c0012t0002g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1646-1346T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39286579 | |||||||
| chr5:39286607 | A | G | 34 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(31): Show |
38 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.1646-1374T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39286607 | |||||||
| chr5:39286715 | TGA | T | 70 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(67): Show |
72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1646-1484_1646-148 others(6): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39286715 | |||||||
| chr5:39286879 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1646-1646C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39286879 | |||||||
| chr5:39286965 | C | T | 1 | a0002c0002t0002g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1646-1732G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39286965 | |||||||
| chr5:39287133 | C | G | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1645+1590G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39287133 | |||||||
| chr5:39287156 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1645+1567T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39287156 | |||||||
| chr5:39287360 | T | G | 1 | a0001c0005t0002g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1645+1363A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39287360 | |||||||
| chr5:39287447 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1645+1276C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39287447 | |||||||
| chr5:39287586 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(146): Show |
159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1645+1137T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39287586 | |||||||
| chr5:39287702 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1645+1021G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39287702 | |||||||
| chr5:39287728 | A | T | 1 | a0008c0011t0001g0324 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1645+995T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39287728 | |||||||
| chr5:39287787 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1645+936G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39287787 | |||||||
| chr5:39287804 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(140): Show |
153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1645+919A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39287804 | |||||||
| chr5:39287937 | C | A | 1 | a0002c0002t0001g0310 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1645+786G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39287937 | |||||||
| chr5:39288012 | T | C | 2 | a0008c0011t0001g0285 a0008c0011t0001g0324 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1645+711A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39288012 | |||||||
| chr5:39288063 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(146): Show |
159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1645+660G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39288063 | |||||||
| chr5:39288250 | A | G | 1 | a0001c0001t0002g0223 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1645+473T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39288250 | |||||||
| chr5:39288316 | C | G | 13 | a0001c0001t0001g0067 a0001c0001t0001g0079 a0001c0001t0001g0170 others(10): Show |
13 | HG00621.hp2 HG00735.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1645+407G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39288316 | |||||||
| chr5:39288417 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1645+306A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39288417 | |||||||
| chr5:39288419 | T | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG00280.hp2 HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1645+304A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39288419 | |||||||
| chr5:39288427 | A | G | 23 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0064 others(20): Show |
24 | HG00323.hp2 HG00558.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1645+296T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39288427 | |||||||
| chr5:39288640 | T | G | 1 | a0001c0001t0001g0252 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1645+83A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39288640 | |||||||
| chr5:39288672 | C | A | 9 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 others(6): Show |
9 | HG01192.hp1 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1645+51G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39288672 | |||||||
| chr5:39288709 | T | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0002c0002t0001g0333 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1645+14A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 10/10 | chr5 | 39288709 | |||||||
| chr5:39289000 | A | G | 2 | a0002c0002t0002g0288 a0002c0002t0002g0352 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1417-49T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39289000 | |||||||
| chr5:39289085 | G | A | 3 | a0001c0005t0002g0023 a0002c0021t0002g0289 a0009c0012t0002g0276 |
3 | HG02723.hp2 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1417-134C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39289085 | |||||||
| chr5:39289441 | G | GT | 188 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(185): Show |
203 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1417-491dupA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39289441 | |||||||
| chr5:39289548 | A | G | 1 | a0002c0002t0001g0336 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1417-597T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39289548 | |||||||
| chr5:39289590 | A | G | 10 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0002c0002t0001g0333 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417-639T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39289590 | |||||||
| chr5:39289630 | G | A | 2 | a0002c0002t0002g0288 a0002c0002t0002g0352 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1417-679C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39289630 | |||||||
| chr5:39289707 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1417-756C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39289707 | |||||||
| chr5:39289834 | T | C | 1 | a0001c0001t0003g0074 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1417-883A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39289834 | |||||||
| chr5:39289929 | T | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | NA18988.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1417-978A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39289929 | |||||||
| chr5:39290089 | G | A | 1 | a0001c0001t0003g0240 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1417-1138C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290089 | |||||||
| chr5:39290100 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1417-1149T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290100 | |||||||
| chr5:39290304 | T | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0251 a0001c0001t0001g0259 |
3 | NA18960.hp1 NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1417-1353A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290304 | |||||||
| chr5:39290347 | G | C | 34 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(31): Show |
38 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.1417-1396C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290347 | |||||||
| chr5:39290379 | A | G | 1 | a0001c0001t0006g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1417-1428T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290379 | |||||||
| chr5:39290440 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1417-1489A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290440 | |||||||
| chr5:39290445 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1417-1494G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290445 | |||||||
| chr5:39290454 | AAAAC | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(185): Show |
203 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1417-1507_1417-150 others(8): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290454 | |||||||
| chr5:39290593 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0252 |
2 | NA18954.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1417-1642T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290593 | |||||||
| chr5:39290635 | C | G | 362 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(359): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.1417-1684G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290635 | |||||||
| chr5:39290703 | C | G | 49 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0033 others(46): Show |
54 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1417-1752G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290703 | |||||||
| chr5:39290716 | G | A | 1 | a0001c0013t0002g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1417-1765C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290716 | |||||||
| chr5:39290810 | C | T | 334 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(331): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1417-1859G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39290810 | |||||||
| chr5:39291029 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1417-2078C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39291029 | |||||||
| chr5:39291046 | C | T | 1 | a0002c0002t0001g0301 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1417-2095G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39291046 | |||||||
| chr5:39291201 | G | A | 40 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(37): Show |
45 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(42): Show |
intron_variant | MODIFIER | c.1417-2250C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39291201 | |||||||
| chr5:39291261 | GA | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(146): Show |
159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1417-2311delT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39291261 | |||||||
| chr5:39291268 | AG | A | 5 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1417-2318delC | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39291268 | |||||||
| chr5:39291453 | A | T | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1417-2502T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39291453 | |||||||
| chr5:39291584 | G | A | 15 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 others(12): Show |
16 | HG01192.hp1 HG02559.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1417-2633C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39291584 | |||||||
| chr5:39291923 | C | A | 1 | a0001c0001t0003g0225 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1417-2972G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39291923 | |||||||
| chr5:39291989 | C | A | 93 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1417-3038G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39291989 | |||||||
| chr5:39292049 | T | C | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1417-3098A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292049 | |||||||
| chr5:39292062 | A | C | 1 | a0001c0001t0004g0362 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1417-3111T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292062 | |||||||
| chr5:39292199 | A | G | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1417-3248T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292199 | |||||||
| chr5:39292252 | A | G | 1 | a0002c0002t0001g0298 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1417-3301T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292252 | |||||||
| chr5:39292300 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1417-3349T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292300 | |||||||
| chr5:39292343 | C | A | 1 | a0001c0001t0003g0036 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1417-3392G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292343 | |||||||
| chr5:39292353 | A | C | 1 | a0002c0002t0001g0305 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1417-3402T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292353 | |||||||
| chr5:39292377 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1417-3426A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292377 | |||||||
| chr5:39292405 | TG | T | 9 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 others(6): Show |
9 | HG01192.hp1 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1417-3455delC | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292405 | |||||||
| chr5:39292416 | C | CT | 49 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0033 others(46): Show |
54 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1417-3466dupA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292416 | |||||||
| chr5:39292465 | G | T | 7 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0161 others(4): Show |
7 | HG00609.hp2 NA18944.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1417-3514C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292465 | |||||||
| chr5:39292492 | T | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0118 |
2 | HG03688.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1417-3541A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292492 | |||||||
| chr5:39292639 | C | T | 2 | a0001c0001t0001g0095 a0004c0003t0005g0218 |
2 | HG02559.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1417-3688G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292639 | |||||||
| chr5:39292668 | T | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0002c0002t0001g0333 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417-3717A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292668 | |||||||
| chr5:39292867 | A | AGTAAAAA others(331): Show |
1 | a0002c0002t0001g0317 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1417-3917_1417-391 others(342): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(330): Show |
1 | a0001c0001t0001g0207 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1417-3917_1417-391 others(341): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(329): Show |
2 | a0001c0001t0001g0088 a0001c0001t0001g0171 |
2 | NA18962.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(340): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(330): Show |
3 | a0001c0001t0001g0170 a0001c0001t0001g0206 a0001c0001t0001g0208 |
3 | HG00621.hp2 NA18966.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(341): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(333): Show |
1 | a0001c0001t0001g0114 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1417-3917_1417-391 others(344): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(328): Show |
1 | a0001c0001t0001g0105 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1417-3917_1417-391 others(339): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(329): Show |
10 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0087 others(7): Show |
10 | HG01081.hp2 HG01943.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(340): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(330): Show |
6 | a0001c0001t0001g0027 a0001c0001t0001g0079 a0001c0001t0001g0082 others(3): Show |
6 | HG00438.hp2 HG01109.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(341): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(331): Show |
6 | a0001c0001t0001g0030 a0001c0001t0001g0065 a0001c0001t0001g0080 others(3): Show |
6 | HG00639.hp1 HG01074.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(342): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(332): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0112 |
2 | HG00280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(343): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(333): Show |
1 | a0001c0001t0001g0113 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1417-3917_1417-391 others(344): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(315): Show |
1 | a0002c0002t0001g0338 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1417-3917_1417-391 others(326): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(327): Show |
1 | a0001c0001t0001g0091 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1417-3917_1417-391 others(338): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(328): Show |
1 | a0001c0001t0001g0184 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1417-3917_1417-391 others(339): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(329): Show |
10 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0097 others(7): Show |
11 | HG00099.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(340): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(329): Show |
1 | a0001c0001t0001g0006 | 2 | NA18973.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(340): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(330): Show |
7 | a0001c0001t0001g0039 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG01123.hp2 HG01175.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(341): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(331): Show |
4 | a0001c0001t0001g0078 a0001c0001t0001g0090 a0001c0001t0001g0141 others(1): Show |
4 | HG00597.hp1 HG00597.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(342): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(316): Show |
1 | a0002c0002t0001g0343 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1417-3917_1417-391 others(327): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(329): Show |
4 | a0001c0001t0001g0067 a0001c0001t0001g0271 a0001c0001t0001g0275 others(1): Show |
4 | HG01099.hp2 HG01884.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(340): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(330): Show |
2 | a0001c0001t0001g0060 a0001c0001t0001g0200 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(341): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292867 | A | AGTAAAAA others(331): Show |
2 | a0001c0001t0001g0059 a0002c0002t0001g0344 |
2 | HG01255.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1417-3917_1417-391 others(342): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292867 | |||||||
| chr5:39292899 | A | C | 1 | a0007c0008t0007g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1417-3948T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292899 | |||||||
| chr5:39292991 | C | T | 2 | a0001c0005t0002g0012 a0001c0005t0002g0272 |
3 | HG01243.hp1 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1417-4040G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39292991 | |||||||
| chr5:39293008 | GT | G | 4 | a0001c0001t0002g0234 a0001c0001t0002g0273 a0001c0001t0002g0274 others(1): Show |
5 | HG02145.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1417-4058delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293008 | |||||||
| chr5:39293009 | T | C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0073 others(27): Show |
32 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1417-4058A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293009 | |||||||
| chr5:39293023 | C | G | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1417-4072G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293023 | |||||||
| chr5:39293040 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG01071.hp1 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1417-4089C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293040 | |||||||
| chr5:39293054 | C | G | 362 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(359): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.1417-4103G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293054 | |||||||
| chr5:39293133 | G | A | 1 | a0002c0002t0001g0321 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1417-4182C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293133 | |||||||
| chr5:39293168 | C | A | 1 | a0002c0002t0002g0303 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1417-4217G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293168 | |||||||
| chr5:39293194 | A | G | 348 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(345): Show |
372 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.1417-4243T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293194 | |||||||
| chr5:39293241 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1417-4290T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293241 | |||||||
| chr5:39293583 | G | A | 49 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0033 others(46): Show |
54 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1417-4632C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293583 | |||||||
| chr5:39293589 | C | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1417-4638G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293589 | |||||||
| chr5:39293739 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1417-4788C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293739 | |||||||
| chr5:39293952 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0002c0002t0001g0361 |
3 | HG01109.hp1 HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1417-5001A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39293952 | |||||||
| chr5:39294075 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1417-5124A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39294075 | |||||||
| chr5:39294476 | A | C | 5 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1417-5525T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39294476 | |||||||
| chr5:39294606 | T | C | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1417-5655A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39294606 | |||||||
| chr5:39294624 | C | G | 1 | a0001c0001t0001g0264 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1417-5673G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39294624 | |||||||
| chr5:39294701 | C | T | 48 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0033 others(45): Show |
53 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1417-5750G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39294701 | |||||||
| chr5:39294758 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1417-5807T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39294758 | |||||||
| chr5:39294831 | A | G | 9 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 others(6): Show |
9 | HG01192.hp1 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1417-5880T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39294831 | |||||||
| chr5:39294891 | C | T | 50 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(47): Show |
56 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1417-5940G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39294891 | |||||||
| chr5:39294959 | A | G | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1417-6008T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39294959 | |||||||
| chr5:39294975 | A | T | 2 | a0002c0002t0002g0288 a0002c0002t0002g0352 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1417-6024T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39294975 | |||||||
| chr5:39295012 | C | T | 1 | a0001c0005t0002g0012 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1417-6061G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39295012 | |||||||
| chr5:39295159 | C | T | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1417-6208G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39295159 | |||||||
| chr5:39295199 | C | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0090 others(4): Show |
8 | HG00099.hp2 HG01123.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1417-6248G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39295199 | |||||||
| chr5:39295199 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(3): Show |
6 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1417-6248G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39295199 | |||||||
| chr5:39295471 | A | G | 4 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1417-6520T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39295471 | |||||||
| chr5:39295877 | T | C | 1 | a0001c0001t0006g0186 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1417-6926A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39295877 | |||||||
| chr5:39296003 | C | T | 3 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 |
3 | HG02572.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1417-7052G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296003 | |||||||
| chr5:39296120 | A | G | 1 | a0002c0002t0001g0312 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1417-7169T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296120 | |||||||
| chr5:39296175 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1417-7224T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296175 | |||||||
| chr5:39296208 | C | T | 23 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0064 others(20): Show |
24 | HG00323.hp2 HG00558.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1417-7257G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296208 | |||||||
| chr5:39296280 | G | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(96): Show |
102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1417-7329C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296280 | |||||||
| chr5:39296372 | AT | A | 34 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(31): Show |
38 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.1417-7422delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296372 | |||||||
| chr5:39296420 | G | A | 3 | a0001c0005t0002g0023 a0002c0021t0002g0289 a0009c0012t0002g0276 |
3 | HG02723.hp2 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1417-7469C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296420 | |||||||
| chr5:39296590 | A | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(96): Show |
102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1417-7639T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296590 | |||||||
| chr5:39296638 | C | T | 49 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0033 others(46): Show |
54 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1417-7687G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296638 | |||||||
| chr5:39296639 | G | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0002c0002t0001g0333 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417-7688C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296639 | |||||||
| chr5:39296760 | G | A | 5 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1417-7809C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296760 | |||||||
| chr5:39296943 | G | C | 69 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(66): Show |
71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1417-7992C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296943 | |||||||
| chr5:39296964 | C | A | 4 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1417-8013G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39296964 | |||||||
| chr5:39297025 | T | A | 2 | a0002c0002t0002g0288 a0002c0002t0002g0352 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1417-8074A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39297025 | |||||||
| chr5:39297121 | A | G | 3 | a0007c0008t0007g0063 a0007c0008t0007g0137 a0007c0008t0007g0230 |
3 | HG01167.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1417-8170T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39297121 | |||||||
| chr5:39297155 | AT | A | 3 | a0007c0008t0007g0063 a0007c0008t0007g0137 a0007c0008t0007g0230 |
3 | HG01167.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1417-8205delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39297155 | |||||||
| chr5:39297623 | T | G | 50 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(47): Show |
56 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1417-8672A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39297623 | |||||||
| chr5:39297639 | A | T | 23 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0064 others(20): Show |
24 | HG00323.hp2 HG00558.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1417-8688T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39297639 | |||||||
| chr5:39297662 | A | G | 1 | a0002c0002t0001g0325 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1417-8711T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39297662 | |||||||
| chr5:39297692 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1417-8741T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39297692 | |||||||
| chr5:39297823 | G | A | 2 | a0001c0001t0001g0047 a0002c0002t0001g0347 |
2 | HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1416+8794C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39297823 | |||||||
| chr5:39297995 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1416+8622T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39297995 | |||||||
| chr5:39298245 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1416+8372G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39298245 | |||||||
| chr5:39298297 | A | G | 2 | a0002c0002t0002g0288 a0002c0002t0002g0352 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1416+8320T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39298297 | |||||||
| chr5:39298306 | A | G | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1416+8311T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39298306 | |||||||
| chr5:39298365 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(146): Show |
159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1416+8252G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39298365 | |||||||
| chr5:39298395 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1416+8222A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39298395 | |||||||
