Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 134359 |
| ensemblid | ENSG00000152359.15 |
| hgncid | 26658 |
| symbol | POC5 |
| name | POC5 centriolar protein |
| refseq_nuc | NM_001099271.2 |
| refseq_prot | NP_001092741.1 |
| ensembl_nuc | ENST00000428202.7 |
| ensembl_prot | ENSP00000410216.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 75674124 |
| end | 75717437 |
| strand | - |
| ver | v1.2 |
| region | chr5:75674124-75717437 |
| region5000 | chr5:75669124-75722437 |
| regionname0 | POC5_chr5_75674124_75717437 |
| regionname5000 | POC5_chr5_75669124_75722437 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 575 | 137 | 45 | 28 | 46 | 5 | 13 | 34 | POC5_chr5_75669124_75722437 | POC5 | MSSDE others(570): Show |
chr5 | 75669124 | 75722437 |
| a0002 | 1/1 | 575 | 111 | 5 | 21 | 65 | 6 | 12 | 52 | POC5_chr5_75669124_75722437 | POC5 | MSSDE others(570): Show |
chr5 | 75669124 | 75722437 |
| a0003 | 0/0 | 575 | 96 | 15 | 11 | 59 | 1 | 10 | 48 | POC5_chr5_75669124_75722437 | POC5 | MSSDE others(570): Show |
chr5 | 75669124 | 75722437 |
| a0004 | 0/0 | 575 | 22 | 17 | 5 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | MSSDE others(570): Show |
chr5 | 75669124 | 75722437 |
| a0005 | 0/0 | 575 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | POC5_chr5_75669124_75722437 | POC5 | MSSDE others(570): Show |
chr5 | 75669124 | 75722437 |
| a0006 | 0/0 | 575 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | POC5_chr5_75669124_75722437 | POC5 | MSSDE others(570): Show |
chr5 | 75669124 | 75722437 |
| a0007 | 0/0 | 575 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | MSSDE others(570): Show |
chr5 | 75669124 | 75722437 |
| a0008 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | MSSDE others(570): Show |
chr5 | 75669124 | 75722437 |
| a0009 | 0/0 | 575 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | MSSDE others(570): Show |
chr5 | 75669124 | 75722437 |
| a0010 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | MSSDE others(570): Show |
chr5 | 75669124 | 75722437 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1725 | 113 | 36 | 24 | 40 | 4 | 9 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0001c0004 | 0/0 | 1725 | 23 | 8 | 4 | 6 | 1 | 4 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0001c0011 | 0/0 | 1725 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0002c0002 | 1/1 | 1725 | 110 | 5 | 21 | 64 | 6 | 12 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0002c0009 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0003c0003 | 0/0 | 1725 | 96 | 15 | 11 | 59 | 1 | 10 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0004c0005 | 0/0 | 1725 | 21 | 16 | 5 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0004c0014 | 0/0 | 1725 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0005c0006 | 0/0 | 1725 | 5 | 0 | 0 | 4 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0006c0007 | 0/0 | 1725 | 4 | 0 | 0 | 4 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0007c0008 | 0/0 | 1725 | 2 | 0 | 1 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0008c0012 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0009c0013 | 0/0 | 1725 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 | ||
| a0010c0010 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | ATGTC others(1720): Show |
chr5 | 75669124 | 75722437 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2185 | 101 | 31 | 23 | 34 | 4 | 9 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0001c0001t0002 | 0/0 | 2185 | 12 | 5 | 1 | 6 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0001c0004t0001 | 0/0 | 2185 | 5 | 2 | 0 | 0 | 0 | 3 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0001c0004t0002 | 0/0 | 2185 | 18 | 6 | 4 | 6 | 1 | 1 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0001c0011t0001 | 0/0 | 2185 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0002c0002t0001 | 1/1 | 2185 | 103 | 5 | 21 | 57 | 6 | 12 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0002c0002t0005 | 0/0 | 2188 | 7 | 0 | 0 | 7 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2183): Show |
chr5 | 75669124 | 75722437 |
| a0002c0009t0001 | 0/0 | 2185 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0003c0003t0001 | 0/0 | 2185 | 4 | 0 | 1 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0003c0003t0002 | 0/0 | 2185 | 77 | 15 | 10 | 43 | 1 | 8 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0003c0003t0004 | 0/0 | 2185 | 15 | 0 | 0 | 13 | 0 | 2 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0004c0005t0003 | 0/0 | 2185 | 21 | 16 | 5 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0004c0014t0003 | 0/0 | 2185 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0005c0006t0002 | 0/0 | 2185 | 5 | 0 | 0 | 4 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0006c0007t0004 | 0/0 | 2185 | 4 | 0 | 0 | 4 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0007c0008t0001 | 0/0 | 2185 | 2 | 0 | 1 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0008c0012t0001 | 0/0 | 2185 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0009c0013t0002 | 0/0 | 2185 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| a0010c0010t0004 | 0/0 | 2185 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | GCAGT others(2180): Show |
chr5 | 75669124 | 75722437 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 2 | 8 | 0 | 2 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0006 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0002g0003 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0004t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0001c0011t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0007 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0005g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0005g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0002t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0002c0009t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0001 | 0/0 | 18 | 0 | 4 | 13 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0004g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0003c0003t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0005t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0004c0014t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0005c0006t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0005c0006t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0005c0006t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0005c0006t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0005c0006t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0006c0007t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0006c0007t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0006c0007t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0006c0007t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0007c0008t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0007c0008t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0008c0012t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0009c0013t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| a0010c0010t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0218 | EUR | GBR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0023 | EUR | GBR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | GBR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00280 | hp1 | a0001 | c0004 | t0002 | g0019 | EUR | FIN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0199 | EUR | FIN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0172 | EUR | FIN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00408 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00423 | hp1 | a0003 | c0003 | t0002 | g0266 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00558 | hp1 | a0003 | c0003 | t0002 | g0254 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00609 | hp2 | a0003 | c0003 | t0002 | g0014 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00621 | hp2 | a0003 | c0003 | t0002 | g0032 | EAS | CHS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0229 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0065 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00735 | hp1 | a0004 | c0005 | t0003 | g0283 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01069 | hp1 | a0003 | c0003 | t0002 | g0030 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01071 | hp1 | a0007 | c0008 | t0001 | g0141 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0030 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01099 | hp1 | a0001 | c0004 | t0002 | g0108 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0235 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01109 | hp1 | a0004 | c0005 | t0003 | g0291 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01167 | hp2 | a0004 | c0005 | t0003 | g0292 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01169 | hp2 | a0004 | c0005 | t0003 | g0290 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01243 | hp1 | a0004 | c0005 | t0003 | g0034 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01255 | hp1 | a0001 | c0004 | t0002 | g0019 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01358 | hp2 | a0003 | c0003 | t0002 | g0066 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01361 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01496 | hp1 | a0003 | c0003 | t0002 | g0256 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0190 | EUR | IBS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01516 | hp2 | a0003 | c0003 | t0002 | g0018 | EUR | IBS | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01884 | hp2 | a0004 | c0005 | t0003 | g0288 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01891 | hp2 | a0004 | c0005 | t0003 | g0008 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01934 | hp2 | a0003 | c0003 | t0002 | g0252 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01943 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01952 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0194 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01975 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01981 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02015 | hp1 | a0008 | c0012 | t0001 | g0117 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02027 | hp2 | a0003 | c0003 | t0002 | g0255 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02040 | hp2 | a0005 | c0006 | t0002 | g0038 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02056 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02080 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02145 | hp1 | a0004 | c0014 | t0003 | g0289 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02145 | hp2 | a0001 | c0004 | t0002 | g0084 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0197 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CDX | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02257 | hp2 | a0004 | c0005 | t0003 | g0035 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02258 | hp1 | a0004 | c0005 | t0003 | g0035 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02293 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0003 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02451 | hp2 | a0003 | c0003 | t0002 | g0259 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0263 | EAS | KHV | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02572 | hp1 | a0004 | c0005 | t0003 | g0282 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02572 | hp2 | a0001 | c0004 | t0002 | g0083 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02602 | hp1 | a0003 | c0003 | t0002 | g0057 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0181 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02647 | hp1 | a0004 | c0005 | t0003 | g0008 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0231 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0053 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02698 | hp2 | a0007 | c0008 | t0001 | g0072 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02723 | hp2 | a0004 | c0005 | t0003 | g0008 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02735 | hp2 | a0003 | c0003 | t0002 | g0064 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02809 | hp2 | a0001 | c0011 | t0001 | g0096 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02818 | hp1 | a0003 | c0003 | t0002 | g0055 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02886 | hp1 | a0003 | c0003 | t0002 | g0258 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0077 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02896 | hp2 | a0004 | c0005 | t0003 | g0284 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02922 | hp2 | a0003 | c0003 | t0002 | g0048 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02970 | hp2 | a0004 | c0005 | t0003 | g0008 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03041 | hp2 | a0004 | c0005 | t0003 | g0281 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03098 | hp2 | a0003 | c0003 | t0002 | g0271 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03130 | hp1 | a0004 | c0005 | t0003 | g0034 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03130 | hp2 | a0004 | c0005 | t0003 | g0286 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03139 | hp2 | a0003 | c0003 | t0002 | g0049 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03195 | hp2 | a0001 | c0004 | t0002 | g0079 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0247 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03453 | hp1 | a0004 | c0005 | t0003 | g0287 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03453 | hp2 | a0003 | c0003 | t0002 | g0267 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0074 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03490 | hp2 | a0001 | c0004 | t0001 | g0165 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03491 | hp1 | a0003 | c0003 | t0002 | g0063 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03492 | hp1 | a0001 | c0004 | t0001 | g0027 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03516 | hp1 | a0003 | c0003 | t0002 | g0047 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03516 | hp2 | a0003 | c0003 | t0002 | g0052 | AFR | ESN | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03540 | hp2 | a0003 | c0003 | t0002 | g0056 | AFR | GWD | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0246 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03688 | hp1 | a0009 | c0013 | t0002 | g0085 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03688 | hp2 | a0003 | c0003 | t0002 | g0078 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03704 | hp2 | a0003 | c0003 | t0004 | g0068 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0150 | SAS | PJL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | BEB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0180 | SAS | BEB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | BEB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03927 | hp2 | a0003 | c0003 | t0004 | g0045 | SAS | BEB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0018 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0221 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG04204 | hp1 | a0001 | c0004 | t0002 | g0081 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG04204 | hp2 | a0003 | c0003 | t0002 | g0001 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG04228 | hp1 | a0003 | c0003 | t0002 | g0031 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG04228 | hp2 | a0001 | c0004 | t0001 | g0027 | SAS | STU | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18522 | hp1 | a0003 | c0003 | t0002 | g0054 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18612 | hp2 | a0003 | c0003 | t0002 | g0251 | EAS | CHB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18747 | hp1 | a0003 | c0003 | t0004 | g0004 | EAS | CHB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18747 | hp2 | a0003 | c0003 | t0002 | g0253 | EAS | CHB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18906 | hp1 | a0003 | c0003 | t0002 | g0264 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18906 | hp2 | a0004 | c0005 | t0003 | g0285 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18940 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18942 | hp1 | a0003 | c0003 | t0004 | g0058 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18942 | hp2 | a0002 | c0002 | t0005 | g0278 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18943 | hp2 | a0003 | c0003 | t0002 | g0265 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18944 | hp1 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18944 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18948 | hp1 | a0006 | c0007 | t0004 | g0070 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18948 | hp2 | a0003 | c0003 | t0002 | g0250 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18950 | hp1 | a0003 | c0003 | t0002 | g0014 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18950 | hp2 | a0002 | c0009 | t0001 | g0227 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18951 | hp2 | a0003 | c0003 | t0001 | g0270 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18953 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18956 | hp2 | a0003 | c0003 | t0002 | g0260 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18959 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18960 | hp2 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18962 | hp1 | a0003 | c0003 | t0004 | g0004 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18963 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18965 | hp1 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18966 | hp1 | a0003 | c0003 | t0002 | g0275 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18966 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18967 | hp2 | a0003 | c0003 | t0004 | g0062 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18968 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18968 | hp2 | a0003 | c0003 | t0004 | g0051 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18970 | hp1 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18971 | hp1 | a0010 | c0010 | t0004 | g0069 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18972 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18972 | hp2 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18973 | hp1 | a0003 | c0003 | t0002 | g0014 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18974 | hp1 | a0005 | c0006 | t0002 | g0037 