Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5395 |
| ensemblid | ENSG00000122512.17 |
| hgncid | 9122 |
| symbol | PMS2 |
| name | PMS1 homolog 2, mismatch repair system component |
| refseq_nuc | NM_000535.7 |
| refseq_prot | NP_000526.2 |
| ensembl_nuc | ENST00000265849.12 |
| ensembl_prot | ENSP00000265849.7 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 5970925 |
| end | 6009049 |
| strand | - |
| ver | v1.2 |
| region | chr7:5970925-6009049 |
| region5000 | chr7:5965925-6014049 |
| regionname0 | PMS2_chr7_5970925_6009049 |
| regionname5000 | PMS2_chr7_5965925_6014049 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 862 | 142 | 22 | 12 | 84 | 2 | 22 | 66 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0002 | 0/0 | 862 | 123 | 24 | 29 | 54 | 8 | 8 | 41 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0003 | 1/0 | 862 | 41 | 8 | 15 | 14 | 1 | 2 | 8 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0004 | 0/1 | 862 | 29 | 8 | 12 | 2 | 2 | 4 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0005 | 0/0 | 862 | 18 | 0 | 2 | 14 | 0 | 2 | 10 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0006 | 0/0 | 862 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0007 | 0/0 | 862 | 9 | 0 | 0 | 9 | 0 | 0 | 8 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0008 | 0/0 | 862 | 6 | 2 | 1 | 3 | 0 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0009 | 0/0 | 862 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0010 | 0/0 | 862 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0011 | 0/0 | 862 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0012 | 0/0 | 862 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0013 | 0/0 | 862 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0014 | 0/0 | 862 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0015 | 0/0 | 862 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0016 | 0/0 | 862 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0017 | 0/0 | 862 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0018 | 0/0 | 862 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0019 | 0/0 | 862 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0020 | 0/0 | 862 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0021 | 0/0 | 862 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0022 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(576): Show |
chr7 | 5965925 | 6014049 |
| a0023 | 0/0 | 862 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0024 | 0/0 | 862 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| a0025 | 0/0 | 862 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | MERAE others(857): Show |
chr7 | 5965925 | 6014049 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2586 | 79 | 1 | 1 | 65 | 0 | 12 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0001c0003 | 0/0 | 2586 | 48 | 8 | 11 | 19 | 2 | 8 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0001c0008 | 0/0 | 2586 | 11 | 11 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0001c0019 | 0/0 | 2586 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0001c0030 | 0/0 | 2586 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0001c0040 | 0/0 | 2586 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0002c0002 | 0/0 | 2586 | 55 | 3 | 10 | 36 | 2 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0002c0004 | 0/0 | 2586 | 48 | 13 | 12 | 13 | 6 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0002c0010 | 0/0 | 2586 | 9 | 8 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0002c0012 | 0/0 | 2586 | 7 | 0 | 3 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0002c0023 | 0/0 | 2586 | 2 | 0 | 2 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0002c0035 | 0/0 | 2586 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0002c0039 | 0/0 | 2586 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0003c0005 | 1/0 | 2586 | 38 | 6 | 14 | 14 | 1 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0003c0020 | 0/0 | 2586 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0003c0028 | 0/0 | 2586 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0004c0006 | 0/1 | 2586 | 29 | 8 | 12 | 2 | 2 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0005c0007 | 0/0 | 2586 | 18 | 0 | 2 | 14 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0006c0009 | 0/0 | 2586 | 10 | 10 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0006c0014 | 0/0 | 2586 | 3 | 2 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0007c0011 | 0/0 | 2586 | 9 | 0 | 0 | 9 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0008c0013 | 0/0 | 2586 | 4 | 2 | 1 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0008c0022 | 0/0 | 2586 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0009c0015 | 0/0 | 2586 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0009c0016 | 0/0 | 2586 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0010c0017 | 0/0 | 2586 | 3 | 0 | 2 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0011c0018 | 0/0 | 2586 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0012c0024 | 0/0 | 2586 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0012c0025 | 0/0 | 2586 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0013c0021 | 0/0 | 2586 | 2 | 0 | 0 | 0 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0014c0036 | 0/0 | 2586 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0015c0042 | 0/0 | 2586 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0016c0033 | 0/0 | 2586 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0017c0037 | 0/0 | 2586 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0018c0032 | 0/0 | 2586 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0019c0026 | 0/0 | 2586 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0020c0029 | 0/0 | 2586 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0021c0041 | 0/0 | 2586 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0022c0034 | 0/0 | 2549 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2544): Show |
chr7 | 5965925 | 6014049 | ||
| a0023c0027 | 0/0 | 2586 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0024c0031 | 0/0 | 2586 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 | ||
| a0025c0038 | 0/0 | 2586 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | ATGGA others(2581): Show |
chr7 | 5965925 | 6014049 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5089 | 71 | 0 | 1 | 59 | 0 | 11 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0001c0001t0002 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0001c0001t0014 | 0/0 | 5090 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5085): Show |
chr7 | 5965925 | 6014049 |
| a0001c0001t0018 | 0/0 | 5089 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0001c0001t0048 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0001c0001t0049 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0001c0001t0051 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0001c0001t0052 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0001c0003t0001 | 0/0 | 5089 | 6 | 1 | 1 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0001c0003t0003 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0001c0003t0004 | 0/0 | 5092 | 28 | 3 | 5 | 13 | 2 | 5 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0001c0003t0008 | 0/0 | 5094 | 2 | 0 | 0 | 0 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0001c0003t0012 | 0/0 | 5094 | 4 | 0 | 4 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0001c0003t0013 | 0/0 | 5092 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0001c0003t0020 | 0/0 | 5092 | 2 | 1 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0001c0003t0044 | 0/0 | 5092 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0001c0003t0045 | 0/0 | 5092 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0001c0008t0007 | 0/0 | 5092 | 10 | 10 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0001c0008t0046 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0001c0019t0053 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0001c0019t0054 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0001c0030t0008 | 0/0 | 5094 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0001c0040t0001 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0002c0002t0002 | 0/0 | 5094 | 46 | 2 | 6 | 32 | 2 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0002t0008 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0002t0015 | 0/0 | 5095 | 2 | 0 | 1 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5090): Show |
chr7 | 5965925 | 6014049 |
| a0002c0002t0028 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0002t0030 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0002t0031 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0002t0032 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0002t0033 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0002t0036 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0004t0001 | 0/0 | 5089 | 36 | 8 | 11 | 8 | 6 | 3 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0002c0004t0002 | 0/0 | 5094 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0004t0008 | 0/0 | 5094 | 3 | 0 | 0 | 3 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0004t0014 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5085): Show |
chr7 | 5965925 | 6014049 |
| a0002c0004t0019 | 0/0 | 5093 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0002c0004t0021 | 0/0 | 5089 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0002c0004t0038 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0002c0004t0039 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0002c0004t0050 | 0/0 | 5089 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0002c0010t0011 | 0/0 | 5093 | 6 | 5 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0002c0010t0014 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5085): Show |
chr7 | 5965925 | 6014049 |
| a0002c0010t0029 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0010t0040 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5091): Show |
chr7 | 5965925 | 6014049 |
| a0002c0012t0001 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0002c0012t0002 | 0/0 | 5094 | 6 | 0 | 3 | 3 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0023t0008 | 0/0 | 5094 | 2 | 0 | 2 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0035t0002 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0002c0039t0001 | 0/0 | 5089 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0003c0005t0001 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0003c0005t0003 | 1/0 | 5093 | 35 | 6 | 14 | 11 | 1 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0003c0005t0041 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0003c0005t0047 | 0/0 | 5092 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0003c0020t0003 | 0/0 | 5093 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0003c0028t0035 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0004c0006t0005 | 0/1 | 5092 | 28 | 7 | 12 | 2 | 2 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0004c0006t0043 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0005c0007t0006 | 0/0 | 5094 | 14 | 0 | 2 | 11 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0005c0007t0022 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0005c0007t0023 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0005c0007t0024 | 0/0 | 5094 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0005c0007t0025 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0006c0009t0009 | 0/0 | 5094 | 8 | 8 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0006c0009t0026 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0006c0009t0037 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0006c0014t0010 | 0/0 | 5094 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0006c0014t0034 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0007c0011t0002 | 0/0 | 5094 | 8 | 0 | 0 | 8 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0007c0011t0016 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0008c0013t0001 | 0/0 | 5089 | 3 | 2 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0008c0013t0042 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0008c0022t0002 | 0/0 | 5094 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0009c0015t0010 | 0/0 | 5094 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0009c0016t0001 | 0/0 | 5089 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0009c0016t0003 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0010c0017t0004 | 0/0 | 5092 | 3 | 0 | 2 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0011c0018t0017 | 0/0 | 5094 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0012c0024t0010 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0012c0025t0001 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0013c0021t0002 | 0/0 | 5094 | 2 | 0 | 0 | 0 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0014c0036t0001 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0015c0042t0005 | 0/0 | 5092 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0016c0033t0010 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0017c0037t0002 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0018c0032t0009 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0019c0026t0006 | 0/0 | 5094 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5089): Show |
chr7 | 5965925 | 6014049 |
| a0020c0029t0003 | 0/0 | 5093 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0021c0041t0001 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5084): Show |
chr7 | 5965925 | 6014049 |
| a0022c0034t0027 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5052): Show |
chr7 | 5965925 | 6014049 |
| a0023c0027t0016 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5088): Show |
chr7 | 5965925 | 6014049 |
| a0024c0031t0005 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| a0025c0038t0004 | 0/0 | 5092 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | AGTCC others(5087): Show |
chr7 | 5965925 | 6014049 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0014g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0018g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0018g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0048g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0049g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0051g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0001t0052g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0004 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0004g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0008g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0008g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0012g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0012g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0012g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0012g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0013g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0013g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0020g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0020g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0044g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0003t0045g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0007g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0007g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0007g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0008t0046g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0019t0053g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0019t0054g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0030t0008g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0001c0040t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0015g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0015g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0028g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0030g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0031g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0032g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0033g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0002t0036g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0005 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0008g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0019g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0021g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0021g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0038g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0039g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0004t0050g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0010t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0010t0011g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0010t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0010t0011g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0010t0011g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0010t0011g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0010t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0010t0029g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0010t0040g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0012t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0012t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0012t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0012t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0012t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0012t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0012t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0023t0008g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0023t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0035t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0002c0039t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0041g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0005t0047g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0020t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0020t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0003c0028t0035g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0004c0006t0043g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0006g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0022g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0023g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0024g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0005c0007t0025g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0009t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0009t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0009t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0009t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0009t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0009t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0009t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0009t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0009t0026g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0009t0037g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0014t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0014t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0006c0014t0034g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0007c0011t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0007c0011t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0007c0011t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0007c0011t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0007c0011t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0007c0011t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0007c0011t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0007c0011t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0007c0011t0016g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0008c0013t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0008c0013t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0008c0013t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0008c0013t0042g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0008c0022t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0008c0022t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0009c0015t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0009c0015t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0009c0015t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0009c0016t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0009c0016t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0009c0016t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0010c0017t0004g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0010c0017t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0011c0018t0017g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0011c0018t0017g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0012c0024t0010g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0012c0025t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0013c0021t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0013c0021t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0014c0036t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0015c0042t0005g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0016c0033t0010g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0017c0037t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0018c0032t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0019c0026t0006g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0020c0029t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0021c0041t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0022c0034t0027g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0023c0027t0016g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0024c0031t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| a0025c0038t0004g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0001 | g0114 | EUR | GBR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00099 | hp2 | a0001 | c0003 | t0004 | g0361 | EUR | GBR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00140 | hp1 | a0014 | c0036 | t0001 | g0080 | EUR | GBR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0238 | EUR | GBR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00280 | hp1 | a0015 | c0042 | t0005 | g0299 | EUR | FIN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00280 | hp2 | a0002 | c0004 | t0001 | g0008 | EUR | FIN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0119 | EUR | FIN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00323 | hp2 | a0002 | c0004 | t0001 | g0091 | EUR | FIN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00423 | hp1 | a0005 | c0007 | t0006 | g0330 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00438 | hp1 | a0003 | c0005 | t0001 | g0059 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00438 | hp2 | a0001 | c0001 | t0018 | g0128 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00544 | hp1 | a0002 | c0004 | t0001 | g0082 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00544 | hp2 | a0002 | c0012 | t0002 | g0188 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00621 | hp2 | a0001 | c0003 | t0004 | g0012 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0175 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00639 | hp2 | a0003 | c0005 | t0003 | g0060 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00642 | hp1 | a0002 | c0004 | t0001 | g0092 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00642 | hp2 | a0004 | c0006 | t0005 | g0301 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00733 | hp1 | a0004 | c0006 | t0005 | g0292 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00733 | hp2 | a0003 | c0005 | t0003 | g0006 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00735 | hp1 | a0002 | c0004 | t0001 | g0071 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00735 | hp2 | a0003 | c0005 | t0003 | g0002 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00738 | hp1 | a0001 | c0003 | t0004 | g0336 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00738 | hp2 | a0005 | c0007 | t0006 | g0371 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00741 | hp1 | a0002 | c0012 | t0002 | g0100 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG00741 | hp2 | a0004 | c0006 | t0005 | g0287 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01069 | hp1 | a0003 | c0005 | t0003 | g0002 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01069 | hp2 | a0010 | c0017 | t0004 | g0013 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01070 | hp1 | a0002 | c0023 | t0008 | g0251 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01070 | hp2 | a0002 | c0004 | t0001 | g0117 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01071 | hp1 | a0002 | c0023 | t0008 | g0256 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01071 | hp2 | a0010 | c0017 | t0004 | g0013 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01074 | hp1 | a0002 | c0039 | t0001 | g0116 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01074 | hp2 | a0001 | c0003 | t0004 | g0349 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01081 | hp1 | a0001 | c0003 | t0045 | g0376 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01081 | hp2 | a0002 | c0004 | t0001 | g0310 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01106 | hp1 | a0002 | c0002 | t0033 | g0248 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01106 | hp2 | a0001 | c0003 | t0012 | g0110 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01109 | hp1 | a0006 | c0014 | t0034 | g0320 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01109 | hp2 | a0004 | c0006 | t0005 | g0295 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01168 | hp1 | a0001 | c0003 | t0012 | g0201 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01168 | hp2 | a0003 | c0005 | t0003 | g0007 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01175 | hp1 | a0002 | c0004 | t0050 | g0076 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01175 | hp2 | a0002 | c0004 | t0001 | g0084 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0118 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01192 | hp2 | a0002 | c0004 | t0001 | g0074 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01243 | hp1 | a0002 | c0002 | t0036 | g0097 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01243 | hp2 | a0008 | c0013 | t0001 | g0073 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01255 | hp1 | a0004 | c0006 | t0005 | g0285 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01256 | hp1 | a0003 | c0005 | t0003 | g0046 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01256 | hp2 | a0002 | c0004 | t0001 | g0075 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01258 | hp1 | a0002 | c0002 | t0008 | g0250 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01258 | hp2 | a0003 | c0005 | t0003 | g0048 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01261 | hp1 | a0001 | c0003 | t0004 | g0348 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01261 | hp2 | a0004 | c0006 | t0005 | g0294 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01346 | hp1 | a0001 | c0003 | t0012 | g0109 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01346 | hp2 | a0016 | c0033 | t0010 | g0105 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01358 | hp1 | a0002 | c0012 | t0002 | g0178 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01358 | hp2 | a0001 | c0003 | t0004 | g0347 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0274 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01361 | hp2 | a0003 | c0005 | t0003 | g0045 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01433 | hp1 | a0002 | c0004 | t0001 | g0086 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01433 | hp2 | a0001 | c0003 | t0012 | g0111 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01496 | hp1 | a0005 | c0007 | t0006 | g0373 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01496 | hp2 | a0002 | c0010 | t0011 | g0034 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01515 | hp1 | a0004 | c0006 | t0005 | g0282 | EUR | IBS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01515 | hp2 | a0001 | c0003 | t0004 | g0004 | EUR | IBS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01517 | hp1 | a0002 | c0004 | t0001 | g0281 | EUR | IBS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01517 | hp2 | a0004 | c0006 | t0005 | g0284 | EUR | IBS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01884 | hp1 | a0001 | c0003 | t0013 | g0014 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01884 | hp2 | a0003 | c0005 | t0003 | g0006 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01891 | hp1 | a0011 | c0018 | t0017 | g0374 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0199 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01928 | hp1 | a0003 | c0005 | t0003 | g0055 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01928 | hp2 | a0004 | c0006 | t0005 | g0300 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01934 | hp1 | a0004 | c0006 | t0005 | g0298 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01934 | hp2 | a0002 | c0004 | t0001 | g0093 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01943 | hp1 | a0004 | c0006 | t0005 | g0311 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01943 | hp2 | a0003 | c0005 | t0003 | g0002 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01952 | hp1 | a0003 | c0028 | t0035 | g0054 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01952 | hp2 | a0003 | c0005 | t0003 | g0001 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01978 | hp1 | a0004 | c0006 | t0005 | g0297 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01978 | hp2 | a0017 | c0037 | t0002 | g0277 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01981 | hp1 | a0004 | c0006 | t0005 | g0283 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01981 | hp2 | a0002 | c0002 | t0015 | g0268 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0247 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01993 | hp2 | a0003 | c0005 | t0003 | g0053 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02004 | hp1 | a0003 | c0005 | t0003 | g0002 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0267 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02015 | hp2 | a0003 | c0005 | t0003 | g0062 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02027 | hp2 | a0001 | c0003 | t0004 | g0351 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02040 | hp1 | a0002 | c0002 | t0030 | g0210 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02055 | hp1 | a0001 | c0008 | t0007 | g0343 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02055 | hp2 | a0002 | c0010 | t0011 | g0035 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02056 | hp1 | a0003 | c0005 | t0047 | g0061 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02056 | hp2 | a0008 | c0022 | t0002 | g0219 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02071 | hp1 | a0003 | c0005 | t0003 | g0016 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0241 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02129 | hp2 | a0005 | c0007 | t0006 | g0367 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02132 | hp1 | a0003 | c0005 | t0003 | g0015 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02132 | hp2 | a0005 | c0007 | t0006 | g0329 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02135 | hp1 | a0005 | c0007 | t0006 | g0318 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02135 | hp2 | a0002 | c0012 | t0002 | g0101 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02145 | hp1 | a0001 | c0008 | t0007 | g0344 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02145 | hp2 | a0004 | c0006 | t0005 | g0296 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02155 | hp1 | a0002 | c0004 | t0001 | g0066 | EAS | CDX | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02155 | hp2 | a0007 | c0011 | t0002 | g0246 | EAS | CDX | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02165 | hp1 | a0003 | c0005 | t0003 | g0050 | EAS | CDX | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CDX | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02257 | hp1 | a0006 | c0009 | t0009 | g0028 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02257 | hp2 | a0001 | c0003 | t0013 | g0363 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02258 | hp1 | a0006 | c0009 | t0009 | g0029 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02258 | hp2 | a0003 | c0005 | t0003 | g0051 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02273 | hp1 | a0002 | c0012 | t0002 | g0177 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0262 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02280 | hp1 | a0009 | c0016 | t0001 | g0106 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02280 | hp2 | a0002 | c0004 | t0019 | g0090 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0261 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02293 | hp2 | a0002 | c0004 | t0001 | g0087 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02300 | hp1 | a0001 | c0003 | t0004 | g0360 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02300 | hp2 | a0003 | c0005 | t0003 | g0002 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02451 | hp1 | a0018 | c0032 | t0009 | g0024 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02451 | hp2 | a0003 | c0005 | t0003 | g0044 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02523 | hp1 | a0004 | c0006 | t0005 | g0303 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02523 | hp2 | a0001 | c0003 | t0004 | g0345 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0273 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02615 | hp2 | a0002 | c0004 | t0001 | g0079 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02622 | hp1 | a0009 | c0016 | t0001 | g0108 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02622 | hp2 | a0002 | c0004 | t0001 | g0088 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02630 | hp1 | a0006 | c0014 | t0010 | g0039 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02630 | hp2 | a0001 | c0001 | t0049 | g0196 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02698 | hp1 | a0004 | c0006 | t0005 | g0288 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02698 | hp2 | a0002 | c0004 | t0001 | g0070 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02717 | hp1 | a0012 | c0025 | t0001 | g0366 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02717 | hp2 | a0001 | c0008 | t0007 | g0339 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02723 | hp1 | a0004 | c0006 | t0005 | g0313 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02723 | hp2 | a0001 | c0008 | t0007 | g0322 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02735 | hp1 | a0019 | c0026 | t0006 | g0372 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0317 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02809 | hp1 | a0002 | c0010 | t0011 | g0032 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02809 | hp2 | a0006 | c0009 | t0026 | g0027 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02818 | hp1 | a0006 | c0009 | t0009 | g0043 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02818 | hp2 | a0002 | c0004 | t0001 | g0067 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02886 | hp1 | a0002 | c0004 | t0001 | g0005 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02886 | hp2 | a0001 | c0003 | t0004 | g0064 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02895 | hp1 | a0006 | c0014 | t0010 | g0018 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02895 | hp2 | a0002 | c0004 | t0039 | g0275 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02897 | hp1 | a0008 | c0013 | t0001 | g0113 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02897 | hp2 | a0002 | c0004 | t0038 | g0276 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02922 | hp1 | a0001 | c0003 | t0013 | g0014 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02922 | hp2 | a0002 | c0010 | t0011 | g0036 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02965 | hp1 | a0001 | c0003 | t0004 | g0335 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02965 | hp2 | a0001 | c0008 | t0007 | g0338 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02970 | hp1 | a0004 | c0006 | t0005 | g0315 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02970 | hp2 | a0004 | c0006 | t0043 | g0314 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02976 | hp1 | a0001 | c0008 | t0007 | g0337 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02976 | hp2 | a0001 | c0003 | t0004 | g0334 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03017 | hp1 | a0004 | c0006 | t0005 | g0304 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03017 | hp2 | a0005 | c0007 | t0024 | g0095 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03041 | hp1 | a0002 | c0004 | t0001 | g0005 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03041 | hp2 | a0002 | c0010 | t0040 | g0030 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03098 | hp1 | a0003 | c0005 | t0003 | g0041 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03098 | hp2 | a0006 | c0009 | t0009 | g0021 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03130 | hp1 | a0003 | c0020 | t0003 | g0307 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03130 | hp2 | a0006 | c0009 | t0009 | g0019 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03139 | hp1 | a0004 | c0006 | t0005 | g0308 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03139 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03195 | hp1 | a0002 | c0010 | t0011 | g0031 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03195 | hp2 | a0008 | c0013 | t0001 | g0025 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03209 | hp1 | a0009 | c0015 | t0010 | g0102 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03209 | hp2 | a0001 | c0008 | t0007 | g0362 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03239 | hp2 | a0005 | c0007 | t0006 | g0370 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03453 | hp1 | a0001 | c0008 | t0007 | g0340 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03453 | hp2 | a0012 | c0024 | t0010 | g0326 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03491 | hp1 | a0002 | c0004 | t0002 | g0249 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03492 | hp2 | a0001 | c0040 | t0001 | g0162 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03516 | hp1 | a0001 | c0008 | t0046 | g0341 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03516 | hp2 | a0009 | c0015 | t0010 | g0107 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0309 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03540 | hp2 | a0006 | c0009 | t0037 | g0026 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03579 | hp1 | a0001 | c0008 | t0007 | g0342 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03579 | hp2 | a0001 | c0008 | t0007 | g0321 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03654 | hp1 | a0001 | c0003 | t0004 | g0004 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03654 | hp2 | a0003 | c0005 | t0003 | g0007 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03669 | hp1 | a0001 | c0003 | t0008 | g0353 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03688 | hp2 | a0001 | c0003 | t0044 | g0381 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03704 | hp1 | a0020 | c0029 | t0003 | g0047 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03704 | hp2 | a0001 | c0003 | t0004 | g0352 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03710 | hp2 | a0001 | c0003 | t0008 | g0354 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0213 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03834 | hp1 | a0004 | c0006 | t0005 | g0290 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03834 | hp2 | a0002 | c0004 | t0001 | g0252 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0242 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03942 | hp2 | a0010 | c0017 | t0004 | g0346 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG04115 | hp1 | a0004 | c0006 | t0005 | g0289 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG04115 | hp2 | a0001 | c0003 | t0004 | g0382 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG04184 | hp1 | a0021 | c0041 | t0001 | g0179 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG04184 | hp2 | a0001 | c0030 | t0008 | g0058 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG04199 | hp1 | a0001 | c0003 | t0004 | g0004 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG04199 | hp2 | a0003 | c0005 | t0003 | g0049 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG04204 | hp1 | a0013 | c0021 | t0002 | g0259 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG04204 | hp2 | a0001 | c0001 | t0051 | g0129 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG04228 | hp1 | a0001 | c0003 | t0004 | g0004 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0263 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0258 | EAS | CHB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18747 | hp2 | a0002 | c0004 | t0001 | g0081 | EAS | CHB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18906 | hp1 | a0001 | c0019 | t0054 | g0365 | AFR | YRI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18906 | hp2 | a0006 | c0009 | t0009 | g0020 | AFR | YRI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18939 | hp1 | a0002 | c0004 | t0001 | g0005 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18942 | hp2 | a0008 | c0022 | t0002 | g0233 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18944 | hp1 | a0001 | c0003 | t0004 | g0383 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18945 | hp1 | a0003 | c0005 | t0003 | g0173 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18947 | hp1 | a0005 | c0007 | t0006 | g0333 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18948 | hp2 | a0001 | c0003 | t0004 | g0379 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18954 | hp2 | a0005 | c0007 | t0006 | g0368 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18957 | hp1 | a0003 | c0005 | t0003 | g0001 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18960 | hp1 | a0008 | c0013 | t0042 | g0094 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18963 | hp1 | a0003 | c0005 | t0003 | g0052 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18969 | hp2 | a0001 | c0003 | t0004 | g0377 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18970 | hp2 | a0001 | c0003 | t0004 | g0378 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18971 | hp1 | a0001 | c0001 | t0052 | g0127 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18971 | hp2 | a0007 | c0011 | t0002 | g0254 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18973 | hp1 | a0002 | c0002 | t0031 | g0270 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18975 | hp2 | a0001 | c0003 | t0004 | g0359 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18977 | hp2 | a0007 | c0011 | t0002 | g0265 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18979 | hp1 | a0002 | c0002 | t0028 | g0224 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18980 | hp2 | a0002 | c0004 | t0001 | g0208 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18981 | hp1 | a0005 | c0007 | t0022 | g0327 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18981 | hp2 | a0001 | c0001 | t0014 | g0171 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18983 | hp1 | a0005 | c0007 | t0006 | g0011 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18983 | hp2 | a0001 | c0001 | t0048 | g0144 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18985 | hp2 | a0002 | c0004 | t0008 | g0209 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18986 | hp2 | a0005 | c0007 | t0025 | g0319 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18989 | hp2 | a0002 | c0004 | t0021 | g0083 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18990 | hp2 | a0003 | c0005 | t0041 | g0056 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18991 | hp1 | a0005 | c0007 | t0006 | g0328 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18994 | hp2 | a0022 | c0034 | t0027 | g0228 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18995 | hp2 | a0002 | c0012 | t0002 | g0187 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18999 | hp1 | a0002 | c0035 | t0002 | g0216 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19001 | hp1 | a0007 | c0011 | t0002 | g0245 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19001 | hp2 | a0001 | c0003 | t0004 | g0380 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19002 | hp2 | a0003 | c0005 | t0003 | g0001 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19003 | hp1 | a0005 | c0007 | t0006 | g0331 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19005 | hp1 | a0001 | c0003 | t0004 | g0358 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19005 | hp2 | a0003 | c0005 | t0003 | g0098 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19007 | hp1 | a0004 | c0006 | t0005 | g0305 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19009 | hp1 | a0002 | c0002 | t0015 | g0218 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19009 | hp2 | a0002 | c0004 | t0001 | g0085 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19010 | hp2 | a0001 | c0003 | t0004 | g0356 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0266 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19012 | hp1 | a0005 | c0007 | t0023 | g0332 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19012 | hp2 | a0001 | c0001 | t0018 | g0150 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19030 | hp1 | a0009 | c0016 | t0003 | g0042 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19030 | hp2 | a0011 | c0018 | t0017 | g0375 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19043 | hp1 | a0002 | c0010 | t0011 | g0033 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19043 | hp2 | a0003 | c0020 | t0003 | g0104 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19056 | hp2 | a0001 | c0003 | t0004 | g0357 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19057 | hp1 | a0023 | c0027 | t0016 | g0234 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19057 | hp2 | a0001 | c0003 | t0003 | g0323 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19065 | hp1 | a0002 | c0004 | t0001 | g0264 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19065 | hp2 | a0005 | c0007 | t0006 | g0369 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19066 | hp2 | a0007 | c0011 | t0002 | g0243 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19067 | hp1 | a0007 | c0011 | t0002 | g0235 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19067 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19068 | hp2 | a0001 | c0003 | t0004 | g0012 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19070 | hp1 | a0007 | c0011 | t0016 | g0253 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19070 | hp2 | a0001 | c0003 | t0020 | g0350 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19074 | hp1 | a0002 | c0004 | t0021 | g0115 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19074 | hp2 | a0002 | c0004 | t0008 | g0223 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19080 | hp2 | a0007 | c0011 | t0002 | g0257 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19081 | hp2 | a0005 | c0007 | t0006 | g0011 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19082 | hp1 | a0002 | c0004 | t0001 | g0065 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19084 | hp2 | a0002 | c0012 | t0001 | g0191 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19088 | hp2 | a0002 | c0004 | t0008 | g0217 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19091 | hp1 | a0007 | c0011 | t0002 | g0255 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19091 | hp2 | a0003 | c0005 | t0003 | g0001 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19240 | hp1 | a0006 | c0009 | t0009 | g0022 | AFR | YRI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA19240 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | YRI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA20129 | hp1 | a0002 | c0002 | t0032 | g0063 | AFR | ASW | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0174 | AFR | ASW | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA20752 | hp1 | a0002 | c0004 | t0001 | g0069 | EUR | TSI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA20752 | hp2 | a0025 | c0038 | t0004 | g0355 | EUR | TSI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA20805 | hp1 | a0002 | c0004 | t0001 | g0078 | EUR | TSI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA20805 | hp2 | a0003 | c0005 | t0003 | g0096 | EUR | TSI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA20905 | hp1 | a0013 | c0021 | t0002 | g0260 | SAS | GIH | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA20905 | hp2 | a0002 | c0004 | t0001 | g0077 | SAS | GIH | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01123 | hp1 | a0004 | c0006 | t0005 | g0291 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG01123 | hp2 | a0002 | c0004 | t0001 | g0008 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02109 | hp1 | a0004 | c0006 | t0005 | g0316 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02109 | hp2 | a0009 | c0015 | t0010 | g0017 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02486 | hp1 | a0001 | c0003 | t0020 | g0306 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02486 | hp2 | a0003 | c0005 | t0003 | g0040 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02559 | hp1 | a0002 | c0004 | t0019 | g0089 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG02559 | hp2 | a0002 | c0010 | t0029 | g0038 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03471 | hp1 | a0002 | c0010 | t0014 | g0037 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG03471 | hp2 | a0001 | c0019 | t0053 | g0364 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG06807 | hp1 | a0004 | c0006 | t0005 | g0293 | AFR | USA | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| HG06807 | hp2 | a0006 | c0009 | t0009 | g0023 | AFR | USA | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18955 | hp1 | a0003 | c0005 | t0003 | g0001 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA20300 | hp1 | a0004 | c0006 | t0005 | g0302 | AFR | USA | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA20300 | hp2 | a0024 | c0031 | t0005 | g0312 | AFR | USA | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA21309 | hp1 | a0003 | c0005 | t0003 | g0120 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| NA21309 | hp2 | a0002 | c0004 | t0014 | g0068 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| homoSapiens | chm13v2 | a0004 | c0006 | t0005 | g0286 | REF | REF | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| homoSapiens | grch38p0 | a0003 | c0005 | t0003 | g0057 | REF | REF | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:5973418 | C | G | 4 | a0004 a0008 a0015 others(1): Show |
36 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(33): Show |
missense_variant | MODERATE | c.2570G>C | p.Gly857Ala | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2600/5093 | 2570/2589 | 857/862 | chr7 | 5973418 | |||
| chr7:5977677 | G | T | 1 | a0013 | 2 | HG04204.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.2356C>A | p.Leu786Met | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/15 | 2386/5093 | 2356/2589 | 786/862 | chr7 | 5977677 | |||
| chr7:5977709 | T | C | 7 | a0005 a0006 a0009 others(4): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
missense_variant | MODERATE | c.2324A>G | p.Asn775Ser | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/15 | 2354/5093 | 2324/2589 | 775/862 | chr7 | 5977709 | |||
| chr7:5982890 | G | A | 1 | a0024 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2108C>T | p.Thr703Met | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/15 | 2138/5093 | 2108/2589 | 703/862 | chr7 | 5982890 | |||
| chr7:5986899 | C | T | 1 | a0020 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.1866G>A | p.Met622Ile | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1896/5093 | 1866/2589 | 622/862 | chr7 | 5986899 | |||
| chr7:5986901 | T | C | 1 | a0019 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1864A>G | p.Met622Val | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1894/5093 | 1864/2589 | 622/862 | chr7 | 5986901 | |||
| chr7:5986976 | T | A | 1 | a0014 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.1789A>T | p.Thr597Ser | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1819/5093 | 1789/2589 | 597/862 | chr7 | 5986976 | |||
| chr7:5987048 | T | A | 1 | a0021 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.1717A>T | p.Thr573Ser | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1747/5093 | 1717/2589 | 573/862 | chr7 | 5987048 | |||
| chr7:5987057 | T | C | 1 | a0018 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1708A>G | p.Asn570Asp | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1738/5093 | 1708/2589 | 570/862 | chr7 | 5987057 | |||
| chr7:5987144 | T | C | 24 | a0001 a0002 a0004 others(21): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
missense_variant | MODERATE | c.1621A>G | p.Lys541Glu | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1651/5093 | 1621/2589 | 541/862 | chr7 | 5987144 | |||
| chr7:5987156 | C | T | 1 | a0016 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.1609G>A | p.Glu537Lys | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1639/5093 | 1609/2589 | 537/862 | chr7 | 5987156 | |||
| chr7:5987206 | G | A | 1 | a0017 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1559C>T | p.Ala520Val | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1589/5093 | 1559/2589 | 520/862 | chr7 | 5987206 | |||
| chr7:5987209 | T | C | 1 | a0017 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1556A>G | p.Tyr519Cys | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1586/5093 | 1556/2589 | 519/862 | chr7 | 5987209 | |||
| chr7:5987233 | G | A | 4 | a0007 a0009 a0011 others(1): Show |
18 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
missense_variant | MODERATE | c.1532C>T | p.Thr511Met | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1562/5093 | 1532/2589 | 511/862 | chr7 | 5987233 | |||
| chr7:5987234 | T | C | 2 | a0010 a0025 |
4 | HG01069.hp2 HG01071.hp2 HG03942.hp2 others(1): Show |
missense_variant | MODERATE | c.1531A>G | p.Thr511Ala | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1561/5093 | 1531/2589 | 511/862 | chr7 | 5987234 | |||
| chr7:5987291 | TCTCCACC others(30): Show |
T | 1 | a0022 | 1 | NA18994.hp2 | frameshift_variant | HIGH | c.1437_1473delCGGACC others(31): Show |
p.His479fs | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1503/5093 | 1437/2589 | 479/862 | chr7 | 5987291 | |||
| chr7:5987311 | G | T | 2 | a0001 a0021 |
87 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(84): Show |
missense_variant | MODERATE | c.1454C>A | p.Thr485Lys | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1484/5093 | 1454/2589 | 485/862 | chr7 | 5987311 | |||
| chr7:5987327 | C | T | 1 | a0001 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.1438G>A | p.Gly480Arg | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1468/5093 | 1438/2589 | 480/862 | chr7 | 5987327 | |||
| chr7:5987328 | G | C | 2 | a0002 a0012 |
2 | HG00642.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.1437C>G | p.His479Gln | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1467/5093 | 1437/2589 | 479/862 | chr7 | 5987328 | |||
| chr7:5987357 | G | A | 8 | a0002 a0007 a0008 others(5): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
missense_variant | MODERATE | c.1408C>T | p.Pro470Ser | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1438/5093 | 1408/2589 | 470/862 | chr7 | 5987357 | |||
| chr7:5987554 | G | C | 1 | a0025 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1211C>G | p.Pro404Arg | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1241/5093 | 1211/2589 | 404/862 | chr7 | 5987554 | |||
| chr7:6002611 | C | T | 1 | a0023 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.379G>A | p.Ala127Thr | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/15 | 409/5093 | 379/2589 | 127/862 | chr7 | 6002611 | |||
| chr7:6005996 | C | T | 4 | a0005 a0011 a0012 others(1): Show |
23 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(20): Show |
missense_variant | MODERATE | c.59G>A | p.Arg20Gln | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/15 | 89/5093 | 59/2589 | 20/862 | chr7 | 6005996 | |||
| chr7:6006003 | T | C | 1 | a0015 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.52A>G | p.Ile18Val | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/15 | 82/5093 | 52/2589 | 18/862 | chr7 | 6006003 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:5973450 | T | C | 1 | a0002c0023 | 2 | HG01070.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.2538A>G | p.Gly846Gly | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2568/5093 | 2538/2589 | 846/862 | chr7 | 5973450 | |||
| chr7:5973522 | A | G | 17 | a0001c0040 a0002c0002 a0002c0023 others(14): Show |