| chr5:39298763 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1416+7854G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39298763 | |||||||
| chr5:39298935 | T | A | 2 | a0002c0002t0001g0300 a0002c0002t0001g0302 |
2 | HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1416+7682A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39298935 | |||||||
| chr5:39298998 | G | A | 1 | a0001c0001t0004g0362 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1416+7619C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39298998 | |||||||
| chr5:39299211 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1416+7406A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299211 | |||||||
| chr5:39299339 | A | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1416+7278T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299339 | |||||||
| chr5:39299378 | G | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0002c0002t0001g0333 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1416+7239C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299378 | |||||||
| chr5:39299457 | CTG | C | 8 | a0001c0001t0001g0102 a0001c0001t0001g0177 a0001c0001t0001g0242 others(5): Show |
11 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1416+7158_1416+715 others(6): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299457 | |||||||
| chr5:39299482 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(186): Show |
204 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1416+7135G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299482 | |||||||
| chr5:39299584 | A | T | 1 | a0012c0019t0001g0306 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1416+7033T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299584 | |||||||
| chr5:39299586 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1416+7031A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299586 | |||||||
| chr5:39299613 | G | A | 357 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(354): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1416+7004C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299613 | |||||||
| chr5:39299678 | T | C | 3 | a0007c0008t0007g0063 a0007c0008t0007g0137 a0007c0008t0007g0230 |
3 | HG01167.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1416+6939A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299678 | |||||||
| chr5:39299742 | G | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(96): Show |
102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1416+6875C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299742 | |||||||
| chr5:39299758 | G | C | 3 | a0001c0009t0002g0227 a0001c0009t0002g0228 a0001c0009t0002g0231 |
3 | HG01167.hp1 HG01169.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1416+6859C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299758 | |||||||
| chr5:39299939 | C | A | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1416+6678G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299939 | |||||||
| chr5:39299940 | T | G | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1416+6677A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39299940 | |||||||
| chr5:39300009 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1416+6608T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39300009 | |||||||
| chr5:39300077 | A | G | 10 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0002c0002t0001g0333 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1416+6540T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39300077 | |||||||
| chr5:39300150 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1416+6467A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39300150 | |||||||
| chr5:39300241 | G | C | 1 | a0001c0001t0001g0207 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1416+6376C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39300241 | |||||||
| chr5:39300363 | G | C | 1 | a0001c0001t0001g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1416+6254C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39300363 | |||||||
| chr5:39300405 | C | T | 1 | a0002c0002t0002g0352 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1416+6212G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39300405 | |||||||
| chr5:39300434 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1416+6183C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39300434 | |||||||
| chr5:39300601 | A | C | 1 | a0001c0001t0002g0223 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1416+6016T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39300601 | |||||||
| chr5:39300717 | A | G | 10 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0002c0002t0001g0333 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1416+5900T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39300717 | |||||||
| chr5:39301029 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1416+5588T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301029 | |||||||
| chr5:39301057 | A | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(146): Show |
159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1416+5560T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301057 | |||||||
| chr5:39301075 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(146): Show |
159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1416+5542T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301075 | |||||||
| chr5:39301256 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1416+5361C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301256 | |||||||
| chr5:39301276 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1416+5341T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301276 | |||||||
| chr5:39301332 | G | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(140): Show |
153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1416+5285C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301332 | |||||||
| chr5:39301392 | A | G | 1 | a0001c0001t0002g0057 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1416+5225T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301392 | |||||||
| chr5:39301453 | G | A | 1 | a0009c0012t0002g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1416+5164C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301453 | |||||||
| chr5:39301580 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1416+5037G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301580 | |||||||
| chr5:39301718 | T | TA | 98 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(95): Show |
101 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1416+4898dupT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301718 | |||||||
| chr5:39301757 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1416+4860T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301757 | |||||||
| chr5:39301773 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1416+4844A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301773 | |||||||
| chr5:39301886 | T | C | 2 | a0001c0001t0002g0198 a0001c0001t0002g0199 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1416+4731A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301886 | |||||||
| chr5:39301998 | C | T | 98 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(95): Show |
101 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1416+4619G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39301998 | |||||||
| chr5:39302111 | G | C | 35 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(32): Show |
39 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.1416+4506C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302111 | |||||||
| chr5:39302128 | G | C | 2 | a0002c0002t0002g0288 a0002c0002t0002g0352 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1416+4489C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302128 | |||||||
| chr5:39302191 | T | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0002c0002t0001g0333 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1416+4426A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302191 | |||||||
| chr5:39302366 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(187): Show |
205 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1416+4251A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302366 | |||||||
| chr5:39302479 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1416+4138G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302479 | |||||||
| chr5:39302745 | A | G | 1 | a0006c0006t0001g0183 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1416+3872T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302745 | |||||||
| chr5:39302828 | T | G | 98 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(95): Show |
101 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1416+3789A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302828 | |||||||
| chr5:39302879 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(187): Show |
205 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1416+3738G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302879 | |||||||
| chr5:39302919 | T | C | 2 | a0002c0002t0002g0288 a0002c0002t0002g0352 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1416+3698A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302919 | |||||||
| chr5:39302927 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1416+3690C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302927 | |||||||
| chr5:39302936 | A | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0139 a0001c0001t0001g0150 others(4): Show |
8 | HG01081.hp1 HG01257.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1416+3681T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302936 | |||||||
| chr5:39302941 | G | A | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1416+3676C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39302941 | |||||||
| chr5:39303214 | A | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0002c0002t0001g0333 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1416+3403T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39303214 | |||||||
| chr5:39303291 | T | C | 2 | a0002c0002t0003g0292 a0002c0002t0003g0293 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1416+3326A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39303291 | |||||||
| chr5:39303357 | G | A | 4 | a0001c0001t0003g0064 a0001c0001t0003g0074 a0002c0002t0003g0292 others(1): Show |
4 | HG00323.hp2 HG02683.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1416+3260C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39303357 | |||||||
| chr5:39303363 | C | G | 50 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0011 others(47): Show |
56 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1416+3254G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39303363 | |||||||
| chr5:39303485 | G | C | 23 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0064 others(20): Show |
24 | HG00323.hp2 HG00558.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1416+3132C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39303485 | |||||||
| chr5:39303705 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1416+2912T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39303705 | |||||||
| chr5:39303823 | T | A | 49 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0033 others(46): Show |
54 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1416+2794A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39303823 | |||||||
| chr5:39303864 | T | C | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1416+2753A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39303864 | |||||||
| chr5:39303865 | G | T | 3 | a0007c0008t0007g0063 a0007c0008t0007g0137 a0007c0008t0007g0230 |
3 | HG01167.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1416+2752C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39303865 | |||||||
| chr5:39303905 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1416+2712G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39303905 | |||||||
| chr5:39304157 | A | G | 5 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1416+2460T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39304157 | |||||||
| chr5:39304471 | T | C | 1 | a0001c0001t0003g0099 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1416+2146A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39304471 | |||||||
| chr5:39304681 | C | T | 10 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0001t0001g0222 others(7): Show |
10 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1416+1936G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39304681 | |||||||
| chr5:39304820 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1416+1797T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39304820 | |||||||
| chr5:39305467 | GT | G | 11 | a0001c0001t0002g0169 a0001c0001t0002g0195 a0001c0001t0002g0209 others(8): Show |
11 | HG00621.hp1 HG02040.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416+1149delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39305467 | |||||||
| chr5:39305492 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1416+1125A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39305492 | |||||||
| chr5:39305644 | T | G | 1 | a0001c0001t0003g0238 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1416+973A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39305644 | |||||||
| chr5:39305782 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1416+835A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39305782 | |||||||
| chr5:39305810 | T | A | 1 | a0002c0002t0001g0334 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1416+807A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39305810 | |||||||
| chr5:39305830 | T | C | 1 | a0007c0008t0007g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1416+787A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39305830 | |||||||
| chr5:39306089 | G | A | 1 | a0001c0001t0006g0221 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1416+528C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306089 | |||||||
| chr5:39306162 | C | CA | 12 | a0001c0001t0001g0029 a0001c0001t0001g0092 a0001c0001t0001g0110 others(9): Show |
12 | HG01981.hp2 HG02258.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1416+454dupT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306162 | |||||||
| chr5:39306162 | CA | C | 39 | a0001c0001t0001g0032 a0001c0001t0001g0105 a0001c0001t0002g0011 others(36): Show |
42 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1416+454delT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306162 | |||||||
| chr5:39306162 | CAA | C | 44 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(41): Show |
49 | HG00438.hp1 HG00609.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1416+453_1416+454d others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306162 | |||||||
| chr5:39306162 | CAAA | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(131): Show |
143 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1416+452_1416+454d others(5): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306162 | |||||||
| chr5:39306333 | T | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1416+284A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306333 | |||||||
| chr5:39306406 | A | T | 9 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 others(6): Show |
9 | HG01192.hp1 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1416+211T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306406 | |||||||
| chr5:39306408 | A | G | 6 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(3): Show |
7 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1416+209T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306408 | |||||||
| chr5:39306413 | G | A | 23 | a0001c0001t0002g0002 a0001c0001t0002g0052 a0001c0001t0002g0054 others(20): Show |
26 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1416+204C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306413 | |||||||
| chr5:39306444 | C | G | 6 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(3): Show |
7 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1416+173G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306444 | |||||||
| chr5:39306520 | G | C | 1 | a0008c0011t0001g0324 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1416+97C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 9/10 | chr5 | 39306520 | |||||||
| chr5:39307026 | T | C | 98 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(95): Show |
101 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1241-234A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39307026 | |||||||
| chr5:39307029 | T | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(95): Show |
101 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1241-237A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39307029 | |||||||
| chr5:39307153 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-361T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39307153 | |||||||
| chr5:39307186 | T | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-394A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39307186 | |||||||
| chr5:39307209 | G | A | 2 | a0002c0002t0001g0318 a0002c0002t0001g0319 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1241-417C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39307209 | |||||||
| chr5:39307250 | T | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-458A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39307250 | |||||||
| chr5:39307584 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1240+646C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39307584 | |||||||
| chr5:39307906 | T | G | 1 | a0001c0001t0001g0145 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1240+324A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39307906 | |||||||
| chr5:39307909 | T | A | 1 | a0001c0001t0001g0029 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1240+321A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39307909 | |||||||
| chr5:39308077 | G | A | 6 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(3): Show |
7 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+153C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39308077 | |||||||
| chr5:39308101 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1240+129C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39308101 | |||||||
| chr5:39308228 | A | G | 1 | a0001c0001t0002g0226 | 1 | HG01891.hp2 | splice_donor_variant&intron_variant | HIGH | c.1240+2T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 8/10 | chr5 | 39308228 | |||||||
| chr5:39308676 | A | G | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1112-318T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39308676 | |||||||
| chr5:39308949 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(184): Show |
203 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1112-591A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39308949 | |||||||
| chr5:39308988 | G | A | 34 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(31): Show |
38 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.1112-630C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39308988 | |||||||
| chr5:39309098 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1112-740G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309098 | |||||||
| chr5:39309164 | A | T | 1 | a0004c0003t0005g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1112-806T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309164 | |||||||
| chr5:39309165 | TA | T | 46 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0033 others(43): Show |
51 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.1112-808delT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309165 | |||||||
| chr5:39309248 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1112-890T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309248 | |||||||
| chr5:39309269 | AAC | A | 3 | a0001c0001t0001g0123 a0002c0002t0001g0307 a0002c0002t0001g0310 |
3 | HG02698.hp2 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1112-913_1112-912d others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309269 | |||||||
| chr5:39309287 | T | C | 11 | a0001c0001t0002g0037 a0001c0001t0002g0198 a0001c0001t0002g0199 others(8): Show |
11 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1112-929A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309287 | |||||||
| chr5:39309311 | T | C | 3 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02970.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1112-953A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309311 | |||||||
| chr5:39309521 | T | C | 11 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0002g0197 others(8): Show |
11 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1112-1163A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309521 | |||||||
| chr5:39309543 | G | A | 2 | a0002c0002t0002g0288 a0002c0002t0002g0352 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1112-1185C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309543 | |||||||
| chr5:39309723 | C | T | 1 | a0001c0013t0002g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1112-1365G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309723 | |||||||
| chr5:39309887 | T | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0052 |
5 | HG00639.hp2 HG00738.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111+1250A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309887 | |||||||
| chr5:39309951 | C | T | 25 | a0001c0001t0002g0195 a0001c0001t0003g0014 a0001c0001t0003g0036 others(22): Show |
26 | HG00323.hp2 HG00558.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1111+1186G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309951 | |||||||
| chr5:39309971 | C | T | 5 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111+1166G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39309971 | |||||||
| chr5:39310081 | C | G | 41 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(38): Show |
46 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.1111+1056G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39310081 | |||||||
| chr5:39310094 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111+1043G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39310094 | |||||||
| chr5:39310221 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1111+916G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39310221 | |||||||
| chr5:39310341 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(184): Show |
203 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1111+796G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39310341 | |||||||
| chr5:39310486 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(3): Show |
6 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111+651T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39310486 | |||||||
| chr5:39310500 | C | T | 8 | a0001c0001t0001g0047 a0002c0002t0001g0016 a0002c0002t0001g0017 others(5): Show |
10 | HG00642.hp2 HG01169.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1111+637G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39310500 | |||||||
| chr5:39310603 | A | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111+534T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39310603 | |||||||
| chr5:39310759 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(143): Show |
157 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1111+378T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39310759 | |||||||
| chr5:39310873 | A | G | 1 | a0002c0002t0002g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1111+264T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39310873 | |||||||
| chr5:39311010 | G | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0139 a0001c0001t0001g0151 others(3): Show |
7 | HG01081.hp1 HG01257.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111+127C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 7/10 | chr5 | 39311010 | |||||||
| chr5:39311404 | G | T | 4 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-27C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39311404 | |||||||
| chr5:39311501 | C | G | 12 | a0001c0001t0002g0004 a0001c0001t0002g0033 a0001c0001t0002g0034 others(9): Show |
13 | HG01192.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.871-124G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39311501 | |||||||
| chr5:39311514 | A | G | 1 | a0002c0002t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.871-137T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39311514 | |||||||
| chr5:39311515 | G | A | 1 | a0007c0008t0007g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.871-138C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39311515 | |||||||
| chr5:39311584 | T | G | 1 | a0001c0001t0001g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.871-207A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39311584 | |||||||
| chr5:39311597 | TAGAC | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-224_871-221del others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39311597 | |||||||
| chr5:39312030 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(183): Show |
202 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.871-653C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312030 | |||||||
| chr5:39312039 | C | T | 53 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(50): Show |
55 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.871-662G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312039 | |||||||
| chr5:39312109 | G | A | 4 | a0002c0002t0001g0318 a0002c0002t0001g0319 a0002c0002t0001g0326 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-732C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312109 | |||||||
| chr5:39312287 | T | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0033 a0001c0001t0002g0034 |
4 | HG02109.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-910A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312287 | |||||||
| chr5:39312345 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(183): Show |
202 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.871-968C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312345 | |||||||
| chr5:39312370 | C | A | 34 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(31): Show |
38 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.871-993G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312370 | |||||||
| chr5:39312371 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.871-994A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312371 | |||||||
| chr5:39312438 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.871-1061T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312438 | |||||||
| chr5:39312451 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-1074A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312451 | |||||||
| chr5:39312479 | T | C | 3 | a0001c0001t0001g0203 a0002c0002t0001g0286 a0002c0002t0001g0287 |
3 | HG02257.hp1 HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.871-1102A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312479 | |||||||
| chr5:39312546 | C | T | 1 | a0001c0001t0010g0364 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.871-1169G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312546 | |||||||
| chr5:39312570 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-1193T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312570 | |||||||
| chr5:39312620 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(146): Show |
160 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.871-1243G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312620 | |||||||
| chr5:39312635 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.871-1258G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312635 | |||||||
| chr5:39312730 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.871-1353G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312730 | |||||||
| chr5:39312765 | G | C | 2 | a0008c0011t0001g0285 a0008c0011t0001g0324 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.871-1388C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312765 | |||||||
| chr5:39312837 | C | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-1460G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312837 | |||||||
| chr5:39312979 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-1602G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39312979 | |||||||
| chr5:39313031 | A | G | 3 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02970.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.871-1654T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313031 | |||||||
| chr5:39313205 | T | C | 27 | a0001c0001t0002g0002 a0001c0001t0002g0052 a0001c0001t0002g0054 others(24): Show |
31 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.871-1828A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313205 | |||||||
| chr5:39313370 | ACTTCTTA others(8): Show |
A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(97): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.871-2008_871-1994d others(17): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313370 | |||||||
| chr5:39313478 | G | A | 35 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(32): Show |
39 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.871-2101C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313478 | |||||||
| chr5:39313536 | T | C | 1 | a0001c0001t0002g0216 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.871-2159A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313536 | |||||||
| chr5:39313571 | C | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0181 |