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18974 | hp2 | a0003 | c0003 | t0004 | g0009 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18975 | hp2 | a0003 | c0003 | t0004 | g0004 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18977 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18978 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18979 | hp1 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18985 | hp1 | a0003 | c0003 | t0002 | g0269 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18985 | hp2 | a0003 | c0003 | t0004 | g0059 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18986 | hp2 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18991 | hp1 | a0006 | c0007 | t0004 | g0060 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18991 | hp2 | a0002 | c0002 | t0005 | g0277 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18992 | hp1 | a0003 | c0003 | t0002 | g0262 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18992 | hp2 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18993 | hp1 | a0003 | c0003 | t0002 | g0032 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18998 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18998 | hp2 | a0003 | c0003 | t0004 | g0009 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19000 | hp2 | a0003 | c0003 | t0002 | g0268 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19001 | hp2 | a0003 | c0003 | t0002 | g0272 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19002 | hp1 | a0003 | c0003 | t0004 | g0004 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19004 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19005 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19005 | hp2 | a0005 | c0006 | t0002 | g0039 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19006 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19007 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19009 | hp1 | a0006 | c0007 | t0004 | g0046 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19011 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | LWK | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19030 | hp2 | a0004 | c0005 | t0003 | g0280 | AFR | LWK | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0080 | AFR | LWK | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0261 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19058 | hp1 | a0002 | c0002 | t0005 | g0033 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19058 | hp2 | a0003 | c0003 | t0004 | g0050 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19059 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19060 | hp2 | a0006 | c0007 | t0004 | g0061 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19063 | hp1 | a0003 | c0003 | t0004 | g0009 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19064 | hp1 | a0002 | c0002 | t0005 | g0033 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19064 | hp2 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19066 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19067 | hp2 | a0005 | c0006 | t0002 | g0040 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19070 | hp1 | a0003 | c0003 | t0004 | g0004 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19075 | hp1 | a0003 | c0003 | t0002 | g0257 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19077 | hp1 | a0001 | c0004 | t0002 | g0075 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19079 | hp2 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19083 | hp2 | a0003 | c0003 | t0001 | g0273 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0274 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19240 | hp1 | a0001 | c0004 | t0002 | g0082 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0156 | EUR | TSI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA20905 | hp1 | a0005 | c0006 | t0002 | g0043 | SAS | GIH | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0217 | SAS | GIH | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0126 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG01123 | hp2 | a0003 | c0003 | t0002 | g0067 | AMR | CLM | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG02559 | hp2 | a0003 | c0003 | t0002 | g0071 | AFR | ACB | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0044 | AFR | MSL | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | USA | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| HG06807 | hp2 | a0003 | c0003 | t0002 | g0031 | AFR | USA | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | USA | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| NA20300 | hp2 | a0004 | c0005 | t0003 | g0279 | AFR | USA | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0144 | REF | REF | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0146 | REF | REF | POC5_chr5_75669124_75722437 | POC5 | chr5 | 75669124 | 75722437 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:75685263 | C | T | 1 | a0009 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1351G>A | p.Val451Ile | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/12 | 1497/2185 | 1351/1728 | 451/575 | chr5 | 75685263 | |||
| chr5:75685328 | G | A | 1 | a0007 | 2 | HG01071.hp1 HG02698.hp2 |
missense_variant | MODERATE | c.1286C>T | p.Ala429Val | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/12 | 1432/2185 | 1286/1728 | 429/575 | chr5 | 75685328 | |||
| chr5:75690483 | A | G | 1 | a0010 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.875T>C | p.Val292Ala | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/12 | 1021/2185 | 875/1728 | 292/575 | chr5 | 75690483 | |||
| chr5:75690501 | T | C | 1 | a0009 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.857A>G | p.Lys286Arg | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/12 | 1003/2185 | 857/1728 | 286/575 | chr5 | 75690501 | |||
| chr5:75690523 | T | C | 1 | a0008 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.835A>G | p.Thr279Ala | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/12 | 981/2185 | 835/1728 | 279/575 | chr5 | 75690523 | |||
| chr5:75692424 | C | T | 1 | a0006 | 4 | NA18948.hp1 NA18991.hp1 NA19009.hp1 others(1): Show |
missense_variant | MODERATE | c.767G>A | p.Arg256Gln | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/12 | 913/2185 | 767/1728 | 256/575 | chr5 | 75692424 | |||
| chr5:75702781 | G | A | 1 | a0005 | 5 | HG02040.hp2 NA18974.hp1 NA19005.hp2 others(2): Show |
missense_variant | MODERATE | c.337C>T | p.Pro113Ser | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/12 | 483/2185 | 337/1728 | 113/575 | chr5 | 75702781 | |||
| chr5:75705757 | A | G | 3 | a0003 a0006 a0010 |
101 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(98): Show |
missense_variant | MODERATE | c.254T>C | p.Ile85Thr | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/12 | 400/2185 | 254/1728 | 85/575 | chr5 | 75705757 | |||
| chr5:75705765 | T | A | 1 | a0004 | 22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
missense_variant | MODERATE | c.246A>T | p.Glu82Asp | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/12 | 392/2185 | 246/1728 | 82/575 | chr5 | 75705765 | |||
| chr5:75707853 | T | C | 8 | a0001 a0003 a0004 others(5): Show |
267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
missense_variant | MODERATE | c.107A>G | p.His36Arg | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/12 | 253/2185 | 107/1728 | 36/575 | chr5 | 75707853 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:75685219 | T | G | 1 | a0002c0009 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.1395A>C | p.Ala465Ala | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/12 | 1541/2185 | 1395/1728 | 465/575 | chr5 | 75685219 | |||
| chr5:75685435 | T | C | 1 | a0001c0011 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1179A>G | p.Gln393Gln | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/12 | 1325/2185 | 1179/1728 | 393/575 | chr5 | 75685435 | |||
| chr5:75702650 | A | G | 1 | a0004c0014 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.468T>C | p.Leu156Leu | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/12 | 614/2185 | 468/1728 | 156/575 | chr5 | 75702650 | |||
| chr5:75702773 | G | A | 2 | a0001c0004 a0009c0013 |
24 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(21): Show |
synonymous_variant | LOW | c.345C>T | p.His115His | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/12 | 491/2185 | 345/1728 | 115/575 | chr5 | 75702773 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:75674199 | T | C | 10 | a0001c0001t0002 a0001c0004t0002 a0003c0003t0002 others(7): Show |
155 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*236A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 12/12 | 236 | chr5 | 75674199 | ||||||
| chr5:75674411 | G | A | 3 | a0003c0003t0004 a0006c0007t0004 a0010c0010t0004 |
20 | HG03704.hp2 HG03927.hp2 NA18747.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*24C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 12/12 | 24 | chr5 | 75674411 | ||||||
| chr5:75717388 | T | TCAG | 1 | a0002c0002t0005 | 7 | NA18942.hp2 NA18944.hp1 NA18960.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-100_-98dupCTG | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/12 | 4452 | chr5 | 75717388 | ||||||
| chr5:75717414 | G | A | 2 | a0004c0005t0003 a0004c0014t0003 |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-123C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/12 | chr5 | 75717414 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:75674731 | T | G | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1585-153A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75674731 | |||||||
| chr5:75674747 | A | T | 14 | a0003c0003t0004g0004 a0003c0003t0004g0009 a0003c0003t0004g0045 others(11): Show |
20 | HG03704.hp2 HG03927.hp2 NA18747.hp1 others(17): Show |
intron_variant | MODIFIER | c.1585-169T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75674747 | |||||||
| chr5:75674834 | C | T | 1 | a0003c0003t0002g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1585-256G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75674834 | |||||||
| chr5:75675025 | G | A | 106 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(103): Show |
154 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1585-447C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675025 | |||||||
| chr5:75675150 | C | G | 107 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(104): Show |
155 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1585-572G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675150 | |||||||
| chr5:75675190 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1585-612T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675190 | |||||||
| chr5:75675193 | T | C | 120 | a0001c0001t0001g0111 a0001c0001t0001g0161 a0001c0001t0001g0166 others(117): Show |
168 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1585-615A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675193 | |||||||
| chr5:75675200 | C | T | 106 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(103): Show |
154 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1585-622G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675200 | |||||||
| chr5:75675203 | A | T | 1 | a0003c0003t0002g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1585-625T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675203 | |||||||
| chr5:75675263 | C | CAT | 107 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(104): Show |
155 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1585-687_1585-686d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675263 | |||||||
| chr5:75675342 | T | C | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1585-764A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675342 | |||||||
| chr5:75675443 | T | G | 1 | a0004c0005t0003g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1585-865A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675443 | |||||||
| chr5:75675549 | A | G | 107 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(104): Show |
155 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1585-971T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675549 | |||||||
| chr5:75675694 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1585-1116G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675694 | |||||||
| chr5:75675884 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1585-1306C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75675884 | |||||||
| chr5:75676021 | A | G | 114 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(111): Show |
134 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1585-1443T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676021 | |||||||
| chr5:75676165 | C | G | 117 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(114): Show |
165 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1585-1587G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676165 | |||||||
| chr5:75676469 | AGGTCCCA others(6): Show |
A | 1 | a0001c0001t0001g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1584+1292_1584+130 others(17): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676469 | |||||||
| chr5:75676503 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1584+1271T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676503 | |||||||
| chr5:75676547 | C | CG | 110 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(107): Show |
129 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1584+1226dupC | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676547 | |||||||
| chr5:75676548 | G | A | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1584+1226C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676548 | |||||||
| chr5:75676548 | G | C | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+1226C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676548 | |||||||
| chr5:75676682 | G | T | 117 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(114): Show |
165 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1584+1092C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676682 | |||||||
| chr5:75676748 | G | A | 15 | a0003c0003t0002g0057 a0003c0003t0004g0004 a0003c0003t0004g0009 others(12): Show |
21 | HG02602.hp1 HG03704.hp2 HG03927.hp2 others(18): Show |
intron_variant | MODIFIER | c.1584+1026C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676748 | |||||||
| chr5:75676759 | T | C | 8 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0132 others(5): Show |
8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1584+1015A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676759 | |||||||
| chr5:75676767 | C | T | 51 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0131 others(48): Show |
79 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1584+1007G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676767 | |||||||
| chr5:75676821 | T | C | 118 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(115): Show |
166 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1584+953A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676821 | |||||||
| chr5:75676826 | CA | C | 6 | a0001c0004t0002g0082 a0001c0004t0002g0083 a0002c0002t0005g0017 others(3): Show |
9 | HG02572.hp2 NA18942.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.1584+947delT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676826 | |||||||
| chr5:75676831 | A | G | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+943T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676831 | |||||||
| chr5:75676836 | AAT | A | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+936_1584+937d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676836 | |||||||
| chr5:75676845 | AAAAT | A | 14 | a0001c0001t0001g0020 a0001c0004t0001g0074 a0001c0004t0001g0077 others(11): Show |
23 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1584+925_1584+928d others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676845 | |||||||
| chr5:75676846 | A | T | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+928T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676846 | |||||||
| chr5:75676849 | T | A | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+925A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676849 | |||||||
| chr5:75676874 | C | A | 1 | a0003c0003t0001g0065 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1584+900G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676874 | |||||||
| chr5:75676924 | A | G | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+850T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676924 | |||||||
| chr5:75676941 | C | A | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1584+833G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75676941 | |||||||
| chr5:75677052 | G | A | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+722C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677052 | |||||||
| chr5:75677217 | T | G | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+557A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677217 | |||||||
| chr5:75677482 | C | T | 1 | a0004c0005t0003g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1584+292G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677482 | |||||||
| chr5:75677574 | C | T | 1 | a0003c0003t0002g0262 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1584+200G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677574 | |||||||
| chr5:75677580 | C | A | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1584+194G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677580 | |||||||
| chr5:75677621 | T | TA | 15 | a0001c0001t0001g0128 a0001c0001t0001g0174 a0001c0001t0001g0179 others(12): Show |
23 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1584+152dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677621 | |||||||
| chr5:75677621 | TA | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(156): Show |
218 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.1584+152delT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677621 | |||||||
| chr5:75677623 | A | T | 26 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(23): Show |
31 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1584+151T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 11/11 | chr5 | 75677623 | |||||||
| chr5:75678054 | C | T | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1408-104G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678054 | |||||||
