Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80012 |
| ensemblid | ENSG00000173889.16 |
| hgncid | 15682 |
| symbol | PHC3 |
| name | polyhomeotic homolog 3 |
| refseq_nuc | NM_024947.4 |
| refseq_prot | NP_079223.3 |
| ensembl_nuc | ENST00000495893.7 |
| ensembl_prot | ENSP00000420294.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 170087584 |
| end | 170181733 |
| strand | - |
| ver | v1.2 |
| region | chr3:170087584-170181733 |
| region5000 | chr3:170082584-170186733 |
| regionname0 | PHC3_chr3_170087584_170181733 |
| regionname5000 | PHC3_chr3_170082584_170186733 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 995 | 319 | 71 | 63 | 147 | 14 | 22 | 106 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| a0002 | 0/0 | 995 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| a0003 | 0/0 | 995 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| a0004 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| a0005 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| a0006 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| a0007 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| a0008 | 0/0 | 995 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| a0009 | 0/0 | 995 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| a0010 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| a0011 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | MAEAE others(990): Show |
chr3 | 170082584 | 170186733 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2985 | 296 | 67 | 63 | 129 | 14 | 21 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0001c0002 | 0/0 | 2985 | 18 | 0 | 0 | 17 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0001c0003 | 0/0 | 2985 | 4 | 4 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0001c0013 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0002c0004 | 0/0 | 2985 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0003c0005 | 0/0 | 2985 | 2 | 1 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0004c0014 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0005c0010 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0006c0008 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0007c0007 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0008c0011 | 0/0 | 2985 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0009c0009 | 0/0 | 2985 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0010c0006 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 | ||
| a0011c0012 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | ATGGC others(2980): Show |
chr3 | 170082584 | 170186733 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 12652 | 71 | 4 | 17 | 40 | 6 | 4 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0002 | 0/0 | 12652 | 54 | 1 | 8 | 33 | 5 | 7 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0003 | 1/0 | 12652 | 39 | 16 | 8 | 11 | 1 | 2 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0004 | 0/1 | 12651 | 32 | 3 | 5 | 23 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12646): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0006 | 0/0 | 12652 | 7 | 7 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0007 | 0/0 | 12651 | 10 | 1 | 7 | 2 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12646): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0008 | 0/0 | 12652 | 9 | 1 | 3 | 0 | 1 | 4 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0009 | 0/0 | 12652 | 8 | 8 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0010 | 0/0 | 12652 | 6 | 2 | 1 | 2 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0011 | 0/0 | 12652 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0012 | 0/0 | 12652 | 5 | 0 | 0 | 5 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0013 | 0/0 | 12652 | 4 | 2 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0014 | 0/0 | 12651 | 4 | 3 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12646): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0015 | 0/0 | 12649 | 3 | 0 | 3 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12644): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0016 | 0/0 | 12650 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12645): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0017 | 0/0 | 12651 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12646): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0018 | 0/0 | 12651 | 2 | 2 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12646): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0019 | 0/0 | 12652 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0020 | 0/0 | 12652 | 2 | 0 | 0 | 0 | 0 | 2 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0021 | 0/0 | 12652 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0022 | 0/0 | 12652 | 2 | 1 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0024 | 0/0 | 12652 | 2 | 0 | 0 | 2 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0028 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0029 | 0/0 | 12652 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0030 | 0/0 | 12652 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0031 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0032 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0033 | 0/0 | 12652 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0034 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0035 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0036 | 0/0 | 12652 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0037 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0038 | 0/0 | 12652 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0039 | 0/0 | 12652 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0040 | 0/0 | 12652 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0042 | 0/0 | 12652 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0043 | 0/0 | 12652 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0044 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0045 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0046 | 0/0 | 12652 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0047 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0048 | 0/0 | 12652 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0049 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0050 | 0/0 | 12652 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0001t0051 | 0/0 | 12651 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12646): Show |
chr3 | 170082584 | 170186733 |
| a0001c0002t0005 | 0/0 | 12652 | 15 | 0 | 0 | 15 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0002t0023 | 0/0 | 12652 | 2 | 0 | 0 | 1 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0002t0041 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0003t0006 | 0/0 | 12652 | 4 | 4 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0001c0013t0002 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0002c0004t0011 | 0/0 | 12652 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0003c0005t0025 | 0/0 | 12657 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12652): Show |
chr3 | 170082584 | 170186733 |
| a0003c0005t0026 | 0/0 | 12657 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12652): Show |
chr3 | 170082584 | 170186733 |
| a0004c0014t0005 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0005c0010t0001 | 0/0 | 12652 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0006c0008t0018 | 0/0 | 12651 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12646): Show |
chr3 | 170082584 | 170186733 |
| a0007c0007t0027 | 0/0 | 12657 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12652): Show |
chr3 | 170082584 | 170186733 |
| a0008c0011t0002 | 0/0 | 12652 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0009c0009t0001 | 0/0 | 12652 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0010c0006t0002 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12647): Show |
chr3 | 170082584 | 170186733 |
| a0011c0012t0004 | 0/0 | 12651 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | AGTGA others(12646): Show |
chr3 | 170082584 | 170186733 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0197 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0012g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0012g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0012g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0012g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0013g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0013g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0014g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0014g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0015g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0015g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0015g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0016g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0017g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0017g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0017g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0019g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0019g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0020g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0020g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0021g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0021g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0022g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0022g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0024g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0024g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0028g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0029g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0030g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0031g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0032g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0033g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0034g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0035g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0036g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0037g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0038g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0039g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0040g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0042g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0043g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0044g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0045g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0046g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0047g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0048g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0049g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0050g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0051g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0023g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0023g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0041g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0003t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0003t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0003t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0003t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0013t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0002c0004t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0002c0004t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0002c0004t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0003c0005t0025g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0003c0005t0026g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0004c0014t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0005c0010t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0006c0008t0018g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0007c0007t0027g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0008c0011t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0009c0009t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0010c0006t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0011c0012t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0226 | EUR | GBR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0215 | EUR | GBR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0122 | EUR | FIN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00408 | hp1 | a0001 | c0002 | t0005 | g0310 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00423 | hp1 | a0001 | c0002 | t0005 | g0316 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00438 | hp1 | a0001 | c0001 | t0012 | g0097 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00558 | hp1 | a0001 | c0002 | t0005 | g0313 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00597 | hp2 | a0001 | c0001 | t0012 | g0290 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00621 | hp1 | a0001 | c0001 | t0024 | g0273 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00639 | hp1 | a0001 | c0001 | t0030 | g0114 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00642 | hp1 | a0001 | c0001 | t0033 | g0303 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00673 | hp2 | a0001 | c0002 | t0005 | g0311 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00735 | hp2 | a0001 | c0001 | t0046 | g0268 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00741 | hp1 | a0001 | c0001 | t0048 | g0242 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0282 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0069 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01109 | hp2 | a0001 | c0001 | t0021 | g0233 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01167 | hp1 | a0001 | c0001 | t0013 | g0102 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01168 | hp1 | a0001 | c0001 | t0015 | g0009 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01168 | hp2 | a0001 | c0001 | t0019 | g0051 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01169 | hp1 | a0001 | c0001 | t0013 | g0101 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01169 | hp2 | a0001 | c0001 | t0019 | g0062 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0125 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01192 | hp2 | a0001 | c0001 | t0015 | g0229 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01243 | hp1 | a0001 | c0001 | t0014 | g0001 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01255 | hp2 | a0001 | c0001 | t0021 | g0008 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0168 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01257 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0135 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0151 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01346 | hp2 | a0001 | c0001 | t0015 | g0181 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0266 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01433 | hp1 | a0003 | c0005 | t0026 | g0324 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0123 | EUR | IBS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0247 | EUR | IBS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0278 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0205 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0194 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02004 | hp2 | a0001 | c0001 | t0007 | g0155 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02015 | hp1 | a0001 | c0002 | t0005 | g0309 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02027 | hp2 | a0004 | c0014 | t0005 | g0320 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02055 | hp1 | a0003 | c0005 | t0025 | g0323 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0326 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02071 | hp2 | a0001 | c0002 | t0023 | g0308 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02132 | hp1 | a0001 | c0001 | t0031 | g0238 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02132 | hp2 | a0001 | c0001 | t0034 | g0025 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02155 | hp1 | a0001 | c0002 | t0005 | g0319 | EAS | CDX | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02257 | hp1 | a0005 | c0010 | t0001 | g0106 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02257 | hp2 | a0001 | c0001 | t0016 | g0110 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0255 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0204 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02273 | hp2 | a0001 | c0001 | t0007 | g0170 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0070 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02451 | hp1 | a0001 | c0001 | t0017 | g0253 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02451 | hp2 | a0001 | c0001 | t0029 | g0113 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0186 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02615 | hp1 | a0001 | c0001 | t0040 | g0031 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02615 | hp2 | a0002 | c0004 | t0011 | g0195 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0148 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0116 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02630 | hp2 | a0001 | c0001 | t0009 | g0174 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0029 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02809 | hp2 | a0001 | c0001 | t0017 | g0254 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02818 | hp1 | a0001 | c0001 | t0042 | g0100 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0115 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02886 | hp1 | a0001 | c0001 | t0038 | g0206 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0279 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02895 | hp2 | a0001 | c0001 | t0016 | g0109 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02896 | hp1 | a0002 | c0004 | t0011 | g0064 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02897 | hp1 | a0002 | c0004 | t0011 | g0063 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02897 | hp2 | a0001 | c0001 | t0016 | g0108 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02922 | hp1 | a0001 | c0001 | t0050 | g0104 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02922 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02965 | hp1 | a0001 | c0001 | t0039 | g0193 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02970 | hp2 | a0006 | c0008 | t0018 | g0149 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0001 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02976 | hp2 | a0001 | c0003 | t0006 | g0294 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0188 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03041 | hp2 | a0001 | c0001 | t0018 | g0169 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0140 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03098 | hp2 | a0001 | c0001 | t0018 | g0139 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0327 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0175 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03239 | hp1 | a0001 | c0001 | t0020 | g0086 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03453 | hp2 | a0001 | c0003 | t0006 | g0293 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0072 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0073 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03492 | hp2 | a0008 | c0011 | t0002 | g0236 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0112 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0065 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0297 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03831 | hp2 | a0001 | c0002 | t0023 | g0312 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03834 | hp1 | a0001 | c0001 | t0043 | g0276 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04184 | hp2 | a0001 | c0001 | t0020 | g0089 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04199 | hp1 | a0009 | c0009 | t0001 | g0020 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0068 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04228 | hp1 | a0001 | c0001 | t0010 | g0021 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | CHB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | CHB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18946 | hp2 | a0001 | c0001 | t0037 | g0049 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18949 | hp2 | a0010 | c0006 | t0002 | g0121 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18951 | hp2 | a0001 | c0002 | t0005 | g0325 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18960 | hp1 | a0001 | c0001 | t0032 | g0090 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18960 | hp2 | a0001 | c0002 | t0005 | g0314 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18964 | hp1 | a0001 | c0002 | t0005 | g0305 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18969 | hp2 | a0001 | c0001 | t0010 | g0094 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18975 | hp1 | a0001 | c0002 | t0005 | g0306 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18975 | hp2 | a0001 | c0001 | t0024 | g0237 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18982 | hp2 | a0001 | c0002 | t0005 | g0317 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18983 | hp2 | a0001 | c0013 | t0002 | g0212 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18985 | hp1 | a0001 | c0002 | t0041 | g0315 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18986 | hp1 | a0001 | c0001 | t0012 | g0077 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18986 | hp2 | a0001 | c0001 | t0045 | g0287 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18991 | hp2 | a0001 | c0002 | t0005 | g0321 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18994 | hp2 | a0001 | c0002 | t0005 | g0307 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18998 | hp2 | a0001 | c0001 | t0044 | g0296 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19003 | hp1 | a0001 | c0001 | t0051 | g0159 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19007 | hp1 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0030 | AFR | LWK | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19030 | hp2 | a0001 | c0001 | t0036 | g0098 | AFR | LWK | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0295 | AFR | LWK | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0099 | AFR | LWK | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19063 | hp1 | a0001 | c0001 | t0049 | g0177 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19063 | hp2 | a0001 | c0001 | t0012 | g0088 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19066 | hp1 | a0001 | c0002 | t0005 | g0318 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19068 | hp1 | a0001 | c0001 | t0012 | g0066 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19078 | hp1 | a0011 | c0012 | t0004 | g0172 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19082 | hp1 | a0001 | c0002 | t0005 | g0304 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19082 | hp2 | a0001 | c0001 | t0035 | g0010 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19085 | hp1 | a0001 | c0001 | t0010 | g0095 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19085 | hp2 | a0001 | c0001 | t0047 | g0244 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0176 | AFR | YRI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | YRI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0103 | AFR | ASW | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20129 | hp2 | a0001 | c0003 | t0006 | g0292 | AFR | ASW | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0239 | EUR | TSI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20752 | hp2 | a0001 | c0001 | t0008 | g0071 | EUR | TSI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20805 | hp1 | a0001 | c0001 | t0022 | g0219 | EUR | TSI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01123 | hp2 | a0001 | c0001 | t0010 | g0015 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0281 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03471 | hp1 | a0007 | c0007 | t0027 | g0322 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | USA | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG06807 | hp2 | a0001 | c0001 | t0022 | g0220 | AFR | USA | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18955 | hp1 | a0001 | c0001 | t0028 | g0048 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18955 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0143 | REF | REF | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0197 | REF | REF | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170113480 | T | C | 1 | a0009 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2233A>G | p.Lys745Glu | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/15 | 2251/12652 | 2233/2988 | 745/995 | chr3 | 170113480 | |||
| chr3:170117321 | T | C | 1 | a0004 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.2098A>G | p.Ile700Val | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/15 | 2116/12652 | 2098/2988 | 700/995 | chr3 | 170117321 | |||
| chr3:170122683 | C | T | 1 | a0006 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1850G>A | p.Arg617Gln | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/15 | 1868/12652 | 1850/2988 | 617/995 | chr3 | 170122683 | |||
| chr3:170128979 | T | C | 1 | a0005 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1493A>G | p.His498Arg | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/15 | 1511/12652 | 1493/2988 | 498/995 | chr3 | 170128979 | |||
| chr3:170129100 | C | G | 2 | a0003 a0007 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.1372G>C | p.Ala458Pro | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/15 | 1390/12652 | 1372/2988 | 458/995 | chr3 | 170129100 | |||
| chr3:170129257 | C | A | 1 | a0008 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.1215G>T | p.Gln405His | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/15 | 1233/12652 | 1215/2988 | 405/995 | chr3 | 170129257 | |||
| chr3:170129294 | G | A | 1 | a0011 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.1178C>T | p.Pro393Leu | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/15 | 1196/12652 | 1178/2988 | 393/995 | chr3 | 170129294 | |||
| chr3:170129337 | C | T | 1 | a0007 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1135G>A | p.Ala379Thr | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/15 | 1153/12652 | 1135/2988 | 379/995 | chr3 | 170129337 | |||
| chr3:170171423 | T | C | 1 | a0002 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.364A>G | p.Thr122Ala | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/15 | 382/12652 | 364/2988 | 122/995 | chr3 | 170171423 | |||
| chr3:170178790 | C | T | 1 | a0010 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.163G>A | p.Asp55Asn | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/15 | 181/12652 | 163/2988 | 55/995 | chr3 | 170178790 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170172686 | G | A | 1 | a0001c0013 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.207C>T | p.Pro69Pro | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/15 | 225/12652 | 207/2988 | 69/995 | chr3 | 170172686 | |||
| chr3:170178803 | G | C | 2 | a0001c0002 a0004c0014 |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
synonymous_variant | LOW | c.150C>G | p.Val50Val | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/15 | 168/12652 | 150/2988 | 50/995 | chr3 | 170178803 | |||
| chr3:170178896 | C | T | 1 | a0001c0003 | 4 | HG02976.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
synonymous_variant | LOW | c.57G>A | p.Pro19Pro | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/15 | 75/12652 | 57/2988 | 19/995 | chr3 | 170178896 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170087659 | A | G | 1 | a0001c0001t0019 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9571T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9571 | chr3 | 170087659 | ||||||
| chr3:170087932 | T | A | 1 | a0001c0002t0041 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9298A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9298 | chr3 | 170087932 | ||||||
| chr3:170088037 | A | C | 1 | a0003c0005t0025 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9193T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9193 | chr3 | 170088037 | ||||||
| chr3:170088044 | A | C | 1 | a0001c0001t0012 | 5 | HG00438.hp1 HG00597.hp2 NA18986.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9186T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9186 | chr3 | 170088044 | ||||||
| chr3:170088121 | T | C | 1 | a0001c0001t0034 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9109A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9109 | chr3 | 170088121 | ||||||
| chr3:170088189 | G | C | 1 | a0001c0001t0035 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9041C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9041 | chr3 | 170088189 | ||||||
| chr3:170088283 | T | C | 1 | a0001c0001t0020 | 2 | HG03239.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8947A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8947 | chr3 | 170088283 | ||||||
| chr3:170088382 | G | A | 6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0018 others(3): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*8848C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8848 | chr3 | 170088382 | ||||||
