Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84675 |
| ensemblid | ENSG00000147573.17 |
| hgncid | 14215 |
| symbol | TRIM55 |
| name | tripartite motif containing 55 |
| refseq_nuc | NM_184085.2 |
| refseq_prot | NP_908973.1 |
| ensembl_nuc | ENST00000315962.9 |
| ensembl_prot | ENSP00000323913.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 66127129 |
| end | 66175485 |
| strand | + |
| ver | v1.2 |
| region | chr8:66127129-66175485 |
| region5000 | chr8:66122129-66180485 |
| regionname0 | TRIM55_chr8_66127129_66175485 |
| regionname5000 | TRIM55_chr8_66122129_66180485 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 548 | 178 | 27 | 40 | 76 | 12 | 21 | 48 | TRIM55_chr8_66122129_66180485 | TRIM55 | MSASL others(543): Show |
chr8 | 66122129 | 66180485 |
| a0002 | 0/0 | 548 | 68 | 58 | 5 | 0 | 0 | 5 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | MSASL others(543): Show |
chr8 | 66122129 | 66180485 |
| a0003 | 0/0 | 548 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | MSASL others(543): Show |
chr8 | 66122129 | 66180485 |
| a0004 | 0/0 | 548 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | MSASL others(543): Show |
chr8 | 66122129 | 66180485 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1644 | 167 | 26 | 39 | 68 | 12 | 20 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 | ||
| a0001c0005 | 0/0 | 1644 | 9 | 0 | 1 | 8 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 | ||
| a0001c0010 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 | ||
| a0001c0011 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 | ||
| a0002c0002 | 0/0 | 1644 | 30 | 27 | 2 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 | ||
| a0002c0003 | 0/0 | 1644 | 25 | 19 | 2 | 0 | 0 | 4 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 | ||
| a0002c0004 | 0/0 | 1644 | 10 | 10 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 | ||
| a0002c0006 | 0/0 | 1644 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 | ||
| a0002c0008 | 0/0 | 1644 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 | ||
| a0003c0009 | 0/0 | 1644 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 | ||
| a0004c0007 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | ATGAG others(1639): Show |
chr8 | 66122129 | 66180485 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2679 | 163 | 26 | 38 | 68 | 11 | 18 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0001c0001t0004 | 0/0 | 2679 | 3 | 0 | 1 | 0 | 1 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0001c0001t0005 | 0/0 | 2679 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0001c0005t0001 | 0/0 | 2679 | 9 | 0 | 1 | 8 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0001c0010t0001 | 0/0 | 2679 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0001c0011t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0002c0002t0001 | 0/0 | 2679 | 22 | 19 | 2 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0002c0002t0002 | 0/0 | 2679 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0002c0002t0003 | 0/0 | 2679 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0002c0003t0001 | 0/0 | 2679 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0002c0003t0002 | 0/0 | 2679 | 20 | 14 | 2 | 0 | 0 | 4 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0002c0004t0001 | 0/0 | 2679 | 10 | 10 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0002c0006t0001 | 0/0 | 2679 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0002c0008t0001 | 0/0 | 2679 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0003c0009t0001 | 0/0 | 2679 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| a0004c0007t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | AGGGC others(2674): Show |
chr8 | 66122129 | 66180485 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0005t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0005t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0005t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0005t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0010t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0001c0011t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0001 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0004t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0004t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0004t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0004t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0006t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0006t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0002c0008t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0003c0009t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| a0004c0007t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00438 | hp2 | a0001 | c0005 | t0001 | g0149 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00544 | hp2 | a0001 | c0005 | t0001 | g0151 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00609 | hp2 | a0001 | c0005 | t0001 | g0153 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00639 | hp2 | a0002 | c0003 | t0002 | g0007 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01167 | hp2 | a0002 | c0008 | t0001 | g0053 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01175 | hp1 | a0002 | c0003 | t0002 | g0028 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0014 | EUR | IBS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01943 | hp1 | a0001 | c0005 | t0001 | g0152 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02004 | hp2 | a0003 | c0009 | t0001 | g0046 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02055 | hp1 | a0002 | c0003 | t0002 | g0027 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02056 | hp1 | a0001 | c0005 | t0001 | g0162 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02074 | hp1 | a0001 | c0005 | t0001 | g0154 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02145 | hp1 | a0002 | c0004 | t0001 | g0208 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02145 | hp2 | a0002 | c0002 | t0003 | g0037 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0064 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02572 | hp2 | a0002 | c0004 | t0001 | g0209 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0122 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02622 | hp1 | a0002 | c0004 | t0001 | g0212 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02622 | hp2 | a0002 | c0003 | t0002 | g0006 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0019 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02647 | hp2 | a0002 | c0004 | t0001 | g0210 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02717 | hp2 | a0004 | c0007 | t0001 | g0057 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02723 | hp2 | a0002 | c0003 | t0002 | g0059 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02809 | hp1 | a0002 | c0004 | t0001 | g0207 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02809 | hp2 | a0002 | c0002 | t0003 | g0032 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02818 | hp1 | a0002 | c0003 | t0002 | g0060 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02818 | hp2 | a0002 | c0003 | t0002 | g0006 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02886 | hp2 | a0002 | c0006 | t0001 | g0145 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0040 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03041 | hp1 | a0002 | c0003 | t0002 | g0011 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03041 | hp2 | a0002 | c0004 | t0001 | g0206 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0010 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03195 | hp1 | a0002 | c0003 | t0002 | g0025 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0063 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03209 | hp2 | a0002 | c0004 | t0001 | g0019 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0030 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03239 | hp1 | a0002 | c0003 | t0002 | g0029 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03486 | hp1 | a0002 | c0003 | t0002 | g0026 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03490 | hp1 | a0002 | c0003 | t0002 | g0008 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03492 | hp2 | a0002 | c0003 | t0002 | g0008 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0010 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03540 | hp2 | a0002 | c0003 | t0002 | g0011 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03579 | hp2 | a0002 | c0003 | t0002 | g0021 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03704 | hp2 | a0001 | c0010 | t0001 | g0147 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0219 | SAS | BEB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG04184 | hp1 | a0002 | c0003 | t0002 | g0007 | SAS | BEB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0088 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18522 | hp2 | a0002 | c0003 | t0002 | g0022 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18940 | hp1 | a0001 | c0005 | t0001 | g0065 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19030 | hp1 | a0002 | c0004 | t0001 | g0211 | AFR | LWK | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19030 | hp2 | a0001 | c0011 | t0001 | g0035 | AFR | LWK | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19043 | hp1 | a0002 | c0003 | t0002 | g0023 | AFR | LWK | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | LWK | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19066 | hp1 | a0001 | c0005 | t0001 | g0016 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19082 | hp1 | a0001 | c0005 | t0001 | g0073 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19240 | hp1 | a0002 | c0006 | t0001 | g0115 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA19240 | hp2 | a0002 | c0002 | t0003 | g0031 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | ASW | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ASW | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | GIH | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02559 | hp1 | a0002 | c0003 | t0002 | g0024 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG02559 | hp2 | a0002 | c0003 | t0001 | g0038 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0039 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | USA | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | USA | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA20300 | hp1 | a0002 | c0004 | t0001 | g0213 | AFR | USA | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| NA20300 | hp2 | a0002 | c0003 | t0002 | g0061 | AFR | USA | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0192 | REF | REF | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0160 | REF | REF | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66135039 | C | T | 1 | a0003 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.391C>T | p.Arg131Cys | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/10 | 531/2679 | 391/1647 | 131/548 | chr8 | 66135039 | |||
| chr8:66149745 | G | A | 1 | a0004 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.704G>A | p.Arg235Gln | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 5/10 | 844/2679 | 704/1647 | 235/548 | chr8 | 66149745 | |||
| chr8:66152419 | A | G | 3 | a0002 a0003 a0004 |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
missense_variant | MODERATE | c.1028A>G | p.Lys343Arg | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/10 | 1168/2679 | 1028/1647 | 343/548 | chr8 | 66152419 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66127274 | C | T | 1 | a0001c0011 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.6C>T | p.Ser2Ser | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/10 | 146/2679 | 6/1647 | 2/548 | chr8 | 66127274 | |||
| chr8:66127277 | A | G | 1 | a0001c0010 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.9A>G | p.Ala3Ala | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/10 | 149/2679 | 9/1647 | 3/548 | chr8 | 66127277 | |||
| chr8:66127370 | G | A | 1 | a0002c0004 | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
synonymous_variant | LOW | c.102G>A | p.Thr34Thr | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/10 | 242/2679 | 102/1647 | 34/548 | chr8 | 66127370 | |||
| chr8:66135149 | A | G | 1 | a0002c0008 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.501A>G | p.Arg167Arg | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/10 | 641/2679 | 501/1647 | 167/548 | chr8 | 66135149 | |||
| chr8:66149812 | C | T | 1 | a0002c0006 | 2 | HG02886.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.771C>T | p.Asn257Asn | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 5/10 | 911/2679 | 771/1647 | 257/548 | chr8 | 66149812 | |||