| chr5:75678056 | G | T | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408-106C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678056 | |||||||
| chr5:75678124 | C | T | 78 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(75): Show |
113 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1408-174G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678124 | |||||||
| chr5:75678157 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1408-207G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678157 | |||||||
| chr5:75678265 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1408-315G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678265 | |||||||
| chr5:75678318 | C | T | 4 | a0002c0002t0001g0028 a0002c0002t0001g0149 a0002c0002t0001g0194 others(1): Show |
5 | HG01952.hp2 HG01975.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408-368G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678318 | |||||||
| chr5:75678328 | C | T | 4 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 others(1): Show |
5 | HG01243.hp1 HG03130.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408-378G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678328 | |||||||
| chr5:75678506 | T | C | 105 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(102): Show |
145 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.1408-556A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678506 | |||||||
| chr5:75678609 | C | CT | 109 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(106): Show |
128 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1408-660dupA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678609 | |||||||
| chr5:75678612 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1408-662A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678612 | |||||||
| chr5:75678629 | C | G | 1 | a0003c0003t0002g0275 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1408-679G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678629 | |||||||
| chr5:75678683 | G | A | 105 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(102): Show |
145 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.1408-733C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678683 | |||||||
| chr5:75678715 | T | C | 105 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(102): Show |
145 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.1408-765A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678715 | |||||||
| chr5:75678812 | T | C | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408-862A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678812 | |||||||
| chr5:75678822 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1408-872A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678822 | |||||||
| chr5:75678829 | C | T | 2 | a0003c0003t0002g0267 a0003c0003t0002g0271 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1408-879G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678829 | |||||||
| chr5:75678853 | A | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408-903T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678853 | |||||||
| chr5:75678913 | C | T | 1 | a0003c0003t0002g0078 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1408-963G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75678913 | |||||||
| chr5:75679057 | C | T | 2 | a0001c0001t0001g0094 a0002c0002t0001g0201 |
2 | HG04115.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1408-1107G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679057 | |||||||
| chr5:75679205 | T | C | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1408-1255A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679205 | |||||||
| chr5:75679443 | C | T | 227 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(224): Show |
294 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1408-1493G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679443 | |||||||
| chr5:75679519 | A | T | 104 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
144 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1408-1569T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679519 | |||||||
| chr5:75679604 | G | A | 77 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(74): Show |
112 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.1408-1654C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679604 | |||||||
| chr5:75679662 | T | C | 1 | a0004c0005t0003g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1408-1712A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679662 | |||||||
| chr5:75679837 | G | C | 4 | a0002c0002t0001g0028 a0002c0002t0001g0149 a0002c0002t0001g0194 others(1): Show |
5 | HG01952.hp2 HG01975.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408-1887C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75679837 | |||||||
| chr5:75680087 | A | G | 215 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(212): Show |
275 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.1408-2137T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680087 | |||||||
| chr5:75680186 | G | T | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1408-2236C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680186 | |||||||
| chr5:75680252 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1408-2302T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680252 | |||||||
| chr5:75680280 | G | A | 25 | a0001c0001t0001g0095 a0001c0001t0001g0115 a0001c0001t0002g0036 others(22): Show |
30 | HG00733.hp2 HG01516.hp2 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.1408-2330C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680280 | |||||||
| chr5:75680404 | G | A | 31 | a0003c0003t0002g0001 a0003c0003t0002g0013 a0003c0003t0002g0014 others(28): Show |
59 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1408-2454C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680404 | |||||||
| chr5:75680468 | C | G | 1 | a0004c0005t0003g0284 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1408-2518G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680468 | |||||||
| chr5:75680782 | T | C | 1 | a0002c0002t0001g0196 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1408-2832A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680782 | |||||||
| chr5:75680989 | A | G | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1408-3039T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75680989 | |||||||
| chr5:75681060 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1408-3110G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681060 | |||||||
| chr5:75681080 | GGAGT | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408-3134_1408-313 others(8): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681080 | |||||||
| chr5:75681236 | T | G | 14 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(11): Show |
22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1408-3286A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681236 | |||||||
| chr5:75681282 | C | T | 1 | a0003c0003t0002g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1408-3332G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681282 | |||||||
| chr5:75681292 | A | G | 9 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(6): Show |
9 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1408-3342T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681292 | |||||||
| chr5:75681324 | A | G | 228 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(225): Show |
290 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.1408-3374T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681324 | |||||||
| chr5:75681358 | A | G | 1 | a0003c0003t0002g0258 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1408-3408T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681358 | |||||||
| chr5:75681374 | T | C | 1 | a0001c0004t0002g0019 | 2 | HG00280.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1408-3424A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681374 | |||||||
| chr5:75681625 | A | AT | 12 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(9): Show |
17 | HG00735.hp1 HG01243.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1407+3581dupA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681625 | |||||||
| chr5:75681632 | A | T | 228 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(225): Show |
290 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.1407+3575T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681632 | |||||||
| chr5:75681633 | A | T | 228 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(225): Show |
290 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.1407+3574T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681633 | |||||||
| chr5:75681774 | T | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1407+3433A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681774 | |||||||
| chr5:75681836 | T | C | 211 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(208): Show |
268 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1407+3371A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681836 | |||||||
| chr5:75681842 | ATC | A | 8 | a0003c0003t0002g0013 a0003c0003t0002g0016 a0003c0003t0002g0253 others(5): Show |
12 | HG02027.hp2 HG02056.hp1 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.1407+3363_1407+336 others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75681842 | |||||||
| chr5:75682020 | T | C | 228 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(225): Show |
290 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.1407+3187A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682020 | |||||||
| chr5:75682029 | T | C | 211 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(208): Show |
268 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1407+3178A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682029 | |||||||
| chr5:75682084 | G | T | 1 | a0001c0001t0001g0242 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1407+3123C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682084 | |||||||
| chr5:75682125 | A | G | 241 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(238): Show |
311 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1407+3082T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682125 | |||||||
| chr5:75682210 | TCAAAA | T | 228 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(225): Show |
290 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.1407+2992_1407+299 others(9): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682210 | |||||||
| chr5:75682509 | A | C | 9 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(6): Show |
9 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1407+2698T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682509 | |||||||
| chr5:75682513 | C | A | 3 | a0002c0002t0001g0170 a0002c0002t0001g0205 a0003c0003t0002g0250 |
3 | HG00438.hp1 NA18940.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1407+2694G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682513 | |||||||
| chr5:75682517 | C | CTT | 198 | a0001c0001t0001g0006 a0001c0001t0001g0122 a0001c0001t0001g0127 others(195): Show |
256 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.1407+2688_1407+268 others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682517 | |||||||
| chr5:75682517 | C | CTTT | 23 | a0001c0001t0001g0076 a0001c0001t0002g0036 a0001c0001t0002g0041 others(20): Show |
27 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.1407+2687_1407+268 others(7): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682517 | |||||||
| chr5:75682688 | T | C | 3 | a0002c0002t0001g0190 a0002c0002t0001g0229 a0002c0002t0001g0235 |
3 | HG00639.hp2 HG01106.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1407+2519A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682688 | |||||||
| chr5:75682724 | C | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0206 a0001c0001t0001g0242 |
3 | HG02615.hp2 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1407+2483G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682724 | |||||||
| chr5:75682759 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1407+2448G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682759 | |||||||
| chr5:75682790 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0242 |
2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1407+2417G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682790 | |||||||
| chr5:75682897 | A | G | 3 | a0003c0003t0002g0258 a0003c0003t0002g0259 a0003c0003t0002g0264 |
3 | HG02451.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1407+2310T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75682897 | |||||||
| chr5:75683032 | G | A | 228 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(225): Show |
290 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.1407+2175C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683032 | |||||||
| chr5:75683054 | G | C | 1 | a0009c0013t0002g0085 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1407+2153C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683054 | |||||||
| chr5:75683137 | A | G | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1407+2070T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683137 | |||||||
| chr5:75683239 | GT | G | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+1967delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683239 | |||||||
| chr5:75683239 | GTT | G | 15 | a0003c0003t0002g0268 a0004c0005t0003g0008 a0004c0005t0003g0035 others(12): Show |
19 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1407+1966_1407+196 others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683239 | |||||||
| chr5:75683239 | GTTT | G | 213 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0122 others(210): Show |
271 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1407+1965_1407+196 others(7): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683239 | |||||||
| chr5:75683335 | A | G | 9 | a0004c0005t0003g0008 a0004c0005t0003g0035 a0004c0005t0003g0281 others(6): Show |
13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1407+1872T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683335 | |||||||
| chr5:75683394 | C | T | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1407+1813G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683394 | |||||||
| chr5:75683445 | G | A | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+1762C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683445 | |||||||
| chr5:75683527 | A | C | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+1680T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683527 | |||||||
| chr5:75683678 | G | A | 2 | a0002c0002t0001g0172 a0002c0002t0001g0173 |
2 | HG00323.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1407+1529C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683678 | |||||||
| chr5:75683703 | T | TA | 10 | a0002c0002t0001g0170 a0004c0005t0003g0008 a0004c0005t0003g0035 others(7): Show |
14 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1407+1503dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683703 | |||||||
| chr5:75683703 | TA | T | 18 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0113 others(15): Show |
26 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.1407+1503delT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683703 | |||||||
| chr5:75683727 | C | T | 1 | a0001c0004t0002g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1407+1480G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683727 | |||||||
| chr5:75683806 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(60): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1407+1401G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683806 | |||||||
| chr5:75683823 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1407+1384G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683823 | |||||||
| chr5:75683867 | C | A | 1 | a0003c0003t0002g0255 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1407+1340G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683867 | |||||||
| chr5:75683912 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1407+1295G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75683912 | |||||||
| chr5:75684041 | G | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1407+1166C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684041 | |||||||
| chr5:75684097 | C | G | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1407+1110G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684097 | |||||||
| chr5:75684194 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1407+1013T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684194 | |||||||
| chr5:75684299 | T | C | 1 | a0004c0005t0003g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1407+908A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684299 | |||||||
| chr5:75684313 | C | T | 1 | a0003c0003t0002g0272 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1407+894G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684313 | |||||||
| chr5:75684315 | T | TAA | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(82): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1407+891_1407+892i others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684315 | |||||||
| chr5:75684363 | A | AT | 17 | a0001c0001t0002g0164 a0001c0001t0002g0213 a0001c0001t0002g0214 others(14): Show |
17 | HG00438.hp1 HG02027.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1407+843dupA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684363 | |||||||
| chr5:75684363 | A | ATTTTTTT others(12): Show |
2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1407+825_1407+843d others(21): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684363 | |||||||
| chr5:75684363 | AT | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(45): Show |
66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1407+843delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684363 | |||||||
| chr5:75684363 | ATT | A | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1407+842_1407+843d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684363 | |||||||
| chr5:75684385 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1407+822C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684385 | |||||||
| chr5:75684427 | A | G | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+780T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684427 | |||||||
| chr5:75684449 | T | TC | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1407+757dupG | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684449 | |||||||
