Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23016 |
| ensemblid | ENSG00000075914.13 |
| hgncid | 28112 |
| symbol | EXOSC7 |
| name | exosome component 7 |
| refseq_nuc | NM_015004.4 |
| refseq_prot | NP_055819.2 |
| ensembl_nuc | ENST00000265564.8 |
| ensembl_prot | ENSP00000265564.7 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 44976244 |
| end | 45011471 |
| strand | + |
| ver | v1.2 |
| region | chr3:44976244-45011471 |
| region5000 | chr3:44971244-45016471 |
| regionname0 | EXOSC7_chr3_44976244_45011471 |
| regionname5000 | EXOSC7_chr3_44971244_45016471 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 291 | 225 | 72 | 38 | 84 | 7 | 24 | 62 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | MASVT others(286): Show |
chr3 | 44971244 | 45016471 |
| a0002 | 1/1 | 291 | 93 | 22 | 29 | 24 | 7 | 9 | 19 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | MASVT others(286): Show |
chr3 | 44971244 | 45016471 |
| a0003 | 0/0 | 291 | 20 | 0 | 7 | 7 | 2 | 4 | 6 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | MASVA others(286): Show |
chr3 | 44971244 | 45016471 |
| a0004 | 0/0 | 291 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | MASVT others(286): Show |
chr3 | 44971244 | 45016471 |
| a0005 | 0/0 | 197 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | MASVT others(192): Show |
chr3 | 44971244 | 45016471 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 873 | 221 | 69 | 38 | 83 | 7 | 24 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | ATGGC others(868): Show |
chr3 | 44971244 | 45016471 | ||
| a0001c0004 | 0/0 | 873 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | ATGGC others(868): Show |
chr3 | 44971244 | 45016471 | ||
| a0001c0008 | 0/0 | 873 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | ATGGC others(868): Show |
chr3 | 44971244 | 45016471 | ||
| a0002c0002 | 1/1 | 873 | 92 | 22 | 28 | 24 | 7 | 9 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | ATGGC others(868): Show |
chr3 | 44971244 | 45016471 | ||
| a0002c0005 | 0/0 | 873 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | ATGGC others(868): Show |
chr3 | 44971244 | 45016471 | ||
| a0003c0003 | 0/0 | 873 | 20 | 0 | 7 | 7 | 2 | 4 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | ATGGC others(868): Show |
chr3 | 44971244 | 45016471 | ||
| a0004c0007 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | ATGGC others(868): Show |
chr3 | 44971244 | 45016471 | ||
| a0005c0006 | 0/0 | 593 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | ATGGC others(588): Show |
chr3 | 44971244 | 45016471 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1042 | 221 | 69 | 38 | 83 | 7 | 24 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | AGATG others(1037): Show |
chr3 | 44971244 | 45016471 |
| a0001c0004t0001 | 0/0 | 1042 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | AGATG others(1037): Show |
chr3 | 44971244 | 45016471 |
| a0001c0008t0001 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | AGATG others(1037): Show |
chr3 | 44971244 | 45016471 |
| a0002c0002t0001 | 1/1 | 1042 | 92 | 22 | 28 | 24 | 7 | 9 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | AGATG others(1037): Show |
chr3 | 44971244 | 45016471 |
| a0002c0005t0001 | 0/0 | 1042 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | AGATG others(1037): Show |
chr3 | 44971244 | 45016471 |
| a0003c0003t0001 | 0/0 | 1042 | 20 | 0 | 7 | 7 | 2 | 4 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | AGATG others(1037): Show |
chr3 | 44971244 | 45016471 |
| a0004c0007t0001 | 0/0 | 1042 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | AGATG others(1037): Show |
chr3 | 44971244 | 45016471 |
| a0005c0006t0001 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | AGATG others(757): Show |
chr3 | 44971244 | 45016471 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 38 | 3 | 10 | 21 | 0 | 4 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0003 | 0/0 | 15 | 0 | 4 | 4 | 1 | 6 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0007 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 3 | 2 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0004t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0001c0008t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0002 | 0/0 | 21 | 2 | 7 | 10 | 2 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0006 | 0/0 | 9 | 3 | 4 | 0 | 1 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0009 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0016 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0020 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0002c0005t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0003c0003t0001g0004 | 0/0 | 11 | 0 | 5 | 3 | 1 | 2 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0003c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0004c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| a0005c0006t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0118 | EUR | GBR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0004 | EUR | GBR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0063 | EUR | GBR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0051 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01074 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0081 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01243 | hp1 | a0002 | c0005 | t0001 | g0021 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0050 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0057 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0094 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0024 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0053 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0024 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03017 | hp2 | a0004 | c0007 | t0001 | g0001 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0079 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0075 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0076 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0024 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0056 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0068 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0067 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG04228 | hp2 | a0003 | c0003 | t0001 | g0004 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18942 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18960 | hp2 | a0001 | c0008 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0052 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19057 | hp1 | a0005 | c0006 | t0001 | g0155 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ASW | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0016 | EUR | TSI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0016 | EUR | TSI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | GIH | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0093 | REF | REF | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0020 | REF | REF | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44976290 | A | G | 1 | a0003 | 20 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(17): Show |
missense_variant | MODERATE | c.13A>G | p.Thr5Ala | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/8 | 47/1042 | 13/876 | 5/291 | chr3 | 44976290 | |||
| chr3:45003609 | TAGCTGGA others(6001): Show |
T | 1 | a0005 | 1 | NA19057.hp1 | exon_loss_variant | HIGH | c.492-1677_772-1614d others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 45003609 | ||||||
| chr3:45005305 | G | A | 1 | a0001 | 13 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(10): Show |
missense_variant | MODERATE | c.506G>A | p.Arg169Gln | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/8 | 540/1042 | 506/876 | 169/291 | chr3 | 45005305 | |||
| chr3:45007424 | G | A | 1 | a0002 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.620G>A | p.Gly207Asp | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/8 | 654/1042 | 620/876 | 207/291 | chr3 | 45007424 | |||
| chr3:45007567 | A | T | 1 | a0001 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.763A>T | p.Met255Leu | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/8 | 797/1042 | 763/876 | 255/291 | chr3 | 45007567 | |||
| chr3:45011245 | G | A | 1 | a0004 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.782G>A | p.Arg261His | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 8/8 | 816/1042 | 782/876 | 261/291 | chr3 | 45011245 | |||
| chr3:45011283 | G | C | 4 | a0001 a0003 a0004 others(1): Show |
247 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
missense_variant | MODERATE | c.820G>C | p.Val274Leu | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 8/8 | 854/1042 | 820/876 | 274/291 | chr3 | 45011283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44976310 | G | A | 1 | a0002c0005 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.33G>A | p.Lys11Lys | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/8 | 67/1042 | 33/876 | 11/291 | chr3 | 44976310 | |||
| chr3:44989160 | C | T | 1 | a0001c0008 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.78C>T | p.Gly26Gly | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/8 | 112/1042 | 78/876 | 26/291 | chr3 | 44989160 | |||
| chr3:45001603 | T | C | 1 | a0001c0004 | 3 | HG02258.hp2 HG02818.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.486T>C | p.Asn162Asn | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/8 | 520/1042 | 486/876 | 162/291 | chr3 | 45001603 | |||
| chr3:45005297 | A | G | 1 | a0003c0003 | 2 | HG00639.hp2 HG01106.hp1 |
synonymous_variant | LOW | c.498A>G | p.Pro166Pro | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/8 | 532/1042 | 498/876 | 166/291 | chr3 | 45005297 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44976366 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+32C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976366 | |||||||
| chr3:44976412 | A | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(81): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.57+78A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976412 | |||||||
| chr3:44976413 | G | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(81): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.57+79G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976413 | |||||||
| chr3:44976494 | C | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+160C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976494 | |||||||
