Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 283208 |
| ensemblid | ENSG00000149380.12 |
| hgncid | 30135 |
| symbol | P4HA3 |
| name | prolyl 4-hydroxylase subunit alpha 3 |
| refseq_nuc | NM_182904.5 |
| refseq_prot | NP_878907.1 |
| ensembl_nuc | ENST00000331597.9 |
| ensembl_prot | ENSP00000332170.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 74266657 |
| end | 74311640 |
| strand | - |
| ver | v1.2 |
| region | chr11:74266657-74311640 |
| region5000 | chr11:74261657-74316640 |
| regionname0 | P4HA3_chr11_74266657_74311640 |
| regionname5000 | P4HA3_chr11_74261657_74316640 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 544 | 297 | 79 | 51 | 119 | 11 | 35 | 93 | P4HA3_chr11_74261657_74316640 | P4HA3 | MGPGA others(539): Show |
chr11 | 74261657 | 74316640 |
| a0002 | 0/0 | 544 | 87 | 7 | 8 | 59 | 3 | 10 | 41 | P4HA3_chr11_74261657_74316640 | P4HA3 | MGPGA others(539): Show |
chr11 | 74261657 | 74316640 |
| a0003 | 0/0 | 544 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | MGPGA others(539): Show |
chr11 | 74261657 | 74316640 |
| a0004 | 0/0 | 544 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | MGPGA others(539): Show |
chr11 | 74261657 | 74316640 |
| a0005 | 0/0 | 544 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | P4HA3_chr11_74261657_74316640 | P4HA3 | MGPGA others(539): Show |
chr11 | 74261657 | 74316640 |
| a0006 | 0/0 | 544 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | MGPGA others(539): Show |
chr11 | 74261657 | 74316640 |
| a0007 | 0/0 | 544 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | MGPGA others(539): Show |
chr11 | 74261657 | 74316640 |
| a0008 | 0/0 | 544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | MGPGA others(539): Show |
chr11 | 74261657 | 74316640 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1632 | 294 | 77 | 50 | 119 | 11 | 35 | P4HA3_chr11_74261657_74316640 | P4HA3 | ATGGG others(1627): Show |
chr11 | 74261657 | 74316640 | ||
| a0001c0004 | 0/0 | 1632 | 2 | 2 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | ATGGG others(1627): Show |
chr11 | 74261657 | 74316640 | ||
| a0001c0007 | 0/0 | 1632 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | ATGGG others(1627): Show |
chr11 | 74261657 | 74316640 | ||
| a0002c0002 | 0/0 | 1632 | 87 | 7 | 8 | 59 | 3 | 10 | P4HA3_chr11_74261657_74316640 | P4HA3 | ATGGG others(1627): Show |
chr11 | 74261657 | 74316640 | ||
| a0003c0003 | 0/0 | 1632 | 7 | 7 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | ATGGG others(1627): Show |
chr11 | 74261657 | 74316640 | ||
| a0004c0006 | 0/0 | 1632 | 2 | 2 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | ATGGG others(1627): Show |
chr11 | 74261657 | 74316640 | ||
| a0005c0005 | 0/0 | 1632 | 2 | 0 | 0 | 2 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | ATGGG others(1627): Show |
chr11 | 74261657 | 74316640 | ||
| a0006c0010 | 0/0 | 1632 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | ATGGG others(1627): Show |
chr11 | 74261657 | 74316640 | ||
| a0007c0009 | 0/0 | 1632 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | ATGGG others(1627): Show |
chr11 | 74261657 | 74316640 | ||
| a0008c0008 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | ATGGG others(1627): Show |
chr11 | 74261657 | 74316640 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2255 | 271 | 64 | 47 | 113 | 11 | 34 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0001c0001t0002 | 0/0 | 2255 | 17 | 10 | 1 | 5 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0001c0001t0003 | 0/0 | 2255 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0001c0001t0004 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0001c0001t0005 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0001c0001t0006 | 0/0 | 2255 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0001c0001t0007 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0001c0001t0008 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0001c0004t0001 | 0/0 | 2255 | 2 | 2 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0001c0007t0001 | 0/0 | 2255 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0002c0002t0002 | 0/0 | 2255 | 87 | 7 | 8 | 59 | 3 | 10 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0003c0003t0002 | 0/0 | 2255 | 7 | 7 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0004c0006t0001 | 0/0 | 2255 | 2 | 2 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0005c0005t0001 | 0/0 | 2255 | 2 | 0 | 0 | 2 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0006c0010t0001 | 0/0 | 2255 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0007c0009t0001 | 0/0 | 2255 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| a0008c0008t0001 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | GTCTG others(2250): Show |
chr11 | 74261657 | 74316640 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 17 | 2 | 5 | 4 | 2 | 4 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0003 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0004 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0004t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0001c0007t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0001 | 0/0 | 23 | 0 | 2 | 18 | 0 | 3 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0005 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0002c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0003c0003t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0003c0003t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0003c0003t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0003c0003t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0003c0003t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0003c0003t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0004c0006t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0004c0006t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0005c0005t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0006c0010t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0007c0009t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| a0008c0008t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0106 | EUR | FIN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0107 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0122 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0246 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0074 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0104 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01433 | hp2 | a0001 | c0007 | t0001 | g0177 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0116 | EUR | IBS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0114 | EUR | IBS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02145 | hp2 | a0003 | c0003 | t0002 | g0145 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0024 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0119 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02300 | hp2 | a0006 | c0010 | t0001 | g0218 | AMR | PEL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0024 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | KHV | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02698 | hp2 | a0007 | c0009 | t0001 | g0063 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0151 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02723 | hp1 | a0003 | c0003 | t0002 | g0144 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0248 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02895 | hp2 | a0004 | c0006 | t0001 | g0238 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02896 | hp1 | a0003 | c0003 | t0002 | g0148 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02897 | hp2 | a0004 | c0006 | t0001 | g0237 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03195 | hp2 | a0003 | c0003 | t0002 | g0032 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03225 | hp2 | a0003 | c0003 | t0002 | g0147 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0128 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0108 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0103 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03540 | hp1 | a0003 | c0003 | t0002 | g0146 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0017 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0136 | SAS | BEB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | STU | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | STU | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | CHB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | CHB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18906 | hp1 | a0008 | c0008 | t0001 | g0141 | AFR | YRI | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18957 | hp1 | a0005 | c0005 | t0001 | g0026 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | LWK | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0247 | AFR | YRI | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA19240 | hp2 | a0003 | c0003 | t0002 | g0032 | AFR | YRI | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ASW | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ASW | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | GIH | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0124 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | MSL | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | USA | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18955 | hp1 | a0005 | c0005 | t0001 | g0026 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | USA | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | USA | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0045 | AFR | LWK | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0232 | REF | REF | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0208 | REF | REF | P4HA3_chr11_74261657_74316640 | P4HA3 | chr11 | 74261657 | 74316640 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74276986 | G | A | 1 | a0005 | 2 | NA18955.hp1 NA18957.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1334C>T | p.Thr445Met | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/13 | 1363/2255 | 1334/1635 | 445/544 | chr11 | 74276986 | |||
| chr11:74277065 | G | A | 1 | a0003 | 7 | HG02145.hp2 HG02723.hp1 HG02896.hp1 others(4): Show |
missense_variant | MODERATE | c.1255C>T | p.Arg419Trp | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/13 | 1284/2255 | 1255/1635 | 419/544 | chr11 | 74277065 | |||
| chr11:74277122 | C | T | 1 | a0002 | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
missense_variant | MODERATE | c.1198G>A | p.Asp400Asn | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/13 | 1227/2255 | 1198/1635 | 400/544 | chr11 | 74277122 | |||
| chr11:74279430 | G | A | 1 | a0004 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.1133C>T | p.Ser378Leu | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/13 | 1162/2255 | 1133/1635 | 378/544 | chr11 | 74279430 | |||
| chr11:74286265 | T | C | 1 | a0007 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.896A>G | p.Asp299Gly | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 6/13 | 925/2255 | 896/1635 | 299/544 | chr11 | 74286265 | |||
| chr11:74298354 | T | C | 1 | a0006 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.575A>G | p.Tyr192Cys | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/13 | 604/2255 | 575/1635 | 192/544 | chr11 | 74298354 | |||
| chr11:74302373 | C | T | 1 | a0008 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.563G>A | p.Gly188Asp | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/13 | 592/2255 | 563/1635 | 188/544 | chr11 | 74302373 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74302459 | A | G | 1 | a0001c0004 | 2 | HG02280.hp1 HG02451.hp2 |
synonymous_variant | LOW | c.477T>C | p.Phe159Phe | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/13 | 506/2255 | 477/1635 | 159/544 | chr11 | 74302459 | |||
| chr11:74302534 | C | T | 1 | a0001c0007 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.402G>A | p.Glu134Glu | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/13 | 431/2255 | 402/1635 | 134/544 | chr11 | 74302534 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74266758 | C | A | 1 | a0001c0001t0004 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*490G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 13/13 | 490 | chr11 | 74266758 | ||||||
| chr11:74266855 | C | A | 1 | a0001c0001t0005 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 13/13 | 393 | chr11 | 74266855 | ||||||
| chr11:74266916 | A | G | 1 | a0001c0001t0008 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*332T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 13/13 | 332 | chr11 | 74266916 | ||||||
| chr11:74267011 | C | A | 1 | a0001c0001t0006 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*237G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 13/13 | 237 | chr11 | 74267011 | ||||||
| chr11:74267013 | C | G | 1 | a0001c0001t0007 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*235G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 13/13 | 235 | chr11 | 74267013 | ||||||
| chr11:74267198 | G | A | 5 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(2): Show |
113 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*50C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 13/13 | 50 | chr11 | 74267198 | ||||||
| chr11:74311628 | C | T | 1 | a0001c0001t0003 | 1 | HG01952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/13 | 17 | chr11 | 74311628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74267654 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0229 others(3): Show |