| chr5:75684489 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1407+718G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684489 | |||||||
| chr5:75684497 | T | C | 1 | a0002c0002t0001g0191 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1407+710A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684497 | |||||||
| chr5:75684521 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1407+686G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684521 | |||||||
| chr5:75684614 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1407+593G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684614 | |||||||
| chr5:75684615 | G | A | 34 | a0003c0003t0001g0270 a0003c0003t0001g0273 a0003c0003t0001g0274 others(31): Show |
62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1407+592C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684615 | |||||||
| chr5:75684651 | C | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1407+556G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684651 | |||||||
| chr5:75684665 | T | C | 2 | a0002c0002t0001g0177 a0002c0002t0001g0226 |
2 | NA19067.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1407+542A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684665 | |||||||
| chr5:75684747 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1407+460T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684747 | |||||||
| chr5:75684809 | AT | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1407+397delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684809 | |||||||
| chr5:75684870 | CT | C | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1407+336delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684870 | |||||||
| chr5:75684870 | CTT | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(45): Show |
66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1407+335_1407+336d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684870 | |||||||
| chr5:75684899 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1407+308C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75684899 | |||||||
| chr5:75685005 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1407+202G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75685005 | |||||||
| chr5:75685050 | G | A | 1 | a0003c0003t0002g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1407+157C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75685050 | |||||||
| chr5:75685067 | C | T | 34 | a0003c0003t0001g0270 a0003c0003t0001g0273 a0003c0003t0001g0274 others(31): Show |
62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1407+140G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75685067 | |||||||
| chr5:75685118 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1407+89G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 10/11 | chr5 | 75685118 | |||||||
| chr5:75685497 | A | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1130-13T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75685497 | |||||||
| chr5:75685519 | C | T | 3 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 |
4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1130-35G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75685519 | |||||||
| chr5:75685720 | T | C | 1 | a0004c0005t0003g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1130-236A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75685720 | |||||||
| chr5:75685978 | C | T | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0211 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1130-494G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75685978 | |||||||
| chr5:75686176 | G | A | 1 | a0001c0004t0002g0083 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1130-692C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686176 | |||||||
| chr5:75686382 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(157): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1130-898A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686382 | |||||||
| chr5:75686657 | T | C | 9 | a0002c0002t0001g0011 a0002c0002t0001g0123 a0002c0002t0001g0153 others(6): Show |
11 | HG00558.hp2 HG00609.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1130-1173A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686657 | |||||||
| chr5:75686842 | G | A | 3 | a0002c0002t0001g0154 a0002c0002t0001g0199 a0002c0002t0001g0200 |
3 | HG00323.hp1 HG01192.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1130-1358C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686842 | |||||||
| chr5:75686865 | C | A | 5 | a0005c0006t0002g0037 a0005c0006t0002g0038 a0005c0006t0002g0039 others(2): Show |
5 | HG02040.hp2 NA18974.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1130-1381G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686865 | |||||||
| chr5:75686961 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1130-1477G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75686961 | |||||||
| chr5:75687033 | AAC | A | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1130-1551_1130-155 others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687033 | |||||||
| chr5:75687037 | A | AT | 14 | a0001c0001t0001g0110 a0001c0004t0001g0074 a0001c0004t0001g0077 others(11): Show |
22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1130-1554dupA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687037 | |||||||
| chr5:75687037 | A | T | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1130-1553T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687037 | |||||||
| chr5:75687055 | T | TAG | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1130-1573_1130-157 others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687055 | |||||||
| chr5:75687112 | C | T | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1130-1628G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687112 | |||||||
| chr5:75687155 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1130-1671A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687155 | |||||||
| chr5:75687192 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1130-1708C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687192 | |||||||
| chr5:75687241 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1130-1757T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687241 | |||||||
| chr5:75687256 | T | G | 35 | a0003c0003t0001g0270 a0003c0003t0001g0273 a0003c0003t0001g0274 others(32): Show |
63 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1129+1756A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687256 | |||||||
| chr5:75687303 | T | C | 1 | a0002c0002t0001g0247 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1129+1709A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687303 | |||||||
| chr5:75687321 | C | T | 3 | a0002c0002t0001g0168 a0002c0002t0001g0183 a0002c0002t0001g0225 |
3 | HG02015.hp2 NA18964.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1129+1691G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687321 | |||||||
| chr5:75687391 | T | TA | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1129+1620dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687391 | |||||||
| chr5:75687736 | G | A | 2 | a0002c0002t0001g0197 a0002c0002t0001g0233 |
2 | HG01256.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1129+1276C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687736 | |||||||
| chr5:75687737 | G | A | 1 | a0003c0003t0002g0263 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1129+1275C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687737 | |||||||
| chr5:75687927 | A | G | 1 | a0002c0002t0001g0201 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1129+1085T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75687927 | |||||||
| chr5:75688204 | T | C | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1129+808A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688204 | |||||||
| chr5:75688255 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0116 |
2 | NA18964.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1129+757C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688255 | |||||||
| chr5:75688263 | G | A | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1129+749C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688263 | |||||||
| chr5:75688444 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1129+568G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688444 | |||||||
| chr5:75688503 | T | A | 1 | a0003c0003t0002g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1129+509A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688503 | |||||||
| chr5:75688583 | A | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1129+429T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688583 | |||||||
| chr5:75688737 | A | G | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129+275T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688737 | |||||||
| chr5:75688794 | G | A | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1129+218C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688794 | |||||||
| chr5:75688878 | T | C | 1 | a0002c0002t0001g0198 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1129+134A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688878 | |||||||
| chr5:75688993 | A | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1129+19T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 9/11 | chr5 | 75688993 | |||||||
| chr5:75689390 | G | C | 1 | a0001c0001t0002g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.976-225C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689390 | |||||||
| chr5:75689479 | G | A | 1 | a0002c0002t0001g0168 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.976-314C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689479 | |||||||
| chr5:75689526 | A | AAAAAT | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.976-366_976-362dup others(5): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689526 | |||||||
| chr5:75689537 | A | G | 1 | a0002c0002t0001g0192 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.976-372T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689537 | |||||||
| chr5:75689591 | G | A | 8 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(5): Show |
8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.976-426C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689591 | |||||||
| chr5:75689635 | T | C | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.976-470A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689635 | |||||||
| chr5:75689689 | A | G | 3 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 |
4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-524T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689689 | |||||||
| chr5:75689918 | C | T | 9 | a0004c0005t0003g0008 a0004c0005t0003g0035 a0004c0005t0003g0281 others(6): Show |
13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.975+465G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689918 | |||||||
| chr5:75689959 | C | T | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.975+424G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75689959 | |||||||
| chr5:75690042 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.975+341A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75690042 | |||||||
| chr5:75690169 | G | A | 1 | a0003c0003t0002g0264 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.975+214C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75690169 | |||||||
| chr5:75690220 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.975+163T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 8/11 | chr5 | 75690220 | |||||||
| chr5:75690656 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(148): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.796-94A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75690656 | |||||||
| chr5:75690751 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.796-189C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75690751 | |||||||
| chr5:75690877 | A | G | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.796-315T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75690877 | |||||||
| chr5:75691152 | G | A | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.796-590C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691152 | |||||||
| chr5:75691176 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.796-614C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691176 | |||||||
| chr5:75691198 | G | A | 1 | a0003c0003t0001g0065 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.796-636C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691198 | |||||||
| chr5:75691283 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.796-721G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691283 | |||||||
| chr5:75691624 | A | T | 1 | a0001c0001t0001g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.795+772T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691624 | |||||||
| chr5:75691708 | C | CAT | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.795+686_795+687dup others(2): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691708 | |||||||
| chr5:75691955 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.795+441G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75691955 | |||||||
| chr5:75692151 | T | A | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.795+245A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692151 | |||||||
| chr5:75692166 | T | A | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.795+230A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692166 | |||||||
| chr5:75692205 | T | C | 1 | a0002c0002t0001g0123 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.795+191A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692205 | |||||||
| chr5:75692241 | C | A | 1 | a0005c0006t0002g0040 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.795+155G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692241 | |||||||
| chr5:75692325 | A | G | 1 | a0002c0002t0001g0199 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.795+71T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692325 | |||||||
| chr5:75692365 | T | C | 1 | a0002c0002t0001g0155 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.795+31A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692365 | |||||||
| chr5:75692373 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.795+23G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 7/11 | chr5 | 75692373 | |||||||
| chr5:75692511 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.691-11G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75692511 | |||||||
| chr5:75692544 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(157): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.691-44T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75692544 | |||||||
| chr5:75692570 | A | C | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.691-70T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75692570 | |||||||
| chr5:75692753 | G | T | 1 | a0005c0006t0002g0040 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.691-253C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75692753 | |||||||
| chr5:75692933 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0110 |
2 | HG03654.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.691-433G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75692933 | |||||||
| chr5:75693014 | TTATATA | T | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.691-520_691-515del others(6): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693014 | |||||||
| chr5:75693026 | CTATATAT | C | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-533_691-527del others(7): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693026 | |||||||
| chr5:75693081 | TTAA | T | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0211 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-584_691-582del others(3): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693081 | |||||||
| chr5:75693097 | C | CATGTT | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.691-598_691-597ins others(5): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693097 | |||||||
| chr5:75693103 | T | C | 1 | a0002c0002t0001g0224 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.691-603A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693103 | |||||||
| chr5:75693161 | CAT | C | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.691-663_691-662del others(2): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693161 | |||||||
| chr5:75693184 | CTAA | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.691-687_691-685del others(3): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693184 | |||||||
| chr5:75693212 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.691-712A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693212 | |||||||
| chr5:75693320 | T | G | 2 | a0002c0002t0001g0199 a0002c0002t0001g0200 |
2 | HG00323.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.691-820A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693320 | |||||||
| chr5:75693532 | T | C | 8 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(5): Show |
8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.691-1032A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693532 | |||||||
| chr5:75693584 | A | C | 1 | a0003c0003t0002g0066 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+1071T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693584 | |||||||
| chr5:75693625 | C | CA | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(60): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.690+1029dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693625 | |||||||
| chr5:75693658 | C | T | 1 | a0004c0005t0003g0281 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.690+997G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693658 | |||||||
| chr5:75693659 | G | A | 8 | a0001c0001t0001g0210 a0001c0001t0002g0131 a0001c0001t0002g0164 others(5): Show |
8 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.690+996C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693659 | |||||||
| chr5:75693806 | G | A | 4 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0215 others(1): Show |
4 | HG02132.hp1 HG02135.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+849C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693806 | |||||||