| chr3:44976556 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0154 |
3 | HG00733.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.57+222C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976556 | |||||||
| chr3:44976688 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.57+354G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976688 | |||||||
| chr3:44976704 | T | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.57+370T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976704 | |||||||
| chr3:44976782 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0151 a0001c0001t0001g0152 |
4 | HG01891.hp2 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+448A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976782 | |||||||
| chr3:44976828 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0149 a0001c0001t0001g0150 |
4 | HG01081.hp2 HG01943.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+494A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976828 | |||||||
| chr3:44976979 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02523.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.57+645T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976979 | |||||||
| chr3:44977034 | C | CA | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+709dupA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44977034 | ||||||
| chr3:44977091 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.57+757A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977091 | |||||||
| chr3:44977213 | A | T | 1 | a0002c0002t0001g0094 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.57+879A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977213 | |||||||
| chr3:44977215 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.57+881C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977215 | |||||||
| chr3:44977568 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.57+1234A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977568 | |||||||
| chr3:44977647 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.57+1313G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977647 | |||||||
| chr3:44977653 | A | C | 1 | a0001c0001t0001g0042 | 2 | HG00673.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.57+1319A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977653 | |||||||
| chr3:44977683 | T | C | 1 | a0002c0002t0001g0062 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57+1349T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977683 | |||||||
| chr3:44978144 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.57+1810A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44978144 | |||||||
| chr3:44978323 | AAG | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
5 | HG01978.hp2 HG01981.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+1991_57+1992del others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44978323 | ||||||
| chr3:44978343 | A | T | 4 | a0002c0002t0001g0023 a0002c0002t0001g0031 a0002c0002t0001g0091 others(1): Show |
7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+2009A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44978343 | |||||||
| chr3:44978488 | T | C | 1 | a0002c0002t0001g0063 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.57+2154T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44978488 | |||||||
| chr3:44978714 | C | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0058 |
9 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+2380C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44978714 | |||||||
| chr3:44979012 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+2678T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979012 | |||||||
| chr3:44979046 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+2712C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979046 | |||||||
| chr3:44979174 | A | G | 1 | a0003c0003t0001g0057 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.57+2840A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979174 | |||||||
| chr3:44979215 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.57+2881T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979215 | |||||||
| chr3:44979301 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.57+2967A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979301 | |||||||
| chr3:44979504 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.57+3170A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979504 | |||||||
| chr3:44979518 | C | A | 1 | a0002c0002t0001g0064 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.57+3184C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979518 | |||||||
| chr3:44979521 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57+3187C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979521 | |||||||
| chr3:44979537 | G | T | 1 | a0001c0001t0001g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57+3203G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979537 | |||||||
| chr3:44979550 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57+3216G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979550 | |||||||
| chr3:44979589 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+3255T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979589 | |||||||
| chr3:44979598 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0095 |
3 | HG01516.hp2 HG01517.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.57+3264T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979598 | |||||||
| chr3:44979598 | T | TTC | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(74): Show |
172 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.57+3264_57+3265ins others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979598 | |||||||
| chr3:44979924 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.57+3590G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979924 | |||||||
| chr3:44980047 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3713T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980047 | |||||||
| chr3:44980048 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3714A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980048 | |||||||
| chr3:44980049 | T | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3715T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980049 | |||||||
| chr3:44980052 | C | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3718C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980052 | |||||||
| chr3:44980053 | C | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3719C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980053 | |||||||
| chr3:44980054 | A | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3720A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980054 | |||||||
| chr3:44980057 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3723T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980057 | |||||||
| chr3:44980058 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3724T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980058 | |||||||
| chr3:44980059 | T | TGCAGTGG others(47): Show |
2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3725_57+3726ins others(54): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980059 | |||||||
| chr3:44980482 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+4148C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980482 | |||||||
| chr3:44980501 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0004t0001g0024 |
5 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+4167G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980501 | |||||||
| chr3:44980544 | A | G | 1 | a0003c0003t0001g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.57+4210A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980544 | |||||||
| chr3:44980604 | C | T | 6 | a0002c0002t0001g0009 a0002c0002t0001g0030 a0002c0002t0001g0087 others(3): Show |
11 | HG00735.hp2 HG00741.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.57+4270C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980604 | |||||||
| chr3:44980624 | C | T | 4 | a0002c0002t0001g0023 a0002c0002t0001g0031 a0002c0002t0001g0091 others(1): Show |
7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+4290C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980624 | |||||||
| chr3:44981656 | A | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+5322A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44981656 | |||||||
| chr3:44982098 | G | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.57+5764G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982098 | |||||||
| chr3:44982127 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.57+5793T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982127 | |||||||
| chr3:44982264 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0095 a0001c0001t0001g0156 others(2): Show |
15 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(12): Show |
intron_variant | MODIFIER | c.57+5930A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982264 | |||||||
| chr3:44982278 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.57+5944C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982278 | |||||||
| chr3:44982278 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.57+5944C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982278 | |||||||
| chr3:44982342 | G | A | 1 | a0002c0002t0001g0062 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57+6008G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982342 | |||||||
| chr3:44982352 | T | C | 10 | a0003c0003t0001g0004 a0003c0003t0001g0047 a0003c0003t0001g0048 others(7): Show |
20 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+6018T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982352 | |||||||
| chr3:44982418 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.57+6084T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982418 | |||||||
| chr3:44982509 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.57+6175A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982509 | |||||||
| chr3:44982563 | G | T | 1 | a0002c0002t0001g0086 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.57+6229G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982563 | |||||||
| chr3:44982583 | G | A | 4 | a0002c0002t0001g0023 a0002c0002t0001g0031 a0002c0002t0001g0091 others(1): Show |
