Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11187 |
| ensemblid | ENSG00000184363.10 |
| hgncid | 9025 |
| symbol | PKP3 |
| name | plakophilin 3 |
| refseq_nuc | NM_007183.4 |
| refseq_prot | NP_009114.1 |
| ensembl_nuc | ENST00000331563.7 |
| ensembl_prot | ENSP00000331678.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 394209 |
| end | 404908 |
| strand | + |
| ver | v1.2 |
| region | chr11:394209-404908 |
| region5000 | chr11:389209-409908 |
| regionname0 | PKP3_chr11_394209_404908 |
| regionname5000 | PKP3_chr11_389209_409908 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 797 | 193 | 59 | 38 | 66 | 6 | 22 | 44 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0002 | 0/0 | 797 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0003 | 0/0 | 797 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0004 | 0/0 | 797 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0005 | 0/0 | 797 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0006 | 0/0 | 797 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0007 | 0/0 | 797 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0008 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0009 | 0/0 | 797 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0010 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0011 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0012 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0013 | 0/0 | 641 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MPTRP others(636): Show |
chr11 | 389209 | 409908 |
| a0014 | 0/0 | 797 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0015 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0016 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0017 | 0/0 | 797 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0018 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(792): Show |
chr11 | 389209 | 409908 |
| a0019 | 0/0 | 370 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | MQDGN others(365): Show |
chr11 | 389209 | 409908 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2391 | 67 | 16 | 10 | 33 | 2 | 6 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0002 | 0/0 | 2391 | 32 | 11 | 5 | 8 | 1 | 7 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0003 | 0/0 | 2391 | 31 | 0 | 12 | 12 | 1 | 6 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0004 | 0/0 | 2391 | 10 | 8 | 1 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0005 | 0/0 | 2391 | 10 | 7 | 1 | 2 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0006 | 1/1 | 2391 | 9 | 0 | 5 | 0 | 2 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0007 | 0/0 | 2391 | 6 | 3 | 2 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0008 | 0/0 | 2391 | 6 | 6 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0009 | 0/0 | 2391 | 6 | 0 | 0 | 6 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0010 | 0/0 | 2391 | 3 | 2 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0011 | 0/0 | 2391 | 3 | 3 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0012 | 0/0 | 2391 | 3 | 0 | 0 | 3 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0016 | 0/0 | 2391 | 2 | 0 | 2 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0018 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0021 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0028 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0030 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0001c0036 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0002c0013 | 0/0 | 2391 | 3 | 3 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0003c0014 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0003c0019 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0004c0015 | 0/0 | 2391 | 2 | 0 | 1 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0005c0022 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0006c0031 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0007c0029 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0008c0025 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0009c0033 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0010c0017 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0011c0024 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0012c0020 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0013c0037 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | GCCGG others(2344): Show |
chr11 | 389209 | 409908 | ||
| a0014c0034 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0015c0026 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0016c0035 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0017c0027 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0018c0023 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2386): Show |
chr11 | 389209 | 409908 | ||
| a0019c0032 | 0/0 | 2402 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | ATGCA others(2397): Show |
chr11 | 389209 | 409908 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2817 | 67 | 16 | 10 | 33 | 2 | 6 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0002t0001 | 0/0 | 2817 | 32 | 11 | 5 | 8 | 1 | 7 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0003t0001 | 0/0 | 2817 | 31 | 0 | 12 | 12 | 1 | 6 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0004t0001 | 0/0 | 2817 | 10 | 8 | 1 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0005t0001 | 0/0 | 2817 | 9 | 6 | 1 | 2 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0005t0004 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0006t0001 | 1/1 | 2817 | 9 | 0 | 5 | 0 | 2 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0007t0001 | 0/0 | 2817 | 6 | 3 | 2 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0008t0001 | 0/0 | 2817 | 6 | 6 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0009t0001 | 0/0 | 2817 | 6 | 0 | 0 | 6 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0010t0001 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0010t0003 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0011t0001 | 0/0 | 2817 | 3 | 3 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0012t0001 | 0/0 | 2817 | 3 | 0 | 0 | 3 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0016t0001 | 0/0 | 2817 | 2 | 0 | 2 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0018t0001 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0021t0001 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0028t0001 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0030t0001 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0001c0036t0001 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0002c0013t0001 | 0/0 | 2817 | 3 | 3 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0003c0014t0001 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0003c0019t0001 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0004c0015t0001 | 0/0 | 2817 | 2 | 0 | 1 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0005c0022t0001 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0006c0031t0001 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0007c0029t0001 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0008c0025t0001 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0009c0033t0001 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0010c0017t0001 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0011c0024t0002 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0012c0020t0001 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0013c0037t0005 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2767): Show |
chr11 | 389209 | 409908 |
| a0014c0034t0001 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0015c0026t0004 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0016c0035t0001 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0017c0027t0001 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0018c0023t0002 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2812): Show |
chr11 | 389209 | 409908 |
| a0019c0032t0001 | 0/0 | 2828 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | AGGGA others(2823): Show |
chr11 | 389209 | 409908 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0004t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0004t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0005t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0005t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0005t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0005t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0005t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0006t0001g0005 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0006t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0006t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0006t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0006t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0006t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0006t0001g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0006t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0007t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0007t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0007t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0007t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0007t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0007t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0008t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0008t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0008t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0008t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0008t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0008t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0009t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0009t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0009t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0009t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0009t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0009t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0010t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0010t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0010t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0011t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0011t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0011t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0012t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0012t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0012t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0016t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0016t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0018t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0021t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0028t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0030t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0001c0036t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0002c0013t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0002c0013t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0002c0013t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0003c0014t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0003c0014t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0003c0019t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0004c0015t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0004c0015t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0005c0022t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0006c0031t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0007c0029t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0008c0025t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0009c0033t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0010c0017t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0011c0024t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0012c0020t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0013c0037t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0014c0034t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0015c0026t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0016c0035t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0017c0027t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0018c0023t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| a0019c0032t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0006 | t0001 | g0068 | EUR | GBR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0132 | EUR | GBR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | CHS | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | CHS | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0027 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | CHS | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00673 | hp2 | a0001 | c0009 | t0001 | g0167 | EAS | CHS | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG00733 | hp2 | a0001 | c0007 | t0001 | g0208 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01175 | hp1 | a0004 | c0015 | t0001 | g0047 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01175 | hp2 | a0001 | c0006 | t0001 | g0049 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01192 | hp2 | a0005 | c0022 | t0001 | g0203 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01243 | hp1 | a0001 | c0005 | t0001 | g0014 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01243 | hp2 | a0001 | c0007 | t0001 | g0010 | AMR | PUR | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0153 | AMR | CLM | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | CLM | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01258 | hp1 | a0001 | c0006 | t0001 | g0038 | AMR | CLM | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | CLM | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01261 | hp1 | a0001 | c0016 | t0001 | g0200 | AMR | CLM | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0115 | AMR | CLM | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01496 | hp1 | a0006 | c0031 | t0001 | g0163 | AMR | CLM | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01515 | hp1 | a0007 | c0029 | t0001 | g0117 | EUR | IBS | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0091 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01891 | hp2 | a0008 | c0025 | t0001 | g0199 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0096 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01943 | hp1 | a0009 | c0033 | t0001 | g0160 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0151 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0095 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0140 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0098 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0111 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02004 | hp2 | a0001 | c0006 | t0001 | g0204 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02027 | hp1 | a0001 | c0012 | t0001 | g0120 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02056 | hp2 | a0001 | c0012 | t0001 | g0119 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02074 | hp2 | a0010 | c0017 | t0001 | g0106 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02132 | hp2 | a0011 | c0024 | t0002 | g0026 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0166 | EAS | KHV | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02145 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0116 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0150 | EAS | CDX | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | CDX | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0023 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02258 | hp2 | a0001 | c0005 | t0001 | g0040 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0113 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02273 | hp2 | a0001 | c0006 | t0001 | g0005 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02300 | hp1 | a0001 | c0016 | t0001 | g0201 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02300 | hp2 | a0001 | c0006 | t0001 | g0035 | AMR | PEL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02622 | hp1 | a0001 | c0008 | t0001 | g0188 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02622 | hp2 | a0001 | c0021 | t0001 | g0086 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02647 | hp2 | a0013 | c0037 | t0005 | g0087 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02683 | hp1 | a0014 | c0034 | t0001 | g0157 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0158 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02717 | hp1 | a0001 | c0007 | t0001 | g0009 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0197 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02723 | hp2 | a0001 | c0010 | t0003 | g0021 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02809 | hp2 | a0001 | c0011 | t0001 | g0050 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02886 | hp1 | a0002 | c0013 | t0001 | g0108 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02886 | hp2 | a0015 | c0026 | t0004 | g0092 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02897 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0172 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0133 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0162 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03130 | hp1 | a0002 | c0013 | t0001 | g0175 | AFR | ESN | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03130 | hp2 | a0001 | c0008 | t0001 | g0189 | AFR | ESN | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03209 | hp2 | a0001 | c0008 | t0001 | g0093 | AFR | MSL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03239 | hp1 | a0001 | c0018 | t0001 | g0045 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | MSL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03486 | hp2 | a0001 | c0008 | t0001 | g0194 | AFR | MSL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03492 | hp1 | a0001 | c0028 | t0001 | g0128 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0161 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03516 | hp1 | a0001 | c0008 | t0001 | g0192 | AFR | ESN | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03516 | hp2 | a0001 | c0005 | t0001 | g0090 | AFR | ESN | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0196 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03540 | hp2 | a0003 | c0019 | t0001 | g0181 | AFR | GWD | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03579 | hp1 | a0001 | c0030 | t0001 | g0174 | AFR | MSL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0114 | SAS | STU | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0147 | SAS | PJL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03834 | hp1 | a0017 | c0027 | t0001 | g0107 | SAS | BEB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03834 | hp2 | a0001 | c0007 | t0001 | g0025 | SAS | BEB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0168 | SAS | BEB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0154 | SAS | STU | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0136 | SAS | STU | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18522 | hp1 | a0001 | c0005 | t0004 | g0006 | AFR | YRI | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0193 | AFR | YRI | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | CHB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18612 | hp2 | a0001 | c0005 | t0001 | g0084 | EAS | CHB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18906 | hp1 | a0003 | c0014 | t0001 | g0187 | AFR | YRI | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | YRI | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18947 | hp1 | a0001 | c0009 | t0001 | g0129 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18947 | hp2 | a0001 | c0005 | t0001 | g0085 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18950 | hp1 | a0018 | c0023 | t0002 | g0037 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18966 | hp2 | a0001 | c0009 | t0001 | g0102 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18994 | hp2 | a0001 | c0009 | t0001 | g0121 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18995 | hp1 | a0001 | c0012 | t0001 | g0156 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19005 | hp1 | a0001 | c0009 | t0001 | g0122 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | LWK | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0032 | AFR | LWK | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19043 | hp1 | a0001 | c0007 | t0001 | g0007 | AFR | LWK | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19043 | hp2 | a0001 | c0011 | t0001 | g0063 | AFR | LWK | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19065 | hp1 | a0019 | c0032 | t0001 | g0144 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19067 | hp2 | a0001 | c0009 | t0001 | g0123 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0094 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19079 | hp2 | a0001 | c0010 | t0001 | g0030 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19240 | hp1 | a0001 | c0008 | t0001 | g0191 | AFR | YRI | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA19240 | hp2 | a0003 | c0014 | t0001 | g0182 | AFR | YRI | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0074 | AFR | ASW | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA20129 | hp2 | a0001 | c0036 | t0001 | g0165 | AFR | ASW | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0097 | EUR | TSI | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA20805 | hp1 | a0004 | c0015 | t0001 | g0058 | EUR | TSI | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA20805 | hp2 | a0001 | c0006 | t0001 | g0207 | EUR | TSI | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | GIH | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0138 | SAS | GIH | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02486 | hp1 | a0001 | c0011 | t0001 | g0001 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02486 | hp2 | a0001 | c0010 | t0003 | g0022 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02559 | hp1 | a0012 | c0020 | t0001 | g0024 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG02559 | hp2 | a0002 | c0013 | t0001 | g0109 | AFR | ACB | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | MSL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG03471 | hp2 | a0016 | c0035 | t0001 | g0180 | AFR | MSL | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | USA | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | USA | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0073 | AFR | USA | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0190 | AFR | USA | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0176 | AFR | LWK | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| homoSapiens | chm13v2 | a0001 | c0006 | t0001 | g0206 | REF | REF | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| homoSapiens | grch38p0 | a0001 | c0006 | t0001 | g0005 | REF | REF | PKP3_chr11_389209_409908 | PKP3 | chr11 | 389209 | 409908 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:394289 | CGCCATGC others(38): Show |
C | 1 | a0013 | 1 | HG02647.hp2 | start_lost&conservative_inframe_deletion | HIGH | c.1_45delATGCAGGACGG others(34): Show |
p.Met1_Ala15del | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/13 | 85/2817 | 1/2394 | 1/797 | INFO_REALIGN_3_PRIME | chr11 | 394289 | ||
| chr11:394449 | C | T | 1 | a0016 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.157C>T | p.Arg53Cys | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/13 | 241/2817 | 157/2394 | 53/797 | chr11 | 394449 | |||
| chr11:394491 | G | A | 1 | a0010 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.199G>A | p.Ala67Thr | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/13 | 283/2817 | 199/2394 | 67/797 | chr11 | 394491 | |||
| chr11:396937 | G | A | 2 | a0003 a0016 |
4 | HG03471.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.436G>A | p.Ala146Thr | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/13 | 520/2817 | 436/2394 | 146/797 | chr11 | 396937 | |||
| chr11:397018 | C | T | 1 | a0015 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.517C>T | p.Arg173Trp | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/13 | 601/2817 | 517/2394 | 173/797 | chr11 | 397018 | |||
| chr11:397054 | C | T | 1 | a0008 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.553C>T | p.Arg185Trp | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/13 | 637/2817 | 553/2394 | 185/797 | chr11 | 397054 | |||
| chr11:397063 | C | A | 1 | a0004 | 2 | HG01175.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.562C>A | p.Pro188Thr | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/13 | 646/2817 | 562/2394 | 188/797 | chr11 | 397063 | |||
| chr11:397117 | G | C | 1 | a0012 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.616G>C | p.Ala206Pro | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/13 | 700/2817 | 616/2394 | 206/797 | chr11 | 397117 | |||
| chr11:397150 | C | T | 1 | a0014 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.649C>T | p.Arg217Cys | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/13 | 733/2817 | 649/2394 | 217/797 | chr11 | 397150 | |||
| chr11:397204 | A | T | 2 | a0011 a0018 |
2 | HG02132.hp2 NA18950.hp1 |
missense_variant | MODERATE | c.703A>T | p.Thr235Ser | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/13 | 787/2817 | 703/2394 | 235/797 | chr11 | 397204 | |||
| chr11:397373 | C | T | 1 | a0009 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.872C>T | p.Ser291Leu | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/13 | 956/2817 | 872/2394 | 291/797 | chr11 | 397373 | |||
| chr11:397390 | G | T | 1 | a0002 | 3 | HG02559.hp2 HG02886.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.889G>T | p.Val297Leu | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/13 | 973/2817 | 889/2394 | 297/797 | chr11 | 397390 | |||
| chr11:397584 | T | TTCAGACC others(4): Show |
1 | a0019 | 1 | NA19065.hp1 | frameshift_variant | HIGH | c.991_1001dupTCAGACC others(4): Show |
p.Leu335fs | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/13 | 1086/2817 | 1002/2394 | 334/797 | INFO_REALIGN_3_PRIME | chr11 | 397584 | ||
| chr11:398981 | T | TGTGCCCG others(17): Show |
1 | a0001 | 1 | HG03492.hp1 | conservative_inframe_insertion | MODERATE | c.1069-9_1083dupTGCC others(20): Show |
p.Gln361_Ala362insCy others(22): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/13 | 1168/2817 | 1084/2394 | 362/797 | INFO_REALIGN_3_PRIME | chr11 | 398981 | ||
| chr11:400024 | C | T | 1 | a0006 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.1331C>T | p.Thr444Met | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 6/13 | 1415/2817 | 1331/2394 | 444/797 | chr11 | 400024 | |||
| chr11:400069 | C | G | 1 | a0007 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.1376C>G | p.Ala459Gly | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 6/13 | 1460/2817 | 1376/2394 | 459/797 | chr11 | 400069 | |||
| chr11:400071 | G | T | 1 | a0007 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.1378G>T | p.Gly460Trp | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 6/13 | 1462/2817 | 1378/2394 | 460/797 | chr11 | 400071 | |||
| chr11:400124 | C | G | 1 | a0005 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.1431C>G | p.Asn477Lys | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 6/13 | 1515/2817 | 1431/2394 | 477/797 | chr11 | 400124 | |||
| chr11:400323 | T | TCGGTCCC others(41): Show |
1 | a0001 | 1 | NA18971.hp2 | disruptive_inframe_insertion | MODERATE | c.1449-10_1486dupCGG others(45): Show |
p.Lys495_Met496insTh others(46): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 7/13 | 1571/2817 | 1487/2394 | 496/797 | INFO_REALIGN_3_PRIME | chr11 | 400323 | ||
| chr11:400641 | T | G | 1 | a0017 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1673T>G | p.Leu558Arg | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/13 | 1757/2817 | 1673/2394 | 558/797 | chr11 | 400641 | |||
| chr11:404095 | G | A | 1 | a0018 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.2230G>A | p.Gly744Arg | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 11/13 | 2314/2817 | 2230/2394 | 744/797 | chr11 | 404095 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:394340 | C | T | 1 | a0001c0036 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.48C>T | p.Gly16Gly | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/13 | 132/2817 | 48/2394 | 16/797 | chr11 | 394340 | |||
| chr11:394514 | G | A | 1 | a0001c0018 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.222G>A | p.Glu74Glu | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/13 | 306/2817 | 222/2394 | 74/797 | chr11 | 394514 | |||
| chr11:396915 | C | T | 15 | a0001c0002 a0001c0003 a0001c0009 others(12): Show |
85 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(82): Show |
synonymous_variant | LOW | c.414C>T | p.Asn138Asn | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/13 | 498/2817 | 414/2394 | 138/797 | chr11 | 396915 | |||
| chr11:400040 | A | G | 8 | a0001c0003 a0001c0005 a0001c0008 others(5): Show |
52 | HG00673.hp1 HG01243.hp1 HG01256.hp1 others(49): Show |
synonymous_variant | LOW | c.1347A>G | p.Thr449Thr | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 6/13 | 1431/2817 | 1347/2394 | 449/797 | chr11 | 400040 | |||
| chr11:400064 | G | A | 1 | a0001c0021 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1371G>A | p.Ser457Ser | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 6/13 | 1455/2817 | 1371/2394 | 457/797 | chr11 | 400064 | |||
| chr11:400070 | T | C | 1 | a0007c0029 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.1377T>C | p.Ala459Ala | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 6/13 | 1461/2817 | 1377/2394 | 459/797 | chr11 | 400070 | |||
| chr11:400109 | A | G | 33 | a0001c0001 a0001c0002 a0001c0003 others(30): Show |
203 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(200): Show |
synonymous_variant | LOW | c.1416A>G | p.Ala472Ala | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 6/13 | 1500/2817 | 1416/2394 | 472/797 | chr11 | 400109 | |||
| chr11:403725 | C | T | 1 | a0001c0028 | 1 | HG03492.hp1 | synonymous_variant | LOW | c.2031C>T | p.Gly677Gly | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 10/13 | 2115/2817 | 2031/2394 | 677/797 | chr11 | 403725 | |||
| chr11:403749 | C | T | 2 | a0001c0011 a0013c0037 |
4 | HG02486.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.2055C>T | p.Asn685Asn | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 10/13 | 2139/2817 | 2055/2394 | 685/797 | chr11 | 403749 | |||
| chr11:403764 | C | T | 2 | a0001c0007 a0001c0012 |
9 | HG00733.hp2 HG01243.hp2 HG02027.hp1 others(6): Show |
synonymous_variant | LOW | c.2070C>T | p.Asp690Asp | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 10/13 | 2154/2817 | 2070/2394 | 690/797 | chr11 | 403764 | |||
| chr11:403980 | G | A | 21 | a0001c0002 a0001c0003 a0001c0004 others(18): Show |
102 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(99): Show |
synonymous_variant | LOW | c.2115G>A | p.Pro705Pro | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 11/13 | 2199/2817 | 2115/2394 | 705/797 | chr11 | 403980 | |||
| chr11:404317 | C | T | 15 | a0001c0002 a0001c0003 a0001c0010 others(12): Show |
81 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(78): Show |
synonymous_variant | LOW | c.2352C>T | p.Phe784Phe | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 12/13 | 2436/2817 | 2352/2394 | 784/797 | chr11 | 404317 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:394256 | G | C | 2 | a0011c0024t0002 a0018c0023t0002 |
2 | HG02132.hp2 NA18950.hp1 |
5_prime_UTR_variant | MODIFIER | c.-37G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/13 | 37 | chr11 | 394256 | ||||||
| chr11:394278 | G | A | 1 | a0001c0010t0003 | 2 | HG02486.hp2 HG02723.hp2 |
5_prime_UTR_variant | MODIFIER | c.-15G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/13 | 15 | chr11 | 394278 | ||||||
| chr11:404727 | G | A | 2 | a0001c0005t0004 a0015c0026t0004 |
2 | HG02886.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*158G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 13/13 | 158 | chr11 | 404727 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:394533 | T | TGGGGACA others(5): Show |
1 | a0001c0005t0004g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.232+15_232+26dupCA others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 394533 | ||||||
| chr11:394584 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.232+60C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 394584 | |||||||
| chr11:394608 | G | C | 4 | a0001c0007t0001g0007 a0001c0007t0001g0008 a0001c0007t0001g0009 others(1): Show |
4 | HG01243.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+84G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 394608 | |||||||
| chr11:394666 | G | GC | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(195): Show |
203 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.232+142_232+143ins others(1): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 394666 | |||||||
| chr11:394700 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(89): Show |
95 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.232+176T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 394700 | |||||||
| chr11:394835 | C | G | 2 | a0001c0004t0001g0196 a0001c0004t0001g0197 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.232+311C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 394835 | |||||||
| chr11:394897 | G | A | 83 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0101 others(80): Show |
85 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.232+373G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 394897 | |||||||
| chr11:394929 | CACGGGAA others(9): Show |
C | 1 | a0002c0013t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.232+406_232+421del others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 394929 | |||||||
| chr11:395015 | G | T | 1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.232+491G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395015 | |||||||
| chr11:395334 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.232+810A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395334 | |||||||
| chr11:395343 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(195): Show |
203 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.232+819T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395343 | |||||||
| chr11:395390 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(85): Show |
91 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.232+866G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395390 | |||||||
| chr11:395406 | G | A | 3 | a0001c0004t0001g0176 a0001c0004t0001g0196 a0001c0004t0001g0197 |
3 | HG02717.hp2 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.232+882G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395406 | |||||||
| chr11:395434 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.232+910C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395434 | |||||||
| chr11:395499 | G | A | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(17): Show |
20 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.232+975G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395499 | |||||||
| chr11:395655 | G | A | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(17): Show |
20 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.233-953G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395655 | |||||||
| chr11:395689 | C | G | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.233-919C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395689 | |||||||
| chr11:395746 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.233-862G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395746 | |||||||
| chr11:395797 | G | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
94 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.233-811G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395797 | |||||||
| chr11:395994 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-614G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 395994 | |||||||
| chr11:396038 | G | T | 2 | a0001c0004t0001g0190 a0001c0008t0001g0191 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.233-570G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396038 | |||||||
| chr11:396039 | A | T | 2 | a0001c0004t0001g0190 a0001c0008t0001g0191 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.233-569A>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396039 | |||||||
| chr11:396051 | G | A | 3 | a0001c0004t0001g0176 a0001c0004t0001g0196 a0001c0004t0001g0197 |
3 | HG02717.hp2 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.233-557G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396051 | |||||||
| chr11:396115 | G | A | 4 | a0001c0001t0001g0209 a0001c0004t0001g0012 a0001c0005t0001g0013 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-493G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396115 | |||||||
| chr11:396243 | C | T | 5 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0172 others(2): Show |
5 | HG02451.hp1 HG02809.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-365C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396243 | |||||||
| chr11:396286 | G | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(1): Show |
4 | HG02129.hp1 NA18943.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-322G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396286 | |||||||
| chr11:396292 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.233-316G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396292 | |||||||
| chr11:396294 | G | A | 4 | a0001c0003t0001g0095 a0001c0003t0001g0096 a0001c0003t0001g0097 others(1): Show |
4 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-314G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396294 | |||||||
| chr11:396308 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(89): Show |
95 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.233-300G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396308 | |||||||
| chr11:396313 | T | TGGCACAT others(9): Show |
1 | a0001c0002t0001g0169 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.233-294_233-279dup others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 396313 | ||||||
| chr11:396330 | C | CGACCAGG others(36): Show |
1 | a0013c0037t0005g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.233-277_233-235dup others(43): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 396330 | ||||||
| chr11:396406 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(195): Show |
203 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.233-202A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396406 | |||||||
| chr11:396473 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(195): Show |
203 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.233-135T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396473 | |||||||
| chr11:396522 | C | T | 1 | a0001c0008t0001g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.233-86C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396522 | |||||||
| chr11:396546 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(103): Show |
109 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.233-62G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 1/12 | chr11 | 396546 | |||||||
| chr11:396701 | C | T | 83 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0101 others(80): Show |
85 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.312+14C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 2/12 | chr11 | 396701 | |||||||
| chr11:396735 | T | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 |
3 | HG02630.hp2 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.312+48T>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 2/12 | chr11 | 396735 | |||||||
| chr11:396794 | C | T | 2 | a0001c0008t0001g0188 a0001c0008t0001g0189 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.313-20C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 2/12 | chr11 | 396794 | |||||||
| chr11:397460 | C | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02148.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.944+15C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/12 | chr11 | 397460 | |||||||
| chr11:397461 | C | CGGCTCAG others(17): Show |
1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.944+17_944+40dupGG others(22): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 397461 | ||||||
| chr11:397685 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1068+23C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397685 | |||||||
| chr11:397706 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(195): Show |
203 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.1068+44T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397706 | |||||||
| chr11:397732 | T | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(195): Show |
203 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.1068+70T>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397732 | |||||||
| chr11:397752 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1068+90C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397752 | |||||||
| chr11:397828 | C | A | 2 | a0001c0010t0003g0021 a0001c0010t0003g0022 |
2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1068+166C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397828 | |||||||
| chr11:397864 | G | GTACCCCC others(310): Show |
1 | a0001c0003t0001g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1068+229_1068+230i others(319): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 397864 | ||||||
| chr11:397877 | T | G | 1 | a0001c0005t0001g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1068+215T>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397877 | |||||||
| chr11:397905 | C | CACCTGCG others(194): Show |
1 | a0001c0009t0001g0102 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1068+392_1068+393i others(203): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 397905 | ||||||
| chr11:397905 | C | T | 80 | a0001c0001t0001g0018 a0001c0001t0001g0209 a0001c0002t0001g0004 others(77): Show |
81 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1068+243C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397905 | |||||||
| chr11:397912 | G | A | 2 | a0001c0010t0003g0021 a0001c0010t0003g0022 |
2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1068+250G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397912 | |||||||
| chr11:397921 | G | C | 2 | a0001c0002t0001g0103 a0001c0003t0001g0099 |
2 | HG03453.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1068+259G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397921 | |||||||
| chr11:397921 | G | GTACCCCC others(252): Show |
1 | a0002c0013t0001g0109 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1068+287_1068+545d others(261): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 397921 | ||||||
| chr11:397938 | T | TCATCACC others(51): Show |
1 | a0001c0002t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1068+295_1068+352d others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 397938 | ||||||
| chr11:397940 | A | ATCACCTC others(599): Show |
1 | a0001c0003t0001g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1068+286_1068+287i others(608): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 397940 | ||||||
| chr11:397949 | A | C | 1 | a0001c0003t0001g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1068+287A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397949 | |||||||
| chr11:397967 | C | G | 1 | a0001c0003t0001g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1068+305C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397967 | |||||||
| chr11:397978 | G | GTACCCCC others(888): Show |
1 | a0010c0017t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1068+450_1068+451i others(897): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 397978 | ||||||
| chr11:397978 | G | GTACCCCC others(625): Show |
1 | a0001c0002t0001g0110 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1068+623_1068+624i others(634): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 397978 | ||||||
| chr11:397986 | G | A | 1 | a0012c0020t0001g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1068+324G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397986 | |||||||
| chr11:397998 | A | G | 2 | a0001c0003t0001g0099 a0001c0021t0001g0086 |
2 | HG02622.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1068+336A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 397998 | |||||||
| chr11:398007 | A | C | 1 | a0001c0003t0001g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1068+345A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398007 | |||||||
| chr11:398007 | A | G | 1 | a0001c0021t0001g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1068+345A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398007 | |||||||
| chr11:398015 | A | ACACACAC others(51): Show |
2 | a0001c0005t0001g0013 a0001c0005t0001g0014 |
2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1068+363_1068+420d others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398015 | ||||||
| chr11:398015 | A | ACACACAC others(138): Show |
1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1068+449_1068+450i others(147): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398015 | ||||||
| chr11:398015 | A | G | 2 | a0001c0003t0001g0099 a0001c0021t0001g0086 |
2 | HG02622.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1068+353A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398015 | |||||||
| chr11:398025 | G | C | 1 | a0001c0021t0001g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1068+363G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398025 | |||||||
| chr11:398025 | G | GCGTCACC others(22): Show |
1 | a0001c0002t0001g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1068+391_1068+392i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398025 | ||||||
| chr11:398025 | GCGTCACC others(51): Show |
G | 3 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0007t0001g0010 |