| chr5:75693823 | C | T | 1 | a0003c0003t0002g0256 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.690+832G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693823 | |||||||
| chr5:75693904 | C | A | 2 | a0003c0003t0002g0066 a0003c0003t0002g0067 |
2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.690+751G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693904 | |||||||
| chr5:75693905 | C | A | 7 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(4): Show |
7 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+750G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75693905 | |||||||
| chr5:75694071 | G | C | 1 | a0002c0002t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.690+584C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694071 | |||||||
| chr5:75694072 | A | C | 1 | a0002c0002t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.690+583T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694072 | |||||||
| chr5:75694073 | G | T | 1 | a0002c0002t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.690+582C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694073 | |||||||
| chr5:75694126 | T | C | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.690+529A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694126 | |||||||
| chr5:75694300 | G | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.690+355C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694300 | |||||||
| chr5:75694313 | T | C | 1 | a0002c0002t0001g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.690+342A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694313 | |||||||
| chr5:75694352 | A | T | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.690+303T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694352 | |||||||
| chr5:75694353 | A | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.690+302T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694353 | |||||||
| chr5:75694389 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.690+266G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694389 | |||||||
| chr5:75694523 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.690+132A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 6/11 | chr5 | 75694523 | |||||||
| chr5:75694910 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.514-79T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75694910 | |||||||
| chr5:75694954 | A | C | 35 | a0003c0003t0001g0270 a0003c0003t0001g0273 a0003c0003t0001g0274 others(32): Show |
63 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.514-123T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75694954 | |||||||
| chr5:75694989 | C | A | 1 | a0005c0006t0002g0040 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.514-158G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75694989 | |||||||
| chr5:75694996 | C | A | 1 | a0002c0002t0001g0221 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.514-165G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75694996 | |||||||
| chr5:75695067 | G | A | 1 | a0002c0002t0001g0126 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.514-236C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695067 | |||||||
| chr5:75695221 | G | A | 1 | a0002c0002t0001g0234 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.514-390C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695221 | |||||||
| chr5:75695297 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.514-466C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695297 | |||||||
| chr5:75695341 | A | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG00639.hp1 HG01109.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.514-510T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695341 | |||||||
| chr5:75695556 | C | T | 1 | a0003c0003t0002g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.514-725G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695556 | |||||||
| chr5:75695618 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-787C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695618 | |||||||
| chr5:75695676 | C | A | 1 | a0005c0006t0002g0040 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.514-845G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695676 | |||||||
| chr5:75695719 | C | T | 1 | a0003c0003t0002g0014 | 3 | HG00609.hp2 NA18950.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.514-888G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695719 | |||||||
| chr5:75695720 | G | A | 9 | a0004c0005t0003g0008 a0004c0005t0003g0035 a0004c0005t0003g0281 others(6): Show |
13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.514-889C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695720 | |||||||
| chr5:75695761 | T | C | 30 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(27): Show |
43 | HG00280.hp1 HG00408.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.514-930A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695761 | |||||||
| chr5:75695770 | C | T | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-939G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695770 | |||||||
| chr5:75695853 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1022T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695853 | |||||||
| chr5:75695854 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1023A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695854 | |||||||
| chr5:75695859 | C | T | 1 | a0005c0006t0002g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.514-1028G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695859 | |||||||
| chr5:75695893 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1062A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695893 | |||||||
| chr5:75695904 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1073A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695904 | |||||||
| chr5:75695923 | C | A | 1 | a0004c0005t0003g0283 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.514-1092G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695923 | |||||||
| chr5:75695969 | C | T | 1 | a0003c0003t0004g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.514-1138G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695969 | |||||||
| chr5:75695985 | G | A | 1 | a0002c0002t0001g0201 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.514-1154C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695985 | |||||||
| chr5:75695993 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.514-1162G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75695993 | |||||||
| chr5:75696021 | G | A | 1 | a0003c0003t0002g0265 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.514-1190C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696021 | |||||||
| chr5:75696024 | A | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(157): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.514-1193T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696024 | |||||||
| chr5:75696039 | C | A | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1208G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696039 | |||||||
| chr5:75696078 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(76): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.514-1247T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696078 | |||||||
| chr5:75696118 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1287G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696118 | |||||||
| chr5:75696142 | A | G | 2 | a0003c0003t0002g0267 a0003c0003t0002g0271 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.514-1311T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696142 | |||||||
| chr5:75696183 | C | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1352G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696183 | |||||||
| chr5:75696183 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.514-1352G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696183 | |||||||
| chr5:75696191 | C | G | 1 | a0003c0003t0002g0255 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.514-1360G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696191 | |||||||
| chr5:75696225 | C | T | 2 | a0001c0004t0002g0079 a0001c0004t0002g0080 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.514-1394G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696225 | |||||||
| chr5:75696238 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1407C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696238 | |||||||
| chr5:75696265 | C | A | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.514-1434G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696265 | |||||||
| chr5:75696328 | A | G | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-1497T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696328 | |||||||
| chr5:75696331 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.514-1500C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696331 | |||||||
| chr5:75696337 | T | C | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.514-1506A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696337 | |||||||
| chr5:75696371 | C | T | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1540G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696371 | |||||||
| chr5:75696378 | C | A | 3 | a0002c0002t0001g0187 a0002c0002t0001g0228 a0002c0009t0001g0227 |
3 | NA18950.hp2 NA18984.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.514-1547G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696378 | |||||||
| chr5:75696418 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-1587G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696418 | |||||||
| chr5:75696420 | T | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.514-1589A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696420 | |||||||
| chr5:75696449 | G | C | 2 | a0003c0003t0002g0055 a0003c0003t0002g0056 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.514-1618C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696449 | |||||||
| chr5:75696452 | T | G | 1 | a0001c0004t0002g0019 | 2 | HG00280.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.514-1621A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696452 | |||||||
| chr5:75696454 | A | G | 1 | a0003c0003t0002g0254 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.514-1623T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696454 | |||||||
| chr5:75696468 | C | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(48): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.514-1637G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696468 | |||||||
| chr5:75696474 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.514-1643G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696474 | |||||||
| chr5:75696582 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.514-1751T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696582 | |||||||
| chr5:75696591 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.514-1760T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696591 | |||||||
| chr5:75696653 | C | T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0224 |
2 | NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.514-1822G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696653 | |||||||
| chr5:75696671 | T | A | 2 | a0002c0002t0001g0202 a0002c0002t0001g0203 |
2 | NA19059.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.514-1840A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696671 | |||||||
| chr5:75696673 | G | A | 8 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(5): Show |
8 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-1842C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696673 | |||||||
| chr5:75696701 | C | A | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1870G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696701 | |||||||
| chr5:75696743 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.514-1912C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696743 | |||||||
| chr5:75696756 | C | T | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1925G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696756 | |||||||
| chr5:75696802 | T | C | 1 | a0002c0002t0001g0126 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.514-1971A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696802 | |||||||
| chr5:75696863 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.514-2032T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696863 | |||||||
| chr5:75696957 | A | C | 1 | a0002c0002t0001g0183 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.514-2126T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696957 | |||||||
| chr5:75696957 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-2126T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75696957 | |||||||
| chr5:75697053 | C | T | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-2222G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697053 | |||||||
| chr5:75697054 | G | A | 1 | a0002c0002t0001g0228 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.514-2223C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697054 | |||||||
| chr5:75697078 | A | G | 1 | a0002c0002t0001g0028 | 2 | HG01981.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.514-2247T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697078 | |||||||
| chr5:75697079 | T | C | 1 | a0002c0002t0001g0235 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.514-2248A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697079 | |||||||
| chr5:75697126 | A | C | 1 | a0003c0003t0002g0253 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.514-2295T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697126 | |||||||
| chr5:75697159 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-2328A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697159 | |||||||
| chr5:75697261 | C | T | 15 | a0001c0001t0002g0132 a0002c0002t0001g0007 a0002c0002t0001g0012 others(12): Show |
21 | HG00423.hp2 HG01257.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.514-2430G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697261 | |||||||
| chr5:75697262 | G | A | 1 | a0004c0005t0003g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.514-2431C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697262 | |||||||
| chr5:75697291 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-2460T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697291 | |||||||
| chr5:75697313 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-2482G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697313 | |||||||
| chr5:75697334 | C | A | 1 | a0002c0002t0001g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.514-2503G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697334 | |||||||
| chr5:75697359 | C | T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0224 |
2 | NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.514-2528G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697359 | |||||||
| chr5:75697360 | A | C | 9 | a0004c0005t0003g0008 a0004c0005t0003g0035 a0004c0005t0003g0281 others(6): Show |
13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.514-2529T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697360 | |||||||
| chr5:75697360 | A | G | 2 | a0002c0002t0001g0123 a0002c0002t0001g0224 |
2 | NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.514-2529T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697360 | |||||||
| chr5:75697387 | GT | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.514-2557delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697387 | |||||||
| chr5:75697454 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.514-2623G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697454 | |||||||
| chr5:75697521 | C | T | 2 | a0003c0003t0002g0055 a0003c0003t0002g0056 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.514-2690G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697521 | |||||||
| chr5:75697563 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.514-2732G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697563 | |||||||
| chr5:75697580 | G | A | 2 | a0003c0003t0002g0030 a0003c0003t0002g0031 |
4 | HG01069.hp1 HG01071.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-2749C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697580 | |||||||
| chr5:75697661 | A | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.514-2830T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697661 | |||||||
| chr5:75697663 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-2832A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697663 | |||||||
| chr5:75697740 | G | A | 3 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 |
4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-2909C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697740 | |||||||
| chr5:75697787 | G | C | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-2956C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697787 | |||||||
| chr5:75697794 | T | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(60): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.514-2963A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697794 | |||||||
| chr5:75697884 | C | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(82): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.514-3053G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697884 | |||||||
| chr5:75697903 | G | A | 1 | a0003c0003t0004g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.514-3072C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697903 | |||||||
| chr5:75697910 | T | C | 2 | a0004c0005t0003g0284 a0004c0005t0003g0285 |
2 | HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.514-3079A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697910 | |||||||
| chr5:75697975 | C | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-3144G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697975 | |||||||
| chr5:75697983 | A | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(82): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.514-3152T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75697983 | |||||||
| chr5:75698032 | T | C | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.514-3201A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698032 | |||||||
| chr5:75698108 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-3277A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698108 | |||||||