| chr3:170088843 | C | T | 1 | a0001c0001t0029 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8387G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8387 | chr3 | 170088843 | ||||||
| chr3:170088892 | G | A | 1 | a0001c0001t0036 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8338C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8338 | chr3 | 170088892 | ||||||
| chr3:170089017 | A | T | 1 | a0001c0001t0024 | 2 | HG00621.hp1 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8213T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8213 | chr3 | 170089017 | ||||||
| chr3:170089028 | A | G | 37 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(34): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*8202T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8202 | chr3 | 170089028 | ||||||
| chr3:170089109 | T | C | 1 | a0001c0001t0043 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8121A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8121 | chr3 | 170089109 | ||||||
| chr3:170089188 | A | G | 3 | a0003c0005t0025 a0003c0005t0026 a0007c0007t0027 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8042T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8042 | chr3 | 170089188 | ||||||
| chr3:170089442 | T | C | 1 | a0001c0001t0008 | 9 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7788A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7788 | chr3 | 170089442 | ||||||
| chr3:170089627 | A | G | 3 | a0003c0005t0025 a0003c0005t0026 a0007c0007t0027 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7603T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7603 | chr3 | 170089627 | ||||||
| chr3:170089635 | G | A | 1 | a0001c0001t0009 | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7595C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7595 | chr3 | 170089635 | ||||||
| chr3:170089745 | C | T | 1 | a0001c0001t0045 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7485G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7485 | chr3 | 170089745 | ||||||
| chr3:170089836 | C | G | 37 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(34): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*7394G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7394 | chr3 | 170089836 | ||||||
| chr3:170089863 | G | A | 1 | a0001c0001t0037 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7367C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7367 | chr3 | 170089863 | ||||||
| chr3:170089927 | A | G | 1 | a0001c0001t0036 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7303T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7303 | chr3 | 170089927 | ||||||
| chr3:170089927 | AAG | A | 3 | a0001c0001t0013 a0001c0001t0042 a0001c0001t0050 |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7301_*7302delCT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7301 | chr3 | 170089927 | ||||||
| chr3:170089928 | A | G | 2 | a0001c0001t0009 a0001c0002t0041 |
9 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7302T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7302 | chr3 | 170089928 | ||||||
| chr3:170089929 | G | A | 3 | a0001c0001t0003 a0001c0001t0009 a0001c0002t0041 |
10 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7301C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7301 | chr3 | 170089929 | ||||||
| chr3:170089929 | G | GA | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 others(3): Show |
13 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7300dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7300 | chr3 | 170089929 | ||||||
| chr3:170089930 | A | G | 3 | a0001c0001t0013 a0001c0001t0042 a0001c0001t0050 |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7300T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7300 | chr3 | 170089930 | ||||||
| chr3:170089972 | G | C | 4 | a0001c0002t0005 a0001c0002t0023 a0001c0002t0041 others(1): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*7258C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7258 | chr3 | 170089972 | ||||||
| chr3:170090020 | A | G | 1 | a0001c0001t0016 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7210T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7210 | chr3 | 170090020 | ||||||
| chr3:170090051 | G | T | 39 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(36): Show |
204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*7179C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7179 | chr3 | 170090051 | ||||||
| chr3:170090077 | A | G | 3 | a0003c0005t0025 a0003c0005t0026 a0007c0007t0027 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7153T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7153 | chr3 | 170090077 | ||||||
| chr3:170090111 | TA | T | 2 | a0001c0001t0014 a0001c0001t0017 |
7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7118delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7118 | chr3 | 170090111 | ||||||
| chr3:170090130 | A | G | 3 | a0001c0001t0013 a0001c0001t0042 a0001c0001t0050 |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7100T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7100 | chr3 | 170090130 | ||||||
| chr3:170090326 | A | C | 12 | a0001c0001t0002 a0001c0001t0022 a0001c0001t0024 others(9): Show |
67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*6904T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 6904 | chr3 | 170090326 | ||||||
| chr3:170090364 | T | C | 2 | a0001c0001t0011 a0002c0004t0011 |
6 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6866A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 6866 | chr3 | 170090364 | ||||||
| chr3:170090417 | AAT | A | 1 | a0001c0001t0016 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6811_*6812delAT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 6811 | chr3 | 170090417 | ||||||
| chr3:170090566 | G | A | 6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0018 others(3): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*6664C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 6664 | chr3 | 170090566 | ||||||
| chr3:170090719 | A | G | 1 | a0001c0001t0039 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6511T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 6511 | chr3 | 170090719 | ||||||
| chr3:170091480 | C | CCTCTT | 3 | a0003c0005t0025 a0003c0005t0026 a0007c0007t0027 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5749_*5750insAAGA others(1): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5749 | chr3 | 170091480 | ||||||
| chr3:170091502 | T | C | 1 | a0001c0001t0039 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5728A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5728 | chr3 | 170091502 | ||||||
| chr3:170091521 | T | C | 1 | a0001c0001t0009 | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5709A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5709 | chr3 | 170091521 | ||||||
| chr3:170091561 | C | G | 1 | a0001c0001t0044 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5669G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5669 | chr3 | 170091561 | ||||||
| chr3:170091771 | A | C | 12 | a0001c0001t0002 a0001c0001t0022 a0001c0001t0024 others(9): Show |
67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5459T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5459 | chr3 | 170091771 | ||||||
| chr3:170091772 | C | A | 12 | a0001c0001t0002 a0001c0001t0022 a0001c0001t0024 others(9): Show |
67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5458G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5458 | chr3 | 170091772 | ||||||
| chr3:170091786 | AAGC | A | 19 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(16): Show |
107 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*5441_*5443delGCT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5441 | chr3 | 170091786 | ||||||
| chr3:170091814 | G | A | 1 | a0001c0001t0046 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5416C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5416 | chr3 | 170091814 | ||||||
| chr3:170091949 | T | C | 1 | a0001c0002t0023 | 2 | HG02071.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5281A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5281 | chr3 | 170091949 | ||||||
| chr3:170092030 | C | T | 1 | a0001c0001t0038 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5200G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5200 | chr3 | 170092030 | ||||||
| chr3:170092135 | A | G | 39 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(36): Show |
204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*5095T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5095 | chr3 | 170092135 | ||||||
| chr3:170092165 | A | C | 3 | a0003c0005t0025 a0003c0005t0026 a0007c0007t0027 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5065T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5065 | chr3 | 170092165 | ||||||
| chr3:170092188 | T | G | 1 | a0001c0001t0039 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5042A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5042 | chr3 | 170092188 | ||||||
| chr3:170092303 | A | G | 1 | a0001c0001t0009 | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4927T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4927 | chr3 | 170092303 | ||||||
| chr3:170092329 | TAAC | T | 1 | a0001c0001t0015 | 3 | HG01168.hp1 HG01192.hp2 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4898_*4900delGTT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4898 | chr3 | 170092329 | ||||||
| chr3:170092366 | T | C | 3 | a0003c0005t0025 a0003c0005t0026 a0007c0007t0027 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4864A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4864 | chr3 | 170092366 | ||||||
| chr3:170092555 | G | A | 1 | a0001c0001t0047 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4675C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4675 | chr3 | 170092555 | ||||||
| chr3:170092753 | T | G | 4 | a0001c0002t0005 a0001c0002t0023 a0001c0002t0041 others(1): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4477A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4477 | chr3 | 170092753 | ||||||
| chr3:170092766 | C | T | 3 | a0003c0005t0025 a0003c0005t0026 a0007c0007t0027 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4464G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4464 | chr3 | 170092766 | ||||||
| chr3:170092896 | A | G | 1 | a0001c0001t0050 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4334T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4334 | chr3 | 170092896 | ||||||
| chr3:170093139 | G | A | 1 | a0001c0001t0040 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4091C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4091 | chr3 | 170093139 | ||||||
| chr3:170093236 | C | T | 1 | a0001c0001t0033 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3994G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3994 | chr3 | 170093236 | ||||||
| chr3:170093251 | G | C | 4 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0051 others(1): Show |
43 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3979C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3979 | chr3 | 170093251 | ||||||
| chr3:170093412 | A | G | 1 | a0001c0001t0031 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3818T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3818 | chr3 | 170093412 | ||||||
| chr3:170093590 | T | C | 1 | a0001c0001t0048 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3640A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3640 | chr3 | 170093590 | ||||||
| chr3:170093612 | T | C | 1 | a0001c0001t0049 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3618A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3618 | chr3 | 170093612 | ||||||
| chr3:170093978 | A | G | 3 | a0003c0005t0025 a0003c0005t0026 a0007c0007t0027 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3252T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3252 | chr3 | 170093978 | ||||||
| chr3:170094269 | A | G | 1 | a0001c0001t0032 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2961T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 2961 | chr3 | 170094269 | ||||||
| chr3:170094327 | A | G | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0009 others(4): Show |
54 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2903T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 2903 | chr3 | 170094327 | ||||||
| chr3:170094363 | C | T | 2 | a0003c0005t0025 a0003c0005t0026 |
2 | HG01433.hp1 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2867G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 2867 | chr3 | 170094363 | ||||||
| chr3:170094530 | C | G | 3 | a0001c0001t0013 a0001c0001t0042 a0001c0001t0050 |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2700G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 2700 | chr3 | 170094530 | ||||||
| chr3:170095162 | T | C | 4 | a0001c0002t0005 a0001c0002t0023 a0001c0002t0041 others(1): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2068A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 2068 | chr3 | 170095162 | ||||||
| chr3:170095234 | T | C | 1 | a0001c0001t0051 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1996A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1996 | chr3 | 170095234 | ||||||
| chr3:170095552 | C | T | 36 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(33): Show |
184 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1678G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1678 | chr3 | 170095552 | ||||||
| chr3:170095689 | T | A | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG00639.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1541A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1541 | chr3 | 170095689 | ||||||
| chr3:170095830 | C | G | 1 | a0001c0001t0031 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1400G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1400 | chr3 | 170095830 | ||||||
| chr3:170095877 | G | A | 2 | a0001c0001t0013 a0001c0001t0050 |
5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1353C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1353 | chr3 | 170095877 | ||||||
| chr3:170096188 | AT | A | 6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0018 others(3): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1041delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1041 | chr3 | 170096188 | ||||||
| chr3:170096330 | C | T | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG00639.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*900G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 900 | chr3 | 170096330 | ||||||
| chr3:170096338 | C | T | 1 | a0001c0001t0028 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*892G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 892 | chr3 | 170096338 | ||||||
| chr3:170096454 | A | C | 3 | a0003c0005t0025 a0003c0005t0026 a0007c0007t0027 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*776T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 776 | chr3 | 170096454 | ||||||
| chr3:170096943 | T | C | 1 | a0001c0001t0014 | 4 | HG01243.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*287A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 287 | chr3 | 170096943 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170097444 | C | T | 7 | a0001c0001t0006g0005 a0001c0001t0006g0140 a0001c0001t0006g0188 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2834-60G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170097444 | |||||||
| chr3:170097621 | T | C | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.2834-237A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170097621 | |||||||
| chr3:170097898 | A | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2834-514T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170097898 | |||||||
| chr3:170098075 | C | T | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2834-691G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098075 | |||||||
| chr3:170098216 | A | T | 1 | a0002c0004t0011g0195 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2834-832T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098216 | |||||||
| chr3:170098551 | A | G | 1 | a0001c0001t0048g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2834-1167T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098551 | |||||||
| chr3:170098559 | A | T | 1 | a0001c0013t0002g0212 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2834-1175T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098559 | |||||||
| chr3:170098560 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2834-1176C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098560 | |||||||
| chr3:170098721 | A | G | 1 | a0001c0001t0004g0150 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2834-1337T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098721 | |||||||
| chr3:170098722 | C | T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.2834-1338G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098722 | |||||||
| chr3:170099141 | T | A | 1 | a0001c0001t0040g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2834-1757A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099141 | |||||||
| chr3:170099500 | G | A | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2834-2116C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099500 | |||||||
| chr3:170099575 | G | A | 1 | a0001c0001t0004g0156 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2834-2191C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099575 | |||||||
| chr3:170099667 | T | C | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2834-2283A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099667 | |||||||
| chr3:170099834 | A | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2834-2450T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099834 | |||||||
| chr3:170099898 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2834-2514G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099898 | |||||||
| chr3:170099973 | T | C | 2 | a0003c0005t0025g0323 a0003c0005t0026g0324 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2833+2506A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099973 | |||||||
| chr3:170100078 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0033g0303 |
2 | HG00323.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.2833+2401T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100078 | |||||||
| chr3:170100079 | C | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(111): Show |
116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2833+2400G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100079 | |||||||
| chr3:170100267 | T | G | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2833+2212A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100267 | |||||||
| chr3:170100377 | G | C | 1 | a0001c0001t0009g0176 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2833+2102C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100377 | |||||||
| chr3:170100589 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2833+1890A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100589 | |||||||
| chr3:170100733 | T | C | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.2833+1746A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100733 | |||||||
| chr3:170100849 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2833+1630A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100849 | |||||||
| chr3:170100868 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2833+1611A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100868 | |||||||
| chr3:170100881 | G | A | 67 | a0001c0001t0002g0117 a0001c0001t0002g0120 a0001c0001t0002g0122 others(64): Show |
67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.2833+1598C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100881 | |||||||
| chr3:170101205 | G | C | 1 | a0001c0001t0003g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2833+1274C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101205 | |||||||
| chr3:170101229 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2833+1250G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101229 | |||||||
| chr3:170101557 | G | A | 2 | a0001c0001t0029g0113 a0001c0001t0030g0114 |
2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2833+922C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101557 | |||||||
| chr3:170101705 | C | G | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2833+774G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101705 | |||||||
| chr3:170101896 | GCTCT | G | 4 | a0001c0001t0006g0140 a0003c0005t0025g0323 a0003c0005t0026g0324 others(1): Show |
4 | HG01433.hp1 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2833+579_2833+582d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101896 | |||||||
| chr3:170101988 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2833+491G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101988 | |||||||
| chr3:170102402 | A | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0085 a0001c0001t0010g0015 |
3 | HG01123.hp2 HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2833+77T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170102402 | |||||||
| chr3:170102403 | A | G | 1 | a0001c0001t0007g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2833+76T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170102403 | |||||||
| chr3:170102798 | A | G | 1 | a0001c0001t0003g0259 | 1 | NA19240.hp2 | splice_region_variant&intron_variant | LOW | c.2601+4T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 13/14 | chr3 | 170102798 | |||||||
| chr3:170103016 | C | T | 1 | a0001c0001t0018g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2469-82G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103016 | |||||||
| chr3:170103019 | TG | T | 4 | a0001c0001t0014g0001 a0003c0005t0025g0323 a0003c0005t0026g0324 others(1): Show |
6 | HG01243.hp1 HG01433.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2469-86delC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103019 | |||||||
| chr3:170103081 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2469-147C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103081 | |||||||
| chr3:170103173 | G | C | 2 | a0001c0001t0008g0002 a0001c0001t0008g0065 |
3 | HG01257.hp2 HG01258.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2469-239C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103173 | |||||||
| chr3:170103238 | C | T | 5 | a0001c0001t0014g0001 a0001c0001t0036g0098 a0003c0005t0025g0323 others(2): Show |
7 | HG01243.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2469-304G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103238 | |||||||
| chr3:170103477 | T | C | 1 | a0001c0001t0004g0158 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2469-543A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103477 | |||||||
| chr3:170103513 | CTCTT | C | 4 | a0001c0001t0014g0001 a0003c0005t0025g0323 a0003c0005t0026g0324 others(1): Show |
6 | HG01243.hp1 HG01433.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2469-583_2469-580d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103513 | |||||||
| chr3:170103577 | A | G | 8 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(5): Show |
8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2469-643T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103577 | |||||||
| chr3:170103887 | C | T | 5 | a0001c0001t0011g0205 a0001c0001t0011g0281 a0002c0004t0011g0063 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2469-953G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103887 | |||||||
| chr3:170103898 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG01256.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2469-964G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103898 | |||||||
| chr3:170103899 | G | A | 1 | a0001c0001t0007g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2469-965C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103899 | |||||||
| chr3:170104413 | T | C | 53 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(50): Show |
54 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.2469-1479A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104413 | |||||||
| chr3:170104604 | A | G | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.2469-1670T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104604 | |||||||
| chr3:170104790 | C | G | 1 | a0001c0001t0003g0201 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2469-1856G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104790 | |||||||
| chr3:170104802 | G | A | 4 | a0001c0001t0014g0001 a0003c0005t0025g0323 a0003c0005t0026g0324 others(1): Show |
6 | HG01243.hp1 HG01433.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2469-1868C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104802 | |||||||
| chr3:170104838 | G | A | 2 | a0001c0003t0006g0292 a0001c0003t0006g0295 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2469-1904C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104838 | |||||||
| chr3:170104966 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2468+1866C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104966 | |||||||
| chr3:170105234 | T | C | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2468+1598A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105234 | |||||||
| chr3:170105308 | T | C | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2468+1524A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105308 | |||||||
| chr3:170105595 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2468+1237G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105595 | |||||||
| chr3:170105699 | G | C | 4 | a0001c0001t0003g0178 a0001c0001t0003g0208 a0001c0001t0003g0209 others(1): Show |
4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2468+1133C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105699 | |||||||
| chr3:170105888 | T | A | 2 | a0001c0001t0004g0164 a0001c0001t0004g0173 |
2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2468+944A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105888 | |||||||
| chr3:170105965 | A | G | 2 | a0001c0001t0020g0086 a0001c0001t0020g0089 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2468+867T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105965 | |||||||
| chr3:170106038 | C | T | 6 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0281 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2468+794G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106038 | |||||||
| chr3:170106139 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2468+693C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106139 | |||||||
| chr3:170106160 | C | A | 4 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 others(1): Show |
4 | NA18747.hp1 NA18942.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.2468+672G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106160 | |||||||
| chr3:170106170 | C | G | 17 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(14): Show |
17 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.2468+662G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106170 | |||||||
| chr3:170106199 | AAG | A | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.2468+631_2468+632d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106199 | |||||||
| chr3:170106293 | A | C | 1 | a0001c0001t0038g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2468+539T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106293 | |||||||
| chr3:170106397 | T | C | 1 | a0001c0001t0017g0254 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2468+435A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106397 | |||||||
| chr3:170106545 | C | A | 1 | a0001c0001t0003g0232 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2468+287G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106545 | |||||||
| chr3:170106639 | G | A | 320 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(317): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.2468+193C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106639 | |||||||
| chr3:170107219 | T | TA | 115 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(112): Show |
117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.2354-274dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107219 | |||||||
| chr3:170107309 | G | C | 1 | a0001c0001t0003g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2354-363C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107309 | |||||||
| chr3:170107417 | T | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(195): Show |
203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.2354-471A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107417 | |||||||
| chr3:170107678 | G | A | 1 | a0001c0001t0007g0141 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2354-732C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107678 | |||||||
| chr3:170107688 | T | TCA | 119 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
123 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2354-744_2354-743d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107688 | |||||||
| chr3:170107857 | C | T | 4 | a0001c0003t0006g0292 a0001c0003t0006g0293 a0001c0003t0006g0294 others(1): Show |
4 | HG02976.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2354-911G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107857 | |||||||
| chr3:170107858 | G | A | 1 | a0001c0001t0031g0238 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2354-912C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107858 | |||||||