104 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(101): Show |
synonymous_variant | LOW | c.2466T>C | p.Leu822Leu | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2496/5093 | 2466/2589 | 822/862 | chr7 | 5973522 | |||
| chr7:5977693 | G | A | 2 | a0005c0007 a0019c0026 |
19 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(16): Show |
synonymous_variant | LOW | c.2340C>T | p.Pro780Pro | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/15 | 2370/5093 | 2340/2589 | 780/862 | chr7 | 5977693 | |||
| chr7:5978618 | A | G | 9 | a0005c0007 a0006c0009 a0006c0014 others(6): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
synonymous_variant | LOW | c.2253T>C | p.Phe751Phe | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/15 | 2283/5093 | 2253/2589 | 751/862 | chr7 | 5978618 | |||
| chr7:5982871 | G | A | 1 | a0002c0035 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.2127C>T | p.Phe709Phe | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/15 | 2157/5093 | 2127/2589 | 709/862 | chr7 | 5982871 | |||
| chr7:5987208 | A | G | 1 | a0001c0019 | 2 | HG03471.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.1557T>C | p.Tyr519Tyr | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1587/5093 | 1557/2589 | 519/862 | chr7 | 5987208 | |||
| chr7:5987277 | G | A | 1 | a0001c0008 | 11 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(8): Show |
synonymous_variant | LOW | c.1488C>T | p.His496His | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1518/5093 | 1488/2589 | 496/862 | chr7 | 5987277 | |||
| chr7:5987499 | C | T | 1 | a0011c0018 | 2 | HG01891.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1266G>A | p.Glu422Glu | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1296/5093 | 1266/2589 | 422/862 | chr7 | 5987499 | |||
| chr7:5997349 | G | C | 37 | a0001c0001 a0001c0003 a0001c0008 others(34): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
synonymous_variant | LOW | c.780C>G | p.Ser260Ser | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/15 | 810/5093 | 780/2589 | 260/862 | chr7 | 5997349 | |||
| chr7:5997391 | G | C | 1 | a0002c0039 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.738C>G | p.Pro246Pro | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/15 | 768/5093 | 738/2589 | 246/862 | chr7 | 5997391 | |||
| chr7:6003755 | G | A | 4 | a0001c0001 a0001c0040 a0002c0012 others(1): Show |
88 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
synonymous_variant | LOW | c.288C>T | p.Ala96Ala | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/15 | 318/5093 | 288/2589 | 96/862 | chr7 | 6003755 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:5971011 | G | C | 26 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0015 others(23): Show |
103 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2388C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2388 | chr7 | 5971011 | ||||||
| chr7:5971019 | G | A | 3 | a0002c0004t0038 a0002c0004t0039 a0002c0010t0011 |
8 | HG01496.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2380C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2380 | chr7 | 5971019 | ||||||
| chr7:5971074 | G | C | 1 | a0004c0006t0043 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2325C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2325 | chr7 | 5971074 | ||||||
| chr7:5971177 | C | T | 9 | a0002c0002t0032 a0002c0004t0021 a0002c0010t0040 others(6): Show |
36 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2222G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2222 | chr7 | 5971177 | ||||||
| chr7:5971231 | G | C | 1 | a0003c0028t0035 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2168C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2168 | chr7 | 5971231 | ||||||
| chr7:5971305 | GATC | G | 3 | a0002c0004t0038 a0002c0004t0039 a0002c0010t0011 |
8 | HG01496.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2091_*2093delGAT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2091 | chr7 | 5971305 | ||||||
| chr7:5971503 | C | A | 1 | a0001c0001t0049 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1896G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1896 | chr7 | 5971503 | ||||||
| chr7:5971512 | A | C | 1 | a0011c0018t0017 | 2 | HG01891.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1887T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1887 | chr7 | 5971512 | ||||||
| chr7:5971540 | C | T | 1 | a0001c0003t0045 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1859G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1859 | chr7 | 5971540 | ||||||
| chr7:5971636 | A | G | 86 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0014 others(83): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
3_prime_UTR_variant | MODIFIER | c.*1763T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1763 | chr7 | 5971636 | ||||||
| chr7:5971721 | A | C | 1 | a0001c0001t0048 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1678T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1678 | chr7 | 5971721 | ||||||
| chr7:5971721 | A | G | 1 | a0002c0002t0036 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1678T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1678 | chr7 | 5971721 | ||||||
| chr7:5971802 | G | A | 24 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0015 others(21): Show |
88 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1597C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1597 | chr7 | 5971802 | ||||||
| chr7:5971805 | C | G | 1 | a0001c0003t0044 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1594G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1594 | chr7 | 5971805 | ||||||
| chr7:5971938 | G | A | 1 | a0002c0002t0033 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1461C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1461 | chr7 | 5971938 | ||||||
| chr7:5972034 | GA | G | 28 | a0001c0001t0001 a0001c0001t0018 a0001c0001t0048 others(25): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1364delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1364 | chr7 | 5972034 | ||||||
| chr7:5972152 | T | C | 1 | a0002c0004t0050 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1247A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1247 | chr7 | 5972152 | ||||||
| chr7:5972202 | GC | G | 11 | a0001c0003t0004 a0001c0003t0013 a0001c0003t0020 others(8): Show |
52 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1196delG | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1196 | chr7 | 5972202 | ||||||
| chr7:5972260 | G | A | 24 | a0001c0003t0004 a0001c0003t0008 a0001c0003t0013 others(21): Show |
81 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1139C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1139 | chr7 | 5972260 | ||||||
| chr7:5972278 | G | A | 2 | a0001c0008t0007 a0001c0008t0046 |
11 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1121C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1121 | chr7 | 5972278 | ||||||
| chr7:5972285 | C | T | 1 | a0002c0002t0031 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1114G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1114 | chr7 | 5972285 | ||||||
| chr7:5972291 | C | G | 18 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0015 others(15): Show |
78 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1108G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1108 | chr7 | 5972291 | ||||||
| chr7:5972367 | T | C | 1 | a0001c0001t0051 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1032A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1032 | chr7 | 5972367 | ||||||
| chr7:5972498 | A | C | 1 | a0001c0019t0053 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 901 | chr7 | 5972498 | ||||||
| chr7:5972550 | C | A | 1 | a0001c0003t0013 | 3 | HG01884.hp1 HG02257.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*849G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 849 | chr7 | 5972550 | ||||||
| chr7:5972550 | C | T | 1 | a0002c0002t0030 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*849G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 849 | chr7 | 5972550 | ||||||
| chr7:5972551 | G | A | 4 | a0006c0009t0009 a0006c0009t0026 a0006c0009t0037 others(1): Show |
11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*848C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 848 | chr7 | 5972551 | ||||||
| chr7:5972674 | C | G | 5 | a0004c0006t0005 a0004c0006t0043 a0008c0013t0042 others(2): Show |
31 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*725G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 725 | chr7 | 5972674 | ||||||
| chr7:5972694 | T | C | 23 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0018 others(20): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*705A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 705 | chr7 | 5972694 | ||||||
| chr7:5972749 | C | T | 63 | a0001c0001t0002 a0001c0003t0004 a0001c0003t0008 others(60): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*650G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 650 | chr7 | 5972749 | ||||||
| chr7:5972750 | A | G | 63 | a0001c0001t0002 a0001c0003t0004 a0001c0003t0008 others(60): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*649T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 649 | chr7 | 5972750 | ||||||
| chr7:5972824 | GTTT | G | 22 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0018 others(19): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*572_*574delAAA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 572 | chr7 | 5972824 | ||||||
| chr7:5972833 | T | G | 48 | a0001c0001t0002 a0001c0003t0008 a0001c0003t0012 others(45): Show |
171 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*566A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 566 | chr7 | 5972833 | ||||||
| chr7:5972833 | T | TG | 2 | a0002c0002t0015 a0008c0013t0042 |
3 | HG01981.hp2 NA18960.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*565_*566insC | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 565 | chr7 | 5972833 | ||||||
| chr7:5972835 | T | G | 1 | a0001c0008t0046 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 564 | chr7 | 5972835 | ||||||
| chr7:5972874 | T | C | 86 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0014 others(83): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
3_prime_UTR_variant | MODIFIER | c.*525A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 525 | chr7 | 5972874 | ||||||
| chr7:5972876 | C | CTA | 4 | a0002c0004t0038 a0002c0004t0039 a0002c0010t0011 others(1): Show |
9 | HG01496.hp2 HG02055.hp2 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*521_*522dupTA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 522 | chr7 | 5972876 | ||||||
| chr7:5972896 | C | T | 11 | a0001c0003t0004 a0001c0003t0013 a0001c0003t0020 others(8): Show |
52 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*503G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 503 | chr7 | 5972896 | ||||||
| chr7:5972929 | C | T | 2 | a0002c0004t0038 a0002c0004t0039 |
2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*470G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 470 | chr7 | 5972929 | ||||||
| chr7:5972938 | G | A | 1 | a0001c0001t0052 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*461C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 461 | chr7 | 5972938 | ||||||
| chr7:5972993 | G | A | 2 | a0001c0019t0053 a0001c0019t0054 |
2 | HG03471.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*406C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 406 | chr7 | 5972993 | ||||||
| chr7:5973069 | C | G | 6 | a0002c0004t0019 a0004c0006t0005 a0004c0006t0043 others(3): Show |
33 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*330G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 330 | chr7 | 5973069 | ||||||
| chr7:5973085 | C | T | 43 | a0001c0001t0002 a0001c0001t0018 a0001c0003t0008 others(40): Show |
135 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*314G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 314 | chr7 | 5973085 | ||||||
| chr7:5973141 | C | A | 1 | a0001c0001t0001 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*258G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 258 | chr7 | 5973141 | ||||||
| chr7:5973196 | C | T | 1 | a0002c0002t0028 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*203G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 203 | chr7 | 5973196 | ||||||
| chr7:5973225 | C | T | 1 | a0003c0005t0041 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*174G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 174 | chr7 | 5973225 | ||||||
| chr7:5973266 | C | T | 1 | a0022c0034t0027 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 133 | chr7 | 5973266 | ||||||
| chr7:5973292 | T | C | 2 | a0001c0019t0053 a0001c0019t0054 |
2 | HG03471.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*107A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 107 | chr7 | 5973292 | ||||||
| chr7:5973306 | G | GT | 46 | a0001c0001t0002 a0001c0003t0008 a0001c0003t0012 others(43): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*92dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 92 | chr7 | 5973306 | ||||||
| chr7:5973306 | G | T | 1 | a0005c0007t0025 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 93 | chr7 | 5973306 | ||||||
| chr7:5973365 | C | T | 1 | a0006c0009t0026 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*34G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 34 | chr7 | 5973365 | ||||||
| chr7:5973382 | C | G | 6 | a0005c0007t0006 a0005c0007t0022 a0005c0007t0023 others(3): Show |
19 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*17G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 17 | chr7 | 5973382 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:5973779 | G | A | 4 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2446-237C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5973779 | |||||||
| chr7:5973861 | C | T | 1 | a0025c0038t0004g0355 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2446-319G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5973861 | |||||||
| chr7:5973970 | G | A | 1 | a0009c0015t0010g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2446-428C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5973970 | |||||||
| chr7:5974010 | C | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0163 |
2 | NA18962.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2446-468G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974010 | |||||||
| chr7:5974135 | C | G | 1 | a0002c0002t0036g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2446-593G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974135 | |||||||
| chr7:5974221 | C | G | 30 | a0004c0006t0005g0282 a0004c0006t0005g0283 a0004c0006t0005g0284 others(27): Show |
30 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.2446-679G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974221 | |||||||
| chr7:5974403 | C | T | 2 | a0006c0014t0010g0018 a0006c0014t0010g0039 |
2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2446-861G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974403 | |||||||
| chr7:5974513 | C | T | 1 | a0002c0004t0001g0085 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2446-971G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974513 | |||||||
| chr7:5974549 | C | A | 3 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 |
3 | HG01106.hp2 HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2446-1007G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974549 | |||||||
| chr7:5974558 | G | C | 6 | a0009c0015t0010g0017 a0009c0015t0010g0102 a0009c0015t0010g0107 others(3): Show |
6 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2446-1016C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974558 | |||||||
| chr7:5974559 | A | C | 1 | a0001c0019t0053g0364 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2446-1017T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974559 | |||||||
| chr7:5974560 | G | A | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2446-1018C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974560 | |||||||
| chr7:5974613 | G | A | 1 | a0008c0013t0042g0094 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2446-1071C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974613 | |||||||
| chr7:5974676 | C | T | 72 | a0002c0002t0002g0072 a0002c0002t0002g0112 a0002c0002t0002g0118 others(69): Show |
72 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.2446-1134G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974676 | |||||||
| chr7:5974709 | A | C | 1 | a0012c0024t0010g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2446-1167T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974709 | |||||||
| chr7:5974718 | C | T | 3 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 |
3 | HG01106.hp2 HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2446-1176G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974718 | |||||||
| chr7:5974719 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2446-1177C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974719 | |||||||
| chr7:5974848 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2446-1306C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974848 | |||||||
| chr7:5974881 | T | C | 32 | a0001c0019t0053g0364 a0001c0019t0054g0365 a0004c0006t0005g0282 others(29): Show |
32 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2446-1339A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974881 | |||||||
| chr7:5974934 | C | T | 5 | a0001c0001t0018g0128 a0001c0001t0018g0150 a0001c0001t0052g0127 others(2): Show |
5 | HG00438.hp2 HG00609.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.2446-1392G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974934 | |||||||
| chr7:5974985 | T | G | 114 | a0001c0001t0002g0146 a0001c0003t0012g0201 a0002c0002t0002g0072 others(111): Show |
115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2446-1443A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974985 | |||||||
| chr7:5975022 | G | T | 2 | a0001c0019t0053g0364 a0001c0019t0054g0365 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2446-1480C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975022 | |||||||
| chr7:5975215 | G | A | 6 | a0001c0008t0007g0338 a0001c0008t0007g0340 a0001c0008t0007g0342 others(3): Show |
6 | HG02055.hp1 HG02965.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2446-1673C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975215 | |||||||
| chr7:5975262 | T | C | 350 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(347): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2446-1720A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975262 | |||||||
| chr7:5975266 | C | T | 1 | a0002c0004t0001g0085 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2446-1724G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975266 | |||||||
| chr7:5975357 | T | C | 80 | a0001c0003t0004g0382 a0001c0003t0044g0381 a0002c0004t0001g0005 others(77): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2446-1815A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975357 | |||||||
| chr7:5975367 | A | T | 31 | a0004c0006t0005g0282 a0004c0006t0005g0283 a0004c0006t0005g0284 others(28): Show |
31 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.2446-1825T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975367 | |||||||
| chr7:5975442 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2446-1900G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975442 | |||||||
| chr7:5975535 | C | CT | 40 | a0002c0004t0001g0005 a0002c0004t0001g0008 a0002c0004t0001g0009 others(37): Show |
44 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2446-1994_2446-199 others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975535 | |||||||
| chr7:5975536 | C | CT | 28 | a0001c0003t0020g0306 a0004c0006t0005g0284 a0004c0006t0005g0285 others(25): Show |
28 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.2446-1995dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975536 | |||||||
| chr7:5975536 | C | T | 42 | a0002c0004t0001g0005 a0002c0004t0001g0008 a0002c0004t0001g0009 others(39): Show |
46 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.2446-1994G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975536 | |||||||
| chr7:5975536 | CT | C | 237 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(234): Show |
247 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.2446-1995delA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975536 | |||||||
| chr7:5975536 | CTT | C | 18 | a0001c0001t0001g0145 a0001c0001t0001g0167 a0001c0003t0004g0336 others(15): Show |
18 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2446-1996_2446-199 others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975536 | |||||||
| chr7:5975556 | A | C | 1 | a0002c0002t0002g0199 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2446-2014T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975556 | |||||||
| chr7:5975598 | G | A | 3 | a0008c0013t0001g0025 a0008c0013t0001g0073 a0008c0013t0001g0113 |
3 | HG01243.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2445+1990C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975598 | |||||||
| chr7:5975721 | C | G | 215 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(212): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2445+1867G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975721 | |||||||
| chr7:5975724 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0147 a0001c0001t0001g0151 |
3 | HG00423.hp2 HG00621.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.2445+1864T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975724 | |||||||
| chr7:5975874 | C | A | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1714G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975874 | |||||||
| chr7:5975895 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1693T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975895 | |||||||
| chr7:5975899 | C | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1689G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975899 | |||||||
| chr7:5975918 | TGTTTTTC others(16): Show |
T | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1647_2445+166 others(27): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975918 | |||||||
| chr7:5975938 | C | A | 1 | a0009c0015t0010g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2445+1650G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975938 | |||||||
| chr7:5975944 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1644G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975944 | |||||||
| chr7:5975949 | C | T | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2445+1639G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975949 | |||||||
| chr7:5975954 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1634A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975954 | |||||||
| chr7:5975956 | T | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1632A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975956 | |||||||
| chr7:5975957 | T | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1631A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975957 | |||||||
| chr7:5975959 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1629C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975959 | |||||||
| chr7:5975968 | C | T | 12 | a0002c0002t0002g0072 a0002c0002t0002g0211 a0002c0002t0002g0226 others(9): Show |
12 | HG00673.hp2 HG02015.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.2445+1620G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975968 | |||||||
| chr7:5976004 | A | G | 238 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(235): Show |
242 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(239): Show |
intron_variant | MODIFIER | c.2445+1584T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976004 | |||||||
| chr7:5976014 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1574C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976014 | |||||||
| chr7:5976015 | C | A | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1573G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976015 | |||||||
| chr7:5976016 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1572T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976016 | |||||||
| chr7:5976024 | AG | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0123 others(92): Show |
99 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.2445+1563delC | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976024 | |||||||
| chr7:5976038 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1550T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976038 | |||||||
| chr7:5976060 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1528C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976060 | |||||||
| chr7:5976062 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1526T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976062 | |||||||
| chr7:5976068 | A | G | 166 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(163): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.2445+1520T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976068 | |||||||
| chr7:5976076 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1512A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976076 | |||||||
| chr7:5976083 | A | T | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1505T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976083 | |||||||
| chr7:5976084 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1504A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976084 | |||||||
| chr7:5976088 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1500T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976088 | |||||||
| chr7:5976100 | G | C | 2 | a0002c0023t0008g0251 a0002c0023t0008g0256 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2445+1488C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976100 | |||||||
| chr7:5976107 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1481C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976107 | |||||||
| chr7:5976108 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(134): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2445+1480A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976108 | |||||||
| chr7:5976129 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1459C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976129 | |||||||
| chr7:5976142 | A | T | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1446T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976142 | |||||||
| chr7:5976145 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1443T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976145 | |||||||
| chr7:5976167 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1421G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976167 | |||||||
| chr7:5976168 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1420C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976168 | |||||||
| chr7:5976175 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1413C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976175 | |||||||
| chr7:5976194 | T | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1394A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976194 | |||||||
| chr7:5976337 | T | C | 8 | a0006c0009t0009g0019 a0006c0009t0009g0021 a0006c0009t0009g0022 others(5): Show |
8 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2445+1251A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976337 | |||||||
| chr7:5976478 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(245): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2445+1110T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976478 | |||||||
| chr7:5976505 | C | A | 1 | a0005c0007t0006g0330 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2445+1083G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976505 | |||||||
| chr7:5976561 | C | A | 1 | a0009c0015t0010g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2445+1027G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976561 | |||||||
| chr7:5976642 | T | G | 2 | a0001c0008t0007g0321 a0009c0016t0003g0042 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2445+946A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976642 | |||||||
| chr7:5976717 | A | G | 43 | a0001c0003t0008g0353 a0001c0003t0008g0354 a0001c0008t0007g0321 others(40): Show |