| chr8:66150348 | G | A | 1 | a0002c0003 | 25 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(22): Show |
synonymous_variant | LOW | c.867G>A | p.Ser289Ser | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/10 | 1007/2679 | 867/1647 | 289/548 | chr8 | 66150348 | |||
| chr8:66152378 | A | G | 1 | a0001c0005 | 9 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.987A>G | p.Glu329Glu | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/10 | 1127/2679 | 987/1647 | 329/548 | chr8 | 66152378 | |||
| chr8:66154277 | G | A | 1 | a0002c0004 | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
synonymous_variant | LOW | c.1467G>A | p.Ala489Ala | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/10 | 1607/2679 | 1467/1647 | 489/548 | chr8 | 66154277 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66127154 | G | A | 2 | a0002c0002t0002 a0002c0003t0002 |
24 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-115G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/10 | 115 | chr8 | 66127154 | ||||||
| chr8:66174875 | C | T | 1 | a0001c0001t0004 | 3 | HG00735.hp2 HG01516.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*282C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 10/10 | 282 | chr8 | 66174875 | ||||||
| chr8:66175023 | G | A | 1 | a0001c0001t0005 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*430G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 10/10 | 430 | chr8 | 66175023 | ||||||
| chr8:66175072 | A | G | 1 | a0002c0002t0003 | 4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*479A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 10/10 | 479 | chr8 | 66175072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66127672 | C | CA | 12 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0008 others(9): Show |
15 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+249dupA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 66127672 | ||||||
| chr8:66127704 | G | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
10 | HG00140.hp1 HG00438.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+268G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66127704 | |||||||
| chr8:66127882 | A | G | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.169-422A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66127882 | |||||||
| chr8:66127895 | A | G | 1 | a0002c0002t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.169-409A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66127895 | |||||||
| chr8:66128005 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.169-299A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66128005 | |||||||
| chr8:66128231 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.169-73A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66128231 | |||||||
| chr8:66128234 | G | A | 44 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(41): Show |
53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.169-70G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66128234 | |||||||
| chr8:66128561 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.341+85G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128561 | |||||||
| chr8:66128562 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.341+86C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128562 | |||||||
| chr8:66128844 | GA | G | 17 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(14): Show |
21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.341+377delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 66128844 | ||||||
| chr8:66128851 | A | C | 8 | a0002c0002t0002g0058 a0002c0002t0002g0062 a0002c0002t0002g0063 others(5): Show |
9 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.341+375A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128851 | |||||||
| chr8:66128852 | A | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0215 |
3 | HG01258.hp2 HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.341+376A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128852 | |||||||
| chr8:66128897 | C | T | 4 | a0002c0002t0001g0054 a0002c0002t0001g0055 a0002c0002t0001g0056 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.341+421C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128897 | |||||||
| chr8:66128950 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.341+474A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128950 | |||||||
| chr8:66129119 | A | G | 1 | a0002c0004t0001g0213 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.341+643A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129119 | |||||||
| chr8:66129150 | A | G | 62 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(59): Show |
73 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.341+674A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129150 | |||||||
| chr8:66129345 | G | A | 1 | a0001c0005t0001g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.341+869G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129345 | |||||||
| chr8:66129403 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.341+927T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129403 | |||||||
| chr8:66129777 | C | T | 1 | a0002c0008t0001g0053 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.341+1301C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129777 | |||||||
| chr8:66129961 | G | C | 1 | a0002c0003t0001g0010 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.341+1485G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129961 | |||||||
| chr8:66130278 | C | T | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.341+1802C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130278 | |||||||
| chr8:66130543 | G | C | 2 | a0002c0002t0001g0043 a0002c0008t0001g0053 |
2 | HG01167.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.341+2067G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130543 | |||||||
| chr8:66130562 | C | CG | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
78 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.341+2094dupG | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 66130562 | ||||||
| chr8:66130659 | C | CT | 21 | a0001c0001t0001g0205 a0002c0002t0002g0062 a0002c0002t0002g0063 others(18): Show |
26 | HG00639.hp2 HG00673.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.341+2202dupT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 66130659 | ||||||
| chr8:66130659 | CTT | C | 16 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(13): Show |
20 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.341+2201_341+2202d others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 66130659 | ||||||
| chr8:66130659 | CTTT | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
22 | HG00140.hp1 HG00438.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.341+2200_341+2202d others(5): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 66130659 | ||||||
| chr8:66130712 | G | C | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.341+2236G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130712 | |||||||
| chr8:66130761 | C | T | 1 | a0002c0004t0001g0019 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.341+2285C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130761 | |||||||
| chr8:66130795 | G | A | 17 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(14): Show |
21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.341+2319G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130795 | |||||||
| chr8:66130883 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18612.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.341+2407G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130883 | |||||||
| chr8:66130888 | C | T | 24 | a0002c0002t0002g0058 a0002c0002t0002g0062 a0002c0002t0002g0063 others(21): Show |
29 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.341+2412C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130888 | |||||||
| chr8:66131109 | A | G | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.341+2633A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131109 | |||||||
| chr8:66131282 | G | A | 62 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(59): Show |
73 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.341+2806G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131282 | |||||||
| chr8:66131293 | G | A | 4 | a0002c0002t0003g0030 a0002c0002t0003g0031 a0002c0002t0003g0032 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.341+2817G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131293 | |||||||
| chr8:66131386 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.341+2910G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131386 | |||||||
| chr8:66131808 | T | C | 61 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
72 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.342-3182T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131808 | |||||||
| chr8:66131922 | C | G | 1 | a0002c0002t0001g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-3068C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131922 | |||||||
| chr8:66132268 | T | C | 4 | a0002c0002t0003g0030 a0002c0002t0003g0031 a0002c0002t0003g0032 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.342-2722T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132268 | |||||||
| chr8:66132344 | T | A | 6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-2646T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132344 | |||||||
| chr8:66132544 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 |
3 | HG03516.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.342-2446G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132544 | |||||||
| chr8:66132558 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.342-2432C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132558 | |||||||
| chr8:66132592 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.342-2398C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132592 | |||||||
| chr8:66132660 | G | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(15): Show |
20 | HG00140.hp1 HG00438.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.342-2330G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132660 | |||||||
| chr8:66132804 | CCTAAA | C | 20 | a0002c0002t0002g0058 a0002c0002t0002g0062 a0002c0002t0002g0063 others(17): Show |
24 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.342-2185_342-2181d others(7): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132804 | |||||||
| chr8:66132841 | T | C | 62 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(59): Show |
73 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.342-2149T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132841 | |||||||
| chr8:66132924 | T | A | 1 | a0002c0004t0001g0019 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.342-2066T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132924 | |||||||
| chr8:66132971 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
6 | HG00140.hp1 HG00438.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-2019C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132971 | |||||||
| chr8:66133039 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0071 others(3): Show |
8 | HG00639.hp1 HG00735.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.342-1951G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133039 | |||||||
| chr8:66133070 | C | T | 1 | a0004c0007t0001g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.342-1920C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133070 | |||||||
| chr8:66133364 | T | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0214 |
3 | HG01123.hp2 HG02300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.342-1626T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133364 | |||||||
| chr8:66133474 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02602.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.342-1516G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133474 | |||||||
| chr8:66133501 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.342-1489G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133501 | |||||||
| chr8:66133550 | A | G | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 |
3 | HG03516.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.342-1440A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133550 | |||||||
| chr8:66133618 | A | C | 1 | a0001c0001t0001g0110 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.342-1372A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133618 | |||||||