| chr5:75698214 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-3383T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698214 | |||||||
| chr5:75698226 | T | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(76): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.514-3395A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698226 | |||||||
| chr5:75698270 | T | C | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.514-3439A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698270 | |||||||
| chr5:75698301 | T | A | 2 | a0004c0005t0003g0290 a0004c0005t0003g0292 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.514-3470A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698301 | |||||||
| chr5:75698429 | A | C | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.514-3598T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698429 | |||||||
| chr5:75698453 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.514-3622C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698453 | |||||||
| chr5:75698498 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0166 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.514-3667T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698498 | |||||||
| chr5:75698518 | C | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0090 |
4 | NA18960.hp1 NA18984.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-3687G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698518 | |||||||
| chr5:75698530 | A | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-3699T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698530 | |||||||
| chr5:75698536 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.514-3705G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698536 | |||||||
| chr5:75698642 | T | A | 1 | a0002c0002t0001g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.514-3811A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698642 | |||||||
| chr5:75698653 | A | T | 1 | a0002c0002t0001g0143 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.514-3822T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698653 | |||||||
| chr5:75698745 | C | T | 8 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(5): Show |
8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+3860G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698745 | |||||||
| chr5:75698746 | A | T | 8 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(5): Show |
8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+3859T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698746 | |||||||
| chr5:75698793 | A | G | 1 | a0002c0002t0001g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.513+3812T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698793 | |||||||
| chr5:75698798 | G | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(76): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.513+3807C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698798 | |||||||
| chr5:75698843 | C | T | 1 | a0003c0003t0004g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.513+3762G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698843 | |||||||
| chr5:75698845 | A | G | 1 | a0002c0002t0001g0223 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.513+3760T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698845 | |||||||
| chr5:75698914 | G | C | 1 | a0001c0001t0001g0020 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.513+3691C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698914 | |||||||
| chr5:75698926 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+3679T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698926 | |||||||
| chr5:75698988 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.513+3617C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75698988 | |||||||
| chr5:75699038 | T | TAGACCAA others(13): Show |
1 | a0005c0006t0002g0040 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.513+3547_513+3566d others(22): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699038 | |||||||
| chr5:75699063 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+3542C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699063 | |||||||
| chr5:75699088 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(117): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.513+3517A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699088 | |||||||
| chr5:75699099 | C | T | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+3506G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699099 | |||||||
| chr5:75699122 | T | C | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+3483A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699122 | |||||||
| chr5:75699184 | T | C | 1 | a0002c0002t0001g0126 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.513+3421A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699184 | |||||||
| chr5:75699236 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.513+3369C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699236 | |||||||
| chr5:75699247 | C | T | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.513+3358G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699247 | |||||||
| chr5:75699365 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.513+3240G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699365 | |||||||
| chr5:75699366 | C | G | 1 | a0001c0004t0002g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513+3239G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699366 | |||||||
| chr5:75699367 | A | G | 13 | a0001c0004t0001g0074 a0001c0004t0001g0077 a0001c0004t0002g0003 others(10): Show |
21 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.513+3238T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699367 | |||||||
| chr5:75699368 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.513+3237G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699368 | |||||||
| chr5:75699418 | A | G | 1 | a0002c0002t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.513+3187T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699418 | |||||||
| chr5:75699443 | A | G | 3 | a0002c0002t0001g0181 a0002c0002t0001g0217 a0002c0002t0001g0246 |
3 | HG02602.hp2 HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.513+3162T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699443 | |||||||
| chr5:75699452 | A | G | 1 | a0002c0002t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.513+3153T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699452 | |||||||
| chr5:75699533 | T | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(157): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.513+3072A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699533 | |||||||
| chr5:75699561 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+3044A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699561 | |||||||
| chr5:75699584 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+3021T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699584 | |||||||
| chr5:75699655 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2950A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699655 | |||||||
| chr5:75699680 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513+2925G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699680 | |||||||
| chr5:75699682 | A | G | 1 | a0003c0003t0002g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513+2923T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699682 | |||||||
| chr5:75699712 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.513+2893C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699712 | |||||||
| chr5:75699722 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.513+2883T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699722 | |||||||
| chr5:75699778 | C | G | 32 | a0001c0001t0002g0132 a0003c0003t0001g0065 a0003c0003t0002g0018 others(29): Show |
39 | HG00733.hp2 HG01123.hp2 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.513+2827G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699778 | |||||||
| chr5:75699793 | C | G | 1 | a0003c0003t0002g0078 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.513+2812G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699793 | |||||||
| chr5:75699793 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(60): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.513+2812G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699793 | |||||||
| chr5:75699794 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.513+2811C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699794 | |||||||
| chr5:75699803 | G | A | 1 | a0003c0003t0002g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513+2802C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699803 | |||||||
| chr5:75699809 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2796G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699809 | |||||||
| chr5:75699816 | AC | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2788delG | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699816 | |||||||
| chr5:75699823 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2782A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699823 | |||||||
| chr5:75699918 | T | C | 1 | a0002c0002t0001g0236 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513+2687A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75699918 | |||||||
| chr5:75700044 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(75): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.513+2561C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700044 | |||||||
| chr5:75700046 | C | A | 1 | a0001c0001t0001g0087 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513+2559G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700046 | |||||||
| chr5:75700184 | C | T | 34 | a0003c0003t0001g0270 a0003c0003t0001g0273 a0003c0003t0001g0274 others(31): Show |
62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.513+2421G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700184 | |||||||
| chr5:75700185 | C | G | 1 | a0001c0001t0001g0248 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.513+2420G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700185 | |||||||
| chr5:75700221 | T | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(48): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.513+2384A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700221 | |||||||
| chr5:75700250 | C | T | 18 | a0003c0003t0002g0252 a0004c0005t0003g0008 a0004c0005t0003g0034 others(15): Show |
23 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.513+2355G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700250 | |||||||
| chr5:75700256 | A | G | 1 | a0003c0003t0002g0013 | 3 | HG02056.hp1 NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.513+2349T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700256 | |||||||
| chr5:75700344 | C | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.513+2261G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700344 | |||||||
| chr5:75700372 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.513+2233A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700372 | |||||||
| chr5:75700374 | T | C | 1 | a0002c0002t0001g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.513+2231A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700374 | |||||||
| chr5:75700413 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(76): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.513+2192G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700413 | |||||||
| chr5:75700470 | A | C | 3 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 |
4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+2135T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700470 | |||||||
| chr5:75700573 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2032T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700573 | |||||||
| chr5:75700589 | A | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+2016T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700589 | |||||||
| chr5:75700626 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513+1979T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700626 | |||||||
| chr5:75700650 | C | T | 8 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(5): Show |
8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+1955G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700650 | |||||||
| chr5:75700655 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.513+1950T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700655 | |||||||
| chr5:75700704 | C | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+1901G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700704 | |||||||
| chr5:75700726 | A | C | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.513+1879T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700726 | |||||||
| chr5:75700757 | C | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+1848G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700757 | |||||||
| chr5:75700793 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(60): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.513+1812G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700793 | |||||||
| chr5:75700801 | A | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.513+1804T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700801 | |||||||
| chr5:75700856 | C | T | 1 | a0004c0005t0003g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+1749G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700856 | |||||||
| chr5:75700880 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+1725C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700880 | |||||||
| chr5:75700900 | G | C | 8 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(5): Show |
8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+1705C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700900 | |||||||
| chr5:75700908 | A | T | 8 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(5): Show |
8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+1697T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700908 | |||||||
| chr5:75700914 | T | C | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.513+1691A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700914 | |||||||
| chr5:75700965 | A | G | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.513+1640T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75700965 | |||||||
| chr5:75701016 | T | C | 31 | a0003c0003t0001g0065 a0003c0003t0002g0018 a0003c0003t0002g0044 others(28): Show |
38 | HG00733.hp2 HG01123.hp2 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.513+1589A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701016 | |||||||
| chr5:75701103 | C | G | 2 | a0004c0005t0003g0035 a0004c0005t0003g0281 |
3 | HG02257.hp2 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.513+1502G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701103 | |||||||
| chr5:75701152 | G | T | 1 | a0003c0003t0002g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.513+1453C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701152 | |||||||
| chr5:75701163 | G | A | 1 | a0003c0003t0002g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513+1442C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701163 | |||||||
| chr5:75701186 | C | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.513+1419G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701186 | |||||||
| chr5:75701216 | C | T | 3 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 |
4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+1389G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701216 | |||||||
| chr5:75701264 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+1341A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701264 | |||||||
| chr5:75701270 | C | G | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.513+1335G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701270 | |||||||
| chr5:75701283 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(58): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.513+1322G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701283 | |||||||
| chr5:75701284 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.513+1321C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701284 | |||||||
| chr5:75701365 | A | G | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+1240T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701365 | |||||||
| chr5:75701435 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.513+1170G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701435 | |||||||
| chr5:75701464 | G | T | 1 | a0001c0001t0002g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.513+1141C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701464 | |||||||
| chr5:75701475 | A | G | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1130T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701475 | |||||||
| chr5:75701480 | C | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(60): Show |
90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.513+1125G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701480 | |||||||
| chr5:75701486 | C | T | 1 | a0003c0003t0002g0251 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.513+1119G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701486 | |||||||
| chr5:75701500 | G | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(59): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.513+1105C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701500 | |||||||
| chr5:75701507 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.513+1098C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701507 | |||||||
| chr5:75701599 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(61): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+1006A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701599 | |||||||
| chr5:75701701 | C | T | 9 | a0004c0005t0003g0008 a0004c0005t0003g0035 a0004c0005t0003g0281 others(6): Show |
13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.513+904G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701701 | |||||||
| chr5:75701708 | C | G | 2 | a0003c0003t0002g0055 a0003c0003t0002g0056 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.513+897G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701708 | |||||||
| chr5:75701728 | A | AAAAT | 3 | a0002c0002t0001g0185 a0007c0008t0001g0072 a0007c0008t0001g0141 |