7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+6249G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982583 | |||||||
| chr3:44982719 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(152): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.57+6385A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982719 | |||||||
| chr3:44982941 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58-6199G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982941 | |||||||
| chr3:44983061 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.58-6079A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983061 | |||||||
| chr3:44983183 | C | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0123 |
2 | HG00423.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.58-5957C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983183 | |||||||
| chr3:44983335 | G | C | 1 | a0005c0006t0001g0155 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.58-5805G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983335 | |||||||
| chr3:44983410 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0040 others(19): Show |
43 | HG00280.hp2 HG00609.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.58-5730C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983410 | |||||||
| chr3:44983448 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.58-5692A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983448 | |||||||
| chr3:44983523 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.58-5617T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983523 | |||||||
| chr3:44983641 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(84): Show |
187 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.58-5499T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983641 | |||||||
| chr3:44983760 | C | T | 1 | a0002c0002t0001g0090 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.58-5380C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983760 | |||||||
| chr3:44983785 | CTG | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.58-5352_58-5351del others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44983785 | ||||||
| chr3:44983848 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0054 |
3 | HG02486.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.58-5292A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983848 | |||||||
| chr3:44983865 | T | TA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(79): Show |
180 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.58-5265dupA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44983865 | ||||||
| chr3:44983913 | T | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.58-5227T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983913 | |||||||
| chr3:44984200 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58-4940G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984200 | |||||||
| chr3:44984319 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.58-4821A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984319 | |||||||
| chr3:44984450 | G | C | 1 | a0001c0001t0001g0040 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.58-4690G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984450 | |||||||
| chr3:44984521 | A | G | 1 | a0002c0002t0001g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.58-4619A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984521 | |||||||
| chr3:44984611 | G | A | 1 | a0001c0001t0001g0012 | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-4529G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984611 | |||||||
| chr3:44984635 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0055 others(1): Show |
13 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-4505A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984635 | |||||||
| chr3:44984719 | A | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.58-4421A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984719 | |||||||
| chr3:44984942 | A | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.58-4198A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984942 | |||||||
| chr3:44985011 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58-4129A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985011 | |||||||
| chr3:44985024 | A | T | 1 | a0001c0001t0001g0012 | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-4116A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985024 | |||||||
| chr3:44985297 | A | G | 1 | a0002c0002t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.58-3843A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985297 | |||||||
| chr3:44985359 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.58-3781T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985359 | |||||||
| chr3:44985418 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58-3722C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985418 | |||||||
| chr3:44985450 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58-3690C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985450 | |||||||
| chr3:44985570 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58-3570G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985570 | |||||||
| chr3:44985597 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-3543G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985597 | |||||||
| chr3:44985619 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-3521C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985619 | |||||||
| chr3:44985652 | A | T | 1 | a0002c0002t0001g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.58-3488A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985652 | |||||||
| chr3:44985721 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.58-3419G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985721 | |||||||
| chr3:44985732 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0133 |
2 | HG03704.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.58-3408G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985732 | |||||||
| chr3:44986017 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.58-3123C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986017 | |||||||
| chr3:44986205 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.58-2935A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986205 | |||||||
| chr3:44986220 | T | TG | 10 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0001t0001g0120 others(7): Show |
11 | HG01192.hp1 HG02135.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-2917dupG | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44986220 | ||||||
| chr3:44986224 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.58-2916A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986224 | |||||||
| chr3:44986243 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.58-2897A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986243 | |||||||
| chr3:44986365 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.58-2775C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986365 | |||||||
| chr3:44986401 | C | T | 11 | a0001c0001t0001g0046 a0003c0003t0001g0004 a0003c0003t0001g0047 others(8): Show |
21 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.58-2739C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986401 | |||||||
| chr3:44986429 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0054 |
3 | HG02486.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.58-2711C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986429 | |||||||
| chr3:44986437 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58-2703C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986437 | |||||||
| chr3:44986450 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58-2690C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986450 | |||||||
| chr3:44986594 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.58-2546G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986594 | |||||||
| chr3:44986619 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.58-2521C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986619 | |||||||
| chr3:44986620 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.58-2520A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986620 | |||||||
| chr3:44986717 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.58-2423A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986717 | |||||||
| chr3:44986719 | C | G | 1 | a0002c0002t0001g0083 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.58-2421C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986719 | |||||||
| chr3:44986759 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0095 a0001c0001t0001g0156 others(2): Show |
15 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-2381C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986759 | |||||||
| chr3:44986807 | G | C | 1 | a0001c0001t0001g0113 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.58-2333G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986807 | |||||||
| chr3:44987015 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-2125A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987015 | |||||||
| chr3:44987085 | TAA | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(89): Show |
196 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.58-2054_58-2053del others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987085 | |||||||
| chr3:44987092 | T | TA | 9 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0002c0002t0001g0023 others(6): Show |
13 | HG02055.hp2 HG02056.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.58-2032dupA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44987092 | ||||||
| chr3:44987092 | TA | T | 15 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0044 others(12): Show |
19 | HG01070.hp2 HG01168.hp2 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.58-2032delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44987092 | ||||||
| chr3:44987098 | AAAAAAAA others(36): Show |
A | 1 | a0001c0001t0001g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.58-2039_58-1997del others(43): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44987098 | ||||||
| chr3:44987132 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0054 |
3 | HG02486.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.58-2008C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987132 | |||||||