| chr8:66133639 | G | A | 62 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(59): Show |
73 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.342-1351G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133639 | |||||||
| chr8:66133685 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.342-1305A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133685 | |||||||
| chr8:66133702 | G | T | 17 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(14): Show |
21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.342-1288G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133702 | |||||||
| chr8:66133743 | A | C | 44 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(41): Show |
53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.342-1247A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133743 | |||||||
| chr8:66133795 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.342-1195A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133795 | |||||||
| chr8:66133948 | C | T | 4 | a0002c0002t0002g0058 a0002c0002t0002g0062 a0002c0002t0002g0063 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.342-1042C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133948 | |||||||
| chr8:66133951 | A | T | 17 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(14): Show |
21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.342-1039A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133951 | |||||||
| chr8:66134081 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0203 |
2 | HG02027.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.342-909A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134081 | |||||||
| chr8:66134124 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.342-866A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134124 | |||||||
| chr8:66134349 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.342-641G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134349 | |||||||
| chr8:66134480 | C | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(46): Show |
59 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.342-510C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134480 | |||||||
| chr8:66134747 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
53 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.342-243C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134747 | |||||||
| chr8:66134959 | G | T | 1 | a0002c0002t0002g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.342-31G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134959 | |||||||
| chr8:66135243 | G | A | 1 | a0002c0003t0002g0007 | 2 | HG00639.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.507+88G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135243 | |||||||
| chr8:66135314 | T | C | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.507+159T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135314 | |||||||
| chr8:66135348 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.507+193C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135348 | |||||||
| chr8:66135418 | C | T | 1 | a0002c0002t0001g0052 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.507+263C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135418 | |||||||
| chr8:66135578 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.507+423T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135578 | |||||||
| chr8:66135588 | C | A | 1 | a0002c0002t0001g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.507+433C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135588 | |||||||
| chr8:66135718 | A | C | 4 | a0002c0003t0002g0011 a0002c0003t0002g0059 a0002c0003t0002g0060 others(1): Show |
5 | HG02723.hp2 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+563A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135718 | |||||||
| chr8:66135746 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG01243.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.507+591C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135746 | |||||||
| chr8:66135929 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02027.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.507+774A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135929 | |||||||
| chr8:66136405 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.508-690T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66136405 | |||||||
| chr8:66136730 | T | C | 1 | a0002c0003t0001g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.508-365T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66136730 | |||||||
| chr8:66136753 | A | G | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.508-342A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66136753 | |||||||
| chr8:66137020 | A | T | 14 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(11): Show |
15 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.508-75A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66137020 | |||||||
| chr8:66137043 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.508-52G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66137043 | |||||||
| chr8:66137063 | A | C | 5 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-32A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66137063 | |||||||
| chr8:66137383 | G | A | 12 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(9): Show |
16 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.603+193G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66137383 | |||||||
| chr8:66137758 | G | GA | 15 | a0001c0001t0001g0066 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
16 | HG01109.hp2 HG01243.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.603+588dupA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66137758 | ||||||
| chr8:66137758 | G | GAA | 8 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(5): Show |
8 | HG02451.hp2 HG02717.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.603+587_603+588dup others(2): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66137758 | ||||||
| chr8:66137758 | GA | G | 68 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0012 others(65): Show |
76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.603+588delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66137758 | ||||||
| chr8:66137758 | GAA | G | 14 | a0001c0001t0001g0103 a0001c0001t0001g0114 a0001c0001t0001g0199 others(11): Show |
16 | HG01167.hp1 HG02083.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.603+587_603+588del others(2): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66137758 | ||||||
| chr8:66137781 | T | A | 44 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(41): Show |
53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.603+591T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66137781 | |||||||
| chr8:66137823 | T | C | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.603+633T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66137823 | |||||||
| chr8:66137964 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.603+774A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66137964 | |||||||
| chr8:66138039 | T | G | 20 | a0002c0002t0002g0058 a0002c0002t0002g0062 a0002c0002t0002g0063 others(17): Show |
24 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.603+849T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138039 | |||||||
| chr8:66138061 | A | C | 1 | a0001c0001t0001g0110 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.603+871A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138061 | |||||||
| chr8:66138330 | C | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
120 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.603+1140C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138330 | |||||||
| chr8:66138413 | G | A | 1 | a0002c0003t0001g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.603+1223G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138413 | |||||||
| chr8:66138532 | G | A | 14 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(11): Show |
15 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.603+1342G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138532 | |||||||
| chr8:66138784 | T | A | 60 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(57): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.603+1594T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138784 | |||||||
| chr8:66138825 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.603+1635T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138825 | |||||||
| chr8:66138952 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.603+1762C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138952 | |||||||
| chr8:66138998 | G | A | 10 | a0001c0001t0001g0140 a0002c0004t0001g0019 a0002c0004t0001g0206 others(7): Show |
11 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.603+1808G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138998 | |||||||
| chr8:66139246 | C | T | 4 | a0002c0003t0002g0011 a0002c0003t0002g0059 a0002c0003t0002g0060 others(1): Show |
5 | HG02723.hp2 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+2056C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139246 | |||||||
| chr8:66139275 | G | A | 1 | a0002c0003t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.603+2085G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139275 | |||||||
| chr8:66139280 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.603+2090T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139280 | |||||||
| chr8:66139476 | TC | T | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.603+2287delC | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139476 | |||||||
| chr8:66139477 | CA | C | 5 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+2288delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139477 | |||||||
| chr8:66139478 | A | T | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.603+2288A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139478 | |||||||
| chr8:66139580 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.603+2390C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139580 | |||||||
| chr8:66139876 | C | T | 58 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(55): Show |
68 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.603+2686C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139876 | |||||||
| chr8:66140055 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG01109.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.603+2865G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140055 | |||||||
| chr8:66140081 | A | C | 60 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(57): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.603+2891A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140081 | |||||||
| chr8:66140160 | A | G | 44 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(41): Show |
53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.603+2970A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140160 | |||||||
| chr8:66140334 | G | A | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.603+3144G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140334 | |||||||
| chr8:66140472 | T | G | 5 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+3282T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140472 | |||||||
| chr8:66140509 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(41): Show |
52 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.603+3319C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140509 | |||||||
| chr8:66140777 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.603+3587G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140777 | |||||||
| chr8:66140787 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0010t0001g0147 |
3 | HG00741.hp1 HG02280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.603+3597G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140787 | |||||||
| chr8:66140913 | A | G | 1 | a0002c0004t0001g0213 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.603+3723A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140913 | |||||||
| chr8:66140966 | A | G | 24 | a0002c0002t0002g0058 a0002c0002t0002g0062 a0002c0002t0002g0063 others(21): Show |
29 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.603+3776A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140966 | |||||||
| chr8:66141007 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.603+3817C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141007 | |||||||
| chr8:66141206 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.603+4016A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141206 | |||||||