3 | HG01243.hp2 HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1068+393_1068+450d others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398025 | ||||||
| chr11:398025 | GCGTCACC others(744): Show |
G | 1 | a0001c0002t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1068+432_1069-148d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398025 | ||||||
| chr11:398036 | G | A | 9 | a0001c0001t0001g0177 a0001c0004t0001g0176 a0001c0004t0001g0196 others(6): Show |
9 | HG02717.hp2 HG03471.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068+374G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398036 | |||||||
| chr11:398043 | C | T | 2 | a0001c0004t0001g0190 a0001c0008t0001g0191 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1068+381C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398043 | |||||||
| chr11:398054 | G | C | 5 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(2): Show |
5 | HG02451.hp1 HG02897.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+392G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398054 | |||||||
| chr11:398054 | GCGTCACC others(22): Show |
G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1068+421_1068+449d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398054 | ||||||
| chr11:398055 | C | T | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1068+393C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398055 | |||||||
| chr11:398065 | G | C | 3 | a0001c0003t0001g0099 a0001c0007t0001g0007 a0001c0021t0001g0086 |
3 | HG02622.hp2 NA18612.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1068+403G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398065 | |||||||
| chr11:398068 | C | A | 1 | a0001c0002t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1068+406C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398068 | |||||||
| chr11:398073 | G | A | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1068+411G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398073 | |||||||
| chr11:398076 | C | T | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1068+414C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398076 | |||||||
| chr11:398078 | C | T | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1068+416C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398078 | |||||||
| chr11:398083 | C | G | 8 | a0001c0001t0001g0018 a0001c0002t0001g0103 a0001c0002t0001g0171 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+421C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398083 | |||||||
| chr11:398085 | G | A | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1068+423G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398085 | |||||||
| chr11:398085 | G | GTCACCTC others(107): Show |
1 | a0001c0007t0001g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1068+450_1068+451i others(116): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398085 | ||||||
| chr11:398102 | G | A | 1 | a0001c0003t0001g0105 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1068+440G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398102 | |||||||
| chr11:398112 | G | C | 6 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(3): Show |
6 | HG02451.hp1 HG02809.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+450G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398112 | |||||||
| chr11:398113 | T | C | 9 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(6): Show |
9 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068+451T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398113 | |||||||
| chr11:398113 | T | TGTCACCT others(224): Show |
1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1068+501_1068+502i others(233): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398113 | ||||||
| chr11:398113 | T | TGTCACCT others(1117): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1068+525_1068+526i others(1126): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398113 | ||||||
| chr11:398113 | T | TGTCACCT others(50): Show |
2 | a0001c0005t0001g0084 a0001c0005t0001g0085 |
2 | NA18612.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1068+492_1068+493i others(59): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398113 | ||||||
| chr11:398113 | TGTCACCT others(512): Show |
T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1068+469_1069-343d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398113 | ||||||
| chr11:398123 | C | G | 5 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0172 others(2): Show |
5 | HG02451.hp1 HG02809.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1068+461C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398123 | |||||||
| chr11:398127 | CCCCACAT others(21): Show |
C | 1 | a0001c0009t0001g0167 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1068+469_1068+496d others(30): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398127 | ||||||
| chr11:398131 | A | G | 8 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+469A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398131 | |||||||
| chr11:398134 | T | C | 8 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+472T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398134 | |||||||
| chr11:398136 | T | C | 8 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+474T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398136 | |||||||
| chr11:398140 | T | TC | 3 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0030t0001g0174 |
3 | HG02897.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1068+479dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398140 | ||||||
| chr11:398140 | T | TCCGTCAC others(23): Show |
1 | a0001c0002t0001g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1068+479_1068+480i others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398140 | ||||||
| chr11:398140 | T | TG | 4 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0021t0001g0086 others(1): Show |
4 | HG02622.hp2 HG02809.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+478_1068+479i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398140 | |||||||
| chr11:398142 | A | G | 8 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+480A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398142 | |||||||
| chr11:398155 | A | C | 8 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+493A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398155 | |||||||
| chr11:398164 | T | C | 12 | a0001c0001t0001g0018 a0001c0002t0001g0100 a0001c0002t0001g0170 others(9): Show |
12 | HG00639.hp1 HG00673.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1068+502T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398164 | |||||||
| chr11:398164 | T | TACCTGCG others(1032): Show |
1 | a0001c0001t0001g0198 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1069-663_1069-662i others(1041): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398164 | ||||||
| chr11:398170 | C | CGTCACCT others(195): Show |
1 | a0001c0036t0001g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1068+574_1068+575i others(204): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398170 | ||||||
| chr11:398171 | GTCACCTC others(21): Show |
G | 1 | a0001c0030t0001g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1068+518_1068+545d others(30): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398171 | ||||||
| chr11:398180 | C | G | 6 | a0001c0001t0001g0018 a0001c0002t0001g0171 a0001c0002t0001g0172 others(3): Show |
6 | HG00673.hp2 HG02622.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+518C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398180 | |||||||
| chr11:398188 | A | G | 8 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(5): Show |
8 | HG00673.hp2 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+526A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398188 | |||||||
| chr11:398191 | T | C | 8 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(5): Show |
8 | HG00673.hp2 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+529T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398191 | |||||||
| chr11:398193 | T | C | 8 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(5): Show |
8 | HG00673.hp2 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+531T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398193 | |||||||
| chr11:398197 | T | TCTGTCAC others(23): Show |
3 | a0001c0001t0001g0018 a0001c0021t0001g0086 a0017c0027t0001g0107 |
3 | HG02622.hp2 HG03834.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1068+536_1068+537i others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398197 | ||||||
| chr11:398197 | T | TG | 4 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0173 others(1): Show |
4 | HG00673.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+535_1068+536i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398197 | |||||||
| chr11:398197 | T | TGCGTCAC others(23): Show |
1 | a0001c0002t0001g0172 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1068+535_1068+536i others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398197 | |||||||
| chr11:398199 | A | ATCACCTC others(22): Show |
1 | a0013c0037t0005g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1068+563_1068+564i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398199 | ||||||
| chr11:398199 | A | ATCACCTC others(22): Show |
1 | a0001c0001t0001g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1068+546_1068+574d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398199 | ||||||
| chr11:398199 | A | ATCACCTC others(1060): Show |
1 | a0001c0003t0001g0003 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1069-663_1069-662i others(1069): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398199 | ||||||
| chr11:398199 | A | ATCACCTC others(800): Show |
1 | a0001c0003t0001g0147 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1069-663_1069-662i others(809): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398199 | ||||||
| chr11:398199 | A | G | 5 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0172 others(2): Show |
5 | HG00673.hp2 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+537A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398199 | |||||||
| chr11:398208 | G | A | 2 | a0002c0013t0001g0108 a0002c0013t0001g0175 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1068+546G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398208 | |||||||
| chr11:398208 | G | C | 1 | a0001c0002t0001g0171 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1068+546G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398208 | |||||||
| chr11:398208 | G | GTACACCC others(370): Show |
1 | a0001c0001t0001g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1068+549_1068+550i others(379): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398208 | ||||||
| chr11:398208 | G | GTACCCCC others(452): Show |
1 | a0001c0002t0001g0101 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1068+615_1068+616i others(461): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398208 | ||||||
| chr11:398212 | C | A | 3 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0011c0024t0002g0026 |
3 | HG01884.hp1 HG02132.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1068+550C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398212 | |||||||
| chr11:398212 | C | CCCCGCAC others(857): Show |
1 | a0001c0003t0001g0095 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1069-663_1069-662i others(866): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398212 | ||||||
| chr11:398221 | C | CACCTCCG others(195): Show |
2 | a0002c0013t0001g0108 a0002c0013t0001g0175 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1068+563_1068+564i others(204): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398221 | ||||||
| chr11:398226 | G | C | 4 | a0001c0002t0001g0170 a0001c0002t0001g0172 a0001c0002t0001g0173 others(1): Show |
4 | HG00673.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+564G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398226 | |||||||
| chr11:398227 | C | T | 3 | a0001c0009t0001g0167 a0003c0014t0001g0187 a0011c0024t0002g0026 |
3 | HG00673.hp2 HG02132.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1068+565C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398227 | |||||||
| chr11:398237 | C | A | 1 | a0001c0021t0001g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1068+575C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398237 | |||||||
| chr11:398237 | C | CTACCCCC others(50): Show |
1 | a0001c0001t0001g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1068+606_1068+607i others(59): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398237 | ||||||
| chr11:398237 | C | G | 6 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(3): Show |
6 | HG02451.hp1 HG02809.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+575C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398237 | |||||||
| chr11:398241 | CCCCACAT others(21): Show |
C | 1 | a0001c0030t0001g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1068+583_1068+610d others(30): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398241 | ||||||
| chr11:398245 | A | G | 9 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(6): Show |
9 | HG00673.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1068+583A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398245 | |||||||
| chr11:398248 | T | C | 9 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(6): Show |
9 | HG00673.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1068+586T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398248 | |||||||
| chr11:398250 | T | C | 9 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(6): Show |
9 | HG00673.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1068+588T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398250 | |||||||
| chr11:398254 | T | TG | 8 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0172 others(5): Show |
8 | HG00673.hp2 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+592_1068+593i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398254 | |||||||
| chr11:398256 | A | ATCACCTC others(863): Show |
1 | a0015c0026t0004g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1068+606_1068+607i others(872): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398256 | ||||||
| chr11:398256 | A | ATCACCTC others(195): Show |
1 | a0001c0001t0001g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1068+606_1068+607i others(204): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398256 | ||||||
| chr11:398256 | A | G | 8 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+594A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398256 | |||||||
| chr11:398265 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1068+603G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398265 | |||||||
| chr11:398265 | G | C | 3 | a0001c0001t0001g0018 a0001c0021t0001g0086 a0017c0027t0001g0107 |
3 | HG02622.hp2 HG03834.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1068+603G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398265 | |||||||
| chr11:398269 | A | ACCCGCAC others(195): Show |
1 | a0001c0003t0001g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1069-663_1069-662i others(204): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398269 | ||||||
| chr11:398269 | A | ACCCGCAC others(857): Show |
1 | a0011c0024t0002g0026 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1068+621_1068+622i others(866): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398269 | ||||||
| chr11:398269 | A | ACCCGCAC others(832): Show |
1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1068+615_1068+616i others(841): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398269 | ||||||
| chr11:398269 | A | C | 13 | a0001c0001t0001g0018 a0001c0002t0001g0170 a0001c0002t0001g0171 others(10): Show |
13 | HG00642.hp1 HG00673.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1068+607A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398269 | |||||||
| chr11:398280 | C | T | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1068+618C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398280 | |||||||
| chr11:398283 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1068+621G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398283 | |||||||
| chr11:398294 | C | CTACCCCC others(281): Show |
3 | a0003c0014t0001g0182 a0003c0019t0001g0181 a0016c0035t0001g0180 |
3 | HG03471.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1068+639_1068+640i others(290): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398294 | ||||||
| chr11:398294 | C | CTACCCCC others(22): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1068+639_1069-663d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398294 | ||||||
| chr11:398294 | C | G | 6 | a0001c0001t0001g0082 a0001c0002t0001g0164 a0001c0002t0001g0171 others(3): Show |
6 | HG00642.hp2 HG00673.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+632C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398294 | |||||||
| chr11:398294 | CTACCCCC others(22): Show |
C | 1 | a0001c0001t0001g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1068+639_1069-663d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398294 | ||||||
| chr11:398294 | CTACCCCC others(51): Show |
C | 1 | a0001c0004t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1068+661_1069-612d others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398294 | ||||||
| chr11:398298 | C | CCCCACAT others(21): Show |
2 | a0002c0013t0001g0108 a0002c0013t0001g0175 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1068+639_1068+640i others(30): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398298 | ||||||
| chr11:398298 | C | CCCCACAT others(78): Show |
1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1068+639_1068+640i others(87): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398298 | ||||||
| chr11:398301 | CGCACACA others(22): Show |
C | 1 | a0001c0008t0001g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1068+650_1069-652d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398301 | ||||||
| chr11:398312 | G | C | 4 | a0001c0004t0001g0190 a0001c0008t0001g0188 a0001c0008t0001g0189 others(1): Show |
4 | HG02622.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+650G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398312 | |||||||
| chr11:398322 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1068+660C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398322 | |||||||
| chr11:398323 | G | C | 19 | a0001c0001t0001g0018 a0001c0001t0001g0046 a0001c0002t0001g0170 others(16): Show |
19 | HG00642.hp1 HG00673.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.1068+661G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398323 | |||||||
| chr11:398326 | C | A | 1 | a0001c0002t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1068+664C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398326 | |||||||
| chr11:398330 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(189): Show |
197 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.1069-662T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398330 | |||||||
| chr11:398341 | C | CCGTCACC others(349): Show |
1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1069-633_1069-632i others(358): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398341 | ||||||
| chr11:398341 | C | CCGTCACC others(860): Show |
1 | a0001c0001t0001g0081 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1069-622_1069-621i others(869): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398341 | ||||||
| chr11:398341 | C | CTGTCACC others(80): Show |
1 | a0003c0014t0001g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1069-651_1069-650i others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398341 | |||||||
| chr11:398341 | C | CTGTCACC others(196): Show |
1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1069-651_1069-650i others(205): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398341 | |||||||
| chr11:398341 | C | G | 14 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0172 others(11): Show |
14 | HG00642.hp1 HG00673.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1069-651C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398341 | |||||||
| chr11:398343 | G | GTCACCTC others(22): Show |
1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1069-621_1069-620i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398343 | ||||||
| chr11:398352 | G | C | 9 | a0001c0001t0001g0082 a0001c0002t0001g0171 a0001c0004t0001g0190 others(6): Show |
9 | HG00673.hp2 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.1069-640G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398352 | |||||||
| chr11:398352 | G | GTACCCCC others(979): Show |
1 | a0001c0004t0001g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1069-623_1069-622i others(988): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398352 | ||||||
| chr11:398356 | C | CCCCGCAC others(365): Show |
1 | a0001c0002t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1069-628_1069-627i others(374): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398356 | ||||||
| chr11:398370 | G | C | 3 | a0001c0004t0001g0027 a0002c0013t0001g0108 a0002c0013t0001g0175 |
3 | HG00642.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1069-622G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398370 | |||||||
| chr11:398372 | G | A | 1 | a0001c0004t0001g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1069-620G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398372 | |||||||
| chr11:398381 | C | CTACCCCC others(396): Show |
1 | a0010c0017t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1069-604_1069-603i others(405): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398381 | ||||||
| chr11:398381 | C | CTACCCCC others(369): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1069-604_1069-603i others(378): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398381 | ||||||
| chr11:398381 | C | CTACCCCC others(829): Show |
1 | a0001c0003t0001g0111 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1069-583_1069-582i others(838): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398381 | ||||||
| chr11:398381 | C | CTACCCCC others(829): Show |
4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0112 others(1): Show |
4 | HG01934.hp2 HG02273.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-583_1069-582i others(838): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398381 | ||||||
| chr11:398381 | C | CTACCCCC others(829): Show |
1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1069-583_1069-582i others(838): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398381 | ||||||
| chr11:398381 | C | CTACCCCC others(858): Show |
1 | a0001c0003t0001g0116 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1069-583_1069-582i others(867): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398381 | ||||||
| chr11:398381 | C | CTACCCCC others(1327): Show |
1 | a0001c0007t0001g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1069-536_1069-535i others(1336): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398381 | ||||||
| chr11:398381 | C | G | 20 | a0001c0001t0001g0018 a0001c0001t0001g0077 a0001c0001t0001g0078 others(17): Show |
20 | HG00642.hp1 HG01261.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.1069-611C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398381 | |||||||
| chr11:398381 | CTACCCCC others(22): Show |
C | 1 | a0008c0025t0001g0199 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1069-582_1069-554d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398381 | ||||||
| chr11:398383 | A | ACCCCCAC others(22): Show |
1 | a0001c0001t0001g0018 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1069-604_1069-603i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398383 | ||||||
| chr11:398389 | G | A | 1 | a0001c0005t0004g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1069-603G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398389 | |||||||
| chr11:398399 | G | C | 8 | a0001c0001t0001g0018 a0001c0004t0001g0196 a0001c0009t0001g0167 others(5): Show |
8 | HG00673.hp2 HG03471.hp2 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-593G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398399 | |||||||
| chr11:398399 | G | GCGTCACC others(685): Show |
1 | a0001c0003t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1069-583_1069-582i others(694): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398399 | ||||||
| chr11:398399 | G | GCGTCACC others(1355): Show |
1 | a0001c0005t0001g0091 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1069-583_1069-582i others(1364): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398399 | ||||||
| chr11:398399 | G | GCGTCACC others(428): Show |
1 | a0001c0001t0001g0031 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1069-583_1069-582i others(437): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398399 | ||||||
| chr11:398399 | G | GCGTCACC others(109): Show |
1 | a0001c0021t0001g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1069-583_1069-582i others(118): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398399 | ||||||
| chr11:398399 | G | GCGTCACC others(22): Show |
1 | a0001c0002t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1069-565_1069-564i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398399 | ||||||
| chr11:398399 | G | GCGTCACC others(805): Show |
1 | a0001c0001t0001g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1069-554_1069-553i others(814): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398399 | ||||||
| chr11:398400 | C | T | 1 | a0001c0004t0001g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1069-592C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398400 | |||||||
| chr11:398401 | G | GTCACCTC others(655): Show |
1 | a0001c0003t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1069-583_1069-582i others(664): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398401 | ||||||
| chr11:398410 | G | A | 1 | a0001c0005t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1069-582G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398410 | |||||||
| chr11:398410 | G | C | 27 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(24): Show |
27 | HG00642.hp1 HG01261.hp2 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.1069-582G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398410 | |||||||
| chr11:398410 | G | GTACCCCC others(80): Show |
4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-565_1069-564i others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398410 | ||||||
| chr11:398410 | G | GTACCCCC others(1703): Show |
1 | a0012c0020t0001g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1069-565_1069-564i others(1712): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398410 | ||||||
| chr11:398410 | G | GTACCCCC others(1472): Show |
1 | a0001c0005t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1069-565_1069-564i others(1481): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398410 | ||||||
| chr11:398410 | G | GTACCCCC others(573): Show |
1 | a0001c0005t0001g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1069-565_1069-564i others(582): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398410 | ||||||
| chr11:398410 | G | GTACCCCC others(22): Show |
1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1069-553_1069-525d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398410 | ||||||
| chr11:398410 | G | GTACCCCC others(196): Show |
1 | a0001c0010t0003g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1069-554_1069-553i others(205): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398410 | ||||||
| chr11:398410 | G | GTACCCCC others(1204): Show |
1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1069-554_1069-553i others(1213): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398410 | ||||||
| chr11:398410 | G | GTACCCCC others(22): Show |
1 | a0001c0001t0001g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1069-556_1069-555i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398410 | ||||||
| chr11:398410 | GTACCCCC others(22): Show |
G | 8 | a0001c0003t0001g0161 a0001c0003t0001g0162 a0001c0004t0001g0073 others(5): Show |
8 | HG01243.hp2 HG02717.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-553_1069-525d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398410 | ||||||
| chr11:398418 | G | GCACACAC others(22): Show |
1 | a0001c0001t0001g0018 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1069-563_1069-562i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398418 | ||||||
| chr11:398428 | G | C | 1 | a0013c0037t0005g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1069-564G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398428 | |||||||
| chr11:398429 | C | CGTCACCT others(80): Show |
2 | a0001c0002t0001g0118 a0007c0029t0001g0117 |
2 | HG00733.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1069-536_1069-535i others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398429 | ||||||
| chr11:398429 | C | T | 1 | a0013c0037t0005g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1069-563C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398429 | |||||||
| chr11:398430 | GTCACCTC others(80): Show |
G | 1 | a0001c0004t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1069-553_1069-467d others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398430 | ||||||
| chr11:398439 | C | CTACCCCC others(22): Show |
1 | a0001c0002t0001g0101 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1069-536_1069-535i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398439 | ||||||
| chr11:398439 | C | CTACCCCC others(225): Show |
1 | a0001c0001t0001g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1069-536_1069-535i others(234): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398439 | ||||||
| chr11:398439 | C | CTACCCCC others(805): Show |
2 | a0001c0005t0001g0013 a0001c0005t0001g0014 |
2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1069-525_1069-524i others(814): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398439 | ||||||
| chr11:398439 | C | CTACCCCC others(51): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1069-525_1069-524i others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398439 | ||||||
| chr11:398439 | C | CTACCCCC others(22): Show |
82 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1069-535_1069-507d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398439 | ||||||
| chr11:398439 | C | CTACCCCC others(51): Show |
1 | a0001c0001t0001g0056 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398439 | ||||||
| chr11:398439 | C | CTACCCCC others(254): Show |
1 | a0001c0010t0003g0021 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1069-507_1069-506i others(263): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398439 | ||||||
| chr11:398439 | C | G | 37 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0077 others(34): Show |
37 | HG00642.hp1 HG00673.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.1069-553C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398439 | |||||||
| chr11:398439 | CTACCCCC others(80): Show |
C | 3 | a0001c0002t0001g0159 a0001c0004t0001g0197 a0009c0033t0001g0160 |
3 | HG01891.hp1 HG01943.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1069-506_1069-420d others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398439 | ||||||
| chr11:398457 | G | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG02723.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1069-535G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398457 | |||||||
| chr11:398459 | G | A | 3 | a0001c0002t0001g0118 a0007c0029t0001g0117 a0013c0037t0005g0087 |
3 | HG00733.hp1 HG01515.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1069-533G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398459 | |||||||
| chr11:398459 | GTCACCTC others(51): Show |
G | 1 | a0001c0001t0001g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1069-506_1069-449d others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398459 | ||||||
| chr11:398468 | G | C | 19 | a0001c0001t0001g0031 a0001c0001t0001g0046 a0001c0001t0001g0075 others(16): Show |
19 | HG00544.hp2 HG00673.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1069-524G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398468 | |||||||
| chr11:398468 | GTACCCCC others(22): Show |
G | 2 | a0001c0004t0001g0196 a0002c0013t0001g0109 |
2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1069-506_1069-478d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398468 | ||||||
| chr11:398468 | GTACCCCC others(138): Show |
G | 1 | a0001c0012t0001g0156 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1069-506_1069-362d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398468 | ||||||
| chr11:398477 | C | CACACACC others(834): Show |
1 | a0001c0001t0001g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1069-507_1069-506i others(843): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398477 | ||||||
| chr11:398485 | T | TGCGTCAC others(397): Show |
1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1069-507_1069-506i others(406): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(542): Show |
1 | a0001c0001t0001g0015 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1069-507_1069-506i others(551): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(136): Show |
1 | a0001c0001t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(145): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(165): Show |
1 | a0004c0015t0001g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(174): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(660): Show |
1 | a0001c0001t0001g0044 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(669): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(397): Show |
1 | a0001c0001t0001g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(406): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(455): Show |
1 | a0018c0023t0002g0037 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(464): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(832): Show |
1 | a0001c0001t0001g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(841): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(745): Show |
1 | a0001c0001t0001g0033 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(754): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(600): Show |
1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1069-507_1069-506i others(609): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(658): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0019 |
3 | HG02148.hp1 HG03704.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1069-507_1069-506i others(667): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(600): Show |
1 | a0001c0018t0001g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(609): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(513): Show |
1 | a0001c0006t0001g0038 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(522): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(542): Show |
1 | a0001c0006t0001g0049 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1069-507_1069-506i others(551): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(658): Show |
1 | a0001c0001t0001g0043 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1069-507_1069-506i others(667): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(1151): Show |
1 | a0001c0010t0001g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1069-507_1069-506i others(1160): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398485 | T | TGCGTCAC others(542): Show |
1 | a0001c0002t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1069-507_1069-506i others(551): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398485 | |||||||
| chr11:398486 | C | G | 37 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0046 others(34): Show |
38 | HG00544.hp2 HG00642.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1069-506C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398486 | |||||||
| chr11:398487 | T | C | 40 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0046 others(37): Show |
41 | HG00544.hp2 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1069-505T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398487 | |||||||
| chr11:398487 | T | TGC | 18 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0019 others(15): Show |
19 | HG00621.hp1 HG01175.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1069-504_1069-503i others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398487 | ||||||
| chr11:398497 | C | A | 2 | a0001c0001t0001g0036 a0013c0037t0005g0087 |
2 | HG02647.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1069-495C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398497 | |||||||
| chr11:398497 | C | G | 19 | a0001c0001t0001g0039 a0001c0001t0001g0082 a0001c0002t0001g0171 others(16): Show |
20 | HG00621.hp1 HG00673.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.1069-495C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398497 | |||||||
| chr11:398515 | G | C | 10 | a0001c0001t0001g0046 a0001c0003t0001g0003 a0001c0003t0001g0095 others(7): Show |
11 | HG01175.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1069-477G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398515 | |||||||
| chr11:398516 | C | T | 4 | a0001c0003t0001g0003 a0001c0003t0001g0095 a0001c0005t0001g0032 others(1): Show |
5 | HG01256.hp2 HG01258.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-476C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398516 | |||||||
| chr11:398517 | A | ATCACCTC others(51): Show |
1 | a0001c0016t0001g0200 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1069-466_1069-409d others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398517 | ||||||
| chr11:398517 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(57): Show |
62 | HG00544.hp2 HG00642.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.1069-475A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398517 | |||||||
| chr11:398525 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1069-467C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398525 | |||||||
| chr11:398526 | G | C | 25 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0034 others(22): Show |
26 | HG01256.hp2 HG01258.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1069-466G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398526 | |||||||
| chr11:398526 | G | GTACCCCC others(22): Show |
2 | a0001c0004t0001g0193 a0001c0008t0001g0194 |
2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1069-438_1069-437i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398526 | ||||||
| chr11:398526 | G | GTACCCCC others(225): Show |
1 | a0003c0014t0001g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1069-438_1069-437i others(234): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398526 | ||||||
| chr11:398526 | G | GTACCCCC others(80): Show |
1 | a0001c0003t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1069-409_1069-408i others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398526 | ||||||
| chr11:398526 | G | GTACCCCC others(22): Show |
1 | a0001c0005t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1069-448_1069-447i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398526 | ||||||
| chr11:398544 | G | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG00621.hp1 HG00673.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-448G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398544 | |||||||
| chr11:398544 | G | GCGTCACC others(22): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG00621.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1069-438_1069-437i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398544 | ||||||
| chr11:398544 | G | GCGTCACC others(138): Show |
2 | a0001c0008t0001g0188 a0001c0008t0001g0189 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1069-438_1069-437i others(147): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398544 | ||||||
| chr11:398545 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(45): Show |
50 | HG00099.hp1 HG00609.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1069-447C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398545 | |||||||
| chr11:398545 | C | TGTCACCT others(544): Show |
1 | a0001c0001t0001g0020 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1069-448_1069-447i others(553): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398545 | |||||||
| chr11:398546 | G | A | 3 | a0001c0003t0001g0003 a0001c0003t0001g0095 a0001c0006t0001g0035 |
4 | HG01256.hp2 HG01258.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-446G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398546 | |||||||
| chr11:398555 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
41 | HG00099.hp1 HG00609.hp2 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.1069-437G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398555 | |||||||
| chr11:398555 | G | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0031 others(27): Show |
31 | HG00544.hp2 HG00673.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1069-437G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398555 | |||||||
| chr11:398555 | GTACCCCC others(22): Show |
G | 2 | a0001c0007t0001g0008 a0001c0007t0001g0208 |
2 | HG00733.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1069-321_1069-293d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398555 | ||||||
| chr11:398562 | C | T | 1 | a0001c0007t0001g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1069-430C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398562 | |||||||
| chr11:398573 | G | C | 8 | a0001c0002t0001g0164 a0001c0002t0001g0170 a0001c0002t0001g0172 others(5): Show |
8 | HG00642.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-419G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398573 | |||||||
| chr11:398574 | C | T | 1 | a0001c0006t0001g0035 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1069-418C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398574 | |||||||
| chr11:398574 | C | TGTCACCT others(80): Show |
1 | a0001c0002t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1069-505_1069-419d others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398574 | |||||||
| chr11:398575 | G | A | 4 | a0001c0009t0001g0167 a0002c0013t0001g0108 a0002c0013t0001g0109 others(1): Show |
4 | HG00673.hp2 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-417G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398575 | |||||||
| chr11:398584 | C | A | 1 | a0001c0006t0001g0035 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1069-408C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398584 | |||||||
| chr11:398584 | C | CTACCCCC others(110): Show |
1 | a0001c0003t0001g0116 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1069-394_1069-393i others(119): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398584 | ||||||
| chr11:398584 | C | CTACCCCC others(1559): Show |
1 | a0001c0001t0001g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1069-362_1069-361i others(1568): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398584 | ||||||
| chr11:398584 | C | CTACCCCC others(167): Show |
1 | a0001c0001t0001g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1069-362_1069-361i others(176): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398584 | ||||||
| chr11:398584 | C | CTACCCCC others(283): Show |
1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1069-380_1069-379i others(292): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398584 | ||||||
| chr11:398584 | C | G | 17 | a0001c0002t0001g0159 a0001c0002t0001g0170 a0001c0002t0001g0172 others(14): Show |
18 | HG00673.hp2 HG01256.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1069-408C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398584 | |||||||
| chr11:398602 | G | C | 8 | a0001c0001t0001g0036 a0001c0001t0001g0072 a0001c0001t0001g0177 others(5): Show |
8 | HG01891.hp1 HG01943.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1069-390G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398602 | |||||||
| chr11:398602 | G | GCGTCACC others(22): Show |
1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1069-380_1069-379i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398602 | ||||||
| chr11:398603 | C | CGTCACCT others(51): Show |
1 | a0001c0003t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1069-380_1069-379i others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398603 | ||||||
| chr11:398603 | C | T | 2 | a0001c0002t0001g0159 a0009c0033t0001g0160 |
2 | HG01891.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1069-389C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398603 | |||||||
| chr11:398613 | C | CTACCCCC others(1735): Show |
1 | a0001c0001t0001g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1069-362_1069-361i others(1744): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398613 | ||||||
| chr11:398613 | C | CTACCCCC others(1501): Show |
1 | a0001c0001t0001g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1069-362_1069-361i others(1510): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398613 | ||||||
| chr11:398613 | C | CTACCCCC others(1530): Show |
1 | a0001c0001t0001g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1069-362_1069-361i others(1539): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398613 | ||||||
| chr11:398613 | C | CTACCCCC others(51): Show |
1 | a0001c0001t0001g0041 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1069-322_1069-321i others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398613 | ||||||
| chr11:398613 | C | G | 18 | a0001c0001t0001g0036 a0001c0001t0001g0177 a0001c0002t0001g0170 others(15): Show |
18 | HG00673.hp2 HG01175.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1069-379C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398613 | |||||||
| chr11:398618 | C | G | 2 | a0001c0008t0001g0188 a0001c0008t0001g0189 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1069-374C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398618 | |||||||