9 | HG02622.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1565-336G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 12/12 | chr11 | 74267654 | |||||||
| chr11:74267655 | G | C | 1 | a0001c0001t0001g0193 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1565-337C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 12/12 | chr11 | 74267655 | |||||||
| chr11:74268046 | G | A | 2 | a0001c0001t0001g0091 a0002c0002t0002g0126 |
2 | HG02040.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1564+99C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 12/12 | chr11 | 74268046 | |||||||
| chr11:74268314 | C | G | 1 | a0006c0010t0001g0218 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1468-73G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74268314 | |||||||
| chr11:74268327 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1468-86C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74268327 | |||||||
| chr11:74268575 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1468-334A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74268575 | |||||||
| chr11:74268598 | G | A | 1 | a0001c0001t0007g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1468-357C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74268598 | |||||||
| chr11:74268601 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
5 | HG01243.hp1 HG02451.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1468-360G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74268601 | |||||||
| chr11:74268843 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1468-602G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74268843 | |||||||
| chr11:74269055 | T | A | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1467+597A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74269055 | |||||||
| chr11:74269183 | TCTC | T | 51 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0240 others(48): Show |
92 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1467+466_1467+468d others(5): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74269183 | |||||||
| chr11:74269204 | C | T | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1467+448G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74269204 | |||||||
| chr11:74269271 | G | C | 1 | a0001c0001t0001g0233 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1467+381C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74269271 | |||||||
| chr11:74269359 | G | A | 1 | a0002c0002t0002g0127 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1467+293C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74269359 | |||||||
| chr11:74269387 | G | A | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0240 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+265C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74269387 | |||||||
| chr11:74269486 | C | A | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+166G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 11/12 | chr11 | 74269486 | |||||||
| chr11:74269875 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1399-155G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74269875 | |||||||
| chr11:74269963 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1399-243T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74269963 | |||||||
| chr11:74270076 | G | C | 5 | a0001c0001t0001g0111 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1399-356C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270076 | |||||||
| chr11:74270081 | A | G | 1 | a0003c0003t0002g0147 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1399-361T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270081 | |||||||
| chr11:74270154 | C | T | 9 | a0001c0001t0001g0113 a0001c0001t0001g0171 a0001c0001t0001g0186 others(6): Show |
9 | HG02165.hp2 HG02523.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.1399-434G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270154 | |||||||
| chr11:74270171 | A | C | 1 | a0002c0002t0002g0105 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1399-451T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270171 | |||||||
| chr11:74270239 | T | C | 3 | a0002c0002t0002g0120 a0002c0002t0002g0128 a0002c0002t0002g0136 |
3 | HG02015.hp2 HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1399-519A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270239 | |||||||
| chr11:74270388 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1399-668A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270388 | |||||||
| chr11:74270401 | A | T | 2 | a0002c0002t0002g0122 a0002c0002t0002g0125 |
2 | HG00738.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1399-681T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270401 | |||||||
| chr11:74270489 | A | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-769T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270489 | |||||||
| chr11:74270490 | A | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-770T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270490 | |||||||
| chr11:74270491 | A | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-771T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270491 | |||||||
| chr11:74270493 | A | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-773T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270493 | |||||||
| chr11:74270494 | A | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-774T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270494 | |||||||
| chr11:74270495 | C | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-775G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270495 | |||||||
| chr11:74270496 | A | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-776T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270496 | |||||||
| chr11:74270497 | A | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-777T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270497 | |||||||
| chr11:74270499 | A | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-779T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270499 | |||||||
| chr11:74270500 | A | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-780T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270500 | |||||||
| chr11:74270503 | A | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-783T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270503 | |||||||
| chr11:74270504 | T | A | 2 | a0002c0002t0002g0131 a0002c0002t0002g0135 |
2 | NA18997.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1399-784A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270504 | |||||||
| chr11:74270504 | T | TTTTTTTT others(245): Show |
1 | a0001c0001t0001g0059 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1399-785_1399-784i others(254): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270504 | |||||||
| chr11:74270504 | T | TTTTTTTT others(261): Show |
1 | a0001c0001t0001g0071 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1399-785_1399-784i others(270): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270504 | |||||||
| chr11:74270504 | T | TTTTTTTT others(263): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02148.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1399-785_1399-784i others(272): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270504 | |||||||
| chr11:74270504 | T | TTTTTTTT others(265): Show |
2 | a0001c0001t0001g0073 a0001c0001t0006g0074 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1399-785_1399-784i others(274): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270504 | |||||||
| chr11:74270504 | T | TTTTTTTT others(266): Show |
1 | a0001c0001t0001g0072 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1399-785_1399-784i others(275): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270504 | |||||||
| chr11:74270504 | T | TTTTTTTT others(267): Show |
1 | a0001c0001t0001g0012 | 4 | HG02083.hp1 NA18950.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-785_1399-784i others(276): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270504 | |||||||
| chr11:74270504 | T | TTTTTTTT others(268): Show |
1 | a0001c0001t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1399-785_1399-784i others(277): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270504 | |||||||
| chr11:74270504 | T | TTTTTTTT others(269): Show |
1 | a0001c0001t0001g0070 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1399-785_1399-784i others(278): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270504 | |||||||
| chr11:74270504 | T | TTTTTTTT others(272): Show |
1 | a0001c0001t0001g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1399-785_1399-784i others(281): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270504 | |||||||
| chr11:74270507 | T | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-787A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270507 | |||||||
| chr11:74270508 | T | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-788A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270508 | |||||||
| chr11:74270511 | A | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1399-791T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270511 | |||||||
| chr11:74270599 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1399-879G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270599 | |||||||
| chr11:74270644 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0240 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-924G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270644 | |||||||
| chr11:74270808 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0240 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-1088G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74270808 | |||||||
| chr11:74271404 | C | T | 104 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0040 others(101): Show |
152 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1399-1684G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74271404 | |||||||
| chr11:74271462 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1399-1742A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74271462 | |||||||
| chr11:74271501 | T | C | 1 | a0002c0002t0002g0129 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1399-1781A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74271501 | |||||||
| chr11:74271554 | G | T | 1 | a0001c0001t0001g0022 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1399-1834C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74271554 | |||||||
| chr11:74271647 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1398+1898G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74271647 | |||||||
| chr11:74271660 | A | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(232): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.1398+1885T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74271660 | |||||||
| chr11:74271680 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | HG02717.hp1 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1398+1865G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74271680 | |||||||
| chr11:74271868 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1398+1677G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74271868 | |||||||
| chr11:74271975 | TC | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1398+1569delG | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74271975 | |||||||
| chr11:74271990 | T | A | 1 | a0001c0001t0001g0037 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1398+1555A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74271990 | |||||||
| chr11:74272024 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1398+1521C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272024 | |||||||
| chr11:74272047 | C | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1398+1498G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272047 | |||||||
| chr11:74272103 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1398+1442C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272103 | |||||||
| chr11:74272172 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1398+1373T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272172 | |||||||
| chr11:74272183 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1398+1362G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272183 | |||||||
| chr11:74272184 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1398+1361T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272184 | |||||||
| chr11:74272197 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398+1348G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272197 | |||||||
| chr11:74272219 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0021 a0001c0001t0001g0242 |
4 | HG01261.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398+1316_1398+132 others(14): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272219 | |||||||
| chr11:74272219 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0244 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1398+1314_1398+132 others(16): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272219 | |||||||
| chr11:74272219 | TAC | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(150): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1398+1324_1398+132 others(6): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272219 | |||||||
| chr11:74272279 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1398+1266G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272279 | |||||||