| chr8:66141329 | C | T | 2 | a0002c0004t0001g0211 a0002c0004t0001g0213 |
2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.603+4139C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141329 | |||||||
| chr8:66141339 | G | A | 3 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0220 |
3 | HG02486.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.603+4149G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141339 | |||||||
| chr8:66141349 | G | T | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.603+4159G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141349 | |||||||
| chr8:66141474 | G | A | 1 | a0002c0002t0001g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.603+4284G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141474 | |||||||
| chr8:66141483 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.603+4293G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141483 | |||||||
| chr8:66141545 | C | G | 1 | a0001c0011t0001g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.603+4355C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141545 | |||||||
| chr8:66141924 | G | A | 58 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(55): Show |
68 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.603+4734G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141924 | |||||||
| chr8:66141947 | T | A | 1 | a0001c0005t0001g0073 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.603+4757T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141947 | |||||||
| chr8:66141993 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG00735.hp1 HG01361.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.603+4803T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141993 | |||||||
| chr8:66142023 | G | A | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.603+4833G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66142023 | |||||||
| chr8:66142100 | C | A | 2 | a0002c0003t0002g0008 a0002c0003t0002g0028 |
3 | HG01175.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.603+4910C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66142100 | |||||||
| chr8:66142326 | G | A | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.603+5136G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66142326 | |||||||
| chr8:66142435 | G | A | 8 | a0002c0002t0002g0058 a0002c0002t0002g0062 a0002c0002t0002g0063 others(5): Show |
9 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.603+5245G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66142435 | |||||||
| chr8:66143003 | TG | T | 17 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(14): Show |
21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.603+5815delG | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66143003 | ||||||
| chr8:66143295 | G | A | 44 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(41): Show |
53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.603+6105G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143295 | |||||||
| chr8:66143582 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.604-6063G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143582 | |||||||
| chr8:66143584 | T | A | 14 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(11): Show |
15 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.604-6061T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143584 | |||||||
| chr8:66143630 | T | G | 6 | a0002c0004t0001g0207 a0002c0004t0001g0208 a0002c0004t0001g0209 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.604-6015T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143630 | |||||||
| chr8:66143738 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.604-5907T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143738 | |||||||
| chr8:66143781 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.604-5864A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143781 | |||||||
| chr8:66143794 | C | A | 5 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-5851C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143794 | |||||||
| chr8:66143800 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.604-5845A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143800 | |||||||
| chr8:66143891 | G | A | 8 | a0002c0002t0002g0058 a0002c0002t0002g0062 a0002c0002t0002g0063 others(5): Show |
9 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.604-5754G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143891 | |||||||
| chr8:66144166 | G | T | 1 | a0001c0005t0001g0162 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.604-5479G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144166 | |||||||
| chr8:66144311 | T | G | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.604-5334T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144311 | |||||||
| chr8:66144412 | T | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG03017.hp2 HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.604-5233T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144412 | |||||||
| chr8:66144505 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.604-5140G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144505 | |||||||
| chr8:66144611 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.604-5034A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144611 | |||||||
| chr8:66144700 | G | C | 42 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(39): Show |
51 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.604-4945G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144700 | |||||||
| chr8:66144909 | T | A | 1 | a0001c0001t0001g0218 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.604-4736T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144909 | |||||||
| chr8:66144979 | G | A | 1 | a0002c0002t0002g0062 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.604-4666G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144979 | |||||||
| chr8:66145025 | A | G | 1 | a0002c0002t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.604-4620A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145025 | |||||||
| chr8:66145035 | T | C | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.604-4610T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145035 | |||||||
| chr8:66145575 | G | A | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.604-4070G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145575 | |||||||
| chr8:66145635 | C | T | 16 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(13): Show |
17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.604-4010C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145635 | |||||||
| chr8:66145639 | A | G | 24 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0033 others(21): Show |
27 | HG00140.hp1 HG00438.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.604-4006A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145639 | |||||||
| chr8:66145660 | G | GT | 5 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-3975dupT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66145660 | ||||||
| chr8:66145714 | G | A | 1 | a0002c0002t0001g0044 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.604-3931G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145714 | |||||||
| chr8:66145722 | G | A | 9 | a0002c0002t0001g0001 a0002c0002t0001g0044 a0002c0002t0001g0045 others(6): Show |
13 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.604-3923G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145722 | |||||||
| chr8:66145986 | G | A | 20 | a0002c0003t0001g0010 a0002c0003t0001g0038 a0002c0003t0001g0039 others(17): Show |
25 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.604-3659G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145986 | |||||||
| chr8:66146101 | G | A | 2 | a0002c0006t0001g0115 a0002c0006t0001g0145 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.604-3544G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66146101 | |||||||
| chr8:66146208 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.604-3437G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66146208 | |||||||
| chr8:66146315 | CT | C | 21 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(18): Show |
25 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.604-3328delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66146315 | ||||||
| chr8:66146740 | T | C | 16 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(13): Show |
17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.604-2905T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66146740 | |||||||
| chr8:66147018 | A | G | 41 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(38): Show |
50 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.604-2627A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147018 | |||||||
| chr8:66147234 | T | C | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.604-2411T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147234 | |||||||
| chr8:66147322 | T | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0010t0001g0147 |
3 | HG00741.hp1 HG02280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.604-2323T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147322 | |||||||
| chr8:66147534 | C | T | 16 | a0002c0003t0002g0006 a0002c0003t0002g0007 a0002c0003t0002g0008 others(13): Show |
20 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-2111C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147534 | |||||||
| chr8:66147562 | C | T | 20 | a0002c0003t0001g0010 a0002c0003t0001g0038 a0002c0003t0001g0039 others(17): Show |
25 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.604-2083C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147562 | |||||||
| chr8:66147651 | C | T | 11 | a0001c0001t0001g0072 a0001c0001t0001g0129 a0001c0001t0001g0134 others(8): Show |
11 | HG00621.hp2 HG00673.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.604-1994C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147651 | |||||||
| chr8:66147688 | A | G | 2 | a0002c0006t0001g0115 a0002c0006t0001g0145 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.604-1957A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147688 | |||||||
| chr8:66147699 | G | A | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.604-1946G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147699 | |||||||
| chr8:66147794 | C | CA | 15 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0075 others(12): Show |
16 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.604-1828dupA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66147794 | ||||||
| chr8:66147794 | CA | C | 13 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(10): Show |
13 | HG00609.hp1 HG00741.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.604-1828delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66147794 | ||||||
| chr8:66147811 | A | AAC | 5 | a0002c0002t0001g0045 a0002c0002t0001g0051 a0002c0002t0001g0054 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.604-1833_604-1832i others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66147811 | ||||||
| chr8:66147811 | A | AC | 16 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(13): Show |
20 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.604-1834_604-1833i others(3): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147811 | |||||||
| chr8:66147813 | A | AAC | 19 | a0002c0003t0001g0010 a0002c0003t0001g0038 a0002c0003t0001g0039 others(16): Show |
24 | HG00639.hp2 HG02055.hp1 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.604-1831_604-1830i others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66147813 | ||||||
| chr8:66147813 | A | C | 36 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(33): Show |
40 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.604-1832A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147813 | |||||||
| chr8:66147913 | A | G | 1 | a0001c0005t0001g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.604-1732A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147913 | |||||||
| chr8:66148226 | ATAAT | A | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.604-1412_604-1409d others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66148226 | ||||||
| chr8:66148286 | A | C | 4 | a0002c0002t0003g0030 a0002c0002t0003g0031 a0002c0002t0003g0032 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.604-1359A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66148286 | |||||||
| chr8:66148330 | A | G | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.604-1315A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66148330 | |||||||