| chr11:398631 | G | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0031 others(12): Show |
16 | HG00544.hp2 HG01192.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.1069-361G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398631 | |||||||
| chr11:398633 | G | A | 4 | a0001c0001t0001g0046 a0001c0002t0001g0159 a0001c0003t0001g0098 others(1): Show |
4 | HG01891.hp1 HG01943.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-359G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398633 | |||||||
| chr11:398642 | C | A | 1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1069-350C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398642 | |||||||
| chr11:398642 | C | CTACCCCC others(22): Show |
1 | a0001c0005t0001g0091 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1069-333_1069-332i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(196): Show |
1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1069-333_1069-332i others(205): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(254): Show |
1 | a0001c0001t0001g0055 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1069-333_1069-332i others(263): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(776): Show |
1 | a0001c0001t0001g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1069-333_1069-332i others(785): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(51): Show |
4 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0169 others(1): Show |
4 | HG03579.hp1 NA18945.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-333_1069-332i others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(80): Show |
1 | a0001c0002t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1069-333_1069-332i others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(1067): Show |
1 | a0001c0012t0001g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1069-333_1069-332i others(1076): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(805): Show |
3 | a0001c0009t0001g0121 a0001c0009t0001g0122 a0001c0009t0001g0123 |
3 | NA18994.hp2 NA19005.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1069-333_1069-332i others(814): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(805): Show |
1 | a0001c0009t0001g0102 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1069-333_1069-332i others(814): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(109): Show |
3 | a0001c0003t0001g0111 a0001c0003t0001g0112 a0001c0003t0001g0113 |
3 | HG01981.hp1 HG02273.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1069-333_1069-332i others(118): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(167): Show |
2 | a0001c0002t0001g0130 a0001c0009t0001g0129 |
2 | HG02735.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1069-333_1069-332i others(176): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(370): Show |
1 | a0001c0002t0001g0138 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1069-333_1069-332i others(379): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | CTACCCCC others(283): Show |
1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1069-333_1069-332i others(292): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398642 | C | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0031 others(29): Show |
33 | HG00544.hp2 HG01192.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1069-350C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398642 | |||||||
| chr11:398642 | CTACCCCC others(51): Show |
C | 1 | a0017c0027t0001g0107 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1069-274_1069-217d others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398642 | ||||||
| chr11:398660 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(131): Show |
138 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1069-332G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398660 | |||||||
| chr11:398660 | G | GCATCACC others(979): Show |
1 | a0001c0001t0001g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1069-331_1069-330i others(988): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398660 | ||||||
| chr11:398660 | G | GCGTCACC others(1095): Show |
1 | a0001c0002t0001g0110 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1069-322_1069-321i others(1104): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398660 | ||||||
| chr11:398660 | G | GCGTCACC others(1182): Show |
1 | a0014c0034t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1069-322_1069-321i others(1191): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398660 | ||||||
| chr11:398660 | G | GCGTCACC others(805): Show |
1 | a0001c0036t0001g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1069-322_1069-321i others(814): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398660 | ||||||
| chr11:398661 | C | T | 4 | a0001c0004t0001g0176 a0001c0004t0001g0196 a0001c0004t0001g0197 others(1): Show |
4 | HG02717.hp2 HG03540.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-331C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398661 | |||||||
| chr11:398662 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1069-330G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398662 | |||||||
| chr11:398671 | C | A | 3 | a0001c0004t0001g0193 a0001c0008t0001g0192 a0001c0008t0001g0194 |
3 | HG03486.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1069-321C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398671 | |||||||
| chr11:398671 | C | CTACCCCC others(22): Show |
4 | a0001c0003t0001g0003 a0001c0003t0001g0095 a0001c0003t0001g0115 others(1): Show |
5 | HG01256.hp2 HG01258.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-304_1069-303i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398671 | ||||||
| chr11:398671 | C | CTACCCCC others(51): Show |
1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1069-304_1069-303i others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398671 | ||||||
| chr11:398671 | C | CTACCCCC others(428): Show |
1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1069-304_1069-303i others(437): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398671 | ||||||
| chr11:398671 | C | CTACCCCC others(573): Show |
1 | a0001c0006t0001g0035 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1069-304_1069-303i others(582): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398671 | ||||||
| chr11:398671 | C | CTACCCCC others(399): Show |
1 | a0013c0037t0005g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1069-304_1069-303i others(408): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398671 | ||||||
| chr11:398671 | C | CTACCCCC others(486): Show |
1 | a0001c0001t0001g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1069-293_1069-292i others(495): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398671 | ||||||
| chr11:398671 | C | CTACCCCC others(254): Show |
1 | a0001c0001t0001g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1069-293_1069-292i others(263): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398671 | ||||||
| chr11:398671 | C | CTACCCCC others(1326): Show |
1 | a0001c0005t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1069-293_1069-292i others(1335): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398671 | ||||||
| chr11:398671 | C | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(140): Show |
147 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1069-321C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398671 | |||||||
| chr11:398671 | CTACCCCC others(22): Show |
C | 3 | a0001c0004t0001g0176 a0001c0004t0001g0196 a0001c0004t0001g0197 |
3 | HG02717.hp2 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1069-292_1069-264d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398671 | ||||||
| chr11:398673 | A | ACCCCCGC others(807): Show |
1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1069-275_1069-274i others(816): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398673 | ||||||
| chr11:398689 | G | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0209 others(8): Show |
11 | HG00621.hp2 HG01175.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1069-303G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398689 | |||||||
| chr11:398689 | G | GCGTCACC others(486): Show |
1 | a0001c0001t0001g0042 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1069-293_1069-292i others(495): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398689 | ||||||
| chr11:398689 | G | GCGTCACC others(424): Show |
1 | a0001c0001t0001g0018 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1069-285_1069-284i others(433): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398689 | ||||||
| chr11:398691 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0043 others(13): Show |
17 | HG01192.hp1 HG01258.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.1069-301G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398691 | |||||||
| chr11:398691 | G | GTCACCTC others(80): Show |
1 | a0001c0010t0001g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1069-293_1069-292i others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(602): Show |
1 | a0001c0001t0001g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1069-293_1069-292i others(611): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(397): Show |
1 | a0001c0011t0001g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1069-293_1069-292i others(406): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(486): Show |
1 | a0001c0001t0001g0036 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1069-293_1069-292i others(495): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(196): Show |
3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG01975.hp1 HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1069-293_1069-292i others(205): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(544): Show |
1 | a0001c0001t0001g0056 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1069-293_1069-292i others(553): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(544): Show |
1 | a0001c0005t0001g0040 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1069-293_1069-292i others(553): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(515): Show |
1 | a0001c0001t0001g0057 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1069-293_1069-292i others(524): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(544): Show |
16 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0028 others(13): Show |
18 | HG01884.hp2 HG02129.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1069-293_1069-292i others(553): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(602): Show |
1 | a0001c0001t0001g0017 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1069-293_1069-292i others(611): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(544): Show |
1 | a0001c0001t0001g0066 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1069-293_1069-292i others(553): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(254): Show |
1 | a0001c0001t0001g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1069-293_1069-292i others(263): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(631): Show |
1 | a0001c0006t0001g0068 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1069-293_1069-292i others(640): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(486): Show |
2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1069-293_1069-292i others(495): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(979): Show |
1 | a0001c0001t0001g0080 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1069-293_1069-292i others(988): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(950): Show |
1 | a0001c0001t0001g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1069-293_1069-292i others(959): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(1095): Show |
1 | a0001c0001t0001g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1069-293_1069-292i others(1104): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(1530): Show |
1 | a0001c0001t0001g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1069-293_1069-292i others(1539): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(457): Show |
2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | NA19007.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1069-293_1069-292i others(466): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398691 | G | GTCACCTC others(747): Show |
1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1069-235_1069-234i others(756): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398691 | ||||||
| chr11:398700 | G | A | 4 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0168 others(1): Show |
4 | HG03927.hp2 NA18945.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-292G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398700 | |||||||
| chr11:398700 | G | C | 25 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0177 others(22): Show |
25 | HG00673.hp2 HG01891.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.1069-292G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398700 | |||||||
| chr11:398700 | G | GTACCCCC others(109): Show |
11 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0131 others(8): Show |
11 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.1069-177_1069-176i others(118): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398700 | ||||||
| chr11:398718 | G | C | 18 | a0001c0001t0001g0186 a0001c0002t0001g0004 a0001c0002t0001g0100 others(15): Show |
19 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.1069-274G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398718 | |||||||
| chr11:398719 | C | CGTCACCT others(80): Show |
2 | a0001c0005t0001g0013 a0001c0005t0001g0014 |
2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1069-246_1069-245i others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398719 | ||||||
| chr11:398720 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0042 others(1): Show |
4 | HG01175.hp2 NA18943.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-272G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398720 | |||||||
| chr11:398729 | C | CTACCCCC others(51): Show |
14 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0126 others(11): Show |
14 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1069-205_1069-148d others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398729 | ||||||
| chr11:398729 | C | CTACCCCC others(225): Show |
1 | a0001c0002t0001g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1069-177_1069-176i others(234): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398729 | ||||||
| chr11:398729 | C | CTACCCCC others(486): Show |
1 | a0010c0017t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1069-217_1069-216i others(495): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398729 | ||||||
| chr11:398729 | C | CTACCCCC others(138): Show |
1 | a0001c0003t0001g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1069-217_1069-216i others(147): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398729 | ||||||
| chr11:398729 | C | G | 24 | a0001c0001t0001g0209 a0001c0002t0001g0004 a0001c0002t0001g0100 others(21): Show |
25 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.1069-263C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398729 | |||||||
| chr11:398731 | A | ACCCCCGC others(924): Show |
1 | a0001c0001t0001g0041 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1069-217_1069-216i others(933): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398731 | ||||||
| chr11:398734 | C | CCCGCACA others(312): Show |
1 | a0001c0001t0001g0054 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1069-235_1069-234i others(321): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398734 | ||||||
| chr11:398747 | G | C | 12 | a0001c0001t0001g0033 a0001c0001t0001g0183 a0001c0001t0001g0184 others(9): Show |
12 | HG01243.hp1 HG01981.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1069-245G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398747 | |||||||
| chr11:398747 | G | GCGTCACC others(138): Show |
1 | a0001c0004t0001g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1069-130_1069-129i others(147): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398747 | ||||||
| chr11:398749 | G | A | 2 | a0011c0024t0002g0026 a0018c0023t0002g0037 |
2 | HG02132.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1069-243G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398749 | |||||||
| chr11:398758 | G | C | 9 | a0001c0001t0001g0054 a0001c0001t0001g0209 a0001c0002t0001g0159 others(6): Show |
9 | HG01891.hp1 HG01943.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1069-234G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398758 | |||||||
| chr11:398758 | G | GTACCCCC others(515): Show |
1 | a0004c0015t0001g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1069-217_1069-216i others(524): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398758 | ||||||
| chr11:398758 | G | GTACCCCC others(51): Show |
1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1069-217_1069-216i others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398758 | ||||||
| chr11:398776 | C | G | 14 | a0001c0001t0001g0054 a0001c0001t0001g0183 a0001c0001t0001g0184 others(11): Show |
14 | HG01981.hp1 HG02109.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1069-216C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398776 | |||||||
| chr11:398777 | C | T | 4 | a0003c0014t0001g0182 a0003c0014t0001g0187 a0003c0019t0001g0181 others(1): Show |
4 | HG03471.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-215C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398777 | |||||||
| chr11:398778 | G | A | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-214G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398778 | |||||||
| chr11:398787 | G | A | 1 | a0001c0002t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1069-205G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398787 | |||||||
| chr11:398787 | G | C | 2 | a0011c0024t0002g0026 a0018c0023t0002g0037 |
2 | HG02132.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1069-205G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398787 | |||||||
| chr11:398787 | G | GTACCCCC others(51): Show |
1 | a0001c0001t0001g0033 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1069-186_1069-185i others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398787 | ||||||
| chr11:398787 | G | GTACCCCC others(51): Show |
2 | a0001c0010t0003g0021 a0001c0010t0003g0022 |
2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1069-177_1069-176i others(60): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398787 | ||||||
| chr11:398792 | C | CCCGCACA others(22): Show |
4 | a0001c0003t0001g0111 a0001c0003t0001g0112 a0001c0003t0001g0113 others(1): Show |
4 | HG01981.hp1 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-188_1069-187i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398792 | ||||||
| chr11:398804 | T | A | 1 | a0014c0034t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1069-188T>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398804 | |||||||
| chr11:398805 | G | C | 3 | a0001c0001t0001g0209 a0001c0004t0001g0190 a0001c0008t0001g0191 |
3 | HG02647.hp1 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1069-187G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398805 | |||||||
| chr11:398816 | G | C | 2 | a0001c0001t0001g0054 a0001c0008t0001g0093 |
2 | HG03209.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1069-176G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398816 | |||||||
| chr11:398816 | G | GTACCCCC others(22): Show |
1 | a0001c0003t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1069-159_1069-158i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398816 | ||||||
| chr11:398834 | C | CCGTCACC others(22): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1069-148_1069-147i others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 398834 | ||||||
| chr11:398834 | C | G | 4 | a0001c0001t0001g0209 a0001c0003t0001g0098 a0001c0004t0001g0190 others(1): Show |
4 | HG01975.hp2 HG02647.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-158C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398834 | |||||||
| chr11:398845 | C | G | 2 | a0001c0001t0001g0209 a0001c0002t0001g0136 |
2 | HG02647.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1069-147C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398845 | |||||||
| chr11:398850 | G | C | 2 | a0001c0001t0001g0209 a0001c0002t0001g0136 |
2 | HG02647.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1069-142G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398850 | |||||||
| chr11:398853 | G | A | 1 | a0001c0021t0001g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1069-139G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398853 | |||||||
| chr11:398865 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1069-127G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398865 | |||||||
| chr11:398889 | C | T | 3 | a0001c0003t0001g0111 a0001c0003t0001g0113 a0001c0003t0001g0116 |
3 | HG01981.hp1 HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1069-103C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398889 | |||||||
| chr11:398957 | T | C | 7 | a0001c0004t0001g0193 a0001c0005t0001g0090 a0001c0005t0001g0091 others(4): Show |
7 | HG01884.hp1 HG02717.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-35T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 4/12 | chr11 | 398957 | |||||||
| chr11:399267 | T | TCCCCACC others(236): Show |
1 | a0001c0002t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1273+311_1273+312i others(245): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 399267 | ||||||
| chr11:399277 | C | CCCCCCTC others(83): Show |
1 | a0001c0001t0001g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1273+161_1273+162i others(92): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 399277 | ||||||
| chr11:399283 | TCCACCTG others(81): Show |
T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0057 |
2 | NA18980.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1273+98_1273+185de others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 399283 | ||||||
| chr11:399341 | T | C | 2 | a0001c0001t0001g0195 a0001c0036t0001g0165 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1273+145T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399341 | |||||||
| chr11:399348 | C | T | 1 | a0001c0007t0001g0208 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1273+152C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399348 | |||||||
| chr11:399366 | A | ACCCCCTC others(172): Show |
1 | a0001c0001t0001g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1273+175_1273+176i others(181): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 399366 | ||||||
| chr11:399366 | ACCCCCCC others(17): Show |
A | 1 | a0001c0002t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1273+174_1273+197d others(26): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 399366 | ||||||
| chr11:399371 | C | CCCACCTG others(82): Show |
2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1273+217_1273+218i others(91): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 399371 | ||||||
| chr11:399371 | C | CT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(63): Show |
67 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1273+175_1273+176i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399371 | |||||||
| chr11:399371 | C | CTCCACCT others(83): Show |
1 | a0001c0001t0001g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1273+175_1273+176i others(92): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399371 | |||||||
| chr11:399371 | C | CTCCACCT others(479): Show |
1 | a0001c0001t0001g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1273+175_1273+176i others(488): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399371 | |||||||
| chr11:399371 | C | T | 7 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
7 | NA18966.hp1 NA18966.hp2 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.1273+175C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399371 | |||||||
| chr11:399372 | C | A | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1273+176C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399372 | |||||||
| chr11:399381 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1273+185C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399381 | |||||||
| chr11:399394 | A | C | 3 | a0001c0004t0001g0027 a0001c0004t0001g0197 a0015c0026t0004g0092 |
3 | HG00642.hp1 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1273+198A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399394 | |||||||
| chr11:399396 | T | C | 3 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0001c0021t0001g0086 |
3 | HG01884.hp1 HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1273+200T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399396 | |||||||
| chr11:399406 | G | GCCCCCTC others(66): Show |
1 | a0001c0008t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1273+239_1273+311d others(75): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 399406 | ||||||
| chr11:399441 | T | C | 1 | a0001c0003t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1273+245T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399441 | |||||||
| chr11:399442 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+246A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399442 | |||||||
| chr11:399465 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+269T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399465 | |||||||
| chr11:399467 | C | T | 16 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0001c0002t0001g0103 others(13): Show |
16 | HG01192.hp1 HG01891.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1273+271C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399467 | |||||||
| chr11:399471 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+275C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399471 | |||||||
| chr11:399476 | T | A | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+280T>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399476 | |||||||
| chr11:399482 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+286C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399482 | |||||||
| chr11:399487 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+291C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399487 | |||||||
| chr11:399488 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+292T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399488 | |||||||
| chr11:399489 | C | G | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+293C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399489 | |||||||
| chr11:399504 | GCCTATCC others(9): Show |
G | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+311_1273+326d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 399504 | ||||||
| chr11:399508 | A | G | 4 | a0001c0004t0001g0176 a0001c0004t0001g0196 a0001c0004t0001g0197 others(1): Show |
4 | HG02717.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+312A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399508 | |||||||
| chr11:399520 | T | TC | 9 | a0001c0001t0001g0019 a0001c0001t0001g0078 a0001c0001t0001g0082 others(6): Show |
9 | HG01192.hp2 HG01261.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1273+331dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 399520 | ||||||
| chr11:399521 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+325C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399521 | |||||||
| chr11:399525 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+329C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399525 | |||||||
| chr11:399547 | T | A | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1273+351T>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399547 | |||||||
| chr11:399643 | TTTGCCGG others(9): Show |
T | 1 | a0001c0002t0001g0110 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1274-322_1274-307d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 399643 | ||||||
| chr11:399765 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1274-202A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399765 | |||||||
| chr11:399851 | G | A | 2 | a0001c0007t0001g0008 a0001c0007t0001g0009 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1274-116G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 5/12 | chr11 | 399851 | |||||||
| chr11:400165 | G | T | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1448+24G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 6/12 | chr11 | 400165 | |||||||
| chr11:400220 | G | C | 1 | a0001c0008t0001g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1448+79G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 6/12 | chr11 | 400220 | |||||||
| chr11:400521 | G | GC | 9 | a0001c0001t0001g0078 a0001c0001t0001g0178 a0001c0002t0001g0103 others(6): Show |
9 | HG00642.hp1 HG01261.hp1 HG01261.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1567-9dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 400521 | ||||||
| chr11:400719 | T | G | 1 | a0001c0002t0001g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1737+14T>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400719 | |||||||
| chr11:400746 | A | AC | 5 | a0001c0001t0001g0051 a0001c0002t0001g0124 a0001c0003t0001g0140 others(2): Show |
5 | HG01175.hp2 HG01952.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+45dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400746 | ||||||
| chr11:400754 | C | G | 1 | a0001c0003t0001g0154 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1737+49C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400754 | |||||||
| chr11:400760 | G | C | 5 | a0001c0002t0001g0004 a0001c0002t0001g0124 a0001c0002t0001g0125 others(2): Show |
6 | HG00642.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+55G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400760 | |||||||
| chr11:400766 | GGCCCCGC others(8): Show |
G | 1 | a0001c0006t0001g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1737+91_1737+105de others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400766 | ||||||
| chr11:400776 | A | AC | 21 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0059 others(18): Show |
21 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1737+76dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400776 | ||||||
| chr11:400776 | A | ACCCCCGC others(9): Show |
1 | a0001c0003t0001g0141 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1737+76_1737+91dup others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400776 | ||||||
| chr11:400777 | CCCCCGCC others(144): Show |
C | 1 | a0001c0001t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1737+77_1737+227de others(1): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400777 | ||||||
| chr11:400783 | C | G | 4 | a0001c0008t0001g0093 a0001c0008t0001g0188 a0001c0008t0001g0189 others(1): Show |
4 | HG02622.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+78C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400783 | |||||||
| chr11:400790 | CA | C | 2 | a0001c0001t0001g0046 a0001c0005t0001g0040 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1737+86delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400790 | |||||||
| chr11:400791 | A | AC | 37 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0053 others(34): Show |
38 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1737+91dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400791 | ||||||
| chr11:400792 | C | CCCCCGCC others(7): Show |
2 | a0001c0003t0001g0142 a0001c0003t0001g0143 |
2 | HG00673.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1737+107_1737+120d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400792 | ||||||
| chr11:400792 | C | G | 2 | a0001c0001t0001g0046 a0001c0005t0001g0040 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1737+87C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400792 | |||||||
| chr11:400804 | T | TCA | 2 | a0001c0001t0001g0046 a0001c0001t0001g0082 |
2 | HG02976.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1737+101_1737+102d others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400804 | ||||||
| chr11:400806 | A | AC | 11 | a0001c0001t0001g0078 a0001c0002t0001g0125 a0001c0003t0001g0115 others(8): Show |
11 | HG00642.hp1 HG01261.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.1737+105dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400806 | ||||||
| chr11:400806 | A | ACCCCGCC others(132): Show |
1 | a0001c0003t0001g0141 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1737+120_1737+121i others(141): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400806 | ||||||
| chr11:400807 | CCCCGCCC others(209): Show |
C | 1 | a0001c0001t0001g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1737+117_1737+332d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400807 | ||||||
| chr11:400807 | CCCCGCCC others(656): Show |
C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0083 |
2 | HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1737+120_1737+782d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400807 | ||||||
| chr11:400808 | CCCGCCCC others(208): Show |
C | 2 | a0001c0005t0001g0091 a0001c0006t0001g0049 |
2 | HG01175.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1737+106_1737+320d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400808 | ||||||
| chr11:400810 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0082 |
2 | HG02976.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1737+105C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400810 | |||||||
| chr11:400810 | CGCCCCGC others(271): Show |
C | 4 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0009t0001g0102 others(1): Show |
4 | NA18612.hp2 NA18947.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+117_1737+394d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400810 | ||||||
| chr11:400810 | CGCCCCGC others(333): Show |
C | 1 | a0001c0001t0001g0066 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1737+117_1737+456d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400810 | ||||||
| chr11:400811 | G | C | 1 | a0001c0003t0001g0155 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1737+106G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400811 | |||||||
| chr11:400811 | G | GC | 4 | a0001c0001t0001g0039 a0001c0001t0001g0059 a0001c0002t0001g0124 others(1): Show |
4 | HG00621.hp1 HG01261.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+110dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400811 | ||||||
| chr11:400816 | G | A | 6 | a0001c0004t0001g0094 a0001c0007t0001g0025 a0001c0007t0001g0208 others(3): Show |
6 | HG00733.hp2 HG02027.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+111G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400816 | |||||||
| chr11:400821 | C | CA | 3 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0009t0001g0122 |
3 | HG00621.hp1 NA19004.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1737+116_1737+117i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400821 | |||||||
| chr11:400822 | C | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(67): Show |
73 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1737+117C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400822 | |||||||
| chr11:400825 | G | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(69): Show |
75 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1737+120G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400825 | |||||||
| chr11:400826 | GACCCCGC others(163): Show |
G | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1737+122_1737+291d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400826 | |||||||
| chr11:400827 | A | C | 2 | a0001c0001t0001g0039 a0001c0009t0001g0122 |
2 | HG00621.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1737+122A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400827 | |||||||
| chr11:400827 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(69): Show |
75 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1737+122A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400827 | |||||||
| chr11:400832 | G | C | 1 | a0001c0002t0001g0148 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1737+127G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400832 | |||||||
| chr11:400836 | A | AC | 23 | a0001c0001t0001g0202 a0001c0001t0001g0205 a0001c0001t0001g0209 others(20): Show |
23 | HG00673.hp1 HG00733.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1737+136dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400836 | ||||||
| chr11:400841 | C | CCG | 9 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp2 HG01261.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+136_1737+137i others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400841 | |||||||
| chr11:400841 | C | CG | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(60): Show |
66 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737+137dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400841 | ||||||
| chr11:400841 | C | CGCCCCCC others(124): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1737+141_1737+142i others(133): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400841 | ||||||
| chr11:400842 | G | C | 1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1737+137G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400842 | |||||||
| chr11:400842 | GCCCCGCT others(301): Show |
G | 1 | a0001c0003t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1737+138_1737+445d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400842 | |||||||
| chr11:400843 | C | G | 1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1737+138C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400843 | |||||||
| chr11:400845 | C | G | 1 | a0001c0036t0001g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1737+140C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400845 | |||||||
| chr11:400850 | C | G | 2 | a0001c0005t0001g0013 a0001c0005t0001g0014 |
2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1737+145C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400850 | |||||||
| chr11:400851 | AC | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(69): Show |
75 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1737+151delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400851 | ||||||
| chr11:400853 | C | A | 82 | a0001c0001t0001g0046 a0001c0002t0001g0004 a0001c0002t0001g0100 others(79): Show |
84 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1737+148C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400853 | |||||||
| chr11:400857 | GACCCCGC others(69): Show |
G | 1 | a0001c0005t0001g0040 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1737+153_1737+228d others(78): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400857 | |||||||
| chr11:400858 | A | ACCCCGCT others(9): Show |
1 | a0001c0002t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1737+163_1737+164i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400858 | ||||||
| chr11:400858 | A | ACCCCGCT others(8): Show |
4 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0130 others(1): Show |
4 | HG00099.hp2 HG00733.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+163_1737+164i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400858 | ||||||
| chr11:400858 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(73): Show |
79 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1737+153A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400858 | |||||||
| chr11:400869 | A | AC | 3 | a0001c0002t0001g0125 a0001c0003t0001g0166 a0001c0004t0001g0027 |
3 | HG00642.hp1 HG02135.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1737+167dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400869 | ||||||
| chr11:400869 | A | C | 20 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0126 others(17): Show |
20 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1737+164A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400869 | |||||||
| chr11:400882 | A | AC | 12 | a0001c0002t0001g0125 a0001c0002t0001g0170 a0001c0002t0001g0172 others(9): Show |
12 | HG01256.hp1 HG01934.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+182dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400882 | ||||||
| chr11:400887 | C | CCG | 10 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0041 others(7): Show |
10 | HG00621.hp1 HG00621.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1737+182_1737+183i others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400887 | |||||||
| chr11:400887 | C | CG | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(53): Show |
59 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1737+183dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400887 | ||||||
| chr11:400887 | C | CGCCCCGC others(26): Show |
1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1737+193_1737+194i others(35): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400887 | ||||||
| chr11:400887 | C | CGCCCCGC others(25): Show |
1 | a0001c0003t0001g0142 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1737+193_1737+194i others(34): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400887 | ||||||
| chr11:400888 | GCCCCGCT others(38): Show |
G | 1 | a0001c0001t0001g0016 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1737+184_1737+228d others(47): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400888 | |||||||
| chr11:400888 | GCCCCGCT others(162): Show |
G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0070 others(2): Show |
5 | HG01243.hp1 HG02135.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+184_1737+352d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400888 | |||||||
| chr11:400893 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1737+188G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400893 | |||||||
| chr11:400897 | A | AC | 6 | a0001c0001t0001g0202 a0001c0002t0001g0125 a0001c0002t0001g0170 others(3): Show |
6 | HG01496.hp2 HG02809.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+197dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400897 | ||||||
| chr11:400897 | AC | A | 13 | a0001c0001t0001g0195 a0001c0001t0001g0209 a0001c0004t0001g0094 others(10): Show |
13 | HG00733.hp2 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1737+197delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400897 | ||||||
| chr11:400898 | C | CCCCGCCC others(67): Show |
1 | a0001c0008t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1737+196_1737+197i others(76): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400898 | ||||||
| chr11:400902 | C | CG | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(61): Show |
67 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1737+198dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400902 | ||||||
| chr11:400902 | C | G | 3 | a0001c0001t0001g0072 a0001c0012t0001g0119 a0001c0012t0001g0120 |
3 | HG02027.hp1 HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1737+197C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400902 | |||||||
| chr11:400903 | G | C | 2 | a0001c0004t0001g0027 a0001c0012t0001g0120 |
2 | HG00642.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1737+198G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400903 | |||||||
| chr11:400912 | A | ACCCCGCC others(8): Show |
1 | a0001c0028t0001g0128 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1737+212_1737+213i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400912 | ||||||
| chr11:400914 | C | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(61): Show |
67 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1737+209C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400914 | |||||||
| chr11:400915 | C | A | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1737+210C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400915 | |||||||
| chr11:400917 | G | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(66): Show |
72 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1737+212G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400917 | |||||||
| chr11:400918 | GA | G | 2 | a0001c0008t0001g0188 a0001c0030t0001g0174 |
2 | HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1737+214delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400918 | |||||||
| chr11:400919 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(63): Show |
69 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1737+214A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400919 | |||||||
| chr11:400919 | ACCCCGCT others(427): Show |
A | 1 | a0001c0001t0001g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1737+218_1737+651d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400919 | ||||||
| chr11:400929 | C | CACCCCGC others(41): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1737+224_1737+225i others(50): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400929 | |||||||
| chr11:400930 | C | A | 5 | a0001c0003t0001g0095 a0001c0003t0001g0096 a0001c0003t0001g0098 others(2): Show |
5 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+225C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400930 | |||||||
| chr11:400933 | C | CGCCCCGC others(9): Show |
1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1737+240_1737+255d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400933 | ||||||
| chr11:400934 | G | GA | 9 | a0001c0001t0001g0046 a0001c0003t0001g0095 a0001c0003t0001g0096 others(6): Show |
9 | HG00642.hp1 HG01934.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+229_1737+230i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400934 | |||||||
| chr11:400934 | G | GCCCCGCT others(9): Show |
1 | a0001c0008t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1737+242_1737+243i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400934 | ||||||
| chr11:400935 | C | G | 1 | a0001c0003t0001g0141 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1737+230C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400935 | |||||||
| chr11:400937 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0209 |