44 | HG00423.hp1 HG01346.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.2445+871T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976717 | |||||||
| chr7:5976786 | G | A | 6 | a0003c0005t0003g0015 a0003c0005t0003g0016 a0003c0005t0003g0050 others(3): Show |
6 | HG02015.hp2 HG02071.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2445+802C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976786 | |||||||
| chr7:5976839 | C | A | 45 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(42): Show |
51 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.2445+749G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976839 | |||||||
| chr7:5976869 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2445+719T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976869 | |||||||
| chr7:5977016 | G | A | 2 | a0004c0006t0005g0283 a0004c0006t0005g0291 |
2 | HG01123.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.2445+572C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977016 | |||||||
| chr7:5977017 | G | A | 1 | a0008c0013t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2445+571C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977017 | |||||||
| chr7:5977029 | TA | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(195): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2445+558delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977029 | |||||||
| chr7:5977047 | G | T | 67 | a0001c0001t0001g0099 a0001c0001t0001g0121 a0001c0001t0001g0122 others(64): Show |
67 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.2445+541C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977047 | |||||||
| chr7:5977056 | G | T | 4 | a0002c0004t0001g0067 a0008c0013t0001g0025 a0008c0013t0001g0073 others(1): Show |
4 | HG01243.hp2 HG02818.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2445+532C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977056 | |||||||
| chr7:5977136 | G | C | 11 | a0001c0040t0001g0162 a0002c0002t0002g0220 a0002c0002t0002g0231 others(8): Show |
11 | HG00642.hp2 HG01891.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.2445+452C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977136 | |||||||
| chr7:5977140 | C | T | 2 | a0002c0002t0002g0199 a0002c0002t0032g0063 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2445+448G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977140 | |||||||
| chr7:5977168 | C | A | 1 | a0001c0001t0049g0196 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2445+420G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977168 | |||||||
| chr7:5977246 | G | A | 4 | a0002c0002t0002g0238 a0002c0002t0002g0247 a0002c0002t0033g0248 others(1): Show |
4 | HG00140.hp2 HG01106.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2445+342C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977246 | |||||||
| chr7:5977258 | T | C | 174 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(171): Show |
178 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.2445+330A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977258 | |||||||
| chr7:5977345 | A | G | 1 | a0006c0014t0034g0320 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2445+243T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977345 | |||||||
| chr7:5977346 | T | C | 1 | a0006c0014t0034g0320 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2445+242A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977346 | |||||||
| chr7:5977375 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2445+213C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977375 | |||||||
| chr7:5977418 | G | A | 122 | a0001c0003t0004g0352 a0002c0002t0002g0072 a0002c0002t0002g0112 others(119): Show |
123 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.2445+170C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977418 | |||||||
| chr7:5977465 | G | A | 1 | a0005c0007t0006g0371 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2445+123C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977465 | |||||||
| chr7:5977494 | G | A | 1 | a0003c0005t0003g0053 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2445+94C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977494 | |||||||
| chr7:5977496 | T | G | 1 | a0001c0003t0020g0306 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2445+92A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977496 | |||||||
| chr7:5977499 | C | T | 1 | a0004c0006t0005g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2445+89G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977499 | |||||||
| chr7:5977532 | C | T | 1 | a0001c0008t0007g0339 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2445+56G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977532 | |||||||
| chr7:5977831 | C | T | 1 | a0002c0004t0001g0081 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2276-74G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977831 | |||||||
| chr7:5977842 | G | A | 2 | a0009c0016t0001g0106 a0009c0016t0001g0108 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2276-85C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977842 | |||||||
| chr7:5977843 | G | C | 1 | a0002c0002t0002g0203 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2276-86C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977843 | |||||||
| chr7:5977857 | C | T | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-100G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977857 | |||||||
| chr7:5977862 | G | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-105C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977862 | |||||||
| chr7:5977885 | T | C | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-128A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977885 | |||||||
| chr7:5977886 | G | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-129C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977886 | |||||||
| chr7:5977891 | C | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-134G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977891 | |||||||
| chr7:5977892 | A | G | 87 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(84): Show |
88 | HG00280.hp1 HG00423.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.2276-135T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977892 | |||||||
| chr7:5977895 | G | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-138C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977895 | |||||||
| chr7:5977916 | C | G | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-159G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977916 | |||||||
| chr7:5977956 | A | G | 1 | a0001c0003t0008g0353 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2276-199T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977956 | |||||||
| chr7:5978028 | G | A | 9 | a0002c0002t0002g0204 a0002c0002t0002g0211 a0002c0002t0002g0215 others(6): Show |
9 | HG00673.hp2 HG02056.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.2276-271C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978028 | |||||||
| chr7:5978033 | T | C | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-276A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978033 | |||||||
| chr7:5978074 | CG | C | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-318delC | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978074 | |||||||
| chr7:5978076 | G | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-319C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978076 | |||||||
| chr7:5978085 | C | T | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-328G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978085 | |||||||
| chr7:5978086 | G | A | 5 | a0007c0011t0002g0255 a0007c0011t0002g0257 a0007c0011t0002g0265 others(2): Show |
5 | HG02717.hp1 NA18977.hp2 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.2276-329C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978086 | |||||||
| chr7:5978120 | C | CAA | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-364_2276-363i others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978120 | |||||||
| chr7:5978132 | A | AAAAAAT | 38 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(35): Show |
39 | HG00423.hp1 HG00738.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.2276-376_2276-375i others(8): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978132 | |||||||
| chr7:5978141 | C | T | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-384G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978141 | |||||||
| chr7:5978155 | A | C | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-398T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978155 | |||||||
| chr7:5978157 | C | G | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-400G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978157 | |||||||
| chr7:5978176 | A | G | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-419T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978176 | |||||||
| chr7:5978180 | A | AC | 40 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(37): Show |
41 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2275+415dupG | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978180 | |||||||
| chr7:5978201 | T | TA | 18 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(15): Show |
19 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.2275+394_2275+395i others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978201 | |||||||
| chr7:5978202 | T | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2275+394A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978202 | |||||||
| chr7:5978211 | C | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2275+385G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978211 | |||||||
| chr7:5978212 | T | C | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2275+384A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978212 | |||||||
| chr7:5978213 | G | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2275+383C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978213 | |||||||
| chr7:5978253 | A | G | 1 | a0001c0003t0045g0376 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2275+343T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978253 | |||||||
| chr7:5978271 | G | A | 319 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(316): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.2275+325C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978271 | |||||||
| chr7:5978272 | A | AT | 9 | a0002c0002t0028g0224 a0002c0004t0001g0085 a0002c0004t0008g0209 others(6): Show |
9 | HG01361.hp2 HG02717.hp1 NA18977.hp2 others(6): Show |
intron_variant | MODIFIER | c.2275+323dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978272 | |||||||
| chr7:5978272 | A | ATT | 14 | a0006c0009t0009g0019 a0006c0009t0009g0020 a0006c0009t0009g0021 others(11): Show |
14 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.2275+322_2275+323d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978272 | |||||||
| chr7:5978272 | A | ATTT | 27 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(24): Show |
28 | HG00423.hp1 HG00738.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.2275+321_2275+323d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978272 | |||||||
| chr7:5978273 | T | A | 1 | a0001c0003t0012g0201 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2275+323A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978273 | |||||||
| chr7:5978302 | C | T | 5 | a0001c0003t0004g0012 a0001c0003t0004g0345 a0001c0003t0004g0351 others(2): Show |
6 | HG00621.hp2 HG02027.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.2275+294G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978302 | |||||||
| chr7:5978340 | G | A | 1 | a0001c0030t0008g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2275+256C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978340 | |||||||
| chr7:5978391 | C | T | 2 | a0006c0014t0010g0018 a0006c0014t0010g0039 |
2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2275+205G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978391 | |||||||
| chr7:5978426 | AC | A | 4 | a0003c0005t0003g0002 a0003c0005t0003g0049 a0003c0005t0003g0055 others(1): Show |
8 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.2275+169delG | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978426 | |||||||
| chr7:5978427 | C | G | 46 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(43): Show |
47 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.2275+169G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978427 | |||||||
| chr7:5978459 | T | C | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2275+137A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978459 | |||||||
| chr7:5978470 | C | G | 2 | a0001c0003t0001g0174 a0001c0003t0001g0175 |
2 | HG00639.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2275+126G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978470 | |||||||
| chr7:5978479 | C | G | 43 | a0001c0003t0004g0347 a0001c0003t0004g0348 a0005c0007t0006g0011 others(40): Show |
44 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2275+117G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978479 | |||||||
| chr7:5978571 | G | A | 2 | a0001c0019t0053g0364 a0001c0019t0054g0365 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2275+25C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978571 | |||||||
| chr7:5978747 | C | G | 9 | a0009c0015t0010g0017 a0009c0015t0010g0102 a0009c0015t0010g0107 others(6): Show |
9 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2175-51G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978747 | |||||||
| chr7:5978813 | A | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(132): Show |
141 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.2175-117T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978813 | |||||||
| chr7:5978822 | C | T | 1 | a0001c0001t0049g0196 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2175-126G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978822 | |||||||
| chr7:5978824 | C | T | 42 | a0003c0028t0035g0054 a0005c0007t0006g0011 a0005c0007t0006g0318 others(39): Show |
43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-128G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978824 | |||||||
| chr7:5978825 | T | A | 42 | a0003c0028t0035g0054 a0005c0007t0006g0011 a0005c0007t0006g0318 others(39): Show |
43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-129A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978825 | |||||||
| chr7:5978827 | C | T | 42 | a0003c0028t0035g0054 a0005c0007t0006g0011 a0005c0007t0006g0318 others(39): Show |
43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-131G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978827 | |||||||
| chr7:5978882 | A | G | 8 | a0006c0009t0009g0019 a0006c0009t0009g0021 a0006c0009t0009g0022 others(5): Show |
8 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2175-186T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978882 | |||||||
| chr7:5978904 | G | A | 42 | a0003c0028t0035g0054 a0005c0007t0006g0011 a0005c0007t0006g0318 others(39): Show |
43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-208C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978904 | |||||||
| chr7:5978958 | C | G | 42 | a0003c0028t0035g0054 a0005c0007t0006g0011 a0005c0007t0006g0318 others(39): Show |
43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-262G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978958 | |||||||
| chr7:5978960 | C | T | 42 | a0003c0028t0035g0054 a0005c0007t0006g0011 a0005c0007t0006g0318 others(39): Show |
43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-264G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978960 | |||||||
| chr7:5978961 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0103 others(29): Show |
36 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.2175-265C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978961 | |||||||
| chr7:5978963 | G | C | 1 | a0004c0006t0005g0292 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2175-267C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978963 | |||||||
| chr7:5978983 | C | T | 1 | a0002c0002t0002g0239 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2175-287G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978983 | |||||||
| chr7:5978988 | A | AGTTTGAG others(8): Show |
1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2175-307_2175-293d others(17): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978988 | |||||||
| chr7:5978997 | C | T | 42 | a0003c0028t0035g0054 a0005c0007t0006g0011 a0005c0007t0006g0318 others(39): Show |
43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-301G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978997 | |||||||
| chr7:5978999 | G | A | 42 | a0003c0028t0035g0054 a0005c0007t0006g0011 a0005c0007t0006g0318 others(39): Show |
43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-303C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978999 | |||||||
| chr7:5979013 | A | G | 42 | a0003c0028t0035g0054 a0005c0007t0006g0011 a0005c0007t0006g0318 others(39): Show |
43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-317T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979013 | |||||||
| chr7:5979016 | G | A | 10 | a0001c0001t0014g0171 a0009c0015t0010g0017 a0009c0015t0010g0102 others(7): Show |
10 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2175-320C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979016 | |||||||
| chr7:5979021 | A | C | 48 | a0001c0003t0008g0353 a0001c0003t0008g0354 a0001c0030t0008g0058 others(45): Show |
49 | HG00099.hp1 HG00423.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2175-325T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979021 | |||||||
| chr7:5979039 | A | G | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-343T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979039 | |||||||
| chr7:5979103 | T | G | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-407A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979103 | |||||||
| chr7:5979140 | T | C | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-444A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979140 | |||||||
| chr7:5979159 | G | A | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-463C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979159 | |||||||
| chr7:5979165 | G | A | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-469C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979165 | |||||||
| chr7:5979179 | G | A | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-483C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979179 | |||||||
| chr7:5979180 | C | T | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-484G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979180 | |||||||
| chr7:5979181 | G | A | 1 | a0002c0002t0002g0231 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2175-485C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979181 | |||||||
| chr7:5979185 | C | T | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-489G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979185 | |||||||
| chr7:5979186 | A | G | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-490T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979186 | |||||||
| chr7:5979201 | C | CA | 116 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(113): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.2175-506dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | |||||||
| chr7:5979201 | C | CAA | 13 | a0001c0001t0001g0324 a0001c0003t0004g0351 a0001c0003t0004g0380 others(10): Show |
13 | HG01175.hp1 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.2175-507_2175-506d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | |||||||
| chr7:5979201 | C | CAAA | 57 | a0001c0001t0001g0003 a0001c0001t0001g0103 a0001c0001t0001g0122 others(54): Show |
60 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.2175-508_2175-506d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | |||||||
| chr7:5979201 | C | CAAAA | 34 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0121 others(31): Show |
35 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2175-509_2175-506d others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | |||||||
| chr7:5979201 | C | CAAAAA | 14 | a0001c0001t0001g0160 a0001c0001t0001g0190 a0005c0007t0006g0373 others(11): Show |
14 | HG01109.hp1 HG01496.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2175-510_2175-506d others(7): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | |||||||
| chr7:5979201 | C | CAAAAAA | 17 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0329 others(14): Show |
18 | HG00738.hp2 HG01346.hp2 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.2175-511_2175-506d others(8): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | |||||||
| chr7:5979217 | A | C | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-521T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979217 | |||||||
| chr7:5979230 | T | C | 41 | a0003c0028t0035g0054 a0005c0007t0006g0011 a0005c0007t0006g0318 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175-534A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979230 | |||||||
| chr7:5979231 | A | C | 1 | a0016c0033t0010g0105 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2175-535T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979231 | |||||||
| chr7:5979236 | C | G | 1 | a0016c0033t0010g0105 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2175-540G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979236 | |||||||
| chr7:5979252 | G | A | 1 | a0016c0033t0010g0105 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2175-556C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979252 | |||||||
| chr7:5979385 | T | C | 8 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(5): Show |
8 | HG02074.hp2 HG02155.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.2175-689A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979385 | |||||||
| chr7:5979387 | T | A | 30 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(27): Show |
31 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.2175-691A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979387 | |||||||
| chr7:5979390 | C | CA | 51 | a0001c0001t0001g0157 a0001c0001t0001g0166 a0001c0001t0001g0190 others(48): Show |
52 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.2175-695dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979390 | |||||||
| chr7:5979409 | C | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175-713G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979409 | |||||||
| chr7:5979410 | A | T | 1 | a0002c0012t0002g0177 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2175-714T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979410 | |||||||
| chr7:5979470 | T | C | 3 | a0006c0009t0009g0020 a0006c0009t0026g0027 a0006c0009t0037g0026 |
3 | HG02809.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2175-774A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979470 | |||||||
| chr7:5979519 | C | T | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175-823G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979519 | |||||||
| chr7:5979532 | C | G | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175-836G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979532 | |||||||
| chr7:5979593 | T | A | 375 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(372): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.2175-897A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979593 | |||||||
| chr7:5979622 | G | C | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175-926C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979622 | |||||||
| chr7:5979643 | C | T | 130 | a0001c0003t0008g0353 a0001c0003t0008g0354 a0001c0030t0008g0058 others(127): Show |
131 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.2175-947G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979643 | |||||||
| chr7:5979665 | T | A | 128 | a0001c0003t0008g0353 a0001c0003t0008g0354 a0001c0030t0008g0058 others(125): Show |
129 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2175-969A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979665 | |||||||
| chr7:5979665 | T | C | 2 | a0002c0002t0002g0239 a0012c0025t0001g0366 |
2 | HG02129.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2175-969A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979665 | |||||||
| chr7:5979666 | T | G | 128 | a0001c0003t0008g0353 a0001c0003t0008g0354 a0001c0030t0008g0058 others(125): Show |
129 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2175-970A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979666 | |||||||
| chr7:5979668 | G | GCTT | 127 | a0001c0003t0008g0353 a0001c0003t0008g0354 a0001c0030t0008g0058 others(124): Show |
128 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.2175-973_2175-972i others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979668 | |||||||
| chr7:5979668 | G | T | 2 | a0002c0002t0002g0239 a0012c0025t0001g0366 |
2 | HG02129.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2175-972C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979668 | |||||||
| chr7:5979713 | G | T | 2 | a0011c0018t0017g0374 a0011c0018t0017g0375 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2175-1017C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979713 | |||||||
| chr7:5979899 | C | G | 11 | a0006c0009t0009g0019 a0006c0009t0009g0020 a0006c0009t0009g0021 others(8): Show |
11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2175-1203G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979899 | |||||||
| chr7:5979924 | G | C | 1 | a0003c0028t0035g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-1228C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979924 | |||||||
| chr7:5979984 | G | A | 1 | a0003c0005t0003g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2175-1288C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979984 | |||||||
| chr7:5980320 | ACAGGGGC others(8): Show |
A | 1 | a0002c0002t0002g0261 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2175-1639_2175-162 others(19): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980320 | |||||||
| chr7:5980342 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175-1646C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980342 | |||||||
| chr7:5980435 | T | C | 44 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0019t0054g0365 others(41): Show |
45 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.2175-1739A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980435 | |||||||
| chr7:5980453 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175-1757C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980453 | |||||||
| chr7:5980482 | G | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175-1786C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980482 | |||||||
| chr7:5980498 | A | G | 318 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(315): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.2175-1802T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980498 | |||||||
| chr7:5980534 | T | C | 1 | a0003c0020t0003g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2175-1838A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980534 | |||||||
| chr7:5980552 | G | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175-1856C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980552 | |||||||
| chr7:5980567 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175-1871G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980567 | |||||||
| chr7:5980705 | A | C | 5 | a0001c0003t0004g0012 a0001c0003t0004g0345 a0001c0003t0004g0351 others(2): Show |
6 | HG00621.hp2 HG02027.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.2175-2009T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980705 | |||||||
| chr7:5980919 | C | CAAACTAC others(137): Show |
1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1904_2174+190 others(148): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980919 | |||||||
| chr7:5980943 | T | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1881A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980943 | |||||||
| chr7:5980956 | A | G | 1 | a0006c0014t0034g0320 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2174+1868T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980956 | |||||||
| chr7:5980967 | C | T | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2174+1857G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980967 | |||||||