| chr8:66148386 | T | C | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.604-1259T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66148386 | |||||||
| chr8:66148863 | A | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0034 |
3 | HG00140.hp1 HG01258.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.604-782A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66148863 | |||||||
| chr8:66149012 | G | A | 1 | a0002c0002t0001g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.604-633G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66149012 | |||||||
| chr8:66149253 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.604-392A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66149253 | |||||||
| chr8:66149402 | A | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.604-243A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66149402 | |||||||
| chr8:66149970 | T | A | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+92T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 5/9 | chr8 | 66149970 | |||||||
| chr8:66150059 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.838-158G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 5/9 | chr8 | 66150059 | |||||||
| chr8:66150134 | G | T | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.838-83G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 5/9 | chr8 | 66150134 | |||||||
| chr8:66150637 | G | C | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.985+171G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66150637 | |||||||
| chr8:66150673 | C | CT | 17 | a0001c0001t0001g0069 a0001c0001t0001g0094 a0001c0001t0001g0095 others(14): Show |
18 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.985+220dupT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66150673 | ||||||
| chr8:66150674 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.985+208T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66150674 | |||||||
| chr8:66150807 | C | G | 16 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(13): Show |
17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.985+341C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66150807 | |||||||
| chr8:66150828 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0171 |
3 | NA18942.hp1 NA18946.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.985+362G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66150828 | |||||||
| chr8:66151057 | T | C | 2 | a0002c0006t0001g0115 a0002c0006t0001g0145 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.985+591T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151057 | |||||||
| chr8:66151143 | T | A | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.985+677T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151143 | |||||||
| chr8:66151182 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.985+716G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151182 | |||||||
| chr8:66151294 | A | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.985+828A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151294 | |||||||
| chr8:66151432 | C | G | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.986-945C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151432 | |||||||
| chr8:66151570 | A | T | 4 | a0002c0002t0003g0030 a0002c0002t0003g0031 a0002c0002t0003g0032 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.986-807A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151570 | |||||||
| chr8:66151666 | A | G | 15 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(12): Show |
19 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.986-711A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151666 | |||||||
| chr8:66151846 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.986-531A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151846 | |||||||
| chr8:66151849 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.986-528A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151849 | |||||||
| chr8:66151850 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.986-527T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151850 | |||||||
| chr8:66151850 | T | TAATA | 6 | a0001c0001t0001g0097 a0001c0001t0001g0129 a0001c0001t0001g0144 others(3): Show |
6 | HG01516.hp1 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.986-484_986-481dup others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66151850 | ||||||
| chr8:66151850 | TAATA | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(68): Show |
78 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.986-484_986-481del others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66151850 | ||||||
| chr8:66151850 | TAATAAAT others(1): Show |
T | 16 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0082 others(13): Show |
18 | HG00140.hp1 HG00735.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.986-488_986-481del others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66151850 | ||||||
| chr8:66151850 | TAATAAAT others(5): Show |
T | 8 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(5): Show |
8 | HG02015.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-492_986-481del others(12): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66151850 | ||||||
| chr8:66151850 | TAATAAAT others(9): Show |
T | 3 | a0002c0002t0003g0030 a0002c0002t0003g0031 a0002c0002t0003g0032 |
3 | HG02809.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.986-496_986-481del others(16): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66151850 | ||||||
| chr8:66151963 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.986-414G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151963 | |||||||
| chr8:66152163 | A | G | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.986-214A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66152163 | |||||||
| chr8:66152288 | CT | C | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.986-87delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66152288 | ||||||
| chr8:66152756 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1236+129G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66152756 | |||||||
| chr8:66152801 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1236+174G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66152801 | |||||||
| chr8:66152903 | T | TTG | 28 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0074 others(25): Show |
32 | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1236+318_1236+319d others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | ||||||
| chr8:66152903 | T | TTGTG | 18 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0092 others(15): Show |
20 | HG01167.hp2 HG01243.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1236+316_1236+319d others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | ||||||
| chr8:66152903 | T | TTGTGTG | 4 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0106 others(1): Show |
4 | HG01243.hp2 HG02809.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+314_1236+319d others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | ||||||
| chr8:66152903 | T | TTGTGTGT others(1): Show |
3 | a0001c0001t0001g0069 a0001c0005t0001g0073 a0002c0002t0003g0037 |
3 | HG02145.hp2 HG06807.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1236+312_1236+319d others(10): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | ||||||
| chr8:66152903 | TTG | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0012 others(40): Show |
54 | HG00140.hp1 HG00438.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1236+318_1236+319d others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | ||||||
| chr8:66152903 | TTGTG | T | 16 | a0001c0001t0001g0084 a0001c0001t0001g0109 a0001c0001t0001g0121 others(13): Show |
18 | HG00544.hp2 HG00639.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1236+316_1236+319d others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | ||||||
| chr8:66152903 | TTGTGTG | T | 19 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0054 others(16): Show |
22 | HG01175.hp1 HG02004.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.1236+314_1236+319d others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | ||||||
| chr8:66152903 | TTGTGTGT others(3): Show |
T | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1236+310_1236+319d others(12): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | ||||||
| chr8:66152903 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0005g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1236+308_1236+319d others(14): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | ||||||
| chr8:66152903 | TTGTGTGT others(13): Show |
T | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1236+300_1236+319d others(22): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | ||||||
| chr8:66152942 | T | A | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1236+315T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66152942 | |||||||
| chr8:66153040 | G | A | 1 | a0002c0003t0001g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1236+413G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153040 | |||||||
| chr8:66153061 | C | T | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1236+434C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153061 | |||||||
| chr8:66153065 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1236+438G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153065 | |||||||
| chr8:66153207 | C | T | 1 | a0002c0004t0001g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1236+580C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153207 | |||||||
| chr8:66153237 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0163 a0001c0001t0001g0166 |
3 | HG01109.hp2 HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1236+610A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153237 | |||||||
| chr8:66153339 | C | T | 1 | a0001c0001t0005g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1237-708C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153339 | |||||||
| chr8:66153539 | G | C | 1 | a0001c0001t0001g0197 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1237-508G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153539 | |||||||
| chr8:66153570 | G | C | 1 | a0002c0002t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1237-477G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153570 | |||||||
| chr8:66153635 | G | A | 1 | a0002c0002t0001g0049 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1237-412G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153635 | |||||||
| chr8:66153649 | AT | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): Show |
45 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1237-397delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153649 | |||||||
| chr8:66153737 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0193 |
2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1237-310T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153737 | |||||||
| chr8:66153859 | A | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG01109.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1237-188A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153859 | |||||||
| chr8:66154003 | CT | C | 38 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(35): Show |
41 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.1237-33delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66154003 | ||||||
| chr8:66154006 | T | C | 7 | a0002c0002t0001g0219 a0002c0003t0002g0006 a0002c0003t0002g0007 others(4): Show |
10 | HG00639.hp2 HG01175.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237-41T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66154006 | |||||||
| chr8:66154349 | A | G | 1 | a0002c0004t0001g0206 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1524+15A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66154349 | |||||||
| chr8:66154387 | C | T | 5 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+53C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66154387 | |||||||
| chr8:66154468 | A | G | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+134A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66154468 | |||||||
| chr8:66154545 | C | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+211C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66154545 | |||||||
| chr8:66155113 | G | A | 5 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+779G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155113 | |||||||
| chr8:66155254 | A | G | 1 | a0002c0004t0001g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1524+920A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155254 | |||||||