| chr3:44987487 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.58-1653G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987487 | |||||||
| chr3:44987494 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.58-1646C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987494 | |||||||
| chr3:44987495 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0120 |
3 | HG02602.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.58-1645G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987495 | |||||||
| chr3:44987565 | A | G | 1 | a0003c0003t0001g0050 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.58-1575A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987565 | |||||||
| chr3:44987683 | C | CT | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.58-1456dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44987683 | ||||||
| chr3:44988056 | C | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0131 |
3 | HG02717.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-1084C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44988056 | |||||||
| chr3:44988175 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.58-965G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44988175 | |||||||
| chr3:44988737 | T | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(17): Show |
42 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.58-403T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44988737 | |||||||
| chr3:44988790 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.58-350A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44988790 | |||||||
| chr3:44988971 | A | G | 8 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0127 others(5): Show |
10 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-169A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44988971 | |||||||
| chr3:44989072 | T | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.58-68T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44989072 | |||||||
| chr3:44989105 | G | C | 4 | a0002c0002t0001g0029 a0002c0002t0001g0067 a0002c0002t0001g0068 others(1): Show |
5 | HG01071.hp1 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-35G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44989105 | |||||||
| chr3:44989106 | G | T | 3 | a0002c0002t0001g0029 a0002c0002t0001g0068 a0002c0002t0001g0081 |
4 | HG01071.hp1 HG01168.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-34G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44989106 | |||||||
| chr3:44989257 | A | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.159+16A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | chr3 | 44989257 | |||||||
| chr3:44989258 | T | C | 1 | a0002c0002t0001g0069 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.159+17T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | chr3 | 44989258 | |||||||
| chr3:44989310 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0119 |
6 | HG00438.hp1 NA18957.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+69C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | chr3 | 44989310 | |||||||
| chr3:44989373 | G | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.159+132G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | chr3 | 44989373 | |||||||
| chr3:44989375 | A | AG | 10 | a0003c0003t0001g0004 a0003c0003t0001g0047 a0003c0003t0001g0048 others(7): Show |
20 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.159+141dupG | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 44989375 | ||||||
| chr3:44989377 | G | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0041 others(12): Show |
35 | HG00609.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.159+136G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | chr3 | 44989377 | |||||||
| chr3:44989858 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
15 | NA18979.hp1 NA18984.hp1 NA18991.hp1 others(12): Show |
intron_variant | MODIFIER | c.254+214C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44989858 | |||||||
| chr3:44989873 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0055 |
4 | HG01934.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+229C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44989873 | |||||||
| chr3:44990241 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.254+597T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990241 | |||||||
| chr3:44990294 | GA | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(84): Show |
187 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.254+651delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990294 | |||||||
| chr3:44990379 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+735T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990379 | |||||||
| chr3:44990512 | G | T | 1 | a0002c0002t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.254+868G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990512 | |||||||
| chr3:44990653 | A | ACTCCTCA others(35): Show |
1 | a0001c0001t0001g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.254+1009_254+1010i others(44): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990653 | |||||||
| chr3:44990730 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.254+1086C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990730 | |||||||
| chr3:44990983 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.254+1339C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990983 | |||||||
| chr3:44991016 | CG | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.254+1373delG | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991016 | |||||||
| chr3:44991362 | A | G | 1 | a0002c0002t0001g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.254+1718A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991362 | |||||||
| chr3:44991572 | C | T | 8 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0127 others(5): Show |
10 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.254+1928C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991572 | |||||||
| chr3:44991704 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.254+2060T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991704 | |||||||
| chr3:44991729 | C | G | 1 | a0002c0002t0001g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.254+2085C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991729 | |||||||
| chr3:44991861 | A | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0046 others(12): Show |
34 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.254+2217A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991861 | |||||||
| chr3:44992001 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.254+2357G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992001 | |||||||
| chr3:44992069 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.254+2425A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992069 | |||||||
| chr3:44992525 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.254+2881T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992525 | |||||||
| chr3:44992527 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.254+2883G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992527 | |||||||
| chr3:44992718 | C | G | 1 | a0002c0002t0001g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.254+3074C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992718 | |||||||
| chr3:44992847 | TAGAG | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.254+3206_254+3209d others(6): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44992847 | ||||||
| chr3:44992919 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.254+3275C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992919 | |||||||
| chr3:44993128 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.254+3484G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44993128 | |||||||
| chr3:44993589 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.255-3498C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44993589 | |||||||
| chr3:44994039 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.255-3048T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994039 | |||||||
| chr3:44994245 | TA | T | 16 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0054 others(13): Show |
27 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.255-2825delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994245 | ||||||
| chr3:44994261 | AAG | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(36): Show |
94 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.255-2824_255-2823d others(4): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994261 | ||||||
| chr3:44994262 | A | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0095 a0001c0001t0001g0156 others(2): Show |
15 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(12): Show |
intron_variant | MODIFIER | c.255-2825A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994262 | |||||||
| chr3:44994263 | GA | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0123 |
5 | HG00423.hp1 HG00423.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.255-2823delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994263 | |||||||
| chr3:44994264 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.255-2823A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994264 | |||||||
| chr3:44994274 | CCTT | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0060 |
3 | HG02809.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.255-2809_255-2807d others(5): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994274 | ||||||
| chr3:44994279 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.255-2808T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994279 | |||||||
| chr3:44994369 | A | AT | 8 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0127 others(5): Show |
10 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.255-2704dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994369 | ||||||
| chr3:44994605 | A | G | 1 | a0002c0002t0001g0076 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.255-2482A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994605 | |||||||
| chr3:44994683 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.255-2404G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994683 | |||||||
| chr3:44994856 | G | GGT | 7 | a0002c0002t0001g0028 a0002c0002t0001g0062 a0002c0002t0001g0070 others(4): Show |