| chr11:74272397 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1398+1148C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272397 | |||||||
| chr11:74272409 | G | A | 48 | a0001c0001t0007g0045 a0001c0007t0001g0177 a0002c0002t0002g0001 others(45): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1398+1136C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272409 | |||||||
| chr11:74272537 | G | A | 7 | a0001c0001t0001g0043 a0001c0001t0001g0249 a0001c0001t0001g0250 others(4): Show |
8 | HG00639.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1398+1008C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272537 | |||||||
| chr11:74272682 | T | A | 1 | a0001c0001t0001g0241 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1398+863A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272682 | |||||||
| chr11:74272876 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1398+669G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272876 | |||||||
| chr11:74272988 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1398+557G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74272988 | |||||||
| chr11:74273044 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1398+501C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74273044 | |||||||
| chr11:74273123 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398+422G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74273123 | |||||||
| chr11:74273190 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1398+355C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74273190 | |||||||
| chr11:74273207 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0221 |
2 | NA18943.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1398+338A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74273207 | |||||||
| chr11:74273244 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1398+301A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74273244 | |||||||
| chr11:74273307 | T | C | 1 | a0001c0007t0001g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1398+238A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74273307 | |||||||
| chr11:74273348 | C | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
280 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.1398+197G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 10/12 | chr11 | 74273348 | |||||||
| chr11:74273680 | A | G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-73T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74273680 | |||||||
| chr11:74273740 | C | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
7 | HG01099.hp1 HG01243.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1336-133G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74273740 | |||||||
| chr11:74273781 | AT | A | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.1336-175delA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74273781 | |||||||
| chr11:74273781 | ATT | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-176_1336-175d others(4): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74273781 | |||||||
| chr11:74273820 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-213C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74273820 | |||||||
| chr11:74273826 | TCTA | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-222_1336-220d others(5): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74273826 | |||||||
| chr11:74273846 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1336-239G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74273846 | |||||||
| chr11:74273950 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-343T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74273950 | |||||||
| chr11:74274169 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-562A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274169 | |||||||
| chr11:74274170 | C | T | 11 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0224 others(8): Show |
14 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1336-563G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274170 | |||||||
| chr11:74274205 | C | T | 1 | a0002c0002t0002g0124 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1336-598G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274205 | |||||||
| chr11:74274219 | C | T | 1 | a0002c0002t0002g0130 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1336-612G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274219 | |||||||
| chr11:74274252 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1336-645C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274252 | |||||||
| chr11:74274293 | G | T | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-686C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274293 | |||||||
| chr11:74274293 | GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0190 |
2 | NA18949.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1336-700_1336-687d others(16): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274293 | |||||||
| chr11:74274304 | G | GT | 20 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0054 others(17): Show |
22 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1336-698dupA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274304 | |||||||
| chr11:74274304 | GT | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(5): Show |
10 | HG00642.hp2 HG01099.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336-698delA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274304 | |||||||
| chr11:74274343 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1336-736A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274343 | |||||||
| chr11:74274367 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-760C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274367 | |||||||
| chr11:74274415 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1336-808G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274415 | |||||||
| chr11:74274472 | A | AT | 13 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0052 others(10): Show |
15 | HG00642.hp2 HG01081.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1336-866dupA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274472 | |||||||
| chr11:74274472 | AT | A | 13 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0194 others(10): Show |
13 | HG01099.hp2 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1336-866delA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274472 | |||||||
| chr11:74274592 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG01123.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1336-985G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274592 | |||||||
| chr11:74274593 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-986T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274593 | |||||||
| chr11:74274600 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1336-993T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274600 | |||||||
| chr11:74274617 | T | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0249 a0001c0001t0001g0250 others(3): Show |
7 | HG00639.hp2 HG02630.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-1010A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274617 | |||||||
| chr11:74274728 | T | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0168 others(3): Show |
8 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1336-1121A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274728 | |||||||
| chr11:74274761 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-1154T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274761 | |||||||
| chr11:74274838 | C | A | 2 | a0003c0003t0002g0032 a0003c0003t0002g0147 |
3 | HG03195.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1336-1231G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274838 | |||||||
| chr11:74274944 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0176 |
2 | HG01070.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1336-1337G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74274944 | |||||||
| chr11:74275079 | T | C | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1336-1472A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275079 | |||||||
| chr11:74275096 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-1489C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275096 | |||||||
| chr11:74275155 | T | G | 1 | a0001c0001t0001g0195 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1336-1548A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275155 | |||||||
| chr11:74275431 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1335+1554A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275431 | |||||||
| chr11:74275466 | G | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(50): Show |
85 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.1335+1519C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275466 | |||||||
| chr11:74275519 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1335+1466A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275519 | |||||||
| chr11:74275572 | G | A | 1 | a0003c0003t0002g0032 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1335+1413C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275572 | |||||||
| chr11:74275624 | C | T | 47 | a0001c0001t0007g0045 a0002c0002t0002g0001 a0002c0002t0002g0005 others(44): Show |
88 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1335+1361G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275624 | |||||||
| chr11:74275691 | A | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1335+1294T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275691 | |||||||
| chr11:74275694 | C | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1335+1291G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275694 | |||||||
| chr11:74275764 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0220 |
2 | NA18945.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1335+1221C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275764 | |||||||
| chr11:74275799 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1335+1186A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275799 | |||||||
| chr11:74275888 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(50): Show |
85 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.1335+1097G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74275888 | |||||||
| chr11:74276043 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0065 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1335+942G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276043 | |||||||
| chr11:74276127 | G | T | 46 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0010 others(43): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1335+858C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276127 | |||||||
| chr11:74276141 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1335+844T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276141 | |||||||
| chr11:74276263 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1335+722A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276263 | |||||||
| chr11:74276343 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1335+642C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276343 | |||||||
| chr11:74276407 | A | AT | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1335+577dupA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276407 | |||||||
| chr11:74276415 | A | T | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1335+570T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276415 | |||||||
| chr11:74276523 | G | T | 1 | a0002c0002t0002g0247 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1335+462C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276523 | |||||||
| chr11:74276524 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0112 |
4 | HG02559.hp2 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335+461G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276524 | |||||||
| chr11:74276545 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0168 others(3): Show |
8 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1335+440G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276545 | |||||||
| chr11:74276634 | T | G | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335+351A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276634 | |||||||
| chr11:74276678 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1335+307G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276678 | |||||||
| chr11:74276737 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1335+248G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 9/12 | chr11 | 74276737 | |||||||
| chr11:74277365 | A | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1176-221T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74277365 | |||||||
| chr11:74277493 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1176-349G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74277493 | |||||||
| chr11:74277612 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1176-468A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74277612 | |||||||
| chr11:74277616 | G | C | 13 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0109 others(10): Show |
15 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1176-472C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74277616 | |||||||
| chr11:74277627 | C | G | 1 | a0001c0001t0001g0241 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1176-483G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74277627 | |||||||