| chr8:66155389 | G | A | 1 | a0002c0002t0001g0052 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1524+1055G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155389 | |||||||
| chr8:66155460 | G | A | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+1126G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155460 | |||||||
| chr8:66155896 | T | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1524+1562T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155896 | |||||||
| chr8:66155921 | A | G | 1 | a0002c0002t0001g0043 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1524+1587A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155921 | |||||||
| chr8:66155998 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1524+1664C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155998 | |||||||
| chr8:66156340 | A | C | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+2006A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156340 | |||||||
| chr8:66156421 | G | A | 2 | a0002c0006t0001g0115 a0002c0006t0001g0145 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1524+2087G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156421 | |||||||
| chr8:66156427 | T | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+2093T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156427 | |||||||
| chr8:66156439 | C | T | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+2105C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156439 | |||||||
| chr8:66156670 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1524+2336C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156670 | |||||||
| chr8:66156687 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1524+2353C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156687 | |||||||
| chr8:66156868 | A | G | 5 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+2534A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156868 | |||||||
| chr8:66157000 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0188 |
5 | HG02015.hp2 HG02071.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+2666C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157000 | |||||||
| chr8:66157097 | A | C | 1 | a0002c0002t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1524+2763A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157097 | |||||||
| chr8:66157153 | T | C | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+2819T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157153 | |||||||
| chr8:66157294 | A | G | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+2960A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157294 | |||||||
| chr8:66157390 | A | C | 1 | a0002c0002t0003g0031 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1524+3056A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157390 | |||||||
| chr8:66157505 | G | A | 1 | a0002c0002t0001g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1524+3171G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157505 | |||||||
| chr8:66157538 | G | A | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+3204G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157538 | |||||||
| chr8:66157599 | G | A | 5 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3265G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157599 | |||||||
| chr8:66157662 | T | C | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+3328T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157662 | |||||||
| chr8:66157743 | C | T | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+3409C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157743 | |||||||
| chr8:66157902 | G | A | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3568G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157902 | |||||||
| chr8:66157920 | C | T | 44 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(41): Show |
53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1524+3586C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157920 | |||||||
| chr8:66157956 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1524+3622C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157956 | |||||||
| chr8:66158065 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1524+3731G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158065 | |||||||
| chr8:66158135 | TCCCCACC others(6): Show |
T | 1 | a0001c0001t0001g0140 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1524+3802_1524+381 others(17): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158135 | |||||||
| chr8:66158136 | C | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0112 a0001c0001t0001g0124 |
3 | HG02300.hp2 NA18998.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1524+3802C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158136 | |||||||
| chr8:66158137 | C | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0184 a0001c0005t0001g0016 |
3 | HG01261.hp1 NA19066.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1524+3803C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158137 | |||||||
| chr8:66158137 | CCCACCAC others(3): Show |
C | 1 | a0001c0001t0001g0103 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1524+3805_1524+381 others(14): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158137 | ||||||
| chr8:66158137 | CCCACCAC others(5): Show |
C | 1 | a0001c0001t0001g0195 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1524+3805_1524+381 others(16): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158137 | ||||||
| chr8:66158138 | CCACCACA others(4): Show |
C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0110 |
2 | NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1524+3808_1524+381 others(15): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158138 | ||||||
| chr8:66158138 | CCACCACA others(16): Show |
C | 1 | a0001c0001t0001g0174 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1524+3808_1524+383 others(27): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158138 | ||||||
| chr8:66158140 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1524+3806A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158140 | |||||||
| chr8:66158141 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1524+3807C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158141 | |||||||
| chr8:66158141 | C | CCA | 17 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0020 others(14): Show |
17 | HG00738.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1524+3867_1524+386 others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | C | CCACA | 11 | a0001c0001t0001g0017 a0001c0001t0001g0068 a0001c0001t0001g0084 others(8): Show |
11 | HG02970.hp1 HG03195.hp2 HG03516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524+3865_1524+386 others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCA | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0072 others(28): Show |
35 | HG00099.hp1 HG00673.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1524+3867_1524+386 others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACA | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0070 others(24): Show |
30 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1524+3865_1524+386 others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACA | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(26): Show |
29 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1524+3863_1524+386 others(10): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACAC others(1): Show |
C | 24 | a0001c0001t0001g0015 a0001c0001t0001g0090 a0001c0001t0001g0117 others(21): Show |
25 | HG00280.hp1 HG00438.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1524+3861_1524+386 others(12): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACAC others(3): Show |
C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0082 others(11): Show |
14 | HG00621.hp1 HG01175.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1524+3859_1524+386 others(14): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACAC others(5): Show |
C | 5 | a0001c0001t0001g0066 a0001c0001t0001g0167 a0002c0003t0001g0039 others(2): Show |
5 | HG01433.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3857_1524+386 others(16): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACAC others(7): Show |
C | 5 | a0002c0003t0002g0011 a0002c0003t0002g0059 a0002c0003t0002g0061 others(2): Show |
6 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+3855_1524+386 others(18): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACAC others(9): Show |
C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0136 a0002c0003t0002g0060 others(1): Show |
5 | HG02630.hp1 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3853_1524+386 others(20): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACAC others(11): Show |
C | 1 | a0002c0004t0001g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1524+3851_1524+386 others(22): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACAC others(13): Show |
C | 2 | a0002c0002t0001g0048 a0002c0002t0003g0031 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1524+3849_1524+386 others(24): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACAC others(15): Show |
C | 5 | a0002c0002t0003g0030 a0002c0002t0003g0032 a0002c0002t0003g0037 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3847_1524+386 others(26): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACAC others(17): Show |
C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0141 others(3): Show |
8 | HG00673.hp1 HG01123.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.1524+3845_1524+386 others(28): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158141 | CCACACAC others(23): Show |
C | 5 | a0002c0002t0001g0052 a0002c0002t0001g0054 a0002c0002t0001g0055 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3839_1524+386 others(34): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | ||||||
| chr8:66158385 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1524+4051T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158385 | |||||||
| chr8:66158386 | C | A | 21 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(18): Show |
25 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1524+4052C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158386 | |||||||
| chr8:66158897 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1524+4563T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158897 | |||||||
| chr8:66159183 | C | T | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1524+4849C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159183 | |||||||
| chr8:66159225 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1524+4891A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159225 | |||||||
| chr8:66159241 | T | C | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+4907T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159241 | |||||||
| chr8:66159265 | G | A | 16 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(13): Show |
17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1524+4931G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159265 | |||||||
| chr8:66159411 | A | G | 5 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+5077A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159411 | |||||||
| chr8:66159486 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0071 |
4 | HG00639.hp1 HG01123.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+5152G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159486 | |||||||
| chr8:66159699 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0034 |
3 | HG00140.hp1 HG01258.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1524+5365T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159699 | |||||||
| chr8:66159703 | A | G | 1 | a0001c0005t0001g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1524+5369A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159703 | |||||||
| chr8:66159929 | C | A | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+5595C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159929 | |||||||
| chr8:66159984 | T | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0108 a0001c0001t0001g0130 others(7): Show |
11 | HG00741.hp2 HG01192.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1524+5650T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159984 | |||||||
| chr8:66160102 | A | C | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1524+5768A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160102 | |||||||