| chr7:5981042 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2174+1782C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981042 | |||||||
| chr7:5981068 | T | C | 1 | a0012c0024t0010g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2174+1756A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981068 | |||||||
| chr7:5981080 | C | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1744G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981080 | |||||||
| chr7:5981127 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1697G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981127 | |||||||
| chr7:5981142 | G | C | 1 | a0004c0006t0043g0314 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2174+1682C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981142 | |||||||
| chr7:5981143 | T | C | 4 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2174+1681A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981143 | |||||||
| chr7:5981150 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1674C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981150 | |||||||
| chr7:5981165 | T | C | 2 | a0002c0012t0002g0101 a0012c0025t0001g0366 |
2 | HG02135.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2174+1659A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981165 | |||||||
| chr7:5981172 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1652C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981172 | |||||||
| chr7:5981179 | G | C | 1 | a0001c0003t0004g0064 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2174+1645C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981179 | |||||||
| chr7:5981234 | A | G | 42 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0005c0007t0006g0011 others(39): Show |
43 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2174+1590T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981234 | |||||||
| chr7:5981348 | G | A | 2 | a0001c0003t0008g0353 a0001c0003t0008g0354 |
2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2174+1476C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981348 | |||||||
| chr7:5981377 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0051g0129 |
2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2174+1447A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981377 | |||||||
| chr7:5981391 | C | T | 87 | a0002c0002t0002g0072 a0002c0002t0002g0112 a0002c0002t0002g0118 others(84): Show |
87 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.2174+1433G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981391 | |||||||
| chr7:5981399 | C | G | 87 | a0002c0002t0002g0072 a0002c0002t0002g0112 a0002c0002t0002g0118 others(84): Show |
87 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.2174+1425G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981399 | |||||||
| chr7:5981412 | T | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1412A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981412 | |||||||
| chr7:5981719 | G | A | 4 | a0002c0002t0002g0226 a0002c0004t0001g0069 a0002c0004t0001g0079 others(1): Show |
4 | HG00673.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2174+1105C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981719 | |||||||
| chr7:5981725 | T | G | 3 | a0002c0004t0001g0069 a0002c0004t0001g0079 a0012c0025t0001g0366 |
3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+1099A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981725 | |||||||
| chr7:5981726 | A | G | 3 | a0002c0004t0001g0069 a0002c0004t0001g0079 a0012c0025t0001g0366 |
3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+1098T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981726 | |||||||
| chr7:5981727 | C | T | 3 | a0002c0004t0001g0069 a0002c0004t0001g0079 a0012c0025t0001g0366 |
3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+1097G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981727 | |||||||
| chr7:5981762 | G | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1062C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981762 | |||||||
| chr7:5981838 | C | T | 3 | a0002c0004t0001g0069 a0002c0004t0001g0079 a0012c0025t0001g0366 |
3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+986G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981838 | |||||||
| chr7:5981839 | C | G | 3 | a0002c0004t0001g0069 a0002c0004t0001g0079 a0012c0025t0001g0366 |
3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+985G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981839 | |||||||
| chr7:5981841 | T | C | 3 | a0002c0004t0001g0069 a0002c0004t0001g0079 a0012c0025t0001g0366 |
3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+983A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981841 | |||||||
| chr7:5981865 | T | A | 1 | a0003c0005t0003g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2174+959A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981865 | |||||||
| chr7:5981910 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+914G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981910 | |||||||
| chr7:5981912 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+912C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981912 | |||||||
| chr7:5981920 | G | T | 1 | a0002c0004t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2174+904C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981920 | |||||||
| chr7:5981973 | T | C | 2 | a0006c0014t0010g0018 a0006c0014t0010g0039 |
2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2174+851A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981973 | |||||||
| chr7:5981992 | A | C | 3 | a0002c0002t0008g0250 a0002c0023t0008g0251 a0002c0023t0008g0256 |
3 | HG01070.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2174+832T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981992 | |||||||
| chr7:5981995 | T | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(81): Show |
88 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2174+829A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981995 | |||||||
| chr7:5982149 | G | A | 1 | a0001c0003t0012g0201 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2174+675C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982149 | |||||||
| chr7:5982177 | A | G | 44 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0005c0007t0006g0011 others(41): Show |
45 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.2174+647T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982177 | |||||||
| chr7:5982291 | C | T | 88 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(85): Show |
88 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.2174+533G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982291 | |||||||
| chr7:5982299 | G | A | 1 | a0004c0006t0005g0305 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2174+525C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982299 | |||||||
| chr7:5982383 | T | C | 2 | a0001c0003t0004g0334 a0001c0003t0004g0335 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2174+441A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982383 | |||||||
| chr7:5982432 | G | A | 13 | a0001c0001t0001g0099 a0001c0001t0001g0121 a0001c0001t0001g0148 others(10): Show |
13 | NA18941.hp2 NA18948.hp1 NA18950.hp1 others(10): Show |
intron_variant | MODIFIER | c.2174+392C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982432 | |||||||
| chr7:5982471 | C | T | 2 | a0001c0001t0014g0171 a0012c0025t0001g0366 |
2 | HG02717.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.2174+353G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982471 | |||||||
| chr7:5982479 | T | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+345A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982479 | |||||||
| chr7:5982483 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+341G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982483 | |||||||
| chr7:5982547 | G | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(83): Show |
90 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.2174+277C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982547 | |||||||
| chr7:5982629 | G | A | 9 | a0009c0015t0010g0017 a0009c0015t0010g0102 a0009c0015t0010g0107 others(6): Show |
9 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2174+195C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982629 | |||||||
| chr7:5982712 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+112C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982712 | |||||||
| chr7:5982721 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+103C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982721 | |||||||
| chr7:5982763 | T | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+61A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982763 | |||||||
| chr7:5982995 | C | T | 83 | a0002c0002t0002g0072 a0002c0002t0002g0112 a0002c0002t0002g0118 others(80): Show |
83 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(80): Show |
splice_region_variant&intron_variant | LOW | c.2007-4G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5982995 | |||||||
| chr7:5982998 | G | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.2007-7C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5982998 | |||||||
| chr7:5983118 | T | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-127A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983118 | |||||||
| chr7:5983142 | T | C | 15 | a0005c0007t0006g0370 a0005c0007t0006g0373 a0006c0009t0009g0019 others(12): Show |
15 | HG01496.hp1 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2007-151A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983142 | |||||||
| chr7:5983144 | G | A | 1 | a0001c0019t0053g0364 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2007-153C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983144 | |||||||
| chr7:5983154 | C | T | 6 | a0004c0006t0005g0308 a0004c0006t0005g0313 a0004c0006t0005g0315 others(3): Show |
6 | HG02109.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2007-163G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983154 | |||||||
| chr7:5983278 | T | C | 53 | a0001c0001t0001g0159 a0002c0002t0036g0097 a0002c0004t0001g0005 others(50): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.2007-287A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983278 | |||||||
| chr7:5983281 | T | C | 5 | a0001c0001t0001g0159 a0002c0004t0008g0209 a0002c0004t0008g0217 others(2): Show |
5 | NA18941.hp2 NA18985.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.2007-290A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983281 | |||||||
| chr7:5983330 | C | T | 186 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(183): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.2007-339G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983330 | |||||||
| chr7:5983347 | G | C | 2 | a0005c0007t0006g0367 a0005c0007t0006g0368 |
2 | HG02129.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.2007-356C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983347 | |||||||
| chr7:5983349 | T | A | 1 | a0020c0029t0003g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2007-358A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983349 | |||||||
| chr7:5983389 | G | A | 11 | a0006c0009t0009g0019 a0006c0009t0009g0020 a0006c0009t0009g0021 others(8): Show |
11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2007-398C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983389 | |||||||
| chr7:5983400 | C | T | 3 | a0002c0004t0001g0264 a0008c0013t0042g0094 a0012c0025t0001g0366 |
3 | HG02717.hp1 NA18960.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2007-409G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983400 | |||||||
| chr7:5983402 | T | C | 99 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0003t0020g0306 others(96): Show |
104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.2007-411A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983402 | |||||||
| chr7:5983527 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-536G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983527 | |||||||
| chr7:5983528 | A | T | 1 | a0002c0002t0015g0218 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2007-537T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983528 | |||||||
| chr7:5983579 | A | G | 1 | a0001c0001t0052g0127 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2007-588T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983579 | |||||||
| chr7:5983591 | C | T | 1 | a0001c0003t0012g0201 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2007-600G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983591 | |||||||
| chr7:5983607 | C | G | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-616G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983607 | |||||||
| chr7:5983609 | A | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-618T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983609 | |||||||
| chr7:5983615 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-624G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983615 | |||||||
| chr7:5983653 | T | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-662A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983653 | |||||||
| chr7:5983681 | A | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-690T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983681 | |||||||
| chr7:5983714 | T | C | 2 | a0002c0002t0030g0210 a0012c0025t0001g0366 |
2 | HG02040.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2007-723A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983714 | |||||||
| chr7:5983719 | G | A | 1 | a0001c0001t0049g0196 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2007-728C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983719 | |||||||
| chr7:5983745 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0195 |
2 | NA18951.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2007-754T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983745 | |||||||
| chr7:5983754 | C | T | 1 | a0003c0005t0003g0050 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2007-763G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983754 | |||||||
| chr7:5983941 | C | T | 94 | a0002c0002t0002g0072 a0002c0002t0002g0112 a0002c0002t0002g0118 others(91): Show |
94 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.2007-950G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983941 | |||||||
| chr7:5983942 | G | A | 41 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(38): Show |
42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2007-951C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983942 | |||||||
| chr7:5983947 | T | C | 44 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0005c0007t0006g0011 others(41): Show |
45 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.2007-956A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983947 | |||||||
| chr7:5983949 | G | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-958C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983949 | |||||||
| chr7:5983990 | C | T | 1 | a0001c0019t0054g0365 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2007-999G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983990 | |||||||
| chr7:5984006 | T | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1015A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984006 | |||||||
| chr7:5984025 | A | G | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1034T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984025 | |||||||
| chr7:5984040 | A | G | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1049T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984040 | |||||||
| chr7:5984061 | C | T | 2 | a0003c0005t0003g0041 a0012c0025t0001g0366 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2007-1070G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984061 | |||||||
| chr7:5984078 | C | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1087G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984078 | |||||||
| chr7:5984088 | T | C | 1 | a0002c0004t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2007-1097A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984088 | |||||||
| chr7:5984138 | G | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1147C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984138 | |||||||
| chr7:5984142 | G | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1151C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984142 | |||||||
| chr7:5984153 | A | G | 1 | a0002c0002t0002g0221 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2007-1162T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984153 | |||||||
| chr7:5984161 | C | T | 2 | a0001c0001t0001g0185 a0012c0025t0001g0366 |
2 | HG02717.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2007-1170G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984161 | |||||||
| chr7:5984295 | T | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1304A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984295 | |||||||
| chr7:5984320 | C | T | 9 | a0009c0015t0010g0017 a0009c0015t0010g0102 a0009c0015t0010g0107 others(6): Show |
9 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2007-1329G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984320 | |||||||
| chr7:5984387 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1396G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984387 | |||||||
| chr7:5984404 | G | A | 48 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(45): Show |
54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.2007-1413C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984404 | |||||||
| chr7:5984407 | G | T | 38 | a0005c0007t0006g0011 a0005c0007t0006g0318 a0005c0007t0006g0328 others(35): Show |
39 | HG00423.hp1 HG00738.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.2007-1416C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984407 | |||||||
| chr7:5984412 | T | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1421A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984412 | |||||||
| chr7:5984433 | G | A | 2 | a0001c0019t0053g0364 a0001c0019t0054g0365 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2007-1442C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984433 | |||||||
| chr7:5984440 | T | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1449A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984440 | |||||||
| chr7:5984517 | C | G | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1526G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984517 | |||||||
| chr7:5984522 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1531C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984522 | |||||||
| chr7:5984646 | A | G | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1655T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984646 | |||||||
| chr7:5984649 | G | A | 1 | a0004c0006t0005g0302 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2007-1658C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984649 | |||||||
| chr7:5984721 | C | G | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1730G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984721 | |||||||
| chr7:5984727 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1736C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984727 | |||||||
| chr7:5984763 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1772G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984763 | |||||||
| chr7:5984794 | A | G | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1803T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984794 | |||||||
| chr7:5984796 | C | G | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1805G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984796 | |||||||
| chr7:5984852 | A | G | 1 | a0012c0024t0010g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2007-1861T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984852 | |||||||
| chr7:5984913 | C | T | 1 | a0001c0003t0004g0361 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2006+1846G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984913 | |||||||
| chr7:5984999 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1760C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984999 | |||||||
| chr7:5985039 | A | G | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1720T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985039 | |||||||
| chr7:5985046 | G | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1713C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985046 | |||||||
| chr7:5985055 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1704C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985055 | |||||||
| chr7:5985105 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1654G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985105 | |||||||
| chr7:5985147 | G | A | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1612C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985147 | |||||||
| chr7:5985163 | T | G | 15 | a0001c0003t0003g0323 a0001c0003t0004g0012 a0001c0003t0004g0345 others(12): Show |
16 | HG00621.hp2 HG02027.hp2 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.2006+1596A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985163 | |||||||
| chr7:5985179 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1580G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985179 | |||||||
| chr7:5985228 | C | T | 9 | a0009c0015t0010g0017 a0009c0015t0010g0102 a0009c0015t0010g0107 others(6): Show |
9 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2006+1531G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985228 | |||||||
| chr7:5985260 | G | C | 1 | a0002c0002t0002g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2006+1499C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985260 | |||||||
| chr7:5985264 | A | AT | 93 | a0001c0001t0001g0158 a0001c0001t0001g0190 a0001c0003t0001g0197 others(90): Show |
99 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.2006+1494dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985264 | |||||||
| chr7:5985264 | A | ATT | 8 | a0001c0001t0001g0099 a0001c0003t0004g0347 a0001c0003t0004g0380 others(5): Show |
8 | HG01261.hp2 HG01358.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2006+1493_2006+149 others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985264 | |||||||
| chr7:5985264 | AT | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0140 a0001c0001t0001g0149 others(5): Show |
8 | HG00558.hp2 HG01168.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.2006+1494delA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985264 | |||||||
| chr7:5985505 | G | A | 43 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0005c0007t0006g0011 others(40): Show |
44 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.2006+1254C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985505 | |||||||
| chr7:5985639 | C | T | 2 | a0002c0004t0038g0276 a0002c0004t0039g0275 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2006+1120G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985639 | |||||||
| chr7:5985647 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(78): Show |
85 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.2006+1112C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985647 | |||||||
| chr7:5985911 | G | A | 1 | a0012c0024t0010g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2006+848C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985911 | |||||||
| chr7:5985914 | C | T | 2 | a0006c0014t0010g0018 a0006c0014t0010g0039 |
2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2006+845G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985914 | |||||||
| chr7:5985982 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2006+777G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985982 | |||||||
| chr7:5986072 | A | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(226): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.2006+687T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986072 | |||||||
| chr7:5986214 | C | T | 137 | a0002c0002t0002g0072 a0002c0002t0002g0112 a0002c0002t0002g0118 others(134): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2006+545G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986214 | |||||||
| chr7:5986263 | C | T | 33 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(30): Show |
39 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2006+496G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986263 | |||||||
| chr7:5986349 | G | A | 24 | a0004c0006t0005g0282 a0004c0006t0005g0283 a0004c0006t0005g0284 others(21): Show |
24 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.2006+410C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986349 | |||||||
| chr7:5986462 | T | C | 3 | a0005c0007t0006g0370 a0005c0007t0006g0373 a0019c0026t0006g0372 |
3 | HG01496.hp1 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2006+297A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986462 | |||||||
| chr7:5986490 | G | A | 4 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2006+269C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986490 | |||||||
| chr7:5986561 | G | A | 1 | a0006c0014t0034g0320 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2006+198C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986561 | |||||||
| chr7:5986591 | C | CTGA | 49 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(46): Show |
55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.2006+165_2006+167d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986591 | |||||||
| chr7:5986597 | C | T | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+162G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986597 | |||||||
| chr7:5986753 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(78): Show |
85 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
splice_region_variant&intron_variant | LOW | c.2006+6G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986753 | |||||||
| chr7:5987736 | G | A | 6 | a0002c0002t0002g0118 a0002c0002t0002g0241 a0002c0002t0002g0261 others(3): Show |
6 | HG01192.hp1 HG01978.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1145-116C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5987736 | |||||||
| chr7:5987818 | G | A | 2 | a0001c0001t0018g0128 a0001c0001t0018g0150 |
2 | HG00438.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1145-198C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5987818 | |||||||
| chr7:5988009 | C | T | 93 | a0002c0002t0002g0112 a0002c0002t0002g0118 a0002c0002t0002g0119 others(90): Show |
93 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1145-389G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988009 | |||||||
| chr7:5988052 | C | CA | 28 | a0001c0003t0004g0360 a0001c0003t0004g0379 a0002c0002t0002g0112 others(25): Show |
28 | HG00673.hp2 HG01071.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.1145-433dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988052 | |||||||
| chr7:5988052 | CA | C | 103 | a0001c0001t0001g0099 a0001c0001t0001g0133 a0001c0001t0001g0134 others(100): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1145-433delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988052 | |||||||
| chr7:5988052 | CAA | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0103 others(104): Show |
111 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1145-434_1145-433d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988052 | |||||||
| chr7:5988071 | A | C | 31 | a0001c0019t0053g0364 a0003c0005t0001g0059 a0003c0005t0003g0001 others(28): Show |
41 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1145-451T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988071 | |||||||
| chr7:5988073 | A | C | 2 | a0001c0003t0013g0014 a0001c0003t0013g0363 |
3 | HG01884.hp1 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1145-453T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988073 | |||||||
| chr7:5988093 | A | G | 1 | a0002c0004t0001g0281 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1145-473T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988093 | |||||||
| chr7:5988094 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1145-474T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988094 | |||||||
| chr7:5988293 | C | T | 2 | a0002c0004t0038g0276 a0002c0004t0039g0275 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1145-673G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988293 | |||||||
| chr7:5988406 | A | T | 1 | a0006c0014t0010g0039 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1145-786T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988406 | |||||||