2 | NA18963.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.871-2194G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313571 | |||||||
| chr5:39313605 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.870+2170T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313605 | |||||||
| chr5:39313624 | C | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0002c0002t0001g0333 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.870+2151G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313624 | |||||||
| chr5:39313755 | C | T | 12 | a0001c0001t0002g0004 a0001c0001t0002g0033 a0001c0001t0002g0034 others(9): Show |
13 | HG01192.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.870+2020G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313755 | |||||||
| chr5:39313818 | C | G | 1 | a0001c0001t0001g0040 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.870+1957G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313818 | |||||||
| chr5:39313867 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.870+1908T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39313867 | |||||||
| chr5:39314102 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.870+1673T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314102 | |||||||
| chr5:39314215 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.870+1560G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314215 | |||||||
| chr5:39314304 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+1471G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314304 | |||||||
| chr5:39314364 | G | T | 4 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+1411C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314364 | |||||||
| chr5:39314389 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+1386A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314389 | |||||||
| chr5:39314448 | T | C | 43 | a0001c0001t0002g0002 a0001c0001t0002g0037 a0001c0001t0002g0052 others(40): Show |
47 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.870+1327A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314448 | |||||||
| chr5:39314457 | A | ATAAATTA others(3): Show |
2 | a0008c0011t0001g0285 a0008c0011t0001g0324 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.870+1308_870+1317d others(12): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314457 | |||||||
| chr5:39314559 | A | G | 1 | a0009c0012t0002g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.870+1216T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314559 | |||||||
| chr5:39314645 | T | C | 9 | a0001c0001t0001g0047 a0002c0002t0001g0016 a0002c0002t0001g0017 others(6): Show |
11 | HG00642.hp2 HG01169.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.870+1130A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314645 | |||||||
| chr5:39314673 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.870+1102G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314673 | |||||||
| chr5:39314753 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+1022T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314753 | |||||||
| chr5:39314948 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.870+827G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39314948 | |||||||
| chr5:39315024 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.870+751T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39315024 | |||||||
| chr5:39315040 | A | G | 35 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(32): Show |
39 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.870+735T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39315040 | |||||||
| chr5:39315075 | G | T | 98 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(95): Show |
101 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.870+700C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39315075 | |||||||
| chr5:39315077 | A | G | 11 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0002g0197 others(8): Show |
11 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.870+698T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39315077 | |||||||
| chr5:39315151 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.870+624C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39315151 | |||||||
| chr5:39315213 | G | A | 25 | a0001c0001t0002g0195 a0001c0001t0003g0014 a0001c0001t0003g0036 others(22): Show |
26 | HG00323.hp2 HG00558.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.870+562C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39315213 | |||||||
| chr5:39315642 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.870+133G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39315642 | |||||||
| chr5:39315643 | G | A | 72 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(69): Show |
74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.870+132C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39315643 | |||||||
| chr5:39315715 | T | TTAAAA | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+59_870+60insTT others(3): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 6/10 | chr5 | 39315715 | |||||||
| chr5:39316172 | T | C | 1 | a0002c0002t0001g0298 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.616-143A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39316172 | |||||||
| chr5:39316248 | A | G | 9 | a0001c0001t0002g0169 a0001c0001t0002g0209 a0001c0001t0002g0210 others(6): Show |
9 | HG00621.hp1 HG02040.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.616-219T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39316248 | |||||||
| chr5:39316320 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(185): Show |
203 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.616-291G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39316320 | |||||||
| chr5:39316343 | CT | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-315delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39316343 | |||||||
| chr5:39316511 | C | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG01071.hp1 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-482G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39316511 | |||||||
| chr5:39316665 | A | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-636T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39316665 | |||||||
| chr5:39316741 | C | T | 1 | a0001c0015t0008g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.616-712G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39316741 | |||||||
| chr5:39316850 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-821A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39316850 | |||||||
| chr5:39316881 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.616-852A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39316881 | |||||||
| chr5:39316957 | C | G | 4 | a0002c0002t0001g0318 a0002c0002t0001g0319 a0002c0002t0001g0326 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-928G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39316957 | |||||||
| chr5:39317064 | T | C | 4 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-1035A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317064 | |||||||
| chr5:39317167 | A | G | 4 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.616-1138T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317167 | |||||||
| chr5:39317176 | C | T | 2 | a0001c0001t0001g0265 a0002c0002t0001g0304 |
2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.616-1147G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317176 | |||||||
| chr5:39317193 | C | T | 10 | a0001c0001t0001g0025 a0001c0001t0002g0197 a0002c0002t0001g0333 others(7): Show |
10 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.616-1164G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317193 | |||||||
| chr5:39317262 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-1233C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317262 | |||||||
| chr5:39317276 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.616-1247T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317276 | |||||||
| chr5:39317315 | T | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-1286A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317315 | |||||||
| chr5:39317330 | G | A | 46 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(43): Show |
51 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.616-1301C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317330 | |||||||
| chr5:39317332 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-1303C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317332 | |||||||
| chr5:39317494 | T | C | 43 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(40): Show |
48 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.616-1465A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317494 | |||||||
| chr5:39317557 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(138): Show |
151 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.616-1528T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317557 | |||||||
| chr5:39317720 | G | A | 43 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(40): Show |
48 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.616-1691C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317720 | |||||||
| chr5:39317741 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-1712G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317741 | |||||||
| chr5:39317742 | G | A | 1 | a0001c0015t0008g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.616-1713C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317742 | |||||||
| chr5:39317761 | C | T | 10 | a0001c0001t0001g0025 a0001c0001t0002g0197 a0002c0002t0001g0333 others(7): Show |
10 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.616-1732G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317761 | |||||||
| chr5:39317762 | G | A | 107 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(104): Show |
111 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.616-1733C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317762 | |||||||
| chr5:39317779 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-1750G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317779 | |||||||
| chr5:39317780 | A | G | 346 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(343): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.616-1751T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317780 | |||||||
| chr5:39317859 | G | GT | 7 | a0001c0001t0002g0223 a0002c0002t0001g0323 a0002c0002t0001g0333 others(4): Show |
8 | HG01192.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.616-1831dupA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317859 | |||||||
| chr5:39317859 | G | T | 41 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(38): Show |
45 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.616-1830C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317859 | |||||||
| chr5:39317859 | GT | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-1831delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317859 | |||||||
| chr5:39317937 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.616-1908C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39317937 | |||||||
| chr5:39318027 | G | C | 1 | a0006c0006t0001g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.616-1998C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318027 | |||||||
| chr5:39318106 | T | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG01071.hp1 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-2077A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318106 | |||||||
| chr5:39318113 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(175): Show |
192 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.616-2084G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318113 | |||||||
| chr5:39318194 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-2165T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318194 | |||||||
| chr5:39318259 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-2230G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318259 | |||||||
| chr5:39318465 | G | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-2436C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318465 | |||||||
| chr5:39318482 | T | C | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | NA18941.hp2 NA18972.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.616-2453A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318482 | |||||||
| chr5:39318557 | CT | C | 11 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0265 others(8): Show |
12 | HG01167.hp2 HG01243.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.616-2529delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318557 | |||||||
| chr5:39318734 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-2705C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318734 | |||||||
| chr5:39318786 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-2757A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318786 | |||||||
| chr5:39318922 | T | C | 3 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02970.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.616-2893A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39318922 | |||||||
| chr5:39319004 | T | C | 1 | a0002c0002t0001g0310 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.616-2975A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319004 | |||||||
| chr5:39319096 | T | C | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.616-3067A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319096 | |||||||
| chr5:39319167 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-3138G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319167 | |||||||
| chr5:39319232 | C | T | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.616-3203G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319232 | |||||||
| chr5:39319454 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-3425A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319454 | |||||||
| chr5:39319469 | T | G | 10 | a0001c0001t0001g0025 a0001c0001t0002g0197 a0002c0002t0001g0333 others(7): Show |
10 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.616-3440A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319469 | |||||||
| chr5:39319472 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.616-3443C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319472 | |||||||
| chr5:39319474 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-3445T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319474 | |||||||
| chr5:39319552 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.616-3523G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319552 | |||||||
| chr5:39319660 | A | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-3631T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319660 | |||||||
| chr5:39319722 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.616-3693A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39319722 | |||||||
| chr5:39320031 | C | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-4002G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320031 | |||||||
| chr5:39320041 | T | G | 183 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0025 others(180): Show |
194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.616-4012A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320041 | |||||||
| chr5:39320197 | T | C | 10 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(7): Show |
11 | HG01243.hp1 HG02615.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.616-4168A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320197 | |||||||
| chr5:39320251 | C | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-4222G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320251 | |||||||
| chr5:39320339 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-4310G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320339 | |||||||
| chr5:39320359 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.616-4330T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320359 | |||||||
| chr5:39320495 | A | G | 47 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(44): Show |
53 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.616-4466T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320495 | |||||||
| chr5:39320573 | A | G | 32 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0203 others(29): Show |
33 | HG00323.hp2 HG00558.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.616-4544T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320573 | |||||||
| chr5:39320605 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-4576T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320605 | |||||||
| chr5:39320648 | GA | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-4620delT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320648 | |||||||
| chr5:39320675 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.616-4646T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320675 | |||||||
| chr5:39320714 | C | A | 2 | a0001c0001t0003g0187 a0001c0001t0003g0190 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.616-4685G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320714 | |||||||
| chr5:39320837 | C | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.616-4808G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320837 | |||||||
| chr5:39320849 | A | T | 1 | a0002c0002t0001g0355 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.616-4820T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320849 | |||||||
| chr5:39320901 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-4872A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320901 | |||||||
| chr5:39320920 | A | G | 1 | a0001c0001t0001g0243 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.616-4891T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39320920 | |||||||
| chr5:39321147 | T | C | 1 | a0002c0021t0002g0289 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.616-5118A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321147 | |||||||
| chr5:39321201 | A | G | 2 | a0001c0001t0001g0265 a0002c0002t0001g0304 |
2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.616-5172T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321201 | |||||||
| chr5:39321207 | T | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-5178A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321207 | |||||||
| chr5:39321386 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.616-5357T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321386 | |||||||
| chr5:39321512 | CA | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-5484delT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321512 | |||||||
| chr5:39321543 | A | C | 2 | a0001c0001t0001g0087 a0001c0001t0002g0086 |
2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.616-5514T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321543 | |||||||
| chr5:39321545 | GA | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0130 others(1): Show |
4 | HG01975.hp1 HG01978.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-5517delT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321545 | |||||||
| chr5:39321602 | T | A | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.616-5573A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321602 | |||||||
| chr5:39321655 | T | C | 36 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(33): Show |
40 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(37): Show |
intron_variant | MODIFIER | c.616-5626A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321655 | |||||||
| chr5:39321665 | A | G | 4 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-5636T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321665 | |||||||
| chr5:39321799 | T | C | 188 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0025 others(185): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.616-5770A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321799 | |||||||
| chr5:39321821 | G | C | 10 | a0001c0001t0001g0025 a0001c0001t0002g0197 a0002c0002t0001g0333 others(7): Show |
10 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.616-5792C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321821 | |||||||
| chr5:39321907 | A | T | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(98): Show |
104 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.616-5878T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321907 | |||||||
| chr5:39321913 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-5884A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321913 | |||||||
| chr5:39321923 | C | T | 10 | a0001c0001t0001g0025 a0001c0001t0002g0197 a0002c0002t0001g0333 others(7): Show |
10 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.616-5894G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321923 | |||||||
| chr5:39321975 | A | T | 3 | a0001c0001t0001g0203 a0002c0002t0001g0286 a0002c0002t0001g0287 |
3 | HG02257.hp1 HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.616-5946T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39321975 | |||||||
| chr5:39322080 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.616-6051C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322080 | |||||||
| chr5:39322099 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-6070C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322099 | |||||||
| chr5:39322173 | G | A | 8 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 others(5): Show |
9 | HG01192.hp1 HG02630.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.616-6144C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322173 | |||||||
| chr5:39322221 | G | A | 3 | a0001c0001t0001g0046 a0002c0002t0002g0288 a0002c0002t0002g0352 |
3 | HG03041.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.616-6192C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322221 | |||||||
| chr5:39322325 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-6296T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322325 | |||||||
| chr5:39322359 | C | T | 234 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(231): Show |
249 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.616-6330G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322359 | |||||||
| chr5:39322585 | C | A | 1 | a0002c0002t0001g0301 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.616-6556G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322585 | |||||||
| chr5:39322690 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.616-6661C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322690 | |||||||
| chr5:39322714 | C | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-6685G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322714 | |||||||
| chr5:39322736 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-6707C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322736 | |||||||
| chr5:39322744 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-6715A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322744 | |||||||
| chr5:39322754 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-6725G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322754 | |||||||
| chr5:39322811 | A | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-6782T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322811 | |||||||
| chr5:39322882 | C | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.616-6853G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322882 | |||||||
| chr5:39322935 | C | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-6906G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39322935 | |||||||
| chr5:39323032 | G | A | 188 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0025 others(185): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.616-7003C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323032 | |||||||
| chr5:39323066 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-7037C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323066 | |||||||
| chr5:39323073 | A | T | 4 | a0001c0001t0003g0064 a0001c0001t0003g0074 a0002c0002t0003g0292 others(1): Show |
4 | HG00323.hp2 HG02683.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-7044T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323073 | |||||||
| chr5:39323111 | G | A | 3 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02970.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.616-7082C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323111 | |||||||
| chr5:39323148 | T | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(65): Show |
70 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.616-7119A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323148 | |||||||
| chr5:39323265 | T | G | 37 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(34): Show |
41 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.616-7236A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323265 | |||||||
| chr5:39323437 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-7408T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323437 | |||||||
| chr5:39323461 | T | A | 9 | a0001c0001t0001g0025 a0002c0002t0001g0333 a0003c0004t0001g0192 others(6): Show |
9 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.616-7432A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323461 | |||||||
| chr5:39323524 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.616-7495G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323524 | |||||||
| chr5:39323616 | C | T | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.616-7587G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323616 | |||||||
| chr5:39323617 | G | A | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.616-7588C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323617 | |||||||
| chr5:39323666 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-7637C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323666 | |||||||
| chr5:39323670 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.616-7641G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323670 | |||||||
| chr5:39323782 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-7753G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323782 | |||||||
| chr5:39323820 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-7791A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323820 | |||||||
| chr5:39323823 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-7794T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323823 | |||||||
| chr5:39323903 | C | A | 1 | a0001c0001t0001g0253 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.615+7773G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323903 | |||||||
| chr5:39323906 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.615+7770A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323906 | |||||||
| chr5:39323907 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.615+7769T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39323907 | |||||||
| chr5:39324000 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+7676A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324000 | |||||||
| chr5:39324087 | A | G | 4 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+7589T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324087 | |||||||
| chr5:39324178 | T | C | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.615+7498A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324178 | |||||||
| chr5:39324198 | A | G | 183 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0025 others(180): Show |
194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.615+7478T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324198 | |||||||
| chr5:39324295 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+7381G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324295 | |||||||
| chr5:39324314 | C | T | 32 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0203 others(29): Show |
33 | HG00323.hp2 HG00558.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.615+7362G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324314 | |||||||
| chr5:39324328 | G | A | 4 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+7348C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324328 | |||||||
| chr5:39324346 | G | T | 4 | a0001c0001t0001g0222 a0001c0001t0002g0004 a0001c0001t0002g0033 others(1): Show |
5 | HG02109.hp2 HG02257.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+7330C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324346 | |||||||
| chr5:39324358 | C | T | 8 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 others(5): Show |
9 | HG01192.hp1 HG02630.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.615+7318G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324358 | |||||||
| chr5:39324439 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+7237T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324439 | |||||||
| chr5:39324567 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+7109C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324567 | |||||||
| chr5:39324690 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+6986C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324690 | |||||||
| chr5:39324730 | A | T | 3 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02970.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.615+6946T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324730 | |||||||
| chr5:39324877 | A | G | 25 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0002g0195 others(22): Show |
26 | HG00323.hp2 HG00558.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.615+6799T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324877 | |||||||
| chr5:39324892 | AG | A | 7 | a0001c0001t0001g0253 a0006c0006t0001g0053 a0006c0006t0001g0120 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.615+6783delC | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324892 | |||||||