| chr3:170107899 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2354-953G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107899 | |||||||
| chr3:170108083 | T | C | 70 | a0001c0001t0002g0117 a0001c0001t0002g0120 a0001c0001t0002g0122 others(67): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.2354-1137A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108083 | |||||||
| chr3:170108122 | T | C | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2354-1176A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108122 | |||||||
| chr3:170108264 | G | A | 1 | a0001c0001t0003g0196 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2354-1318C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108264 | |||||||
| chr3:170108312 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0302 a0009c0009t0001g0020 |
3 | HG01256.hp2 HG01978.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2354-1366A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108312 | |||||||
| chr3:170108351 | A | C | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2354-1405T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108351 | |||||||
| chr3:170108357 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0045 others(4): Show |
7 | HG01433.hp2 HG02300.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.2354-1411A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108357 | |||||||
| chr3:170108518 | A | G | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2354-1572T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108518 | |||||||
| chr3:170108565 | A | G | 2 | a0001c0002t0005g0305 a0001c0002t0005g0318 |
2 | NA18964.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2354-1619T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108565 | |||||||
| chr3:170108660 | A | G | 1 | a0001c0001t0024g0273 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2354-1714T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108660 | |||||||
| chr3:170108871 | C | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2354-1925G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108871 | |||||||
| chr3:170108984 | GAGT | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2354-2041_2354-203 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108984 | |||||||
| chr3:170109317 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0289 |
2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2354-2371G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170109317 | |||||||
| chr3:170109365 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(112): Show |
117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.2354-2419C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170109365 | |||||||
| chr3:170109404 | A | G | 3 | a0001c0001t0016g0108 a0001c0001t0016g0109 a0001c0001t0016g0110 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2354-2458T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170109404 | |||||||
| chr3:170109884 | C | G | 8 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(5): Show |
8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2354-2938G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170109884 | |||||||
| chr3:170109966 | TA | T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.2354-3021delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170109966 | |||||||
| chr3:170110165 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+3195A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110165 | |||||||
| chr3:170110221 | G | A | 7 | a0001c0001t0003g0252 a0001c0001t0003g0291 a0001c0001t0014g0001 others(4): Show |
9 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2353+3139C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110221 | |||||||
| chr3:170110299 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+3061A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110299 | |||||||
| chr3:170110327 | G | A | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2353+3033C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110327 | |||||||
| chr3:170110346 | AC | A | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2353+3013delG | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110346 | |||||||
| chr3:170110499 | T | C | 5 | a0001c0001t0014g0001 a0001c0001t0014g0186 a0001c0001t0017g0253 others(2): Show |
7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2353+2861A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110499 | |||||||
| chr3:170110500 | C | T | 2 | a0001c0001t0002g0213 a0001c0001t0002g0285 |
2 | HG00609.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2353+2860G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110500 | |||||||
| chr3:170110583 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+2777G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110583 | |||||||
| chr3:170110595 | T | A | 1 | a0001c0001t0029g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2353+2765A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110595 | |||||||
| chr3:170110855 | C | T | 2 | a0001c0001t0029g0113 a0001c0001t0030g0114 |
2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2353+2505G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110855 | |||||||
| chr3:170111261 | A | AAAAG | 16 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0018 others(13): Show |
16 | HG00323.hp2 HG00558.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.2353+2098_2353+209 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | |||||||
| chr3:170111261 | A | AGAAG | 10 | a0001c0001t0002g0234 a0001c0001t0002g0240 a0001c0001t0002g0241 others(7): Show |
10 | HG00423.hp2 HG02280.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.2353+2095_2353+209 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | |||||||
| chr3:170111261 | A | AGAAGGAA others(5): Show |
1 | a0001c0001t0002g0132 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2353+2087_2353+209 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | |||||||
| chr3:170111261 | AGAAG | A | 78 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(75): Show |
79 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.2353+2095_2353+209 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | |||||||
| chr3:170111261 | AGAAGGAA others(1): Show |
A | 36 | a0001c0001t0001g0107 a0001c0001t0002g0128 a0001c0001t0002g0129 others(33): Show |
38 | HG00140.hp2 HG00621.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.2353+2091_2353+209 others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | |||||||
| chr3:170111261 | AGAAGGAA others(5): Show |
A | 32 | a0001c0001t0001g0032 a0001c0001t0001g0080 a0001c0001t0002g0180 others(29): Show |
32 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.2353+2087_2353+209 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | |||||||
| chr3:170111261 | AGAAGGAA others(9): Show |
A | 18 | a0001c0001t0002g0213 a0001c0001t0002g0235 a0001c0001t0003g0207 others(15): Show |
18 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.2353+2083_2353+209 others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | |||||||
| chr3:170111261 | AGAAGGAA others(13): Show |
A | 11 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(8): Show |
11 | HG02027.hp2 HG02055.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2353+2079_2353+209 others(24): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | |||||||
| chr3:170111261 | AGAAGGAA others(17): Show |
A | 1 | a0001c0001t0009g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2353+2075_2353+209 others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | |||||||
| chr3:170111262 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0016 others(33): Show |
38 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.2353+2098C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111262 | |||||||
| chr3:170111266 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0075 others(1): Show |
4 | HG02293.hp2 NA18973.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2353+2094C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111266 | |||||||
| chr3:170111274 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2353+2086C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111274 | |||||||
| chr3:170111297 | GGAAGGAA others(21): Show |
G | 1 | a0007c0007t0027g0322 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2353+2035_2353+206 others(32): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111297 | |||||||
| chr3:170111301 | GGAAGGAA others(17): Show |
G | 2 | a0003c0005t0025g0323 a0003c0005t0026g0324 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2353+2035_2353+205 others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111301 | |||||||
| chr3:170111305 | G | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0018 others(17): Show |
20 | HG00323.hp2 HG00558.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.2353+2055C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111305 | |||||||
| chr3:170111309 | G | C | 67 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(64): Show |
67 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.2353+2051C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111309 | |||||||
| chr3:170111309 | G | GGAACGAA others(1): Show |
17 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(14): Show |
18 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.2353+2050_2353+205 others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111309 | |||||||
| chr3:170111309 | G | GGAACGAA others(5): Show |
1 | a0001c0001t0012g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2353+2050_2353+205 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111309 | |||||||
| chr3:170111309 | GGAAGGAA others(5): Show |
G | 1 | a0001c0001t0003g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2353+2039_2353+205 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111309 | |||||||
| chr3:170111313 | G | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): Show |
101 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2353+2047C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111313 | |||||||
| chr3:170111313 | G | GGAACGAA others(1): Show |
4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0105 others(1): Show |
4 | HG01255.hp1 HG02056.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.2353+2046_2353+204 others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111313 | |||||||
| chr3:170111313 | G | GGAACGAA others(5): Show |
6 | a0001c0001t0001g0016 a0001c0001t0008g0002 a0001c0001t0008g0065 others(3): Show |
7 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2353+2046_2353+204 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111313 | |||||||
| chr3:170111313 | GGAAGGAA others(1): Show |
G | 9 | a0001c0001t0003g0227 a0001c0001t0003g0231 a0001c0001t0003g0266 others(6): Show |
9 | HG00735.hp2 HG01106.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.2353+2039_2353+204 others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111313 | |||||||
| chr3:170111317 | G | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(123): Show |
128 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.2353+2043C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111317 | |||||||
| chr3:170111317 | G | GGAACGAA others(9): Show |
1 | a0001c0001t0001g0081 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2353+2042_2353+204 others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111317 | |||||||
| chr3:170111317 | GGAAC | G | 8 | a0001c0001t0003g0230 a0001c0001t0003g0232 a0001c0001t0003g0260 others(5): Show |
8 | HG01081.hp1 HG01109.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.2353+2039_2353+204 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111317 | |||||||
| chr3:170111321 | C | G | 3 | a0001c0001t0003g0178 a0001c0001t0003g0210 a0001c0001t0003g0226 |
3 | HG00140.hp1 HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2353+2039G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111321 | |||||||
| chr3:170111325 | C | A | 2 | a0001c0001t0003g0261 a0001c0001t0003g0264 |
2 | HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2353+2035G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111325 | |||||||
| chr3:170111330 | G | A | 2 | a0001c0001t0003g0261 a0001c0001t0003g0264 |
2 | HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2353+2030C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111330 | |||||||
| chr3:170111341 | A | G | 2 | a0001c0001t0003g0261 a0001c0001t0003g0264 |
2 | HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2353+2019T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111341 | |||||||
| chr3:170111345 | C | A | 2 | a0001c0001t0003g0261 a0001c0001t0003g0264 |
2 | HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2353+2015G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111345 | |||||||
| chr3:170111345 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2353+2015G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111345 | |||||||
| chr3:170111348 | A | G | 2 | a0001c0001t0003g0261 a0001c0001t0003g0264 |
2 | HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2353+2012T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111348 | |||||||
| chr3:170111352 | G | GAAAGGGA others(8): Show |
1 | a0001c0001t0003g0262 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2353+1993_2353+200 others(19): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111352 | |||||||
| chr3:170111378 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1982T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111378 | |||||||
| chr3:170111384 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1976C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111384 | |||||||
| chr3:170111392 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1968T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111392 | |||||||
| chr3:170111393 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1967T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111393 | |||||||
| chr3:170111394 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1966C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | |||||||
| chr3:170111394 | G | GAGGAAGG others(9): Show |
1 | a0001c0002t0005g0310 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2353+1950_2353+196 others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | |||||||
| chr3:170111394 | G | GAGGAAGG others(17): Show |
2 | a0001c0002t0041g0315 a0004c0014t0005g0320 |
2 | HG02027.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2353+1942_2353+196 others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | |||||||
| chr3:170111394 | G | GAGGAAGG others(21): Show |
10 | a0001c0002t0005g0304 a0001c0002t0005g0306 a0001c0002t0005g0307 others(7): Show |
10 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.2353+1965_2353+196 others(32): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | |||||||
| chr3:170111394 | G | GAGGAAGG others(25): Show |
5 | a0001c0002t0005g0309 a0001c0002t0005g0317 a0001c0002t0005g0318 others(2): Show |
5 | HG02015.hp1 NA18951.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.2353+1965_2353+196 others(36): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | |||||||
| chr3:170111394 | G | GAGGAAGG others(29): Show |
1 | a0001c0002t0005g0305 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2353+1965_2353+196 others(40): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | |||||||
| chr3:170111723 | TAAAACGG others(15): Show |
T | 8 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(5): Show |
8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2353+1615_2353+163 others(26): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111723 | |||||||
| chr3:170111756 | A | C | 1 | a0001c0001t0036g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2353+1604T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111756 | |||||||
| chr3:170111796 | G | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1564C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111796 | |||||||
| chr3:170112021 | T | C | 1 | a0001c0001t0009g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2353+1339A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112021 | |||||||
| chr3:170112067 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1293G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112067 | |||||||
| chr3:170112080 | T | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(111): Show |
116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2353+1280A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112080 | |||||||
| chr3:170112144 | C | T | 8 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(5): Show |
8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2353+1216G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112144 | |||||||
| chr3:170112190 | A | G | 1 | a0001c0001t0018g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2353+1170T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112190 | |||||||
| chr3:170112379 | TTA | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+979_2353+980d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112379 | |||||||
| chr3:170112386 | T | C | 53 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(50): Show |
54 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.2353+974A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112386 | |||||||
| chr3:170112392 | TA | T | 5 | a0001c0001t0012g0088 a0001c0001t0016g0108 a0001c0001t0016g0109 others(2): Show |
5 | HG02132.hp2 HG02257.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2353+967delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112392 | |||||||
| chr3:170112394 | TA | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(150): Show |
156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.2353+965delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112394 | |||||||
| chr3:170112395 | A | T | 12 | a0001c0001t0002g0129 a0001c0001t0002g0183 a0001c0001t0002g0184 others(9): Show |
12 | HG00609.hp1 HG02080.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.2353+965T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112395 | |||||||
| chr3:170112395 | AT | A | 22 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0030g0114 others(19): Show |
22 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.2353+964delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112395 | |||||||
| chr3:170112439 | G | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+921C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112439 | |||||||
| chr3:170112486 | G | C | 1 | a0001c0001t0003g0259 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2353+874C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112486 | |||||||
| chr3:170112505 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+855T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112505 | |||||||
| chr3:170112513 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2353+847C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112513 | |||||||
| chr3:170112524 | A | AT | 111 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(108): Show |
113 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2353+835dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112524 | |||||||
| chr3:170112524 | AT | A | 7 | a0001c0001t0002g0275 a0001c0001t0004g0127 a0001c0001t0004g0147 others(4): Show |
7 | HG01168.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2353+835delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112524 | |||||||
| chr3:170112610 | G | A | 1 | a0001c0001t0032g0090 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2353+750C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112610 | |||||||
| chr3:170112671 | A | G | 53 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(50): Show |
54 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.2353+689T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112671 | |||||||
| chr3:170112807 | A | G | 1 | a0001c0001t0029g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2353+553T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112807 | |||||||
| chr3:170113153 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+207C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170113153 | |||||||
| chr3:170113714 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0302 a0009c0009t0001g0020 |
3 | HG01256.hp2 HG01978.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2194-195G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170113714 | |||||||
| chr3:170113895 | A | C | 1 | a0001c0001t0002g0123 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2194-376T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170113895 | |||||||
| chr3:170114164 | C | T | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2194-645G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114164 | |||||||
| chr3:170114165 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2194-646C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114165 | |||||||
| chr3:170114304 | C | T | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2194-785G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114304 | |||||||
| chr3:170114314 | T | C | 4 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 others(1): Show |
4 | NA18747.hp1 NA18942.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.2194-795A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114314 | |||||||
| chr3:170114328 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(115): Show |
120 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2194-809G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114328 | |||||||
| chr3:170114558 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2194-1039G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114558 | |||||||
| chr3:170114727 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2194-1208C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114727 | |||||||
| chr3:170114758 | C | G | 1 | a0001c0001t0050g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2194-1239G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114758 | |||||||
| chr3:170114766 | T | A | 1 | a0001c0001t0001g0038 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2194-1247A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114766 | |||||||
| chr3:170114971 | A | G | 1 | a0001c0001t0042g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2194-1452T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114971 | |||||||
| chr3:170115152 | T | C | 1 | a0001c0001t0009g0176 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2194-1633A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115152 | |||||||
| chr3:170115319 | AAGG | A | 46 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(43): Show |
47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.2194-1803_2194-180 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115319 | |||||||
| chr3:170115350 | ATATG | A | 5 | a0001c0001t0002g0277 a0001c0001t0003g0260 a0001c0001t0009g0112 others(2): Show |
5 | HG02486.hp1 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2194-1835_2194-183 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115350 | |||||||
| chr3:170115405 | A | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+1821T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115405 | |||||||
| chr3:170115459 | A | G | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2193+1767T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115459 | |||||||
| chr3:170115540 | T | C | 3 | a0001c0001t0016g0108 a0001c0001t0016g0109 a0001c0001t0016g0110 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2193+1686A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115540 | |||||||
| chr3:170115877 | T | TCA | 17 | a0001c0001t0002g0214 a0001c0001t0002g0243 a0001c0001t0002g0245 others(14): Show |
19 | HG01243.hp1 HG01884.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.2193+1347_2193+134 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | |||||||
| chr3:170115877 | T | TCACA | 9 | a0001c0001t0001g0087 a0001c0001t0006g0005 a0001c0001t0006g0140 others(6): Show |
9 | HG00741.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2193+1345_2193+134 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | |||||||
| chr3:170115877 | T | TCACACAC others(1): Show |
125 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.2193+1341_2193+134 others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | |||||||
| chr3:170115877 | T | TCACACAC others(3): Show |
34 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(31): Show |
34 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.2193+1339_2193+134 others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | |||||||
| chr3:170115877 | T | TCACACAC others(5): Show |
4 | a0001c0001t0001g0056 a0001c0001t0001g0111 a0001c0001t0013g0103 others(1): Show |
4 | HG01361.hp2 HG03098.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.2193+1337_2193+134 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | |||||||
| chr3:170115877 | T | TCACACAC others(9): Show |
3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2193+1333_2193+134 others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | |||||||
| chr3:170115877 | T | TCACACAC others(13): Show |
3 | a0001c0002t0005g0306 a0001c0002t0005g0307 a0001c0002t0005g0313 |
3 | HG00558.hp1 NA18975.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2193+1329_2193+134 others(24): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | |||||||
| chr3:170115877 | T | TCACACAC others(17): Show |
1 | a0001c0002t0005g0325 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2193+1325_2193+134 others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | |||||||
| chr3:170115877 | T | TCTCACAC others(5): Show |
1 | a0001c0001t0010g0021 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2193+1348_2193+134 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | |||||||
| chr3:170115877 | TCA | T | 16 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0309 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.2193+1347_2193+134 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | |||||||
| chr3:170115909 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+1317A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115909 | |||||||
| chr3:170116006 | A | C | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2193+1220T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116006 | |||||||
| chr3:170116069 | T | C | 7 | a0001c0001t0006g0005 a0001c0001t0006g0140 a0001c0001t0006g0188 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2193+1157A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116069 | |||||||
| chr3:170116111 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2193+1115C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116111 | |||||||
| chr3:170116132 | G | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(194): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.2193+1094C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116132 | |||||||
| chr3:170116319 | C | A | 1 | a0001c0003t0006g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2193+907G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116319 | |||||||
| chr3:170116320 | T | C | 25 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(22): Show |
25 | HG00673.hp1 HG01261.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.2193+906A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116320 | |||||||
| chr3:170116381 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+845A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116381 | |||||||
| chr3:170116486 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+740T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116486 | |||||||
| chr3:170116517 | A | C | 1 | a0001c0001t0004g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2193+709T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116517 | |||||||
| chr3:170116570 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2193+656T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116570 | |||||||
| chr3:170116654 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+572G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116654 | |||||||
| chr3:170116672 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+554T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116672 | |||||||
| chr3:170116720 | A | G | 323 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(320): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.2193+506T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116720 | |||||||
| chr3:170116806 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2193+420C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116806 | |||||||
| chr3:170116865 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+361G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116865 | |||||||
| chr3:170116909 | TA | T | 313 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(310): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.2193+316delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116909 | |||||||
| chr3:170117069 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2193+157A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170117069 | |||||||
| chr3:170117164 | G | A | 5 | a0001c0001t0014g0001 a0001c0001t0014g0186 a0001c0001t0017g0253 others(2): Show |
7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2193+62C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170117164 | |||||||