| chr11:74277880 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1176-736A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74277880 | |||||||
| chr11:74277980 | T | A | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0240 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176-836A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74277980 | |||||||
| chr11:74278110 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1176-966T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278110 | |||||||
| chr11:74278184 | CA | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0047 |
10 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1176-1041delT | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278184 | |||||||
| chr11:74278352 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1175+1036G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278352 | |||||||
| chr11:74278353 | A | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
260 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1175+1035T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278353 | |||||||
| chr11:74278378 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1175+1010A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278378 | |||||||
| chr11:74278483 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1175+905C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278483 | |||||||
| chr11:74278591 | C | G | 1 | a0001c0001t0001g0042 | 2 | HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1175+797G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278591 | |||||||
| chr11:74278669 | A | T | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1175+719T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278669 | |||||||
| chr11:74278701 | A | T | 1 | a0001c0001t0007g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1175+687T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278701 | |||||||
| chr11:74278710 | T | C | 1 | a0002c0002t0002g0137 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175+678A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278710 | |||||||
| chr11:74278812 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+576A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278812 | |||||||
| chr11:74278866 | T | TA | 5 | a0001c0001t0001g0111 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175+521_1175+522i others(3): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278866 | |||||||
| chr11:74278986 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1175+402T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74278986 | |||||||
| chr11:74279007 | C | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+381G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74279007 | |||||||
| chr11:74279236 | C | T | 1 | a0002c0002t0002g0246 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1175+152G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74279236 | |||||||
| chr11:74279284 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1175+104A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74279284 | |||||||
| chr11:74279297 | A | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+91T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74279297 | |||||||
| chr11:74279300 | T | C | 1 | a0002c0002t0002g0094 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1175+88A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 8/12 | chr11 | 74279300 | |||||||
| chr11:74279618 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1111-166T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74279618 | |||||||
| chr11:74279654 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1111-202C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74279654 | |||||||
| chr11:74279690 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-238G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74279690 | |||||||
| chr11:74279691 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1111-239C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74279691 | |||||||
| chr11:74279759 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-307A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74279759 | |||||||
| chr11:74279827 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1111-375C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74279827 | |||||||
| chr11:74280123 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1111-671A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280123 | |||||||
| chr11:74280142 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1111-690C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280142 | |||||||
| chr11:74280153 | A | G | 1 | a0001c0007t0001g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1111-701T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280153 | |||||||
| chr11:74280217 | G | A | 1 | a0002c0002t0002g0119 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1111-765C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280217 | |||||||
| chr11:74280246 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1111-794A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280246 | |||||||
| chr11:74280323 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1111-871A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280323 | |||||||
| chr11:74280351 | G | A | 1 | a0003c0003t0002g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1111-899C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280351 | |||||||
| chr11:74280490 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-1038A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280490 | |||||||
| chr11:74280808 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1111-1356T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280808 | |||||||
| chr11:74280939 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0190 |
2 | NA18949.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1111-1487G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280939 | |||||||
| chr11:74280965 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-1513A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280965 | |||||||
| chr11:74280998 | C | T | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-1546G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74280998 | |||||||
| chr11:74281060 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1111-1608C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281060 | |||||||
| chr11:74281250 | A | G | 1 | a0001c0001t0001g0036 | 2 | NA18968.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1111-1798T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281250 | |||||||
| chr11:74281297 | A | C | 1 | a0002c0002t0002g0029 | 2 | NA18948.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1111-1845T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281297 | |||||||
| chr11:74281418 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1111-1966A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281418 | |||||||
| chr11:74281552 | T | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0168 others(3): Show |
8 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-2100A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281552 | |||||||
| chr11:74281666 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1111-2214A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281666 | |||||||
| chr11:74281730 | G | A | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-2278C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281730 | |||||||
| chr11:74281732 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-2280T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281732 | |||||||
| chr11:74281753 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
6 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-2301A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281753 | |||||||
| chr11:74281797 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-2345G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281797 | |||||||
| chr11:74281814 | T | C | 1 | a0002c0002t0002g0118 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1111-2362A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281814 | |||||||
| chr11:74281820 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0167 |
3 | HG00597.hp2 HG03831.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1111-2368G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281820 | |||||||
| chr11:74281869 | T | TATA | 10 | a0001c0001t0001g0043 a0001c0001t0001g0165 a0001c0001t0001g0167 others(7): Show |
11 | HG00639.hp2 HG02630.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1111-2420_1111-241 others(7): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281869 | |||||||
| chr11:74281869 | T | TATAATA | 6 | a0001c0001t0001g0225 a0001c0001t0002g0156 a0001c0001t0002g0157 others(3): Show |
8 | HG01099.hp2 HG02280.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-2423_1111-241 others(10): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281869 | |||||||
| chr11:74281869 | T | TATAATAA others(2): Show |
22 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0168 others(19): Show |
24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1111-2426_1111-241 others(13): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281869 | |||||||
| chr11:74281869 | T | TATAATAA others(5): Show |
35 | a0001c0001t0001g0226 a0001c0001t0001g0236 a0001c0001t0002g0101 others(32): Show |
58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1111-2429_1111-241 others(16): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281869 | |||||||
| chr11:74281869 | T | TATAATAA others(8): Show |
21 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0241 others(18): Show |
38 | HG00597.hp1 HG00733.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1111-2432_1111-241 others(19): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281869 | |||||||
| chr11:74281869 | T | TATAATAA others(11): Show |
3 | a0001c0001t0001g0240 a0001c0001t0007g0045 a0002c0002t0002g0121 |
3 | HG00558.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1111-2435_1111-241 others(22): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281869 | |||||||
| chr11:74281869 | TATA | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(71): Show |
118 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1111-2420_1111-241 others(7): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281869 | |||||||
| chr11:74281925 | AT | A | 48 | a0001c0001t0001g0230 a0001c0001t0007g0045 a0002c0002t0002g0001 others(45): Show |
89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1111-2474delA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281925 | |||||||
| chr11:74281926 | T | A | 63 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(60): Show |
74 | HG00639.hp2 HG00642.hp2 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.1111-2474A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74281926 | |||||||
| chr11:74282095 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-2643G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282095 | |||||||
| chr11:74282130 | T | TA | 56 | a0001c0001t0001g0047 a0001c0001t0001g0055 a0001c0001t0001g0072 others(53): Show |
97 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1111-2679dupT | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282130 | |||||||
| chr11:74282143 | C | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01099.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1111-2691G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282143 | |||||||
| chr11:74282160 | G | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0046 others(1): Show |
11 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111-2708C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282160 | |||||||
| chr11:74282187 | T | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
260 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1111-2735A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282187 | |||||||
| chr11:74282292 | T | A | 1 | a0001c0001t0001g0250 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111-2840A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282292 | |||||||
| chr11:74282534 | G | A | 47 | a0001c0001t0007g0045 a0002c0002t0002g0001 a0002c0002t0002g0005 others(44): Show |
88 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1111-3082C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282534 | |||||||
| chr11:74282538 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-3086C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282538 | |||||||
| chr11:74282595 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-3143T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282595 | |||||||
| chr11:74282611 | G | A | 109 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0031 others(106): Show |
159 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1111-3159C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282611 | |||||||
| chr11:74282612 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-3160A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282612 | |||||||
| chr11:74282640 | T | TAC | 5 | a0001c0001t0001g0111 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+3168_1110+316 others(6): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282640 | |||||||
| chr11:74282895 | TG | T | 6 | a0002c0002t0002g0103 a0002c0002t0002g0104 a0002c0002t0002g0105 others(3): Show |