7 | HG01975.hp2 HG01981.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.255-2182_255-2181d others(4): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | G | GGTGT | 8 | a0001c0001t0001g0007 a0002c0002t0001g0002 a0002c0002t0001g0009 others(5): Show |
11 | HG00280.hp1 HG01256.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.255-2184_255-2181d others(6): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | G | GGTGTGT | 5 | a0001c0001t0001g0007 a0002c0002t0001g0023 a0002c0002t0001g0030 others(2): Show |
5 | HG02145.hp1 HG03041.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.255-2186_255-2181d others(8): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | G | GGTGTGTG others(1): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0002c0002t0001g0092 |
4 | HG01167.hp2 HG01169.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-2188_255-2181d others(10): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | G | GGTGTGTG others(3): Show |
1 | a0002c0002t0001g0002 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.255-2190_255-2181d others(12): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | G | GGTGTGTG others(5): Show |
1 | a0002c0002t0001g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.255-2192_255-2181d others(14): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | GGT | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0027 others(17): Show |
35 | HG00140.hp2 HG00735.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.255-2182_255-2181d others(4): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | GGTGT | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
28 | HG00609.hp1 HG00639.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.255-2184_255-2181d others(6): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | GGTGTGT | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(9): Show |
25 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.255-2186_255-2181d others(8): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | GGTGTGTG others(1): Show |
G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(30): Show |
44 | HG00280.hp2 HG00609.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.255-2188_255-2181d others(10): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | GGTGTGTG others(3): Show |
G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(52): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.255-2190_255-2181d others(12): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | GGTGTGTG others(5): Show |
G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0131 others(2): Show |
5 | HG01109.hp2 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-2192_255-2181d others(14): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | GGTGTGTG others(7): Show |
G | 2 | a0001c0001t0001g0145 a0003c0003t0001g0004 |
2 | NA19030.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.255-2194_255-2181d others(16): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994856 | GGTGTGTG others(11): Show |
G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0140 |
2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.255-2198_255-2181d others(20): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | ||||||
| chr3:44994870 | T | G | 1 | a0001c0001t0001g0114 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.255-2217T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994870 | |||||||
| chr3:44994944 | A | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0124 a0001c0001t0001g0131 others(1): Show |
5 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-2143A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994944 | |||||||
| chr3:44994947 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.255-2140C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994947 | |||||||
| chr3:44994954 | C | CA | 6 | a0001c0001t0001g0037 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
9 | HG02258.hp2 HG02818.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.255-2124dupA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994954 | ||||||
| chr3:44995047 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0025 others(5): Show |
20 | HG00642.hp1 HG01109.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.255-2040C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44995047 | |||||||
| chr3:44995230 | G | A | 1 | a0002c0002t0001g0016 | 4 | HG00733.hp2 HG03491.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.255-1857G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44995230 | |||||||
| chr3:44995308 | G | A | 22 | a0002c0002t0001g0002 a0002c0002t0001g0016 a0002c0002t0001g0022 others(19): Show |
49 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.255-1779G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44995308 | |||||||
| chr3:44996018 | A | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0046 others(12): Show |
34 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.255-1069A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996018 | |||||||
| chr3:44996158 | G | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(110): Show |
247 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.255-929G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996158 | |||||||
| chr3:44996178 | T | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(82): Show |
183 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.255-909T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996178 | |||||||
| chr3:44996277 | T | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.255-810T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996277 | |||||||
| chr3:44996299 | CA | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
209 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.255-783delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44996299 | ||||||
| chr3:44996412 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.255-675G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996412 | |||||||
| chr3:44996556 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0058 |
9 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.255-531A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996556 | |||||||
| chr3:44996753 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.255-334A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996753 | |||||||
| chr3:44996847 | A | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0004t0001g0024 |
5 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-240A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996847 | |||||||
| chr3:44996852 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0119 |
6 | HG00438.hp1 NA18957.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-235A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996852 | |||||||
| chr3:44996963 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.255-124A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996963 | |||||||
| chr3:44997002 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0119 |
6 | HG00438.hp1 NA18957.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-85A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44997002 | |||||||
| chr3:44997050 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.255-37A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44997050 | |||||||
| chr3:44997852 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.420+600A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44997852 | |||||||
| chr3:44997886 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0004t0001g0024 |
5 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+634C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44997886 | |||||||
| chr3:44997991 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.420+739G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44997991 | |||||||
| chr3:44998031 | G | GT | 12 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0058 others(9): Show |
27 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.420+786dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 44998031 | ||||||
| chr3:44998031 | G | GTT | 5 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0055 others(2): Show |
5 | HG01934.hp2 HG02818.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.420+785_420+786dup others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 44998031 | ||||||
| chr3:44998039 | G | GT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0104 a0001c0001t0001g0157 others(2): Show |
6 | HG01261.hp1 HG03209.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+801dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 44998039 | ||||||
| chr3:44998039 | G | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(15): Show |
37 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.420+787G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998039 | |||||||
| chr3:44998060 | G | A | 1 | a0003c0003t0001g0048 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.420+808G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998060 | |||||||
| chr3:44998093 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.420+841T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998093 | |||||||
| chr3:44998396 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.420+1144C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998396 | |||||||
| chr3:44998596 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0054 |
3 | HG02486.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.420+1344T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998596 | |||||||
| chr3:44998828 | A | G | 1 | a0001c0001t0001g0018 | 4 | HG01928.hp1 HG01975.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1576A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998828 | |||||||
| chr3:44998969 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0105 a0001c0001t0001g0106 |
5 | HG00642.hp1 HG01192.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+1717G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998969 | |||||||
| chr3:44999015 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(83): Show |
186 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.420+1763G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999015 | |||||||
| chr3:44999148 | GC | G | 10 | a0003c0003t0001g0004 a0003c0003t0001g0047 a0003c0003t0001g0048 others(7): Show |
20 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.420+1898delC | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 44999148 | ||||||