| chr3:170117479 | G | GA | 24 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0084 others(21): Show |
24 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.1943-4dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117479 | |||||||
| chr3:170117480 | A | G | 1 | a0001c0001t0003g0231 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.1943-4T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117480 | |||||||
| chr3:170117732 | G | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-256C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117732 | |||||||
| chr3:170117785 | G | GAGA | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-312_1943-310d others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117785 | |||||||
| chr3:170117832 | T | TA | 21 | a0001c0001t0039g0193 a0001c0002t0005g0304 a0001c0002t0005g0305 others(18): Show |
21 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1943-357dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117832 | |||||||
| chr3:170117843 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-367G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117843 | |||||||
| chr3:170117844 | C | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0013 |
2 | NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1943-368G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117844 | |||||||
| chr3:170117844 | C | CA | 9 | a0001c0001t0001g0050 a0001c0001t0002g0180 a0001c0001t0003g0261 others(6): Show |
9 | HG01175.hp1 HG01934.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1943-369dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117844 | |||||||
| chr3:170118337 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-861G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170118337 | |||||||
| chr3:170118344 | C | G | 4 | a0001c0001t0003g0178 a0001c0001t0003g0208 a0001c0001t0003g0209 others(1): Show |
4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943-868G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170118344 | |||||||
| chr3:170118434 | C | T | 3 | a0001c0001t0016g0108 a0001c0001t0016g0109 a0001c0001t0016g0110 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1943-958G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170118434 | |||||||
| chr3:170118562 | C | A | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1943-1086G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170118562 | |||||||
| chr3:170118575 | A | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-1099T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170118575 | |||||||
| chr3:170119021 | C | A | 2 | a0001c0003t0006g0292 a0001c0003t0006g0295 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1943-1545G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119021 | |||||||
| chr3:170119036 | T | TA | 49 | a0001c0001t0002g0241 a0001c0001t0003g0133 a0001c0001t0004g0006 others(46): Show |
50 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1943-1561dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119036 | |||||||
| chr3:170119036 | T | TAAA | 18 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(15): Show |
18 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.1943-1563_1943-156 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119036 | |||||||
| chr3:170119036 | TA | T | 17 | a0001c0001t0002g0117 a0001c0001t0002g0218 a0001c0001t0002g0250 others(14): Show |
17 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1943-1561delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119036 | |||||||
| chr3:170119432 | T | C | 7 | a0001c0001t0006g0005 a0001c0001t0006g0140 a0001c0001t0006g0188 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1943-1956A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119432 | |||||||
| chr3:170119627 | C | T | 1 | a0001c0001t0004g0163 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1943-2151G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119627 | |||||||
| chr3:170119711 | C | T | 2 | a0001c0001t0020g0086 a0001c0001t0020g0089 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1943-2235G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119711 | |||||||
| chr3:170119731 | C | T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1943-2255G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119731 | |||||||
| chr3:170119745 | T | C | 1 | a0001c0001t0004g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1943-2269A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119745 | |||||||
| chr3:170119756 | A | G | 4 | a0001c0001t0002g0117 a0001c0001t0002g0288 a0001c0001t0045g0287 others(1): Show |
4 | NA18959.hp2 NA18983.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1943-2280T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119756 | |||||||
| chr3:170119830 | T | TA | 55 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(52): Show |
56 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1943-2355dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119830 | |||||||
| chr3:170119830 | T | TAA | 7 | a0001c0001t0007g0125 a0001c0001t0013g0099 a0001c0001t0013g0101 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1943-2356_1943-235 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119830 | |||||||
| chr3:170119830 | T | TAAA | 9 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0016g0108 others(6): Show |
9 | HG00639.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1943-2357_1943-235 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119830 | |||||||
| chr3:170119830 | TA | T | 6 | a0001c0001t0003g0178 a0001c0001t0003g0210 a0001c0001t0031g0238 others(3): Show |
6 | HG02132.hp1 HG02145.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1943-2355delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119830 | |||||||
| chr3:170119844 | A | AAAG | 18 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(15): Show |
18 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.1943-2369_1943-236 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119844 | |||||||
| chr3:170119850 | C | T | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1943-2374G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119850 | |||||||
| chr3:170119907 | G | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-2431C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119907 | |||||||
| chr3:170119999 | A | G | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1943-2523T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119999 | |||||||
| chr3:170120212 | A | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(150): Show |
156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1942+2379T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120212 | |||||||
| chr3:170120415 | G | A | 14 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0013g0099 others(11): Show |
14 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1942+2176C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120415 | |||||||
| chr3:170120519 | G | A | 5 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1942+2072C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120519 | |||||||
| chr3:170120625 | T | C | 2 | a0001c0001t0001g0107 a0005c0010t0001g0106 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1942+1966A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120625 | |||||||
| chr3:170120943 | T | C | 1 | a0010c0006t0002g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1942+1648A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120943 | |||||||
| chr3:170120994 | C | T | 1 | a0001c0001t0012g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1942+1597G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120994 | |||||||
| chr3:170121082 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1942+1509T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121082 | |||||||
| chr3:170121317 | A | G | 1 | a0001c0001t0003g0267 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1942+1274T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121317 | |||||||
| chr3:170121318 | G | C | 1 | a0007c0007t0027g0322 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1942+1273C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121318 | |||||||
| chr3:170121430 | C | T | 2 | a0003c0005t0025g0323 a0003c0005t0026g0324 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1942+1161G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121430 | |||||||
| chr3:170121447 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1942+1144G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121447 | |||||||
| chr3:170121451 | G | C | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1942+1140C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121451 | |||||||
| chr3:170121540 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1942+1051A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121540 | |||||||
| chr3:170121719 | T | C | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1942+872A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121719 | |||||||
| chr3:170121806 | T | C | 1 | a0001c0001t0003g0232 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1942+785A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121806 | |||||||
| chr3:170121910 | T | C | 1 | a0001c0001t0002g0271 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1942+681A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121910 | |||||||
| chr3:170121992 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1942+599G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121992 | |||||||
| chr3:170122049 | T | C | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1942+542A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170122049 | |||||||
| chr3:170122303 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1942+288A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170122303 | |||||||
| chr3:170122540 | ATTAACAT | A | 4 | a0001c0001t0003g0178 a0001c0001t0003g0208 a0001c0001t0003g0209 others(1): Show |
4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1942+44_1942+50del others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170122540 | |||||||
| chr3:170122778 | T | G | 1 | a0001c0001t0003g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1789-34A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170122778 | |||||||
| chr3:170122826 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1789-82G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170122826 | |||||||
| chr3:170122861 | ACTACT | A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0085 a0001c0001t0003g0230 others(1): Show |
4 | HG01123.hp2 HG01192.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789-122_1789-118d others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170122861 | |||||||
| chr3:170122866 | TCTAA | T | 5 | a0001c0001t0002g0243 a0001c0001t0002g0245 a0001c0001t0002g0246 others(2): Show |
5 | NA18943.hp2 NA18944.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1789-126_1789-123d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170122866 | |||||||
| chr3:170122874 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1789-130T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170122874 | |||||||
| chr3:170123139 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1789-395C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123139 | |||||||
| chr3:170123263 | C | A | 1 | a0001c0003t0006g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1789-519G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123263 | |||||||
| chr3:170123356 | T | TACACACA others(1): Show |
97 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
99 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1789-620_1789-613d others(10): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | |||||||
| chr3:170123356 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0083 a0001c0001t0003g0230 |
2 | HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1789-622_1789-613d others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | |||||||
| chr3:170123356 | T | TACACACA others(5): Show |
107 | a0001c0001t0002g0120 a0001c0001t0002g0122 a0001c0001t0002g0123 others(104): Show |
109 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1789-624_1789-613d others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | |||||||
| chr3:170123356 | T | TACACACA others(7): Show |
27 | a0001c0001t0002g0117 a0001c0001t0002g0179 a0001c0001t0002g0288 others(24): Show |
27 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1789-626_1789-613d others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | |||||||
| chr3:170123356 | T | TACACACA others(9): Show |
8 | a0001c0001t0006g0005 a0001c0001t0006g0188 a0001c0001t0006g0189 others(5): Show |
8 | HG02109.hp1 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1789-628_1789-613d others(18): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | |||||||
| chr3:170123356 | T | TACACACA others(11): Show |
59 | a0001c0001t0002g0271 a0001c0001t0004g0006 a0001c0001t0004g0007 others(56): Show |
59 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1789-630_1789-613d others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | |||||||
| chr3:170123356 | T | TACACACA others(13): Show |
19 | a0001c0001t0004g0126 a0001c0001t0004g0164 a0001c0001t0004g0173 others(16): Show |
20 | HG00408.hp1 HG00423.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1789-613_1789-612i others(22): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | |||||||
| chr3:170123356 | T | TACACACA others(15): Show |
1 | a0003c0005t0026g0324 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1789-613_1789-612i others(24): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | |||||||
| chr3:170123356 | T | TACACACA others(19): Show |
1 | a0007c0007t0027g0322 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1789-613_1789-612i others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | |||||||
| chr3:170123645 | T | C | 1 | a0001c0001t0038g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1789-901A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123645 | |||||||
| chr3:170123772 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1789-1028T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123772 | |||||||
| chr3:170123836 | G | A | 6 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0016g0108 others(3): Show |
6 | HG02257.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1789-1092C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123836 | |||||||
| chr3:170123918 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1789-1174G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123918 | |||||||
| chr3:170124138 | G | A | 53 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(50): Show |
54 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1789-1394C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170124138 | |||||||
| chr3:170124196 | G | T | 1 | a0001c0001t0003g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1789-1452C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170124196 | |||||||
| chr3:170124439 | G | A | 6 | a0001c0001t0002g0128 a0001c0001t0002g0180 a0001c0001t0002g0218 others(3): Show |
6 | HG01943.hp2 HG01981.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789-1695C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170124439 | |||||||
| chr3:170124493 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1789-1749C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170124493 | |||||||
| chr3:170124838 | A | G | 10 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 others(7): Show |
10 | HG01175.hp1 HG01255.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1789-2094T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170124838 | |||||||
| chr3:170125007 | G | A | 1 | a0001c0001t0003g0198 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1789-2263C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125007 | |||||||
| chr3:170125130 | G | A | 1 | a0001c0001t0002g0246 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1789-2386C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125130 | |||||||
| chr3:170125130 | G | T | 4 | a0001c0001t0003g0178 a0001c0001t0003g0208 a0001c0001t0003g0209 others(1): Show |
4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789-2386C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125130 | |||||||
| chr3:170125380 | T | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1789-2636A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125380 | |||||||
| chr3:170125400 | T | C | 1 | a0001c0001t0002g0274 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1789-2656A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125400 | |||||||
| chr3:170125589 | AT | A | 2 | a0001c0001t0007g0004 a0001c0001t0007g0151 |
3 | HG01257.hp1 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1789-2846delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125589 | |||||||
| chr3:170125636 | C | T | 1 | a0001c0001t0003g0259 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1789-2892G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125636 | |||||||
| chr3:170125643 | A | G | 1 | a0001c0001t0004g0160 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1789-2899T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125643 | |||||||
| chr3:170125924 | A | G | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1788+2760T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125924 | |||||||
| chr3:170125925 | TA | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1788+2758delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125925 | |||||||
| chr3:170126053 | T | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1788+2631A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126053 | |||||||
| chr3:170126065 | A | C | 1 | a0001c0001t0002g0221 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1788+2619T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126065 | |||||||
| chr3:170126394 | G | A | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1788+2290C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126394 | |||||||
| chr3:170126468 | T | C | 1 | a0001c0001t0003g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1788+2216A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126468 | |||||||
| chr3:170126504 | G | GTA | 11 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0111 others(8): Show |
11 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.1788+2178_1788+217 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126504 | |||||||
| chr3:170126504 | G | GTATA | 4 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0032g0090 others(1): Show |
4 | HG00558.hp2 NA18946.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1788+2176_1788+217 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126504 | |||||||
| chr3:170126504 | G | GTATATAT others(21): Show |
2 | a0001c0001t0016g0108 a0001c0001t0016g0109 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1788+2179_1788+218 others(32): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126504 | |||||||
| chr3:170126504 | G | GTGTATAT others(17): Show |
1 | a0001c0001t0042g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1788+2179_1788+218 others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126504 | |||||||
| chr3:170126504 | GTA | G | 15 | a0001c0001t0003g0187 a0001c0001t0003g0226 a0001c0001t0003g0227 others(12): Show |
15 | HG00140.hp1 HG01081.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1788+2178_1788+217 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126504 | |||||||
| chr3:170126506 | A | G | 7 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1788+2178T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126506 | |||||||
| chr3:170126508 | A | G | 1 | a0001c0001t0003g0256 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1788+2176T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126508 | |||||||
| chr3:170126510 | A | G | 1 | a0007c0007t0027g0322 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1788+2174T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126510 | |||||||
| chr3:170126524 | A | T | 1 | a0001c0001t0033g0303 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1788+2160T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126524 | |||||||
| chr3:170126525 | TA | T | 14 | a0001c0001t0003g0257 a0001c0001t0003g0258 a0001c0001t0003g0260 others(11): Show |
14 | HG01256.hp1 HG01258.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1788+2158delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126525 | |||||||
| chr3:170126526 | A | T | 3 | a0001c0001t0006g0278 a0001c0001t0006g0279 a0001c0001t0033g0303 |
3 | HG00642.hp1 HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1788+2158T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126526 | |||||||
| chr3:170126527 | TA | T | 34 | a0001c0001t0002g0234 a0001c0001t0002g0241 a0001c0001t0003g0252 others(31): Show |
35 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1788+2156delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126527 | |||||||
| chr3:170126528 | A | AT | 15 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0002g0129 others(12): Show |
15 | HG00408.hp2 HG01175.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.1788+2155dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | ATAT | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(13): Show |
16 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1788+2155_1788+215 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | ATATATAT others(6): Show |
1 | a0001c0001t0036g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1788+2155_1788+215 others(17): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | ATATATAT others(20): Show |
3 | a0001c0001t0013g0101 a0001c0001t0013g0102 a0001c0001t0013g0103 |
3 | HG01167.hp1 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1788+2155_1788+215 others(31): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | ATATATAT others(21): Show |
1 | a0001c0001t0016g0110 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1788+2155_1788+215 others(32): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | ATATATAT others(26): Show |
1 | a0001c0001t0010g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1788+2155_1788+215 others(37): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | ATATATAT others(32): Show |
1 | a0001c0001t0040g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1788+2155_1788+215 others(43): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | ATATATAT others(5): Show |
1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1788+2155_1788+215 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | ATATT | 8 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(5): Show |
8 | HG01106.hp2 HG01256.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.1788+2155_1788+215 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | ATT | 24 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0040 others(21): Show |
24 | HG00673.hp1 HG01123.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1788+2154_1788+215 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | ATTT | 32 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(29): Show |
33 | HG00280.hp1 HG00438.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1788+2153_1788+215 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | A | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0055 others(26): Show |
29 | HG00642.hp1 HG01081.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1788+2156T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126528 | AT | A | 70 | a0001c0001t0002g0117 a0001c0001t0002g0120 a0001c0001t0002g0122 others(67): Show |
70 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1788+2155delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | |||||||
| chr3:170126529 | T | TA | 18 | a0001c0001t0002g0243 a0001c0001t0002g0245 a0001c0001t0002g0246 others(15): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1788+2154_1788+215 others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126529 | |||||||
| chr3:170126529 | T | TATATATA others(4): Show |
1 | a0001c0001t0050g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1788+2154_1788+215 others(15): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126529 | |||||||
| chr3:170126529 | T | TATATATA others(10): Show |
1 | a0001c0001t0013g0099 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1788+2154_1788+215 others(21): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126529 | |||||||
| chr3:170126530 | T | A | 19 | a0001c0001t0002g0284 a0001c0001t0003g0118 a0001c0001t0003g0202 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1788+2154A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126530 | |||||||
| chr3:170126531 | T | A | 20 | a0001c0001t0002g0122 a0001c0001t0002g0128 a0001c0001t0002g0130 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1788+2153A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126531 | |||||||
| chr3:170126533 | T | A | 2 | a0001c0001t0003g0178 a0001c0001t0003g0210 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1788+2151A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126533 | |||||||
| chr3:170126742 | T | C | 1 | a0008c0011t0002g0236 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1788+1942A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126742 | |||||||
| chr3:170126929 | TG | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1788+1754delC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126929 | |||||||
| chr3:170126930 | G | T | 79 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(76): Show |
80 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1788+1754C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126930 | |||||||
| chr3:170126953 | A | T | 1 | a0010c0006t0002g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1788+1731T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126953 | |||||||
| chr3:170127019 | T | C | 2 | a0001c0001t0029g0113 a0001c0001t0030g0114 |
2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1788+1665A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127019 | |||||||
| chr3:170127086 | T | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1788+1598A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127086 | |||||||
| chr3:170127136 | A | C | 1 | a0001c0001t0003g0202 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1788+1548T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127136 | |||||||
| chr3:170127145 | T | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(142): Show |
148 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.1788+1539A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127145 | |||||||
| chr3:170127166 | A | T | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1788+1518T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127166 | |||||||
| chr3:170127234 | T | G | 3 | a0001c0001t0007g0148 a0001c0001t0018g0169 a0006c0008t0018g0149 |
3 | HG02622.hp1 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1788+1450A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127234 | |||||||
| chr3:170127339 | T | C | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1788+1345A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127339 | |||||||
| chr3:170127382 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1788+1302C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127382 | |||||||
| chr3:170127386 | C | A | 1 | a0001c0001t0003g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1788+1298G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127386 | |||||||
| chr3:170127497 | G | A | 18 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0013g0099 others(15): Show |
18 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.1788+1187C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127497 | |||||||
| chr3:170127512 | C | CTT | 190 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1788+1171_1788+117 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127512 | |||||||
| chr3:170127711 | G | C | 1 | a0001c0001t0003g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1788+973C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127711 | |||||||
| chr3:170127816 | T | G | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1788+868A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127816 | |||||||
| chr3:170128097 | C | A | 5 | a0001c0001t0002g0243 a0001c0001t0002g0245 a0001c0001t0002g0246 others(2): Show |
5 | NA18943.hp2 NA18944.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1788+587G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128097 | |||||||
| chr3:170128097 | C | T | 1 | a0001c0001t0012g0097 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1788+587G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128097 | |||||||
| chr3:170128234 | A | C | 5 | a0001c0001t0002g0117 a0001c0001t0002g0288 a0001c0001t0031g0238 others(2): Show |
5 | HG02132.hp1 NA18959.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1788+450T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128234 | |||||||
| chr3:170128270 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1788+414C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128270 | |||||||
| chr3:170128272 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1788+412A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128272 | |||||||
| chr3:170128290 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1788+394G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128290 | |||||||