6 | HG00280.hp1 HG00733.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+2913delC | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282895 | |||||||
| chr11:74282898 | A | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
9 | HG00597.hp2 HG02040.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1110+2911T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282898 | |||||||
| chr11:74282942 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
392 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.1110+2867C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74282942 | |||||||
| chr11:74283093 | A | G | 46 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0010 others(43): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1110+2716T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283093 | |||||||
| chr11:74283177 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+2632T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283177 | |||||||
| chr11:74283205 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1110+2604A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283205 | |||||||
| chr11:74283240 | A | T | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1110+2569T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283240 | |||||||
| chr11:74283276 | G | A | 4 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0073 others(1): Show |
4 | HG01074.hp2 HG01515.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+2533C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283276 | |||||||
| chr11:74283283 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1110+2526A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283283 | |||||||
| chr11:74283498 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1110+2311G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283498 | |||||||
| chr11:74283589 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+2220G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283589 | |||||||
| chr11:74283590 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1110+2219C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283590 | |||||||
| chr11:74283892 | ACT | A | 46 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0010 others(43): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1110+1915_1110+191 others(6): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283892 | |||||||
| chr11:74283923 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1110+1886T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74283923 | |||||||
| chr11:74284060 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1110+1749G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284060 | |||||||
| chr11:74284165 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1110+1644A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284165 | |||||||
| chr11:74284191 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1110+1618A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284191 | |||||||
| chr11:74284231 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1110+1578G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284231 | |||||||
| chr11:74284281 | G | T | 1 | a0001c0001t0001g0241 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1110+1528C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284281 | |||||||
| chr11:74284313 | C | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+1496G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284313 | |||||||
| chr11:74284432 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1110+1377C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284432 | |||||||
| chr11:74284437 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0046 others(1): Show |
11 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1372A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284437 | |||||||
| chr11:74284520 | T | C | 1 | a0002c0002t0002g0010 | 5 | HG02258.hp2 HG02486.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+1289A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284520 | |||||||
| chr11:74284582 | A | C | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1110+1227T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284582 | |||||||
| chr11:74284651 | G | A | 34 | a0001c0001t0001g0021 a0001c0001t0001g0111 a0001c0001t0001g0167 others(31): Show |
38 | HG00642.hp2 HG01099.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.1110+1158C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284651 | |||||||
| chr11:74284664 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1110+1145C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284664 | |||||||
| chr11:74284734 | G | A | 17 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0050 others(14): Show |
20 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1110+1075C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74284734 | |||||||
| chr11:74285354 | G | A | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1110+455C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74285354 | |||||||
| chr11:74285464 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1110+345C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74285464 | |||||||
| chr11:74285570 | G | A | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0240 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+239C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74285570 | |||||||
| chr11:74285589 | G | A | 10 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(7): Show |
10 | HG01099.hp2 HG02280.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+220C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74285589 | |||||||
| chr11:74285629 | T | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1110+180A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74285629 | |||||||
| chr11:74285633 | G | T | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1110+176C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74285633 | |||||||
| chr11:74285689 | ATTCTGAA others(5): Show |
A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0202 a0001c0001t0001g0221 others(1): Show |
4 | NA18943.hp2 NA18964.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+108_1110+119d others(14): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 7/12 | chr11 | 74285689 | |||||||
| chr11:74286193 | C | T | 10 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(7): Show |
10 | HG01099.hp2 HG02280.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.933+35G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 6/12 | chr11 | 74286193 | |||||||
| chr11:74286773 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.770-382G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74286773 | |||||||
| chr11:74286967 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
6 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-576A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74286967 | |||||||
| chr11:74287027 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.770-636G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74287027 | |||||||
| chr11:74287200 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.770-809T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74287200 | |||||||
| chr11:74287348 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.770-957T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74287348 | |||||||
| chr11:74287371 | A | G | 1 | a0002c0002t0002g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.770-980T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74287371 | |||||||
| chr11:74287409 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.770-1018C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74287409 | |||||||
| chr11:74287420 | T | C | 1 | a0003c0003t0002g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.770-1029A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74287420 | |||||||
| chr11:74287432 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.770-1041G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74287432 | |||||||
| chr11:74287437 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0168 others(1): Show |
6 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-1046G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74287437 | |||||||
| chr11:74287467 | A | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0023 others(6): Show |
18 | HG00642.hp2 HG01106.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.770-1076T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74287467 | |||||||
| chr11:74287476 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.770-1085A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74287476 | |||||||
| chr11:74288114 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0023 others(6): Show |
18 | HG00642.hp2 HG01106.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.769+965A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288114 | |||||||
| chr11:74288157 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.769+922C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288157 | |||||||
| chr11:74288228 | G | T | 1 | a0001c0001t0002g0156 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.769+851C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288228 | |||||||
| chr11:74288246 | G | C | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.769+833C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288246 | |||||||
| chr11:74288247 | G | C | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.769+832C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288247 | |||||||
| chr11:74288252 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.769+827C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288252 | |||||||
| chr11:74288365 | G | C | 1 | a0001c0001t0001g0037 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.769+714C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288365 | |||||||
| chr11:74288408 | C | A | 1 | a0001c0001t0003g0044 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.769+671G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288408 | |||||||
| chr11:74288514 | T | C | 1 | a0002c0002t0002g0102 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.769+565A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288514 | |||||||
| chr11:74288527 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.769+552T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288527 | |||||||
| chr11:74288822 | G | A | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.769+257C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288822 | |||||||
| chr11:74288848 | C | T | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+231G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288848 | |||||||
| chr11:74288948 | C | CA | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(116): Show |
212 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.769+130dupT | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288948 | |||||||
| chr11:74288948 | C | CAA | 7 | a0001c0001t0001g0182 a0001c0001t0001g0204 a0001c0001t0001g0215 others(4): Show |
8 | HG00423.hp2 HG01978.hp2 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.769+129_769+130dup others(2): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288948 | |||||||
| chr11:74288948 | CA | C | 35 | a0001c0001t0001g0043 a0001c0001t0001g0111 a0001c0001t0001g0112 others(32): Show |
38 | HG00639.hp2 HG01099.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.769+130delT | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288948 | |||||||
| chr11:74288948 | CAA | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+129_769+130del others(2): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74288948 | |||||||
| chr11:74289024 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.769+55C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 5/12 | chr11 | 74289024 | |||||||
| chr11:74289135 | T | TAA | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.718-7_718-6dupTT | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289135 | |||||||
| chr11:74289195 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.718-65G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289195 | |||||||
| chr11:74289204 | T | TA | 194 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(191): Show |
306 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.718-75dupT | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289204 | |||||||
| chr11:74289359 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-229C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289359 | |||||||
| chr11:74289379 | T | C | 22 | a0001c0001t0002g0033 a0001c0001t0002g0100 a0001c0001t0002g0101 others(19): Show |
24 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.718-249A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289379 | |||||||
| chr11:74289441 | C | T | 34 | a0001c0001t0001g0021 a0001c0001t0001g0111 a0001c0001t0001g0167 others(31): Show |
38 | HG00642.hp2 HG01099.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.718-311G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289441 | |||||||
| chr11:74289536 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.718-406G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289536 | |||||||
| chr11:74289552 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-422C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289552 | |||||||
| chr11:74289734 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-604G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289734 | |||||||