2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1737+232C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400937 | |||||||
| chr11:400944 | C | CA | 2 | a0001c0003t0001g0116 a0001c0003t0001g0166 |
2 | HG02135.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1737+239_1737+240i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400944 | |||||||
| chr11:400945 | C | A | 79 | a0001c0001t0001g0046 a0001c0002t0001g0004 a0001c0002t0001g0100 others(76): Show |
81 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1737+240C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400945 | |||||||
| chr11:400947 | CCGGCCCC others(7): Show |
C | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1737+244_1737+257d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400947 | ||||||
| chr11:400947 | CCGGCCCC others(162): Show |
C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0183 |
2 | HG02145.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1737+244_1737+412d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400947 | ||||||
| chr11:400948 | CG | C | 10 | a0001c0001t0001g0046 a0001c0003t0001g0095 a0001c0003t0001g0096 others(7): Show |
10 | HG00642.hp1 HG01515.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.1737+245delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400948 | ||||||
| chr11:400949 | G | C | 1 | a0001c0001t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1737+244G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400949 | |||||||
| chr11:400949 | G | GA | 3 | a0001c0002t0001g0103 a0001c0002t0001g0168 a0001c0003t0001g0114 |
3 | HG03453.hp1 HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1737+244_1737+245i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400949 | |||||||
| chr11:400949 | GGCCCCGC others(163): Show |
G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(51): Show |
57 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1737+256_1737+425d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400949 | ||||||
| chr11:400950 | G | A | 69 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0101 others(66): Show |
71 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1737+245G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400950 | |||||||
| chr11:400950 | G | C | 6 | a0001c0001t0001g0071 a0001c0002t0001g0103 a0001c0002t0001g0133 others(3): Show |
6 | HG02135.hp2 HG03017.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+245G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400950 | |||||||
| chr11:400959 | A | AC | 4 | a0001c0004t0001g0012 a0001c0007t0001g0010 a0001c0030t0001g0174 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+255dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400959 | ||||||
| chr11:400960 | CACCCGCC others(162): Show |
C | 1 | a0001c0001t0001g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1737+256_1737+424d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400960 | |||||||
| chr11:400961 | A | C | 46 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(43): Show |
46 | HG00609.hp1 HG00642.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1737+256A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400961 | |||||||
| chr11:400961 | ACCCGCCC others(163): Show |
A | 2 | a0001c0006t0001g0035 a0001c0006t0001g0204 |
2 | HG02004.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1737+261_1737+430d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400961 | ||||||
| chr11:400964 | C | CG | 7 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0006t0001g0038 others(4): Show |
7 | HG00099.hp1 HG01175.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+260dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400964 | ||||||
| chr11:400964 | C | G | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1737+259C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400964 | |||||||
| chr11:400966 | C | A | 2 | a0001c0001t0001g0089 a0001c0005t0001g0040 |
2 | HG02258.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1737+261C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400966 | |||||||
| chr11:400974 | A | AC | 5 | a0001c0001t0001g0209 a0001c0002t0001g0168 a0001c0003t0001g0155 others(2): Show |
5 | HG01261.hp1 HG02647.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+274dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400974 | ||||||
| chr11:400976 | C | A | 6 | a0001c0001t0001g0034 a0001c0006t0001g0038 a0001c0006t0001g0068 others(3): Show |
6 | HG00099.hp1 HG01175.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+271C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400976 | |||||||
| chr11:400976 | C | CCCCGCCC others(518): Show |
1 | a0001c0003t0001g0141 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1737+288_1737+289i others(527): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400976 | ||||||
| chr11:400979 | C | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0089 a0001c0005t0001g0040 others(1): Show |
4 | HG01515.hp1 HG02258.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+274C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400979 | |||||||
| chr11:400980 | GCCCCGCT others(9): Show |
G | 6 | a0001c0004t0001g0197 a0001c0007t0001g0008 a0001c0007t0001g0009 others(3): Show |
6 | HG02717.hp1 HG02717.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+302_1737+317d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400980 | ||||||
| chr11:400981 | C | A | 5 | a0001c0001t0001g0034 a0001c0006t0001g0038 a0001c0006t0001g0068 others(2): Show |
5 | HG00099.hp1 HG01175.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+276C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400981 | |||||||
| chr11:400991 | C | A | 2 | a0001c0002t0001g0104 a0001c0003t0001g0166 |
2 | HG02135.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1737+286C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400991 | |||||||
| chr11:400994 | G | C | 82 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0064 others(79): Show |
84 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1737+289G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400994 | |||||||
| chr11:400994 | GGACCCCG others(149): Show |
G | 3 | a0001c0006t0001g0038 a0001c0006t0001g0068 a0001c0021t0001g0086 |
3 | HG00099.hp1 HG01258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1737+291_1737+446d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400994 | ||||||
| chr11:400995 | G | C | 5 | a0001c0002t0001g0134 a0001c0003t0001g0155 a0001c0008t0001g0093 others(2): Show |
5 | HG01515.hp1 HG02074.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+290G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400995 | |||||||
| chr11:400995 | G | GCCCCGCT others(176): Show |
1 | a0014c0034t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1737+290_1737+291i others(185): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400995 | |||||||
| chr11:400995 | GA | G | 70 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0002t0001g0004 others(67): Show |
72 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1737+291delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400995 | |||||||
| chr11:400996 | A | C | 1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+291A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400996 | |||||||
| chr11:400996 | A | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0001g0089 others(10): Show |
13 | HG00609.hp1 HG01515.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1737+291A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 400996 | |||||||
| chr11:400996 | ACCCCGCT others(411): Show |
A | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1737+302_1737+719d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 400996 | ||||||
| chr11:401005 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1737+300A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401005 | |||||||
| chr11:401006 | C | CA | 3 | a0001c0004t0001g0027 a0001c0004t0001g0073 a0001c0004t0001g0074 |
3 | HG00642.hp1 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1737+301_1737+302i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401006 | |||||||
| chr11:401006 | C | CACCCGG | 3 | a0001c0003t0001g0095 a0001c0003t0001g0096 a0001c0003t0001g0098 |
3 | HG01934.hp2 HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1737+301_1737+302i others(8): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401006 | |||||||
| chr11:401007 | C | A | 24 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0081 others(21): Show |
24 | HG00733.hp2 HG01243.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1737+302C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401007 | |||||||
| chr11:401008 | CCGGACCC others(69): Show |
C | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1737+305_1737+380d others(78): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401008 | ||||||
| chr11:401008 | CCGGACCC others(147): Show |
C | 1 | a0004c0015t0001g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1737+305_1737+458d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401008 | ||||||
| chr11:401010 | G | C | 33 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(30): Show |
33 | HG00733.hp2 HG01243.hp2 HG01515.hp1 others(30): Show |
intron_variant | MODIFIER | c.1737+305G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401010 | |||||||
| chr11:401010 | G | GCTCACAC others(2): Show |
3 | a0001c0003t0001g0095 a0001c0003t0001g0096 a0001c0003t0001g0098 |
3 | HG01934.hp2 HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1737+305_1737+306i others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401010 | |||||||
| chr11:401011 | G | C | 1 | a0001c0012t0001g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1737+306G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401011 | |||||||
| chr11:401011 | GA | G | 22 | a0001c0001t0001g0064 a0001c0001t0001g0177 a0001c0001t0001g0178 others(19): Show |
22 | HG00733.hp2 HG01243.hp2 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.1737+307delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401011 | |||||||
| chr11:401011 | GAC | G | 3 | a0001c0004t0001g0027 a0001c0004t0001g0073 a0001c0004t0001g0074 |
3 | HG00642.hp1 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1737+307_1737+308d others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401011 | |||||||
| chr11:401012 | A | G | 12 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(9): Show |
12 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.1737+307A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401012 | |||||||
| chr11:401013 | C | G | 1 | a0001c0003t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1737+308C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401013 | |||||||
| chr11:401017 | G | C | 1 | a0001c0003t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1737+312G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401017 | |||||||
| chr11:401023 | A | C | 5 | a0001c0001t0001g0048 a0001c0003t0001g0166 a0001c0008t0001g0093 others(2): Show |
5 | HG02135.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+318A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401023 | |||||||
| chr11:401026 | C | CG | 27 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(24): Show |
27 | HG00733.hp2 HG01243.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.1737+322dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401026 | ||||||
| chr11:401026 | C | G | 3 | a0001c0001t0001g0048 a0001c0008t0001g0188 a0001c0030t0001g0174 |
3 | HG02622.hp1 HG03579.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1737+321C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401026 | |||||||
| chr11:401027 | G | C | 1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1737+322G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401027 | |||||||
| chr11:401028 | C | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0005t0001g0040 |
3 | HG02129.hp1 HG02258.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1737+323C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401028 | |||||||
| chr11:401028 | C | G | 60 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0101 others(57): Show |
62 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1737+323C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401028 | |||||||
| chr11:401037 | CA | C | 5 | a0001c0001t0001g0016 a0001c0003t0001g0095 a0001c0003t0001g0096 others(2): Show |
5 | HG01515.hp1 HG01934.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+333delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401037 | |||||||
| chr11:401038 | A | C | 8 | a0001c0001t0001g0046 a0001c0001t0001g0064 a0001c0001t0001g0089 others(5): Show |
8 | HG02258.hp2 HG02622.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1737+333A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401038 | |||||||
| chr11:401041 | CG | C | 27 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0081 others(24): Show |
27 | HG00642.hp1 HG00733.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1737+338delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401041 | ||||||
| chr11:401042 | G | C | 5 | a0001c0001t0001g0048 a0001c0003t0001g0095 a0001c0003t0001g0096 others(2): Show |
5 | HG01515.hp1 HG01934.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+337G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401042 | |||||||
| chr11:401042 | G | GCCCCGCT others(115): Show |
1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1737+337_1737+338i others(124): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401042 | |||||||
| chr11:401042 | G | GGCCCCGC others(8): Show |
54 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0101 others(51): Show |
56 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1737+348_1737+349i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401042 | ||||||
| chr11:401042 | G | GGCCCCGC others(9): Show |
1 | a0001c0003t0001g0116 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1737+349_1737+350i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401042 | ||||||
| chr11:401042 | G | GGCCCCGC others(9): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+352_1737+353i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401042 | ||||||
| chr11:401052 | A | ACACCCGC others(9): Show |
3 | a0001c0002t0001g0125 a0001c0002t0001g0172 a0001c0016t0001g0200 |
3 | HG01261.hp1 HG02897.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1737+348_1737+349i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401052 | ||||||
| chr11:401054 | C | A | 22 | a0001c0002t0001g0104 a0001c0002t0001g0110 a0001c0002t0001g0126 others(19): Show |
22 | HG00609.hp1 HG00642.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.1737+349C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401054 | |||||||
| chr11:401057 | C | CG | 7 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0048 others(4): Show |
7 | HG01175.hp2 HG01884.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+353dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401057 | ||||||
| chr11:401057 | C | G | 2 | a0001c0001t0001g0046 a0001c0003t0001g0141 |
2 | HG02129.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1737+352C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401057 | |||||||
| chr11:401058 | GCCCCGCT others(7): Show |
G | 1 | a0001c0001t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1737+354_1737+367d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401058 | |||||||
| chr11:401058 | GCCCCGCT others(209): Show |
G | 1 | a0001c0005t0001g0040 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1737+354_1737+569d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401058 | |||||||
| chr11:401059 | C | G | 2 | a0001c0006t0001g0005 a0001c0006t0001g0207 |
2 | HG02273.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1737+354C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401059 | |||||||
| chr11:401060 | CCCGCTCA others(132): Show |
C | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1737+358_1737+496d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401060 | ||||||
| chr11:401063 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1737+358G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401063 | |||||||
| chr11:401067 | A | ACCCCCGC others(9): Show |
4 | a0001c0003t0001g0155 a0001c0003t0001g0161 a0006c0031t0001g0163 others(1): Show |
4 | HG01496.hp1 HG02559.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+368_1737+369i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401067 | ||||||
| chr11:401069 | C | A | 3 | a0001c0001t0001g0046 a0001c0003t0001g0141 a0001c0003t0001g0150 |
3 | HG02129.hp2 HG02165.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1737+364C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401069 | |||||||
| chr11:401069 | CCCCGGCC others(225): Show |
C | 1 | a0001c0004t0001g0197 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1737+369_1737+600d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401069 | ||||||
| chr11:401070 | CCCGGCCC others(224): Show |
C | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1737+368_1737+598d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401070 | ||||||
| chr11:401072 | C | G | 4 | a0001c0001t0001g0019 a0001c0005t0001g0091 a0001c0006t0001g0049 others(1): Show |
4 | HG01175.hp2 HG01515.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+367C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401072 | |||||||
| chr11:401073 | G | GA | 2 | a0001c0001t0001g0016 a0007c0029t0001g0117 |
2 | HG01515.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1737+368_1737+369i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401073 | |||||||
| chr11:401073 | G | GCCCCGCT others(9): Show |
3 | a0001c0002t0001g0145 a0001c0002t0001g0168 a0019c0032t0001g0144 |
3 | HG00609.hp1 HG03927.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1737+368_1737+369i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401073 | |||||||
| chr11:401074 | G | C | 90 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(87): Show |
92 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1737+369G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401074 | |||||||
| chr11:401074 | G | GC | 11 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0070 others(8): Show |
11 | HG01243.hp1 HG01934.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.1737+372dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401074 | ||||||
| chr11:401074 | G | GCCCCGCT others(8): Show |
1 | a0001c0001t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1737+372_1737+373i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401074 | ||||||
| chr11:401077 | CG | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0081 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1737+373delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401077 | |||||||
| chr11:401080 | T | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0081 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1737+375T>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401080 | |||||||
| chr11:401082 | A | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0081 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1737+377A>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401082 | |||||||
| chr11:401083 | CA | C | 4 | a0001c0001t0001g0089 a0001c0002t0001g0110 a0001c0008t0001g0188 others(1): Show |
4 | HG02622.hp1 HG02735.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+379delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401083 | |||||||
| chr11:401084 | A | C | 29 | a0001c0001t0001g0046 a0001c0001t0001g0177 a0001c0001t0001g0178 others(26): Show |
29 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1737+379A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401084 | |||||||
| chr11:401087 | CG | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0003t0001g0166 others(3): Show |
6 | HG01175.hp2 HG01884.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+384delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401087 | ||||||
| chr11:401088 | G | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0001t0001g0089 others(5): Show |
8 | HG02622.hp1 HG02723.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1737+383G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401088 | |||||||
| chr11:401088 | G | GCCCCGCT others(288): Show |
1 | a0001c0002t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1737+383_1737+384i others(297): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401088 | |||||||
| chr11:401088 | G | GCCCCGCT others(285): Show |
1 | a0001c0002t0001g0126 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1737+383_1737+384i others(294): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401088 | |||||||
| chr11:401089 | GC | G | 4 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0008t0001g0191 others(1): Show |
4 | HG01515.hp1 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+388delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401089 | ||||||
| chr11:401090 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1737+385C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401090 | |||||||
| chr11:401099 | C | A | 1 | a0001c0003t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1737+394C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401099 | |||||||
| chr11:401099 | CA | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0089 others(1): Show |
4 | HG03209.hp2 HG03688.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+395delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401099 | |||||||
| chr11:401100 | A | ACCCGGCC others(646): Show |
1 | a0001c0010t0001g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1737+415_1737+416i others(655): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401100 | ||||||
| chr11:401100 | A | C | 33 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(30): Show |
33 | HG00642.hp2 HG01175.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1737+395A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401100 | |||||||
| chr11:401102 | CCGGCCCC others(147): Show |
C | 1 | a0001c0007t0001g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1737+399_1737+552d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401102 | ||||||
| chr11:401103 | C | G | 1 | a0001c0030t0001g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1737+398C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401103 | |||||||
| chr11:401103 | CG | C | 4 | a0001c0002t0001g0104 a0001c0003t0001g0095 a0001c0003t0001g0096 others(1): Show |
4 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+400delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401103 | ||||||
| chr11:401104 | G | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0048 others(4): Show |
7 | HG02135.hp1 HG03209.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+399G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401104 | |||||||
| chr11:401104 | GGCCCCGC others(8): Show |
G | 1 | a0001c0008t0001g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1737+411_1737+425d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401104 | ||||||
| chr11:401104 | GGCCCCGC others(39): Show |
G | 2 | a0001c0007t0001g0008 a0001c0007t0001g0009 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1737+416_1737+461d others(48): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401104 | ||||||
| chr11:401105 | G | A | 2 | a0001c0001t0001g0034 a0001c0030t0001g0174 |
2 | HG02056.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1737+400G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401105 | |||||||
| chr11:401106 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1737+401C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401106 | |||||||
| chr11:401106 | C | CCCCGCTC others(458): Show |
1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1737+444_1737+445i others(467): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401106 | ||||||
| chr11:401110 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1737+405G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401110 | |||||||
| chr11:401116 | A | C | 21 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(18): Show |
21 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1737+411A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401116 | |||||||
| chr11:401119 | C | CG | 17 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(14): Show |
17 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1737+415dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401119 | ||||||
| chr11:401119 | C | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0082 a0001c0001t0001g0183 |
3 | HG02145.hp1 HG03453.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1737+414C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401119 | |||||||
| chr11:401120 | G | GCCCCGCT others(38): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1737+429_1737+430i others(47): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401120 | ||||||
| chr11:401120 | GCCCCGCT others(408): Show |
G | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1737+416_1737+830d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401120 | |||||||
| chr11:401121 | C | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0089 |
2 | HG02056.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1737+416C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401121 | |||||||
| chr11:401125 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1737+420G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401125 | |||||||
| chr11:401129 | AC | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0005t0001g0084 others(3): Show |
6 | HG02723.hp1 HG03579.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+429delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401129 | ||||||
| chr11:401131 | C | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0002t0001g0145 others(4): Show |
7 | HG00609.hp1 HG01175.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+426C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401131 | |||||||
| chr11:401131 | C | CCCCGGCC others(240): Show |
1 | a0001c0002t0001g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1737+444_1737+445i others(249): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401131 | ||||||
| chr11:401131 | CCCCGGCC others(209): Show |
C | 1 | a0003c0014t0001g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1737+445_1737+660d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401131 | ||||||
| chr11:401134 | C | G | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1737+429C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401134 | |||||||
| chr11:401136 | G | A | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1737+431G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401136 | |||||||
| chr11:401137 | CCCCGCTC others(408): Show |
C | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1737+442_1737+856d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401137 | ||||||
| chr11:401145 | A | AC | 6 | a0001c0001t0001g0028 a0001c0002t0001g0164 a0001c0003t0001g0166 others(3): Show |
6 | HG00642.hp2 HG02135.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+441dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401145 | ||||||
| chr11:401145 | A | ACCCCCGG others(170): Show |
1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1737+441_1737+442i others(179): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401145 | ||||||
| chr11:401146 | CACCTGCC others(54): Show |
C | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1737+442_1737+502d others(63): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401146 | |||||||
| chr11:401147 | A | ACCCGCCC others(276): Show |
1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1737+444_1737+445i others(285): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401147 | ||||||
| chr11:401147 | A | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0028 others(11): Show |
14 | HG00642.hp1 HG00642.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1737+442A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401147 | |||||||
| chr11:401150 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(170): Show |
178 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.1737+445T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401150 | |||||||
| chr11:401150 | T | G | 9 | a0001c0001t0001g0028 a0001c0002t0001g0126 a0001c0002t0001g0164 others(6): Show |
9 | HG00642.hp1 HG00642.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1737+445T>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401150 | |||||||
| chr11:401150 | T | TGCCCCGC others(9): Show |
1 | a0001c0006t0001g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1737+456_1737+457i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401150 | ||||||
| chr11:401152 | C | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(64): Show |
70 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1737+447C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401152 | |||||||
| chr11:401160 | A | AC | 3 | a0001c0001t0001g0028 a0001c0003t0001g0143 a0010c0017t0001g0106 |
3 | HG00673.hp1 HG02074.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1737+456dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401160 | ||||||
| chr11:401161 | CA | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(63): Show |
69 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1737+457delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401161 | |||||||
| chr11:401162 | A | C | 105 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0029 others(102): Show |
107 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1737+457A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401162 | |||||||
| chr11:401166 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1737+461G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401166 | |||||||
| chr11:401166 | GGCCCCGC others(424): Show |
G | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1737+498_1737+928d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401166 | ||||||
| chr11:401167 | G | A | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1737+462G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401167 | |||||||
| chr11:401167 | G | C | 1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1737+462G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401167 | |||||||
| chr11:401168 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1737+463C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401168 | |||||||
| chr11:401178 | A | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(164): Show |
172 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.1737+473A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401178 | |||||||
| chr11:401179 | C | CCCCGGCC others(9): Show |
1 | a0005c0022t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1737+476_1737+477i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401179 | ||||||
| chr11:401179 | C | CCGGCCCC others(7): Show |
1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1737+475_1737+476i others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401179 | ||||||
| chr11:401180 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1737+475C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401180 | |||||||
| chr11:401181 | CG | C | 12 | a0001c0001t0001g0016 a0001c0002t0001g0126 a0001c0002t0001g0164 others(9): Show |
12 | HG00642.hp1 HG00642.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+478delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401181 | ||||||
| chr11:401182 | G | C | 3 | a0001c0002t0001g0118 a0001c0002t0001g0168 a0005c0022t0001g0203 |
3 | HG00733.hp1 HG01192.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1737+477G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401182 | |||||||
| chr11:401182 | G | GCCCCGCT others(258): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+477_1737+478i others(267): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401182 | |||||||
| chr11:401182 | G | GGCCCCGC others(8): Show |
2 | a0001c0006t0001g0005 a0017c0027t0001g0107 |
2 | HG02273.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1737+479_1737+493d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401182 | ||||||
| chr11:401182 | G | T | 1 | a0001c0008t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1737+477G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401182 | |||||||
| chr11:401182 | GGCCCCGC others(23): Show |
G | 3 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0003c0014t0001g0187 |
3 | HG03471.hp1 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1737+489_1737+518d others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401182 | ||||||
| chr11:401182 | GGCCCCGC others(284): Show |
G | 3 | a0001c0004t0001g0196 a0003c0019t0001g0181 a0016c0035t0001g0180 |
3 | HG03471.hp2 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1737+489_1737+779d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401182 | ||||||
| chr11:401183 | G | A | 5 | a0001c0006t0001g0038 a0001c0006t0001g0068 a0001c0008t0001g0093 others(2): Show |
5 | HG00099.hp1 HG01175.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+478G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401183 | |||||||
| chr11:401183 | G | C | 1 | a0001c0010t0001g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1737+478G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401183 | |||||||
| chr11:401184 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0089 |
2 | HG02129.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1737+479C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401184 | |||||||
| chr11:401184 | CCCCGCTC others(361): Show |
C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0004t0001g0176 others(1): Show |
4 | HG03209.hp1 HG03486.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+489_1737+856d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401184 | ||||||
| chr11:401194 | A | ACCCACCC others(23): Show |
1 | a0001c0002t0001g0110 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1737+492_1737+493i others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401194 | ||||||
| chr11:401194 | A | ACCCGCCC others(23): Show |
34 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0124 others(31): Show |
36 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1737+493_1737+494i others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401194 | ||||||
| chr11:401194 | A | ACCCGCCC others(24): Show |
1 | a0001c0028t0001g0128 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1737+493_1737+494i others(33): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401194 | ||||||
| chr11:401194 | A | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(77): Show |
83 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1737+489A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401194 | |||||||
| chr11:401197 | C | CGCCCCGC others(427): Show |
1 | a0001c0002t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1737+493_1737+494i others(436): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401197 | ||||||
| chr11:401197 | C | CGCCCCGC others(535): Show |
1 | a0001c0003t0001g0142 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1737+493_1737+494i others(544): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401197 | ||||||
| chr11:401197 | C | CGCCCCGC others(537): Show |
1 | a0001c0003t0001g0155 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1737+493_1737+494i others(546): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401197 | ||||||
| chr11:401197 | C | CGCCCCGC others(534): Show |
1 | a0001c0003t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1737+493_1737+494i others(543): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401197 | ||||||
| chr11:401197 | C | CGCCCCGC others(9): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1737+493_1737+494i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401197 | ||||||
| chr11:401197 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1737+492C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401197 | |||||||
| chr11:401197 | C | T | 2 | a0001c0007t0001g0008 a0001c0007t0001g0009 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1737+492C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401197 | |||||||
| chr11:401198 | G | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0056 |
3 | HG00621.hp2 NA18966.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1737+493G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401198 | |||||||
| chr11:401198 | G | GA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(59): Show |
65 | HG00544.hp2 HG00621.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.1737+493_1737+494i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401198 | |||||||
| chr11:401198 | GGCCCGCT others(7): Show |
G | 1 | a0001c0008t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1737+498_1737+511d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401198 | ||||||
| chr11:401199 | G | A | 7 | a0001c0001t0001g0019 a0001c0005t0001g0091 a0001c0006t0001g0038 others(4): Show |
7 | HG00099.hp1 HG01175.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+494G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401199 | |||||||
| chr11:401199 | G | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(103): Show |
110 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1737+494G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401199 | |||||||
| chr11:401199 | G | CCCCGCTC others(23): Show |
12 | a0001c0002t0001g0103 a0001c0002t0001g0132 a0001c0002t0001g0133 others(9): Show |
12 | HG00099.hp2 HG00673.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1737+493_1737+494i others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401199 | |||||||
| chr11:401199 | G | GAC | 3 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0056 |
3 | HG00621.hp2 NA18966.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1737+494_1737+495i others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401199 | |||||||
| chr11:401199 | G | GC | 17 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0001t0001g0089 others(14): Show |
17 | HG00642.hp2 HG01952.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1737+497dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401199 | ||||||
| chr11:401199 | G | GCCCGCTC others(256): Show |
1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1737+503_1737+504i others(265): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401199 | ||||||
| chr11:401208 | C | CCCCGCCC others(132): Show |
1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1737+503_1737+504i others(141): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401208 | |||||||
| chr11:401209 | A | C | 19 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0028 others(16): Show |
19 | HG00099.hp1 HG01175.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1737+504A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401209 | |||||||
| chr11:401212 | C | CG | 7 | a0001c0001t0001g0028 a0001c0006t0001g0038 a0001c0006t0001g0049 others(4): Show |
7 | HG00099.hp1 HG01175.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+508dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401212 | ||||||
| chr11:401212 | C | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0005t0001g0091 |
3 | HG01884.hp1 HG02056.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1737+507C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401212 | |||||||
| chr11:401213 | G | GA | 2 | a0001c0002t0001g0168 a0001c0003t0001g0166 |
2 | HG02135.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1737+508_1737+509i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401213 | |||||||
| chr11:401214 | C | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(66): Show |
72 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1737+509C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401214 | |||||||
| chr11:401214 | C | CCCCGCTC others(274): Show |
1 | a0001c0016t0001g0200 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1737+523_1737+524i others(283): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401214 | ||||||
| chr11:401214 | C | CCCCGCTC others(272): Show |
2 | a0001c0003t0001g0149 a0001c0004t0001g0073 |
2 | NA19004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1737+527_1737+528i others(281): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401214 | ||||||
| chr11:401214 | C | CCCCGCTC others(178): Show |
1 | a0001c0003t0001g0141 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1737+527_1737+528i others(187): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401214 | ||||||
| chr11:401214 | C | CCCCGCTC others(255): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1737+527_1737+528i others(264): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401214 | ||||||
| chr11:401214 | C | CCCCGCTC others(271): Show |
1 | a0001c0002t0001g0101 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1737+527_1737+528i others(280): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401214 | ||||||
| chr11:401214 | C | CCCCGCTC others(271): Show |
7 | a0001c0002t0001g0148 a0001c0002t0001g0170 a0001c0002t0001g0172 others(4): Show |
7 | HG00544.hp1 HG01981.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+527_1737+528i others(280): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401214 | ||||||
| chr11:401214 | C | CCCCGCTC others(271): Show |
2 | a0001c0002t0001g0127 a0001c0002t0001g0169 |
2 | NA19065.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1737+527_1737+528i others(280): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401214 | ||||||
| chr11:401214 | C | G | 2 | a0001c0002t0001g0118 a0001c0002t0001g0126 |
2 | HG00733.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1737+509C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401214 | |||||||
| chr11:401218 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1737+513G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401218 | |||||||
| chr11:401222 | A | ACCCCCGG others(24): Show |
1 | a0001c0002t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1737+527_1737+528i others(33): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401222 | ||||||
| chr11:401224 | C | A | 6 | a0001c0002t0001g0137 a0001c0007t0001g0008 a0001c0007t0001g0009 others(3): Show |
6 | HG00733.hp2 HG02717.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+519C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401224 | |||||||
| chr11:401225 | C | CCCAGCCC others(7): Show |
1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1737+522_1737+523i others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401225 | ||||||
| chr11:401227 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1737+522C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401227 | |||||||
| chr11:401228 | G | A | 5 | a0001c0007t0001g0007 a0001c0007t0001g0025 a0001c0007t0001g0208 others(2): Show |
5 | HG00733.hp2 HG02056.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+523G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401228 | |||||||
| chr11:401228 | G | C | 2 | a0001c0003t0001g0114 a0001c0004t0001g0094 |
2 | HG03688.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1737+523G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401228 | |||||||
| chr11:401228 | G | GGCCCGCT others(445): Show |
1 | a0001c0003t0001g0116 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1737+527_1737+528i others(454): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401228 | ||||||
| chr11:401229 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1737+524G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401229 | |||||||
| chr11:401229 | GC | G | 4 | a0001c0003t0001g0097 a0001c0007t0001g0208 a0001c0012t0001g0119 others(1): Show |
4 | HG00733.hp2 HG02056.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+528delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401229 | ||||||
| chr11:401229 | GCCCCGCT others(117): Show |
G | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1737+528_1737+651d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401229 | ||||||
| chr11:401229 | GCCCCGCT others(148): Show |
G | 1 | a0001c0007t0001g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1737+528_1737+682d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401229 | ||||||
| chr11:401234 | G | A | 5 | a0001c0001t0001g0066 a0001c0006t0001g0038 a0001c0006t0001g0068 others(2): Show |
5 | HG00099.hp1 HG00609.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+529G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401234 | |||||||
| chr11:401235 | CTCACACC others(9): Show |
C | 1 | a0001c0006t0001g0005 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1737+540_1737+555d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401235 | ||||||
| chr11:401238 | A | AC | 3 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0184 |
3 | HG00621.hp1 HG00621.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1737+534dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401238 | ||||||
| chr11:401239 | C | CCCCCGAC others(7): Show |
1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1737+534_1737+535i others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401239 | |||||||
| chr11:401239 | CA | C | 21 | a0001c0001t0001g0066 a0001c0002t0001g0101 a0001c0002t0001g0118 others(18): Show |
21 | HG00544.hp1 HG00609.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1737+535delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401239 | |||||||
| chr11:401240 | A | ACCCGACC others(23): Show |
1 | a0001c0001t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1737+539_1737+540i others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401240 | ||||||
| chr11:401240 | A | ACCCGGCC others(23): Show |
1 | a0001c0002t0001g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1737+543_1737+544i others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401240 | ||||||
| chr11:401240 | A | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(138): Show |
146 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1737+535A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401240 | |||||||