| chr3:170129705 | A | T | 1 | a0001c0001t0002g0184 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.920-153T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129705 | |||||||
| chr3:170129787 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-235G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129787 | |||||||
| chr3:170129841 | A | C | 1 | a0001c0001t0009g0176 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.920-289T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129841 | |||||||
| chr3:170129866 | A | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.920-314T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129866 | |||||||
| chr3:170129889 | G | A | 3 | a0001c0001t0016g0108 a0001c0001t0016g0109 a0001c0001t0016g0110 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.920-337C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129889 | |||||||
| chr3:170129901 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-349G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129901 | |||||||
| chr3:170129990 | C | T | 1 | a0001c0001t0007g0141 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.920-438G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129990 | |||||||
| chr3:170130039 | T | C | 1 | a0007c0007t0027g0322 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.920-487A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130039 | |||||||
| chr3:170130069 | T | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-517A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130069 | |||||||
| chr3:170130214 | T | C | 2 | a0001c0001t0029g0113 a0001c0001t0030g0114 |
2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.920-662A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130214 | |||||||
| chr3:170130292 | G | A | 1 | a0001c0001t0002g0283 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.920-740C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130292 | |||||||
| chr3:170130399 | T | C | 1 | a0001c0001t0031g0238 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.920-847A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130399 | |||||||
| chr3:170130514 | A | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-962T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130514 | |||||||
| chr3:170130566 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.920-1014A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130566 | |||||||
| chr3:170130602 | AT | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-1051delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130602 | |||||||
| chr3:170130884 | A | G | 1 | a0003c0005t0025g0323 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.920-1332T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130884 | |||||||
| chr3:170130943 | G | GA | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-1392dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130943 | |||||||
| chr3:170131002 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-1450T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131002 | |||||||
| chr3:170131116 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-1564C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131116 | |||||||
| chr3:170131145 | TA | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(196): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.920-1594delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131145 | |||||||
| chr3:170131145 | TAA | T | 95 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0046 others(92): Show |
96 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.920-1595_920-1594d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131145 | |||||||
| chr3:170131148 | A | T | 18 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(15): Show |
18 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.920-1596T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131148 | |||||||
| chr3:170131149 | A | T | 1 | a0001c0002t0005g0307 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.920-1597T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131149 | |||||||
| chr3:170131194 | TA | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-1643delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131194 | |||||||
| chr3:170131299 | T | TAACAAAA others(363): Show |
1 | a0001c0001t0010g0021 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.920-1748_920-1747i others(372): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131299 | |||||||
| chr3:170131308 | C | A | 8 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(5): Show |
8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-1756G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131308 | |||||||
| chr3:170131324 | G | A | 2 | a0001c0001t0011g0205 a0001c0001t0011g0281 |
2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.920-1772C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131324 | |||||||
| chr3:170131618 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.920-2066C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131618 | |||||||
| chr3:170131691 | G | A | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-2139C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131691 | |||||||
| chr3:170131735 | G | A | 1 | a0001c0001t0051g0159 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.920-2183C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131735 | |||||||
| chr3:170131963 | G | A | 1 | a0001c0001t0038g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.920-2411C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131963 | |||||||
| chr3:170131974 | G | C | 5 | a0001c0001t0014g0001 a0001c0001t0014g0186 a0001c0001t0017g0253 others(2): Show |
7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.920-2422C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131974 | |||||||
| chr3:170132082 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-2530C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132082 | |||||||
| chr3:170132082 | G | GA | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.920-2531dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132082 | |||||||
| chr3:170132183 | CAT | C | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.920-2633_920-2632d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132183 | |||||||
| chr3:170132301 | G | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-2749C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132301 | |||||||
| chr3:170132392 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-2840G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132392 | |||||||
| chr3:170132524 | A | C | 1 | a0001c0001t0036g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.920-2972T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132524 | |||||||
| chr3:170132660 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-3108C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132660 | |||||||
| chr3:170132709 | C | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0119 |
3 | NA18992.hp1 NA19066.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.920-3157G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132709 | |||||||
| chr3:170132748 | G | A | 7 | a0001c0002t0005g0304 a0001c0002t0005g0310 a0001c0002t0005g0311 others(4): Show |
7 | HG00408.hp1 HG00423.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-3196C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132748 | |||||||
| chr3:170132839 | A | C | 1 | a0001c0001t0037g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.920-3287T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132839 | |||||||
| chr3:170133112 | A | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+3307T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133112 | |||||||
| chr3:170133159 | A | G | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.919+3260T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133159 | |||||||
| chr3:170133182 | CT | C | 9 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(6): Show |
9 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+3236delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133182 | |||||||
| chr3:170133323 | A | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+3096T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133323 | |||||||
| chr3:170133368 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0002g0277 |
2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.919+3051C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133368 | |||||||
| chr3:170133384 | G | C | 1 | a0001c0002t0005g0309 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.919+3035C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133384 | |||||||
| chr3:170133441 | T | C | 1 | a0001c0001t0036g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.919+2978A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133441 | |||||||
| chr3:170133651 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.919+2768A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133651 | |||||||
| chr3:170133803 | G | A | 3 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 |
3 | HG02622.hp2 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.919+2616C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133803 | |||||||
| chr3:170133817 | A | T | 67 | a0001c0001t0002g0117 a0001c0001t0002g0120 a0001c0001t0002g0122 others(64): Show |
67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.919+2602T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133817 | |||||||
| chr3:170133864 | C | T | 2 | a0001c0001t0029g0113 a0001c0001t0030g0114 |
2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.919+2555G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133864 | |||||||
| chr3:170134079 | C | T | 1 | a0001c0001t0047g0244 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.919+2340G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170134079 | |||||||
| chr3:170134379 | G | A | 1 | a0001c0001t0012g0290 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.919+2040C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170134379 | |||||||
| chr3:170134512 | C | T | 7 | a0001c0003t0006g0292 a0001c0003t0006g0293 a0001c0003t0006g0294 others(4): Show |
7 | HG01433.hp1 HG02055.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+1907G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170134512 | |||||||
| chr3:170135082 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.919+1337A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135082 | |||||||
| chr3:170135111 | C | T | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.919+1308G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135111 | |||||||
| chr3:170135137 | T | A | 1 | a0001c0001t0002g0247 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.919+1282A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135137 | |||||||
| chr3:170135139 | TTTTG | T | 7 | a0001c0001t0003g0178 a0001c0001t0003g0208 a0001c0001t0003g0209 others(4): Show |
7 | HG02145.hp1 HG02630.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+1276_919+1279d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135139 | |||||||
| chr3:170135139 | TTTTGTTT others(1): Show |
T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+1272_919+1279d others(10): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135139 | |||||||
| chr3:170135253 | T | C | 1 | a0001c0001t0044g0296 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.919+1166A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135253 | |||||||
| chr3:170135343 | T | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+1076A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135343 | |||||||
| chr3:170135421 | G | A | 15 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0013g0099 others(12): Show |
15 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+998C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135421 | |||||||
| chr3:170135453 | A | AT | 100 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.919+965dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135453 | |||||||
| chr3:170135488 | A | T | 1 | a0001c0001t0029g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.919+931T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135488 | |||||||
| chr3:170135506 | T | TA | 15 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0013g0099 others(12): Show |
15 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+912dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135506 | |||||||
| chr3:170135512 | T | TACACAC | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+901_919+906dup others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135512 | |||||||
| chr3:170135654 | TACTA | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(12): Show |
15 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.919+761_919+764del others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135654 | |||||||
| chr3:170135747 | CT | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+671delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135747 | |||||||
| chr3:170135808 | A | G | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.919+611T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135808 | |||||||
| chr3:170135851 | G | C | 1 | a0001c0001t0021g0008 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.919+568C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135851 | |||||||
| chr3:170135975 | GACA | G | 15 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0013g0099 others(12): Show |
15 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+441_919+443del others(3): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135975 | |||||||
| chr3:170136031 | T | G | 1 | a0001c0001t0002g0179 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.919+388A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136031 | |||||||
| chr3:170136155 | T | C | 1 | a0001c0001t0006g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.919+264A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136155 | |||||||
| chr3:170136210 | A | T | 2 | a0001c0001t0002g0130 a0001c0001t0002g0214 |
2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.919+209T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136210 | |||||||
| chr3:170136252 | CT | C | 3 | a0002c0004t0011g0063 a0002c0004t0011g0064 a0002c0004t0011g0195 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.919+166delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136252 | |||||||
| chr3:170136289 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+130C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136289 | |||||||
| chr3:170136413 | T | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0043 |
2 | NA18940.hp1 NA19091.hp1 |
splice_region_variant&intron_variant | LOW | c.919+6A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136413 | |||||||
| chr3:170136796 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.673-131T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170136796 | |||||||
| chr3:170136808 | A | G | 1 | a0001c0001t0004g0158 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.673-143T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170136808 | |||||||
| chr3:170136883 | T | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(150): Show |
156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.673-218A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170136883 | |||||||
| chr3:170136977 | A | G | 5 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(2): Show |
5 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-312T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170136977 | |||||||
| chr3:170137208 | G | GT | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.673-544dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170137208 | |||||||
| chr3:170137438 | G | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-773C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170137438 | |||||||
| chr3:170137450 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.673-785C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170137450 | |||||||
| chr3:170137562 | A | G | 1 | a0001c0001t0003g0259 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.673-897T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170137562 | |||||||
| chr3:170137641 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-976G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170137641 | |||||||
| chr3:170138152 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-1487C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138152 | |||||||
| chr3:170138227 | A | T | 2 | a0001c0001t0004g0153 a0001c0001t0004g0161 |
2 | NA18943.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.673-1562T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138227 | |||||||
| chr3:170138306 | G | A | 6 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-1641C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138306 | |||||||
| chr3:170138412 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-1747G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138412 | |||||||
| chr3:170138539 | AATTAGCC others(2): Show |
A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-1883_673-1875d others(11): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138539 | |||||||
| chr3:170138586 | A | G | 1 | a0001c0001t0001g0011 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.673-1921T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138586 | |||||||
| chr3:170138597 | G | A | 1 | a0001c0002t0005g0306 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.673-1932C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138597 | |||||||
| chr3:170138689 | C | CA | 15 | a0001c0001t0002g0129 a0001c0001t0002g0183 a0001c0001t0002g0184 others(12): Show |
15 | HG00609.hp1 HG02040.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.673-2025dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138689 | |||||||
| chr3:170138689 | CA | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(168): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.673-2025delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138689 | |||||||
| chr3:170138689 | CAA | C | 13 | a0001c0001t0004g0162 a0001c0001t0006g0188 a0001c0001t0012g0066 others(10): Show |
13 | HG00438.hp1 HG01433.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.673-2026_673-2025d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138689 | |||||||
| chr3:170138776 | G | A | 1 | a0001c0001t0050g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.673-2111C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138776 | |||||||
| chr3:170138886 | A | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-2221T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138886 | |||||||
| chr3:170138915 | A | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-2250T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138915 | |||||||
| chr3:170138965 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0289 |
2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.673-2300A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138965 | |||||||
| chr3:170139000 | G | A | 1 | a0001c0001t0011g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.673-2335C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139000 | |||||||
| chr3:170139189 | A | G | 7 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(4): Show |
7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-2524T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139189 | |||||||
| chr3:170139199 | G | GACTTAAT others(3): Show |
1 | a0001c0001t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.673-2535_673-2534i others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139199 | |||||||
| chr3:170139201 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.673-2536A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139201 | |||||||
| chr3:170139202 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.673-2537G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139202 | |||||||
| chr3:170139219 | C | T | 306 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(303): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.673-2554G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139219 | |||||||
| chr3:170139564 | G | C | 1 | a0001c0001t0001g0011 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.673-2899C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139564 | |||||||
| chr3:170139702 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.673-3037A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139702 | |||||||
| chr3:170140216 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0045 others(4): Show |
7 | HG01433.hp2 HG02300.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.673-3551A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140216 | |||||||
| chr3:170140222 | A | G | 1 | a0009c0009t0001g0020 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.673-3557T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140222 | |||||||
| chr3:170140440 | G | A | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.673-3775C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140440 | |||||||
| chr3:170140451 | G | A | 3 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0264 |
3 | HG01175.hp1 HG01934.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.673-3786C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140451 | |||||||
| chr3:170140582 | T | C | 1 | a0001c0001t0003g0231 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.673-3917A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140582 | |||||||
| chr3:170140584 | C | CT | 34 | a0001c0001t0001g0026 a0001c0001t0002g0185 a0001c0001t0002g0191 others(31): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.673-3920dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140584 | |||||||
| chr3:170140584 | CT | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
97 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.673-3920delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140584 | |||||||
| chr3:170140584 | CTT | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0085 a0001c0001t0001g0105 others(9): Show |
12 | HG00639.hp1 HG01256.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.673-3921_673-3920d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140584 | |||||||
| chr3:170140584 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0002g0213 a0001c0001t0002g0285 |
2 | HG00609.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.673-3932_673-3920d others(15): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140584 | |||||||
| chr3:170140587 | T | C | 7 | a0001c0001t0006g0005 a0001c0001t0006g0140 a0001c0001t0006g0188 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.673-3922A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140587 | |||||||
| chr3:170140619 | A | T | 1 | a0001c0001t0001g0055 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.673-3954T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140619 | |||||||
| chr3:170140627 | C | T | 306 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(303): Show |
311 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.673-3962G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140627 | |||||||
| chr3:170140645 | C | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-3980G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140645 | |||||||
| chr3:170140650 | G | A | 1 | a0001c0001t0036g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.673-3985C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140650 | |||||||
| chr3:170140687 | G | A | 1 | a0001c0001t0003g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.673-4022C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140687 | |||||||
| chr3:170140703 | C | T | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.673-4038G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140703 | |||||||
| chr3:170140730 | G | A | 1 | a0001c0001t0003g0261 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.673-4065C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140730 | |||||||
| chr3:170140925 | C | T | 1 | a0006c0008t0018g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.673-4260G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140925 | |||||||
| chr3:170141015 | A | G | 2 | a0001c0001t0007g0004 a0001c0001t0007g0151 |
3 | HG01257.hp1 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.673-4350T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141015 | |||||||
| chr3:170141286 | T | C | 5 | a0001c0001t0014g0001 a0001c0001t0014g0186 a0001c0001t0017g0253 others(2): Show |
7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+4137A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141286 | |||||||
| chr3:170141370 | C | G | 5 | a0001c0001t0014g0001 a0001c0001t0014g0186 a0001c0001t0017g0253 others(2): Show |
7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+4053G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141370 | |||||||
| chr3:170141505 | T | C | 1 | a0001c0001t0029g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672+3918A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141505 | |||||||
| chr3:170141768 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.672+3655G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141768 | |||||||
| chr3:170141792 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+3631A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141792 | |||||||
| chr3:170141902 | C | G | 4 | a0001c0001t0003g0118 a0001c0001t0003g0196 a0001c0001t0003g0200 others(1): Show |
4 | HG00438.hp2 NA18959.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+3521G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141902 | |||||||
| chr3:170142082 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+3341A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142082 | |||||||
| chr3:170142099 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.672+3324G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142099 | |||||||
| chr3:170142451 | C | T | 48 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(45): Show |
49 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.672+2972G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142451 | |||||||
| chr3:170142661 | G | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+2762C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142661 | |||||||
| chr3:170142744 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+2679A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142744 | |||||||
| chr3:170142912 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+2511T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142912 | |||||||
| chr3:170143378 | A | T | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.672+2045T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143378 | |||||||
| chr3:170143505 | AT | A | 19 | a0001c0001t0003g0118 a0001c0001t0003g0178 a0001c0001t0003g0196 others(16): Show |
19 | HG00438.hp2 HG01884.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.672+1917delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143505 | |||||||
| chr3:170143533 | A | G | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.672+1890T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143533 | |||||||
| chr3:170143570 | C | T | 193 | a0001c0001t0002g0117 a0001c0001t0002g0120 a0001c0001t0002g0122 others(190): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.672+1853G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143570 | |||||||
| chr3:170143804 | T | C | 1 | a0007c0007t0027g0322 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.672+1619A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143804 | |||||||
| chr3:170143807 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+1616A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143807 | |||||||
| chr3:170143969 | G | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+1454C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143969 | |||||||
| chr3:170143993 | T | C | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.672+1430A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143993 | |||||||
| chr3:170144145 | C | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+1278G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144145 | |||||||
| chr3:170144158 | T | TA | 55 | a0001c0001t0001g0105 a0001c0001t0001g0289 a0001c0001t0004g0006 others(52): Show |
56 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.672+1264dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144158 | |||||||
| chr3:170144159 | A | C | 1 | a0003c0005t0025g0323 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.672+1264T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144159 | |||||||
| chr3:170144169 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.672+1254T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144169 | |||||||
| chr3:170144201 | C | T | 1 | a0001c0001t0034g0025 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.672+1222G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144201 | |||||||
| chr3:170144202 | G | A | 7 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(4): Show |
7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.672+1221C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144202 | |||||||
| chr3:170144297 | T | C | 7 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(4): Show |