3 | HG01071.hp1 HG02698.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.513+873_513+876dup others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701728 | |||||||
| chr5:75701728 | AAAAT | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(150): Show |
220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.513+873_513+876del others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701728 | |||||||
| chr5:75701839 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.513+766G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701839 | |||||||
| chr5:75701911 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(61): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+694A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701911 | |||||||
| chr5:75701931 | T | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(150): Show |
220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.513+674A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75701931 | |||||||
| chr5:75702007 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(61): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+598A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702007 | |||||||
| chr5:75702016 | A | G | 9 | a0004c0005t0003g0008 a0004c0005t0003g0035 a0004c0005t0003g0281 others(6): Show |
13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.513+589T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702016 | |||||||
| chr5:75702170 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(61): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+435T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702170 | |||||||
| chr5:75702172 | G | A | 1 | a0003c0003t0002g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.513+433C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702172 | |||||||
| chr5:75702358 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513+247T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702358 | |||||||
| chr5:75702438 | C | T | 1 | a0002c0002t0001g0184 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.513+167G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702438 | |||||||
| chr5:75702439 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(61): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+166C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702439 | |||||||
| chr5:75702444 | T | G | 3 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 |
4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+161A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702444 | |||||||
| chr5:75702509 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(61): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.513+96C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702509 | |||||||
| chr5:75702560 | C | T | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+45G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702560 | |||||||
| chr5:75702601 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
splice_region_variant&intron_variant | LOW | c.513+4C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 5/11 | chr5 | 75702601 | |||||||
| chr5:75703067 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.308-257G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703067 | |||||||
| chr5:75703285 | T | C | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.308-475A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703285 | |||||||
| chr5:75703350 | G | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0120 others(1): Show |
4 | HG01943.hp2 HG02148.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-540C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703350 | |||||||
| chr5:75703464 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.308-654T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703464 | |||||||
| chr5:75703573 | C | G | 9 | a0004c0005t0003g0008 a0004c0005t0003g0035 a0004c0005t0003g0281 others(6): Show |
13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.308-763G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703573 | |||||||
| chr5:75703580 | C | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-770G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703580 | |||||||
| chr5:75703739 | G | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.308-929C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703739 | |||||||
| chr5:75703751 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(160): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.308-941C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703751 | |||||||
| chr5:75703875 | G | A | 1 | a0001c0004t0002g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.308-1065C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703875 | |||||||
| chr5:75703889 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.308-1079G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703889 | |||||||
| chr5:75703930 | C | T | 7 | a0001c0001t0002g0131 a0001c0001t0002g0158 a0001c0001t0002g0164 others(4): Show |
7 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.308-1120G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703930 | |||||||
| chr5:75703972 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.308-1162C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75703972 | |||||||
| chr5:75704026 | G | A | 1 | a0010c0010t0004g0069 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.308-1216C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704026 | |||||||
| chr5:75704110 | G | A | 13 | a0001c0004t0001g0027 a0001c0004t0001g0165 a0001c0004t0002g0003 others(10): Show |
22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.308-1300C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704110 | |||||||
| chr5:75704140 | C | T | 1 | a0002c0002t0001g0183 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.308-1330G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704140 | |||||||
| chr5:75704153 | C | CA | 8 | a0001c0001t0001g0162 a0002c0002t0001g0157 a0002c0002t0001g0170 others(5): Show |
8 | HG00423.hp1 HG02896.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.308-1344dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704153 | |||||||
| chr5:75704153 | CA | C | 23 | a0001c0001t0001g0099 a0001c0001t0001g0118 a0001c0001t0002g0131 others(20): Show |
27 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.308-1344delT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704153 | |||||||
| chr5:75704153 | CAA | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(43): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.308-1345_308-1344d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704153 | |||||||
| chr5:75704925 | C | G | 1 | a0002c0002t0001g0140 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.307+779G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704925 | |||||||
| chr5:75704931 | G | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.307+773C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704931 | |||||||
| chr5:75704967 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.307+737C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704967 | |||||||
| chr5:75704981 | C | T | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.307+723G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75704981 | |||||||
| chr5:75705094 | G | T | 1 | a0002c0002t0001g0182 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.307+610C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705094 | |||||||
| chr5:75705103 | C | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0139 a0001c0001t0001g0174 others(3): Show |
6 | HG01192.hp2 HG01261.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.307+601G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705103 | |||||||
| chr5:75705173 | G | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.307+531C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705173 | |||||||
| chr5:75705200 | C | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(69): Show |
95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.307+504G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705200 | |||||||
| chr5:75705209 | T | TA | 23 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(20): Show |
28 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.307+494_307+495ins others(1): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705209 | |||||||
| chr5:75705209 | T | TAA | 46 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(43): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.307+494_307+495ins others(2): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705209 | |||||||
| chr5:75705210 | T | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(69): Show |
95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.307+494A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705210 | |||||||
| chr5:75705211 | A | T | 13 | a0001c0004t0001g0027 a0001c0004t0001g0165 a0001c0004t0002g0003 others(10): Show |
22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.307+493T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705211 | |||||||
| chr5:75705218 | T | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(69): Show |
95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.307+486A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705218 | |||||||
| chr5:75705236 | C | A | 1 | a0003c0003t0002g0272 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.307+468G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705236 | |||||||
| chr5:75705427 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.307+277A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705427 | |||||||
| chr5:75705496 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.307+208G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705496 | |||||||
| chr5:75705569 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18954.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.307+135T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705569 | |||||||
| chr5:75705607 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(84): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.307+97T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 4/11 | chr5 | 75705607 | |||||||
| chr5:75705852 | A | G | 1 | a0003c0003t0004g0045 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.224-65T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75705852 | |||||||
| chr5:75705891 | A | G | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.224-104T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75705891 | |||||||
| chr5:75705934 | G | A | 1 | a0002c0002t0001g0222 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.224-147C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75705934 | |||||||
| chr5:75705969 | GACTT | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.224-186_224-183del others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75705969 | |||||||
| chr5:75706562 | GTTTT | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(44): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.224-779_224-776del others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706562 | |||||||
| chr5:75706565 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.224-778A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706565 | |||||||
| chr5:75706570 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.224-783A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706570 | |||||||
| chr5:75706638 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.224-851T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706638 | |||||||
| chr5:75706736 | A | C | 1 | a0002c0002t0001g0222 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.224-949T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706736 | |||||||
| chr5:75706807 | T | C | 1 | a0003c0003t0002g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.223+930A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706807 | |||||||
| chr5:75706810 | G | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(69): Show |
95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.223+927C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706810 | |||||||
| chr5:75706867 | T | C | 1 | a0003c0003t0002g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.223+870A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75706867 | |||||||
| chr5:75707018 | T | C | 2 | a0002c0002t0001g0170 a0002c0002t0001g0205 |
2 | HG00438.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.223+719A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707018 | |||||||
| chr5:75707020 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.223+717G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707020 | |||||||
| chr5:75707023 | C | T | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+714G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707023 | |||||||
| chr5:75707070 | G | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(69): Show |
95 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.223+667C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707070 | |||||||
| chr5:75707111 | T | C | 1 | a0003c0003t0002g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.223+626A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707111 | |||||||
| chr5:75707134 | T | C | 2 | a0003c0003t0002g0030 a0003c0003t0002g0031 |
4 | HG01069.hp1 HG01071.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+603A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707134 | |||||||
| chr5:75707141 | T | C | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0211 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+596A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707141 | |||||||
| chr5:75707185 | C | T | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+552G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707185 | |||||||
| chr5:75707231 | A | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(150): Show |
220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.223+506T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707231 | |||||||
| chr5:75707384 | C | CT | 3 | a0002c0002t0001g0181 a0002c0002t0001g0217 a0002c0002t0001g0246 |
3 | HG02602.hp2 HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.223+352dupA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707384 | |||||||
| chr5:75707588 | A | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.223+149T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707588 | |||||||
| chr5:75707624 | A | T | 13 | a0001c0004t0001g0027 a0001c0004t0001g0165 a0001c0004t0002g0003 others(10): Show |
22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.223+113T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707624 | |||||||
| chr5:75707626 | A | T | 13 | a0001c0004t0001g0027 a0001c0004t0001g0165 a0001c0004t0002g0003 others(10): Show |
22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.223+111T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707626 | |||||||
| chr5:75707627 | T | TC | 13 | a0001c0004t0001g0027 a0001c0004t0001g0165 a0001c0004t0002g0003 others(10): Show |
22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.223+109_223+110ins others(1): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707627 | |||||||
| chr5:75707644 | T | C | 13 | a0001c0004t0001g0027 a0001c0004t0001g0165 a0001c0004t0002g0003 others(10): Show |
22 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.223+93A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 3/11 | chr5 | 75707644 | |||||||
| chr5:75707906 | G | A | 4 | a0001c0001t0001g0087 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | NA18999.hp1 NA19059.hp2 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-31C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75707906 | |||||||
| chr5:75707964 | CCA | C | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-91_85-90delTG | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75707964 | |||||||
| chr5:75708053 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.85-178A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75708053 | |||||||
| chr5:75708282 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.85-407T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75708282 | |||||||
| chr5:75708350 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.85-475C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75708350 | |||||||
| chr5:75709154 | C | G | 1 | a0004c0005t0003g0288 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.85-1279G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709154 | |||||||
| chr5:75709270 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.85-1395C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709270 | |||||||
| chr5:75709492 | T | TA | 66 | a0003c0003t0001g0065 a0003c0003t0001g0270 a0003c0003t0001g0273 others(63): Show |
101 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.85-1618dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709492 | |||||||
| chr5:75709515 | A | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-1640T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709515 | |||||||
| chr5:75709781 | G | T | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.85-1906C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709781 | |||||||
| chr5:75709790 | T | C | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-1915A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709790 | |||||||
| chr5:75709969 | T | C | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.85-2094A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75709969 | |||||||
| chr5:75710074 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.85-2199T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710074 | |||||||
| chr5:75710288 | T | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(82): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.85-2413A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710288 | |||||||
| chr5:75710331 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.85-2456A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710331 | |||||||
| chr5:75710448 | G | A | 8 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(5): Show |
8 | HG01243.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+2406C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710448 | |||||||
| chr5:75710451 | C | A | 2 | a0003c0003t0002g0267 a0003c0003t0002g0271 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.84+2403G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710451 | |||||||