| chr11:401242 | C | G | 1 | a0001c0001t0001g0016 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1737+537C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401242 | |||||||
| chr11:401243 | CG | C | 4 | a0001c0007t0001g0208 a0001c0008t0001g0093 a0001c0012t0001g0119 others(1): Show |
4 | HG00733.hp2 HG02056.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+540delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401243 | ||||||
| chr11:401244 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1737+539G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401244 | |||||||
| chr11:401245 | G | A | 3 | a0001c0001t0001g0019 a0001c0005t0001g0091 a0001c0006t0001g0049 |
3 | HG01175.hp2 HG01884.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1737+540G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401245 | |||||||
| chr11:401246 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1737+541C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401246 | |||||||
| chr11:401250 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(56): Show |
62 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1737+545G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401250 | |||||||
| chr11:401251 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.1737+546T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401251 | |||||||
| chr11:401256 | A | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1737+551A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401256 | |||||||
| chr11:401259 | C | CG | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(71): Show |
77 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1737+555dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401259 | ||||||
| chr11:401259 | C | G | 2 | a0001c0001t0001g0089 a0001c0007t0001g0010 |
2 | HG01243.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1737+554C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401259 | |||||||
| chr11:401261 | C | A | 12 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0034 others(9): Show |
12 | HG00609.hp2 HG01175.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+556C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401261 | |||||||
| chr11:401264 | C | T | 5 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+559C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401264 | |||||||
| chr11:401265 | G | A | 1 | a0001c0012t0001g0156 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1737+560G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401265 | |||||||
| chr11:401271 | A | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(77): Show |
83 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1737+566A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401271 | |||||||
| chr11:401274 | C | CG | 5 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0003t0001g0097 others(2): Show |
5 | HG01175.hp2 HG01884.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+570dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401274 | ||||||
| chr11:401274 | C | G | 6 | a0001c0001t0001g0081 a0001c0001t0001g0209 a0001c0005t0001g0084 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+569C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401274 | |||||||
| chr11:401274 | C | T | 2 | a0001c0008t0001g0188 a0001c0030t0001g0174 |
2 | HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1737+569C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401274 | |||||||
| chr11:401276 | C | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0034 others(7): Show |
10 | HG00099.hp1 HG00609.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.1737+571C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401276 | |||||||
| chr11:401280 | G | A | 1 | a0001c0005t0001g0040 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1737+575G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401280 | |||||||
| chr11:401286 | C | A | 9 | a0001c0003t0001g0097 a0001c0003t0001g0166 a0001c0004t0001g0094 others(6): Show |
9 | HG00099.hp1 HG00733.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+581C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401286 | |||||||
| chr11:401288 | CCGGCCCG others(6): Show |
C | 3 | a0001c0005t0001g0091 a0001c0006t0001g0049 a0001c0009t0001g0123 |
3 | HG01175.hp2 HG01884.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1737+585_1737+597d others(15): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401288 | ||||||
| chr11:401289 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0089 |
3 | HG02129.hp1 HG03453.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1737+584C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401289 | |||||||
| chr11:401289 | C | T | 1 | a0001c0007t0001g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1737+584C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401289 | |||||||
| chr11:401290 | G | A | 2 | a0001c0007t0001g0008 a0001c0007t0001g0009 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1737+585G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401290 | |||||||
| chr11:401290 | G | GA | 2 | a0001c0001t0001g0016 a0001c0001t0001g0089 |
2 | HG02129.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1737+585_1737+586i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401290 | |||||||
| chr11:401290 | GGCCCGCT others(7): Show |
G | 2 | a0001c0001t0001g0019 a0001c0009t0001g0102 |
2 | HG02148.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1737+590_1737+603d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401290 | ||||||
| chr11:401291 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(66): Show |
72 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1737+586G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401291 | |||||||
| chr11:401291 | G | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0089 others(4): Show |
7 | HG00733.hp2 HG02056.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+586G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401291 | |||||||
| chr11:401291 | G | GC | 13 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0001t0001g0209 others(10): Show |
13 | HG01243.hp2 HG01261.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.1737+589dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401291 | ||||||
| chr11:401292 | CCCGCTCA others(22): Show |
C | 5 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+590_1737+618d others(31): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401292 | ||||||
| chr11:401301 | A | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(11): Show |
14 | HG00099.hp1 HG00609.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1737+596A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401301 | |||||||
| chr11:401304 | C | CG | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0081 others(3): Show |
6 | HG00733.hp2 HG02056.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+600dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401304 | ||||||
| chr11:401304 | C | G | 3 | a0001c0005t0001g0091 a0001c0006t0001g0049 a0001c0009t0001g0123 |
3 | HG01175.hp2 HG01884.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1737+599C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401304 | |||||||
| chr11:401305 | G | C | 1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1737+600G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401305 | |||||||
| chr11:401305 | G | GA | 3 | a0001c0001t0001g0209 a0001c0005t0001g0084 a0001c0005t0001g0085 |
3 | HG02647.hp1 NA18612.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1737+600_1737+601i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401305 | |||||||
| chr11:401306 | C | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(66): Show |
72 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1737+601C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401306 | |||||||
| chr11:401306 | C | G | 5 | a0001c0006t0001g0038 a0001c0006t0001g0068 a0001c0021t0001g0086 others(2): Show |
5 | HG00099.hp1 HG01175.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+601C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401306 | |||||||
| chr11:401310 | G | A | 3 | a0001c0001t0001g0019 a0001c0005t0001g0091 a0001c0006t0001g0049 |
3 | HG01175.hp2 HG01884.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1737+605G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401310 | |||||||
| chr11:401315 | C | CCCCGGAC others(288): Show |
1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1737+613_1737+614i others(297): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401315 | ||||||
| chr11:401315 | CCCCCGGC others(54): Show |
C | 1 | a0001c0001t0001g0043 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1737+615_1737+675d others(63): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401315 | ||||||
| chr11:401316 | C | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0001t0001g0209 others(12): Show |
15 | HG00733.hp2 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.1737+611C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401316 | |||||||
| chr11:401316 | CCCCGGCC others(24): Show |
C | 1 | a0005c0022t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1737+620_1737+650d others(33): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401316 | ||||||
| chr11:401319 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0089 |
2 | HG02129.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1737+614C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401319 | |||||||
| chr11:401320 | G | GA | 3 | a0001c0001t0001g0089 a0001c0009t0001g0102 a0001c0009t0001g0123 |
3 | HG03688.hp2 NA18966.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1737+615_1737+616i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401320 | |||||||
| chr11:401320 | GGCCCGCT others(39): Show |
G | 1 | a0001c0005t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1737+620_1737+665d others(48): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401320 | ||||||
| chr11:401320 | GGCCCGCT others(146): Show |
G | 1 | a0001c0001t0001g0066 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1737+620_1737+772d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401320 | ||||||
| chr11:401321 | G | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0001t0001g0209 others(6): Show |
9 | HG00099.hp1 HG01175.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+616G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401321 | |||||||
| chr11:401321 | G | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0089 others(8): Show |
11 | HG00642.hp1 HG00733.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1737+616G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401321 | |||||||
| chr11:401321 | G | GC | 75 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0002t0001g0004 others(72): Show |
77 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1737+619dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(131): Show |
1 | a0001c0010t0001g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1737+619_1737+620i others(140): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(322): Show |
1 | a0019c0032t0001g0144 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1737+619_1737+620i others(331): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(362): Show |
1 | a0014c0034t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1737+619_1737+620i others(371): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(336): Show |
1 | a0001c0002t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1737+619_1737+620i others(345): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(319): Show |
3 | a0001c0003t0001g0099 a0001c0003t0001g0139 a0001c0003t0001g0153 |
3 | HG01256.hp1 NA18612.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1737+619_1737+620i others(328): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(210): Show |
1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1737+619_1737+620i others(219): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(321): Show |
1 | a0001c0002t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1737+619_1737+620i others(330): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(320): Show |
1 | a0001c0002t0001g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1737+619_1737+620i others(329): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(194): Show |
1 | a0001c0002t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1737+619_1737+620i others(203): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(288): Show |
1 | a0001c0003t0001g0152 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1737+619_1737+620i others(297): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | G | GCCCCGCT others(117): Show |
1 | a0001c0002t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1737+619_1737+620i others(126): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401321 | GCCCGCTC others(25): Show |
G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0031 others(4): Show |
7 | HG00544.hp2 HG01515.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+631_1737+662d others(34): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401321 | ||||||
| chr11:401330 | CA | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(66): Show |
72 | HG00621.hp1 HG00673.hp2 HG01175.hp2 others(69): Show |
intron_variant | MODIFIER | c.1737+626delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401330 | |||||||
| chr11:401331 | A | C | 49 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0041 others(46): Show |
49 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1737+626A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401331 | |||||||
| chr11:401333 | C | G | 1 | a0001c0021t0001g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1737+628C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401333 | |||||||
| chr11:401334 | CG | C | 38 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0110 others(35): Show |
40 | HG00099.hp2 HG00639.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1737+631delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401334 | ||||||
| chr11:401335 | G | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(60): Show |
66 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.1737+630G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401335 | |||||||
| chr11:401335 | G | GCCCCGCT others(178): Show |
1 | a0001c0002t0001g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1737+630_1737+631i others(187): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401335 | |||||||
| chr11:401335 | G | GCCCCGCT others(256): Show |
1 | a0012c0020t0001g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1737+630_1737+631i others(265): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401335 | |||||||
| chr11:401336 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1737+631G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401336 | |||||||
| chr11:401336 | G | C | 2 | a0001c0002t0001g0124 a0001c0028t0001g0128 |
2 | HG02109.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1737+631G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401336 | |||||||
| chr11:401337 | C | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(59): Show |
65 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.1737+632C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401337 | |||||||
| chr11:401340 | C | T | 1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1737+635C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401340 | |||||||
| chr11:401346 | CA | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0089 a0001c0004t0001g0012 others(7): Show |
10 | HG01175.hp2 HG01884.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.1737+642delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401346 | |||||||
| chr11:401347 | A | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(110): Show |
118 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.1737+642A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401347 | |||||||
| chr11:401349 | C | G | 3 | a0001c0006t0001g0038 a0001c0006t0001g0068 a0004c0015t0001g0047 |
3 | HG00099.hp1 HG01175.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1737+644C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401349 | |||||||
| chr11:401350 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1737+645C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401350 | |||||||
| chr11:401350 | CG | C | 35 | a0001c0001t0001g0016 a0001c0002t0001g0101 a0001c0002t0001g0118 others(32): Show |
35 | HG00544.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1737+647delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401350 | ||||||
| chr11:401351 | G | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0089 a0001c0003t0001g0114 others(4): Show |
7 | HG01175.hp2 HG01884.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+646G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401351 | |||||||
| chr11:401351 | GGCCCCGC others(8): Show |
G | 3 | a0001c0001t0001g0209 a0001c0005t0001g0084 a0001c0005t0001g0085 |
3 | HG02647.hp1 NA18612.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1737+658_1737+672d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401351 | ||||||
| chr11:401351 | GGCCCCGC others(115): Show |
G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0053 |
3 | HG00621.hp2 HG02004.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1737+658_1737+779d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401351 | ||||||
| chr11:401352 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1737+647G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401352 | |||||||
| chr11:401353 | C | A | 6 | a0001c0001t0001g0019 a0001c0005t0001g0091 a0001c0006t0001g0038 others(3): Show |
6 | HG00099.hp1 HG01175.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+648C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401353 | |||||||
| chr11:401363 | A | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(75): Show |
81 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1737+658A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401363 | |||||||
| chr11:401364 | C | CG | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(51): Show |
57 | HG00621.hp1 HG00673.hp2 HG01192.hp1 others(54): Show |
intron_variant | MODIFIER | c.1737+659_1737+660i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401364 | |||||||
| chr11:401366 | C | CG | 27 | a0001c0001t0001g0089 a0001c0002t0001g0101 a0001c0002t0001g0118 others(24): Show |
27 | HG00544.hp1 HG00642.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.1737+662dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401366 | ||||||
| chr11:401366 | C | CGCCCCGC others(9): Show |
1 | a0001c0002t0001g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1737+673_1737+688d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401366 | ||||||
| chr11:401366 | C | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(53): Show |
59 | HG00621.hp1 HG00673.hp2 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.1737+661C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401366 | |||||||
| chr11:401367 | GCCCCGCT others(69): Show |
G | 3 | a0001c0006t0001g0038 a0001c0006t0001g0068 a0004c0015t0001g0047 |
3 | HG00099.hp1 HG01175.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1737+663_1737+738d others(78): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401367 | |||||||
| chr11:401368 | C | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(63): Show |
69 | HG00544.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1737+663C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401368 | |||||||
| chr11:401368 | C | G | 1 | a0012c0020t0001g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1737+663C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401368 | |||||||
| chr11:401372 | G | A | 6 | a0001c0001t0001g0209 a0001c0005t0001g0013 a0001c0005t0001g0084 others(3): Show |
6 | HG02145.hp2 HG02647.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+667G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401372 | |||||||
| chr11:401377 | C | CA | 2 | a0001c0002t0001g0164 a0001c0003t0001g0166 |
2 | HG00642.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1737+672_1737+673i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401377 | |||||||
| chr11:401378 | C | A | 30 | a0001c0001t0001g0016 a0001c0002t0001g0101 a0001c0002t0001g0104 others(27): Show |
30 | HG00544.hp1 HG00733.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1737+673C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401378 | |||||||
| chr11:401378 | C | CCCCGGCC others(240): Show |
1 | a0001c0002t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1737+693_1737+694i others(249): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401378 | ||||||
| chr11:401378 | C | CCCCGGCC others(242): Show |
1 | a0001c0002t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1737+688_1737+689i others(251): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401378 | ||||||
| chr11:401378 | C | CCCCGGCC others(241): Show |
6 | a0001c0002t0001g0004 a0001c0002t0001g0125 a0001c0003t0001g0003 others(3): Show |
7 | HG01256.hp2 HG01258.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+688_1737+689i others(250): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401378 | ||||||
| chr11:401378 | C | CCCCGGCC others(241): Show |
1 | a0001c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1737+688_1737+689i others(250): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401378 | ||||||
| chr11:401378 | C | CCCCGGCC others(239): Show |
2 | a0001c0003t0001g0142 a0001c0003t0001g0150 |
2 | HG02165.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1737+681_1737+682i others(248): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401378 | ||||||
| chr11:401380 | CCGGCCCC others(53): Show |
C | 1 | a0013c0037t0005g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1737+677_1737+736d others(62): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401380 | ||||||
| chr11:401381 | C | G | 8 | a0001c0001t0001g0034 a0001c0004t0001g0012 a0001c0004t0001g0190 others(5): Show |
8 | HG02056.hp1 HG02622.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1737+676C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401381 | |||||||
| chr11:401381 | CG | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(2): Show |
5 | HG02129.hp1 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+678delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401381 | ||||||
| chr11:401382 | G | A | 1 | a0001c0007t0001g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1737+677G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401382 | |||||||
| chr11:401382 | GGCCCCGC others(54): Show |
G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(29): Show |
35 | HG01358.hp1 HG01884.hp2 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.1737+709_1737+769d others(63): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401382 | ||||||
| chr11:401382 | GGCCCCGC others(84): Show |
G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0031 others(5): Show |
8 | HG00544.hp2 HG01515.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1737+689_1737+779d others(93): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401382 | ||||||
| chr11:401383 | G | A | 8 | a0001c0001t0001g0034 a0001c0004t0001g0012 a0001c0004t0001g0190 others(5): Show |
8 | HG02056.hp1 HG02622.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1737+678G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401383 | |||||||
| chr11:401383 | GC | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0072 others(7): Show |
10 | HG01175.hp2 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1737+682delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401383 | ||||||
| chr11:401384 | C | CCCGCTCA others(350): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1737+681_1737+682i others(359): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401384 | ||||||
| chr11:401384 | CCCCGCTC others(53): Show |
C | 1 | a0001c0011t0001g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1737+683_1737+742d others(62): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401384 | ||||||
| chr11:401394 | A | C | 53 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0028 others(50): Show |
53 | HG00673.hp1 HG00733.hp2 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.1737+689A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401394 | |||||||
| chr11:401397 | C | CG | 33 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0110 others(30): Show |
33 | HG00099.hp2 HG00673.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1737+693dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401397 | ||||||
| chr11:401397 | C | CGCCCCGC others(40): Show |
1 | a0001c0001t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1737+703_1737+704i others(49): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401397 | ||||||
| chr11:401397 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 |
3 | HG02129.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1737+692C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401397 | |||||||
| chr11:401398 | G | GA | 3 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 |
3 | HG02129.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1737+693_1737+694i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401398 | |||||||
| chr11:401398 | GCCCCGCT others(53): Show |
G | 3 | a0001c0007t0001g0208 a0001c0012t0001g0119 a0001c0012t0001g0156 |
3 | HG00733.hp2 HG02056.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1737+694_1737+753d others(62): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401398 | |||||||
| chr11:401399 | C | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0043 others(14): Show |
17 | HG01175.hp2 HG01884.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.1737+694C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401399 | |||||||
| chr11:401407 | ACACCCGG others(70): Show |
A | 1 | a0001c0001t0001g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1737+704_1737+780d others(79): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401407 | ||||||
| chr11:401408 | CA | C | 16 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0081 others(13): Show |
16 | HG02145.hp2 HG02622.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.1737+704delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401408 | |||||||
| chr11:401409 | A | ACCCGGCC others(70): Show |
1 | a0002c0013t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1737+724_1737+725i others(79): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401409 | ||||||
| chr11:401409 | A | C | 39 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0039 others(36): Show |
39 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1737+704A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401409 | |||||||
| chr11:401412 | C | G | 18 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0055 others(15): Show |
18 | HG00621.hp1 HG00673.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1737+707C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401412 | |||||||
| chr11:401412 | CG | C | 8 | a0001c0002t0001g0159 a0001c0003t0001g0114 a0001c0005t0001g0084 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1737+709delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401412 | ||||||
| chr11:401412 | CGGCCCCG others(147): Show |
C | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1737+709_1737+862d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401412 | ||||||
| chr11:401413 | G | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0001t0001g0209 others(3): Show |
6 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+708G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401413 | |||||||
| chr11:401413 | G | GCCCCGCT others(7): Show |
1 | a0001c0003t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1737+708_1737+709i others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401413 | |||||||
| chr11:401414 | G | A | 18 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0055 others(15): Show |
18 | HG00621.hp1 HG00673.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1737+709G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401414 | |||||||
| chr11:401414 | G | GCCCCCGC others(356): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1737+713_1737+714i others(365): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401414 | ||||||
| chr11:401415 | C | A | 7 | a0001c0001t0001g0209 a0001c0003t0001g0114 a0001c0005t0001g0013 others(4): Show |
7 | HG02145.hp2 HG02647.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+710C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401415 | |||||||
| chr11:401425 | A | C | 55 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(52): Show |
55 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1737+720A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401425 | |||||||
| chr11:401427 | C | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0072 others(2): Show |
5 | HG01175.hp2 HG01884.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+722C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401427 | |||||||
| chr11:401428 | C | A | 5 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(2): Show |
5 | HG03471.hp1 NA18906.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+723C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401428 | |||||||
| chr11:401428 | C | G | 3 | a0001c0002t0001g0104 a0001c0008t0001g0194 a0001c0021t0001g0086 |
3 | HG02622.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1737+723C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401428 | |||||||
| chr11:401428 | CGGCCCGC others(178): Show |
C | 1 | a0001c0005t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1737+725_1737+909d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401428 | ||||||
| chr11:401430 | G | A | 26 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0048 others(23): Show |
26 | HG00621.hp1 HG00673.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1737+725G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401430 | |||||||
| chr11:401430 | G | C | 47 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0195 others(44): Show |
47 | HG00099.hp2 HG00673.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.1737+725G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401430 | |||||||
| chr11:401430 | G | GA | 5 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0072 others(2): Show |
5 | HG01175.hp2 HG01884.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+725_1737+726i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401430 | |||||||
| chr11:401430 | G | GC | 55 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0001t0001g0089 others(52): Show |
56 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1737+728dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401430 | ||||||
| chr11:401430 | G | GCCCCGCT others(411): Show |
1 | a0001c0002t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1737+728_1737+729i others(420): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401430 | ||||||
| chr11:401430 | G | GCCCCGCT others(410): Show |
1 | a0001c0002t0001g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1737+728_1737+729i others(419): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401430 | ||||||
| chr11:401430 | GCCCGCTC others(8): Show |
G | 1 | a0005c0022t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1737+765_1737+779d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401430 | ||||||
| chr11:401431 | CCCGCTCA others(114): Show |
C | 1 | a0001c0004t0001g0197 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1737+729_1737+849d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401431 | ||||||
| chr11:401438 | ACACCCGC others(39): Show |
A | 3 | a0001c0005t0004g0006 a0001c0006t0001g0204 a0001c0009t0001g0167 |
3 | HG00673.hp2 HG02004.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1737+735_1737+780d others(48): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401438 | ||||||
| chr11:401438 | ACACCCGC others(55): Show |
A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0055 a0001c0001t0001g0059 others(2): Show |
5 | HG01192.hp1 HG01243.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+735_1737+796d others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401438 | ||||||
| chr11:401440 | A | C | 31 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0028 others(28): Show |
31 | HG00621.hp1 HG01175.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.1737+735A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401440 | |||||||
| chr11:401443 | C | CG | 16 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0043 others(13): Show |
16 | HG00609.hp1 HG01175.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1737+739dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401443 | ||||||
| chr11:401443 | C | CGGACCCG others(226): Show |
2 | a0001c0003t0001g0161 a0001c0003t0001g0162 |
2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1737+739_1737+740i others(235): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401443 | ||||||
| chr11:401443 | C | CGGCCCCG others(226): Show |
1 | a0001c0002t0001g0110 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1737+739_1737+740i others(235): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401443 | ||||||
| chr11:401443 | C | CGGCCCCG others(227): Show |
1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1737+739_1737+740i others(236): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401443 | ||||||
| chr11:401443 | C | CGGCCCCG others(226): Show |
15 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0171 others(12): Show |
15 | HG01934.hp2 HG01943.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1737+739_1737+740i others(235): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401443 | ||||||
| chr11:401443 | C | CGGCCCCG others(226): Show |
2 | a0001c0010t0003g0021 a0001c0010t0003g0022 |
2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1737+739_1737+740i others(235): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401443 | ||||||
| chr11:401443 | C | CGGCCCCG others(226): Show |
4 | a0001c0002t0001g0132 a0001c0002t0001g0133 a0001c0002t0001g0134 others(1): Show |
4 | HG00099.hp2 HG02074.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+739_1737+740i others(235): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401443 | ||||||
| chr11:401443 | C | G | 13 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0064 others(10): Show |
13 | HG00621.hp1 HG00642.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1737+738C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401443 | |||||||
| chr11:401443 | CGCCCCGC others(116): Show |
C | 1 | a0001c0007t0001g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1737+755_1737+877d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401443 | ||||||
| chr11:401444 | G | GA | 2 | a0001c0001t0001g0089 a0001c0004t0001g0094 |
2 | HG03688.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1737+739_1737+740i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401444 | |||||||
| chr11:401444 | GCCCCGCT others(7): Show |
G | 1 | a0017c0027t0001g0107 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1737+740_1737+753d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401444 | |||||||
| chr11:401445 | C | A | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1737+740C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401445 | |||||||
| chr11:401445 | C | G | 6 | a0001c0001t0001g0209 a0001c0005t0001g0013 a0001c0005t0001g0084 others(3): Show |
6 | HG02145.hp2 HG02647.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+740C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401445 | |||||||
| chr11:401452 | C | CA | 3 | a0001c0002t0001g0136 a0001c0008t0001g0188 a0001c0030t0001g0174 |
3 | HG02622.hp1 HG03579.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1737+748dupA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401452 | ||||||
| chr11:401455 | A | C | 68 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(65): Show |
69 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1737+750A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401455 | |||||||
| chr11:401457 | C | G | 6 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(3): Show |
6 | HG03471.hp1 HG03486.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+752C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401457 | |||||||
| chr11:401458 | C | A | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1737+753C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401458 | |||||||
| chr11:401458 | C | CG | 38 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0002t0001g0004 others(35): Show |
39 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.1737+754dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401458 | ||||||
| chr11:401458 | C | CGACCCGC others(242): Show |
1 | a0001c0003t0001g0155 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1737+754_1737+755i others(251): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401458 | ||||||
| chr11:401458 | C | CGCCCCGC others(9): Show |
2 | a0001c0002t0001g0171 a0001c0002t0001g0173 |
2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1737+754_1737+769d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401458 | ||||||
| chr11:401458 | C | CGCCCCGC others(9): Show |
23 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0110 others(20): Show |
23 | HG00099.hp2 HG01891.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.1737+764_1737+765i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401458 | ||||||
| chr11:401458 | C | CGGCCCCG others(25): Show |
1 | a0001c0002t0001g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1737+754_1737+755i others(34): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401458 | ||||||
| chr11:401458 | C | CGGCCCGC others(244): Show |
1 | a0001c0028t0001g0128 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1737+754_1737+755i others(253): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401458 | ||||||
| chr11:401458 | C | G | 23 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0064 others(20): Show |
23 | HG00621.hp1 HG01261.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.1737+753C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401458 | |||||||
| chr11:401459 | G | GA | 7 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(4): Show |
7 | HG02622.hp2 HG03471.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+754_1737+755i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401459 | |||||||
| chr11:401460 | C | A | 9 | a0001c0001t0001g0089 a0001c0001t0001g0209 a0001c0004t0001g0094 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+755C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401460 | |||||||
| chr11:401460 | C | CCCCGCTC others(8): Show |
8 | a0001c0002t0001g0135 a0001c0003t0001g0099 a0001c0003t0001g0139 others(5): Show |
8 | HG00642.hp1 HG01256.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.1737+764_1737+765i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401460 | ||||||
| chr11:401460 | C | CCCCGCTC others(102): Show |
1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1737+764_1737+765i others(111): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401460 | ||||||
| chr11:401460 | C | CCCCGCTC others(101): Show |
3 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0003t0001g0151 |
3 | HG00609.hp1 HG01943.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1737+764_1737+765i others(110): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401460 | ||||||
| chr11:401460 | C | G | 1 | a0002c0013t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1737+755C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401460 | |||||||
| chr11:401460 | CCCCGCTC others(54): Show |
C | 1 | a0001c0001t0001g0015 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1737+759_1737+819d others(63): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401460 | ||||||
| chr11:401469 | CACCCGCC others(56): Show |
C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(36): Show |
42 | HG00099.hp1 HG01175.hp2 HG01258.hp1 others(39): Show |
intron_variant | MODIFIER | c.1737+765_1737+827d others(65): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401469 | |||||||
| chr11:401470 | A | C | 19 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0081 others(16): Show |
19 | HG00642.hp1 HG01175.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.1737+765A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401470 | |||||||
| chr11:401473 | C | CG | 12 | a0001c0001t0001g0089 a0001c0001t0001g0209 a0001c0004t0001g0094 others(9): Show |
12 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+769dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401473 | ||||||
| chr11:401473 | C | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0081 others(2): Show |
5 | HG01175.hp1 HG02723.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+768C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401473 | |||||||
| chr11:401474 | G | A | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1737+769G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401474 | |||||||
| chr11:401474 | G | C | 1 | a0001c0028t0001g0128 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1737+769G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401474 | |||||||
| chr11:401474 | G | GA | 4 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0081 others(1): Show |
4 | HG01175.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+769_1737+770i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401474 | |||||||
| chr11:401475 | C | A | 9 | a0001c0001t0001g0016 a0001c0003t0001g0114 a0001c0003t0001g0166 others(6): Show |
9 | HG00733.hp2 HG02056.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+770C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401475 | |||||||
| chr11:401475 | C | G | 2 | a0001c0002t0001g0104 a0001c0012t0001g0120 |
2 | HG02027.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1737+770C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401475 | |||||||
| chr11:401483 | A | ACCCCGGC others(630): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+782_1737+783i others(639): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401483 | ||||||
| chr11:401483 | AC | A | 7 | a0001c0001t0001g0016 a0001c0007t0001g0008 a0001c0007t0001g0009 others(4): Show |
7 | HG00733.hp2 HG02056.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+783delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401483 | ||||||
| chr11:401485 | C | A | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0080 others(6): Show |
9 | HG02027.hp1 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+780C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401485 | |||||||
| chr11:401485 | CCCCGGCC others(86): Show |
C | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1737+796_1737+888d others(95): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401485 | ||||||
| chr11:401487 | C | G | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0031 others(15): Show |
18 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.1737+782C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401487 | |||||||
| chr11:401488 | C | G | 18 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0070 others(15): Show |
18 | HG01261.hp2 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1737+783C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401488 | |||||||
| chr11:401488 | CG | C | 5 | a0001c0001t0001g0056 a0001c0002t0001g0104 a0001c0008t0001g0188 others(2): Show |
5 | HG01175.hp1 HG02622.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+785delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401488 | ||||||
| chr11:401490 | G | A | 18 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0070 others(15): Show |
18 | HG01261.hp2 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1737+785G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401490 | |||||||
| chr11:401490 | G | C | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1737+785G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401490 | |||||||
| chr11:401490 | G | GCCCCGCT others(62): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+795_1737+796i others(71): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401490 | ||||||
| chr11:401491 | C | A | 20 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0031 others(17): Show |
20 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1737+786C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401491 | |||||||
| chr11:401495 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0195 a0001c0004t0001g0094 |
3 | HG03688.hp2 NA19079.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1737+790G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401495 | |||||||
| chr11:401499 | AC | A | 4 | a0001c0001t0001g0056 a0001c0003t0001g0166 a0004c0015t0001g0047 others(1): Show |
4 | HG01175.hp1 HG02135.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+799delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401499 | ||||||
| chr11:401500 | CCCCCGGC others(71): Show |
C | 4 | a0001c0001t0001g0034 a0001c0005t0004g0006 a0001c0006t0001g0204 others(1): Show |
4 | HG00673.hp2 HG02004.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+799_1737+876d others(80): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401500 | ||||||
| chr11:401501 | C | A | 24 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0064 others(21): Show |
24 | HG01261.hp2 HG02145.hp1 HG02148.hp2 others(21): Show |
intron_variant | MODIFIER | c.1737+796C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401501 | |||||||
| chr11:401504 | C | G | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1737+799C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401504 | |||||||
| chr11:401504 | CG | C | 15 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0070 others(12): Show |
15 | HG01261.hp2 HG02145.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.1737+801delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401504 | ||||||
| chr11:401504 | CGGCCCCG others(102): Show |