| chr11:74289802 | T | A | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.718-672A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289802 | |||||||
| chr11:74289842 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-712C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289842 | |||||||
| chr11:74289869 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.718-739C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74289869 | |||||||
| chr11:74290092 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-962G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290092 | |||||||
| chr11:74290120 | T | C | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-990A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290120 | |||||||
| chr11:74290129 | C | T | 2 | a0002c0002t0002g0103 a0002c0002t0002g0108 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.718-999G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290129 | |||||||
| chr11:74290130 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.718-1000C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290130 | |||||||
| chr11:74290264 | A | G | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-1134T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290264 | |||||||
| chr11:74290266 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.718-1136G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290266 | |||||||
| chr11:74290286 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.718-1156C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290286 | |||||||
| chr11:74290335 | T | C | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.718-1205A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290335 | |||||||
| chr11:74290355 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-1225C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290355 | |||||||
| chr11:74290369 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-1239C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290369 | |||||||
| chr11:74290390 | A | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
7 | HG01099.hp1 HG01243.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-1260T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290390 | |||||||
| chr11:74290395 | G | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0162 others(9): Show |
15 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-1265C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290395 | |||||||
| chr11:74290472 | T | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.718-1342A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290472 | |||||||
| chr11:74290488 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0047 |
10 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.718-1358G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290488 | |||||||
| chr11:74290507 | T | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-1377A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290507 | |||||||
| chr11:74290569 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
96 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.718-1439G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290569 | |||||||
| chr11:74290570 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.718-1440C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290570 | |||||||
| chr11:74290662 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.718-1532A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290662 | |||||||
| chr11:74290746 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.718-1616C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290746 | |||||||
| chr11:74290763 | G | A | 4 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0073 others(1): Show |
4 | HG01074.hp2 HG01515.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-1633C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290763 | |||||||
| chr11:74290844 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(50): Show |
85 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.718-1714C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290844 | |||||||
| chr11:74290895 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
7 | HG01099.hp1 HG01243.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-1765A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290895 | |||||||
| chr11:74290947 | T | A | 1 | a0002c0002t0002g0107 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.718-1817A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290947 | |||||||
| chr11:74290959 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.718-1829A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290959 | |||||||
| chr11:74290979 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.718-1849T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74290979 | |||||||
| chr11:74291033 | G | A | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0240 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-1903C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291033 | |||||||
| chr11:74291069 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.718-1939T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291069 | |||||||
| chr11:74291092 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.718-1962G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291092 | |||||||
| chr11:74291119 | C | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-1989G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291119 | |||||||
| chr11:74291159 | C | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0143 |
3 | HG01243.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.718-2029G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291159 | |||||||
| chr11:74291257 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.718-2127C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291257 | |||||||
| chr11:74291258 | G | C | 1 | a0001c0001t0001g0023 | 2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.718-2128C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291258 | |||||||
| chr11:74291456 | G | A | 3 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0008g0151 |
3 | HG02717.hp2 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.718-2326C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291456 | |||||||
| chr11:74291493 | G | A | 21 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(18): Show |
23 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.718-2363C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291493 | |||||||
| chr11:74291621 | C | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
7 | HG01099.hp1 HG01243.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-2491G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291621 | |||||||
| chr11:74291658 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.718-2528A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291658 | |||||||
| chr11:74291705 | T | A | 1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.718-2575A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291705 | |||||||
| chr11:74291706 | G | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0249 a0001c0001t0001g0250 others(4): Show |
8 | HG00639.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-2576C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291706 | |||||||
| chr11:74291762 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.718-2632A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291762 | |||||||
| chr11:74291797 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.718-2667T>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291797 | |||||||
| chr11:74291802 | G | A | 168 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.718-2672C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291802 | |||||||
| chr11:74291835 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.718-2705C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291835 | |||||||
| chr11:74291840 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-2710C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291840 | |||||||
| chr11:74291993 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-2863A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74291993 | |||||||
| chr11:74292082 | T | G | 1 | a0001c0001t0001g0217 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.718-2952A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292082 | |||||||
| chr11:74292209 | C | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
6 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.718-3079G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292209 | |||||||
| chr11:74292217 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.718-3087C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292217 | |||||||
| chr11:74292282 | G | A | 13 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(10): Show |
15 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-3152C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292282 | |||||||
| chr11:74292292 | T | A | 1 | a0001c0001t0001g0019 | 3 | HG01515.hp1 HG01517.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.718-3162A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292292 | |||||||
| chr11:74292502 | T | A | 1 | a0001c0001t0001g0206 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.718-3372A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292502 | |||||||
| chr11:74292623 | C | T | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-3493G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292623 | |||||||
| chr11:74292658 | T | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0249 a0001c0001t0001g0250 others(4): Show |
8 | HG00639.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-3528A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292658 | |||||||
| chr11:74292723 | C | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-3593G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292723 | |||||||
| chr11:74292751 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02148.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.718-3621G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292751 | |||||||
| chr11:74292791 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-3661G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74292791 | |||||||
| chr11:74293163 | G | C | 1 | a0001c0001t0001g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.718-4033C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293163 | |||||||
| chr11:74293241 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.718-4111G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293241 | |||||||
| chr11:74293241 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-4111G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293241 | |||||||
| chr11:74293256 | C | T | 13 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0109 others(10): Show |
15 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-4126G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293256 | |||||||
| chr11:74293336 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.718-4206C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293336 | |||||||
| chr11:74293447 | T | C | 1 | a0002c0002t0002g0132 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.718-4317A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293447 | |||||||
| chr11:74293502 | G | C | 21 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(18): Show |
23 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.718-4372C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293502 | |||||||
| chr11:74293552 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.718-4422A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293552 | |||||||
| chr11:74293601 | T | G | 1 | a0002c0002t0002g0133 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.718-4471A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293601 | |||||||
| chr11:74293658 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-4528G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293658 | |||||||
| chr11:74293926 | T | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0067 others(8): Show |
14 | HG01074.hp2 HG01515.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.717+4286A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293926 | |||||||
| chr11:74293935 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.717+4277A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293935 | |||||||
| chr11:74293959 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+4253G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74293959 | |||||||
| chr11:74294045 | C | T | 6 | a0001c0001t0001g0111 a0001c0001t0001g0167 a0001c0001t0001g0234 others(3): Show |
6 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+4167G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294045 | |||||||
| chr11:74294198 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+4014G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294198 | |||||||
| chr11:74294199 | G | A | 1 | a0001c0004t0001g0024 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.717+4013C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294199 | |||||||
| chr11:74294229 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.717+3983A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294229 | |||||||
| chr11:74294359 | T | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+3853A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294359 | |||||||