| chr5:39324915 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.615+6761G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324915 | |||||||
| chr5:39324948 | C | T | 3 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02970.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.615+6728G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324948 | |||||||
| chr5:39324995 | T | C | 1 | a0008c0011t0001g0324 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.615+6681A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39324995 | |||||||
| chr5:39325027 | C | T | 24 | a0001c0001t0001g0046 a0001c0001t0002g0035 a0001c0001t0002g0042 others(21): Show |
26 | HG01167.hp2 HG01192.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.615+6649G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325027 | |||||||
| chr5:39325030 | G | C | 9 | a0001c0001t0001g0025 a0002c0002t0001g0333 a0003c0004t0001g0192 others(6): Show |
9 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.615+6646C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325030 | |||||||
| chr5:39325085 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+6591T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325085 | |||||||
| chr5:39325159 | C | T | 12 | a0001c0001t0001g0067 a0001c0001t0001g0079 a0001c0001t0001g0170 others(9): Show |
12 | HG00621.hp2 HG00735.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.615+6517G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325159 | |||||||
| chr5:39325177 | T | C | 1 | a0002c0002t0001g0317 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.615+6499A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325177 | |||||||
| chr5:39325178 | A | G | 48 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(45): Show |
54 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.615+6498T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325178 | |||||||
| chr5:39325216 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0037 a0001c0001t0002g0201 others(1): Show |
5 | HG02055.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+6460A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325216 | |||||||
| chr5:39325240 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(281): Show |
305 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.615+6436A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325240 | |||||||
| chr5:39325264 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.615+6412G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325264 | |||||||
| chr5:39325322 | A | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+6354T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325322 | |||||||
| chr5:39325550 | G | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+6126C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325550 | |||||||
| chr5:39325581 | T | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0052 |
5 | HG00639.hp2 HG00738.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.615+6095A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325581 | |||||||
| chr5:39325602 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.615+6074T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325602 | |||||||
| chr5:39325622 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.615+6054T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325622 | |||||||
| chr5:39325634 | C | T | 3 | a0007c0008t0007g0063 a0007c0008t0007g0137 a0007c0008t0007g0230 |
3 | HG01167.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.615+6042G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325634 | |||||||
| chr5:39325641 | G | A | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.615+6035C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325641 | |||||||
| chr5:39325686 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+5990G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325686 | |||||||
| chr5:39325709 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+5967A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325709 | |||||||
| chr5:39325728 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+5948G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325728 | |||||||
| chr5:39325729 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(113): Show |
123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.615+5947C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325729 | |||||||
| chr5:39325771 | C | CA | 69 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0102 others(66): Show |
76 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.615+5904dupT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325771 | |||||||
| chr5:39325771 | C | CAA | 71 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(68): Show |
73 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.615+5903_615+5904d others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325771 | |||||||
| chr5:39325771 | CA | C | 9 | a0001c0001t0001g0159 a0001c0001t0001g0250 a0001c0001t0001g0253 others(6): Show |
9 | HG02080.hp2 HG02647.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.615+5904delT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325771 | |||||||
| chr5:39325966 | T | G | 1 | a0001c0001t0001g0279 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.615+5710A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39325966 | |||||||
| chr5:39326047 | G | GT | 5 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 others(2): Show |
5 | HG01496.hp2 HG01928.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.615+5628dupA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326047 | |||||||
| chr5:39326088 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+5588T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326088 | |||||||
| chr5:39326130 | T | C | 16 | a0001c0001t0001g0025 a0001c0001t0002g0035 a0001c0001t0002g0042 others(13): Show |
17 | HG01192.hp1 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.615+5546A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326130 | |||||||
| chr5:39326168 | T | C | 11 | a0001c0001t0001g0025 a0001c0001t0002g0035 a0001c0001t0002g0042 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.615+5508A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326168 | |||||||
| chr5:39326181 | T | C | 248 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(245): Show |
264 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.615+5495A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326181 | |||||||
| chr5:39326215 | T | A | 8 | a0001c0001t0001g0046 a0001c0001t0001g0200 a0001c0001t0002g0035 others(5): Show |
8 | HG02717.hp2 HG02970.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.615+5461A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326215 | |||||||
| chr5:39326249 | T | G | 35 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(32): Show |
39 | HG00609.hp1 HG01358.hp1 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.615+5427A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326249 | |||||||
| chr5:39326303 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+5373A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326303 | |||||||
| chr5:39326401 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.615+5275G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326401 | |||||||
| chr5:39326481 | T | C | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.615+5195A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326481 | |||||||
| chr5:39326516 | T | C | 1 | a0002c0002t0001g0334 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.615+5160A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326516 | |||||||
| chr5:39326530 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+5146A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326530 | |||||||
| chr5:39326815 | G | C | 4 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+4861C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326815 | |||||||
| chr5:39326875 | A | T | 1 | a0001c0001t0003g0142 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.615+4801T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326875 | |||||||
| chr5:39326899 | A | G | 3 | a0001c0001t0001g0203 a0002c0002t0001g0286 a0002c0002t0001g0287 |
3 | HG02257.hp1 HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.615+4777T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326899 | |||||||
| chr5:39326984 | A | AT | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+4691dupA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39326984 | |||||||
| chr5:39327016 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+4660C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327016 | |||||||
| chr5:39327063 | C | CA | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+4612dupT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327063 | |||||||
| chr5:39327084 | C | A | 5 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.615+4592G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327084 | |||||||
| chr5:39327181 | C | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+4495G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327181 | |||||||
| chr5:39327265 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+4411A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327265 | |||||||
| chr5:39327347 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.615+4329A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327347 | |||||||
| chr5:39327542 | G | A | 1 | a0001c0001t0003g0239 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.615+4134C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327542 | |||||||
| chr5:39327708 | T | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+3968A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327708 | |||||||
| chr5:39327712 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+3964G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327712 | |||||||
| chr5:39327771 | T | C | 329 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(326): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.615+3905A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327771 | |||||||
| chr5:39327782 | T | C | 8 | a0001c0001t0001g0025 a0003c0004t0001g0192 a0003c0004t0001g0193 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.615+3894A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327782 | |||||||
| chr5:39327784 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.615+3892A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39327784 | |||||||
| chr5:39328054 | C | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0127 |
3 | HG03831.hp1 HG03927.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.615+3622G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328054 | |||||||
| chr5:39328074 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+3602C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328074 | |||||||
| chr5:39328209 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+3467G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328209 | |||||||
| chr5:39328292 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.615+3384G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328292 | |||||||
| chr5:39328343 | C | T | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.615+3333G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328343 | |||||||
| chr5:39328404 | A | G | 175 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(172): Show |
187 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.615+3272T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328404 | |||||||
| chr5:39328452 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+3224A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328452 | |||||||
| chr5:39328529 | C | T | 1 | a0002c0002t0001g0334 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.615+3147G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328529 | |||||||
| chr5:39328534 | C | A | 4 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+3142G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328534 | |||||||
| chr5:39328661 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+3015G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328661 | |||||||
| chr5:39328957 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.615+2719G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39328957 | |||||||
| chr5:39329029 | A | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+2647T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329029 | |||||||
| chr5:39329069 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+2607G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329069 | |||||||
| chr5:39329188 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+2488A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329188 | |||||||
| chr5:39329211 | C | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+2465G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329211 | |||||||
| chr5:39329336 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0024 others(143): Show |
157 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.615+2340C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329336 | |||||||
| chr5:39329347 | G | C | 1 | a0009c0012t0002g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.615+2329C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329347 | |||||||
| chr5:39329355 | C | T | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.615+2321G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329355 | |||||||
| chr5:39329407 | T | A | 2 | a0001c0001t0001g0159 a0011c0014t0001g0178 |
2 | HG03942.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.615+2269A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329407 | |||||||
| chr5:39329442 | A | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+2234T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329442 | |||||||
| chr5:39329572 | T | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(3): Show |
6 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+2104A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329572 | |||||||
| chr5:39329643 | A | C | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.615+2033T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329643 | |||||||
| chr5:39329722 | G | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+1954C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329722 | |||||||
| chr5:39329875 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.615+1801T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329875 | |||||||
| chr5:39329891 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+1785C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39329891 | |||||||
| chr5:39330165 | A | AT | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+1510dupA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330165 | |||||||
| chr5:39330316 | G | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+1360C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330316 | |||||||
| chr5:39330349 | G | A | 2 | a0001c0001t0002g0209 a0001c0001t0002g0212 |
2 | NA18961.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.615+1327C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330349 | |||||||
| chr5:39330398 | C | T | 47 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(44): Show |
52 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.615+1278G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330398 | |||||||
| chr5:39330470 | G | A | 8 | a0001c0001t0001g0025 a0003c0004t0001g0192 a0003c0004t0001g0193 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.615+1206C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330470 | |||||||
| chr5:39330525 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+1151C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330525 | |||||||
| chr5:39330527 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.615+1149G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330527 | |||||||
| chr5:39330556 | C | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+1120G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330556 | |||||||
| chr5:39330653 | G | C | 1 | a0004c0003t0005g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.615+1023C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330653 | |||||||
| chr5:39330670 | T | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+1006A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330670 | |||||||
| chr5:39330720 | C | CTT | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+955_615+956ins others(2): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39330720 | |||||||
| chr5:39331075 | T | A | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.615+601A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39331075 | |||||||
| chr5:39331114 | G | A | 56 | a0001c0001t0001g0025 a0001c0001t0001g0222 a0001c0001t0002g0002 others(53): Show |
62 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.615+562C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39331114 | |||||||
| chr5:39331199 | T | C | 1 | a0001c0013t0002g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.615+477A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39331199 | |||||||
| chr5:39331206 | T | TATAAATC others(6): Show |
1 | a0003c0004t0001g0266 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.615+457_615+469dup others(13): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39331206 | |||||||
| chr5:39331274 | G | A | 26 | a0001c0001t0001g0046 a0001c0001t0001g0200 a0001c0001t0002g0035 others(23): Show |
28 | HG01167.hp2 HG01192.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.615+402C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39331274 | |||||||
| chr5:39331287 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0105 |
2 | HG00323.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.615+389G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39331287 | |||||||
| chr5:39331292 | G | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+384C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 5/10 | chr5 | 39331292 | |||||||
| chr5:39332086 | G | T | 1 | a0002c0002t0001g0338 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.477-272C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332086 | |||||||
| chr5:39332197 | G | A | 2 | a0001c0001t0001g0159 a0011c0014t0001g0178 |
2 | HG03942.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.477-383C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332197 | |||||||
| chr5:39332210 | G | T | 1 | a0001c0001t0002g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.477-396C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332210 | |||||||
| chr5:39332211 | G | T | 1 | a0012c0019t0001g0306 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.477-397C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332211 | |||||||
| chr5:39332224 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-410C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332224 | |||||||
| chr5:39332304 | C | T | 64 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(61): Show |
66 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.477-490G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332304 | |||||||
| chr5:39332505 | T | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-691A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332505 | |||||||
| chr5:39332535 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-721T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332535 | |||||||
| chr5:39332661 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.477-847G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332661 | |||||||
| chr5:39332804 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-990A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332804 | |||||||
| chr5:39332813 | G | A | 5 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.477-999C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332813 | |||||||
| chr5:39332819 | T | A | 4 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(1): Show |
4 | HG02040.hp2 HG02165.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-1005A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332819 | |||||||
| chr5:39332887 | A | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0275 |
3 | HG01884.hp1 HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.477-1073T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332887 | |||||||
| chr5:39332978 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-1164A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39332978 | |||||||
| chr5:39333132 | T | G | 175 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(172): Show |
187 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.477-1318A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333132 | |||||||
| chr5:39333202 | C | T | 1 | a0006c0006t0001g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.477-1388G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333202 | |||||||
| chr5:39333269 | C | T | 1 | a0002c0002t0001g0361 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.477-1455G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333269 | |||||||
| chr5:39333392 | C | G | 330 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(327): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.477-1578G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333392 | |||||||
| chr5:39333441 | C | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-1627G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333441 | |||||||
| chr5:39333554 | A | ATCTCCC | 74 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(71): Show |
82 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.477-1746_477-1741d others(8): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333554 | |||||||
| chr5:39333554 | A | ATCTCCCT others(5): Show |
36 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0093 others(33): Show |
38 | HG00609.hp2 HG01192.hp1 HG02056.hp2 others(35): Show |
intron_variant | MODIFIER | c.477-1752_477-1741d others(14): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333554 | |||||||
| chr5:39333554 | A | ATCTCCCT others(17): Show |
5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0073 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.477-1764_477-1741d others(26): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333554 | |||||||
| chr5:39333554 | A | ATCTCCCT others(23): Show |
1 | a0002c0002t0001g0310 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.477-1741_477-1740i others(32): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333554 | |||||||
| chr5:39333554 | A | ATCTCCCT others(29): Show |
1 | a0001c0001t0001g0153 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.477-1741_477-1740i others(38): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333554 | |||||||
| chr5:39333554 | ATCTCCC | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0105 a0001c0001t0001g0167 |
3 | HG00323.hp1 HG01070.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.477-1746_477-1741d others(8): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333554 | |||||||
| chr5:39333584 | G | A | 5 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.477-1770C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333584 | |||||||
| chr5:39333584 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0024 others(136): Show |
150 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.477-1770C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333584 | |||||||
| chr5:39333596 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.477-1782C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333596 | |||||||
| chr5:39333596 | G | C | 128 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0026 others(125): Show |
135 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.477-1782C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333596 | |||||||
| chr5:39333602 | C | G | 17 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0051 others(14): Show |
17 | HG00408.hp2 HG01123.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.477-1788G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333602 | |||||||
| chr5:39333606 | C | CCGTCTCC others(31): Show |
11 | a0001c0001t0001g0001 a0001c0001t0001g0050 a0001c0001t0001g0247 others(8): Show |
15 | HG06807.hp1 NA18612.hp1 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.477-1793_477-1792i others(40): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333606 | |||||||
| chr5:39333606 | C | CCGTCTCC others(44): Show |
1 | a0001c0001t0001g0176 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.477-1793_477-1792i others(53): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333606 | |||||||
| chr5:39333606 | C | CCGTCTCC others(43): Show |
28 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0061 others(25): Show |
30 | HG00408.hp1 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.477-1793_477-1792i others(52): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333606 | |||||||
| chr5:39333606 | C | CCGTCTCC others(69): Show |
1 | a0002c0002t0001g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477-1793_477-1792i others(78): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333606 | |||||||
| chr5:39333608 | C | CTCTCCCT others(67): Show |
1 | a0001c0001t0001g0154 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.477-1795_477-1794i others(76): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333608 | |||||||
| chr5:39333608 | C | CTCTCCCT others(61): Show |
8 | a0001c0001t0001g0038 a0001c0001t0001g0129 a0001c0001t0001g0131 others(5): Show |
8 | HG01071.hp1 HG01081.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.477-1795_477-1794i others(70): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333608 | |||||||
| chr5:39333608 | C | CTCTCCCT others(55): Show |
8 | a0001c0001t0001g0009 a0001c0001t0001g0106 a0001c0001t0001g0107 others(5): Show |
9 | HG00280.hp2 HG01257.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.477-1795_477-1794i others(64): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333608 | |||||||
| chr5:39333608 | C | CTCTCCGT others(37): Show |
17 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0051 others(14): Show |
17 | HG00408.hp2 HG01123.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.477-1795_477-1794i others(46): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333608 | |||||||
| chr5:39333608 | C | CTCTCCGT others(49): Show |
64 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(61): Show |
68 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.477-1795_477-1794i others(58): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333608 | |||||||
| chr5:39333608 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0047 others(38): Show |
47 | HG00408.hp1 HG00558.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.477-1794G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333608 | |||||||
| chr5:39333616 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0024 others(142): Show |
156 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.477-1802A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333616 | |||||||
| chr5:39333616 | T | TGGTCTCC others(19): Show |
14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.477-1828_477-1803d others(28): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333616 | |||||||
| chr5:39333642 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0184 |
2 | HG00735.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.477-1828G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333642 | |||||||
| chr5:39333659 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.477-1845G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333659 | |||||||
| chr5:39333684 | G | A | 1 | a0003c0004t0001g0266 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.477-1870C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333684 | |||||||
| chr5:39333685 | C | A | 1 | a0002c0002t0002g0015 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.477-1871G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333685 | |||||||
| chr5:39333737 | G | C | 3 | a0001c0001t0001g0253 a0002c0002t0001g0313 a0002c0002t0001g0342 |
3 | NA18993.hp2 NA18997.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.477-1923C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333737 | |||||||
| chr5:39333756 | C | T | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.477-1942G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333756 | |||||||
| chr5:39333758 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-1944G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333758 | |||||||
| chr5:39333761 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-1947T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333761 | |||||||
| chr5:39333764 | G | A | 8 | a0001c0001t0001g0025 a0003c0004t0001g0192 a0003c0004t0001g0193 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.477-1950C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333764 | |||||||
| chr5:39333806 | GT | G | 46 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(43): Show |
51 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.477-1993delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333806 | |||||||
| chr5:39333815 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2001A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333815 | |||||||
| chr5:39333821 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2007G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333821 | |||||||
| chr5:39333845 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.477-2031G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333845 | |||||||
| chr5:39333863 | C | T | 141 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(138): Show |