| chr3:44999181 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.420+1929G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999181 | |||||||
| chr3:44999190 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(88): Show |
195 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.420+1938T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999190 | |||||||
| chr3:44999236 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.420+1984G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999236 | |||||||
| chr3:44999243 | A | T | 1 | a0002c0002t0001g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.420+1991A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999243 | |||||||
| chr3:44999277 | T | C | 1 | a0002c0002t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.420+2025T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999277 | |||||||
| chr3:44999295 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.420+2043T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999295 | |||||||
| chr3:44999354 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.420+2102G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999354 | |||||||
| chr3:44999397 | G | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0025 others(6): Show |
21 | HG00642.hp1 HG01109.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.421-2141G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999397 | |||||||
| chr3:44999513 | A | C | 2 | a0002c0002t0001g0031 a0002c0002t0001g0092 |
3 | HG02056.hp2 NA18952.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.421-2025A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999513 | |||||||
| chr3:44999689 | TA | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0117 a0002c0002t0001g0022 others(1): Show |
7 | HG02129.hp1 HG02922.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-1836delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 44999689 | ||||||
| chr3:45000001 | T | TA | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.421-1536dupA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 45000001 | ||||||
| chr3:45000459 | C | T | 1 | a0002c0002t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.421-1079C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000459 | |||||||
| chr3:45000555 | G | C | 2 | a0002c0002t0001g0029 a0002c0002t0001g0081 |
3 | HG01071.hp1 HG01168.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.421-983G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000555 | |||||||
| chr3:45000560 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.421-978G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000560 | |||||||
| chr3:45000571 | T | C | 11 | a0002c0002t0001g0083 a0003c0003t0001g0004 a0003c0003t0001g0047 others(8): Show |
21 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.421-967T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000571 | |||||||
| chr3:45000629 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.421-909A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000629 | |||||||
| chr3:45000805 | C | G | 2 | a0002c0002t0001g0075 a0002c0002t0001g0076 |
2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.421-733C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000805 | |||||||
| chr3:45001145 | G | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(32): Show |
63 | HG00280.hp2 HG00609.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.421-393G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001145 | |||||||
| chr3:45001228 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG01070.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.421-310G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001228 | |||||||
| chr3:45001229 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.421-309G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001229 | |||||||
| chr3:45001239 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG00673.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.421-299G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001239 | |||||||
| chr3:45001314 | A | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.421-224A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001314 | |||||||
| chr3:45001335 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.421-203C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001335 | |||||||
| chr3:45002187 | CTGAT | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.491+583_491+586del others(4): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45002187 | ||||||
| chr3:45002278 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.491+670A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002278 | |||||||
| chr3:45002338 | C | A | 1 | a0002c0002t0001g0092 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.491+730C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002338 | |||||||
| chr3:45002363 | T | C | 1 | a0002c0002t0001g0066 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.491+755T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002363 | |||||||
| chr3:45002370 | A | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0123 |
2 | HG00423.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.491+762A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002370 | |||||||
| chr3:45002403 | C | T | 1 | a0002c0002t0001g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.491+795C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002403 | |||||||
| chr3:45002435 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.491+827A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002435 | |||||||
| chr3:45002501 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(80): Show |
181 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.491+893A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002501 | |||||||
| chr3:45002707 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.491+1099A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002707 | |||||||
| chr3:45002908 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.491+1300G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002908 | |||||||
| chr3:45002992 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0121 |
2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.491+1384A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002992 | |||||||
| chr3:45003326 | TGTGC | T | 44 | a0001c0001t0001g0148 a0002c0002t0001g0002 a0002c0002t0001g0006 others(41): Show |
88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.491+1742_491+1745d others(6): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003326 | ||||||
| chr3:45003326 | TGTGCGTG others(1): Show |
T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(38): Show |
77 | HG00639.hp1 HG00738.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.491+1738_491+1745d others(10): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003326 | ||||||
| chr3:45003326 | TGTGCGTG others(5): Show |
T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(34): Show |
90 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.491+1734_491+1745d others(14): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003326 | ||||||
| chr3:45003334 | CGTGCGTG others(11): Show |
C | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.491+1730_491+1747d others(20): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003334 | ||||||
| chr3:45003335 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.491+1727G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003335 | |||||||
| chr3:45003340 | TGCGTGCG others(3): Show |
T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0156 others(3): Show |
20 | HG00642.hp2 HG02602.hp1 NA18953.hp1 others(17): Show |
intron_variant | MODIFIER | c.491+1734_491+1743d others(12): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003340 | ||||||
| chr3:45003342 | CGTGCGTG others(3): Show |
C | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.491+1738_491+1747d others(12): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003342 | ||||||
| chr3:45003342 | CGTGCGTG others(5): Show |
C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0004t0001g0024 |
9 | HG02145.hp2 HG02258.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.491+1738_491+1749d others(14): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003342 | ||||||
| chr3:45003344 | TGCGTGC | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0019 others(22): Show |
50 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.491+1738_491+1743d others(8): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003344 | ||||||
| chr3:45003350 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.491+1742C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003350 | |||||||
| chr3:45003351 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.491+1743G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003351 | |||||||
| chr3:45003363 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
210 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.491+1755A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003363 | |||||||
| chr3:45003381 | T | C | 8 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0127 others(5): Show |
10 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.491+1773T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003381 | |||||||
| chr3:45003386 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
254 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.491+1778A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003386 | |||||||
| chr3:45003775 | G | A | 1 | a0003c0003t0001g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.492-1516G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003775 | |||||||
| chr3:45004227 | A | G | 1 | a0002c0002t0001g0064 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.492-1064A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004227 | |||||||
| chr3:45004324 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.492-967C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004324 | |||||||
| chr3:45004325 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0151 a0001c0001t0001g0152 |
4 | HG01891.hp2 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-966A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004325 | |||||||
| chr3:45004475 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.492-816C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004475 | |||||||
| chr3:45004502 | C | T | 4 | a0002c0002t0001g0023 a0002c0002t0001g0031 a0002c0002t0001g0091 others(1): Show |