C | 1 | a0001c0005t0001g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1737+801_1737+909d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401504 | ||||||
| chr11:401505 | GGCCCCGT others(23): Show |
G | 2 | a0001c0007t0001g0025 a0001c0021t0001g0086 |
2 | HG02622.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1737+807_1737+836d others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401505 | ||||||
| chr11:401506 | G | A | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1737+801G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401506 | |||||||
| chr11:401512 | T | C | 144 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(141): Show |
146 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1737+807T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401512 | |||||||
| chr11:401517 | A | C | 38 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0028 others(35): Show |
38 | HG00733.hp2 HG01175.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1737+812A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401517 | |||||||
| chr11:401520 | C | CG | 5 | a0001c0002t0001g0104 a0001c0003t0001g0097 a0001c0003t0001g0114 others(2): Show |
5 | HG02148.hp2 HG03130.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+816dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401520 | ||||||
| chr11:401520 | C | CGCCCCGC others(9): Show |
1 | a0001c0002t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1737+826_1737+827i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401520 | ||||||
| chr11:401520 | C | G | 25 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0048 others(22): Show |
25 | HG01175.hp1 HG01192.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1737+815C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401520 | |||||||
| chr11:401521 | G | A | 6 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(3): Show |
6 | HG03471.hp1 HG03486.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+816G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401521 | |||||||
| chr11:401521 | G | GA | 15 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0064 others(12): Show |
15 | HG00733.hp2 HG01261.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1737+816_1737+817i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401521 | |||||||
| chr11:401522 | C | G | 2 | a0001c0008t0001g0188 a0001c0030t0001g0174 |
2 | HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1737+817C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401522 | |||||||
| chr11:401525 | C | T | 2 | a0003c0019t0001g0181 a0016c0035t0001g0180 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1737+820C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401525 | |||||||
| chr11:401532 | A | C | 33 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(30): Show |
33 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1737+827A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401532 | |||||||
| chr11:401535 | C | CG | 13 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0070 others(10): Show |
13 | HG01261.hp2 HG01952.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1737+831dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401535 | ||||||
| chr11:401535 | C | CGCCCCGC others(303): Show |
1 | a0001c0003t0001g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1737+841_1737+842i others(312): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401535 | ||||||
| chr11:401535 | C | CGGCCCCG others(59): Show |
1 | a0001c0003t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1737+831_1737+832i others(68): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401535 | ||||||
| chr11:401535 | C | G | 25 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(22): Show |
25 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1737+830C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401535 | |||||||
| chr11:401536 | G | GA | 19 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(16): Show |
19 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.1737+831_1737+832i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401536 | |||||||
| chr11:401536 | G | GGA | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(36): Show |
42 | HG00099.hp1 HG01175.hp2 HG01258.hp1 others(39): Show |
intron_variant | MODIFIER | c.1737+831_1737+832i others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401536 | |||||||
| chr11:401536 | GCCCCGCT others(1): Show |
G | 5 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(2): Show |
5 | HG03471.hp1 NA18906.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+832_1737+839d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401536 | |||||||
| chr11:401536 | GCCCCGCT others(32): Show |
G | 1 | a0001c0008t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1737+832_1737+870d others(41): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401536 | |||||||
| chr11:401537 | C | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0195 others(7): Show |
10 | HG00733.hp2 HG02056.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1737+832C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401537 | |||||||
| chr11:401537 | C | G | 1 | a0002c0013t0001g0109 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1737+832C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401537 | |||||||
| chr11:401547 | C | A | 14 | a0001c0001t0001g0089 a0001c0002t0001g0104 a0001c0002t0001g0145 others(11): Show |
14 | HG00609.hp1 HG01952.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.1737+842C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401547 | |||||||
| chr11:401547 | CCCCGGCC others(55): Show |
C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0055 a0001c0001t0001g0059 others(1): Show |
4 | HG01243.hp1 NA18952.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+851_1737+912d others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401547 | ||||||
| chr11:401550 | C | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0076 a0001c0001t0001g0195 |
3 | HG01192.hp1 NA18966.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1737+845C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401550 | |||||||
| chr11:401551 | G | GA | 9 | a0001c0001t0001g0056 a0001c0001t0001g0076 a0001c0001t0001g0195 others(6): Show |
9 | HG01192.hp1 HG03471.hp1 NA18906.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+846_1737+847i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401551 | |||||||
| chr11:401552 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(58): Show |
64 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1737+847G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401552 | |||||||
| chr11:401552 | G | C | 27 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0056 others(24): Show |
27 | HG01192.hp1 HG01261.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.1737+847G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401552 | |||||||
| chr11:401552 | G | GC | 19 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(16): Show |
19 | HG00733.hp2 HG02027.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.1737+850dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCCGCT others(25): Show |
1 | a0001c0002t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1737+850_1737+851i others(34): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(8): Show |
9 | a0001c0002t0001g0100 a0001c0002t0001g0110 a0001c0002t0001g0159 others(6): Show |
9 | HG00639.hp1 HG01891.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+856_1737+857i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(410): Show |
1 | a0001c0003t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(419): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(383): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(392): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(317): Show |
1 | a0019c0032t0001g0144 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(326): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(55): Show |
1 | a0017c0027t0001g0107 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(178): Show |
1 | a0001c0003t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(187): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(178): Show |
4 | a0001c0003t0001g0095 a0001c0003t0001g0147 a0001c0003t0001g0154 others(1): Show |
4 | HG01952.hp1 HG02074.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+856_1737+857i others(187): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(302): Show |
1 | a0001c0003t0001g0111 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(311): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(317): Show |
2 | a0001c0003t0001g0112 a0001c0003t0001g0113 |
2 | HG02273.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1737+856_1737+857i others(326): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(348): Show |
1 | a0001c0003t0001g0003 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1737+856_1737+857i others(357): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(459): Show |
1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(468): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(163): Show |
1 | a0001c0003t0001g0105 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(172): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(333): Show |
1 | a0009c0033t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(342): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(392): Show |
1 | a0001c0010t0001g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(401): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(438): Show |
1 | a0001c0003t0001g0155 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(447): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(409): Show |
2 | a0001c0002t0001g0148 a0001c0003t0001g0142 |
2 | HG00544.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1737+856_1737+857i others(418): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(532): Show |
1 | a0001c0003t0001g0141 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(541): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(301): Show |
1 | a0001c0003t0001g0149 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(310): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(394): Show |
1 | a0001c0002t0001g0172 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(403): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(164): Show |
1 | a0001c0002t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(173): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(395): Show |
1 | a0001c0002t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(404): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(442): Show |
1 | a0001c0002t0001g0126 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(451): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(133): Show |
3 | a0001c0002t0001g0132 a0001c0002t0001g0133 a0001c0002t0001g0138 |
3 | HG00099.hp2 HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1737+856_1737+857i others(142): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(364): Show |
1 | a0001c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(373): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(425): Show |
1 | a0001c0002t0001g0101 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(434): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(409): Show |
1 | a0001c0028t0001g0128 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(418): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(362): Show |
1 | a0001c0002t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(371): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(163): Show |
1 | a0002c0013t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(172): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401552 | G | GCCCGCTC others(411): Show |
1 | a0001c0003t0001g0158 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1737+856_1737+857i others(420): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401552 | ||||||
| chr11:401560 | A | ACACCCGC others(351): Show |
1 | a0001c0016t0001g0200 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(360): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401560 | ||||||
| chr11:401560 | AC | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(58): Show |
64 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1737+860delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401560 | ||||||
| chr11:401561 | C | A | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1737+856C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401561 | |||||||
| chr11:401561 | C | CACCCGCC others(7): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1737+856_1737+857i others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401561 | |||||||
| chr11:401562 | C | A | 55 | a0001c0001t0001g0056 a0001c0001t0001g0076 a0001c0001t0001g0195 others(52): Show |
56 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1737+857C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401562 | |||||||
| chr11:401565 | CG | C | 18 | a0001c0001t0001g0056 a0001c0001t0001g0076 a0001c0001t0001g0195 others(15): Show |
18 | HG00609.hp1 HG00673.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1737+862delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401565 | ||||||
| chr11:401566 | G | GCCCCGCT others(41): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1737+861_1737+862i others(50): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(117): Show |
1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1737+861_1737+862i others(126): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(287): Show |
1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1737+861_1737+862i others(296): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(209): Show |
1 | a0001c0003t0001g0096 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1737+861_1737+862i others(218): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(115): Show |
1 | a0001c0003t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1737+861_1737+862i others(124): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(378): Show |
5 | a0001c0002t0001g0103 a0001c0002t0001g0171 a0001c0002t0001g0173 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+861_1737+862i others(387): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(378): Show |
1 | a0001c0036t0001g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1737+861_1737+862i others(387): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(363): Show |
1 | a0001c0002t0001g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1737+861_1737+862i others(372): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(347): Show |
3 | a0001c0002t0001g0127 a0001c0002t0001g0137 a0001c0002t0001g0169 |
3 | NA19065.hp2 NA19087.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1737+861_1737+862i others(356): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(362): Show |
1 | a0001c0002t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1737+861_1737+862i others(371): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(399): Show |
1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1737+861_1737+862i others(408): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(378): Show |
1 | a0001c0002t0001g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1737+861_1737+862i others(387): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(379): Show |
1 | a0001c0002t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1737+861_1737+862i others(388): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | G | GCCCCGCT others(378): Show |
1 | a0001c0002t0001g0004 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1737+861_1737+862i others(387): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401566 | GGCCCCGC others(2): Show |
G | 5 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(2): Show |
5 | HG03471.hp1 NA18906.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+862_1737+870d others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401566 | |||||||
| chr11:401568 | C | A | 2 | a0001c0003t0001g0097 a0001c0003t0001g0114 |
2 | HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1737+863C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401568 | |||||||
| chr11:401568 | C | CCCGCTCA others(39): Show |
1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1737+865_1737+866i others(48): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401568 | ||||||
| chr11:401572 | G | A | 6 | a0001c0001t0001g0016 a0001c0007t0001g0008 a0001c0007t0001g0009 others(3): Show |
6 | HG00733.hp2 HG02056.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+867G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401572 | |||||||
| chr11:401577 | CA | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(60): Show |
66 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1737+873delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401577 | |||||||
| chr11:401578 | A | C | 52 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0056 others(49): Show |
53 | HG00609.hp1 HG00639.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.1737+873A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401578 | |||||||
| chr11:401581 | C | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0056 a0001c0001t0001g0076 others(3): Show |
6 | HG00621.hp1 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+876C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401581 | |||||||
| chr11:401581 | CG | C | 7 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0126 others(4): Show |
7 | HG00639.hp2 HG00733.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+878delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401581 | ||||||
| chr11:401582 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1737+877G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401582 | |||||||
| chr11:401582 | G | C | 2 | a0001c0004t0001g0094 a0001c0008t0001g0189 |
2 | HG03130.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1737+877G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401582 | |||||||
| chr11:401583 | G | A | 10 | a0001c0001t0001g0039 a0001c0001t0001g0056 a0001c0001t0001g0076 others(7): Show |
10 | HG00621.hp1 HG01175.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1737+878G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401583 | |||||||
| chr11:401584 | C | A | 1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1737+879C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401584 | |||||||
| chr11:401591 | CACACCCG others(187): Show |
C | 1 | a0001c0001t0001g0205 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1737+889_1737+1082 others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401591 | ||||||
| chr11:401594 | A | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(11): Show |
14 | HG00733.hp2 HG02056.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.1737+889A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401594 | |||||||
| chr11:401594 | A | T | 1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1737+889A>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401594 | |||||||
| chr11:401597 | C | CG | 18 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0076 others(15): Show |
19 | HG00642.hp1 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1737+893dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401597 | ||||||
| chr11:401599 | C | A | 14 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0064 others(11): Show |
14 | HG00733.hp2 HG01261.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1737+894C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401599 | |||||||
| chr11:401602 | C | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0004t0001g0193 |
3 | HG03209.hp1 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1737+897C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401602 | |||||||
| chr11:401607 | ACACCCGG others(88): Show |
A | 1 | a0001c0011t0001g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1737+904_1737+998d others(97): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401607 | ||||||
| chr11:401608 | CA | C | 24 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0046 others(21): Show |
24 | HG00733.hp2 HG01175.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.1737+904delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401608 | |||||||
| chr11:401609 | A | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(86): Show |
92 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1737+904A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401609 | |||||||
| chr11:401611 | C | G | 1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1737+906C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401611 | |||||||
| chr11:401612 | C | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(69): Show |
75 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1737+907C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401612 | |||||||
| chr11:401612 | CG | C | 30 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0002t0001g0004 others(27): Show |
32 | HG00642.hp1 HG00642.hp2 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.1737+909delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401612 | ||||||
| chr11:401613 | G | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0056 a0001c0001t0001g0076 others(8): Show |
11 | HG00733.hp2 HG01175.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1737+908G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401613 | |||||||
| chr11:401613 | G | GCCCCGCT others(7): Show |
2 | a0001c0002t0001g0127 a0001c0002t0001g0169 |
2 | NA19065.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1737+908_1737+909i others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401613 | |||||||
| chr11:401613 | G | GCCCCGCT others(7): Show |
1 | a0001c0002t0001g0110 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1737+908_1737+909i others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401613 | |||||||
| chr11:401613 | G | GCCCCGCT others(298): Show |
1 | a0001c0004t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1737+908_1737+909i others(307): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401613 | |||||||
| chr11:401613 | G | GCCCCGCT others(302): Show |
1 | a0001c0004t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1737+908_1737+909i others(311): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401613 | |||||||
| chr11:401614 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(69): Show |
75 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1737+909G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401614 | |||||||
| chr11:401614 | G | C | 4 | a0001c0001t0001g0078 a0001c0002t0001g0145 a0001c0002t0001g0146 others(1): Show |
4 | HG00609.hp1 HG01261.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+909G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401614 | |||||||
| chr11:401615 | C | A | 7 | a0001c0001t0001g0016 a0001c0003t0001g0097 a0001c0004t0001g0094 others(4): Show |
7 | HG00733.hp2 HG02129.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+910C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401615 | |||||||
| chr11:401615 | C | CCCCCGCT others(9): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+913_1737+914i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401615 | ||||||
| chr11:401615 | C | G | 1 | a0001c0002t0001g0110 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1737+910C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401615 | |||||||
| chr11:401623 | A | AC | 3 | a0001c0001t0001g0183 a0001c0006t0001g0035 a0001c0012t0001g0120 |
3 | HG02027.hp1 HG02145.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1737+919dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401623 | ||||||
| chr11:401624 | CA | C | 6 | a0001c0001t0001g0089 a0001c0003t0001g0096 a0001c0004t0001g0196 others(3): Show |
6 | HG01934.hp2 HG02056.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+920delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401624 | |||||||
| chr11:401625 | A | ACCCGACC others(8): Show |
6 | a0001c0002t0001g0124 a0001c0003t0001g0095 a0001c0003t0001g0098 others(3): Show |
6 | HG01952.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+924_1737+925i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401625 | ||||||
| chr11:401625 | A | ACCCGACC others(193): Show |
1 | a0001c0003t0001g0116 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1737+924_1737+925i others(202): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401625 | ||||||
| chr11:401625 | A | C | 31 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0001g0048 others(28): Show |
31 | HG01175.hp1 HG01192.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.1737+920A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401625 | |||||||
| chr11:401628 | C | G | 2 | a0001c0005t0001g0023 a0001c0005t0001g0032 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1737+923C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401628 | |||||||
| chr11:401628 | CG | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(86): Show |
92 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1737+925delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401628 | ||||||
| chr11:401628 | CGGCCCCG others(72): Show |
C | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1737+925_1737+1003 others(82): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401628 | ||||||
| chr11:401629 | G | A | 1 | a0001c0028t0001g0128 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1737+924G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401629 | |||||||
| chr11:401629 | G | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0089 a0001c0004t0001g0196 others(3): Show |
6 | HG02004.hp1 HG02056.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+924G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401629 | |||||||
| chr11:401629 | G | GACCCGCT others(223): Show |
1 | a0001c0002t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1737+924_1737+925i others(232): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401629 | |||||||
| chr11:401629 | G | GACCCGCT others(145): Show |
1 | a0002c0013t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+924_1737+925i others(154): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401629 | |||||||
| chr11:401629 | G | GACCCGCT others(177): Show |
5 | a0001c0003t0001g0139 a0001c0003t0001g0143 a0001c0003t0001g0151 others(2): Show |
5 | HG00673.hp1 HG01256.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+924_1737+925i others(186): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401629 | |||||||
| chr11:401629 | G | GACCCGCT others(144): Show |
3 | a0001c0002t0001g0132 a0001c0002t0001g0133 a0001c0002t0001g0138 |
3 | HG00099.hp2 HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1737+924_1737+925i others(153): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401629 | |||||||
| chr11:401629 | G | GACCCGCT others(146): Show |
1 | a0010c0017t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1737+924_1737+925i others(155): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401629 | |||||||
| chr11:401629 | G | GCCCCGCT others(271): Show |
1 | a0014c0034t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1737+924_1737+925i others(280): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401629 | |||||||
| chr11:401629 | GGCCCCGC others(24): Show |
G | 1 | a0001c0005t0001g0085 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1737+936_1737+966d others(33): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401629 | ||||||
| chr11:401630 | G | A | 2 | a0001c0005t0001g0023 a0001c0005t0001g0032 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1737+925G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401630 | |||||||
| chr11:401630 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1737+925G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401630 | |||||||
| chr11:401630 | GCCCCGCT others(25): Show |
G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0083 |
2 | HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1737+929_1737+960d others(34): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401630 | ||||||
| chr11:401631 | C | A | 12 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0003t0001g0097 others(9): Show |
12 | HG00733.hp2 HG02056.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+926C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401631 | |||||||
| chr11:401640 | CA | C | 19 | a0001c0001t0001g0018 a0001c0001t0001g0089 a0001c0001t0001g0177 others(16): Show |
19 | HG01243.hp2 HG01952.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.1737+936delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401640 | |||||||
| chr11:401641 | A | ACCCGCCC others(69): Show |
1 | a0001c0003t0001g0142 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1737+940_1737+941i others(78): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401641 | ||||||
| chr11:401641 | A | ACCCGGCC others(350): Show |
1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1737+955_1737+956i others(359): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401641 | ||||||
| chr11:401641 | A | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(104): Show |
110 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1737+936A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401641 | |||||||
| chr11:401644 | C | CGCCCCGC others(85): Show |
1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1737+940_1737+941i others(94): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401644 | ||||||
| chr11:401644 | C | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(61): Show |
67 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.1737+939C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401644 | |||||||
| chr11:401644 | C | T | 1 | a0001c0005t0001g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1737+939C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401644 | |||||||
| chr11:401644 | CG | C | 14 | a0001c0001t0001g0028 a0001c0002t0001g0104 a0001c0002t0001g0148 others(11): Show |
14 | HG00544.hp1 HG01981.hp1 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.1737+941delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401644 | ||||||
| chr11:401645 | G | A | 3 | a0001c0002t0001g0101 a0001c0002t0001g0126 a0001c0028t0001g0128 |
3 | HG01069.hp2 HG03492.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1737+940G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401645 | |||||||
| chr11:401645 | G | C | 6 | a0001c0001t0001g0039 a0001c0003t0001g0096 a0001c0003t0001g0097 others(3): Show |
6 | HG00621.hp1 HG01243.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+940G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401645 | |||||||
| chr11:401645 | G | GCCCCGCT others(69): Show |
1 | a0001c0003t0001g0158 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1737+940_1737+941i others(78): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401645 | |||||||
| chr11:401645 | G | GCCCCGCT others(69): Show |
3 | a0001c0003t0001g0099 a0001c0003t0001g0112 a0001c0003t0001g0115 |
3 | HG01358.hp2 NA18612.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1737+940_1737+941i others(78): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401645 | |||||||
| chr11:401645 | G | GCCCCGCT others(69): Show |
1 | a0001c0002t0001g0172 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1737+940_1737+941i others(78): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401645 | |||||||
| chr11:401645 | G | GGCCCCGC others(65): Show |
1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1737+966_1737+967i others(74): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401645 | ||||||
| chr11:401646 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(73): Show |
79 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1737+941G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401646 | |||||||
| chr11:401646 | GC | G | 6 | a0001c0001t0001g0016 a0001c0007t0001g0008 a0001c0007t0001g0009 others(3): Show |
6 | HG00733.hp2 HG02056.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+945delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401646 | ||||||
| chr11:401647 | C | A | 3 | a0001c0001t0001g0028 a0001c0003t0001g0097 a0001c0003t0001g0114 |
3 | HG03453.hp2 HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1737+942C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401647 | |||||||
| chr11:401657 | A | C | 34 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(31): Show |
34 | HG00621.hp1 HG00733.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1737+952A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401657 | |||||||
| chr11:401660 | C | A | 4 | a0001c0001t0001g0089 a0001c0004t0001g0196 a0003c0019t0001g0181 others(1): Show |
4 | HG03471.hp2 HG03540.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+955C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401660 | |||||||
| chr11:401660 | C | CG | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(84): Show |
90 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1737+956dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401660 | ||||||
| chr11:401660 | C | CGCCCCGC others(55): Show |
2 | a0001c0003t0001g0111 a0001c0003t0001g0113 |
2 | HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1737+966_1737+967i others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401660 | ||||||
| chr11:401660 | C | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0177 a0001c0001t0001g0179 others(3): Show |
6 | HG02717.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+955C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401660 | |||||||
| chr11:401662 | C | A | 21 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0048 others(18): Show |
21 | HG00733.hp2 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1737+957C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401662 | |||||||
| chr11:401665 | C | T | 2 | a0001c0001t0001g0178 a0001c0008t0001g0192 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1737+960C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401665 | |||||||
| chr11:401670 | A | ACACCCGC others(71): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1737+966_1737+967i others(80): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401670 | ||||||
| chr11:401670 | A | ACACCCGC others(71): Show |
2 | a0001c0002t0001g0127 a0001c0002t0001g0169 |
2 | NA19065.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1737+966_1737+967i others(80): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401670 | ||||||
| chr11:401670 | A | ACACCCGG others(134): Show |
1 | a0001c0003t0001g0003 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1737+966_1737+967i others(143): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401670 | ||||||
| chr11:401670 | A | ACACCCGG others(133): Show |
1 | a0001c0003t0001g0003 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1737+966_1737+967i others(142): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401670 | ||||||
| chr11:401671 | C | CA | 8 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0002t0001g0125 others(5): Show |
8 | HG01261.hp1 HG01943.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1737+966_1737+967i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401671 | |||||||
| chr11:401672 | C | A | 59 | a0001c0001t0001g0089 a0001c0001t0001g0177 a0001c0001t0001g0178 others(56): Show |
60 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1737+967C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401672 | |||||||
| chr11:401672 | C | CCCCAGCC others(9): Show |
1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1737+970_1737+971i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401672 | ||||||
| chr11:401675 | C | A | 1 | a0001c0003t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1737+970C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401675 | |||||||
| chr11:401675 | C | CG | 42 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0039 others(39): Show |
42 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1737+971dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401675 | ||||||
| chr11:401675 | C | G | 17 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0076 others(14): Show |
18 | HG00733.hp1 HG01175.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1737+970C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401675 | |||||||
| chr11:401677 | C | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0083 |
2 | HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1737+972C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401677 | |||||||
| chr11:401677 | C | G | 1 | a0001c0003t0001g0096 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1737+972C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401677 | |||||||
| chr11:401687 | C | A | 45 | a0001c0001t0001g0039 a0001c0002t0001g0004 a0001c0002t0001g0100 others(42): Show |
46 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1737+982C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401687 | |||||||
| chr11:401689 | C | A | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1737+984C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401689 | |||||||
| chr11:401689 | C | G | 9 | a0001c0001t0001g0016 a0001c0004t0001g0196 a0001c0007t0001g0008 others(6): Show |
9 | HG00733.hp2 HG02056.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+984C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401689 | |||||||
| chr11:401690 | C | G | 15 | a0001c0001t0001g0089 a0001c0001t0001g0177 a0001c0001t0001g0179 others(12): Show |
15 | HG02027.hp1 HG02717.hp2 HG03209.hp1 others(12): Show |
intron_variant | MODIFIER | c.1737+985C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401690 | |||||||
| chr11:401690 | CG | C | 34 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0081 others(31): Show |
35 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1737+987delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401690 | ||||||
| chr11:401691 | G | C | 2 | a0001c0003t0001g0140 a0001c0008t0001g0188 |
2 | HG01952.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1737+986G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401691 | |||||||
| chr11:401692 | G | A | 11 | a0001c0001t0001g0028 a0001c0001t0001g0076 a0001c0001t0001g0089 others(8): Show |
11 | HG01192.hp1 HG02717.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.1737+987G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401692 | |||||||
| chr11:401692 | G | C | 1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1737+987G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401692 | |||||||
| chr11:401692 | GC | G | 6 | a0001c0002t0001g0124 a0001c0003t0001g0095 a0001c0003t0001g0098 others(3): Show |
6 | HG01952.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+991delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401692 | ||||||
| chr11:401693 | C | A | 17 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0003t0001g0097 others(14): Show |
17 | HG00621.hp1 HG00733.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1737+988C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401693 | |||||||
| chr11:401693 | C | G | 1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+988C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401693 | |||||||
| chr11:401694 | C | G | 4 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0173 others(1): Show |
4 | HG02135.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+989C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401694 | |||||||
| chr11:401697 | G | A | 11 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0064 others(8): Show |
11 | HG01261.hp2 HG02145.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.1737+992G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401697 | |||||||
| chr11:401701 | A | AC | 5 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0202 others(2): Show |
5 | HG01243.hp1 HG01496.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+1001dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401701 | ||||||
| chr11:401701 | AC | A | 12 | a0001c0001t0001g0039 a0001c0001t0001g0178 a0001c0004t0001g0012 others(9): Show |
12 | HG00621.hp1 HG01243.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+1001delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401701 | ||||||
| chr11:401702 | C | CACCCGCC others(101): Show |
2 | a0001c0002t0001g0131 a0001c0002t0001g0137 |
2 | HG00639.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1737+997_1737+998i others(110): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401702 | |||||||
| chr11:401703 | C | A | 39 | a0001c0001t0001g0028 a0001c0001t0001g0076 a0001c0001t0001g0089 others(36): Show |
39 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1737+998C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401703 | |||||||
| chr11:401705 | C | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0083 |
2 | HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1737+1000C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401705 | |||||||
| chr11:401706 | C | G | 1 | a0001c0003t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1737+1001C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401706 | |||||||
| chr11:401706 | CG | C | 27 | a0001c0001t0001g0028 a0001c0001t0001g0076 a0001c0001t0001g0177 others(24): Show |
27 | HG00609.hp1 HG00673.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.1737+1003delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401706 | ||||||
| chr11:401707 | G | A | 1 | a0001c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1737+1002G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401707 | |||||||
| chr11:401707 | G | GCCCCGCT others(22): Show |
1 | a0009c0033t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1737+1002_1737+100 others(33): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401707 | |||||||
| chr11:401707 | G | GCCCCGCT others(23): Show |
1 | a0001c0002t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1737+1002_1737+100 others(34): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401707 | |||||||
| chr11:401708 | G | A | 9 | a0001c0001t0001g0056 a0001c0003t0001g0097 a0001c0004t0001g0012 others(6): Show |
9 | HG01175.hp1 HG02027.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+1003G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401708 | |||||||
| chr11:401708 | G | GA | 2 | a0001c0002t0001g0131 a0001c0002t0001g0137 |
2 | HG00639.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1737+1003_1737+100 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401708 | |||||||
| chr11:401708 | G | GCCCCGCT others(466): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1737+1013_1737+101 others(477): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401708 | ||||||
| chr11:401709 | C | A | 11 | a0001c0001t0001g0028 a0001c0001t0001g0076 a0001c0001t0001g0080 others(8): Show |
11 | HG00609.hp1 HG01192.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1737+1004C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401709 | |||||||
| chr11:401715 | T | C | 1 | a0001c0003t0001g0003 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1737+1010T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401715 | |||||||
| chr11:401716 | CACCCCCG others(85): Show |
C | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1737+1019_1737+111 others(96): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401716 | ||||||
| chr11:401716 | CACCCCCG others(280): Show |
C | 5 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0004t0001g0176 others(2): Show |
5 | HG02717.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+1017_1738-107 others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401716 | ||||||
| chr11:401717 | ACCCCCGA others(156): Show |
A | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1737+1017_1737+117 others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401717 | ||||||
| chr11:401719 | C | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(104): Show |
111 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1737+1014C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401719 | |||||||
| chr11:401721 | C | G | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1737+1016C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401721 | |||||||
| chr11:401722 | C | CGGCCCCG others(9): Show |
3 | a0001c0003t0001g0111 a0001c0003t0001g0112 a0001c0003t0001g0113 |
3 | HG01981.hp1 HG02273.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1737+1018_1737+101 others(20): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401722 | ||||||
| chr11:401722 | C | G | 12 | a0001c0001t0001g0209 a0001c0003t0001g0003 a0001c0003t0001g0097 others(9): Show |
13 | HG01256.hp2 HG01258.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1737+1017C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401722 | |||||||
| chr11:401723 | GA | G | 43 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0048 others(40): Show |
44 | HG00544.hp1 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1737+1019delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401723 | |||||||
| chr11:401724 | A | G | 58 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0039 others(55): Show |
58 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1737+1019A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401724 | |||||||
| chr11:401724 | AC | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(71): Show |
77 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1737+1023delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401724 | ||||||
| chr11:401724 | ACCCCGCT others(10): Show |
A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0005t0001g0084 others(1): Show |
4 | HG02135.hp1 HG02148.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+1023_1737+103 others(21): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401724 | ||||||
| chr11:401731 | T | C | 3 | a0001c0003t0001g0099 a0001c0003t0001g0115 a0001c0003t0001g0116 |
3 | HG01358.hp2 HG02148.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1737+1026T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401731 | |||||||