151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.477-2049G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333863 | |||||||
| chr5:39333865 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2051A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333865 | |||||||
| chr5:39333877 | T | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2063A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333877 | |||||||
| chr5:39333881 | C | T | 1 | a0012c0019t0001g0306 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.477-2067G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333881 | |||||||
| chr5:39333882 | G | A | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.477-2068C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333882 | |||||||
| chr5:39333953 | G | A | 3 | a0001c0001t0002g0195 a0001c0001t0003g0142 a0002c0002t0002g0339 |
3 | NA18939.hp2 NA18975.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.477-2139C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333953 | |||||||
| chr5:39333957 | C | T | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.477-2143G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333957 | |||||||
| chr5:39333981 | G | A | 1 | a0001c0001t0003g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.477-2167C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333981 | |||||||
| chr5:39333996 | C | G | 8 | a0001c0001t0001g0025 a0003c0004t0001g0192 a0003c0004t0001g0193 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.477-2182G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39333996 | |||||||
| chr5:39334005 | C | T | 3 | a0001c0001t0001g0067 a0007c0008t0007g0137 a0007c0008t0007g0230 |
3 | HG01167.hp2 HG03195.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.477-2191G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334005 | |||||||
| chr5:39334029 | G | A | 3 | a0005c0007t0001g0013 a0005c0007t0001g0168 a0005c0007t0001g0233 |
4 | HG02056.hp2 NA18966.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-2215C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334029 | |||||||
| chr5:39334032 | A | AC | 15 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0045 others(12): Show |
15 | HG00741.hp2 HG01099.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.477-2219dupG | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334032 | |||||||
| chr5:39334040 | T | G | 1 | a0002c0002t0003g0322 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.477-2226A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334040 | |||||||
| chr5:39334081 | A | G | 173 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(170): Show |
185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.477-2267T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334081 | |||||||
| chr5:39334128 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.477-2314T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334128 | |||||||
| chr5:39334138 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2324G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334138 | |||||||
| chr5:39334158 | G | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(83): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.477-2344C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334158 | |||||||
| chr5:39334176 | T | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0139 a0001c0001t0001g0151 others(2): Show |
6 | HG01081.hp1 HG01257.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.477-2362A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334176 | |||||||
| chr5:39334190 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2376G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334190 | |||||||
| chr5:39334210 | C | A | 1 | a0001c0013t0002g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.477-2396G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334210 | |||||||
| chr5:39334221 | G | A | 167 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(164): Show |
179 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.477-2407C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334221 | |||||||
| chr5:39334224 | G | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2410C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334224 | |||||||
| chr5:39334250 | G | T | 2 | a0001c0001t0001g0038 a0010c0020t0001g0309 |
2 | HG03490.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.477-2436C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334250 | |||||||
| chr5:39334263 | C | T | 6 | a0001c0001t0002g0223 a0001c0001t0006g0185 a0001c0001t0006g0186 others(3): Show |
6 | HG01192.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.477-2449G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334263 | |||||||
| chr5:39334269 | G | A | 9 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.477-2455C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334269 | |||||||
| chr5:39334296 | C | G | 55 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(52): Show |
61 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.477-2482G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334296 | |||||||
| chr5:39334302 | C | CG | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2489_477-2488i others(3): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334302 | |||||||
| chr5:39334304 | A | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2490T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334304 | |||||||
| chr5:39334308 | C | T | 1 | a0004c0003t0005g0044 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.477-2494G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334308 | |||||||
| chr5:39334309 | G | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(83): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.477-2495C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334309 | |||||||
| chr5:39334333 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.477-2519C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334333 | |||||||
| chr5:39334335 | C | T | 86 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(83): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.477-2521G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334335 | |||||||
| chr5:39334341 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.477-2527C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334341 | |||||||
| chr5:39334346 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2532T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334346 | |||||||
| chr5:39334369 | T | C | 8 | a0001c0001t0001g0062 a0002c0002t0001g0350 a0006c0006t0001g0053 others(5): Show |
8 | HG00642.hp1 HG01074.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.477-2555A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334369 | |||||||
| chr5:39334373 | T | C | 2 | a0001c0001t0001g0062 a0002c0002t0001g0350 |
2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.477-2559A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334373 | |||||||
| chr5:39334374 | G | A | 2 | a0001c0001t0001g0062 a0002c0002t0001g0350 |
2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.477-2560C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334374 | |||||||
| chr5:39334385 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.477-2571G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334385 | |||||||
| chr5:39334385 | C | T | 4 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.477-2571G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334385 | |||||||
| chr5:39334386 | G | A | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.477-2572C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334386 | |||||||
| chr5:39334413 | C | T | 7 | a0002c0002t0001g0286 a0006c0006t0001g0053 a0006c0006t0001g0120 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.477-2599G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334413 | |||||||
| chr5:39334420 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(151): Show |
165 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.477-2606G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334420 | |||||||
| chr5:39334421 | G | A | 3 | a0001c0001t0001g0165 a0004c0003t0005g0218 a0004c0003t0005g0219 |
3 | HG02559.hp2 NA19070.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.477-2607C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334421 | |||||||
| chr5:39334450 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2636C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334450 | |||||||
| chr5:39334453 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2639A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334453 | |||||||
| chr5:39334455 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2641C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334455 | |||||||
| chr5:39334466 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2652T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334466 | |||||||
| chr5:39334484 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2670C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334484 | |||||||
| chr5:39334485 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2671A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334485 | |||||||
| chr5:39334489 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2675A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334489 | |||||||
| chr5:39334493 | A | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2679T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334493 | |||||||
| chr5:39334501 | ACCCCGTC others(39): Show |
A | 26 | a0001c0001t0001g0046 a0001c0001t0001g0200 a0001c0001t0002g0035 others(23): Show |
28 | HG01167.hp2 HG01192.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.477-2733_477-2688d others(48): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334501 | |||||||
| chr5:39334506 | G | A | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.477-2692C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334506 | |||||||
| chr5:39334506 | G | C | 2 | a0001c0001t0002g0195 a0002c0002t0002g0339 |
2 | NA18975.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.477-2692C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334506 | |||||||
| chr5:39334534 | C | CCGCCCGG others(72): Show |
6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2721_477-2720i others(81): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334534 | |||||||
| chr5:39334538 | A | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2724T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334538 | |||||||
| chr5:39334551 | C | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2737G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334551 | |||||||
| chr5:39334567 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.477-2753C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334567 | |||||||
| chr5:39334587 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2773G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334587 | |||||||
| chr5:39334595 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2781A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334595 | |||||||
| chr5:39334596 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2782C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334596 | |||||||
| chr5:39334601 | G | A | 1 | a0001c0005t0002g0272 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.477-2787C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334601 | |||||||
| chr5:39334604 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2790A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334604 | |||||||
| chr5:39334618 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2804G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334618 | |||||||
| chr5:39334621 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2807G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334621 | |||||||
| chr5:39334625 | G | T | 3 | a0001c0001t0001g0203 a0002c0002t0001g0286 a0002c0002t0001g0287 |
3 | HG02257.hp1 HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.477-2811C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334625 | |||||||
| chr5:39334628 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2814A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334628 | |||||||
| chr5:39334633 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2819T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334633 | |||||||
| chr5:39334666 | G | A | 9 | a0001c0001t0001g0265 a0001c0013t0002g0119 a0002c0002t0001g0304 others(6): Show |
9 | HG02572.hp1 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.477-2852C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334666 | |||||||
| chr5:39334675 | C | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(151): Show |
165 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.477-2861G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334675 | |||||||
| chr5:39334678 | A | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2864T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334678 | |||||||
| chr5:39334698 | C | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2884G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334698 | |||||||
| chr5:39334705 | C | T | 9 | a0001c0001t0001g0046 a0001c0001t0001g0200 a0001c0001t0002g0035 others(6): Show |
9 | HG02717.hp2 HG02970.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.477-2891G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334705 | |||||||
| chr5:39334710 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(48): Show |
53 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.477-2896G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334710 | |||||||
| chr5:39334714 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2900A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334714 | |||||||
| chr5:39334722 | C | T | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.477-2908G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334722 | |||||||
| chr5:39334723 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2909T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334723 | |||||||
| chr5:39334728 | G | A | 7 | a0001c0001t0002g0011 a0006c0006t0001g0053 a0006c0006t0001g0120 others(4): Show |
8 | HG02572.hp1 HG02818.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.477-2914C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334728 | |||||||
| chr5:39334731 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0096 others(3): Show |
7 | HG00099.hp2 HG01123.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.477-2917G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334731 | |||||||
| chr5:39334732 | G | A | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.477-2918C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334732 | |||||||
| chr5:39334755 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.477-2941G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334755 | |||||||
| chr5:39334759 | C | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(83): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.477-2945G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334759 | |||||||
| chr5:39334762 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.477-2948G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334762 | |||||||
| chr5:39334805 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-2991T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334805 | |||||||
| chr5:39334839 | G | A | 1 | a0002c0002t0001g0298 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.477-3025C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334839 | |||||||
| chr5:39334908 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-3094T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334908 | |||||||
| chr5:39334994 | G | GA | 323 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(320): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.477-3181dupT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39334994 | |||||||
| chr5:39335013 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-3199T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335013 | |||||||
| chr5:39335038 | G | A | 16 | a0001c0001t0001g0046 a0001c0001t0001g0200 a0001c0001t0002g0035 others(13): Show |
17 | HG01167.hp2 HG01243.hp1 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.477-3224C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335038 | |||||||
| chr5:39335194 | T | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-3380A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335194 | |||||||
| chr5:39335260 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.477-3446T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335260 | |||||||
| chr5:39335284 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-3470T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335284 | |||||||
| chr5:39335314 | T | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-3500A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335314 | |||||||
| chr5:39335505 | T | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-3691A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335505 | |||||||
| chr5:39335805 | G | A | 6 | a0001c0001t0001g0222 a0001c0001t0002g0004 a0001c0001t0002g0033 others(3): Show |
7 | HG02109.hp2 HG02257.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.477-3991C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335805 | |||||||
| chr5:39335839 | G | T | 10 | a0001c0001t0002g0223 a0001c0001t0006g0185 a0001c0001t0006g0186 others(7): Show |
11 | HG01192.hp1 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.477-4025C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335839 | |||||||
| chr5:39335949 | G | A | 2 | a0002c0002t0001g0323 a0004c0003t0005g0005 |
3 | HG02630.hp2 HG02738.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.477-4135C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335949 | |||||||
| chr5:39335956 | A | G | 9 | a0001c0001t0001g0025 a0001c0001t0002g0011 a0003c0004t0001g0192 others(6): Show |
10 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.477-4142T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335956 | |||||||
| chr5:39335995 | C | T | 4 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-4181G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39335995 | |||||||
| chr5:39336056 | ATGT | A | 4 | a0001c0001t0001g0191 a0001c0001t0003g0036 a0001c0001t0003g0187 others(1): Show |
4 | HG01346.hp2 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-4245_477-4243d others(5): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336056 | |||||||
| chr5:39336256 | A | G | 1 | a0006c0006t0001g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.477-4442T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336256 | |||||||
| chr5:39336264 | A | C | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-4450T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336264 | |||||||
| chr5:39336287 | T | C | 7 | a0001c0005t0002g0012 a0001c0005t0002g0023 a0001c0005t0002g0272 others(4): Show |
8 | HG01167.hp2 HG01243.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.477-4473A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336287 | |||||||
| chr5:39336299 | C | A | 16 | a0001c0001t0001g0046 a0001c0001t0001g0200 a0001c0001t0002g0035 others(13): Show |
17 | HG01167.hp2 HG01243.hp1 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.477-4485G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336299 | |||||||
| chr5:39336329 | T | A | 4 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-4515A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336329 | |||||||
| chr5:39336398 | T | C | 2 | a0007c0008t0007g0137 a0007c0008t0007g0230 |
2 | HG01167.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.477-4584A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336398 | |||||||
| chr5:39336509 | G | C | 1 | a0002c0002t0002g0352 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.476+4637C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336509 | |||||||
| chr5:39336537 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02040.hp2 HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.476+4609A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336537 | |||||||
| chr5:39336538 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.476+4608C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336538 | |||||||
| chr5:39336708 | G | T | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.476+4438C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336708 | |||||||
| chr5:39336715 | G | A | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.476+4431C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336715 | |||||||
| chr5:39336722 | G | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(83): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.476+4424C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336722 | |||||||
| chr5:39336747 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0264 |
2 | NA18961.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.476+4399C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336747 | |||||||
| chr5:39336784 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.476+4362T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336784 | |||||||
| chr5:39336826 | T | A | 41 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(38): Show |
46 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.476+4320A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336826 | |||||||
| chr5:39336848 | T | TGGTGGCT others(291): Show |
1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.476+4297_476+4298i others(300): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336848 | |||||||
| chr5:39336849 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.476+4297G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336849 | |||||||
| chr5:39336862 | T | C | 41 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(38): Show |
46 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.476+4284A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336862 | |||||||
| chr5:39336916 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.476+4230T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336916 | |||||||
| chr5:39336977 | G | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.476+4169C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336977 | |||||||
| chr5:39336982 | G | GT | 7 | a0002c0002t0002g0337 a0006c0006t0001g0053 a0006c0006t0001g0120 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.476+4163dupA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39336982 | |||||||
| chr5:39337010 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.476+4136C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39337010 | |||||||
| chr5:39337166 | T | C | 1 | a0006c0006t0001g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.476+3980A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39337166 | |||||||
| chr5:39337218 | C | A | 8 | a0001c0001t0001g0025 a0003c0004t0001g0192 a0003c0004t0001g0193 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.476+3928G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39337218 | |||||||
| chr5:39337268 | T | A | 168 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(165): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.476+3878A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39337268 | |||||||
| chr5:39337490 | A | G | 6 | a0001c0001t0002g0223 a0001c0001t0006g0185 a0001c0001t0006g0186 others(3): Show |
6 | HG01192.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.476+3656T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39337490 | |||||||
| chr5:39337544 | A | G | 1 | a0005c0007t0001g0233 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.476+3602T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39337544 | |||||||
| chr5:39337551 | C | T | 2 | a0001c0009t0002g0227 a0001c0009t0002g0228 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.476+3595G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39337551 | |||||||
| chr5:39337661 | T | C | 3 | a0004c0003t0005g0041 a0004c0003t0005g0044 a0004c0003t0005g0204 |
3 | HG02723.hp1 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.476+3485A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39337661 | |||||||
| chr5:39337748 | A | G | 1 | a0006c0006t0001g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.476+3398T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39337748 | |||||||
| chr5:39337751 | A | C | 5 | a0001c0005t0002g0012 a0001c0005t0002g0023 a0001c0005t0002g0272 others(2): Show |
6 | HG01243.hp1 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.476+3395T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39337751 | |||||||
| chr5:39338028 | G | A | 5 | a0001c0001t0001g0046 a0004c0003t0005g0005 a0004c0003t0005g0041 others(2): Show |
6 | HG02630.hp2 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.476+3118C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338028 | |||||||
| chr5:39338168 | T | C | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.476+2978A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338168 | |||||||
| chr5:39338256 | G | A | 41 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(38): Show |
46 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.476+2890C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338256 | |||||||
| chr5:39338296 | C | T | 2 | a0007c0008t0007g0137 a0007c0008t0007g0230 |
2 | HG01167.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.476+2850G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338296 | |||||||
| chr5:39338323 | G | C | 1 | a0001c0001t0002g0057 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.476+2823C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338323 | |||||||
| chr5:39338452 | G | A | 1 | a0008c0011t0001g0324 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.476+2694C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338452 | |||||||
| chr5:39338559 | C | T | 2 | a0008c0011t0001g0285 a0008c0011t0001g0324 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.476+2587G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338559 | |||||||
| chr5:39338586 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.476+2560T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338586 | |||||||
| chr5:39338618 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.476+2528T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338618 | |||||||
| chr5:39338667 | A | T | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.476+2479T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338667 | |||||||
| chr5:39338685 | G | T | 62 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(59): Show |
64 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.476+2461C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338685 | |||||||
| chr5:39338730 | C | T | 8 | a0001c0001t0001g0025 a0003c0004t0001g0192 a0003c0004t0001g0193 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.476+2416G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338730 | |||||||
| chr5:39338919 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.476+2227C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338919 | |||||||
| chr5:39338922 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.476+2224G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39338922 | |||||||
| chr5:39339279 | A | T | 1 | a0002c0002t0001g0360 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.476+1867T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339279 | |||||||
| chr5:39339576 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.476+1570C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339576 | |||||||
| chr5:39339580 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.476+1566T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339580 | |||||||
| chr5:39339651 | CT | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(155): Show |
169 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.476+1494delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339651 | |||||||
| chr5:39339651 | CTT | C | 90 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0028 others(87): Show |
98 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.476+1493_476+1494d others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339651 | |||||||
| chr5:39339651 | CTTT | C | 63 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(60): Show |
65 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.476+1492_476+1494d others(5): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339651 | |||||||
| chr5:39339651 | CTTTT | C | 7 | a0001c0001t0001g0046 a0001c0009t0002g0228 a0004c0003t0005g0005 others(4): Show |
8 | HG01169.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.476+1491_476+1494d others(6): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339651 | |||||||
| chr5:39339752 | T | C | 1 | a0002c0002t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.476+1394A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339752 | |||||||
| chr5:39339774 | C | T | 1 | a0002c0002t0001g0316 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.476+1372G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339774 | |||||||
| chr5:39339861 | G | A | 62 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(59): Show |
64 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.476+1285C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339861 | |||||||
| chr5:39339894 | C | A | 1 | a0002c0002t0001g0298 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.476+1252G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339894 | |||||||
| chr5:39339905 | C | T | 86 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(83): Show |
90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.476+1241G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339905 | |||||||