| chr7:5988506 | C | T | 1 | a0002c0004t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1145-886G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988506 | |||||||
| chr7:5988548 | G | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0088 |
3 | HG02622.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1145-928C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988548 | |||||||
| chr7:5988556 | C | T | 1 | a0020c0029t0003g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1145-936G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988556 | |||||||
| chr7:5988559 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(80): Show |
87 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1145-939A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988559 | |||||||
| chr7:5988755 | A | C | 1 | a0001c0003t0045g0376 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1144+1045T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988755 | |||||||
| chr7:5988850 | TTTTG | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(79): Show |
86 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1144+946_1144+949d others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988850 | |||||||
| chr7:5988879 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1144+921C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988879 | |||||||
| chr7:5988946 | C | G | 4 | a0002c0002t0002g0238 a0002c0002t0002g0247 a0002c0002t0033g0248 others(1): Show |
4 | HG00140.hp2 HG01106.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+854G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988946 | |||||||
| chr7:5988969 | A | C | 1 | a0005c0007t0024g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1144+831T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988969 | |||||||
| chr7:5989005 | G | A | 2 | a0001c0003t0001g0174 a0001c0003t0001g0175 |
2 | HG00639.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1144+795C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989005 | |||||||
| chr7:5989016 | C | T | 136 | a0001c0003t0001g0266 a0002c0002t0002g0072 a0002c0002t0002g0112 others(133): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1144+784G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989016 | |||||||
| chr7:5989056 | C | T | 78 | a0001c0003t0001g0266 a0002c0002t0002g0112 a0002c0002t0002g0118 others(75): Show |
78 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1144+744G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989056 | |||||||
| chr7:5989065 | T | C | 23 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0002c0004t0021g0115 others(20): Show |
24 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1144+735A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989065 | |||||||
| chr7:5989088 | G | A | 1 | a0006c0014t0034g0320 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1144+712C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989088 | |||||||
| chr7:5989120 | G | T | 5 | a0001c0003t0004g0012 a0001c0003t0004g0345 a0001c0003t0004g0351 others(2): Show |
6 | HG00621.hp2 HG02027.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144+680C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989120 | |||||||
| chr7:5989130 | A | G | 3 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 |
3 | HG01106.hp2 HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1144+670T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989130 | |||||||
| chr7:5989137 | G | A | 309 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(306): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1144+663C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989137 | |||||||
| chr7:5989141 | C | A | 1 | a0002c0039t0001g0116 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1144+659G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989141 | |||||||
| chr7:5989220 | C | T | 1 | a0002c0002t0032g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1144+580G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989220 | |||||||
| chr7:5989274 | T | C | 4 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+526A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989274 | |||||||
| chr7:5989354 | G | T | 1 | a0002c0004t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1144+446C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989354 | |||||||
| chr7:5989381 | T | C | 305 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(302): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1144+419A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989381 | |||||||
| chr7:5989387 | C | T | 1 | a0009c0015t0010g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1144+413G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989387 | |||||||
| chr7:5989514 | C | T | 4 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+286G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989514 | |||||||
| chr7:5989658 | C | T | 1 | a0003c0005t0003g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1144+142G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989658 | |||||||
| chr7:5989784 | A | C | 1 | a0006c0014t0010g0018 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1144+16T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989784 | |||||||
| chr7:5990033 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.989-78G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990033 | |||||||
| chr7:5990059 | G | GT | 17 | a0002c0004t0001g0008 a0002c0004t0001g0069 a0002c0004t0001g0070 others(14): Show |
18 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.989-105dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990059 | |||||||
| chr7:5990117 | C | T | 131 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0002c0002t0002g0072 others(128): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.989-162G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990117 | |||||||
| chr7:5990211 | T | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(78): Show |
85 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.989-256A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990211 | |||||||
| chr7:5990254 | C | T | 2 | a0002c0010t0011g0033 a0002c0010t0011g0034 |
2 | HG01496.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.989-299G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990254 | |||||||
| chr7:5990297 | C | G | 1 | a0005c0007t0006g0370 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.989-342G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990297 | |||||||
| chr7:5990327 | G | T | 1 | a0001c0003t0004g0360 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.989-372C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990327 | |||||||
| chr7:5990389 | C | T | 1 | a0012c0024t0010g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.989-434G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990389 | |||||||
| chr7:5990453 | A | T | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.989-498T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990453 | |||||||
| chr7:5990473 | C | T | 2 | a0001c0001t0001g0156 a0002c0002t0036g0097 |
2 | HG01243.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.989-518G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990473 | |||||||
| chr7:5990513 | A | G | 1 | a0005c0007t0006g0318 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.989-558T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990513 | |||||||
| chr7:5990656 | G | A | 129 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0002c0002t0002g0072 others(126): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.989-701C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990656 | |||||||
| chr7:5990757 | T | A | 1 | a0002c0002t0031g0270 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.989-802A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990757 | |||||||
| chr7:5990806 | G | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(78): Show |
85 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.989-851C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990806 | |||||||
| chr7:5990834 | C | T | 7 | a0002c0012t0001g0191 a0002c0012t0002g0100 a0002c0012t0002g0101 others(4): Show |
7 | HG00544.hp2 HG00741.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.989-879G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990834 | |||||||
| chr7:5990842 | C | T | 7 | a0002c0012t0001g0191 a0002c0012t0002g0100 a0002c0012t0002g0101 others(4): Show |
7 | HG00544.hp2 HG00741.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.989-887G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990842 | |||||||
| chr7:5990860 | A | T | 1 | a0001c0030t0008g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.989-905T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990860 | |||||||
| chr7:5990957 | G | C | 4 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-1002C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990957 | |||||||
| chr7:5991011 | T | C | 3 | a0001c0003t0045g0376 a0002c0004t0038g0276 a0002c0004t0039g0275 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.988+962A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991011 | |||||||
| chr7:5991091 | A | G | 36 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(33): Show |
36 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.988+882T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991091 | |||||||
| chr7:5991152 | T | A | 1 | a0003c0020t0003g0307 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.988+821A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991152 | |||||||
| chr7:5991347 | C | T | 2 | a0003c0005t0003g0046 a0003c0005t0003g0048 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.988+626G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991347 | |||||||
| chr7:5991401 | AT | A | 6 | a0002c0012t0002g0100 a0002c0012t0002g0101 a0002c0012t0002g0177 others(3): Show |
6 | HG00544.hp2 HG00741.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.988+571delA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991401 | |||||||
| chr7:5991447 | C | T | 1 | a0012c0024t0010g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.988+526G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991447 | |||||||
| chr7:5991470 | TA | T | 129 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0002c0002t0002g0072 others(126): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.988+502delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991470 | |||||||
| chr7:5991524 | C | T | 1 | a0002c0002t0002g0212 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.988+449G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991524 | |||||||
| chr7:5991537 | TA | T | 47 | a0001c0001t0001g0164 a0001c0003t0003g0323 a0001c0003t0004g0004 others(44): Show |
53 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.988+435delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991537 | |||||||
| chr7:5991610 | C | T | 1 | a0002c0004t0001g0085 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.988+363G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991610 | |||||||
| chr7:5991655 | C | T | 1 | a0003c0005t0003g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.988+318G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991655 | |||||||
| chr7:5991664 | C | A | 2 | a0001c0003t0004g0334 a0001c0003t0004g0335 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.988+309G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991664 | |||||||
| chr7:5991667 | G | A | 1 | a0016c0033t0010g0105 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.988+306C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991667 | |||||||
| chr7:5991767 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.988+206T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991767 | |||||||
| chr7:5991787 | C | T | 8 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(5): Show |
8 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.988+186G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991787 | |||||||
| chr7:5991796 | G | A | 3 | a0001c0001t0001g0184 a0002c0004t0001g0065 a0002c0004t0001g0066 |
3 | HG02155.hp1 NA18965.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.988+177C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991796 | |||||||
| chr7:5991814 | G | A | 2 | a0001c0003t0001g0174 a0001c0003t0001g0175 |
2 | HG00639.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.988+159C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991814 | |||||||
| chr7:5992173 | G | GT | 21 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0156 others(18): Show |
22 | HG00423.hp1 HG00673.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.904-117dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992173 | |||||||
| chr7:5992173 | G | T | 1 | a0002c0002t0002g0211 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.904-116C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992173 | |||||||
| chr7:5992203 | C | T | 1 | a0002c0002t0030g0210 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.904-146G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992203 | |||||||
| chr7:5992269 | G | T | 1 | a0002c0012t0001g0191 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.904-212C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992269 | |||||||
| chr7:5992316 | A | AT | 9 | a0001c0001t0001g0154 a0002c0002t0002g0226 a0002c0002t0002g0231 others(6): Show |
9 | HG00673.hp2 HG01175.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-260dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992316 | |||||||
| chr7:5992326 | C | T | 129 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0002c0002t0002g0072 others(126): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.904-269G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992326 | |||||||
| chr7:5992332 | T | G | 1 | a0001c0003t0012g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.904-275A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992332 | |||||||
| chr7:5992333 | T | C | 3 | a0006c0009t0009g0020 a0006c0009t0026g0027 a0006c0009t0037g0026 |
3 | HG02809.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.904-276A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992333 | |||||||
| chr7:5992412 | G | A | 1 | a0001c0003t0045g0376 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.904-355C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992412 | |||||||
| chr7:5992456 | A | C | 2 | a0013c0021t0002g0259 a0013c0021t0002g0260 |
2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.904-399T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992456 | |||||||
| chr7:5992522 | G | A | 10 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(7): Show |
10 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.904-465C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992522 | |||||||
| chr7:5992562 | C | T | 9 | a0002c0004t0014g0068 a0002c0010t0011g0031 a0002c0010t0011g0032 others(6): Show |
9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-505G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992562 | |||||||
| chr7:5992566 | C | T | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0154 others(1): Show |
4 | HG04184.hp1 NA18979.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-509G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992566 | |||||||
| chr7:5992567 | G | A | 1 | a0004c0006t0005g0313 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.904-510C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992567 | |||||||
| chr7:5992700 | A | C | 3 | a0001c0008t0007g0338 a0001c0008t0007g0342 a0001c0008t0046g0341 |
3 | HG02965.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.904-643T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992700 | |||||||
| chr7:5992787 | A | G | 1 | a0001c0003t0003g0323 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.904-730T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992787 | |||||||
| chr7:5992875 | T | C | 3 | a0006c0009t0009g0020 a0006c0009t0026g0027 a0006c0009t0037g0026 |
3 | HG02809.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.904-818A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992875 | |||||||
| chr7:5992880 | G | C | 6 | a0002c0002t0002g0118 a0002c0002t0002g0241 a0002c0002t0002g0261 others(3): Show |
6 | HG01192.hp1 HG01978.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-823C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992880 | |||||||
| chr7:5993002 | T | C | 1 | a0009c0015t0010g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.904-945A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993002 | |||||||
| chr7:5993026 | T | C | 2 | a0013c0021t0002g0259 a0013c0021t0002g0260 |
2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.904-969A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993026 | |||||||
| chr7:5993069 | A | C | 1 | a0002c0010t0040g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.904-1012T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993069 | |||||||
| chr7:5993072 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.904-1015G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993072 | |||||||
| chr7:5993117 | T | A | 51 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(48): Show |
57 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.904-1060A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993117 | |||||||
| chr7:5993155 | G | A | 1 | a0002c0002t0032g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.904-1098C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993155 | |||||||
| chr7:5993201 | T | C | 1 | a0009c0016t0003g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.904-1144A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993201 | |||||||
| chr7:5993233 | T | C | 2 | a0002c0004t0038g0276 a0002c0004t0039g0275 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.904-1176A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993233 | |||||||
| chr7:5993290 | G | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0280 |
3 | HG02735.hp2 HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.904-1233C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993290 | |||||||
| chr7:5993370 | C | CA | 142 | a0001c0001t0001g0137 a0001c0001t0001g0157 a0001c0001t0001g0189 others(139): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.904-1314dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993370 | |||||||
| chr7:5993370 | C | CAA | 84 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(81): Show |
88 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.904-1315_904-1314d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993370 | |||||||
| chr7:5993387 | A | AG | 52 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(49): Show |
58 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.904-1331_904-1330i others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993387 | |||||||
| chr7:5993387 | A | G | 1 | a0001c0008t0007g0337 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.904-1330T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993387 | |||||||
| chr7:5993409 | C | A | 1 | a0022c0034t0027g0228 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.904-1352G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993409 | |||||||
| chr7:5993429 | A | ATGT | 377 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(374): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.904-1375_904-1373d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993429 | |||||||
| chr7:5993464 | T | A | 6 | a0002c0002t0002g0118 a0002c0002t0002g0241 a0002c0002t0002g0261 others(3): Show |
6 | HG01192.hp1 HG01978.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-1407A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993464 | |||||||
| chr7:5993556 | A | T | 2 | a0002c0002t0002g0206 a0002c0002t0030g0210 |
2 | HG02027.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.904-1499T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993556 | |||||||
| chr7:5993588 | C | T | 1 | a0002c0002t0002g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.904-1531G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993588 | |||||||
| chr7:5993633 | C | T | 4 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-1576G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993633 | |||||||
| chr7:5993658 | C | T | 2 | a0002c0002t0002g0244 a0002c0002t0002g0272 |
2 | HG02080.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.904-1601G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993658 | |||||||
| chr7:5993720 | G | C | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.904-1663C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993720 | |||||||
| chr7:5993741 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.904-1684C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993741 | |||||||
| chr7:5993838 | G | A | 33 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(30): Show |
39 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.903+1696C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993838 | |||||||
| chr7:5993849 | C | T | 5 | a0001c0001t0001g0135 a0001c0003t0012g0109 a0001c0003t0012g0110 others(2): Show |
5 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+1685G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993849 | |||||||
| chr7:5993862 | C | CA | 44 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0154 others(41): Show |
49 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.903+1671dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993862 | |||||||
| chr7:5993862 | C | CAA | 13 | a0001c0003t0001g0197 a0002c0002t0002g0205 a0002c0004t0001g0008 others(10): Show |
14 | HG00280.hp2 HG01123.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.903+1670_903+1671d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993862 | |||||||
| chr7:5993862 | C | CAAA | 90 | a0001c0003t0001g0258 a0002c0002t0002g0072 a0002c0002t0002g0118 others(87): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.903+1669_903+1671d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993862 | |||||||
| chr7:5993862 | C | CAAAA | 32 | a0001c0003t0001g0266 a0002c0002t0002g0112 a0002c0002t0002g0200 others(29): Show |
32 | HG00544.hp2 HG00673.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.903+1668_903+1671d others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993862 | |||||||
| chr7:5993862 | CA | C | 21 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0280 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.903+1671delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993862 | |||||||
| chr7:5994237 | C | T | 3 | a0002c0002t0002g0119 a0002c0002t0002g0273 a0002c0002t0002g0274 |
3 | HG00323.hp1 HG01361.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.903+1297G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994237 | |||||||
| chr7:5994250 | G | A | 1 | a0002c0012t0002g0101 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.903+1284C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994250 | |||||||
| chr7:5994252 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(78): Show |
85 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.903+1282C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994252 | |||||||
| chr7:5994296 | G | A | 2 | a0001c0003t0004g0334 a0001c0003t0004g0335 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.903+1238C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994296 | |||||||
| chr7:5994389 | A | C | 1 | a0012c0024t0010g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.903+1145T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994389 | |||||||
| chr7:5994432 | G | A | 2 | a0002c0002t0002g0269 a0002c0002t0031g0270 |
2 | NA18968.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.903+1102C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994432 | |||||||
| chr7:5994486 | T | C | 2 | a0009c0016t0001g0106 a0009c0016t0001g0108 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.903+1048A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994486 | |||||||
| chr7:5994521 | T | C | 2 | a0002c0004t0038g0276 a0002c0004t0039g0275 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.903+1013A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994521 | |||||||
| chr7:5994526 | C | T | 7 | a0009c0015t0010g0017 a0009c0015t0010g0102 a0009c0015t0010g0107 others(4): Show |
7 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+1008G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994526 | |||||||
| chr7:5994539 | C | T | 12 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(9): Show |
12 | HG01109.hp1 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.903+995G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994539 | |||||||
| chr7:5994555 | C | T | 1 | a0009c0015t0010g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.903+979G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994555 | |||||||
| chr7:5994572 | A | G | 22 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0005c0007t0006g0011 others(19): Show |
23 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.903+962T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994572 | |||||||
| chr7:5994630 | A | G | 1 | a0002c0039t0001g0116 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.903+904T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994630 | |||||||
| chr7:5994662 | G | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(83): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.903+872C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994662 | |||||||
| chr7:5994693 | G | A | 8 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(5): Show |
8 | HG02055.hp2 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.903+841C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994693 | |||||||
| chr7:5994715 | G | T | 7 | a0009c0015t0010g0017 a0009c0015t0010g0102 a0009c0015t0010g0107 others(4): Show |
7 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+819C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994715 | |||||||
| chr7:5994731 | A | G | 1 | a0007c0011t0002g0243 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.903+803T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994731 | |||||||
| chr7:5994769 | C | T | 9 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(6): Show |
9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+765G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994769 | |||||||
| chr7:5994952 | C | T | 9 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(6): Show |
9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+582G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994952 | |||||||
| chr7:5995039 | T | A | 49 | a0001c0003t0003g0323 a0001c0003t0004g0357 a0001c0003t0004g0358 others(46): Show |
53 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.903+495A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995039 | |||||||
| chr7:5995041 | T | A | 2 | a0002c0004t0038g0276 a0002c0004t0039g0275 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.903+493A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995041 | |||||||
| chr7:5995048 | A | T | 2 | a0001c0001t0001g0165 a0002c0002t0036g0097 |
2 | HG01243.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.903+486T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995048 | |||||||
| chr7:5995187 | A | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(260): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.903+347T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995187 | |||||||
| chr7:5995188 | A | C | 263 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(260): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.903+346T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995188 | |||||||
| chr7:5995236 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.903+298G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995236 | |||||||
| chr7:5995288 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.903+246G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995288 | |||||||
| chr7:5995289 | G | A | 3 | a0002c0010t0011g0036 a0002c0010t0014g0037 a0002c0010t0029g0038 |
3 | HG02559.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.903+245C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995289 | |||||||
| chr7:5995333 | G | A | 6 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0036 others(3): Show |
6 | HG02559.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.903+201C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995333 | |||||||
| chr7:5995390 | C | A | 48 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(45): Show |