7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.672+1126A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144297 | |||||||
| chr3:170144308 | T | C | 2 | a0003c0005t0025g0323 a0003c0005t0026g0324 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.672+1115A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144308 | |||||||
| chr3:170144341 | CA | C | 6 | a0001c0001t0002g0274 a0001c0001t0003g0267 a0001c0001t0007g0194 others(3): Show |
6 | HG00639.hp1 HG01168.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.672+1081delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144341 | |||||||
| chr3:170144478 | G | A | 2 | a0002c0004t0011g0063 a0002c0004t0011g0064 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.672+945C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144478 | |||||||
| chr3:170144691 | G | A | 1 | a0001c0001t0030g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.672+732C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144691 | |||||||
| chr3:170144711 | T | C | 1 | a0007c0007t0027g0322 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.672+712A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144711 | |||||||
| chr3:170144810 | ATCC | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+610_672+612del others(3): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144810 | |||||||
| chr3:170144896 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+527G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144896 | |||||||
| chr3:170145042 | C | A | 1 | a0001c0001t0007g0194 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.672+381G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170145042 | |||||||
| chr3:170145150 | G | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+273C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170145150 | |||||||
| chr3:170145346 | A | C | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.672+77T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170145346 | |||||||
| chr3:170145822 | C | T | 1 | a0001c0002t0005g0321 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.574-301G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170145822 | |||||||
| chr3:170145879 | G | GAAGTTA | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.574-359_574-358ins others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170145879 | |||||||
| chr3:170146100 | C | T | 3 | a0001c0001t0016g0108 a0001c0001t0016g0109 a0001c0001t0016g0110 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.574-579G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146100 | |||||||
| chr3:170146101 | G | A | 1 | a0001c0001t0003g0256 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.574-580C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146101 | |||||||
| chr3:170146308 | G | A | 48 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(45): Show |
49 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.574-787C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146308 | |||||||
| chr3:170146366 | C | A | 48 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(45): Show |
49 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.574-845G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146366 | |||||||
| chr3:170146535 | C | CT | 12 | a0001c0001t0002g0122 a0001c0001t0002g0183 a0001c0001t0002g0239 others(9): Show |
12 | HG00280.hp2 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-1015dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146535 | |||||||
| chr3:170146535 | CT | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(157): Show |
163 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.574-1015delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146535 | |||||||
| chr3:170146767 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.574-1246T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146767 | |||||||
| chr3:170146869 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.574-1348A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146869 | |||||||
| chr3:170146877 | C | CT | 12 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0055 others(9): Show |
12 | HG00735.hp1 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-1357dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146877 | |||||||
| chr3:170146877 | CT | C | 30 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0093 others(27): Show |
30 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.574-1357delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146877 | |||||||
| chr3:170146877 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0016g0108 a0001c0001t0016g0109 a0001c0001t0016g0110 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.574-1369_574-1357d others(15): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146877 | |||||||
| chr3:170146943 | C | A | 1 | a0001c0001t0003g0118 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.574-1422G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146943 | |||||||
| chr3:170147096 | C | T | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.574-1575G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147096 | |||||||
| chr3:170147278 | T | C | 1 | a0001c0001t0036g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-1757A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147278 | |||||||
| chr3:170147282 | A | T | 1 | a0001c0001t0010g0094 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.574-1761T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147282 | |||||||
| chr3:170147359 | T | TA | 50 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(47): Show |
51 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.573+1726dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147359 | |||||||
| chr3:170147376 | G | C | 5 | a0001c0001t0002g0243 a0001c0001t0002g0245 a0001c0001t0002g0246 others(2): Show |
5 | NA18943.hp2 NA18944.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+1710C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147376 | |||||||
| chr3:170147554 | CTTG | C | 3 | a0001c0001t0016g0108 a0001c0001t0016g0109 a0001c0001t0016g0110 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.573+1529_573+1531d others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147554 | |||||||
| chr3:170147631 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.573+1455G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147631 | |||||||
| chr3:170147634 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.573+1452A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147634 | |||||||
| chr3:170147863 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.573+1223G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147863 | |||||||
| chr3:170147950 | T | C | 5 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(2): Show |
5 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+1136A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147950 | |||||||
| chr3:170148061 | G | A | 1 | a0001c0001t0002g0243 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.573+1025C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148061 | |||||||
| chr3:170148121 | T | C | 7 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(4): Show |
7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.573+965A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148121 | |||||||
| chr3:170148225 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(189): Show |
195 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.573+861A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148225 | |||||||
| chr3:170148226 | G | A | 3 | a0001c0001t0016g0108 a0001c0001t0016g0109 a0001c0001t0016g0110 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.573+860C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148226 | |||||||
| chr3:170148278 | TAAC | T | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.573+805_573+807del others(3): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148278 | |||||||
| chr3:170148617 | T | C | 1 | a0001c0001t0003g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.573+469A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148617 | |||||||
| chr3:170148836 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.573+250G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148836 | |||||||
| chr3:170148843 | G | T | 1 | a0001c0001t0009g0175 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.573+243C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148843 | |||||||
| chr3:170148884 | T | C | 1 | a0001c0001t0003g0266 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.573+202A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148884 | |||||||
| chr3:170149008 | CTT | C | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.573+76_573+77delAA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170149008 | |||||||
| chr3:170149024 | A | T | 19 | a0001c0001t0003g0118 a0001c0001t0003g0178 a0001c0001t0003g0196 others(16): Show |
19 | HG00438.hp2 HG01884.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.573+62T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170149024 | |||||||
| chr3:170149472 | A | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
121 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.415-228T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149472 | |||||||
| chr3:170149517 | C | T | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415-273G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149517 | |||||||
| chr3:170149529 | A | G | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-285T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149529 | |||||||
| chr3:170149608 | C | T | 1 | a0001c0001t0008g0069 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.415-364G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149608 | |||||||
| chr3:170149676 | G | A | 42 | a0001c0001t0002g0130 a0001c0001t0004g0006 a0001c0001t0004g0007 others(39): Show |
43 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.415-432C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149676 | |||||||
| chr3:170149714 | C | T | 1 | a0003c0005t0026g0324 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.415-470G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149714 | |||||||
| chr3:170149778 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0024g0237 |
2 | HG02015.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.415-534T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149778 | |||||||
| chr3:170149856 | C | T | 7 | a0001c0001t0006g0005 a0001c0001t0006g0140 a0001c0001t0006g0188 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-612G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149856 | |||||||
| chr3:170149956 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-712T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149956 | |||||||
| chr3:170149985 | A | G | 1 | a0001c0013t0002g0212 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.415-741T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149985 | |||||||
| chr3:170150182 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-938G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150182 | |||||||
| chr3:170150200 | T | A | 1 | a0001c0002t0005g0325 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.415-956A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150200 | |||||||
| chr3:170150201 | T | C | 1 | a0001c0001t0003g0291 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.415-957A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150201 | |||||||
| chr3:170150231 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
121 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.415-987G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150231 | |||||||
| chr3:170150245 | A | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-1001T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150245 | |||||||
| chr3:170150247 | G | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-1003C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150247 | |||||||
| chr3:170150471 | G | A | 4 | a0001c0003t0006g0292 a0001c0003t0006g0293 a0001c0003t0006g0294 others(1): Show |
4 | HG02976.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1227C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150471 | |||||||
| chr3:170150531 | T | TA | 12 | a0001c0001t0002g0183 a0001c0001t0002g0185 a0001c0001t0002g0283 others(9): Show |
12 | HG02080.hp1 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-1288dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | |||||||
| chr3:170150531 | T | TAAAAAAA others(3): Show |
65 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.415-1297_415-1288d others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | |||||||
| chr3:170150531 | T | TAAAAAAA others(4): Show |
35 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0027 others(32): Show |
35 | HG00597.hp2 HG01109.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.415-1298_415-1288d others(13): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | |||||||
| chr3:170150531 | T | TAAAAAAA others(5): Show |
13 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0010g0029 others(10): Show |
13 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-1299_415-1288d others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | |||||||
| chr3:170150531 | T | TAAAAAAA others(6): Show |
3 | a0001c0001t0001g0107 a0001c0001t0040g0031 a0005c0010t0001g0106 |
3 | HG02257.hp1 HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.415-1300_415-1288d others(15): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | |||||||
| chr3:170150531 | TA | T | 19 | a0001c0001t0002g0117 a0001c0001t0002g0131 a0001c0001t0002g0240 others(16): Show |
19 | HG01168.hp1 HG01433.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.415-1288delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | |||||||
| chr3:170150555 | T | A | 1 | a0011c0012t0004g0172 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.415-1311A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150555 | |||||||
| chr3:170150555 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-1311A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150555 | |||||||
| chr3:170150557 | A | T | 1 | a0011c0012t0004g0172 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.415-1313T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150557 | |||||||
| chr3:170150637 | T | C | 1 | a0001c0001t0018g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.415-1393A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150637 | |||||||
| chr3:170150691 | C | T | 2 | a0001c0003t0006g0293 a0001c0003t0006g0294 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.415-1447G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150691 | |||||||
| chr3:170150719 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-1475C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150719 | |||||||
| chr3:170150817 | T | C | 1 | a0001c0001t0009g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.415-1573A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150817 | |||||||
| chr3:170150932 | G | T | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.415-1688C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150932 | |||||||
| chr3:170150949 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-1705G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150949 | |||||||
| chr3:170150996 | A | G | 2 | a0001c0001t0002g0239 a0001c0001t0002g0247 |
2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.415-1752T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150996 | |||||||
| chr3:170151016 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.415-1772C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151016 | |||||||
| chr3:170151055 | A | G | 7 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0258 others(4): Show |
7 | HG01255.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-1811T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151055 | |||||||
| chr3:170151061 | A | C | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.415-1817T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151061 | |||||||
| chr3:170151303 | T | A | 1 | a0001c0001t0002g0221 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.415-2059A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151303 | |||||||
| chr3:170151335 | T | C | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-2091A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151335 | |||||||
| chr3:170151368 | T | C | 2 | a0001c0001t0001g0107 a0005c0010t0001g0106 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.415-2124A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151368 | |||||||
| chr3:170151384 | T | C | 1 | a0001c0001t0012g0290 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.415-2140A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151384 | |||||||
| chr3:170151743 | G | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(120): Show |
125 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.415-2499C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151743 | |||||||
| chr3:170152337 | A | AT | 42 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0033 others(39): Show |
43 | HG00597.hp1 HG00609.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.415-3094dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152337 | |||||||
| chr3:170152337 | A | ATT | 6 | a0001c0001t0002g0277 a0001c0001t0004g0138 a0001c0001t0007g0151 others(3): Show |
6 | HG01346.hp1 HG01433.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-3095_415-3094d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152337 | |||||||
| chr3:170152337 | A | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0060 |
3 | NA19065.hp1 NA19074.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.415-3093T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152337 | |||||||
| chr3:170152337 | AT | A | 26 | a0001c0001t0002g0183 a0001c0001t0006g0005 a0001c0001t0006g0188 others(23): Show |
26 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.415-3094delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152337 | |||||||
| chr3:170152385 | A | C | 1 | a0001c0001t0003g0256 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.415-3141T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152385 | |||||||
| chr3:170152427 | C | G | 1 | a0001c0002t0005g0319 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.415-3183G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152427 | |||||||
| chr3:170152564 | A | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-3320T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152564 | |||||||
| chr3:170152573 | A | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-3329T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152573 | |||||||
| chr3:170152677 | T | C | 5 | a0001c0001t0003g0187 a0001c0001t0003g0232 a0001c0001t0003g0266 others(2): Show |
5 | HG01081.hp1 HG01361.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-3433A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152677 | |||||||
| chr3:170152861 | CATGT | C | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-3621_415-3618d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152861 | |||||||
| chr3:170152867 | G | A | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-3623C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152867 | |||||||
| chr3:170152868 | C | CAA | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-3625_415-3624i others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152868 | |||||||
| chr3:170152877 | G | C | 1 | a0001c0001t0001g0299 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.415-3633C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152877 | |||||||
| chr3:170153032 | C | T | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415-3788G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153032 | |||||||
| chr3:170153123 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-3879A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153123 | |||||||
| chr3:170153321 | T | G | 2 | a0003c0005t0025g0323 a0003c0005t0026g0324 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.415-4077A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153321 | |||||||
| chr3:170153356 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-4112G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153356 | |||||||
| chr3:170153444 | G | A | 1 | a0001c0001t0004g0136 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.415-4200C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153444 | |||||||
| chr3:170153530 | G | A | 15 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0309 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.415-4286C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153530 | |||||||
| chr3:170153539 | G | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(96): Show |
101 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.415-4295C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153539 | |||||||
| chr3:170153595 | C | G | 31 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0127 others(28): Show |
32 | HG00597.hp1 HG00609.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.415-4351G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153595 | |||||||
| chr3:170153622 | G | A | 1 | a0001c0001t0018g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.415-4378C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153622 | |||||||
| chr3:170153653 | C | T | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-4409G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153653 | |||||||
| chr3:170153655 | C | A | 1 | a0001c0001t0002g0217 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.415-4411G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153655 | |||||||
| chr3:170153672 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.415-4428T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153672 | |||||||
| chr3:170153680 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.415-4436C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153680 | |||||||
| chr3:170153719 | C | T | 1 | a0001c0001t0008g0069 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.415-4475G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153719 | |||||||
| chr3:170153762 | C | CA | 106 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.415-4519dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153762 | |||||||
| chr3:170153804 | CT | C | 3 | a0001c0001t0001g0035 a0001c0001t0020g0086 a0001c0001t0020g0089 |
3 | HG03239.hp1 HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.415-4561delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153804 | |||||||
| chr3:170153839 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-4595G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153839 | |||||||
| chr3:170153914 | G | A | 1 | a0010c0006t0002g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.415-4670C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153914 | |||||||
| chr3:170153994 | C | G | 2 | a0001c0001t0002g0213 a0001c0001t0002g0285 |
2 | HG00609.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.415-4750G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153994 | |||||||
| chr3:170154359 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.415-5115G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154359 | |||||||
| chr3:170154428 | T | A | 1 | a0001c0001t0003g0199 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.415-5184A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154428 | |||||||
| chr3:170154459 | CAGTA | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-5219_415-5216d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154459 | |||||||
| chr3:170154543 | T | C | 1 | a0001c0001t0043g0276 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.415-5299A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154543 | |||||||
| chr3:170154560 | A | T | 1 | a0001c0001t0024g0273 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.415-5316T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154560 | |||||||
| chr3:170154587 | T | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-5343A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154587 | |||||||
| chr3:170154638 | G | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-5394C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154638 | |||||||
| chr3:170154712 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.415-5468A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154712 | |||||||
| chr3:170154811 | G | T | 2 | a0001c0001t0004g0164 a0001c0001t0004g0173 |
2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.415-5567C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154811 | |||||||
| chr3:170154961 | A | G | 1 | a0001c0001t0049g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.415-5717T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154961 | |||||||
| chr3:170155013 | T | C | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415-5769A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155013 | |||||||
| chr3:170155024 | A | G | 1 | a0001c0001t0003g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.415-5780T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155024 | |||||||
| chr3:170155046 | C | T | 48 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(45): Show |
49 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.415-5802G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155046 | |||||||
| chr3:170155142 | A | G | 2 | a0003c0005t0025g0323 a0003c0005t0026g0324 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.415-5898T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155142 | |||||||
| chr3:170155282 | A | G | 2 | a0001c0001t0004g0150 a0011c0012t0004g0172 |
2 | NA18944.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.415-6038T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155282 | |||||||
| chr3:170155461 | C | T | 1 | a0001c0001t0004g0137 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.415-6217G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155461 | |||||||
| chr3:170155501 | G | A | 2 | a0003c0005t0025g0323 a0003c0005t0026g0324 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.415-6257C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155501 | |||||||
| chr3:170155618 | C | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(186): Show |
192 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.415-6374G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155618 | |||||||
| chr3:170155631 | A | AG | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-6388dupC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155631 | |||||||
| chr3:170155682 | C | A | 1 | a0010c0006t0002g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.415-6438G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155682 | |||||||
| chr3:170156201 | T | C | 2 | a0001c0001t0001g0107 a0005c0010t0001g0106 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.415-6957A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156201 | |||||||
| chr3:170156441 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.415-7197C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156441 | |||||||
| chr3:170156504 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-7260C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156504 | |||||||
| chr3:170156609 | T | G | 1 | a0008c0011t0002g0236 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.415-7365A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156609 | |||||||
| chr3:170156717 | C | A | 2 | a0001c0001t0010g0029 a0001c0001t0010g0030 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-7473G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156717 | |||||||
| chr3:170156846 | C | T | 40 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(37): Show |
41 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.415-7602G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156846 | |||||||
| chr3:170156859 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.415-7615A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156859 | |||||||
| chr3:170156884 | C | T | 1 | a0001c0001t0038g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415-7640G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156884 | |||||||
| chr3:170157028 | A | G | 1 | a0001c0001t0002g0179 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.415-7784T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157028 | |||||||
| chr3:170157180 | T | C | 41 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(38): Show |
42 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.415-7936A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157180 | |||||||
| chr3:170157378 | T | A | 1 | a0001c0001t0051g0159 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.415-8134A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157378 | |||||||
| chr3:170157457 | G | A | 1 | a0001c0001t0004g0166 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.415-8213C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157457 | |||||||
| chr3:170157578 | A | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-8334T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157578 | |||||||
| chr3:170157601 | A | T | 1 | a0001c0001t0001g0041 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.415-8357T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157601 | |||||||