7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.492-789C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004502 | |||||||
| chr3:45004555 | G | GT | 42 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(39): Show |
64 | HG00735.hp1 HG00735.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.492-723dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45004555 | ||||||
| chr3:45004555 | G | GTT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0034 others(5): Show |
10 | HG00609.hp1 HG00639.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.492-724_492-723dup others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45004555 | ||||||
| chr3:45004555 | GT | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0046 others(12): Show |
33 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.492-723delT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45004555 | ||||||
| chr3:45004557 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.492-734T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004557 | |||||||
| chr3:45004569 | G | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0034 others(43): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.492-722G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004569 | |||||||
| chr3:45004573 | T | G | 1 | a0001c0001t0001g0012 | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.492-718T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004573 | |||||||
| chr3:45004575 | T | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.492-716T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004575 | |||||||
| chr3:45004680 | TCAGA | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0055 others(1): Show |
13 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.492-607_492-604del others(4): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45004680 | ||||||
| chr3:45005123 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 |
13 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(10): Show |
intron_variant | MODIFIER | c.492-168G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45005123 | |||||||
| chr3:45005138 | TTGACAGG others(2): Show |
T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 |
13 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(10): Show |
intron_variant | MODIFIER | c.492-140_492-132del others(9): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45005138 | ||||||
| chr3:45005620 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.615+206T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45005620 | |||||||
| chr3:45005949 | C | T | 1 | a0003c0003t0001g0004 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.615+535C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45005949 | |||||||
| chr3:45006068 | C | CT | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(47): Show |
94 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.615+683dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | ||||||
| chr3:45006068 | C | CTT | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(34): Show |
69 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.615+682_615+683dup others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | ||||||
| chr3:45006068 | CT | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0025 others(29): Show |
62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.615+683delT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | ||||||
| chr3:45006068 | CTT | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0095 a0001c0001t0001g0156 others(4): Show |
17 | HG02056.hp2 NA18952.hp1 NA18970.hp2 others(14): Show |
intron_variant | MODIFIER | c.615+682_615+683del others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | ||||||
| chr3:45006068 | CTTTTTTT others(1): Show |
C | 8 | a0001c0008t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0047 others(5): Show |
18 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.615+676_615+683del others(8): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | ||||||
| chr3:45006068 | CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.615+672_615+683del others(12): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | ||||||
| chr3:45006068 | CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG00280.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.615+666_615+683del others(18): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | ||||||
| chr3:45006116 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(83): Show |
186 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.615+702C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006116 | |||||||
| chr3:45006120 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.615+706C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006120 | |||||||
| chr3:45006126 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.615+712G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006126 | |||||||
| chr3:45006139 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(83): Show |
186 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.615+725G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006139 | |||||||
| chr3:45006229 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.615+815C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006229 | |||||||
| chr3:45006266 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.615+852C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006266 | |||||||
| chr3:45006267 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(35): Show |
95 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.615+853G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006267 | |||||||
| chr3:45006345 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.615+931C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006345 | |||||||
| chr3:45006404 | G | GT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0002c0002t0001g0002 others(4): Show |
9 | HG00280.hp1 HG01106.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.616-993dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006404 | ||||||
| chr3:45006404 | GT | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(79): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.616-993delT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006404 | ||||||
| chr3:45006404 | GTT | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(42): Show |
86 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.616-994_616-993del others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006404 | ||||||
| chr3:45006404 | GTTT | G | 7 | a0001c0001t0001g0043 a0001c0001t0001g0128 a0001c0001t0001g0130 others(4): Show |
10 | HG02056.hp2 HG02559.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.616-995_616-993del others(3): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006404 | ||||||
| chr3:45006411 | T | G | 1 | a0001c0001t0001g0007 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.615+997T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006411 | |||||||
| chr3:45006412 | T | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0055 others(2): Show |
13 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.615+998T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006412 | |||||||
| chr3:45006440 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.616-980C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006440 | |||||||
| chr3:45006449 | G | A | 1 | a0003c0003t0001g0053 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.616-971G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006449 | |||||||
| chr3:45006458 | G | A | 2 | a0002c0002t0001g0075 a0002c0002t0001g0076 |
2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.616-962G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006458 | |||||||
| chr3:45006477 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
246 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.616-943T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006477 | |||||||
| chr3:45006478 | G | A | 1 | a0001c0008t0001g0001 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.616-942G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006478 | |||||||
| chr3:45006495 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
253 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.616-925T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006495 | |||||||
| chr3:45006502 | C | T | 11 | a0001c0001t0001g0046 a0003c0003t0001g0004 a0003c0003t0001g0047 others(8): Show |
21 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.616-918C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006502 | |||||||
| chr3:45006568 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 |
13 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-852C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006568 | |||||||
| chr3:45006597 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0114 |
2 | HG00609.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.616-823T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006597 | |||||||
| chr3:45006648 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.616-772C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006648 | |||||||
| chr3:45006648 | C | T | 1 | a0002c0002t0001g0002 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.616-772C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006648 | |||||||
| chr3:45006658 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
253 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.616-762T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006658 | |||||||
| chr3:45006659 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
253 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.616-761G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006659 | |||||||
| chr3:45006690 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.616-730A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006690 | |||||||
| chr3:45006703 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.616-717A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006703 | |||||||
| chr3:45006711 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0004t0001g0024 |
5 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.616-709C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006711 | |||||||
| chr3:45006795 | A | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.616-625A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006795 | |||||||