| chr8:66160191 | A | G | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1524+5857A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160191 | |||||||
| chr8:66160227 | A | G | 5 | a0002c0002t0001g0052 a0002c0002t0001g0054 a0002c0002t0001g0055 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+5893A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160227 | |||||||
| chr8:66160356 | G | GGT | 14 | a0001c0001t0001g0034 a0001c0001t0001g0104 a0001c0001t0001g0110 others(11): Show |
14 | HG00738.hp2 HG01070.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1524+6051_1524+605 others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | ||||||
| chr8:66160356 | G | GGTGT | 19 | a0001c0001t0001g0098 a0001c0001t0001g0173 a0001c0005t0001g0154 others(16): Show |
20 | HG01167.hp2 HG01891.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524+6049_1524+605 others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | ||||||
| chr8:66160356 | G | GGTGTGT | 12 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0044 others(9): Show |
16 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1524+6047_1524+605 others(10): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | ||||||
| chr8:66160356 | G | GGTGTGTG others(3): Show |
4 | a0002c0003t0001g0038 a0002c0003t0002g0059 a0002c0006t0001g0115 others(1): Show |
4 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+6043_1524+605 others(14): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | ||||||
| chr8:66160356 | G | GGTGTGTG others(5): Show |
12 | a0002c0003t0001g0039 a0002c0003t0002g0006 a0002c0003t0002g0007 others(9): Show |
15 | HG00639.hp2 HG01175.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1524+6041_1524+605 others(16): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | ||||||
| chr8:66160356 | G | GGTGTGTG others(7): Show |
4 | a0002c0003t0002g0011 a0002c0003t0002g0024 a0002c0003t0002g0027 others(1): Show |
5 | HG02055.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+6039_1524+605 others(18): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | ||||||
| chr8:66160356 | G | GGTGTGTG others(9): Show |
6 | a0002c0003t0001g0010 a0002c0003t0001g0040 a0002c0003t0002g0023 others(3): Show |
7 | HG02145.hp1 HG02622.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+6037_1524+605 others(20): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | ||||||
| chr8:66160356 | G | GGTGTGTG others(11): Show |
2 | a0002c0004t0001g0209 a0002c0004t0001g0211 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1524+6035_1524+605 others(22): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | ||||||
| chr8:66160514 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1524+6180C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160514 | |||||||
| chr8:66160564 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1524+6230G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160564 | |||||||
| chr8:66160792 | C | T | 16 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(13): Show |
17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1524+6458C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160792 | |||||||
| chr8:66160866 | G | GTT | 12 | a0002c0002t0001g0036 a0002c0004t0001g0019 a0002c0004t0001g0206 others(9): Show |
13 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1524+6544_1524+654 others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160866 | ||||||
| chr8:66160866 | GT | G | 5 | a0001c0001t0001g0003 a0002c0002t0001g0054 a0002c0002t0001g0055 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+6545delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160866 | ||||||
| chr8:66161183 | A | T | 1 | a0002c0002t0002g0062 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1524+6849A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161183 | |||||||
| chr8:66161461 | A | T | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1524+7127A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161461 | |||||||
| chr8:66161526 | A | G | 2 | a0001c0001t0001g0130 a0002c0002t0001g0052 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1524+7192A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161526 | |||||||
| chr8:66161557 | A | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+7223A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161557 | |||||||
| chr8:66161635 | C | T | 1 | a0002c0002t0001g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1524+7301C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161635 | |||||||
| chr8:66161648 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1524+7314A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161648 | |||||||
| chr8:66161694 | CA | C | 16 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(13): Show |
17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1524+7361delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161694 | |||||||
| chr8:66161701 | T | C | 2 | a0002c0003t0002g0021 a0002c0003t0002g0027 |
2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1524+7367T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161701 | |||||||
| chr8:66161740 | A | C | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1524+7406A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161740 | |||||||
| chr8:66161755 | G | GT | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1524+7437dupT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66161755 | ||||||
| chr8:66161755 | G | GTT | 36 | a0001c0001t0001g0068 a0001c0001t0001g0098 a0001c0005t0001g0154 others(33): Show |
41 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1524+7436_1524+743 others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66161755 | ||||||
| chr8:66161755 | G | GTTT | 5 | a0002c0002t0001g0051 a0002c0002t0001g0056 a0002c0003t0001g0010 others(2): Show |
6 | HG02572.hp1 HG02896.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1524+7435_1524+743 others(7): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66161755 | ||||||
| chr8:66161755 | GT | G | 5 | a0001c0001t0001g0165 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG00738.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+7437delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66161755 | ||||||
| chr8:66161776 | G | C | 44 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(41): Show |
53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1524+7442G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161776 | |||||||
| chr8:66161819 | C | T | 1 | a0002c0002t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1524+7485C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161819 | |||||||
| chr8:66161859 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1524+7525T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161859 | |||||||
| chr8:66162017 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0171 |
3 | NA18942.hp1 NA18946.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1524+7683C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162017 | |||||||
| chr8:66162102 | CA | C | 15 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(12): Show |
19 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1524+7769delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162102 | |||||||
| chr8:66162159 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1524+7825G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162159 | |||||||
| chr8:66162487 | T | C | 1 | a0001c0001t0001g0005 | 3 | HG00673.hp1 HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1524+8153T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162487 | |||||||
| chr8:66162599 | A | G | 20 | a0002c0003t0001g0010 a0002c0003t0001g0038 a0002c0003t0001g0039 others(17): Show |
25 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1524+8265A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162599 | |||||||
| chr8:66162905 | A | T | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+8571A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162905 | |||||||
| chr8:66162920 | A | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+8586A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162920 | |||||||
| chr8:66163111 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1524+8777C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163111 | |||||||
| chr8:66163310 | T | C | 44 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(41): Show |
53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1524+8976T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163310 | |||||||
| chr8:66163351 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1524+9017G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163351 | |||||||
| chr8:66163556 | C | T | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+9222C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163556 | |||||||
| chr8:66163557 | G | A | 5 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(2): Show |
5 | HG02486.hp1 HG03017.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+9223G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163557 | |||||||
| chr8:66163906 | A | G | 1 | a0002c0002t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1524+9572A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163906 | |||||||
| chr8:66163947 | G | T | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1524+9613G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163947 | |||||||
| chr8:66164008 | GT | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(41): Show |
52 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1524+9686delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164008 | ||||||
| chr8:66164358 | G | A | 15 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(12): Show |
19 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1524+10024G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66164358 | |||||||
| chr8:66164532 | G | T | 2 | a0001c0001t0004g0014 a0001c0001t0004g0122 |
3 | HG00735.hp2 HG01516.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1525-9939G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66164532 | |||||||
| chr8:66164535 | G | A | 1 | a0002c0003t0002g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1525-9936G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66164535 | |||||||
| chr8:66164876 | G | A | 2 | a0002c0006t0001g0115 a0002c0006t0001g0145 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1525-9595G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66164876 | |||||||
| chr8:66164933 | A | AGAAG | 9 | a0001c0001t0001g0094 a0001c0001t0001g0121 a0001c0001t0001g0144 others(6): Show |
9 | HG00609.hp2 HG01109.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1525-9499_1525-949 others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | ||||||
| chr8:66164933 | A | G | 2 | a0001c0001t0001g0016 a0001c0005t0001g0016 |
2 | NA18962.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1525-9538A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66164933 | |||||||
| chr8:66164933 | AGAAG | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(46): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.1525-9499_1525-949 others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | ||||||
| chr8:66164933 | AGAAGGAA others(1): Show |
A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(39): Show |
50 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1525-9503_1525-949 others(12): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | ||||||
| chr8:66164933 | AGAAGGAA others(5): Show |
A | 8 | a0001c0001t0001g0100 a0001c0001t0001g0136 a0001c0001t0001g0193 others(5): Show |
8 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-9507_1525-949 others(16): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | ||||||
| chr8:66164933 | AGAAGGAA others(9): Show |
A | 54 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(51): Show |
64 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.1525-9511_1525-949 others(20): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | ||||||
| chr8:66164933 | AGAAGGAA others(17): Show |
A | 1 | a0002c0002t0001g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-9519_1525-949 others(28): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | ||||||
| chr8:66165223 | G | A | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1525-9248G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165223 | |||||||
| chr8:66165268 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1525-9203G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165268 | |||||||
| chr8:66165501 | TATTTA | T | 3 | a0002c0003t0001g0010 a0002c0003t0001g0039 a0002c0003t0001g0040 |
4 | HG02896.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-8965_1525-896 others(9): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66165501 | ||||||