| chr3:170157927 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-8683G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157927 | |||||||
| chr3:170157942 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.415-8698G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157942 | |||||||
| chr3:170158150 | G | A | 7 | a0001c0001t0006g0005 a0001c0001t0006g0140 a0001c0001t0006g0188 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-8906C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158150 | |||||||
| chr3:170158202 | A | G | 1 | a0001c0001t0036g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.415-8958T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158202 | |||||||
| chr3:170158203 | T | G | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415-8959A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158203 | |||||||
| chr3:170158480 | T | C | 4 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 others(1): Show |
4 | NA18747.hp1 NA18942.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-9236A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158480 | |||||||
| chr3:170158499 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-9255C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158499 | |||||||
| chr3:170158560 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-9316T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158560 | |||||||
| chr3:170158626 | G | GA | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.415-9383dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158626 | |||||||
| chr3:170158666 | C | T | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415-9422G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158666 | |||||||
| chr3:170158673 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-9429G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158673 | |||||||
| chr3:170158708 | C | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-9464G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158708 | |||||||
| chr3:170158927 | G | GA | 31 | a0001c0001t0004g0134 a0001c0001t0004g0135 a0001c0001t0004g0144 others(28): Show |
31 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.415-9684dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158927 | |||||||
| chr3:170158970 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-9726C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158970 | |||||||
| chr3:170158977 | C | T | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.415-9733G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158977 | |||||||
| chr3:170159129 | C | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG00280.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.415-9885G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159129 | |||||||
| chr3:170159164 | CG | C | 6 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 others(3): Show |
6 | HG01433.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-9921delC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159164 | |||||||
| chr3:170159168 | C | A | 2 | a0001c0003t0006g0293 a0001c0003t0006g0294 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.415-9924G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159168 | |||||||
| chr3:170159251 | C | CA | 26 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0019 others(23): Show |
26 | HG00408.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.415-10008dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159251 | |||||||
| chr3:170159251 | CA | C | 73 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0096 others(70): Show |
74 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.415-10008delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159251 | |||||||
| chr3:170159251 | CAAAAA | C | 6 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 others(3): Show |
6 | HG01433.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-10012_415-1000 others(9): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159251 | |||||||
| chr3:170159251 | CAAAAAAA others(5): Show |
C | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-10019_415-1000 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159251 | |||||||
| chr3:170159274 | A | T | 3 | a0002c0004t0011g0063 a0002c0004t0011g0064 a0002c0004t0011g0195 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.415-10030T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159274 | |||||||
| chr3:170159542 | G | C | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415-10298C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159542 | |||||||
| chr3:170159653 | A | C | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10409T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159653 | |||||||
| chr3:170159666 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.415-10422G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159666 | |||||||
| chr3:170159672 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-10428T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159672 | |||||||
| chr3:170159695 | C | T | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10451G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159695 | |||||||
| chr3:170159710 | A | T | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10466T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159710 | |||||||
| chr3:170159751 | C | T | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10507G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159751 | |||||||
| chr3:170159752 | A | C | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10508T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159752 | |||||||
| chr3:170159753 | G | T | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10509C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159753 | |||||||
| chr3:170159773 | G | GGGTGGGG others(3): Show |
1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10530_415-1052 others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159773 | |||||||
| chr3:170159775 | A | G | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10531T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159775 | |||||||
| chr3:170159780 | A | T | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10536T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159780 | |||||||
| chr3:170159794 | C | A | 1 | a0001c0001t0012g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10550G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159794 | |||||||
| chr3:170159831 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.415-10587A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159831 | |||||||
| chr3:170159974 | C | T | 1 | a0007c0007t0027g0322 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-10730G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159974 | |||||||
| chr3:170160039 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.415-10795C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160039 | |||||||
| chr3:170160057 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.415-10813T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160057 | |||||||
| chr3:170160126 | T | C | 7 | a0001c0001t0006g0005 a0001c0001t0006g0140 a0001c0001t0006g0188 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-10882A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160126 | |||||||
| chr3:170160200 | T | C | 1 | a0001c0002t0041g0315 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.415-10956A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160200 | |||||||
| chr3:170160232 | T | G | 5 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(2): Show |
5 | HG00741.hp1 HG01517.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-10988A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160232 | |||||||
| chr3:170160934 | A | G | 1 | a0001c0001t0003g0198 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414+10439T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160934 | |||||||
| chr3:170161132 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+10241G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161132 | |||||||
| chr3:170161302 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.414+10071G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161302 | |||||||
| chr3:170161325 | T | C | 1 | a0001c0001t0003g0200 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.414+10048A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161325 | |||||||
| chr3:170161375 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+9998G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161375 | |||||||
| chr3:170161415 | C | T | 2 | a0001c0001t0004g0147 a0001c0001t0004g0160 |
2 | NA18942.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.414+9958G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161415 | |||||||
| chr3:170161527 | G | C | 1 | a0001c0001t0001g0034 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.414+9846C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161527 | |||||||
| chr3:170161565 | G | A | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+9808C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161565 | |||||||
| chr3:170161570 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(194): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.414+9803T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161570 | |||||||
| chr3:170161636 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+9737C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161636 | |||||||
| chr3:170161685 | G | A | 1 | a0001c0001t0004g0167 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.414+9688C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161685 | |||||||
| chr3:170161866 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+9507G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161866 | |||||||
| chr3:170161907 | C | T | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.414+9466G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161907 | |||||||
| chr3:170161959 | A | C | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+9414T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161959 | |||||||
| chr3:170161974 | T | C | 1 | a0008c0011t0002g0236 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.414+9399A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161974 | |||||||
| chr3:170162072 | T | C | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.414+9301A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162072 | |||||||
| chr3:170162131 | T | C | 1 | a0001c0002t0005g0321 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.414+9242A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162131 | |||||||
| chr3:170162296 | T | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(194): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.414+9077A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162296 | |||||||
| chr3:170162356 | T | C | 1 | a0001c0001t0048g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.414+9017A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162356 | |||||||
| chr3:170162500 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0091 others(5): Show |
9 | HG00323.hp1 NA18945.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+8873A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162500 | |||||||
| chr3:170162645 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.414+8728G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162645 | |||||||
| chr3:170162721 | C | G | 1 | a0001c0001t0050g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.414+8652G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162721 | |||||||
| chr3:170162783 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.414+8590A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162783 | |||||||
| chr3:170162799 | T | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+8574A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162799 | |||||||
| chr3:170162832 | C | G | 3 | a0001c0001t0013g0101 a0001c0001t0013g0102 a0001c0001t0013g0103 |
3 | HG01167.hp1 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.414+8541G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162832 | |||||||
| chr3:170162860 | G | A | 1 | a0001c0001t0008g0069 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414+8513C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162860 | |||||||
| chr3:170162873 | T | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(96): Show |
101 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.414+8500A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162873 | |||||||
| chr3:170162972 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.414+8401A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162972 | |||||||
| chr3:170162975 | C | T | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.414+8398G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162975 | |||||||
| chr3:170162984 | TCTC | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(96): Show |
101 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.414+8386_414+8388d others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162984 | |||||||
| chr3:170163044 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+8329G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163044 | |||||||
| chr3:170163045 | G | A | 1 | a0001c0001t0011g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.414+8328C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163045 | |||||||
| chr3:170163133 | T | C | 1 | a0002c0004t0011g0195 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.414+8240A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163133 | |||||||
| chr3:170163216 | C | A | 3 | a0001c0001t0003g0226 a0001c0001t0021g0233 a0001c0001t0046g0268 |
3 | HG00140.hp1 HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.414+8157G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163216 | |||||||
| chr3:170163268 | G | T | 1 | a0001c0001t0002g0184 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.414+8105C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163268 | |||||||
| chr3:170163461 | A | AGT | 36 | a0001c0001t0001g0059 a0001c0001t0002g0270 a0001c0001t0002g0271 others(33): Show |
37 | HG00597.hp1 HG00609.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+7910_414+7911d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163461 | A | AGTGT | 22 | a0001c0001t0001g0036 a0001c0001t0002g0269 a0001c0001t0002g0274 others(19): Show |
22 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.414+7908_414+7911d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163461 | A | AGTGTGT | 6 | a0001c0001t0009g0326 a0001c0001t0009g0327 a0001c0001t0016g0108 others(3): Show |
6 | HG00639.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+7906_414+7911d others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163461 | AGT | A | 62 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0023 others(59): Show |
62 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.414+7910_414+7911d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163461 | AGTGT | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0058 others(90): Show |
94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.414+7908_414+7911d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163461 | AGTGTGT | A | 54 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0018 others(51): Show |
57 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.414+7906_414+7911d others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163461 | AGTGTGTG others(1): Show |
A | 4 | a0001c0001t0001g0075 a0001c0001t0004g0164 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02486.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+7904_414+7911d others(10): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163461 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0040g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.414+7900_414+7911d others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163461 | AGTGTGTG others(7): Show |
A | 4 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0018g0139 others(1): Show |
4 | HG02717.hp2 HG03098.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+7898_414+7911d others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163461 | AGTGTGTG others(11): Show |
A | 5 | a0001c0001t0002g0243 a0001c0001t0002g0245 a0001c0001t0002g0246 others(2): Show |
5 | NA18943.hp2 NA18944.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+7894_414+7911d others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163461 | AGTGTGTG others(15): Show |
A | 1 | a0001c0002t0005g0309 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.414+7890_414+7911d others(24): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | |||||||
| chr3:170163463 | T | A | 1 | a0003c0005t0026g0324 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.414+7910A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163463 | |||||||
| chr3:170163514 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+7859A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163514 | |||||||
| chr3:170163562 | C | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(194): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.414+7811G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163562 | |||||||
| chr3:170163585 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.414+7788C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163585 | |||||||
| chr3:170163590 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+7783G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163590 | |||||||
| chr3:170163766 | C | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.414+7607G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163766 | |||||||
| chr3:170163766 | C | T | 9 | a0001c0001t0003g0201 a0001c0001t0003g0203 a0001c0001t0006g0005 others(6): Show |
9 | HG01884.hp1 HG02080.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+7607G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163766 | |||||||
| chr3:170163767 | G | A | 1 | a0001c0001t0015g0009 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.414+7606C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163767 | |||||||
| chr3:170163861 | C | CA | 18 | a0001c0001t0002g0120 a0001c0001t0002g0184 a0001c0001t0002g0191 others(15): Show |
18 | HG00621.hp1 HG01346.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.414+7511dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | |||||||
| chr3:170163861 | C | CAAA | 16 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.414+7509_414+7511d others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | |||||||
| chr3:170163861 | CA | C | 14 | a0001c0001t0002g0269 a0001c0001t0003g0196 a0001c0001t0003g0200 others(11): Show |
16 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.414+7511delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | |||||||
| chr3:170163861 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+7503_414+7511d others(11): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | |||||||
| chr3:170163861 | CAAAAAAA others(3): Show |
C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(108): Show |
113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.414+7502_414+7511d others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | |||||||
| chr3:170163861 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.414+7501_414+7511d others(13): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | |||||||
| chr3:170163883 | A | AAAAAAAG others(22): Show |
2 | a0003c0005t0025g0323 a0003c0005t0026g0324 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.414+7489_414+7490i others(31): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163883 | |||||||
| chr3:170163883 | A | AAAAAGGC others(20): Show |
1 | a0007c0007t0027g0322 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.414+7489_414+7490i others(29): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163883 | |||||||
| chr3:170164036 | T | TA | 4 | a0001c0001t0002g0184 a0001c0001t0010g0029 a0001c0001t0010g0030 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+7336dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164036 | |||||||
| chr3:170164161 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+7212G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164161 | |||||||
| chr3:170164169 | C | A | 1 | a0001c0001t0003g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.414+7204G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164169 | |||||||
| chr3:170164222 | A | C | 1 | a0001c0001t0003g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.414+7151T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164222 | |||||||
| chr3:170164262 | A | G | 1 | a0001c0001t0044g0296 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.414+7111T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164262 | |||||||
| chr3:170164417 | A | G | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+6956T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164417 | |||||||
| chr3:170164560 | G | A | 1 | a0001c0001t0009g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.414+6813C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164560 | |||||||
| chr3:170164587 | A | G | 1 | a0001c0001t0002g0222 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.414+6786T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164587 | |||||||
| chr3:170164830 | C | A | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+6543G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164830 | |||||||
| chr3:170165031 | T | A | 1 | a0001c0001t0002g0274 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.414+6342A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165031 | |||||||
| chr3:170165041 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.414+6332C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165041 | |||||||
| chr3:170165165 | T | TC | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+6207dupG | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165165 | |||||||
| chr3:170165208 | T | C | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+6165A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165208 | |||||||
| chr3:170165379 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+5994C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165379 | |||||||
| chr3:170165490 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0035g0010 |
2 | NA18973.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.414+5883A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165490 | |||||||
| chr3:170165577 | A | C | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.414+5796T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165577 | |||||||
| chr3:170165583 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0119 |
3 | NA18992.hp1 NA19066.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.414+5790C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165583 | |||||||
| chr3:170165614 | C | T | 1 | a0001c0001t0018g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.414+5759G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165614 | |||||||
| chr3:170165742 | A | T | 1 | a0001c0001t0002g0184 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.414+5631T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165742 | |||||||
| chr3:170165751 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.414+5622G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165751 | |||||||
| chr3:170165753 | C | CA | 30 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0035 others(27): Show |
30 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.414+5619dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165753 | |||||||
| chr3:170165753 | CA | C | 46 | a0001c0001t0002g0222 a0001c0001t0002g0234 a0001c0001t0003g0118 others(43): Show |
46 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.414+5619delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165753 | |||||||
| chr3:170165753 | CAA | C | 41 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(38): Show |
42 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.414+5618_414+5619d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165753 | |||||||
| chr3:170165815 | C | CAAAGAAG others(2852): Show |
1 | a0001c0001t0002g0183 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.414+5557_414+5558i others(2861): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165815 | |||||||
| chr3:170165815 | C | CAAAGAAG others(3073): Show |
1 | a0001c0001t0002g0249 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.414+5557_414+5558i others(3082): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165815 | |||||||
| chr3:170165815 | C | CAAAGAAG others(3342): Show |
1 | a0001c0001t0002g0184 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.414+5557_414+5558i others(3351): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165815 | |||||||
| chr3:170165815 | C | CAAAGAAG others(3509): Show |
1 | a0001c0001t0002g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.414+5557_414+5558i others(3518): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165815 | |||||||
| chr3:170165981 | T | TA | 7 | a0001c0001t0001g0289 a0001c0001t0002g0185 a0001c0001t0002g0222 others(4): Show |
7 | HG01255.hp2 HG02056.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+5391dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165981 | |||||||
| chr3:170165981 | T | TAA | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+5390_414+5391d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165981 | |||||||
| chr3:170165999 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.414+5374G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165999 | |||||||
| chr3:170166102 | T | C | 1 | a0001c0001t0010g0095 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.414+5271A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166102 | |||||||
| chr3:170166179 | G | A | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+5194C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166179 | |||||||
| chr3:170166375 | A | T | 1 | a0001c0001t0007g0142 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.414+4998T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166375 | |||||||
| chr3:170166470 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+4903A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166470 | |||||||
| chr3:170166675 | C | CT | 67 | a0001c0001t0002g0117 a0001c0001t0002g0120 a0001c0001t0002g0122 others(64): Show |
67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.414+4697dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166675 | |||||||
| chr3:170166692 | C | T | 1 | a0001c0001t0032g0090 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.414+4681G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166692 | |||||||
| chr3:170166826 | G | A | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+4547C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166826 | |||||||
| chr3:170166940 | C | A | 1 | a0001c0001t0002g0223 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.414+4433G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166940 | |||||||
| chr3:170167293 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.414+4080G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167293 | |||||||
| chr3:170167315 | A | G | 51 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(48): Show |
52 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.414+4058T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167315 | |||||||
| chr3:170167429 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.414+3944A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167429 | |||||||
| chr3:170167738 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.414+3635G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167738 | |||||||
| chr3:170167750 | G | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
119 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.414+3623C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167750 | |||||||
| chr3:170167759 | C | CA | 160 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(157): Show |
163 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.414+3613dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167759 | |||||||
| chr3:170167759 | C | CAA | 12 | a0001c0001t0001g0035 a0001c0001t0009g0112 a0001c0001t0009g0115 others(9): Show |
12 | HG00438.hp1 HG00597.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.414+3612_414+3613d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167759 | |||||||
| chr3:170167759 | CA | C | 19 | a0001c0001t0002g0228 a0001c0001t0003g0187 a0001c0001t0003g0200 others(16): Show |
19 | HG00140.hp1 HG00735.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+3613delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167759 | |||||||
| chr3:170167795 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.414+3578G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167795 | |||||||
| chr3:170167912 | C | T | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+3461G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167912 | |||||||
| chr3:170168034 | C | T | 1 | a0001c0001t0007g0142 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.414+3339G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168034 | |||||||
| chr3:170168172 | T | C | 1 | a0001c0001t0003g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.414+3201A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168172 | |||||||