54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.903+144G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995390 | |||||||
| chr7:5995434 | A | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(83): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.903+100T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995434 | |||||||
| chr7:5995450 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(83): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.903+84C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995450 | |||||||
| chr7:5995759 | A | G | 1 | a0002c0002t0028g0224 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.804-126T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995759 | |||||||
| chr7:5995797 | A | C | 123 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0002c0002t0002g0072 others(120): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.804-164T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995797 | |||||||
| chr7:5995876 | C | T | 49 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(46): Show |
55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.804-243G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995876 | |||||||
| chr7:5995890 | T | C | 1 | a0008c0013t0042g0094 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.804-257A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995890 | |||||||
| chr7:5995905 | C | T | 7 | a0009c0015t0010g0017 a0009c0015t0010g0102 a0009c0015t0010g0107 others(4): Show |
7 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-272G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995905 | |||||||
| chr7:5995910 | C | T | 1 | a0002c0002t0002g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.804-277G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995910 | |||||||
| chr7:5996055 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.804-422C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996055 | |||||||
| chr7:5996125 | G | C | 9 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(6): Show |
9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-492C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996125 | |||||||
| chr7:5996140 | C | T | 1 | a0009c0015t0010g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.804-507G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996140 | |||||||
| chr7:5996313 | A | G | 296 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(293): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.804-680T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996313 | |||||||
| chr7:5996317 | GC | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(83): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.804-685delG | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996317 | |||||||
| chr7:5996368 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.804-735T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996368 | |||||||
| chr7:5996374 | C | T | 49 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(46): Show |
55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.804-741G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996374 | |||||||
| chr7:5996429 | C | G | 1 | a0004c0006t0043g0314 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.804-796G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996429 | |||||||
| chr7:5996571 | C | G | 2 | a0001c0003t0004g0382 a0001c0003t0044g0381 |
2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.803+755G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996571 | |||||||
| chr7:5996575 | G | A | 49 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(46): Show |
55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.803+751C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996575 | |||||||
| chr7:5996577 | T | TAA | 7 | a0001c0001t0001g0124 a0002c0002t0002g0240 a0002c0002t0002g0241 others(4): Show |
7 | HG00673.hp1 HG02080.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+747_803+748dup others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996577 | |||||||
| chr7:5996577 | T | TAAA | 87 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0002c0002t0002g0112 others(84): Show |
90 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.803+746_803+748dup others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996577 | |||||||
| chr7:5996585 | A | C | 11 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(8): Show |
11 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.803+741T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996585 | |||||||
| chr7:5996588 | A | T | 1 | a0001c0030t0008g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.803+738T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996588 | |||||||
| chr7:5996590 | A | AAAAAT | 6 | a0002c0002t0002g0206 a0002c0002t0002g0239 a0002c0004t0001g0008 others(3): Show |
7 | HG00280.hp2 HG01123.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+735_803+736ins others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996590 | |||||||
| chr7:5996590 | A | AAAATAT | 77 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(74): Show |
81 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.803+735_803+736ins others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996590 | |||||||
| chr7:5996590 | A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0151 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.803+735_803+736ins others(10): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996590 | |||||||
| chr7:5996590 | A | AAAT | 7 | a0002c0002t0002g0072 a0002c0002t0002g0238 a0002c0004t0001g0067 others(4): Show |
7 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+735_803+736ins others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996590 | |||||||
| chr7:5996590 | A | T | 21 | a0001c0030t0008g0058 a0003c0005t0001g0059 a0003c0005t0003g0001 others(18): Show |
28 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.803+736T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996590 | |||||||
| chr7:5996591 | AT | A | 20 | a0001c0003t0004g0334 a0001c0003t0012g0109 a0001c0003t0012g0110 others(17): Show |
20 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.803+734delA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996591 | |||||||
| chr7:5996591 | ATAT | A | 19 | a0001c0008t0007g0321 a0001c0008t0007g0322 a0001c0008t0007g0337 others(16): Show |
19 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.803+732_803+734del others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996591 | |||||||
| chr7:5996592 | T | A | 66 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0003t0003g0323 others(63): Show |
73 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.803+734A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996592 | |||||||
| chr7:5996594 | T | A | 39 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(36): Show |
45 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.803+732A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996594 | |||||||
| chr7:5996596 | T | A | 13 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(10): Show |
13 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.803+730A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996596 | |||||||
| chr7:5996598 | T | A | 9 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(6): Show |
9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+728A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996598 | |||||||
| chr7:5996600 | T | A | 10 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(7): Show |
10 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.803+726A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996600 | |||||||
| chr7:5996606 | TATATATA others(1): Show |
T | 6 | a0009c0015t0010g0017 a0009c0015t0010g0102 a0009c0016t0001g0106 others(3): Show |
6 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.803+712_803+719del others(8): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996606 | |||||||
| chr7:5996612 | T | C | 2 | a0001c0001t0001g0151 a0003c0005t0003g0098 |
2 | HG00621.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.803+714A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996612 | |||||||
| chr7:5996612 | TAC | T | 79 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0003t0003g0323 others(76): Show |
86 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.803+712_803+713del others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996612 | |||||||
| chr7:5996614 | C | T | 178 | a0001c0001t0001g0124 a0001c0003t0001g0258 a0001c0003t0001g0266 others(175): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.803+712G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996614 | |||||||
| chr7:5996616 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.803+710G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996616 | |||||||
| chr7:5996620 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.803+706C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996620 | |||||||
| chr7:5996622 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.803+704A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996622 | |||||||
| chr7:5996638 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.803+688G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996638 | |||||||
| chr7:5996884 | C | A | 107 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(104): Show |
113 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.803+442G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996884 | |||||||
| chr7:5997030 | C | T | 1 | a0002c0002t0002g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.803+296G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5997030 | |||||||
| chr7:5997077 | G | A | 1 | a0002c0002t0002g0199 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803+249C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5997077 | |||||||
| chr7:5997112 | G | A | 2 | a0002c0004t0019g0089 a0002c0004t0019g0090 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.803+214C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5997112 | |||||||
| chr7:5997171 | A | G | 96 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(93): Show |
102 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.803+155T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5997171 | |||||||
| chr7:5997426 | G | GA | 34 | a0001c0003t0020g0306 a0002c0004t0001g0309 a0002c0004t0001g0310 others(31): Show |
34 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(31): Show |
splice_region_variant&intron_variant | LOW | c.706-4dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997426 | |||||||
| chr7:5997426 | GA | G | 210 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(207): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
splice_region_variant&intron_variant | LOW | c.706-4delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997426 | |||||||
| chr7:5997529 | A | C | 1 | a0001c0019t0053g0364 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.706-106T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997529 | |||||||
| chr7:5997537 | G | T | 12 | a0006c0009t0009g0019 a0006c0009t0009g0020 a0006c0009t0009g0021 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.706-114C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997537 | |||||||
| chr7:5997601 | A | G | 34 | a0001c0003t0020g0306 a0002c0004t0001g0309 a0002c0004t0001g0310 others(31): Show |
34 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.706-178T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997601 | |||||||
| chr7:5997878 | G | C | 11 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(8): Show |
11 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-455C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997878 | |||||||
| chr7:5998010 | G | T | 12 | a0006c0009t0009g0019 a0006c0009t0009g0020 a0006c0009t0009g0021 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.706-587C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998010 | |||||||
| chr7:5998077 | G | GT | 12 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(9): Show |
12 | HG00741.hp2 HG01256.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.706-655dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998077 | |||||||
| chr7:5998084 | T | G | 119 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0002c0002t0002g0072 others(116): Show |
123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.706-661A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998084 | |||||||
| chr7:5998092 | T | G | 119 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0002c0002t0002g0072 others(116): Show |
123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.706-669A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998092 | |||||||
| chr7:5998331 | C | T | 6 | a0001c0003t0004g0004 a0001c0003t0004g0361 a0001c0003t0012g0109 others(3): Show |
9 | HG00099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.705+777G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998331 | |||||||
| chr7:5998359 | C | T | 1 | a0003c0020t0003g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.705+749G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998359 | |||||||
| chr7:5998360 | G | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(85): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.705+748C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998360 | |||||||
| chr7:5998376 | G | A | 1 | a0002c0012t0002g0187 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.705+732C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998376 | |||||||
| chr7:5998414 | T | C | 122 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0001c0003t0004g0064 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.705+694A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998414 | |||||||
| chr7:5998520 | C | A | 1 | a0004c0006t0005g0297 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.705+588G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998520 | |||||||
| chr7:5998529 | C | T | 1 | a0001c0003t0012g0201 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.705+579G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998529 | |||||||
| chr7:5998548 | G | C | 46 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(43): Show |
52 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.705+560C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998548 | |||||||
| chr7:5998651 | G | A | 1 | a0002c0002t0002g0271 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.705+457C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998651 | |||||||
| chr7:5998664 | A | C | 35 | a0001c0003t0020g0306 a0002c0004t0001g0309 a0002c0004t0001g0310 others(32): Show |
35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.705+444T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998664 | |||||||
| chr7:5998693 | C | CA | 55 | a0001c0001t0001g0126 a0001c0001t0001g0158 a0001c0001t0001g0159 others(52): Show |
55 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.705+414dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998693 | |||||||
| chr7:5998727 | C | T | 1 | a0012c0024t0010g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.705+381G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998727 | |||||||
| chr7:5998763 | T | C | 49 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(46): Show |
55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.705+345A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998763 | |||||||
| chr7:5998819 | G | A | 12 | a0006c0009t0009g0019 a0006c0009t0009g0020 a0006c0009t0009g0021 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.705+289C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998819 | |||||||
| chr7:5998852 | G | A | 48 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(45): Show |
54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.705+256C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998852 | |||||||
| chr7:5998989 | CA | C | 312 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(309): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.705+118delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998989 | |||||||
| chr7:5999072 | G | A | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0280 |
3 | HG02735.hp2 HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.705+36C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5999072 | |||||||
| chr7:5999091 | T | C | 122 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0001c0003t0004g0064 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.705+17A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5999091 | |||||||
| chr7:5999301 | T | C | 1 | a0003c0005t0003g0062 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.538-26A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999301 | |||||||
| chr7:5999355 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.538-80G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999355 | |||||||
| chr7:5999448 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.538-173G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999448 | |||||||
| chr7:5999449 | G | A | 11 | a0001c0008t0007g0321 a0001c0008t0007g0322 a0001c0008t0007g0337 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.538-174C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999449 | |||||||
| chr7:5999498 | T | C | 45 | a0001c0003t0004g0064 a0002c0002t0002g0072 a0002c0002t0032g0063 others(42): Show |
49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.538-223A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999498 | |||||||
| chr7:5999635 | T | G | 2 | a0002c0004t0001g0092 a0002c0004t0001g0117 |
2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.538-360A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999635 | |||||||
| chr7:5999636 | T | TA | 42 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(39): Show |
48 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.538-362dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999636 | |||||||
| chr7:5999697 | G | A | 1 | a0009c0016t0001g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.538-422C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999697 | |||||||
| chr7:5999753 | A | C | 26 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0180 others(23): Show |
26 | HG00544.hp2 HG00741.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.538-478T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999753 | |||||||
| chr7:5999773 | G | A | 1 | a0002c0002t0036g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.538-498C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999773 | |||||||
| chr7:5999857 | G | T | 1 | a0001c0001t0018g0128 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.538-582C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999857 | |||||||
| chr7:5999870 | G | A | 1 | a0001c0003t0004g0336 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.538-595C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999870 | |||||||
| chr7:5999898 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(85): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.538-623A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999898 | |||||||
| chr7:6000117 | G | A | 1 | a0006c0009t0009g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.538-842C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000117 | |||||||
| chr7:6000163 | C | G | 1 | a0003c0005t0003g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.538-888G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000163 | |||||||
| chr7:6000310 | G | T | 48 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(45): Show |
54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.538-1035C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000310 | |||||||
| chr7:6000321 | C | T | 1 | a0003c0005t0003g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.538-1046G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000321 | |||||||
| chr7:6000377 | T | TA | 6 | a0004c0006t0005g0302 a0004c0006t0005g0313 a0004c0006t0005g0315 others(3): Show |
6 | HG02109.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.538-1103dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000377 | |||||||
| chr7:6000377 | TA | T | 262 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(259): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.538-1103delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000377 | |||||||
| chr7:6000377 | TAA | T | 22 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0001g0195 others(19): Show |
22 | HG01106.hp2 HG01168.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.538-1104_538-1103d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000377 | |||||||
| chr7:6000455 | T | C | 1 | a0006c0014t0034g0320 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.538-1180A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000455 | |||||||
| chr7:6000488 | T | C | 1 | a0001c0003t0004g0336 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.538-1213A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000488 | |||||||
| chr7:6000704 | T | C | 1 | a0001c0003t0004g0360 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.538-1429A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000704 | |||||||
| chr7:6000717 | G | A | 1 | a0001c0019t0053g0364 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.538-1442C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000717 | |||||||
| chr7:6000856 | T | G | 82 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0002c0002t0002g0112 others(79): Show |
82 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.538-1581A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000856 | |||||||
| chr7:6001000 | A | C | 124 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0001c0003t0004g0064 others(121): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.537+1453T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001000 | |||||||
| chr7:6001094 | T | A | 1 | a0002c0002t0002g0202 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.537+1359A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001094 | |||||||
| chr7:6001159 | G | A | 2 | a0006c0014t0010g0018 a0006c0014t0010g0039 |
2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.537+1294C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001159 | |||||||
| chr7:6001189 | G | T | 1 | a0005c0007t0006g0318 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.537+1264C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001189 | |||||||
| chr7:6001213 | CTTG | C | 12 | a0006c0009t0009g0019 a0006c0009t0009g0020 a0006c0009t0009g0021 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.537+1237_537+1239d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001213 | |||||||
| chr7:6001373 | C | CT | 327 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(324): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.537+1079dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001373 | |||||||
| chr7:6001373 | C | CTT | 19 | a0001c0001t0001g0165 a0002c0002t0002g0112 a0002c0004t0001g0067 others(16): Show |
19 | HG01496.hp2 HG01981.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.537+1078_537+1079d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001373 | |||||||
| chr7:6001466 | A | G | 53 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(50): Show |
59 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.537+987T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001466 | |||||||
| chr7:6001487 | C | A | 1 | a0006c0014t0034g0320 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.537+966G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001487 | |||||||
| chr7:6001488 | A | G | 1 | a0006c0014t0034g0320 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.537+965T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001488 | |||||||
| chr7:6001541 | T | C | 34 | a0001c0003t0020g0306 a0002c0004t0001g0309 a0002c0004t0001g0310 others(31): Show |
34 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.537+912A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001541 | |||||||
| chr7:6001579 | C | T | 1 | a0012c0024t0010g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.537+874G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001579 | |||||||
| chr7:6001610 | C | G | 2 | a0001c0003t0004g0382 a0001c0003t0044g0381 |
2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.537+843G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001610 | |||||||
| chr7:6001668 | C | T | 1 | a0001c0003t0020g0306 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.537+785G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001668 | |||||||
| chr7:6001875 | T | C | 55 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(52): Show |
61 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.537+578A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001875 | |||||||
| chr7:6002013 | A | T | 1 | a0002c0002t0002g0203 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.537+440T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002013 | |||||||
| chr7:6002020 | A | T | 1 | a0012c0024t0010g0326 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.537+433T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002020 | |||||||
| chr7:6002022 | T | A | 11 | a0006c0009t0009g0019 a0006c0009t0009g0020 a0006c0009t0009g0021 others(8): Show |
11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.537+431A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002022 | |||||||
| chr7:6002156 | A | G | 1 | a0012c0025t0001g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.537+297T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002156 | |||||||
| chr7:6002181 | C | T | 9 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(6): Show |
9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.537+272G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002181 | |||||||
| chr7:6002187 | G | A | 120 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0001c0003t0004g0064 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.537+266C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002187 | |||||||
| chr7:6002204 | T | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.537+249A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002204 | |||||||
| chr7:6002205 | T | A | 122 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0001c0003t0004g0064 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.537+248A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002205 | |||||||
| chr7:6002266 | T | C | 49 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(46): Show |
55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.537+187A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002266 | |||||||
| chr7:6002344 | C | G | 1 | a0001c0001t0014g0171 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.537+109G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002344 | |||||||
| chr7:6002384 | A | G | 1 | a0001c0001t0014g0171 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.537+69T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002384 | |||||||
| chr7:6002891 | C | T | 122 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0001c0003t0004g0064 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.354-255G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6002891 | |||||||
| chr7:6002932 | C | G | 11 | a0006c0009t0009g0019 a0006c0009t0009g0020 a0006c0009t0009g0021 others(8): Show |
11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.354-296G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6002932 | |||||||
| chr7:6003004 | A | G | 4 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-368T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003004 | |||||||
| chr7:6003020 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(83): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.354-384C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003020 | |||||||
| chr7:6003234 | C | T | 1 | a0001c0003t0004g0064 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.353+456G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003234 | |||||||
| chr7:6003299 | A | G | 42 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(39): Show |
48 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.353+391T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003299 | |||||||
| chr7:6003306 | G | GAT | 59 | a0002c0002t0002g0112 a0002c0002t0002g0200 a0002c0002t0002g0203 others(56): Show |
59 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.353+382_353+383dup others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003306 | |||||||