| chr11:401733 | AC | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(61): Show |
67 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1737+1033delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401733 | ||||||
| chr11:401735 | C | A | 35 | a0001c0001t0001g0029 a0001c0001t0001g0080 a0001c0001t0001g0081 others(32): Show |
35 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1737+1030C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401735 | |||||||
| chr11:401738 | C | G | 23 | a0001c0001t0001g0016 a0001c0002t0001g0101 a0001c0002t0001g0118 others(20): Show |
23 | HG00733.hp1 HG00733.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1737+1033C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401738 | |||||||
| chr11:401738 | CGACCCCG others(171): Show |
C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0083 |
2 | HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1737+1035_1738-116 others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401738 | ||||||
| chr11:401738 | CGACCCCG others(706): Show |
C | 5 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(2): Show |
5 | HG03471.hp1 NA18906.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+1035_1738-626 others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401738 | ||||||
| chr11:401739 | G | A | 11 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0125 others(8): Show |
12 | HG00642.hp2 HG02074.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+1034G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401739 | |||||||
| chr11:401739 | G | C | 2 | a0001c0001t0001g0082 a0001c0003t0001g0166 |
2 | HG02135.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1737+1034G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401739 | |||||||
| chr11:401739 | G | GCCCCGCT others(162): Show |
1 | a0001c0003t0001g0096 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1737+1034_1737+103 others(173): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401739 | |||||||
| chr11:401739 | GA | G | 23 | a0001c0001t0001g0078 a0001c0002t0001g0132 a0001c0002t0001g0133 others(20): Show |
23 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1737+1035delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401739 | |||||||
| chr11:401740 | A | C | 1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+1035A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401740 | |||||||
| chr11:401740 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(116): Show |
123 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.1737+1035A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401740 | |||||||
| chr11:401740 | AC | A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0048 others(8): Show |
11 | HG02145.hp1 HG02300.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1737+1039delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401740 | ||||||
| chr11:401741 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1737+1036C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401741 | |||||||
| chr11:401745 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0076 |
2 | HG01192.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1737+1040G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401745 | |||||||
| chr11:401747 | T | C | 1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1737+1042T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401747 | |||||||
| chr11:401750 | CCCCCGCC others(84): Show |
C | 1 | a0001c0001t0001g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1737+1051_1737+114 others(95): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401750 | ||||||
| chr11:401750 | CCCCCGCC others(154): Show |
C | 1 | a0001c0001t0001g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1737+1051_1738-116 others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401750 | ||||||
| chr11:401751 | C | A | 66 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0048 others(63): Show |
67 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1737+1046C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401751 | |||||||
| chr11:401751 | CCCCGCCC others(153): Show |
C | 1 | a0001c0009t0001g0102 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1737+1050_1738-116 others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401751 | ||||||
| chr11:401753 | CCGCCCCG others(543): Show |
C | 3 | a0001c0004t0001g0196 a0003c0019t0001g0181 a0016c0035t0001g0180 |
3 | HG03471.hp2 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1737+1049_1738-775 others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401753 | |||||||
| chr11:401754 | C | CA | 2 | a0001c0003t0001g0096 a0009c0033t0001g0160 |
2 | HG01934.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1737+1049_1737+105 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401754 | |||||||
| chr11:401754 | C | CG | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(88): Show |
95 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1737+1050dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401754 | ||||||
| chr11:401754 | C | G | 12 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0044 others(9): Show |
12 | HG01358.hp2 HG01496.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+1049C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401754 | |||||||
| chr11:401754 | C | T | 1 | a0001c0003t0001g0141 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1737+1049C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401754 | |||||||
| chr11:401755 | G | GA | 4 | a0001c0003t0001g0099 a0001c0003t0001g0114 a0001c0003t0001g0115 others(1): Show |
4 | HG01358.hp2 HG01496.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+1050_1737+105 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401755 | |||||||
| chr11:401756 | C | A | 24 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0046 others(21): Show |
24 | HG00621.hp1 HG00733.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1737+1051C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401756 | |||||||
| chr11:401756 | C | G | 2 | a0001c0003t0001g0149 a0017c0027t0001g0107 |
2 | HG03834.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1737+1051C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401756 | |||||||
| chr11:401760 | G | A | 3 | a0001c0001t0001g0056 a0004c0015t0001g0047 a0008c0025t0001g0199 |
3 | HG01175.hp1 HG01891.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1737+1055G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401760 | |||||||
| chr11:401763 | CACCCCCG others(38): Show |
C | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1737+1066_1737+111 others(49): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401763 | ||||||
| chr11:401763 | CACCCCCG others(108): Show |
C | 1 | a0001c0007t0001g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1737+1066_1737+118 others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401763 | ||||||
| chr11:401765 | C | CA | 11 | a0001c0002t0001g0100 a0001c0002t0001g0110 a0001c0002t0001g0148 others(8): Show |
11 | HG00544.hp1 HG00639.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1737+1060_1737+106 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401765 | |||||||
| chr11:401765 | CCCCCGCC others(14): Show |
C | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1737+1065_1737+108 others(25): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401765 | ||||||
| chr11:401766 | C | A | 27 | a0001c0001t0001g0078 a0001c0002t0001g0124 a0001c0002t0001g0133 others(24): Show |
27 | HG00609.hp1 HG00673.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1737+1061C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401766 | |||||||
| chr11:401766 | CCCCGCCC others(36): Show |
C | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1737+1065_1737+110 others(47): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401766 | ||||||
| chr11:401769 | C | CG | 50 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0044 others(47): Show |
52 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1737+1065dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401769 | ||||||
| chr11:401769 | C | G | 21 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0209 others(18): Show |
21 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1737+1064C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401769 | |||||||
| chr11:401769 | CGCCCCGC others(16): Show |
C | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1737+1104_1737+112 others(27): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401769 | ||||||
| chr11:401770 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0209 |
2 | HG02647.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1737+1065G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401770 | |||||||
| chr11:401770 | G | GA | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(57): Show |
63 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1737+1065_1737+106 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401770 | |||||||
| chr11:401770 | GCCCCGCT others(934): Show |
G | 1 | a0001c0008t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1737+1066_1738-367 others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401770 | |||||||
| chr11:401771 | C | A | 6 | a0001c0001t0001g0078 a0001c0002t0001g0104 a0001c0002t0001g0131 others(3): Show |
6 | HG00639.hp2 HG01261.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+1066C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401771 | |||||||
| chr11:401771 | C | G | 13 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0070 others(10): Show |
13 | HG00642.hp1 HG02145.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.1737+1066C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401771 | |||||||
| chr11:401778 | CACCCCCG | C | 2 | a0001c0008t0001g0188 a0017c0027t0001g0107 |
2 | HG02622.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1737+1081_1737+108 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401778 | ||||||
| chr11:401778 | CACCCCCG others(23): Show |
C | 1 | a0001c0011t0001g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1737+1081_1737+111 others(34): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401778 | ||||||
| chr11:401779 | ACCCCCGA others(1): Show |
A | 7 | a0001c0001t0001g0016 a0001c0003t0001g0114 a0001c0007t0001g0008 others(4): Show |
7 | HG00733.hp2 HG02056.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+1079_1737+108 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401779 | ||||||
| chr11:401781 | C | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(80): Show |
86 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1737+1076C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401781 | |||||||
| chr11:401784 | C | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0209 a0001c0002t0001g0104 |
3 | HG02647.hp1 HG03688.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1737+1079C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401784 | |||||||
| chr11:401784 | CGACCCCC others(257): Show |
C | 2 | a0001c0001t0001g0056 a0004c0015t0001g0047 |
2 | HG01175.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1737+1081_1738-102 others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401784 | ||||||
| chr11:401785 | G | A | 2 | a0001c0002t0001g0133 a0001c0002t0001g0138 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1737+1080G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401785 | G | GACCCGCT others(1): Show |
7 | a0001c0002t0001g0100 a0001c0002t0001g0159 a0001c0003t0001g0097 others(4): Show |
7 | HG00639.hp1 HG01891.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+1084_1737+108 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401785 | ||||||
| chr11:401785 | G | GCCCCGCT others(1): Show |
10 | a0001c0002t0001g0132 a0001c0002t0001g0148 a0001c0003t0001g0142 others(7): Show |
10 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1737+1080_1737+108 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401785 | G | GCCCCGCT others(32): Show |
1 | a0010c0017t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1737+1080_1737+108 others(43): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401785 | G | GCCCGCTC others(354): Show |
1 | a0001c0003t0001g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1737+1080_1737+108 others(365): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401785 | G | GGCCCCCG others(3): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1737+1080_1737+108 others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401785 | G | GGCCCCGC others(2): Show |
17 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0125 others(14): Show |
18 | HG00642.hp2 HG01496.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.1737+1080_1737+108 others(13): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401785 | G | GGCCCCGC others(155): Show |
1 | a0001c0010t0001g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1737+1080_1737+108 others(166): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401785 | G | GGCCCCGC others(149): Show |
1 | a0019c0032t0001g0144 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1737+1080_1737+108 others(160): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401785 | G | GGCCCCGC others(172): Show |
3 | a0001c0003t0001g0095 a0001c0003t0001g0098 a0001c0003t0001g0147 |
3 | HG01952.hp1 HG01975.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1737+1080_1737+108 others(183): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401785 | G | GGCCCCGC others(277): Show |
1 | a0001c0002t0001g0169 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1737+1080_1737+108 others(288): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401785 | G | GGCCCGCT others(687): Show |
1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1737+1080_1737+108 others(698): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401785 | |||||||
| chr11:401786 | A | C | 2 | a0001c0002t0001g0168 a0001c0008t0001g0093 |
2 | HG03209.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1737+1081A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401786 | |||||||
| chr11:401786 | A | G | 25 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0124 others(22): Show |
25 | HG00609.hp1 HG00733.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1737+1081A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401786 | |||||||
| chr11:401786 | ACCCCCGG | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0044 others(5): Show |
8 | HG02135.hp1 HG02148.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1737+1086_1737+109 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401786 | ||||||
| chr11:401786 | ACCCCCGG others(1): Show |
A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(56): Show |
62 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1737+1085_1737+109 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401786 | ||||||
| chr11:401786 | ACCCCCGG others(55): Show |
A | 3 | a0001c0001t0001g0070 a0001c0007t0001g0025 a0001c0021t0001g0086 |
3 | HG02622.hp2 HG03834.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1737+1085_1737+114 others(66): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401786 | ||||||
| chr11:401786 | ACCCCCGG others(141): Show |
A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0183 a0001c0006t0001g0035 others(1): Show |
4 | HG02145.hp1 HG02300.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+1085_1738-114 others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401786 | ||||||
| chr11:401786 | ACCCCCGG others(218): Show |
A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0082 |
2 | HG03927.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1737+1085_1738-106 others(4): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401786 | ||||||
| chr11:401787 | C | CCCCGCTC others(1): Show |
6 | a0001c0002t0001g0126 a0001c0002t0001g0172 a0001c0003t0001g0099 others(3): Show |
6 | HG01358.hp2 HG02683.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+1085_1737+108 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401787 | C | CCCCGCTC others(92): Show |
1 | a0001c0002t0001g0127 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1737+1085_1737+108 others(103): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401787 | C | CCCCGCTC others(446): Show |
2 | a0001c0002t0001g0101 a0001c0028t0001g0128 |
2 | HG01069.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1737+1085_1737+108 others(457): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401787 | C | CCCCGCTC others(431): Show |
1 | a0001c0002t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1737+1085_1737+108 others(442): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401787 | C | CCCCGCTC others(449): Show |
1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1737+1085_1737+108 others(460): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401787 | C | CCCGCTCA | 4 | a0001c0002t0001g0130 a0001c0003t0001g0111 a0001c0003t0001g0112 others(1): Show |
4 | HG01981.hp1 HG02273.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+1084_1737+108 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401787 | C | CCCGCTCA others(437): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1737+1084_1737+108 others(448): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401787 | C | CCCGCTCA others(430): Show |
1 | a0001c0003t0001g0003 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1737+1084_1737+108 others(441): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401787 | C | CCCGCTCA others(415): Show |
1 | a0001c0002t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1737+1084_1737+108 others(426): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401787 | C | CCCGCTCA others(415): Show |
1 | a0001c0002t0001g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1737+1084_1737+108 others(426): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401787 | C | CCCGCTCA others(431): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1737+1084_1737+108 others(442): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401787 | ||||||
| chr11:401788 | C | A | 4 | a0001c0002t0001g0148 a0001c0002t0001g0169 a0001c0003t0001g0105 others(1): Show |
4 | HG00544.hp1 NA18952.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+1083C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401788 | |||||||
| chr11:401789 | C | CCGCTCAC others(1): Show |
4 | a0001c0002t0001g0133 a0001c0002t0001g0138 a0001c0030t0001g0174 others(1): Show |
4 | HG02559.hp2 HG03017.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+1085_1737+108 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401789 | ||||||
| chr11:401789 | C | CCGCTCAC others(140): Show |
1 | a0001c0003t0001g0154 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1737+1085_1737+108 others(151): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401789 | ||||||
| chr11:401789 | C | CGCTCACA | 8 | a0001c0001t0001g0028 a0001c0002t0001g0145 a0001c0002t0001g0146 others(5): Show |
8 | HG00609.hp1 HG01256.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1737+1084_1737+108 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401789 | |||||||
| chr11:401789 | C | CGCTCACA others(62): Show |
1 | a0014c0034t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1737+1084_1737+108 others(73): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401789 | |||||||
| chr11:401789 | C | CGCTCACC others(309): Show |
1 | a0001c0002t0001g0110 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1737+1084_1737+108 others(320): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401789 | |||||||
| chr11:401791 | C | G | 2 | a0001c0001t0001g0205 a0001c0003t0001g0097 |
2 | HG01069.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1737+1086C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401791 | |||||||
| chr11:401792 | G | A | 6 | a0001c0002t0001g0132 a0001c0007t0001g0008 a0001c0007t0001g0009 others(3): Show |
6 | HG00099.hp2 HG00733.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+1087G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401792 | |||||||
| chr11:401792 | G | C | 26 | a0001c0001t0001g0028 a0001c0002t0001g0110 a0001c0002t0001g0126 others(23): Show |
26 | HG00609.hp1 HG01256.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.1737+1087G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401792 | |||||||
| chr11:401792 | G | GCTCACAC others(353): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+1087_1737+108 others(364): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401792 | |||||||
| chr11:401792 | G | GCTCACAC others(158): Show |
1 | a0001c0002t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1737+1087_1737+108 others(169): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401792 | |||||||
| chr11:401793 | G | A | 13 | a0001c0001t0001g0089 a0001c0001t0001g0205 a0001c0001t0001g0209 others(10): Show |
14 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1737+1088G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401793 | |||||||
| chr11:401793 | G | GCCCCGCT others(63): Show |
1 | a0001c0006t0001g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1738-1176_1738-110 others(74): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401793 | ||||||
| chr11:401794 | C | A | 12 | a0001c0001t0001g0028 a0001c0002t0001g0126 a0001c0002t0001g0127 others(9): Show |
12 | HG01358.hp2 HG01981.hp1 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+1089C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401794 | |||||||
| chr11:401794 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1737+1089C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401794 | |||||||
| chr11:401795 | C | T | 1 | a0001c0008t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1737+1090C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401795 | |||||||
| chr11:401801 | CACCCCCG | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(59): Show |
65 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1737+1104_1737+111 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401801 | ||||||
| chr11:401804 | C | A | 24 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0044 others(21): Show |
24 | HG00099.hp2 HG00544.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1737+1099C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401804 | |||||||
| chr11:401807 | C | CCGGCCCC others(3): Show |
1 | a0001c0003t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1737+1102_1737+110 others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401807 | |||||||
| chr11:401807 | C | G | 19 | a0001c0002t0001g0100 a0001c0002t0001g0101 a0001c0002t0001g0118 others(16): Show |
20 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1737+1102C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401807 | |||||||
| chr11:401807 | CGACCCCC others(1): Show |
C | 6 | a0001c0005t0001g0023 a0001c0007t0001g0008 a0001c0007t0001g0009 others(3): Show |
6 | HG00733.hp2 HG02056.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+1104_1737+111 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401807 | ||||||
| chr11:401808 | G | C | 1 | a0001c0003t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1737+1103G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GACCCGCT others(1): Show |
10 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0044 others(7): Show |
10 | HG01358.hp2 HG02135.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.1737+1107_1737+110 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401808 | ||||||
| chr11:401808 | G | GACCCGCT others(17): Show |
1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1737+1107_1737+110 others(28): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401808 | ||||||
| chr11:401808 | G | GCCCCGCT others(1): Show |
3 | a0001c0002t0001g0132 a0001c0003t0001g0097 a0002c0013t0001g0108 |
3 | HG00099.hp2 HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1737+1103_1737+110 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GCCCCGCT others(326): Show |
1 | a0001c0002t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(337): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GCCCCGCT others(279): Show |
2 | a0001c0003t0001g0161 a0001c0003t0001g0162 |
2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1737+1103_1737+110 others(290): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GCCCCGCT others(309): Show |
1 | a0001c0016t0001g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(320): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GCCCCGCT others(309): Show |
1 | a0001c0002t0001g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(320): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GCCCCGCT others(155): Show |
1 | a0001c0003t0001g0105 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(166): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GCCCCGCT others(730): Show |
1 | a0001c0003t0001g0149 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(741): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GCCCCGCT others(48): Show |
1 | a0001c0003t0001g0142 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(59): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGCCCCCG others(3): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGCCCCGC others(313): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(324): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGCCCCGC others(2): Show |
15 | a0001c0002t0001g0104 a0001c0002t0001g0110 a0001c0002t0001g0124 others(12): Show |
15 | HG00609.hp1 HG01261.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1737+1103_1737+110 others(13): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGCCCCGC others(125): Show |
2 | a0001c0002t0001g0148 a0001c0003t0001g0155 |
2 | HG00544.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1737+1103_1737+110 others(136): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGCCCCGC others(420): Show |
1 | a0001c0003t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(431): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGCCCCGC others(62): Show |
2 | a0001c0004t0001g0073 a0001c0004t0001g0074 |
2 | NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1737+1103_1737+110 others(73): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGCCCCGC others(325): Show |
1 | a0012c0020t0001g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(336): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGCCCCGC others(34): Show |
1 | a0009c0033t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(45): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGCCCCGC others(759): Show |
1 | a0001c0003t0001g0153 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(770): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGCCCCGC others(743): Show |
1 | a0001c0003t0001g0139 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(754): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401808 | G | GGGCCCCG others(3): Show |
1 | a0019c0032t0001g0144 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1737+1103_1737+110 others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401808 | |||||||
| chr11:401809 | A | C | 4 | a0001c0003t0001g0151 a0001c0008t0001g0188 a0001c0030t0001g0174 others(1): Show |
4 | HG01943.hp1 HG01943.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+1104A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401809 | |||||||
| chr11:401809 | A | G | 8 | a0001c0001t0001g0028 a0001c0002t0001g0168 a0001c0003t0001g0111 others(5): Show |
8 | HG00642.hp1 HG01981.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.1737+1104A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401809 | |||||||
| chr11:401809 | ACCCCCGG others(32): Show |
A | 1 | a0001c0001t0001g0078 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1737+1108_1737+114 others(43): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401809 | ||||||
| chr11:401810 | C | CCCGCTCA | 16 | a0001c0001t0001g0028 a0001c0002t0001g0004 a0001c0002t0001g0103 others(13): Show |
17 | HG00642.hp2 HG01496.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1737+1107_1737+110 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401810 | ||||||
| chr11:401811 | C | A | 2 | a0001c0003t0001g0097 a0001c0008t0001g0093 |
2 | HG03209.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1737+1106C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401811 | |||||||
| chr11:401812 | C | CCGCTCAC others(1): Show |
6 | a0001c0002t0001g0168 a0001c0003t0001g0111 a0001c0003t0001g0112 others(3): Show |
6 | HG00642.hp1 HG01981.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+1108_1737+110 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401812 | ||||||
| chr11:401812 | C | CGCTCACA | 6 | a0001c0001t0001g0016 a0001c0002t0001g0169 a0001c0003t0001g0151 others(3): Show |
6 | HG01943.hp2 HG02129.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+1107_1737+110 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401812 | |||||||
| chr11:401813 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1737+1108C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401813 | |||||||
| chr11:401814 | C | G | 6 | a0001c0002t0001g0126 a0001c0002t0001g0172 a0001c0003t0001g0099 others(3): Show |
6 | HG01358.hp2 HG02027.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+1109C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401814 | |||||||
| chr11:401815 | G | A | 1 | a0001c0002t0001g0127 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1737+1110G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401815 | |||||||
| chr11:401815 | G | C | 17 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0002t0001g0168 others(14): Show |
17 | HG00642.hp1 HG01496.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1737+1110G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401815 | |||||||
| chr11:401816 | G | A | 12 | a0001c0001t0001g0089 a0001c0001t0001g0209 a0001c0002t0001g0101 others(9): Show |
13 | HG00639.hp2 HG00733.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1737+1111G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401816 | |||||||
| chr11:401816 | G | GA | 12 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0125 others(9): Show |
13 | HG00642.hp2 HG02074.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.1737+1111_1737+111 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401816 | |||||||
| chr11:401817 | C | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0046 others(4): Show |
7 | HG01496.hp1 HG02129.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+1112C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401817 | |||||||
| chr11:401821 | G | A | 2 | a0001c0007t0001g0007 a0001c0011t0001g0063 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1737+1116G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401821 | |||||||
| chr11:401826 | C | CA | 2 | a0001c0001t0001g0060 a0001c0003t0001g0143 |
2 | HG00673.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1737+1121_1737+112 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401826 | |||||||
| chr11:401827 | C | A | 20 | a0001c0001t0001g0089 a0001c0001t0001g0209 a0001c0002t0001g0126 others(17): Show |
20 | HG00609.hp1 HG00642.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1737+1122C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401827 | |||||||
| chr11:401827 | CCCCGGCT others(7): Show |
C | 1 | a0001c0006t0001g0049 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1737+1126_1737+113 others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401827 | ||||||
| chr11:401829 | C | G | 5 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0007t0001g0208 others(2): Show |
5 | HG00733.hp2 HG02056.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+1124C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401829 | |||||||
| chr11:401830 | C | G | 10 | a0001c0003t0001g0116 a0001c0003t0001g0166 a0001c0007t0001g0008 others(7): Show |
10 | HG00733.hp2 HG01496.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.1737+1125C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401830 | |||||||
| chr11:401830 | CG | C | 11 | a0001c0001t0001g0089 a0001c0001t0001g0209 a0001c0002t0001g0136 others(8): Show |
11 | HG00609.hp1 HG01358.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1737+1127delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401830 | ||||||
| chr11:401830 | CGGCTCCA others(9): Show |
C | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1737+1127_1737+114 others(20): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401830 | ||||||
| chr11:401831 | G | A | 1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1737+1126G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401831 | |||||||
| chr11:401831 | G | C | 1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1737+1126G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401831 | |||||||
| chr11:401832 | G | A | 15 | a0001c0002t0001g0104 a0001c0002t0001g0126 a0001c0002t0001g0127 others(12): Show |
15 | HG01981.hp1 HG02056.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1737+1127G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401832 | |||||||
| chr11:401832 | G | C | 2 | a0001c0007t0001g0208 a0001c0012t0001g0120 |
2 | HG00733.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.1737+1127G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401832 | |||||||
| chr11:401833 | CT | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0002t0001g0104 others(8): Show |
11 | HG01981.hp1 HG02129.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1737+1129delT | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401833 | |||||||
| chr11:401834 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(139): Show |
146 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1737+1129T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401834 | |||||||
| chr11:401834 | T | G | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1737+1129T>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401834 | |||||||
| chr11:401834 | T | TCACACCC others(3): Show |
3 | a0001c0002t0001g0172 a0001c0003t0001g0097 a0001c0003t0001g0158 |
3 | HG02683.hp2 HG02897.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1737+1130_1737+113 others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401834 | ||||||
| chr11:401837 | A | G | 92 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0046 others(89): Show |
93 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1737+1132A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401837 | |||||||
| chr11:401839 | T | C | 5 | a0001c0003t0001g0095 a0001c0003t0001g0096 a0001c0003t0001g0098 others(2): Show |
5 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+1134T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401839 | |||||||
| chr11:401840 | G | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(154): Show |
161 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.1737+1135G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401840 | |||||||
| chr11:401841 | A | AC | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(86): Show |
93 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1737+1140dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401841 | ||||||
| chr11:401841 | A | ACCCCCGA others(423): Show |
1 | a0001c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1737+1140_1737+114 others(434): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401841 | ||||||
| chr11:401841 | A | ACCCCCGG others(23): Show |
1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1737+1140_1737+114 others(34): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401841 | ||||||
| chr11:401843 | C | A | 26 | a0001c0001t0001g0046 a0001c0002t0001g0126 a0001c0002t0001g0145 others(23): Show |
26 | HG00609.hp1 HG00733.hp2 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.1737+1138C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401843 | |||||||
| chr11:401846 | G | C | 52 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0002t0001g0100 others(49): Show |
52 | HG00544.hp1 HG00609.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1737+1141G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401846 | |||||||
| chr11:401846 | G | T | 1 | a0001c0008t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1737+1141G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401846 | |||||||
| chr11:401847 | G | GA | 5 | a0001c0002t0001g0127 a0001c0003t0001g0095 a0001c0003t0001g0096 others(2): Show |
5 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+1142_1737+114 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401847 | |||||||
| chr11:401848 | C | A | 35 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0002t0001g0100 others(32): Show |
35 | HG00544.hp1 HG00639.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.1737+1143C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401848 | |||||||
| chr11:401851 | C | T | 1 | a0001c0002t0001g0127 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1737+1146C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401851 | |||||||
| chr11:401852 | G | A | 2 | a0001c0001t0001g0195 a0001c0006t0001g0049 |
2 | HG01175.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1737+1147G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401852 | |||||||
| chr11:401855 | C | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0209 |
2 | HG02647.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1737+1150C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401855 | |||||||
| chr11:401857 | C | CCCCCGGC others(8): Show |
1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1737+1155_1737+115 others(19): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401857 | ||||||
| chr11:401858 | C | A | 14 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0003t0001g0099 others(11): Show |
14 | HG00642.hp1 HG01358.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1737+1153C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401858 | |||||||
| chr11:401860 | CG | C | 12 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0130 others(9): Show |
13 | HG00639.hp2 HG00733.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1737+1157delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401860 | ||||||
| chr11:401861 | G | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(119): Show |
126 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1737+1156G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401861 | |||||||
| chr11:401862 | GA | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(73): Show |
79 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1737+1158delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401862 | |||||||
| chr11:401863 | A | C | 1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1737+1158A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401863 | |||||||
| chr11:401863 | A | G | 26 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0070 others(23): Show |
27 | HG00609.hp1 HG00642.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1737+1158A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401863 | |||||||
| chr11:401863 | AC | A | 20 | a0001c0001t0001g0043 a0001c0001t0001g0089 a0001c0001t0001g0209 others(17): Show |
20 | HG00099.hp2 HG01358.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.1737+1162delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401863 | ||||||
| chr11:401863 | ACCCCGCT others(86): Show |
A | 1 | a0001c0006t0001g0005 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1738-1106_1738-101 others(97): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401863 | ||||||
| chr11:401864 | C | A | 1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1737+1159C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401864 | |||||||
| chr11:401864 | C | CCCCGCTC others(53): Show |
1 | a0001c0002t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1737+1168_1737+116 others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401864 | ||||||
| chr11:401864 | C | CCCGCTCA others(7): Show |
2 | a0001c0003t0001g0116 a0006c0031t0001g0163 |
2 | HG01496.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1737+1161_1737+116 others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401864 | ||||||
| chr11:401864 | C | G | 2 | a0001c0005t0001g0023 a0001c0005t0001g0032 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1737+1159C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401864 | |||||||
| chr11:401871 | CACCCCCG | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0070 others(10): Show |
13 | HG00733.hp2 HG01261.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1737+1174_1737+118 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401871 | ||||||
| chr11:401873 | CCCCCGAC others(30): Show |
C | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1737+1169_1738-116 others(41): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401873 | |||||||
| chr11:401874 | C | A | 10 | a0001c0001t0001g0028 a0001c0002t0001g0127 a0001c0002t0001g0169 others(7): Show |
10 | HG00642.hp1 HG01943.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1737+1169C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401874 | |||||||
| chr11:401877 | C | CCGGCCCC others(3): Show |
1 | a0001c0003t0001g0149 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1737+1172_1737+117 others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401877 | |||||||
| chr11:401877 | C | G | 6 | a0001c0002t0001g0110 a0001c0002t0001g0130 a0001c0002t0001g0132 others(3): Show |
6 | HG00099.hp2 HG02735.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1737+1172C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401877 | |||||||
| chr11:401877 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1737+1172C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401877 | |||||||
| chr11:401877 | CGACCCCC others(1): Show |
C | 3 | a0001c0001t0001g0195 a0001c0002t0001g0169 a0001c0006t0001g0049 |
3 | HG01175.hp2 NA19065.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1737+1174_1737+118 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401877 | ||||||
| chr11:401878 | G | C | 1 | a0001c0003t0001g0149 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1737+1173G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401878 | |||||||
| chr11:401878 | G | GACCCCGC others(2): Show |
4 | a0001c0002t0001g0110 a0001c0002t0001g0132 a0001c0003t0001g0161 others(1): Show |
4 | HG00099.hp2 HG02735.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+1178_1737+117 others(13): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401878 | ||||||
| chr11:401878 | G | GGCCCCCG others(3): Show |
1 | a0001c0016t0001g0200 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1737+1173_1737+117 others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401878 | |||||||
| chr11:401878 | G | GGCCCCGC others(2): Show |
27 | a0001c0002t0001g0100 a0001c0002t0001g0124 a0001c0002t0001g0133 others(24): Show |
27 | HG00544.hp1 HG00639.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1737+1173_1737+117 others(13): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401878 | |||||||
| chr11:401878 | G | GGCCCCGC others(373): Show |
1 | a0001c0002t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1737+1173_1737+117 others(384): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401878 | |||||||
| chr11:401878 | G | GGCCCCGC others(357): Show |
1 | a0001c0002t0001g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1737+1173_1737+117 others(368): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401878 | |||||||
| chr11:401878 | G | GGCCCCGC others(327): Show |
1 | a0001c0003t0001g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1737+1173_1737+117 others(338): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401878 | |||||||
| chr11:401878 | G | GGCCCCGC others(128): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+1173_1737+117 others(139): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401878 | |||||||
| chr11:401878 | G | GGCCCGCT others(712): Show |
1 | a0001c0003t0001g0152 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1737+1173_1737+117 others(723): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401878 | |||||||
| chr11:401879 | A | G | 3 | a0001c0002t0001g0127 a0001c0003t0001g0097 a0001c0004t0001g0027 |
3 | HG00642.hp1 NA19087.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1737+1174A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401879 | |||||||
| chr11:401879 | ACCCCCGG others(1): Show |
A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(59): Show |
65 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1737+1178_1737+118 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401879 | ||||||
| chr11:401880 | C | CCCGCTCA | 21 | a0001c0001t0001g0046 a0001c0002t0001g0104 a0001c0002t0001g0125 others(18): Show |
21 | HG01496.hp1 HG01981.hp1 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.1737+1177_1737+117 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401880 | ||||||
| chr11:401881 | C | A | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1737+1176C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401881 | |||||||
| chr11:401882 | C | CGCTCACA | 6 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0044 others(3): Show |
6 | HG02135.hp1 HG02135.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+1177_1737+117 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401882 | |||||||
| chr11:401882 | C | CGCTCACC others(186): Show |
1 | a0001c0002t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1737+1177_1737+117 others(197): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401882 | |||||||
| chr11:401882 | C | CGCTCACC others(261): Show |
1 | a0001c0003t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1737+1177_1737+117 others(272): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401882 | |||||||
| chr11:401882 | C | CGCTCACC others(355): Show |
1 | a0001c0002t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1737+1177_1737+117 others(366): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401882 | |||||||
| chr11:401882 | C | CGCTCACC others(338): Show |
1 | a0001c0002t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1737+1177_1737+117 others(349): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401882 | |||||||
| chr11:401882 | C | CGCTCACC others(184): Show |