| chr5:39339969 | G | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0050 others(27): Show |
34 | HG00408.hp2 HG00558.hp1 HG02080.hp2 others(31): Show |
intron_variant | MODIFIER | c.476+1177C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339969 | |||||||
| chr5:39339972 | G | C | 4 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0179 others(1): Show |
4 | HG00609.hp2 NA18944.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+1174C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39339972 | |||||||
| chr5:39340033 | C | A | 87 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(84): Show |
91 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.476+1113G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340033 | |||||||
| chr5:39340180 | G | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.476+966C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340180 | |||||||
| chr5:39340347 | C | CCAACAAA others(20): Show |
1 | a0008c0011t0001g0324 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.476+772_476+798dup others(27): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340347 | |||||||
| chr5:39340372 | T | TAGCAACA others(20): Show |
1 | a0002c0002t0001g0298 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.476+773_476+774ins others(27): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340372 | |||||||
| chr5:39340459 | G | A | 168 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(165): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.476+687C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340459 | |||||||
| chr5:39340477 | T | C | 1 | a0001c0001t0002g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.476+669A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340477 | |||||||
| chr5:39340515 | T | G | 1 | a0007c0008t0007g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.476+631A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340515 | |||||||
| chr5:39340542 | T | TC | 4 | a0004c0003t0005g0005 a0004c0003t0005g0041 a0004c0003t0005g0044 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.476+603dupG | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340542 | |||||||
| chr5:39340564 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.476+582G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340564 | |||||||
| chr5:39340573 | G | T | 41 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0004 others(38): Show |
46 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.476+573C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340573 | |||||||
| chr5:39340639 | C | T | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.476+507G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340639 | |||||||
| chr5:39340690 | G | C | 1 | a0001c0013t0002g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.476+456C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340690 | |||||||
| chr5:39340699 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.476+447G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340699 | |||||||
| chr5:39340740 | G | A | 1 | a0002c0002t0001g0358 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.476+406C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340740 | |||||||
| chr5:39340792 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.476+354C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340792 | |||||||
| chr5:39340804 | C | A | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.476+342G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340804 | |||||||
| chr5:39340842 | G | T | 1 | a0001c0001t0001g0241 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.476+304C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340842 | |||||||
| chr5:39340907 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.476+239A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340907 | |||||||
| chr5:39340910 | T | C | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.476+236A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340910 | |||||||
| chr5:39340931 | A | G | 1 | a0002c0002t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.476+215T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340931 | |||||||
| chr5:39340946 | G | A | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.476+200C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 4/10 | chr5 | 39340946 | |||||||
| chr5:39341335 | A | G | 1 | a0002c0002t0001g0340 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.329-42T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 3/10 | chr5 | 39341335 | |||||||
| chr5:39341395 | A | G | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.329-102T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 3/10 | chr5 | 39341395 | |||||||
| chr5:39341765 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.184-65C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 2/10 | chr5 | 39341765 | |||||||
| chr5:39341811 | A | G | 5 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0220 others(2): Show |
5 | HG02615.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-111T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 2/10 | chr5 | 39341811 | |||||||
| chr5:39342017 | A | G | 6 | a0006c0006t0001g0053 a0006c0006t0001g0120 a0006c0006t0001g0121 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+74T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 2/10 | chr5 | 39342017 | |||||||
| chr5:39342071 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.183+20C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 2/10 | chr5 | 39342071 | |||||||
| chr5:39342206 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(231): Show |
253 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.78-10G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39342206 | |||||||
| chr5:39342391 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(243): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.78-195A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39342391 | |||||||
| chr5:39342408 | T | G | 2 | a0002c0002t0001g0320 a0002c0002t0001g0336 |
2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.78-212A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39342408 | |||||||
| chr5:39342459 | G | A | 1 | a0001c0005t0002g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.78-263C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39342459 | |||||||
| chr5:39342590 | C | T | 2 | a0008c0011t0001g0285 a0008c0011t0001g0324 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.78-394G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39342590 | |||||||
| chr5:39342887 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.78-691A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39342887 | |||||||
| chr5:39342916 | T | C | 332 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(329): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.78-720A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39342916 | |||||||
| chr5:39343061 | A | G | 76 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(73): Show |
80 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.78-865T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343061 | |||||||
| chr5:39343090 | C | T | 2 | a0001c0001t0002g0011 a0007c0008t0007g0137 |
3 | HG01167.hp2 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.78-894G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343090 | |||||||
| chr5:39343260 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.78-1064C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343260 | |||||||
| chr5:39343293 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(175): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.78-1097T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343293 | |||||||
| chr5:39343362 | A | G | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.78-1166T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343362 | |||||||
| chr5:39343411 | C | T | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78-1215G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343411 | |||||||
| chr5:39343412 | A | T | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78-1216T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343412 | |||||||
| chr5:39343436 | T | C | 2 | a0001c0001t0001g0071 a0002c0002t0001g0327 |
2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.78-1240A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343436 | |||||||
| chr5:39343463 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0072 a0001c0001t0001g0096 others(4): Show |
8 | HG00099.hp2 HG00733.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-1267G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343463 | |||||||
| chr5:39343524 | A | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0051 others(26): Show |
33 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.78-1328T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343524 | |||||||
| chr5:39343565 | G | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(175): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.78-1369C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343565 | |||||||
| chr5:39343570 | C | T | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0203 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-1374G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343570 | |||||||
| chr5:39343595 | G | A | 1 | a0012c0019t0001g0306 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.78-1399C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343595 | |||||||
| chr5:39343819 | T | G | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.78-1623A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343819 | |||||||
| chr5:39343844 | A | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(330): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.78-1648T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343844 | |||||||
| chr5:39343850 | A | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.78-1654T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343850 | |||||||
| chr5:39343864 | A | G | 2 | a0001c0005t0002g0023 a0009c0012t0002g0276 |
2 | HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.78-1668T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343864 | |||||||
| chr5:39343874 | A | G | 331 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(328): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.78-1678T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343874 | |||||||
| chr5:39343880 | C | T | 15 | a0001c0001t0001g0232 a0001c0001t0001g0265 a0001c0001t0002g0197 others(12): Show |
15 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.78-1684G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343880 | |||||||
| chr5:39343896 | T | TGATACCC others(15): Show |
17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.78-1722_78-1701dup others(22): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343896 | |||||||
| chr5:39343905 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.78-1709C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343905 | |||||||
| chr5:39343941 | A | G | 2 | a0001c0001t0002g0201 a0001c0005t0002g0012 |
3 | HG02451.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.78-1745T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39343941 | |||||||
| chr5:39344007 | C | G | 1 | a0001c0001t0002g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.78-1811G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344007 | |||||||
| chr5:39344068 | G | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.78-1872C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344068 | |||||||
| chr5:39344109 | A | T | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0203 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-1913T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344109 | |||||||
| chr5:39344164 | C | G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0030 others(101): Show |
110 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.78-1968G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344164 | |||||||
| chr5:39344215 | A | G | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.78-2019T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344215 | |||||||
| chr5:39344254 | C | A | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-2058G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344254 | |||||||
| chr5:39344370 | T | C | 18 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(15): Show |
18 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.78-2174A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344370 | |||||||
| chr5:39344392 | T | C | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.78-2196A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344392 | |||||||
| chr5:39344398 | G | A | 12 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(9): Show |
12 | HG01934.hp1 HG01943.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.78-2202C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344398 | |||||||
| chr5:39344494 | C | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0093 others(31): Show |
36 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.78-2298G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344494 | |||||||
| chr5:39344630 | T | C | 1 | a0002c0002t0001g0302 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.78-2434A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344630 | |||||||
| chr5:39344637 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.78-2441C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344637 | |||||||
| chr5:39344713 | A | G | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-2517T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344713 | |||||||
| chr5:39344736 | T | A | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-2540A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344736 | |||||||
| chr5:39344826 | G | A | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0203 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-2630C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344826 | |||||||
| chr5:39344858 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.78-2662C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344858 | |||||||
| chr5:39344929 | C | T | 366 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(363): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.78-2733G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344929 | |||||||
| chr5:39344979 | T | A | 1 | a0009c0012t0002g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.78-2783A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39344979 | |||||||
| chr5:39345037 | G | C | 1 | a0001c0010t0001g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.78-2841C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345037 | |||||||
| chr5:39345070 | G | C | 69 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(66): Show |
73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.78-2874C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345070 | |||||||
| chr5:39345070 | G | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.78-2874C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345070 | |||||||
| chr5:39345077 | G | A | 69 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(66): Show |
73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.78-2881C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345077 | |||||||
| chr5:39345084 | T | C | 69 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(66): Show |
73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.78-2888A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345084 | |||||||
| chr5:39345089 | A | G | 69 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(66): Show |
73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.78-2893T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345089 | |||||||
| chr5:39345091 | T | G | 69 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(66): Show |
73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.78-2895A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345091 | |||||||
| chr5:39345094 | C | T | 69 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(66): Show |
73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.78-2898G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345094 | |||||||
| chr5:39345203 | C | T | 2 | a0001c0001t0002g0011 a0007c0008t0007g0137 |
3 | HG01167.hp2 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.78-3007G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345203 | |||||||
| chr5:39345224 | T | C | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.78-3028A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345224 | |||||||
| chr5:39345244 | A | C | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0203 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-3048T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345244 | |||||||
| chr5:39345250 | C | G | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.78-3054G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345250 | |||||||
| chr5:39345264 | T | C | 69 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(66): Show |
73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.78-3068A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345264 | |||||||
| chr5:39345338 | C | T | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-3142G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345338 | |||||||
| chr5:39345405 | A | G | 2 | a0002c0002t0001g0017 a0002c0002t0001g0356 |
3 | HG01256.hp2 HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.78-3209T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345405 | |||||||
| chr5:39345414 | A | G | 17 | a0001c0001t0001g0232 a0001c0001t0001g0265 a0001c0001t0002g0011 others(14): Show |
18 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.78-3218T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345414 | |||||||
| chr5:39345437 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.78-3241A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345437 | |||||||
| chr5:39345440 | C | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.78-3244G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345440 | |||||||
| chr5:39345705 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.78-3509T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345705 | |||||||
| chr5:39345756 | C | T | 1 | a0007c0008t0007g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78-3560G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345756 | |||||||
| chr5:39345757 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.78-3561C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345757 | |||||||
| chr5:39345786 | A | C | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(16): Show |
19 | HG00733.hp1 HG00741.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.78-3590T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345786 | |||||||
| chr5:39345838 | A | T | 15 | a0001c0001t0001g0232 a0001c0001t0001g0265 a0001c0001t0002g0197 others(12): Show |
15 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.78-3642T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345838 | |||||||
| chr5:39345888 | A | G | 1 | a0001c0001t0002g0109 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.78-3692T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345888 | |||||||
| chr5:39345903 | C | T | 2 | a0001c0001t0002g0037 a0002c0021t0002g0289 |
2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.78-3707G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345903 | |||||||
| chr5:39345922 | T | A | 2 | a0003c0004t0001g0192 a0003c0004t0001g0193 |
2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.78-3726A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345922 | |||||||
| chr5:39345942 | G | A | 3 | a0001c0001t0002g0201 a0001c0005t0002g0012 a0001c0005t0002g0272 |
4 | HG01243.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-3746C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345942 | |||||||
| chr5:39345945 | AGAAATAA others(11): Show |
A | 1 | a0007c0008t0007g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78-3767_78-3750del others(18): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345945 | |||||||
| chr5:39345991 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-3795A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39345991 | |||||||
| chr5:39346030 | G | C | 1 | a0002c0002t0001g0347 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.78-3834C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346030 | |||||||
| chr5:39346043 | C | A | 1 | a0007c0008t0007g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78-3847G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346043 | |||||||
| chr5:39346074 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.78-3878T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346074 | |||||||
| chr5:39346171 | A | G | 17 | a0001c0001t0001g0232 a0001c0001t0001g0265 a0001c0001t0002g0011 others(14): Show |
18 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.78-3975T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346171 | |||||||
| chr5:39346190 | T | C | 1 | a0001c0001t0001g0264 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.78-3994A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346190 | |||||||
| chr5:39346247 | A | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-4051T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346247 | |||||||
| chr5:39346452 | T | C | 6 | a0001c0001t0002g0223 a0001c0001t0006g0185 a0001c0001t0006g0186 others(3): Show |
6 | HG01192.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-4256A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346452 | |||||||
| chr5:39346493 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.78-4297C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346493 | |||||||
| chr5:39346666 | T | G | 7 | a0001c0001t0001g0200 a0001c0001t0002g0035 a0001c0001t0002g0042 others(4): Show |
7 | HG02717.hp2 HG02970.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.78-4470A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346666 | |||||||
| chr5:39346700 | C | A | 1 | a0001c0001t0002g0199 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-4504G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346700 | |||||||
| chr5:39346714 | A | T | 2 | a0001c0001t0001g0217 a0001c0001t0002g0052 |
2 | HG00099.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.78-4518T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346714 | |||||||
| chr5:39346730 | T | C | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.78-4534A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346730 | |||||||
| chr5:39346824 | T | C | 1 | a0004c0003t0005g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.78-4628A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346824 | |||||||
| chr5:39346825 | G | A | 1 | a0004c0003t0005g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.78-4629C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346825 | |||||||
| chr5:39346838 | T | G | 1 | a0004c0003t0005g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.78-4642A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346838 | |||||||
| chr5:39346853 | AAGGCTGG others(974): Show |
A | 1 | a0004c0003t0005g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.78-5638_78-4658del | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346853 | |||||||
| chr5:39346951 | G | A | 17 | a0001c0001t0001g0232 a0001c0001t0001g0265 a0001c0001t0002g0011 others(14): Show |
18 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.78-4755C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39346951 | |||||||
| chr5:39347015 | C | T | 1 | a0002c0002t0002g0303 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.78-4819G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347015 | |||||||
| chr5:39347016 | G | A | 4 | a0006c0006t0001g0120 a0006c0006t0001g0121 a0006c0006t0001g0183 others(1): Show |
4 | HG02818.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-4820C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347016 | |||||||
| chr5:39347130 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.78-4934G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347130 | |||||||
| chr5:39347137 | C | A | 1 | a0002c0002t0002g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.78-4941G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347137 | |||||||
| chr5:39347264 | G | T | 331 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(328): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.78-5068C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347264 | |||||||
| chr5:39347323 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(4): Show |
7 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.78-5127C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347323 | |||||||
| chr5:39347413 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.78-5217G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347413 | |||||||
| chr5:39347420 | C | G | 17 | a0001c0001t0001g0232 a0001c0001t0001g0265 a0001c0001t0002g0011 others(14): Show |
18 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.78-5224G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347420 | |||||||
| chr5:39347495 | A | G | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78-5299T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347495 | |||||||
| chr5:39347530 | C | T | 332 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(329): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.78-5334G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347530 | |||||||
| chr5:39347576 | G | A | 1 | a0001c0001t0003g0036 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.78-5380C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347576 | |||||||
| chr5:39347588 | G | A | 315 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(312): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.78-5392C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347588 | |||||||
| chr5:39347652 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.78-5456A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347652 | |||||||
| chr5:39347737 | G | A | 4 | a0006c0006t0001g0120 a0006c0006t0001g0121 a0006c0006t0001g0183 others(1): Show |
4 | HG02818.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-5541C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347737 | |||||||
| chr5:39347748 | C | A | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78-5552G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347748 | |||||||
| chr5:39347771 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.78-5575T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347771 | |||||||
| chr5:39347840 | G | T | 1 | a0004c0003t0005g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.78-5644C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347840 | |||||||
| chr5:39347874 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.78-5678G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347874 | |||||||
| chr5:39347901 | G | C | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78-5705C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347901 | |||||||
| chr5:39347937 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.78-5741A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347937 | |||||||
| chr5:39347942 | G | T | 332 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(329): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.78-5746C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347942 | |||||||
| chr5:39347948 | G | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(330): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.78-5752C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347948 | |||||||
| chr5:39347951 | A | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(172): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.78-5755T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347951 | |||||||
| chr5:39347965 | T | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(330): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.78-5769A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347965 | |||||||
| chr5:39347983 | C | T | 333 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(330): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.78-5787G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347983 | |||||||
| chr5:39347992 | T | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(330): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.78-5796A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347992 | |||||||
| chr5:39347999 | T | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(330): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.78-5803A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39347999 | |||||||
| chr5:39348001 | T | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(330): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.78-5805A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348001 | |||||||
| chr5:39348042 | T | A | 1 | a0009c0012t0002g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.78-5846A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348042 | |||||||
| chr5:39348049 | C | A | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-5853G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348049 | |||||||
| chr5:39348049 | C | T | 3 | a0006c0006t0001g0120 a0006c0006t0001g0121 a0006c0006t0001g0183 |
3 | HG02818.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.78-5853G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348049 | |||||||
| chr5:39348101 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01070.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.78-5905A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348101 | |||||||