| chr7:6003306 | G | GATAT | 7 | a0002c0010t0011g0033 a0002c0010t0011g0034 a0002c0010t0011g0035 others(4): Show |
7 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.353+380_353+383dup others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003306 | |||||||
| chr7:6003306 | G | GATATAT | 3 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0040g0030 |
3 | HG02809.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.353+378_353+383dup others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003306 | |||||||
| chr7:6003306 | G | T | 1 | a0004c0006t0005g0305 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.353+384C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003306 | |||||||
| chr7:6003306 | GAT | G | 53 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(50): Show |
59 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.353+382_353+383del others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003306 | |||||||
| chr7:6003308 | T | G | 3 | a0002c0004t0038g0276 a0002c0004t0039g0275 a0005c0007t0024g0095 |
3 | HG02895.hp2 HG02897.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.353+382A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003308 | |||||||
| chr7:6003324 | T | A | 1 | a0001c0001t0001g0279 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.353+366A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003324 | |||||||
| chr7:6003324 | T | TATATATA others(1): Show |
79 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(76): Show |
83 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.353+365_353+366ins others(8): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003324 | |||||||
| chr7:6003324 | T | TATATATA others(3): Show |
5 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
5 | HG00558.hp2 HG00673.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+365_353+366ins others(10): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003324 | |||||||
| chr7:6003324 | T | TATATATA others(9): Show |
1 | a0002c0012t0001g0191 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.353+365_353+366ins others(16): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003324 | |||||||
| chr7:6003369 | C | T | 1 | a0004c0006t0005g0300 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.353+321G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003369 | |||||||
| chr7:6003426 | A | G | 53 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(50): Show |
59 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.353+264T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003426 | |||||||
| chr7:6003434 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(83): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.353+256G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003434 | |||||||
| chr7:6003481 | C | T | 263 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(260): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.353+209G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003481 | |||||||
| chr7:6003836 | A | G | 1 | a0002c0002t0032g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.251-44T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 3/14 | chr7 | 6003836 | |||||||
| chr7:6003864 | T | C | 4 | a0001c0003t0012g0109 a0001c0003t0012g0110 a0001c0003t0012g0111 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-72A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 3/14 | chr7 | 6003864 | |||||||
| chr7:6004120 | T | C | 3 | a0002c0010t0011g0036 a0002c0010t0014g0037 a0002c0010t0029g0038 |
3 | HG02559.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.164-62A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004120 | |||||||
| chr7:6004166 | C | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(83): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.164-108G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004166 | |||||||
| chr7:6004290 | T | C | 2 | a0001c0019t0053g0364 a0001c0019t0054g0365 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.164-232A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004290 | |||||||
| chr7:6004333 | CTG | C | 75 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0003t0003g0323 others(72): Show |
82 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.164-277_164-276del others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004333 | |||||||
| chr7:6004468 | C | A | 1 | a0002c0010t0029g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.164-410G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004468 | |||||||
| chr7:6004490 | C | T | 1 | a0001c0019t0053g0364 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-432G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004490 | |||||||
| chr7:6004620 | C | T | 1 | a0002c0002t0002g0202 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.164-562G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004620 | |||||||
| chr7:6004693 | C | T | 9 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(6): Show |
9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-635G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004693 | |||||||
| chr7:6004715 | C | CA | 32 | a0001c0003t0004g0334 a0001c0003t0004g0335 a0001c0003t0045g0376 others(29): Show |
32 | HG00280.hp1 HG00733.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.164-658dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004715 | |||||||
| chr7:6004715 | C | CAA | 32 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(29): Show |
38 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.164-659_164-658dup others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004715 | |||||||
| chr7:6004797 | G | A | 2 | a0001c0003t0004g0004 a0001c0003t0004g0361 |
5 | HG00099.hp2 HG01515.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-739C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004797 | |||||||
| chr7:6004884 | C | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(283): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.164-826G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004884 | |||||||
| chr7:6004889 | G | T | 1 | a0006c0009t0009g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.164-831C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004889 | |||||||
| chr7:6004890 | T | G | 76 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0003t0003g0323 others(73): Show |
83 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-832A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004890 | |||||||
| chr7:6004897 | T | A | 4 | a0002c0002t0002g0119 a0002c0002t0002g0273 a0002c0002t0002g0274 others(1): Show |
4 | HG00323.hp1 HG01361.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-839A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004897 | |||||||
| chr7:6005019 | T | C | 342 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(339): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.163+873A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005019 | |||||||
| chr7:6005268 | G | A | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
6 | NA18950.hp1 NA18953.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+624C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005268 | |||||||
| chr7:6005361 | G | C | 1 | a0001c0001t0014g0171 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.163+531C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005361 | |||||||
| chr7:6005561 | T | C | 7 | a0003c0020t0003g0104 a0009c0015t0010g0017 a0009c0015t0010g0102 others(4): Show |
7 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+331A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005561 | |||||||
| chr7:6005589 | G | A | 2 | a0001c0003t0004g0004 a0001c0003t0004g0361 |
5 | HG00099.hp2 HG01515.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+303C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005589 | |||||||
| chr7:6005754 | T | C | 124 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0001c0003t0004g0064 others(121): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.163+138A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005754 | |||||||
| chr7:6005760 | C | G | 1 | a0006c0009t0009g0019 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.163+132G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005760 | |||||||
| chr7:6005884 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG02602.hp1 | splice_region_variant&intron_variant | LOW | c.163+8T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005884 | |||||||
| chr7:6006152 | T | C | 1 | a0008c0013t0042g0094 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.24-121A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006152 | |||||||
| chr7:6006189 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-158T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006189 | |||||||
| chr7:6006191 | C | CTTAGTCT others(4): Show |
1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-161_24-160insTG others(9): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006191 | |||||||
| chr7:6006192 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-161T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006192 | |||||||
| chr7:6006197 | T | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-166A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006197 | |||||||
| chr7:6006199 | T | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-168A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006199 | |||||||
| chr7:6006200 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-169T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006200 | |||||||
| chr7:6006203 | A | C | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-172T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006203 | |||||||
| chr7:6006205 | C | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-174G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006205 | |||||||
| chr7:6006209 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-178T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006209 | |||||||
| chr7:6006210 | A | C | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-179T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006210 | |||||||
| chr7:6006211 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-180T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006211 | |||||||
| chr7:6006212 | C | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-181G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006212 | |||||||
| chr7:6006213 | A | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-182T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006213 | |||||||
| chr7:6006214 | T | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-183A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006214 | |||||||
| chr7:6006217 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-186T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006217 | |||||||
| chr7:6006220 | C | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-189G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006220 | |||||||
| chr7:6006221 | A | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-190T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006221 | |||||||
| chr7:6006225 | T | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-194A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006225 | |||||||
| chr7:6006229 | T | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-198A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006229 | |||||||
| chr7:6006230 | C | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-199G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006230 | |||||||
| chr7:6006231 | T | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-200A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006231 | |||||||
| chr7:6006232 | G | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-201C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006232 | |||||||
| chr7:6006238 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-207T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006238 | |||||||
| chr7:6006242 | T | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-211A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006242 | |||||||
| chr7:6006246 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-215T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006246 | |||||||
| chr7:6006247 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-216T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006247 | |||||||
| chr7:6006250 | C | T | 48 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(45): Show |
54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.24-219G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006250 | |||||||
| chr7:6006251 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-220T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006251 | |||||||
| chr7:6006255 | G | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-224C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006255 | |||||||
| chr7:6006258 | C | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-227G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006258 | |||||||
| chr7:6006262 | A | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-231T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006262 | |||||||
| chr7:6006271 | T | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-240A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006271 | |||||||
| chr7:6006272 | T | C | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-241A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006272 | |||||||
| chr7:6006273 | A | C | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-242T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006273 | |||||||
| chr7:6006276 | C | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-245G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006276 | |||||||
| chr7:6006277 | T | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-246A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006277 | |||||||
| chr7:6006279 | A | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-248T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006279 | |||||||
| chr7:6006292 | G | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-261C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006292 | |||||||
| chr7:6006294 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-263T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006294 | |||||||
| chr7:6006297 | C | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-266G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006297 | |||||||
| chr7:6006302 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-271T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006302 | |||||||
| chr7:6006303 | T | C | 49 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(46): Show |
55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.24-272A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006303 | |||||||
| chr7:6006307 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-276T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006307 | |||||||
| chr7:6006321 | C | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-290G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006321 | |||||||
| chr7:6006322 | A | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-291T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006322 | |||||||
| chr7:6006323 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-292T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006323 | |||||||
| chr7:6006324 | A | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-293T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006324 | |||||||
| chr7:6006325 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-294T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006325 | |||||||
| chr7:6006327 | C | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-296G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006327 | |||||||
| chr7:6006333 | C | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-302G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006333 | |||||||
| chr7:6006335 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-304T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006335 | |||||||
| chr7:6006337 | A | C | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-306T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006337 | |||||||
| chr7:6006338 | A | C | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-307T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006338 | |||||||
| chr7:6006339 | T | C | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-308A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006339 | |||||||
| chr7:6006350 | T | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-319A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006350 | |||||||
| chr7:6006352 | C | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-321G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006352 | |||||||
| chr7:6006355 | G | C | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-324C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006355 | |||||||
| chr7:6006361 | T | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-330A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006361 | |||||||
| chr7:6006362 | G | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-331C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006362 | |||||||
| chr7:6006366 | G | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-335C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006366 | |||||||
| chr7:6006367 | C | G | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-336G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006367 | |||||||
| chr7:6006374 | G | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-343C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006374 | |||||||
| chr7:6006376 | C | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-345G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006376 | |||||||
| chr7:6006377 | T | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-346A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006377 | |||||||
| chr7:6006378 | G | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-347C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006378 | |||||||
| chr7:6006380 | G | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-349C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006380 | |||||||
| chr7:6006384 | G | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-353C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006384 | |||||||
| chr7:6006385 | C | A | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-354G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006385 | |||||||
| chr7:6006394 | G | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-363C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006394 | |||||||
| chr7:6006399 | C | T | 1 | a0002c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-368G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006399 | |||||||
| chr7:6006431 | A | G | 1 | a0006c0014t0034g0320 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.24-400T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006431 | |||||||
| chr7:6006511 | G | C | 1 | a0002c0002t0002g0119 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.24-480C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006511 | |||||||
| chr7:6006610 | G | A | 9 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(6): Show |
9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.24-579C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006610 | |||||||
| chr7:6006638 | C | CA | 24 | a0004c0006t0005g0316 a0005c0007t0006g0011 a0005c0007t0006g0318 others(21): Show |
25 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.24-608dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006638 | |||||||
| chr7:6006666 | T | A | 2 | a0001c0019t0053g0364 a0001c0019t0054g0365 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.24-635A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006666 | |||||||
| chr7:6006846 | G | A | 4 | a0001c0001t0001g0103 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG02083.hp2 HG02165.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-815C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006846 | |||||||
| chr7:6006899 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.24-868T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006899 | |||||||
| chr7:6006996 | C | A | 9 | a0002c0010t0011g0031 a0002c0010t0011g0032 a0002c0010t0011g0033 others(6): Show |
9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.24-965G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006996 | |||||||
| chr7:6006998 | A | G | 1 | a0001c0003t0004g0336 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.24-967T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006998 | |||||||
| chr7:6007083 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.24-1052G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007083 | |||||||
| chr7:6007087 | C | CATT | 30 | a0001c0001t0001g0103 a0001c0001t0001g0172 a0001c0001t0001g0176 others(27): Show |
30 | HG00544.hp2 HG00639.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.24-1059_24-1057dup others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | |||||||
| chr7:6007087 | C | CATTATT | 55 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0099 others(52): Show |
59 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.24-1062_24-1057dup others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | |||||||
| chr7:6007087 | C | CATTATTA others(5): Show |
1 | a0001c0001t0001g0122 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.24-1068_24-1057dup others(12): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | |||||||
| chr7:6007087 | CATT | C | 244 | a0001c0003t0001g0258 a0001c0003t0001g0266 a0001c0003t0003g0323 others(241): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.24-1059_24-1057del others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | |||||||
| chr7:6007087 | CATTATT | C | 3 | a0003c0005t0003g0096 a0003c0005t0003g0120 a0006c0014t0010g0039 |
3 | HG02630.hp1 NA20805.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.24-1062_24-1057del others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | |||||||
| chr7:6007087 | CATTATTA others(2): Show |
C | 3 | a0001c0003t0013g0014 a0001c0003t0013g0363 a0001c0008t0007g0362 |
4 | HG01884.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.24-1065_24-1057del others(9): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | |||||||
| chr7:6007103 | ATTATTAT others(5): Show |
A | 1 | a0002c0002t0036g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.24-1084_24-1073del others(12): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007103 | |||||||
| chr7:6007152 | G | A | 69 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(66): Show |
76 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.24-1121C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007152 | |||||||
| chr7:6007175 | G | A | 2 | a0001c0019t0053g0364 a0001c0019t0054g0365 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.24-1144C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007175 | |||||||
| chr7:6007302 | G | A | 1 | a0003c0005t0003g0098 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.24-1271C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007302 | |||||||
| chr7:6007359 | G | A | 56 | a0001c0003t0020g0306 a0002c0004t0001g0309 a0002c0004t0001g0310 others(53): Show |
56 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.24-1328C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007359 | |||||||
| chr7:6007403 | A | G | 2 | a0001c0003t0004g0334 a0001c0003t0004g0335 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.24-1372T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007403 | |||||||
| chr7:6007442 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.24-1411G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007442 | |||||||
| chr7:6007500 | C | T | 48 | a0001c0003t0003g0323 a0001c0003t0004g0004 a0001c0003t0004g0012 others(45): Show |
54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.24-1469G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007500 | |||||||
| chr7:6007551 | C | T | 1 | a0006c0014t0010g0018 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.23+1446G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007551 | |||||||
| chr7:6007672 | G | C | 1 | a0001c0003t0045g0376 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.23+1325C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007672 | |||||||
| chr7:6007856 | AT | A | 43 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0003t0012g0109 others(40): Show |
43 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.23+1140delA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007856 | |||||||
| chr7:6007856 | ATT | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0121 others(204): Show |
212 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.23+1139_23+1140del others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007856 | |||||||
| chr7:6007856 | ATTT | A | 63 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(60): Show |
69 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.23+1138_23+1140del others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007856 | |||||||
| chr7:6007945 | C | T | 56 | a0001c0003t0020g0306 a0002c0004t0001g0309 a0002c0004t0001g0310 others(53): Show |
56 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.23+1052G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007945 | |||||||
| chr7:6008134 | G | A | 1 | a0002c0004t0001g0281 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.23+863C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008134 | |||||||
| chr7:6008336 | T | C | 4 | a0001c0003t0004g0377 a0001c0003t0004g0378 a0001c0003t0004g0379 others(1): Show |
4 | NA18948.hp2 NA18969.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+661A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008336 | |||||||
| chr7:6008504 | C | A | 2 | a0001c0003t0004g0382 a0001c0003t0044g0381 |
2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.23+493G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008504 | |||||||
| chr7:6008555 | G | C | 71 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0003t0003g0323 others(68): Show |
78 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.23+442C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008555 | |||||||
| chr7:6008649 | G | A | 1 | a0001c0003t0004g0383 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.23+348C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008649 | |||||||
| chr7:6008728 | C | T | 71 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0003t0003g0323 others(68): Show |
78 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.23+269G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008728 | |||||||
| chr7:6008731 | GTCT | G | 34 | a0001c0003t0020g0306 a0002c0004t0001g0309 a0002c0004t0001g0310 others(31): Show |
34 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.23+263_23+265delAG others(1): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008731 | |||||||
| chr7:6008735 | G | C | 34 | a0001c0003t0020g0306 a0002c0004t0001g0309 a0002c0004t0001g0310 others(31): Show |
34 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.23+262C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008735 | |||||||
| chr7:6008736 | G | A | 34 | a0001c0003t0020g0306 a0002c0004t0001g0309 a0002c0004t0001g0310 others(31): Show |
34 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.23+261C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008736 | |||||||
| chr7:6008741 | G | A | 1 | a0002c0002t0002g0317 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.23+256C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008741 | |||||||
| chr7:6008796 | A | C | 1 | a0009c0015t0010g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.23+201T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008796 | |||||||
| chr7:6008891 | C | T | 2 | a0003c0005t0003g0015 a0003c0005t0003g0016 |
2 | HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.23+106G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008891 | |||||||
| chr7:6008925 | G | A | 71 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0003t0003g0323 others(68): Show |
78 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.23+72C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008925 |