| chr11:74294409 | G | A | 1 | a0002c0002t0002g0107 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.717+3803C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294409 | |||||||
| chr11:74294466 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0249 a0001c0001t0001g0250 others(3): Show |
7 | HG00639.hp2 HG02630.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+3746G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294466 | |||||||
| chr11:74294479 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.717+3733C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294479 | |||||||
| chr11:74294493 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+3719C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294493 | |||||||
| chr11:74294623 | G | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0162 others(9): Show |
15 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.717+3589C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294623 | |||||||
| chr11:74294671 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.717+3541G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294671 | |||||||
| chr11:74294858 | C | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+3354G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294858 | |||||||
| chr11:74294858 | C | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(225): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.717+3354G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294858 | |||||||
| chr11:74294997 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
6 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+3215C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74294997 | |||||||
| chr11:74295039 | T | C | 2 | a0002c0002t0002g0018 a0002c0002t0002g0134 |
4 | HG02056.hp1 HG02523.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+3173A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74295039 | |||||||
| chr11:74295109 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
9 | HG00642.hp2 HG01261.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.717+3103G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74295109 | |||||||
| chr11:74295228 | G | A | 14 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0109 others(11): Show |
16 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.717+2984C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74295228 | |||||||
| chr11:74295314 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.717+2898G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74295314 | |||||||
| chr11:74295445 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.717+2767A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74295445 | |||||||
| chr11:74295504 | G | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+2708C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74295504 | |||||||
| chr11:74295880 | C | T | 46 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0010 others(43): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.717+2332G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74295880 | |||||||
| chr11:74295914 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
6 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+2298A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74295914 | |||||||
| chr11:74296012 | T | C | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.717+2200A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296012 | |||||||
| chr11:74296090 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.717+2122A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296090 | |||||||
| chr11:74296146 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.717+2066A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296146 | |||||||
| chr11:74296366 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.717+1846A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296366 | |||||||
| chr11:74296470 | C | T | 28 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(25): Show |
32 | HG00642.hp2 HG01099.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.717+1742G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296470 | |||||||
| chr11:74296680 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.717+1532A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296680 | |||||||
| chr11:74296729 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.717+1483T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296729 | |||||||
| chr11:74296788 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1424A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296788 | |||||||
| chr11:74296789 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1423C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296789 | |||||||
| chr11:74296837 | C | T | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.717+1375G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296837 | |||||||
| chr11:74296915 | G | GT | 2 | a0001c0001t0001g0007 a0001c0001t0001g0182 |
6 | HG00733.hp2 HG02015.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+1296dupA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296915 | |||||||
| chr11:74296934 | C | CT | 60 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(57): Show |
93 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.717+1277dupA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296934 | |||||||
| chr11:74296934 | C | CTT | 16 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0050 others(13): Show |
19 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.717+1276_717+1277d others(4): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296934 | |||||||
| chr11:74296964 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1248T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296964 | |||||||
| chr11:74296990 | A | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
260 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.717+1222T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74296990 | |||||||
| chr11:74297017 | C | T | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.717+1195G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74297017 | |||||||
| chr11:74297145 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.717+1067C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74297145 | |||||||
| chr11:74297340 | C | A | 1 | a0001c0001t0008g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.717+872G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74297340 | |||||||
| chr11:74297365 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+847A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74297365 | |||||||
| chr11:74297504 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG01123.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.717+708A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74297504 | |||||||
| chr11:74297510 | A | G | 13 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0109 others(10): Show |
15 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.717+702T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74297510 | |||||||
| chr11:74297818 | T | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.717+394A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74297818 | |||||||
| chr11:74297862 | T | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.717+350A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 4/12 | chr11 | 74297862 | |||||||
| chr11:74298650 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.568-289A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74298650 | |||||||
| chr11:74298760 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.568-399G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74298760 | |||||||
| chr11:74298891 | G | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0168 others(3): Show |
8 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.568-530C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74298891 | |||||||
| chr11:74298912 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.568-551G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74298912 | |||||||
| chr11:74298924 | T | C | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.568-563A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74298924 | |||||||
| chr11:74298969 | G | C | 5 | a0003c0003t0002g0032 a0003c0003t0002g0145 a0003c0003t0002g0146 others(2): Show |
6 | HG02145.hp2 HG02896.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-608C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74298969 | |||||||
| chr11:74298999 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
6 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-638A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74298999 | |||||||
| chr11:74299137 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0166 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.568-776C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299137 | |||||||
| chr11:74299284 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.568-923A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299284 | |||||||
| chr11:74299440 | C | T | 1 | a0002c0002t0002g0118 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.568-1079G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299440 | |||||||
| chr11:74299620 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.568-1259C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299620 | |||||||
| chr11:74299660 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.568-1299A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299660 | |||||||
| chr11:74299667 | G | GA | 28 | a0001c0001t0001g0079 a0001c0001t0001g0113 a0001c0001t0001g0162 others(25): Show |
29 | HG01099.hp2 HG02145.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.568-1307dupT | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299667 | |||||||
| chr11:74299667 | GA | G | 75 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0020 others(72): Show |
125 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.568-1307delT | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299667 | |||||||
| chr11:74299667 | GAA | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(3): Show |
8 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.568-1308_568-1307d others(4): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299667 | |||||||
| chr11:74299668 | A | G | 1 | a0002c0002t0002g0136 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.568-1307T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299668 | |||||||
| chr11:74299684 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.568-1323G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299684 | |||||||
| chr11:74299687 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.568-1326G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299687 | |||||||
| chr11:74299758 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.568-1397A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299758 | |||||||
| chr11:74299886 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.568-1525A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299886 | |||||||
| chr11:74299895 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.568-1534G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74299895 | |||||||
| chr11:74300112 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.568-1751A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74300112 | |||||||
| chr11:74300201 | C | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.568-1840G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74300201 | |||||||
| chr11:74300433 | C | T | 5 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
5 | HG01361.hp1 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.567+1936G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74300433 | |||||||
| chr11:74300650 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.567+1719A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74300650 | |||||||
| chr11:74300697 | A | G | 4 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(1): Show |
5 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.567+1672T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74300697 | |||||||
| chr11:74300765 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.567+1604G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74300765 | |||||||
| chr11:74300908 | T | C | 72 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
115 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.567+1461A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74300908 | |||||||
| chr11:74301093 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.567+1276G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74301093 | |||||||
| chr11:74301293 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0096 others(2): Show |
23 | HG00733.hp2 HG02015.hp1 HG02165.hp1 others(20): Show |
intron_variant | MODIFIER | c.567+1076T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74301293 | |||||||
| chr11:74301403 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.567+966G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74301403 | |||||||
| chr11:74301562 | C | A | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.567+807G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74301562 | |||||||
| chr11:74301758 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.567+611G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74301758 | |||||||
| chr11:74302152 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.567+217G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74302152 | |||||||