| chr5:39348120 | C | A | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-5924G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348120 | |||||||
| chr5:39348193 | A | T | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.78-5997T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348193 | |||||||
| chr5:39348221 | G | C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-6025C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348221 | |||||||
| chr5:39348224 | C | T | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-6028G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348224 | |||||||
| chr5:39348231 | G | A | 4 | a0006c0006t0001g0120 a0006c0006t0001g0121 a0006c0006t0001g0183 others(1): Show |
4 | HG02818.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-6035C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348231 | |||||||
| chr5:39348514 | G | T | 1 | a0001c0001t0002g0235 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.78-6318C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348514 | |||||||
| chr5:39348589 | C | T | 15 | a0001c0001t0001g0232 a0001c0001t0001g0265 a0001c0001t0002g0197 others(12): Show |
15 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.78-6393G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348589 | |||||||
| chr5:39348603 | G | C | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0203 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-6407C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348603 | |||||||
| chr5:39348640 | A | G | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-6444T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348640 | |||||||
| chr5:39348761 | C | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0093 others(31): Show |
35 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.78-6565G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348761 | |||||||
| chr5:39348810 | G | T | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-6614C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348810 | |||||||
| chr5:39348982 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.78-6786C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39348982 | |||||||
| chr5:39349034 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.78-6838T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349034 | |||||||
| chr5:39349048 | G | A | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0203 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-6852C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349048 | |||||||
| chr5:39349131 | G | A | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.78-6935C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349131 | |||||||
| chr5:39349136 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.78-6940G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349136 | |||||||
| chr5:39349137 | G | A | 3 | a0001c0001t0001g0045 a0002c0002t0001g0329 a0002c0002t0001g0351 |
3 | HG02602.hp1 HG02965.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.78-6941C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349137 | |||||||
| chr5:39349181 | A | C | 1 | a0007c0008t0007g0230 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.78-6985T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349181 | |||||||
| chr5:39349183 | G | GA | 68 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(65): Show |
72 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.78-6988dupT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349183 | |||||||
| chr5:39349183 | GA | G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-6988delT | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349183 | |||||||
| chr5:39349251 | C | T | 2 | a0001c0001t0001g0027 a0002c0002t0003g0357 |
2 | HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.78-7055G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349251 | |||||||
| chr5:39349309 | A | G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-7113T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349309 | |||||||
| chr5:39349360 | A | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(36): Show |
40 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.78-7164T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349360 | |||||||
| chr5:39349361 | A | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(36): Show |
40 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.78-7165T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349361 | |||||||
| chr5:39349362 | A | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(36): Show |
40 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.78-7166T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349362 | |||||||
| chr5:39349389 | C | T | 7 | a0001c0001t0001g0200 a0001c0001t0002g0035 a0001c0001t0002g0042 others(4): Show |
7 | HG02717.hp2 HG02970.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.78-7193G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349389 | |||||||
| chr5:39349495 | A | G | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0203 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-7299T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349495 | |||||||
| chr5:39349581 | G | A | 2 | a0004c0003t0005g0218 a0004c0003t0005g0219 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.78-7385C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349581 | |||||||
| chr5:39349590 | G | T | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-7394C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349590 | |||||||
| chr5:39349602 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.78-7406C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349602 | |||||||
| chr5:39349653 | G | A | 3 | a0001c0001t0001g0265 a0002c0002t0001g0304 a0002c0002t0002g0291 |
3 | HG01109.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.78-7457C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349653 | |||||||
| chr5:39349723 | T | G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-7527A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349723 | |||||||
| chr5:39349794 | T | C | 7 | a0001c0001t0001g0200 a0001c0001t0002g0035 a0001c0001t0002g0042 others(4): Show |
7 | HG02717.hp2 HG02970.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.78-7598A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349794 | |||||||
| chr5:39349890 | G | A | 17 | a0001c0001t0001g0232 a0001c0001t0001g0265 a0001c0001t0002g0011 others(14): Show |
18 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.78-7694C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349890 | |||||||
| chr5:39349920 | C | G | 1 | a0001c0001t0001g0020 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.78-7724G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39349920 | |||||||
| chr5:39350044 | G | T | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0203 others(10): Show |
14 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-7848C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350044 | |||||||
| chr5:39350154 | A | G | 2 | a0002c0002t0001g0331 a0002c0002t0001g0332 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.78-7958T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350154 | |||||||
| chr5:39350182 | G | A | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | NA18941.hp2 NA18972.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.78-7986C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350182 | |||||||
| chr5:39350261 | C | T | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(12): Show |
15 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.78-8065G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350261 | |||||||
| chr5:39350369 | T | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(12): Show |
15 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.78-8173A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350369 | |||||||
| chr5:39350479 | T | C | 2 | a0002c0002t0001g0282 a0002c0002t0001g0283 |
2 | HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.78-8283A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350479 | |||||||
| chr5:39350503 | C | T | 2 | a0001c0001t0002g0011 a0007c0008t0007g0137 |
3 | HG01167.hp2 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.78-8307G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350503 | |||||||
| chr5:39350549 | A | AAGGTACA others(4): Show |
14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-8354_78-8353ins others(11): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350549 | |||||||
| chr5:39350722 | G | A | 1 | a0007c0008t0007g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78-8526C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350722 | |||||||
| chr5:39350816 | G | C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-8620C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350816 | |||||||
| chr5:39350841 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.78-8645C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39350841 | |||||||
| chr5:39351088 | G | A | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-8892C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351088 | |||||||
| chr5:39351089 | T | G | 1 | a0004c0003t0005g0044 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.78-8893A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351089 | |||||||
| chr5:39351113 | G | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0093 others(31): Show |
36 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.78-8917C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351113 | |||||||
| chr5:39351326 | C | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-9130G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351326 | |||||||
| chr5:39351364 | T | C | 69 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(66): Show |
73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.78-9168A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351364 | |||||||
| chr5:39351401 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.78-9205G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351401 | |||||||
| chr5:39351450 | C | A | 34 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0093 others(31): Show |
36 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.78-9254G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351450 | |||||||
| chr5:39351502 | G | A | 11 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0002c0002t0001g0016 others(8): Show |
13 | HG00642.hp2 HG01169.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-9306C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351502 | |||||||
| chr5:39351553 | T | G | 2 | a0001c0001t0001g0067 a0001c0001t0002g0245 |
2 | HG02040.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.78-9357A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351553 | |||||||
| chr5:39351588 | A | T | 1 | a0004c0003t0005g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.78-9392T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351588 | |||||||
| chr5:39351601 | C | T | 333 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(330): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.78-9405G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351601 | |||||||
| chr5:39351721 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0116 a0001c0001t0001g0246 others(3): Show |
6 | HG00438.hp2 HG00558.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-9525G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351721 | |||||||
| chr5:39351779 | G | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-9583C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351779 | |||||||
| chr5:39351836 | T | A | 34 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0093 others(31): Show |
36 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.78-9640A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351836 | |||||||
| chr5:39351864 | C | G | 17 | a0001c0001t0001g0232 a0001c0001t0001g0265 a0001c0001t0002g0011 others(14): Show |
18 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.78-9668G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351864 | |||||||
| chr5:39351950 | C | T | 1 | a0001c0001t0003g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.78-9754G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39351950 | |||||||
| chr5:39352228 | T | A | 1 | a0002c0002t0001g0330 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-10032A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352228 | |||||||
| chr5:39352276 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.78-10080C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352276 | |||||||
| chr5:39352292 | C | A | 1 | a0001c0001t0001g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.78-10096G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352292 | |||||||
| chr5:39352440 | C | T | 1 | a0007c0008t0007g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78-10244G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352440 | |||||||
| chr5:39352666 | T | C | 2 | a0001c0001t0004g0365 a0001c0001t0004g0367 |
2 | NA18964.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.78-10470A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352666 | |||||||
| chr5:39352670 | G | A | 1 | a0007c0008t0007g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78-10474C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352670 | |||||||
| chr5:39352736 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01070.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.78-10540C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352736 | |||||||
| chr5:39352823 | A | G | 3 | a0006c0006t0001g0120 a0006c0006t0001g0121 a0006c0006t0001g0183 |
3 | HG02818.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.78-10627T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352823 | |||||||
| chr5:39352834 | GT | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(16): Show |
19 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.78-10639delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352834 | |||||||
| chr5:39352841 | T | TG | 23 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0028 others(20): Show |
24 | HG00741.hp2 HG01256.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.78-10646_78-10645i others(3): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352841 | |||||||
| chr5:39352842 | T | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(287): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.78-10646A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352842 | |||||||
| chr5:39352843 | T | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(16): Show |
19 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.78-10647A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39352843 | |||||||
| chr5:39353315 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.77+11073C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353315 | |||||||
| chr5:39353429 | C | A | 2 | a0001c0001t0002g0037 a0002c0021t0002g0289 |
2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.77+10959G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353429 | |||||||
| chr5:39353460 | A | G | 34 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0093 others(31): Show |
36 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.77+10928T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353460 | |||||||
| chr5:39353620 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0065 others(36): Show |
40 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.77+10768A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353620 | |||||||
| chr5:39353754 | AAGAGTTT others(2): Show |
A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0051 others(25): Show |
32 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.77+10625_77+10633d others(11): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353754 | |||||||
| chr5:39353759 | T | C | 1 | a0002c0002t0001g0330 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.77+10629A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353759 | |||||||
| chr5:39353808 | G | C | 1 | a0001c0015t0008g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.77+10580C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353808 | |||||||
| chr5:39353927 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.77+10461G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353927 | |||||||
| chr5:39353937 | C | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.77+10451G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353937 | |||||||
| chr5:39353967 | G | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
17 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.77+10421C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353967 | |||||||
| chr5:39353988 | G | A | 1 | a0002c0002t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.77+10400C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39353988 | |||||||
| chr5:39354137 | G | A | 2 | a0001c0001t0001g0030 a0002c0002t0001g0294 |
2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.77+10251C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39354137 | |||||||
| chr5:39354440 | C | A | 34 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(31): Show |
36 | HG00609.hp2 HG00621.hp1 HG02056.hp2 others(33): Show |
intron_variant | MODIFIER | c.77+9948G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39354440 | |||||||
| chr5:39354551 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.77+9837T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39354551 | |||||||
| chr5:39354601 | C | T | 1 | a0001c0010t0001g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.77+9787G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39354601 | |||||||
| chr5:39354615 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.77+9773C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39354615 | |||||||
| chr5:39354657 | A | C | 11 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0202 others(8): Show |
11 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.77+9731T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39354657 | |||||||
| chr5:39354660 | A | T | 11 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0202 others(8): Show |
11 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.77+9728T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39354660 | |||||||
| chr5:39354716 | T | C | 2 | a0001c0001t0001g0040 a0002c0002t0003g0357 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.77+9672A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39354716 | |||||||
| chr5:39354811 | A | G | 105 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0026 others(102): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.77+9577T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39354811 | |||||||
| chr5:39355033 | A | T | 185 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(182): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.77+9355T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355033 | |||||||
| chr5:39355065 | G | A | 2 | a0001c0001t0002g0195 a0003c0004t0001g0267 |
2 | HG03098.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.77+9323C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355065 | |||||||
| chr5:39355187 | T | C | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.77+9201A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355187 | |||||||
| chr5:39355188 | C | T | 2 | a0001c0001t0004g0369 a0002c0002t0001g0296 |
2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.77+9200G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355188 | |||||||
| chr5:39355409 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG03490.hp1 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.77+8979A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355409 | |||||||
| chr5:39355461 | G | GT | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.77+8926dupA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355461 | |||||||
| chr5:39355489 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0039 others(123): Show |
137 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.77+8899C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355489 | |||||||
| chr5:39355545 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(44): Show |
52 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.77+8843G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355545 | |||||||
| chr5:39355546 | G | A | 75 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0017 others(72): Show |
81 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.77+8842C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355546 | |||||||
| chr5:39355836 | T | G | 1 | a0002c0002t0002g0337 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.77+8552A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355836 | |||||||
| chr5:39355897 | C | T | 1 | a0001c0005t0002g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.77+8491G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355897 | |||||||
| chr5:39355898 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(123): Show |
137 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.77+8490C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39355898 | |||||||
| chr5:39356024 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.77+8364T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356024 | |||||||
| chr5:39356053 | C | G | 5 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0004c0003t0005g0005 others(2): Show |
6 | HG02630.hp2 HG02895.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+8335G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356053 | |||||||
| chr5:39356176 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.77+8212C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356176 | |||||||
| chr5:39356232 | A | G | 1 | a0003c0004t0001g0268 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.77+8156T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356232 | |||||||
| chr5:39356339 | C | A | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.77+8049G>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356339 | |||||||
| chr5:39356406 | G | C | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.77+7982C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356406 | |||||||
| chr5:39356407 | C | G | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.77+7981G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356407 | |||||||
| chr5:39356415 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.77+7973G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356415 | |||||||
| chr5:39356489 | G | A | 79 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0017 others(76): Show |
85 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.77+7899C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356489 | |||||||
| chr5:39356492 | C | G | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.77+7896G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356492 | |||||||
| chr5:39356493 | G | C | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.77+7895C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356493 | |||||||
| chr5:39356512 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG03490.hp1 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.77+7876C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356512 | |||||||
| chr5:39356624 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+7764C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356624 | |||||||
| chr5:39356652 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+7736G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356652 | |||||||
| chr5:39356699 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.77+7689A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356699 | |||||||
| chr5:39356725 | A | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG03490.hp1 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.77+7663T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356725 | |||||||
| chr5:39356828 | C | T | 1 | a0001c0001t0002g0011 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.77+7560G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356828 | |||||||
| chr5:39356964 | G | A | 14 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0001t0002g0042 others(11): Show |
16 | HG01361.hp1 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+7424C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39356964 | |||||||
| chr5:39357022 | C | T | 1 | a0001c0001t0001g0007 | 2 | NA18955.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.77+7366G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357022 | |||||||
| chr5:39357073 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(135): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.77+7315T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357073 | |||||||
| chr5:39357081 | A | T | 1 | a0002c0002t0001g0330 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.77+7307T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357081 | |||||||
| chr5:39357311 | C | T | 2 | a0001c0001t0002g0201 a0001c0005t0002g0012 |
3 | HG02451.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.77+7077G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357311 | |||||||
| chr5:39357326 | C | T | 1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.77+7062G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357326 | |||||||
| chr5:39357329 | G | C | 1 | a0002c0002t0001g0304 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.77+7059C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357329 | |||||||
| chr5:39357475 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(2): Show |
5 | HG01123.hp1 HG01192.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+6913T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357475 | |||||||
| chr5:39357551 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.77+6837C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357551 | |||||||
| chr5:39357557 | AT | A | 80 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0017 others(77): Show |
86 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.77+6830delA | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357557 | |||||||
| chr5:39357637 | C | G | 1 | a0006c0006t0001g0183 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.77+6751G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357637 | |||||||
| chr5:39357683 | G | A | 1 | a0006c0006t0001g0183 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.77+6705C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357683 | |||||||
| chr5:39357756 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.77+6632G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357756 | |||||||
| chr5:39357759 | T | A | 1 | a0011c0014t0001g0178 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.77+6629A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357759 | |||||||
| chr5:39357765 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(48): Show |
57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.77+6623C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357765 | |||||||
| chr5:39357837 | A | T | 1 | a0007c0008t0007g0137 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.77+6551T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357837 | |||||||
| chr5:39357942 | G | A | 1 | a0002c0002t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+6446C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357942 | |||||||
| chr5:39357995 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02055.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.77+6393G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39357995 | |||||||
| chr5:39358018 | G | A | 1 | a0007c0008t0007g0137 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.77+6370C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358018 | |||||||
| chr5:39358122 | A | G | 1 | a0007c0008t0007g0137 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.77+6266T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358122 | |||||||
| chr5:39358233 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.77+6155T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358233 | |||||||
| chr5:39358455 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(131): Show |
146 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.77+5933A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358455 | |||||||
| chr5:39358841 | C | T | 1 | a0001c0005t0002g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.77+5547G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358841 | |||||||
| chr5:39358844 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG00609.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.77+5544C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358844 | |||||||
| chr5:39358910 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.77+5478C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358910 | |||||||
| chr5:39358923 | T | C | 83 | a0001c0015t0008g0138 a0002c0002t0001g0003 a0002c0002t0001g0016 others(80): Show |
89 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.77+5465A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358923 | |||||||
| chr5:39358933 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.77+5455G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358933 | |||||||
| chr5:39358934 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.77+5454C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358934 | |||||||
| chr5:39358963 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0039 others(133): Show |
148 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.77+5425A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358963 | |||||||
| chr5:39358988 | A | AAAAT | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG01123.hp1 HG01192.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+5396_77+5399dup others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358988 | |||||||