| chr3:45006796 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.616-624C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006796 | |||||||
| chr3:45006802 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.616-618C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006802 | |||||||
| chr3:45006811 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0046 others(12): Show |
34 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.616-609C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006811 | |||||||
| chr3:45006912 | A | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.616-508A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006912 | |||||||
| chr3:45006960 | A | C | 1 | a0001c0001t0001g0001 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.616-460A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006960 | |||||||
| chr3:45006980 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): Show |
245 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.616-440T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006980 | |||||||
| chr3:45007119 | T | A | 1 | a0001c0001t0001g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.616-301T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45007119 | |||||||
| chr3:45007129 | T | C | 1 | a0001c0001t0001g0041 | 2 | HG01070.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.616-291T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45007129 | |||||||
| chr3:45007315 | T | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0025 others(6): Show |
21 | HG00642.hp1 HG01109.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.616-105T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45007315 | |||||||
| chr3:45007400 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 |
13 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-20C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45007400 | |||||||
| chr3:45007408 | C | T | 4 | a0002c0002t0001g0023 a0002c0002t0001g0031 a0002c0002t0001g0091 others(1): Show |
7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.616-12C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45007408 | |||||||
| chr3:45007581 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02451.hp1 | splice_region_variant&intron_variant | LOW | c.771+6G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007581 | |||||||
| chr3:45007694 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
253 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.771+119A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007694 | |||||||
| chr3:45007799 | A | C | 1 | a0002c0002t0001g0031 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.771+224A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007799 | |||||||
| chr3:45007822 | C | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(83): Show |
186 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.771+247C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007822 | |||||||
| chr3:45007879 | C | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 |
13 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(10): Show |
intron_variant | MODIFIER | c.771+304C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007879 | |||||||
| chr3:45007882 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771+307G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007882 | |||||||
| chr3:45008098 | C | G | 2 | a0003c0003t0001g0004 a0003c0003t0001g0051 |
3 | HG01070.hp2 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.771+523C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008098 | |||||||
| chr3:45008109 | A | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0004t0001g0024 |
5 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+534A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008109 | |||||||
| chr3:45008161 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02523.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.771+586T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008161 | |||||||
| chr3:45008217 | G | C | 1 | a0003c0003t0001g0004 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.771+642G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008217 | |||||||
| chr3:45008473 | T | C | 1 | a0001c0001t0001g0010 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.771+898T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008473 | |||||||
| chr3:45008802 | A | C | 1 | a0001c0001t0001g0008 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.771+1227A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008802 | |||||||
| chr3:45008900 | A | G | 1 | a0003c0003t0001g0053 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.771+1325A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008900 | |||||||
| chr3:45008971 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.771+1396T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008971 | |||||||
| chr3:45008991 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.771+1416G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008991 | |||||||
| chr3:45009080 | T | C | 1 | a0002c0002t0001g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.771+1505T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009080 | |||||||
| chr3:45009218 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
246 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.771+1643G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009218 | |||||||
| chr3:45009267 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.771+1692T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009267 | |||||||
| chr3:45009360 | G | A | 1 | a0001c0001t0001g0010 | 4 | NA18953.hp1 NA18961.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+1785G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009360 | |||||||
| chr3:45009472 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.772-1763A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009472 | |||||||
| chr3:45009509 | C | CT | 13 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0009 others(10): Show |
22 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.772-1718dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 45009509 | ||||||
| chr3:45009510 | T | A | 4 | a0002c0002t0001g0023 a0002c0002t0001g0031 a0002c0002t0001g0091 others(1): Show |
7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-1725T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009510 | |||||||
| chr3:45009556 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.772-1679T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009556 | |||||||
| chr3:45009587 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.772-1648C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009587 | |||||||
| chr3:45009634 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0059 others(2): Show |
9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.772-1601C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009634 | |||||||
| chr3:45009642 | T | TGGTTCAA others(37): Show |
1 | a0002c0002t0001g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-1592_772-1549d others(46): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 45009642 | ||||||
| chr3:45009653 | A | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0026 others(14): Show |
37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.772-1582A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009653 | |||||||
| chr3:45009683 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.772-1552T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009683 | |||||||
| chr3:45009848 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.772-1387C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009848 | |||||||
| chr3:45010291 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.772-944A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45010291 | |||||||
| chr3:45010330 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.772-905C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45010330 | |||||||
| chr3:45010335 | A | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(110): Show |
247 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.772-900A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45010335 | |||||||
| chr3:45010387 | A | G | 1 | a0003c0003t0001g0057 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.772-848A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45010387 | |||||||
| chr3:45010862 | AG | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0089 |
3 | HG00741.hp2 HG01346.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.772-372delG | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45010862 | |||||||
| chr3:45011018 | T | A | 1 | a0002c0002t0001g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-217T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011018 | |||||||
| chr3:45011029 | T | A | 1 | a0002c0002t0001g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-206T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011029 | |||||||
| chr3:45011034 | A | T | 1 | a0002c0002t0001g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-201A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011034 | |||||||
| chr3:45011047 | C | A | 1 | a0002c0002t0001g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-188C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011047 | |||||||
| chr3:45011057 | T | G | 1 | a0002c0002t0001g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-178T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011057 | |||||||
| chr3:45011066 | G | T | 1 | a0002c0002t0001g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-169G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011066 | |||||||
| chr3:45011072 | T | A | 1 | a0002c0002t0001g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-163T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011072 | |||||||
| chr3:45011076 | G | T | 1 | a0002c0002t0001g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-159G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011076 | |||||||
| chr3:45011078 | TTTTGTTT others(54): Show |
T | 1 | a0002c0002t0001g0088 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-155_772-95delT others(60): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 45011078 | ||||||
| chr3:45011131 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.772-104T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011131 |