| chr3:170168185 | T | TCAAAGG | 196 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(193): Show |
199 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.414+3182_414+3187d others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168185 | |||||||
| chr3:170168186 | C | CAAAGGCA others(5): Show |
1 | a0001c0002t0005g0304 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.414+3186_414+3187i others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168186 | |||||||
| chr3:170168204 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+3169T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168204 | |||||||
| chr3:170168219 | CCT | C | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+3152_414+3153d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168219 | |||||||
| chr3:170168234 | G | GA | 9 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(6): Show |
10 | HG00323.hp1 NA18945.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+3138dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168234 | |||||||
| chr3:170168484 | G | A | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+2889C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168484 | |||||||
| chr3:170168540 | T | C | 323 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(320): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.414+2833A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168540 | |||||||
| chr3:170168544 | T | A | 1 | a0001c0001t0002g0223 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.414+2829A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168544 | |||||||
| chr3:170168626 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG01256.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+2747G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168626 | |||||||
| chr3:170168703 | G | A | 1 | a0001c0001t0009g0176 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.414+2670C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168703 | |||||||
| chr3:170168707 | T | C | 1 | a0001c0001t0002g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.414+2666A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168707 | |||||||
| chr3:170168710 | C | A | 1 | a0001c0001t0003g0266 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.414+2663G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168710 | |||||||
| chr3:170168753 | C | CA | 167 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(164): Show |
170 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.414+2619dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168753 | |||||||
| chr3:170168753 | C | CAA | 22 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0027 others(19): Show |
22 | HG00438.hp1 HG00597.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.414+2618_414+2619d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168753 | |||||||
| chr3:170168753 | C | CAAA | 14 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(11): Show |
14 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.414+2617_414+2619d others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168753 | |||||||
| chr3:170168820 | T | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0028 |
2 | NA19066.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.414+2553A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168820 | |||||||
| chr3:170168900 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.414+2473T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168900 | |||||||
| chr3:170168938 | G | T | 3 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 |
3 | HG02622.hp2 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.414+2435C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168938 | |||||||
| chr3:170169041 | C | T | 21 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0128 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.414+2332G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169041 | |||||||
| chr3:170169068 | G | A | 4 | a0001c0001t0003g0178 a0001c0001t0003g0208 a0001c0001t0003g0209 others(1): Show |
4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+2305C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169068 | |||||||
| chr3:170169095 | C | T | 2 | a0001c0001t0002g0213 a0001c0001t0002g0285 |
2 | HG00609.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.414+2278G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169095 | |||||||
| chr3:170169282 | C | T | 2 | a0003c0005t0025g0323 a0003c0005t0026g0324 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.414+2091G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169282 | |||||||
| chr3:170169299 | T | C | 1 | a0001c0002t0005g0307 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.414+2074A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169299 | |||||||
| chr3:170169326 | A | G | 120 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.414+2047T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169326 | |||||||
| chr3:170169614 | T | C | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.414+1759A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169614 | |||||||
| chr3:170170043 | C | A | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.414+1330G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170170043 | |||||||
| chr3:170170150 | C | G | 2 | a0001c0001t0010g0029 a0001c0001t0010g0030 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.414+1223G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170170150 | |||||||
| chr3:170170472 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+901C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170170472 | |||||||
| chr3:170170704 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+669A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170170704 | |||||||
| chr3:170171159 | A | T | 1 | a0001c0002t0041g0315 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.414+214T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170171159 | |||||||
| chr3:170171187 | C | CA | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+185dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170171187 | |||||||
| chr3:170171258 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.414+115G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170171258 | |||||||
| chr3:170171276 | A | C | 2 | a0001c0003t0006g0293 a0001c0003t0006g0294 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.414+97T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170171276 | |||||||
| chr3:170171543 | T | A | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.337-93A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170171543 | |||||||
| chr3:170171917 | G | C | 1 | a0001c0001t0043g0276 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.337-467C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170171917 | |||||||
| chr3:170171976 | C | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.337-526G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170171976 | |||||||
| chr3:170172115 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.336+442G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170172115 | |||||||
| chr3:170172374 | T | TA | 120 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.336+182dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170172374 | |||||||
| chr3:170172397 | T | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.336+160A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170172397 | |||||||
| chr3:170172487 | C | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.336+70G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170172487 | |||||||
| chr3:170172545 | T | C | 1 | a0001c0001t0010g0021 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.336+12A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170172545 | |||||||
| chr3:170172799 | T | C | 5 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-87A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170172799 | |||||||
| chr3:170172864 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-152T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170172864 | |||||||
| chr3:170172934 | GT | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-223delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170172934 | |||||||
| chr3:170172950 | T | C | 45 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(42): Show |
46 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.181-238A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170172950 | |||||||
| chr3:170172966 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.181-254C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170172966 | |||||||
| chr3:170173016 | C | A | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.181-304G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173016 | |||||||
| chr3:170173019 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.181-307G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173019 | |||||||
| chr3:170173134 | G | A | 1 | a0001c0001t0036g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.181-422C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173134 | |||||||
| chr3:170173172 | G | A | 4 | a0001c0001t0001g0067 a0003c0005t0025g0323 a0003c0005t0026g0324 others(1): Show |
4 | HG01433.hp1 HG02055.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-460C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173172 | |||||||
| chr3:170173202 | A | C | 1 | a0001c0001t0040g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.181-490T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173202 | |||||||
| chr3:170173206 | A | G | 1 | a0001c0001t0010g0021 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.181-494T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173206 | |||||||
| chr3:170173245 | C | G | 1 | a0001c0013t0002g0212 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.181-533G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173245 | |||||||
| chr3:170173284 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-572T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173284 | |||||||
| chr3:170173391 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-679A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173391 | |||||||
| chr3:170173397 | G | A | 2 | a0001c0001t0006g0278 a0001c0001t0006g0279 |
2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.181-685C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173397 | |||||||
| chr3:170173414 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-702G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173414 | |||||||
| chr3:170173451 | C | G | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.181-739G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173451 | |||||||
| chr3:170173458 | G | A | 48 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0126 others(45): Show |
49 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.181-746C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173458 | |||||||
| chr3:170173673 | T | C | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.181-961A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173673 | |||||||
| chr3:170173844 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-1132G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173844 | |||||||
| chr3:170173854 | T | C | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.181-1142A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173854 | |||||||
| chr3:170173935 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-1223C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173935 | |||||||
| chr3:170174123 | G | A | 1 | a0001c0001t0050g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.181-1411C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174123 | |||||||
| chr3:170174166 | C | CTCT | 6 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-1455_181-1454i others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174166 | |||||||
| chr3:170174277 | A | T | 7 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(4): Show |
7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-1565T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174277 | |||||||
| chr3:170174278 | A | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
121 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.181-1566T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174278 | |||||||
| chr3:170174439 | A | G | 3 | a0002c0004t0011g0063 a0002c0004t0011g0064 a0002c0004t0011g0195 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.181-1727T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174439 | |||||||
| chr3:170174510 | G | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(186): Show |
192 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.181-1798C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174510 | |||||||
| chr3:170174958 | A | G | 2 | a0001c0002t0005g0305 a0001c0002t0005g0318 |
2 | NA18964.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.181-2246T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174958 | |||||||
| chr3:170175027 | A | G | 3 | a0001c0001t0016g0108 a0001c0001t0016g0109 a0001c0001t0016g0110 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.181-2315T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175027 | |||||||
| chr3:170175269 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.181-2557A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175269 | |||||||
| chr3:170175394 | T | G | 1 | a0001c0001t0030g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.181-2682A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175394 | |||||||
| chr3:170175610 | C | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(186): Show |
192 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.181-2898G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175610 | |||||||
| chr3:170175636 | A | G | 6 | a0001c0001t0003g0211 a0001c0001t0013g0099 a0001c0001t0013g0101 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-2924T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175636 | |||||||
| chr3:170175637 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-2925C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175637 | |||||||
| chr3:170175747 | G | A | 304 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(301): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.180+3026C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175747 | |||||||
| chr3:170175760 | T | C | 1 | a0001c0001t0010g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.180+3013A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175760 | |||||||
| chr3:170175838 | C | T | 3 | a0001c0001t0009g0174 a0001c0001t0009g0175 a0001c0001t0009g0176 |
3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.180+2935G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175838 | |||||||
| chr3:170175902 | C | T | 1 | a0001c0001t0049g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.180+2871G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175902 | |||||||
| chr3:170175908 | G | A | 5 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(2): Show |
5 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+2865C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175908 | |||||||
| chr3:170175923 | C | CA | 29 | a0001c0001t0002g0191 a0001c0001t0002g0283 a0001c0001t0002g0284 others(26): Show |
29 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.180+2849dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175923 | |||||||
| chr3:170175938 | C | A | 1 | a0003c0005t0026g0324 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.180+2835G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175938 | |||||||
| chr3:170175966 | G | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+2807C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175966 | |||||||
| chr3:170176205 | G | A | 2 | a0001c0002t0005g0314 a0004c0014t0005g0320 |
2 | HG02027.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.180+2568C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176205 | |||||||
| chr3:170176218 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+2555A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176218 | |||||||
| chr3:170176225 | C | CA | 120 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(117): Show |
122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.180+2547dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176225 | |||||||
| chr3:170176245 | AG | A | 3 | a0001c0001t0002g0288 a0001c0001t0003g0286 a0001c0001t0045g0287 |
3 | NA18959.hp1 NA18986.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.180+2527delC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176245 | |||||||
| chr3:170176421 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+2352T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176421 | |||||||
| chr3:170176437 | G | C | 1 | a0007c0007t0027g0322 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.180+2336C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176437 | |||||||
| chr3:170176440 | G | A | 1 | a0001c0002t0005g0316 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.180+2333C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176440 | |||||||
| chr3:170176452 | T | C | 1 | a0001c0001t0036g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.180+2321A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176452 | |||||||
| chr3:170176509 | G | A | 1 | a0010c0006t0002g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.180+2264C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176509 | |||||||
| chr3:170176552 | G | A | 1 | a0001c0001t0006g0140 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.180+2221C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176552 | |||||||
| chr3:170176555 | C | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(184): Show |
190 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.180+2218G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176555 | |||||||
| chr3:170176726 | G | A | 5 | a0001c0001t0013g0099 a0001c0001t0013g0101 a0001c0001t0013g0102 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.180+2047C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176726 | |||||||
| chr3:170176892 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(184): Show |
190 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.180+1881C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176892 | |||||||
| chr3:170176918 | T | C | 3 | a0001c0001t0013g0101 a0001c0001t0013g0102 a0001c0001t0013g0103 |
3 | HG01167.hp1 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.180+1855A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176918 | |||||||
| chr3:170176929 | A | T | 1 | a0009c0009t0001g0020 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.180+1844T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176929 | |||||||
| chr3:170176954 | A | G | 1 | a0001c0001t0007g0141 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.180+1819T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176954 | |||||||
| chr3:170177022 | A | G | 1 | a0001c0001t0039g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.180+1751T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177022 | |||||||
| chr3:170177203 | A | G | 8 | a0001c0001t0008g0002 a0001c0001t0008g0065 a0001c0001t0008g0068 others(5): Show |
9 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+1570T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177203 | |||||||
| chr3:170177214 | T | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+1559A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177214 | |||||||
| chr3:170177230 | G | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(184): Show |
190 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.180+1543C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177230 | |||||||
| chr3:170177236 | A | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.180+1537T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177236 | |||||||
| chr3:170177417 | A | T | 2 | a0001c0003t0006g0293 a0001c0003t0006g0294 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.180+1356T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177417 | |||||||
| chr3:170177428 | G | A | 1 | a0001c0001t0015g0009 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.180+1345C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177428 | |||||||
| chr3:170177489 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.180+1284G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177489 | |||||||
| chr3:170177609 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+1164G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177609 | |||||||
| chr3:170177658 | C | T | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+1115G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177658 | |||||||
| chr3:170177666 | A | AT | 157 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(154): Show |
160 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.180+1106dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177666 | |||||||
| chr3:170177666 | A | ATT | 43 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(40): Show |
43 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.180+1105_180+1106d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177666 | |||||||
| chr3:170177696 | G | C | 1 | a0001c0001t0003g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.180+1077C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177696 | |||||||
| chr3:170177859 | T | TG | 112 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(109): Show |
114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.180+913dupC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177859 | |||||||
| chr3:170178140 | A | AT | 12 | a0001c0001t0001g0011 a0001c0001t0002g0128 a0001c0001t0002g0129 others(9): Show |
12 | HG01175.hp2 HG02080.hp2 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.180+632dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178140 | |||||||
| chr3:170178143 | T | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+630A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178143 | |||||||
| chr3:170178144 | T | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+629A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178144 | |||||||
| chr3:170178185 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+588A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178185 | |||||||
| chr3:170178210 | C | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+563G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178210 | |||||||
| chr3:170178221 | G | A | 3 | a0001c0001t0010g0029 a0001c0001t0010g0030 a0001c0001t0040g0031 |
3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.180+552C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178221 | |||||||
| chr3:170178235 | C | G | 42 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0033 others(39): Show |
42 | HG00323.hp2 HG00408.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.180+538G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178235 | |||||||
| chr3:170178266 | C | A | 2 | a0001c0001t0001g0107 a0005c0010t0001g0106 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.180+507G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178266 | |||||||
| chr3:170178366 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.180+407G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178366 | |||||||
| chr3:170178572 | A | T | 2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | HG00280.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.180+201T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178572 | |||||||
| chr3:170178709 | A | G | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+64T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178709 | |||||||
| chr3:170179161 | T | G | 1 | a0004c0014t0005g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.15-223A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170179161 | |||||||
| chr3:170179372 | C | A | 3 | a0001c0001t0016g0108 a0001c0001t0016g0109 a0001c0001t0016g0110 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.15-434G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170179372 | |||||||
| chr3:170180133 | T | TA | 5 | a0001c0001t0040g0031 a0001c0002t0005g0321 a0003c0005t0025g0323 others(2): Show |
5 | HG01433.hp1 HG02055.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-1196dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180133 | |||||||
| chr3:170180148 | CA | C | 23 | a0001c0001t0002g0120 a0001c0001t0010g0029 a0001c0001t0010g0030 others(20): Show |
23 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.15-1211delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180148 | |||||||
| chr3:170180217 | G | C | 1 | a0001c0001t0003g0291 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.15-1279C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180217 | |||||||
| chr3:170180263 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.15-1325A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180263 | |||||||
| chr3:170180305 | C | T | 1 | a0001c0003t0006g0292 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15-1367G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180305 | |||||||
| chr3:170180316 | G | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(12): Show |
15 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.15-1378C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180316 | |||||||
| chr3:170180404 | G | A | 7 | a0001c0001t0009g0112 a0001c0001t0009g0115 a0001c0001t0009g0116 others(4): Show |
7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+1298C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180404 | |||||||
| chr3:170180469 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0003g0118 |
2 | NA18959.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.14+1233T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180469 | |||||||
| chr3:170180564 | G | GT | 111 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(108): Show |
113 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.14+1137dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180564 | |||||||
| chr3:170180564 | G | GTT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
6 | HG00741.hp2 HG01123.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+1136_14+1137dup others(2): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180564 | |||||||
| chr3:170180564 | GT | G | 6 | a0001c0001t0003g0297 a0001c0001t0044g0296 a0001c0003t0006g0292 others(3): Show |
6 | HG02976.hp2 HG03453.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+1137delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180564 | |||||||
| chr3:170180631 | T | C | 4 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(1): Show |
4 | HG01261.hp2 HG01934.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+1071A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180631 | |||||||
| chr3:170181184 | T | C | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.14+518A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181184 | |||||||
| chr3:170181196 | G | T | 1 | a0001c0001t0015g0009 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.14+506C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181196 | |||||||
| chr3:170181197 | A | T | 1 | a0001c0001t0015g0009 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.14+505T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181197 | |||||||
| chr3:170181406 | C | A | 1 | a0001c0001t0001g0302 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.14+296G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181406 | |||||||
| chr3:170181407 | G | A | 1 | a0001c0001t0033g0303 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.14+295C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181407 | |||||||
| chr3:170181432 | G | C | 19 | a0001c0002t0005g0304 a0001c0002t0005g0305 a0001c0002t0005g0306 others(16): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.14+270C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181432 | |||||||
| chr3:170181466 | C | A | 3 | a0003c0005t0025g0323 a0003c0005t0026g0324 a0007c0007t0027g0322 |
3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.14+236G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181466 | |||||||
| chr3:170181484 | G | C | 2 | a0003c0005t0025g0323 a0003c0005t0026g0324 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.14+218C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181484 | |||||||
| chr3:170181490 | G | C | 1 | a0001c0002t0005g0325 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.14+212C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181490 | |||||||
| chr3:170181514 | C | T | 1 | a0001c0001t0021g0008 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.14+188G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181514 | |||||||
| chr3:170181521 | C | G | 2 | a0001c0001t0004g0006 a0001c0001t0004g0007 |
2 | HG00597.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.14+181G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181521 | |||||||
| chr3:170181535 | C | T | 1 | a0001c0001t0006g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.14+167G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181535 | |||||||
| chr3:170181665 | C | A | 2 | a0001c0001t0009g0326 a0001c0001t0009g0327 |
2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.14+37G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181665 |