| chr5:75710558 | C | T | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+2296G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710558 | |||||||
| chr5:75710559 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.84+2295T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710559 | |||||||
| chr5:75710624 | T | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.84+2230A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710624 | |||||||
| chr5:75710824 | T | C | 1 | a0003c0003t0002g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.84+2030A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710824 | |||||||
| chr5:75710828 | C | T | 5 | a0004c0005t0003g0288 a0004c0005t0003g0290 a0004c0005t0003g0291 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+2026G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710828 | |||||||
| chr5:75710858 | T | C | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.84+1996A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710858 | |||||||
| chr5:75710986 | T | C | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.84+1868A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710986 | |||||||
| chr5:75710996 | T | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+1858A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75710996 | |||||||
| chr5:75711033 | G | A | 3 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 |
4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+1821C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711033 | |||||||
| chr5:75711119 | T | A | 1 | a0001c0001t0002g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84+1735A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711119 | |||||||
| chr5:75711581 | T | A | 33 | a0003c0003t0001g0270 a0003c0003t0001g0273 a0003c0003t0001g0274 others(30): Show |
60 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.84+1273A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711581 | |||||||
| chr5:75711632 | A | C | 34 | a0003c0003t0001g0270 a0003c0003t0001g0273 a0003c0003t0001g0274 others(31): Show |
62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.84+1222T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711632 | |||||||
| chr5:75711731 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.84+1123T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711731 | |||||||
| chr5:75711753 | A | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(52): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.84+1101T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711753 | |||||||
| chr5:75711768 | A | G | 1 | a0003c0003t0002g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.84+1086T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711768 | |||||||
| chr5:75711776 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.84+1078C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711776 | |||||||
| chr5:75711833 | A | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+1021T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711833 | |||||||
| chr5:75711896 | A | G | 1 | a0003c0003t0002g0078 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.84+958T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711896 | |||||||
| chr5:75711943 | G | A | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+911C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75711943 | |||||||
| chr5:75712033 | C | T | 2 | a0002c0002t0001g0180 a0002c0002t0001g0221 |
2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.84+821G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712033 | |||||||
| chr5:75712107 | G | A | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.84+747C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712107 | |||||||
| chr5:75712323 | A | G | 6 | a0001c0001t0001g0122 a0001c0001t0001g0139 a0001c0001t0001g0174 others(3): Show |
6 | HG01192.hp2 HG01261.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+531T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712323 | |||||||
| chr5:75712368 | T | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(87): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.84+486A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712368 | |||||||
| chr5:75712461 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.84+393A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712461 | |||||||
| chr5:75712490 | A | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+364T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712490 | |||||||
| chr5:75712556 | T | A | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.84+298A>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712556 | |||||||
| chr5:75712683 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.84+171A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712683 | |||||||
| chr5:75712684 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.84+170C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712684 | |||||||
| chr5:75712694 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.84+160A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712694 | |||||||
| chr5:75712703 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.84+151C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712703 | |||||||
| chr5:75712789 | TTTTCCCT others(8): Show |
T | 1 | a0001c0001t0001g0106 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.84+50_84+64delTGAA others(11): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712789 | |||||||
| chr5:75712851 | T | G | 1 | a0004c0005t0003g0287 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.84+3A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 2/11 | chr5 | 75712851 | |||||||
| chr5:75713133 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-14-182G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713133 | |||||||
| chr5:75713242 | C | A | 1 | a0009c0013t0002g0085 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-14-291G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713242 | |||||||
| chr5:75713255 | G | C | 1 | a0002c0002t0001g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-14-304C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713255 | |||||||
| chr5:75713259 | A | ACTTT | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-312_-14-309dup others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713259 | |||||||
| chr5:75713288 | G | C | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-337C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713288 | |||||||
| chr5:75713473 | T | C | 66 | a0003c0003t0001g0065 a0003c0003t0001g0270 a0003c0003t0001g0273 others(63): Show |
101 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-14-522A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713473 | |||||||
| chr5:75713486 | A | T | 11 | a0001c0004t0002g0003 a0001c0004t0002g0019 a0001c0004t0002g0075 others(8): Show |
19 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-535T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713486 | |||||||
| chr5:75713636 | A | T | 3 | a0002c0002t0001g0138 a0002c0002t0001g0163 a0002c0002t0001g0220 |
3 | NA18971.hp2 NA18989.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-14-685T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713636 | |||||||
| chr5:75713698 | G | A | 1 | a0003c0003t0002g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-14-747C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713698 | |||||||
| chr5:75713814 | G | A | 9 | a0004c0005t0003g0008 a0004c0005t0003g0035 a0004c0005t0003g0281 others(6): Show |
13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-863C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713814 | |||||||
| chr5:75713864 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-14-913T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713864 | |||||||
| chr5:75713866 | G | A | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG00741.hp1 HG02004.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-915C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75713866 | |||||||
| chr5:75714009 | C | G | 6 | a0001c0001t0002g0131 a0001c0001t0002g0164 a0001c0001t0002g0213 others(3): Show |
6 | HG02027.hp1 HG02056.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-1058G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714009 | |||||||
| chr5:75714087 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-14-1136T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714087 | |||||||
| chr5:75714089 | G | C | 1 | a0002c0002t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-14-1138C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714089 | |||||||
| chr5:75714177 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(158): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-14-1226A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714177 | |||||||
| chr5:75714242 | C | G | 1 | a0002c0002t0001g0177 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-14-1291G>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714242 | |||||||
| chr5:75714255 | G | T | 34 | a0003c0003t0001g0270 a0003c0003t0001g0273 a0003c0003t0001g0274 others(31): Show |
62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-14-1304C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714255 | |||||||
| chr5:75714284 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-14-1333T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714284 | |||||||
| chr5:75714285 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-14-1334C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714285 | |||||||
| chr5:75714392 | G | A | 1 | a0006c0007t0004g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-14-1441C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714392 | |||||||
| chr5:75714694 | C | T | 31 | a0003c0003t0001g0065 a0003c0003t0002g0018 a0003c0003t0002g0044 others(28): Show |
38 | HG00733.hp2 HG01123.hp2 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.-14-1743G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714694 | |||||||
| chr5:75714708 | C | T | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-1757G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714708 | |||||||
| chr5:75714727 | T | G | 1 | a0003c0003t0002g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-14-1776A>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714727 | |||||||
| chr5:75714859 | G | C | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-1908C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714859 | |||||||
| chr5:75714936 | G | A | 2 | a0001c0004t0001g0027 a0001c0004t0001g0165 |
3 | HG03490.hp2 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-14-1985C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714936 | |||||||
| chr5:75714988 | CCTGTATT others(28): Show |
C | 2 | a0001c0004t0001g0074 a0001c0004t0001g0077 |
2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-2072_-14-2038d others(37): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75714988 | |||||||
| chr5:75715028 | C | T | 3 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 |
4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-2077G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715028 | |||||||
| chr5:75715067 | CT | C | 3 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 |
4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-2117delA | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715067 | |||||||
| chr5:75715087 | A | C | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-2136T>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715087 | |||||||
| chr5:75715234 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-15+2072G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715234 | |||||||
| chr5:75715264 | C | T | 1 | a0002c0002t0001g0024 | 2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-15+2042G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715264 | |||||||
| chr5:75715301 | C | T | 73 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(70): Show |
108 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+2005G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715301 | |||||||
| chr5:75715309 | C | CA | 13 | a0001c0001t0001g0076 a0001c0001t0001g0166 a0001c0001t0001g0167 others(10): Show |
13 | HG00099.hp1 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+1996dupT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715309 | |||||||
| chr5:75715309 | C | CAA | 14 | a0001c0004t0001g0077 a0001c0004t0002g0003 a0001c0004t0002g0019 others(11): Show |
23 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-15+1995_-15+1996d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715309 | |||||||
| chr5:75715309 | C | CAAAAAA | 4 | a0004c0005t0003g0008 a0004c0005t0003g0035 a0004c0005t0003g0286 others(1): Show |
8 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+1991_-15+1996d others(8): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715309 | |||||||
| chr5:75715309 | CA | C | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0107 others(5): Show |
8 | HG01256.hp2 HG01943.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+1996delT | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715309 | |||||||
| chr5:75715476 | TGA | T | 15 | a0001c0001t0001g0076 a0001c0004t0001g0074 a0001c0004t0001g0077 others(12): Show |
23 | HG00280.hp1 HG00408.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-15+1828_-15+1829d others(4): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715476 | |||||||
| chr5:75715724 | C | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG00639.hp1 HG01109.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.-15+1582G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715724 | |||||||
| chr5:75715738 | A | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-15+1568T>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715738 | |||||||
| chr5:75715948 | G | A | 9 | a0004c0005t0003g0008 a0004c0005t0003g0035 a0004c0005t0003g0281 others(6): Show |
13 | HG00735.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+1358C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715948 | |||||||
| chr5:75715989 | G | A | 8 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 others(5): Show |
9 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+1317C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75715989 | |||||||
| chr5:75716003 | T | C | 2 | a0002c0002t0001g0172 a0002c0002t0001g0173 |
2 | HG00323.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.-15+1303A>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716003 | |||||||
| chr5:75716383 | T | TG | 56 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(53): Show |
67 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-15+922dupC | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716383 | |||||||
| chr5:75716383 | T | TGG | 34 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(31): Show |
39 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15+921_-15+922dup others(2): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716383 | |||||||
| chr5:75716383 | TG | T | 52 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0109 others(49): Show |
63 | HG00280.hp2 HG00408.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.-15+922delC | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716383 | |||||||
| chr5:75716383 | TGG | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0086 others(31): Show |
47 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.-15+921_-15+922del others(2): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716383 | |||||||
| chr5:75716383 | TGGG | T | 44 | a0001c0001t0001g0076 a0001c0001t0002g0036 a0001c0004t0001g0074 others(41): Show |
79 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-15+920_-15+922del others(3): Show |
POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716383 | |||||||
| chr5:75716384 | G | C | 9 | a0003c0003t0002g0018 a0003c0003t0002g0047 a0003c0003t0002g0048 others(6): Show |
10 | HG01516.hp2 HG02698.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+922C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716384 | |||||||
| chr5:75716385 | G | C | 19 | a0003c0003t0001g0065 a0003c0003t0002g0055 a0003c0003t0002g0056 others(16): Show |
25 | HG00733.hp2 HG01123.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.-15+921C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716385 | |||||||
| chr5:75716388 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-15+918C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716388 | |||||||
| chr5:75716392 | G | C | 1 | a0003c0003t0002g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-15+914C>G | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716392 | |||||||
| chr5:75716396 | G | T | 2 | a0002c0002t0001g0073 a0007c0008t0001g0072 |
2 | HG00642.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-15+910C>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716396 | |||||||
| chr5:75716492 | C | T | 73 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0042 others(70): Show |
108 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+814G>A | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716492 | |||||||
| chr5:75716999 | C | A | 17 | a0004c0005t0003g0008 a0004c0005t0003g0034 a0004c0005t0003g0035 others(14): Show |
22 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-15+307G>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75716999 | |||||||
| chr5:75717008 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-15+298T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75717008 | |||||||
| chr5:75717009 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-15+297C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75717009 | |||||||
| chr5:75717211 | G | A | 34 | a0003c0003t0001g0270 a0003c0003t0001g0273 a0003c0003t0001g0274 others(31): Show |
62 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-15+95C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75717211 | |||||||
| chr5:75717253 | A | G | 3 | a0004c0005t0003g0034 a0004c0005t0003g0279 a0004c0005t0003g0280 |
4 | HG01243.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+53T>C | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75717253 | |||||||
| chr5:75717290 | G | A | 1 | a0002c0002t0001g0276 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-15+16C>T | POC5 | ENSG00000152359.15 | transcript | ENST00000428202.7 | protein_coding | 1/11 | chr5 | 75717290 |