| chr5:39358988 | A | T | 82 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0017 others(79): Show |
88 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.77+5400T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39358988 | |||||||
| chr5:39359009 | A | T | 1 | a0001c0001t0002g0034 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+5379T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359009 | |||||||
| chr5:39359010 | AAT | A | 5 | a0001c0001t0002g0004 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
6 | HG01346.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+5376_77+5377del others(2): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359010 | |||||||
| chr5:39359015 | AAAAT | A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0003g0124 others(3): Show |
6 | HG01256.hp1 HG01891.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+5369_77+5372del others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359015 | |||||||
| chr5:39359015 | AAAATAT | A | 24 | a0001c0001t0001g0184 a0001c0001t0001g0188 a0001c0001t0001g0191 others(21): Show |
26 | HG00735.hp1 HG01167.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.77+5367_77+5372del others(6): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359015 | |||||||
| chr5:39359015 | AAAATATA others(1): Show |
A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0236 a0001c0001t0001g0237 others(31): Show |
40 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.77+5365_77+5372del others(8): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359015 | |||||||
| chr5:39359016 | A | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0038 others(3): Show |
6 | HG02055.hp1 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+5372T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359016 | |||||||
| chr5:39359017 | A | T | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.77+5371T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359017 | |||||||
| chr5:39359017 | AAT | A | 16 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(13): Show |
16 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+5369_77+5370del others(2): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359017 | |||||||
| chr5:39359017 | AATAT | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.77+5367_77+5370del others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359017 | |||||||
| chr5:39359017 | AATATAT | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0002g0042 others(4): Show |
8 | HG02630.hp2 HG02895.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+5365_77+5370del others(6): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359017 | |||||||
| chr5:39359017 | AATATATA others(1): Show |
A | 98 | a0001c0001t0001g0232 a0001c0001t0001g0265 a0001c0001t0001g0271 others(95): Show |
104 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.77+5363_77+5370del others(8): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359017 | |||||||
| chr5:39359019 | T | A | 29 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0026 others(26): Show |
32 | HG00438.hp1 HG00621.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.77+5369A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359019 | |||||||
| chr5:39359021 | T | A | 15 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
16 | HG01123.hp1 HG01192.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+5367A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359021 | |||||||
| chr5:39359023 | T | A | 8 | a0001c0001t0001g0006 a0001c0001t0002g0004 a0001c0001t0002g0033 others(5): Show |
10 | HG01346.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+5365A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359023 | |||||||
| chr5:39359025 | T | A | 1 | a0001c0001t0002g0235 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.77+5363A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359025 | |||||||
| chr5:39359036 | A | G | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG01123.hp1 HG01192.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+5352T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359036 | |||||||
| chr5:39359038 | G | T | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.77+5350C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359038 | |||||||
| chr5:39359048 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+5340C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359048 | |||||||
| chr5:39359050 | A | G | 3 | a0001c0001t0001g0275 a0001c0001t0002g0273 a0001c0001t0002g0274 |
3 | HG01884.hp1 HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.77+5338T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359050 | |||||||
| chr5:39359060 | G | T | 1 | a0001c0001t0002g0197 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.77+5328C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359060 | |||||||
| chr5:39359060 | GTA | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG03139.hp2 HG03225.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+5326_77+5327del others(2): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359060 | |||||||
| chr5:39359070 | A | G | 1 | a0002c0002t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+5318T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359070 | |||||||
| chr5:39359078 | G | A | 1 | a0002c0002t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+5310C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359078 | |||||||
| chr5:39359078 | GTA | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG01123.hp1 HG01192.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+5308_77+5309del others(2): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359078 | |||||||
| chr5:39359084 | A | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.77+5304T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359084 | |||||||
| chr5:39359088 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0039 others(55): Show |
64 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.77+5300T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359088 | |||||||
| chr5:39359088 | ATG | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0047 others(64): Show |
72 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.77+5298_77+5299del others(2): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359088 | |||||||
| chr5:39359088 | ATGTG | A | 4 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0004c0003t0005g0218 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+5296_77+5299del others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359088 | |||||||
| chr5:39359090 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(3): Show |
6 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+5298C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359090 | |||||||
| chr5:39359098 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0002g0223 a0001c0001t0006g0224 |
3 | HG01192.hp1 HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.77+5290C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359098 | |||||||
| chr5:39359098 | G | GTA | 4 | a0001c0001t0001g0126 a0001c0001t0001g0134 a0001c0001t0002g0125 others(1): Show |
4 | HG01952.hp1 HG04204.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+5289_77+5290ins others(2): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359098 | |||||||
| chr5:39359098 | G | GTATATAT others(1): Show |
3 | a0001c0001t0002g0042 a0004c0003t0005g0005 a0004c0003t0005g0041 |
4 | HG02630.hp2 HG02895.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+5289_77+5290ins others(8): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359098 | |||||||
| chr5:39359098 | G | GTATATAT others(7): Show |
1 | a0001c0001t0002g0043 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.77+5289_77+5290ins others(14): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359098 | |||||||
| chr5:39359098 | G | GTATATAT others(11): Show |
1 | a0004c0003t0005g0044 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.77+5289_77+5290ins others(18): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359098 | |||||||
| chr5:39359100 | G | A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0046 others(60): Show |
66 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.77+5288C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359100 | |||||||
| chr5:39359100 | G | GTA | 8 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0200 others(5): Show |
9 | HG01361.hp1 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+5287_77+5288ins others(2): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359100 | |||||||
| chr5:39359100 | G | GTATA | 10 | a0001c0001t0001g0203 a0001c0001t0002g0004 a0001c0001t0002g0034 others(7): Show |
12 | HG01346.hp2 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+5287_77+5288ins others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359100 | |||||||
| chr5:39359100 | G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0040 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.77+5287_77+5288ins others(18): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359100 | |||||||
| chr5:39359102 | G | A | 152 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.77+5286C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTA | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0009t0002g0227 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+5284_77+5285dup others(2): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTATA | 4 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0009t0002g0231 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+5282_77+5285dup others(4): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTATATAT others(3): Show |
30 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0236 others(27): Show |
36 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.77+5276_77+5285dup others(10): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTATATAT others(5): Show |
4 | a0001c0001t0001g0032 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
4 | HG03486.hp1 NA18747.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+5274_77+5285dup others(12): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0019 a0001c0001t0003g0263 |
2 | HG00733.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.77+5272_77+5285dup others(14): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTATATAT others(11): Show |
3 | a0001c0001t0001g0264 a0003c0004t0001g0266 a0003c0004t0001g0267 |
3 | HG03098.hp2 HG03471.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.77+5268_77+5285dup others(18): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTATATAT others(13): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0265 others(4): Show |
7 | HG00741.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+5266_77+5285dup others(20): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTATATAT others(15): Show |
1 | a0001c0001t0001g0022 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.77+5264_77+5285dup others(22): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTATAT others(7): Show |
1 | a0002c0002t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+5285_77+5286ins others(14): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTATAT others(17): Show |
1 | a0002c0002t0003g0357 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.77+5285_77+5286ins others(24): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTAT others(7): Show |
1 | a0008c0011t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.77+5285_77+5286ins others(14): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTAT others(9): Show |
7 | a0002c0002t0001g0321 a0002c0002t0001g0323 a0002c0002t0001g0325 others(4): Show |
7 | HG02738.hp2 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(16): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTAT others(11): Show |
5 | a0002c0002t0001g0330 a0002c0002t0001g0331 a0002c0002t0001g0332 others(2): Show |
6 | HG01070.hp1 HG01071.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(18): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTAT others(13): Show |
2 | a0002c0002t0001g0016 a0002c0002t0001g0338 |
3 | HG00735.hp2 HG01169.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(20): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTAT others(15): Show |
7 | a0002c0002t0001g0343 a0002c0002t0001g0344 a0002c0002t0001g0345 others(4): Show |
7 | HG00642.hp2 HG01255.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(22): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTAT others(17): Show |
4 | a0002c0002t0001g0349 a0002c0002t0001g0350 a0002c0002t0001g0351 others(1): Show |
4 | HG01074.hp1 HG01109.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(24): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTAT others(19): Show |
3 | a0002c0002t0001g0354 a0002c0002t0001g0355 a0002c0002t0001g0356 |
3 | HG01099.hp2 HG01261.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(26): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTAT others(21): Show |
1 | a0002c0002t0001g0017 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(28): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(7): Show |
1 | a0002c0002t0001g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.77+5285_77+5286ins others(14): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(9): Show |
6 | a0002c0002t0001g0299 a0002c0002t0001g0300 a0002c0002t0001g0301 others(3): Show |
6 | HG01928.hp2 HG01975.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(16): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(11): Show |
16 | a0002c0002t0001g0283 a0002c0002t0001g0307 a0002c0002t0001g0308 others(13): Show |
16 | HG01071.hp1 HG02165.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(18): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(13): Show |
3 | a0002c0002t0001g0328 a0002c0002t0001g0329 a0002c0002t0001g0360 |
3 | HG02451.hp1 HG03927.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(20): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(15): Show |
5 | a0002c0002t0001g0333 a0002c0002t0001g0334 a0002c0002t0001g0335 others(2): Show |
5 | HG01515.hp2 NA18969.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(22): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(17): Show |
6 | a0002c0002t0001g0340 a0002c0002t0001g0342 a0002c0002t0001g0359 others(3): Show |
6 | HG01109.hp1 HG01934.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(24): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(19): Show |
2 | a0002c0002t0001g0003 a0002c0002t0001g0348 |
5 | HG01978.hp1 NA18953.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(26): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(21): Show |
2 | a0002c0002t0002g0352 a0002c0002t0002g0353 |
2 | HG01943.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(28): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(23): Show |
1 | a0002c0002t0001g0358 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.77+5285_77+5286ins others(30): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(11): Show |
5 | a0002c0002t0001g0282 a0002c0002t0001g0296 a0002c0002t0001g0298 others(2): Show |
5 | HG00408.hp1 HG01175.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+5285_77+5286ins others(18): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(13): Show |
1 | a0002c0002t0001g0305 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.77+5285_77+5286ins others(20): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359102 | G | GTGTGTGT others(9): Show |
1 | a0002c0002t0001g0294 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.77+5285_77+5286ins others(16): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359102 | |||||||
| chr5:39359174 | G | A | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.77+5214C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359174 | |||||||
| chr5:39359221 | A | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(130): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.77+5167T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359221 | |||||||
| chr5:39359301 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(266): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.77+5087G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359301 | |||||||
| chr5:39359513 | C | T | 6 | a0001c0001t0002g0226 a0001c0009t0002g0227 a0001c0009t0002g0228 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+4875G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359513 | |||||||
| chr5:39359529 | G | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG03490.hp1 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.77+4859C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359529 | |||||||
| chr5:39359671 | G | C | 81 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0017 others(78): Show |
87 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.77+4717C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359671 | |||||||
| chr5:39359806 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.77+4582A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359806 | |||||||
| chr5:39359813 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+4575A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359813 | |||||||
| chr5:39359885 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02055.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.77+4503G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359885 | |||||||
| chr5:39359902 | A | G | 1 | a0007c0008t0007g0137 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.77+4486T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39359902 | |||||||
| chr5:39360127 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+4261T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360127 | |||||||
| chr5:39360380 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(130): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.77+4008G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360380 | |||||||
| chr5:39360398 | G | A | 1 | a0002c0002t0001g0359 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.77+3990C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360398 | |||||||
| chr5:39360417 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.77+3971A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360417 | |||||||
| chr5:39360425 | A | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0039 others(133): Show |
148 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.77+3963T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360425 | |||||||
| chr5:39360431 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0039 others(133): Show |
148 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.77+3957T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360431 | |||||||
| chr5:39360466 | T | C | 1 | a0007c0008t0007g0137 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.77+3922A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360466 | |||||||
| chr5:39360652 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.77+3736G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360652 | |||||||
| chr5:39360723 | A | G | 1 | a0001c0001t0003g0225 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.77+3665T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360723 | |||||||
| chr5:39360750 | T | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(48): Show |
57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.77+3638A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360750 | |||||||
| chr5:39360783 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+3605T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39360783 | |||||||
| chr5:39361053 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(135): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.77+3335G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361053 | |||||||
| chr5:39361161 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.77+3227T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361161 | |||||||
| chr5:39361201 | G | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.77+3187C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361201 | |||||||
| chr5:39361296 | C | T | 5 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0004c0003t0005g0005 others(2): Show |
6 | HG02630.hp2 HG02895.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+3092G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361296 | |||||||
| chr5:39361407 | T | G | 1 | a0001c0001t0004g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.77+2981A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361407 | |||||||
| chr5:39361454 | A | G | 82 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0017 others(79): Show |
88 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.77+2934T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361454 | |||||||
| chr5:39361700 | C | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(131): Show |
146 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.77+2688G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361700 | |||||||
| chr5:39361753 | G | A | 26 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0184 others(23): Show |
28 | HG00735.hp1 HG01167.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.77+2635C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361753 | |||||||
| chr5:39361777 | G | C | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG01433.hp1 HG01952.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+2611C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361777 | |||||||
| chr5:39361937 | C | T | 82 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0017 others(79): Show |
88 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.77+2451G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361937 | |||||||
| chr5:39361971 | C | G | 82 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0017 others(79): Show |
88 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.77+2417G>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361971 | |||||||
| chr5:39361987 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.77+2401A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361987 | |||||||
| chr5:39361992 | T | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0004 others(6): Show |
10 | HG01346.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+2396A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39361992 | |||||||
| chr5:39362065 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0039 others(138): Show |
153 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.77+2323C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362065 | |||||||
| chr5:39362079 | A | G | 1 | a0007c0008t0007g0137 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.77+2309T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362079 | |||||||
| chr5:39362185 | T | G | 3 | a0001c0001t0001g0046 a0004c0003t0005g0218 a0004c0003t0005g0219 |
3 | HG02559.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.77+2203A>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362185 | |||||||
| chr5:39362237 | T | C | 6 | a0001c0001t0001g0271 a0003c0004t0001g0266 a0003c0004t0001g0267 others(3): Show |
6 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+2151A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362237 | |||||||
| chr5:39362265 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.77+2123G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362265 | |||||||
| chr5:39362311 | G | T | 3 | a0001c0001t0001g0275 a0001c0001t0002g0273 a0001c0001t0002g0274 |
3 | HG01884.hp1 HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.77+2077C>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362311 | |||||||
| chr5:39362331 | A | C | 1 | a0001c0001t0002g0002 | 4 | HG00639.hp2 HG00738.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+2057T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362331 | |||||||
| chr5:39362444 | AGGAGGGA others(16): Show |
A | 1 | a0002c0002t0001g0360 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.77+1921_77+1943del others(23): Show |
C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362444 | |||||||
| chr5:39362479 | G | C | 75 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0017 others(72): Show |
80 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.77+1909C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362479 | |||||||
| chr5:39362616 | C | T | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.77+1772G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362616 | |||||||
| chr5:39362650 | C | T | 5 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0004c0003t0005g0005 others(2): Show |
6 | HG02630.hp2 HG02895.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+1738G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362650 | |||||||
| chr5:39362918 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02055.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.77+1470C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362918 | |||||||
| chr5:39362986 | C | T | 6 | a0001c0001t0002g0004 a0001c0001t0002g0033 a0001c0001t0002g0034 others(3): Show |
7 | HG01346.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+1402G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39362986 | |||||||
| chr5:39363003 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+1385G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363003 | |||||||
| chr5:39363140 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0005t0002g0023 |
3 | HG02055.hp1 HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.77+1248G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363140 | |||||||
| chr5:39363152 | G | A | 1 | a0001c0005t0002g0272 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.77+1236C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363152 | |||||||
| chr5:39363224 | A | T | 2 | a0002c0002t0001g0282 a0002c0002t0001g0283 |
2 | HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.77+1164T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363224 | |||||||
| chr5:39363250 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.77+1138C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363250 | |||||||
| chr5:39363331 | G | C | 11 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(8): Show |
11 | HG00621.hp2 HG02074.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.77+1057C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363331 | |||||||
| chr5:39363366 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.77+1022C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363366 | |||||||
| chr5:39363389 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+999G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363389 | |||||||
| chr5:39363526 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.77+862T>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363526 | |||||||
| chr5:39363592 | C | T | 5 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0004c0003t0005g0005 others(2): Show |
6 | HG02630.hp2 HG02895.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+796G>A | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363592 | |||||||
| chr5:39363628 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0236 others(48): Show |
57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.77+760C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363628 | |||||||
| chr5:39363680 | T | A | 9 | a0001c0001t0004g0018 a0001c0001t0004g0362 a0001c0001t0004g0363 others(6): Show |
10 | HG00438.hp1 HG02056.hp1 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.77+708A>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363680 | |||||||
| chr5:39363712 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.77+676C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363712 | |||||||
| chr5:39363809 | A | G | 5 | a0001c0001t0001g0222 a0001c0001t0002g0223 a0001c0001t0006g0220 others(2): Show |
5 | HG01192.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+579T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363809 | |||||||
| chr5:39363935 | G | C | 1 | a0002c0002t0001g0361 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.77+453C>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363935 | |||||||
| chr5:39363999 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG00733.hp1 HG00741.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+389T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39363999 | |||||||
| chr5:39364039 | T | C | 5 | a0001c0001t0001g0222 a0001c0001t0002g0223 a0001c0001t0006g0220 others(2): Show |
5 | HG01192.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+349A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39364039 | |||||||
| chr5:39364111 | G | A | 7 | a0001c0001t0001g0222 a0001c0001t0002g0223 a0001c0001t0006g0220 others(4): Show |
7 | HG01192.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+277C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39364111 | |||||||
| chr5:39364237 | T | C | 92 | a0001c0001t0001g0275 a0001c0001t0001g0277 a0001c0001t0001g0278 others(89): Show |
98 | HG00408.hp1 HG00558.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.77+151A>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39364237 | |||||||
| chr5:39364256 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0039 others(149): Show |
165 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.77+132C>T | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39364256 | |||||||
| chr5:39364351 | A | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG03490.hp1 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.77+37T>G | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39364351 | |||||||
| chr5:39364372 | A | G | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(17): Show |
21 | HG00733.hp1 HG00741.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+16T>C | C9 | ENSG00000113600.12 | transcript | ENST00000263408.5 | protein_coding | 1/10 | chr5 | 39364372 |