| chr11:74302260 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.567+109A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 3/12 | chr11 | 74302260 | |||||||
| chr11:74302813 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.344-221G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74302813 | |||||||
| chr11:74303101 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.344-509C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303101 | |||||||
| chr11:74303292 | C | CT | 17 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0080 others(14): Show |
20 | HG01070.hp2 HG01255.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.344-701dupA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303292 | |||||||
| chr11:74303292 | C | CTT | 58 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(55): Show |
99 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.344-702_344-701dup others(2): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303292 | |||||||
| chr11:74303292 | CT | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0223 a0001c0001t0001g0239 others(8): Show |
13 | HG00642.hp2 HG01261.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.344-701delA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303292 | |||||||
| chr11:74303296 | T | C | 5 | a0001c0001t0001g0111 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.344-704A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303296 | |||||||
| chr11:74303376 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.344-784G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303376 | |||||||
| chr11:74303423 | T | G | 7 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(4): Show |
8 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.344-831A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303423 | |||||||
| chr11:74303435 | C | T | 6 | a0001c0001t0001g0111 a0001c0001t0001g0167 a0001c0001t0001g0234 others(3): Show |
6 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.343+835G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303435 | |||||||
| chr11:74303585 | C | CT | 59 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
100 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.343+684dupA | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303585 | |||||||
| chr11:74303613 | C | G | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.343+657G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303613 | |||||||
| chr11:74303658 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.343+612A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303658 | |||||||
| chr11:74303883 | G | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0224 others(8): Show |
14 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.343+387C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303883 | |||||||
| chr11:74303900 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.343+370T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74303900 | |||||||
| chr11:74304164 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.343+106G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74304164 | |||||||
| chr11:74304236 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0231 |
3 | HG00735.hp1 HG01175.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.343+34A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 2/12 | chr11 | 74304236 | |||||||
| chr11:74304549 | A | G | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-137T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74304549 | |||||||
| chr11:74304554 | G | C | 46 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0010 others(43): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.201-142C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74304554 | |||||||
| chr11:74304649 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0240 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-237G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74304649 | |||||||
| chr11:74304948 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.201-536G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74304948 | |||||||
| chr11:74304963 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0240 others(1): Show |
4 | HG02572.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-551G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74304963 | |||||||
| chr11:74305027 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.201-615C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74305027 | |||||||
| chr11:74305102 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.201-690G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74305102 | |||||||
| chr11:74305114 | G | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.201-702C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74305114 | |||||||
| chr11:74305356 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.201-944A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74305356 | |||||||
| chr11:74305584 | C | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0047 |
10 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.201-1172G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74305584 | |||||||
| chr11:74305664 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.201-1252T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74305664 | |||||||
| chr11:74305895 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.201-1483T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74305895 | |||||||
| chr11:74305942 | C | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0046 others(1): Show |
11 | HG01106.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.201-1530G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74305942 | |||||||
| chr11:74306004 | A | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01099.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.201-1592T>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306004 | |||||||
| chr11:74306227 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.201-1815A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306227 | |||||||
| chr11:74306274 | C | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(50): Show |
85 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.201-1862G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306274 | |||||||
| chr11:74306536 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.201-2124T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306536 | |||||||
| chr11:74306558 | T | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG01884.hp2 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.201-2146A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306558 | |||||||
| chr11:74306609 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(3): Show |
8 | HG00642.hp2 HG01261.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-2197G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306609 | |||||||
| chr11:74306634 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(3): Show |
8 | HG00642.hp2 HG01261.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-2222T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306634 | |||||||
| chr11:74306795 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(3): Show |
8 | HG00642.hp2 HG01261.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-2383T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306795 | |||||||
| chr11:74306871 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.201-2459G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306871 | |||||||
| chr11:74306920 | C | T | 6 | a0002c0002t0002g0103 a0002c0002t0002g0104 a0002c0002t0002g0105 others(3): Show |
6 | HG00280.hp1 HG00733.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.201-2508G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306920 | |||||||
| chr11:74306931 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.201-2519C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306931 | |||||||
| chr11:74306973 | G | A | 29 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(26): Show |
33 | HG00642.hp2 HG01099.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.201-2561C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74306973 | |||||||
| chr11:74307164 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
5 | HG01243.hp1 HG02451.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.201-2752C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74307164 | |||||||
| chr11:74307221 | T | G | 23 | a0001c0001t0002g0033 a0001c0001t0002g0099 a0001c0001t0002g0100 others(20): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.201-2809A>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74307221 | |||||||
| chr11:74307277 | C | A | 10 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(7): Show |
10 | HG01099.hp2 HG02280.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.201-2865G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74307277 | |||||||
| chr11:74307374 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.201-2962G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74307374 | |||||||
| chr11:74307703 | G | A | 5 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
5 | HG01361.hp1 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-3291C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74307703 | |||||||
| chr11:74308129 | G | T | 1 | a0002c0002t0002g0102 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.200+3283C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74308129 | |||||||
| chr11:74308252 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.200+3160G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74308252 | |||||||
| chr11:74308608 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
96 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.200+2804G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74308608 | |||||||
| chr11:74308649 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.200+2763G>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74308649 | |||||||
| chr11:74308682 | TG | T | 3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG02257.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.200+2729delC | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74308682 | |||||||
| chr11:74308758 | T | TTAAAA | 8 | a0001c0001t0001g0021 a0001c0001t0001g0239 a0001c0001t0001g0242 others(5): Show |
10 | HG00642.hp2 HG01261.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.200+2649_200+2653d others(7): Show |
P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74308758 | |||||||
| chr11:74308875 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.200+2537G>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74308875 | |||||||
| chr11:74309149 | G | T | 3 | a0002c0002t0002g0246 a0002c0002t0002g0247 a0002c0002t0002g0248 |
3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.200+2263C>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74309149 | |||||||
| chr11:74309491 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.200+1921C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74309491 | |||||||
| chr11:74309500 | T | A | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.200+1912A>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74309500 | |||||||
| chr11:74309606 | G | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0096 others(2): Show |
23 | HG00733.hp2 HG02015.hp1 HG02165.hp1 others(20): Show |
intron_variant | MODIFIER | c.200+1806C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74309606 | |||||||
| chr11:74310004 | T | C | 1 | a0002c0002t0002g0163 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.200+1408A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74310004 | |||||||
| chr11:74310525 | G | A | 11 | a0001c0001t0001g0043 a0001c0001t0001g0249 a0001c0001t0001g0250 others(8): Show |
16 | HG00639.hp2 HG01074.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.200+887C>T | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74310525 | |||||||
| chr11:74310559 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0164 |
6 | HG02083.hp2 HG04184.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.200+853T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74310559 | |||||||
| chr11:74310601 | G | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0242 a0001c0001t0001g0243 others(2): Show |
7 | HG00642.hp2 HG01261.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.200+811C>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74310601 | |||||||
| chr11:74310666 | T | C | 11 | a0001c0001t0001g0043 a0001c0001t0001g0249 a0001c0001t0001g0250 others(8): Show |
16 | HG00639.hp2 HG01074.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.200+746A>G | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74310666 | |||||||
| chr11:74311118 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(139): Show |
225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.200+294T>C | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74311118 | |||||||
| chr11:74311384 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(64): Show |
108 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.200+28G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74311384 | |||||||
| chr11:74311411 | C | T | 1 | a0001c0001t0007g0045 | 1 | NA21309.hp1 | splice_donor_variant&intron_variant | HIGH | c.200+1G>A | P4HA3 | ENSG00000149380.12 | transcript | ENST00000331597.9 | protein_coding | 1/12 | chr11 | 74311411 |