| chr8:66165502 | AT | A | 4 | a0002c0002t0003g0030 a0002c0002t0003g0031 a0002c0002t0003g0032 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-8966delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66165502 | ||||||
| chr8:66165508 | T | A | 4 | a0002c0002t0003g0030 a0002c0002t0003g0031 a0002c0002t0003g0032 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-8963T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165508 | |||||||
| chr8:66165760 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1525-8711A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165760 | |||||||
| chr8:66165856 | C | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1525-8615C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165856 | |||||||
| chr8:66165924 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1525-8547C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165924 | |||||||
| chr8:66165952 | CT | C | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1525-8508delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66165952 | ||||||
| chr8:66166045 | TCTC | T | 11 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(8): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1525-8422_1525-842 others(7): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66166045 | ||||||
| chr8:66166537 | C | T | 1 | a0002c0003t0002g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1525-7934C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66166537 | |||||||
| chr8:66166556 | G | A | 2 | a0002c0003t0002g0006 a0002c0003t0002g0024 |
3 | HG02559.hp1 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1525-7915G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66166556 | |||||||
| chr8:66167031 | A | G | 4 | a0002c0002t0003g0030 a0002c0002t0003g0031 a0002c0002t0003g0032 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-7440A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167031 | |||||||
| chr8:66167051 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1525-7420A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167051 | |||||||
| chr8:66167533 | A | G | 44 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(41): Show |
53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1525-6938A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167533 | |||||||
| chr8:66167870 | C | G | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1525-6601C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167870 | |||||||
| chr8:66167891 | G | T | 2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1525-6580G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167891 | |||||||
| chr8:66167934 | G | A | 15 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(12): Show |
19 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1525-6537G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167934 | |||||||
| chr8:66167950 | A | G | 21 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(18): Show |
25 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1525-6521A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167950 | |||||||
| chr8:66168408 | C | T | 3 | a0002c0003t0001g0010 a0002c0003t0001g0039 a0002c0003t0001g0040 |
4 | HG02896.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-6063C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66168408 | |||||||
| chr8:66168493 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1525-5978G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66168493 | |||||||
| chr8:66168807 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1525-5664G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66168807 | |||||||
| chr8:66168912 | G | C | 5 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-5559G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66168912 | |||||||
| chr8:66169147 | C | A | 1 | a0002c0002t0001g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-5324C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169147 | |||||||
| chr8:66169232 | G | A | 1 | a0002c0002t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1525-5239G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169232 | |||||||
| chr8:66169290 | C | T | 2 | a0002c0002t0001g0052 a0002c0002t0001g0055 |
2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1525-5181C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169290 | |||||||
| chr8:66169475 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 |
3 | HG03516.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1525-4996T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169475 | |||||||
| chr8:66169504 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0171 |
3 | NA18942.hp1 NA18946.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1525-4967C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169504 | |||||||
| chr8:66169593 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1525-4878A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169593 | |||||||
| chr8:66169646 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1525-4825C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169646 | |||||||
| chr8:66169896 | T | A | 48 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(45): Show |
57 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1525-4575T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169896 | |||||||
| chr8:66169897 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1525-4574A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169897 | |||||||
| chr8:66170016 | A | G | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1525-4455A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170016 | |||||||
| chr8:66170455 | A | T | 2 | a0002c0003t0002g0021 a0002c0003t0002g0027 |
2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1525-4016A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170455 | |||||||
| chr8:66170497 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
125 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.1525-3974T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170497 | |||||||
| chr8:66170538 | G | A | 1 | a0002c0004t0001g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1525-3933G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170538 | |||||||
| chr8:66170563 | A | G | 1 | a0002c0003t0002g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1525-3908A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170563 | |||||||
| chr8:66170639 | C | T | 4 | a0002c0002t0003g0030 a0002c0002t0003g0031 a0002c0002t0003g0032 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-3832C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170639 | |||||||
| chr8:66170685 | G | A | 1 | a0001c0001t0004g0122 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1525-3786G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170685 | |||||||
| chr8:66170760 | A | G | 15 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(12): Show |
19 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1525-3711A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170760 | |||||||
| chr8:66170893 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1525-3578A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170893 | |||||||
| chr8:66171040 | G | A | 4 | a0002c0002t0002g0058 a0002c0002t0002g0062 a0002c0002t0002g0063 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-3431G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66171040 | |||||||
| chr8:66171534 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1525-2937T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66171534 | |||||||
| chr8:66171793 | G | A | 25 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(22): Show |
30 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1525-2678G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66171793 | |||||||
| chr8:66171889 | C | T | 2 | a0002c0002t0003g0030 a0002c0002t0003g0032 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1525-2582C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66171889 | |||||||
| chr8:66171970 | G | GGGGTC | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
125 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.1525-2499_1525-249 others(9): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66171970 | ||||||
| chr8:66172009 | G | A | 9 | a0002c0004t0001g0019 a0002c0004t0001g0206 a0002c0004t0001g0207 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1525-2462G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172009 | |||||||
| chr8:66172038 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1525-2433A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172038 | |||||||
| chr8:66172060 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0175 a0001c0001t0001g0177 |
3 | HG01261.hp2 HG04228.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1525-2411G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172060 | |||||||
| chr8:66172067 | GGAAGGAA others(9): Show |
G | 25 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(22): Show |
30 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.1525-2388_1525-237 others(20): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66172067 | ||||||
| chr8:66172096 | G | A | 1 | a0002c0002t0001g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-2375G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172096 | |||||||
| chr8:66172144 | T | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(38): Show |
49 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1525-2327T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172144 | |||||||
| chr8:66172170 | G | A | 35 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(32): Show |
40 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.1525-2301G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172170 | |||||||
| chr8:66172423 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1525-2048C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172423 | |||||||
| chr8:66172845 | G | A | 21 | a0002c0002t0001g0036 a0002c0003t0001g0010 a0002c0003t0001g0038 others(18): Show |
26 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525-1626G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172845 | |||||||
| chr8:66172934 | T | G | 25 | a0002c0002t0001g0036 a0002c0002t0003g0030 a0002c0002t0003g0031 others(22): Show |
30 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1525-1537T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172934 | |||||||
| chr8:66172972 | T | C | 1 | a0002c0002t0001g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-1499T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172972 | |||||||
| chr8:66173032 | C | T | 35 | a0002c0002t0001g0001 a0002c0002t0001g0041 a0002c0002t0001g0042 others(32): Show |
40 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.1525-1439C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66173032 | |||||||
| chr8:66173067 | T | G | 21 | a0002c0002t0001g0001 a0002c0002t0001g0043 a0002c0002t0001g0044 others(18): Show |
25 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1525-1404T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66173067 | |||||||
| chr8:66173601 | C | T | 1 | a0002c0004t0001g0210 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1525-870C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66173601 | |||||||
| chr8:66173615 | G | C | 1 | a0002c0002t0002g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1525-856G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66173615 | |||||||
| chr8:66173629 | G | A | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1525-842G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66173629 | |||||||
| chr8:66174115 | G | A | 60 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0041 others(57): Show |
70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1525-356G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66174115 | |||||||
| chr8:66174170 | TA | T | 5 | a0002c0002t0001g0036 a0002c0002t0001g0041 a0002c0002t0001g0042 others(2): Show |
5 | HG02486.hp1 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-287delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66174170 | ||||||
| chr8:66174256 | A | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG01109.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1525-215A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66174256 | |||||||
| chr8:66174349 | TATTGTTA others(11): Show |
T | 1 | a0001c0001t0001g0125 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1525-110_1525-93de others(19): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66174349 |