1 | a0001c0010t0003g0021 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1737+1177_1737+117 others(195): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401882 | |||||||
| chr11:401882 | C | CGCTCACC others(352): Show |
1 | a0001c0002t0001g0004 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1737+1177_1737+117 others(363): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401882 | |||||||
| chr11:401882 | C | CGCTCACC others(322): Show |
1 | a0009c0033t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1737+1177_1737+117 others(333): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401882 | |||||||
| chr11:401882 | C | CGCTCACC others(337): Show |
1 | a0002c0013t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1737+1177_1737+117 others(348): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401882 | |||||||
| chr11:401882 | C | CGCTCACC others(353): Show |
1 | a0001c0003t0001g0141 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1737+1177_1737+117 others(364): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401882 | |||||||
| chr11:401883 | C | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0070 a0001c0001t0001g0078 others(2): Show |
5 | HG01261.hp2 HG02129.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+1178C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401883 | |||||||
| chr11:401884 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1737+1179C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401884 | |||||||
| chr11:401885 | G | A | 9 | a0001c0002t0001g0104 a0001c0002t0001g0126 a0001c0002t0001g0172 others(6): Show |
9 | HG01496.hp1 HG01981.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1737+1180G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401885 | |||||||
| chr11:401885 | G | C | 30 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0044 others(27): Show |
31 | HG00642.hp1 HG00642.hp2 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.1737+1180G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401885 | |||||||
| chr11:401886 | G | A | 4 | a0001c0001t0001g0028 a0001c0002t0001g0130 a0001c0003t0001g0140 others(1): Show |
4 | HG01952.hp2 HG02735.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+1181G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401886 | |||||||
| chr11:401887 | C | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0029 others(20): Show |
23 | HG00642.hp2 HG01261.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.1737+1182C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401887 | |||||||
| chr11:401887 | C | CCCCGCTC others(295): Show |
1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-1182_1738-118 others(306): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401887 | ||||||
| chr11:401896 | CCCCCGGC others(8): Show |
C | 6 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0007t0001g0208 others(3): Show |
6 | HG00733.hp2 HG02056.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-1174_1738-116 others(19): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401896 | ||||||
| chr11:401897 | C | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(58): Show |
64 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1738-1181C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401897 | |||||||
| chr11:401899 | C | G | 9 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0134 others(6): Show |
10 | HG01358.hp2 HG01943.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738-1179C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401899 | |||||||
| chr11:401900 | C | CGACCCGC others(376): Show |
1 | a0001c0003t0001g0096 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1738-1177_1738-117 others(387): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401900 | ||||||
| chr11:401900 | C | CGACCCGC others(377): Show |
1 | a0001c0002t0001g0148 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1738-1177_1738-117 others(388): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401900 | ||||||
| chr11:401900 | C | G | 16 | a0001c0002t0001g0004 a0001c0002t0001g0103 a0001c0002t0001g0125 others(13): Show |
17 | HG01358.hp2 HG01943.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1738-1178C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401900 | |||||||
| chr11:401900 | C | T | 1 | a0001c0003t0001g0105 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1738-1178C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401900 | |||||||
| chr11:401900 | CGGCTCCA others(9): Show |
C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(50): Show |
56 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1738-1176_1738-116 others(20): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401900 | ||||||
| chr11:401901 | G | A | 2 | a0001c0003t0001g0116 a0001c0003t0001g0140 |
2 | HG01952.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1738-1177G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401901 | |||||||
| chr11:401901 | G | C | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1738-1177G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401901 | |||||||
| chr11:401901 | G | GACCCGCT others(22): Show |
1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1738-1177_1738-117 others(33): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401901 | |||||||
| chr11:401902 | G | A | 48 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0039 others(45): Show |
49 | HG00544.hp1 HG00621.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.1738-1176G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401902 | |||||||
| chr11:401903 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1738-1175C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401903 | |||||||
| chr11:401903 | CT | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0033 others(39): Show |
42 | HG00621.hp1 HG00642.hp2 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.1738-1174delT | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401903 | |||||||
| chr11:401904 | T | C | 69 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0046 others(66): Show |
71 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1738-1174T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401904 | |||||||
| chr11:401907 | A | C | 1 | a0001c0003t0001g0147 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1738-1171A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401907 | |||||||
| chr11:401907 | A | G | 109 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0028 others(106): Show |
111 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1738-1171A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401907 | |||||||
| chr11:401909 | T | C | 1 | a0001c0003t0001g0147 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1738-1169T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401909 | |||||||
| chr11:401910 | G | C | 112 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0028 others(109): Show |
114 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1738-1168G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401910 | |||||||
| chr11:401911 | A | AC | 11 | a0001c0001t0001g0072 a0001c0002t0001g0110 a0001c0002t0001g0132 others(8): Show |
11 | HG00099.hp2 HG00642.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1738-1163dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401911 | ||||||
| chr11:401911 | ACCCCGGC others(636): Show |
A | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1738-1147_1738-505 others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401911 | ||||||
| chr11:401912 | C | A | 1 | a0001c0008t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1738-1166C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401912 | |||||||
| chr11:401912 | C | CA | 2 | a0001c0001t0001g0078 a0014c0034t0001g0157 |
2 | HG01261.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1738-1166_1738-116 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401912 | |||||||
| chr11:401913 | C | A | 29 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0070 others(26): Show |
30 | HG00544.hp1 HG01175.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.1738-1165C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401913 | |||||||
| chr11:401913 | C | CCCCGACC others(393): Show |
1 | a0001c0002t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1738-1163_1738-116 others(404): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401913 | ||||||
| chr11:401913 | C | CCCCGACC others(391): Show |
2 | a0001c0002t0001g0133 a0001c0002t0001g0138 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1738-1163_1738-116 others(402): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401913 | ||||||
| chr11:401913 | C | CCCCGACC others(392): Show |
1 | a0012c0020t0001g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1738-1163_1738-116 others(403): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401913 | ||||||
| chr11:401913 | C | CCCCGACC others(391): Show |
7 | a0001c0002t0001g0100 a0001c0002t0001g0159 a0001c0003t0001g0105 others(4): Show |
7 | HG00639.hp1 HG01891.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-1163_1738-116 others(402): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401913 | ||||||
| chr11:401916 | G | C | 78 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0029 others(75): Show |
79 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1738-1162G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401916 | |||||||
| chr11:401916 | G | GCTCACCC others(370): Show |
1 | a0001c0003t0001g0147 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1738-1162_1738-116 others(381): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401916 | |||||||
| chr11:401916 | G | T | 2 | a0001c0004t0001g0094 a0001c0030t0001g0174 |
2 | HG03579.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1738-1162G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401916 | |||||||
| chr11:401917 | G | A | 10 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0131 others(7): Show |
11 | HG00639.hp2 HG00733.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1738-1161G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401917 | |||||||
| chr11:401917 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1738-1161G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401917 | |||||||
| chr11:401917 | G | GA | 9 | a0001c0002t0001g0104 a0001c0002t0001g0126 a0001c0002t0001g0172 others(6): Show |
9 | HG01496.hp1 HG01981.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-1161_1738-116 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401917 | |||||||
| chr11:401918 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(82): Show |
88 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.1738-1160C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401918 | |||||||
| chr11:401918 | C | G | 8 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0043 others(5): Show |
8 | HG00621.hp1 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-1160C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401918 | |||||||
| chr11:401927 | C | CCCCCGAC others(262): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1738-1148_1738-114 others(273): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401927 | ||||||
| chr11:401927 | C | CCCCCGAC others(262): Show |
1 | a0001c0002t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1738-1148_1738-114 others(273): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401927 | ||||||
| chr11:401927 | C | CCCCCGAC others(261): Show |
5 | a0001c0002t0001g0101 a0001c0002t0001g0135 a0001c0002t0001g0137 others(2): Show |
6 | HG01069.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-1148_1738-114 others(272): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401927 | ||||||
| chr11:401927 | C | CCCCCGGC others(8): Show |
1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1738-1148_1738-114 others(19): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401927 | ||||||
| chr11:401928 | C | A | 20 | a0001c0002t0001g0104 a0001c0002t0001g0125 a0001c0002t0001g0126 others(17): Show |
20 | HG00642.hp1 HG01981.hp1 HG02273.hp1 others(17): Show |
intron_variant | MODIFIER | c.1738-1150C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401928 | |||||||
| chr11:401930 | C | G | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-1148C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401930 | |||||||
| chr11:401930 | CG | C | 7 | a0001c0002t0001g0130 a0001c0007t0001g0008 a0001c0007t0001g0009 others(4): Show |
7 | HG00733.hp2 HG02056.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-1146delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401930 | ||||||
| chr11:401931 | G | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(101): Show |
108 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1738-1147G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401931 | |||||||
| chr11:401932 | G | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0060 |
2 | HG01884.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1738-1146G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401932 | |||||||
| chr11:401932 | GA | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(59): Show |
65 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1738-1145delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401932 | |||||||
| chr11:401933 | A | G | 28 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0029 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1738-1145A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401933 | |||||||
| chr11:401933 | AC | A | 19 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0053 others(16): Show |
19 | HG00099.hp2 HG00621.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1738-1141delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401933 | ||||||
| chr11:401934 | C | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0060 |
2 | HG01884.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1738-1144C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401934 | |||||||
| chr11:401934 | C | CCCCCGGC others(260): Show |
1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1738-1141_1738-114 others(271): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401934 | ||||||
| chr11:401934 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(51): Show |
57 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1738-1144C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401934 | |||||||
| chr11:401941 | CACCCCCG | C | 18 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0039 others(15): Show |
18 | HG00621.hp1 HG01192.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1738-1129_1738-112 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401941 | ||||||
| chr11:401944 | C | A | 40 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0002t0001g0104 others(37): Show |
40 | HG00642.hp2 HG01256.hp1 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.1738-1134C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401944 | |||||||
| chr11:401946 | C | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0081 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-1132C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401946 | |||||||
| chr11:401947 | C | G | 16 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0131 others(13): Show |
17 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1738-1131C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401947 | |||||||
| chr11:401947 | CGACCCCC others(1): Show |
C | 3 | a0001c0001t0001g0046 a0001c0003t0001g0166 a0001c0008t0001g0192 |
3 | HG02135.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1738-1129_1738-112 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401947 | ||||||
| chr11:401948 | G | GACCCGCT others(1098): Show |
2 | a0001c0004t0001g0073 a0001c0004t0001g0074 |
2 | NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1738-1126_1738-112 others(1109): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401948 | ||||||
| chr11:401948 | G | GCCCCGCT others(1): Show |
4 | a0001c0001t0001g0028 a0001c0002t0001g0127 a0001c0002t0001g0164 others(1): Show |
4 | HG00642.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-1130_1738-112 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401948 | |||||||
| chr11:401948 | G | GCCCCGCT others(199): Show |
1 | a0001c0003t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1738-1130_1738-112 others(210): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401948 | |||||||
| chr11:401948 | G | GCCCCGCT others(215): Show |
3 | a0001c0003t0001g0095 a0001c0003t0001g0098 a0010c0017t0001g0106 |
3 | HG01952.hp1 HG01975.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.1738-1130_1738-112 others(226): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401948 | |||||||
| chr11:401948 | G | GCCCCGCT others(231): Show |
4 | a0001c0003t0001g0139 a0001c0003t0001g0142 a0001c0003t0001g0149 others(1): Show |
4 | HG01256.hp1 NA18971.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-1130_1738-112 others(242): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401948 | |||||||
| chr11:401948 | G | GCCCCGCT others(217): Show |
1 | a0001c0010t0001g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1738-1130_1738-112 others(228): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401948 | |||||||
| chr11:401948 | G | GGCCCCGC others(2): Show |
5 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0148 others(2): Show |
5 | HG00544.hp1 HG00609.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-1130_1738-112 others(13): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401948 | |||||||
| chr11:401948 | G | GGCCCCGC others(3): Show |
1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1738-1130_1738-112 others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401948 | |||||||
| chr11:401948 | G | GGCCCCGC others(78): Show |
6 | a0001c0002t0001g0104 a0001c0002t0001g0126 a0001c0003t0001g0111 others(3): Show |
6 | HG01981.hp1 HG02273.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-1130_1738-112 others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401948 | |||||||
| chr11:401948 | G | GGCCCCGC others(232): Show |
1 | a0001c0016t0001g0200 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1738-1130_1738-112 others(243): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401948 | |||||||
| chr11:401949 | A | C | 5 | a0001c0002t0001g0168 a0001c0003t0001g0097 a0001c0004t0001g0027 others(2): Show |
5 | HG00642.hp1 HG03209.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-1129A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401949 | |||||||
| chr11:401949 | A | G | 26 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(23): Show |
27 | HG00639.hp1 HG01358.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1738-1129A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401949 | |||||||
| chr11:401949 | ACCCCCGG others(1): Show |
A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0051 others(10): Show |
13 | HG01243.hp2 HG01981.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.1738-1125_1738-111 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401949 | ||||||
| chr11:401949 | ACCCCCGG others(55): Show |
A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(48): Show |
54 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.1738-1125_1738-106 others(66): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401949 | ||||||
| chr11:401949 | ACCCCCGG others(71): Show |
A | 2 | a0001c0005t0001g0023 a0001c0005t0001g0032 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1738-1125_1738-104 others(82): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401949 | ||||||
| chr11:401950 | C | CCCCGCTC others(1): Show |
22 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(19): Show |
23 | HG00639.hp1 HG01358.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1738-1125_1738-112 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401950 | ||||||
| chr11:401950 | C | CCCGCTCA | 7 | a0001c0002t0001g0125 a0001c0002t0001g0170 a0001c0002t0001g0171 others(4): Show |
7 | HG02451.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-1126_1738-112 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401950 | ||||||
| chr11:401950 | C | CCCGCTCA others(390): Show |
1 | a0019c0032t0001g0144 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1738-1126_1738-112 others(401): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401950 | ||||||
| chr11:401950 | C | CCCGCTCA others(415): Show |
1 | a0001c0003t0001g0161 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1738-1126_1738-112 others(426): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401950 | ||||||
| chr11:401951 | C | A | 19 | a0001c0002t0001g0104 a0001c0002t0001g0126 a0001c0002t0001g0127 others(16): Show |
19 | HG00642.hp2 HG01256.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1738-1127C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401951 | |||||||
| chr11:401951 | C | CCGCTCAC others(231): Show |
1 | a0001c0003t0001g0155 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1738-1126_1738-112 others(242): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401951 | ||||||
| chr11:401951 | C | CCGCTCAC others(246): Show |
1 | a0001c0002t0001g0132 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1738-1126_1738-112 others(257): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401951 | ||||||
| chr11:401951 | C | CCGCTCAC others(246): Show |
2 | a0001c0002t0001g0110 a0001c0003t0001g0162 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1738-1126_1738-112 others(257): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401951 | ||||||
| chr11:401952 | C | CCGCTCAC others(310): Show |
1 | a0014c0034t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1738-1125_1738-112 others(321): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401952 | ||||||
| chr11:401952 | C | CGCTCACA others(483): Show |
1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1738-1126_1738-112 others(494): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401952 | |||||||
| chr11:401953 | C | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0005t0001g0084 others(2): Show |
5 | HG02135.hp1 HG02148.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-1125C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401953 | |||||||
| chr11:401954 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1738-1124C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401954 | |||||||
| chr11:401955 | G | C | 14 | a0001c0001t0001g0078 a0001c0002t0001g0125 a0001c0002t0001g0170 others(11): Show |
14 | HG00642.hp1 HG00673.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1738-1123G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401955 | |||||||
| chr11:401955 | G | T | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1738-1123G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401955 | |||||||
| chr11:401956 | G | A | 32 | a0001c0001t0001g0028 a0001c0002t0001g0004 a0001c0002t0001g0100 others(29): Show |
33 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.1738-1122G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401956 | |||||||
| chr11:401957 | C | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0078 others(12): Show |
15 | HG01261.hp2 HG01496.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.1738-1121C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401957 | |||||||
| chr11:401964 | CACCCCCG | C | 23 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1738-1106_1738-110 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401964 | ||||||
| chr11:401965 | A | ACCCCCGC others(325): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1738-1107_1738-110 others(336): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401965 | ||||||
| chr11:401965 | ACCCCCGA others(1): Show |
A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0070 a0001c0001t0001g0078 others(5): Show |
8 | HG01261.hp2 HG02129.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-1108_1738-110 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401965 | ||||||
| chr11:401966 | CCCCCGAC others(31): Show |
C | 1 | a0017c0027t0001g0107 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1738-1106_1738-106 others(42): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401966 | ||||||
| chr11:401967 | C | A | 31 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
31 | HG00099.hp2 HG00642.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1738-1111C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401967 | |||||||
| chr11:401969 | C | G | 2 | a0001c0003t0001g0143 a0001c0003t0001g0166 |
2 | HG00673.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1738-1109C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401969 | |||||||
| chr11:401970 | C | G | 30 | a0001c0001t0001g0046 a0001c0002t0001g0004 a0001c0002t0001g0100 others(27): Show |
31 | HG00544.hp1 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1738-1108C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401970 | |||||||
| chr11:401971 | G | GACCCGCT others(308): Show |
1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1738-1103_1738-110 others(319): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401971 | ||||||
| chr11:401971 | G | GACCCGCT others(323): Show |
1 | a0001c0003t0001g0152 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1738-1103_1738-110 others(334): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401971 | ||||||
| chr11:401971 | G | GACCCGCT others(307): Show |
1 | a0001c0002t0001g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1738-1103_1738-110 others(318): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401971 | ||||||
| chr11:401971 | G | GCCCCGCT others(1): Show |
3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0081 |
3 | HG02723.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-1107_1738-110 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401971 | |||||||
| chr11:401971 | G | GCCCCGCT others(16): Show |
1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-1107_1738-110 others(27): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401971 | |||||||
| chr11:401971 | G | GGCCCCGC others(2): Show |
5 | a0001c0004t0001g0027 a0001c0004t0001g0073 a0001c0004t0001g0074 others(2): Show |
5 | HG00642.hp1 HG02683.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-1107_1738-110 others(13): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401971 | |||||||
| chr11:401971 | G | GGCCCCGC others(254): Show |
1 | a0001c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1738-1107_1738-110 others(265): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401971 | |||||||
| chr11:401972 | ACCCCCGG others(32): Show |
A | 1 | a0001c0001t0001g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1738-1102_1738-106 others(43): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401972 | ||||||
| chr11:401973 | C | CCCGCTCA | 9 | a0001c0002t0001g0125 a0001c0002t0001g0170 a0001c0002t0001g0171 others(6): Show |
9 | HG01496.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-1103_1738-110 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401973 | ||||||
| chr11:401973 | C | CCCGCTCA others(106): Show |
1 | a0001c0002t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1738-1103_1738-110 others(117): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401973 | ||||||
| chr11:401973 | C | CCCGCTCA others(30): Show |
1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1738-1103_1738-110 others(41): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401973 | ||||||
| chr11:401974 | C | A | 2 | a0001c0003t0001g0114 a0001c0008t0001g0093 |
2 | HG03209.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1738-1104C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401974 | |||||||
| chr11:401974 | C | CCCCGCTC others(3): Show |
1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-1100_1738-109 others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401974 | ||||||
| chr11:401975 | C | CGCTCACA | 23 | a0001c0002t0001g0104 a0001c0002t0001g0110 a0001c0002t0001g0126 others(20): Show |
23 | HG00099.hp2 HG00642.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.1738-1103_1738-110 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401975 | |||||||
| chr11:401975 | C | CGCTCACC others(46): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1738-1103_1738-110 others(57): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401975 | |||||||
| chr11:401975 | C | CGCTCACC others(185): Show |
1 | a0001c0003t0001g0116 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1738-1103_1738-110 others(196): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401975 | |||||||
| chr11:401975 | C | CGCTCACC others(245): Show |
1 | a0001c0003t0001g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1738-1103_1738-110 others(256): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401975 | |||||||
| chr11:401975 | C | CGCTCACC others(153): Show |
1 | a0001c0003t0001g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1738-1103_1738-110 others(164): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401975 | |||||||
| chr11:401976 | C | G | 14 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0043 others(11): Show |
14 | HG00621.hp1 HG01192.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1738-1102C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401976 | |||||||
| chr11:401977 | C | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0081 others(1): Show |
4 | HG02723.hp1 HG02735.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-1101C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401977 | |||||||
| chr11:401978 | G | A | 7 | a0001c0002t0001g0125 a0001c0002t0001g0145 a0001c0002t0001g0170 others(4): Show |
7 | HG00609.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-1100G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401978 | |||||||
| chr11:401978 | G | C | 31 | a0001c0002t0001g0104 a0001c0002t0001g0110 a0001c0002t0001g0126 others(28): Show |
31 | HG00099.hp2 HG00642.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.1738-1100G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401978 | |||||||
| chr11:401978 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1738-1100G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401978 | |||||||
| chr11:401979 | G | A | 42 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0081 others(39): Show |
44 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1738-1099G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401979 | |||||||
| chr11:401979 | G | C | 1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-1099G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401979 | |||||||
| chr11:401980 | C | A | 41 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0043 others(38): Show |
41 | HG00099.hp2 HG00621.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1738-1098C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401980 | |||||||
| chr11:401988 | AC | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0070 a0001c0001t0001g0078 others(8): Show |
11 | HG01261.hp2 HG02129.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1738-1085delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401988 | ||||||
| chr11:401989 | CCCCCGGC others(7): Show |
C | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1738-1088_1738-107 others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401989 | |||||||
| chr11:401990 | C | A | 21 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0044 others(18): Show |
22 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1738-1088C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401990 | |||||||
| chr11:401992 | C | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0195 |
3 | HG01981.hp2 HG02056.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1738-1086C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401992 | |||||||
| chr11:401993 | C | G | 8 | a0001c0001t0001g0089 a0001c0002t0001g0172 a0001c0003t0001g0099 others(5): Show |
8 | HG00673.hp1 HG01496.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-1085C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401993 | |||||||
| chr11:401993 | CG | C | 12 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0135 others(9): Show |
13 | HG00733.hp1 HG00733.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1738-1083delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401993 | ||||||
| chr11:401993 | CGGCTCCA others(9): Show |
C | 2 | a0001c0001t0001g0044 a0001c0005t0001g0084 |
2 | HG02135.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1738-1083_1738-106 others(20): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401993 | ||||||
| chr11:401993 | CGGCTCCA others(79): Show |
C | 2 | a0001c0001t0001g0019 a0001c0011t0001g0063 |
2 | HG02148.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1738-1083_1738-998 others(89): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 401993 | ||||||
| chr11:401994 | G | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0078 a0001c0001t0001g0080 others(4): Show |
7 | HG01261.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-1084G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401994 | |||||||
| chr11:401994 | G | C | 1 | a0001c0002t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1738-1084G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401994 | |||||||
| chr11:401995 | G | A | 14 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0002t0001g0125 others(11): Show |
14 | HG00609.hp1 HG02135.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.1738-1083G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401995 | |||||||
| chr11:401996 | C | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0195 |
3 | HG01981.hp2 HG02056.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1738-1082C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401996 | |||||||
| chr11:401996 | CT | C | 11 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0002t0001g0125 others(8): Show |
11 | HG00609.hp1 HG01243.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1738-1081delT | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401996 | |||||||
| chr11:401997 | T | C | 86 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0033 others(83): Show |
87 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1738-1081T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 401997 | |||||||
| chr11:402000 | A | G | 97 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(94): Show |
98 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1738-1078A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402000 | |||||||
| chr11:402003 | G | C | 98 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(95): Show |
99 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1738-1075G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402003 | |||||||
| chr11:402004 | A | AC | 22 | a0001c0001t0001g0034 a0001c0001t0001g0089 a0001c0001t0001g0195 others(19): Show |
23 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1738-1070dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402004 | ||||||
| chr11:402005 | C | CA | 2 | a0001c0003t0001g0140 a0001c0003t0001g0151 |
2 | HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1738-1073_1738-107 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402005 | |||||||
| chr11:402006 | C | A | 27 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0039 others(24): Show |
27 | HG00621.hp1 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1738-1072C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402006 | |||||||
| chr11:402009 | G | C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0033 others(29): Show |
32 | HG00621.hp1 HG01192.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1738-1069G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402009 | |||||||
| chr11:402010 | G | A | 2 | a0001c0002t0001g0130 a0001c0008t0001g0192 |
2 | HG02735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1738-1068G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402010 | |||||||
| chr11:402010 | G | C | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1738-1068G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402010 | |||||||
| chr11:402010 | G | GA | 9 | a0001c0002t0001g0125 a0001c0002t0001g0145 a0001c0002t0001g0170 others(6): Show |
9 | HG00609.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-1068_1738-106 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402010 | |||||||
| chr11:402011 | C | A | 4 | a0001c0007t0001g0010 a0001c0008t0001g0093 a0001c0008t0001g0188 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-1067C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402011 | |||||||
| chr11:402016 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1738-1062C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402016 | |||||||
| chr11:402018 | C | G | 13 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0131 others(10): Show |
14 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1738-1060C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402018 | |||||||
| chr11:402021 | C | A | 20 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0195 others(17): Show |
20 | HG00609.hp1 HG01496.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.1738-1057C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402021 | |||||||
| chr11:402023 | C | G | 2 | a0001c0001t0001g0178 a0001c0007t0001g0025 |
2 | HG02630.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1738-1055C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402023 | |||||||
| chr11:402023 | CG | C | 30 | a0001c0001t0001g0089 a0001c0002t0001g0004 a0001c0002t0001g0100 others(27): Show |
31 | HG00544.hp1 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1738-1053delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402023 | ||||||
| chr11:402024 | G | A | 5 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0004t0001g0176 others(2): Show |
5 | HG02717.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-1054G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402024 | |||||||
| chr11:402024 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(83): Show |
90 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1738-1054G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402024 | |||||||
| chr11:402024 | G | GGCCCCGC others(85): Show |
7 | a0001c0002t0001g0104 a0001c0002t0001g0126 a0001c0002t0001g0127 others(4): Show |
7 | HG01981.hp1 HG02273.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-1053_1738-105 others(96): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402024 | ||||||
| chr11:402025 | G | A | 1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1738-1053G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402025 | |||||||
| chr11:402025 | GA | G | 30 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0051 others(27): Show |
30 | HG00099.hp2 HG00642.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.1738-1052delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402025 | |||||||
| chr11:402026 | A | C | 2 | a0001c0001t0001g0048 a0001c0003t0001g0166 |
2 | HG02135.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1738-1052A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402026 | |||||||
| chr11:402026 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(57): Show |
63 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1738-1052A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402026 | |||||||
| chr11:402026 | AC | A | 15 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0131 others(12): Show |
16 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1738-1048delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402026 | ||||||
| chr11:402027 | CCCCGCTC others(551): Show |
C | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-1047_1738-490 others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402027 | ||||||
| chr11:402032 | C | T | 2 | a0001c0003t0001g0096 a0001c0003t0001g0097 |
2 | HG01934.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1738-1046C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402032 | |||||||
| chr11:402034 | CACCCCCG | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(56): Show |
62 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1738-1036_1738-103 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402034 | ||||||
| chr11:402037 | C | A | 40 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(37): Show |
40 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1738-1041C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402037 | |||||||
| chr11:402039 | C | G | 4 | a0001c0002t0001g0146 a0001c0002t0001g0168 a0001c0003t0001g0152 others(1): Show |
4 | HG02165.hp2 HG02723.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-1039C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402039 | |||||||
| chr11:402040 | C | G | 18 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0195 others(15): Show |
18 | HG00673.hp1 HG01981.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.1738-1038C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402040 | |||||||
| chr11:402040 | C | T | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1738-1038C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402040 | |||||||
| chr11:402040 | CGACCCCC others(1): Show |
C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0177 a0001c0001t0001g0179 others(3): Show |
6 | HG02129.hp1 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-1036_1738-102 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402040 | ||||||
| chr11:402040 | CGACCCCC others(32): Show |
C | 1 | a0001c0007t0001g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1738-1036_1738-998 others(42): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402040 | ||||||
| chr11:402040 | CGACCCCC others(404): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1738-1036_1738-626 others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402040 | ||||||
| chr11:402041 | G | GACCCGCT others(1): Show |
2 | a0001c0003t0001g0140 a0001c0003t0001g0151 |
2 | HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1738-1033_1738-103 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402041 | ||||||
| chr11:402041 | G | GACCCGCT others(108): Show |
1 | a0001c0002t0001g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1738-1033_1738-103 others(119): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402041 | ||||||
| chr11:402041 | G | GCCCCGCT others(1): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0008t0001g0093 |
3 | HG02723.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-1037_1738-103 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402041 | |||||||
| chr11:402041 | G | GGCCCCGC others(2): Show |
3 | a0001c0004t0001g0073 a0001c0004t0001g0074 a0014c0034t0001g0157 |
3 | HG02683.hp1 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1738-1037_1738-103 others(13): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402041 | |||||||
| chr11:402041 | G | GGCCCCGC others(125): Show |
1 | a0001c0002t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1738-1037_1738-103 others(136): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402041 | |||||||
| chr11:402041 | G | GGCCCCGC others(124): Show |
4 | a0001c0002t0001g0171 a0001c0002t0001g0173 a0001c0010t0003g0022 others(1): Show |
4 | HG02451.hp1 HG02486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-1037_1738-103 others(135): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402041 | |||||||
| chr11:402042 | A | C | 16 | a0001c0002t0001g0110 a0001c0002t0001g0132 a0001c0002t0001g0164 others(13): Show |
16 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.1738-1036A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402042 | |||||||
| chr11:402042 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0002t0001g0125 others(1): Show |
4 | HG02976.hp2 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-1036A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402042 | |||||||
| chr11:402042 | ACCCCCGG others(1): Show |
A | 6 | a0001c0001t0001g0064 a0001c0001t0001g0183 a0001c0005t0001g0023 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-1032_1738-102 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402042 | ||||||
| chr11:402042 | ACCCCCGG others(48): Show |
A | 1 | a0001c0009t0001g0102 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1738-1032_1738-978 others(58): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402042 | ||||||
| chr11:402042 | ACCCCCGG others(70): Show |
A | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1738-1031_1738-955 others(80): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402042 | ||||||
| chr11:402042 | ACCCCCGG others(102): Show |
A | 7 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG01884.hp2 HG02135.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-1032_1738-924 others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402042 | ||||||
| chr11:402043 | C | CCCCGCTC others(203): Show |
1 | a0001c0002t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1738-1032_1738-103 others(214): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402043 | ||||||
| chr11:402043 | C | CCCGCTCA | 7 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0076 others(4): Show |
7 | HG00621.hp1 HG01192.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-1033_1738-103 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402043 | ||||||
| chr11:402043 | C | T | 1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1738-1035C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402043 | |||||||
| chr11:402043 | CCCCCGGC others(87): Show |
C | 2 | a0001c0001t0001g0072 a0001c0009t0001g0122 |
2 | HG02027.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1738-1032_1738-939 others(97): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402043 | ||||||
| chr11:402044 | C | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0078 a0001c0001t0001g0080 others(2): Show |
5 | HG01261.hp2 HG02622.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-1034C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402044 | |||||||
| chr11:402045 | C | CCGCTCAC others(1): Show |
7 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0002t0001g0146 others(4): Show |
7 | HG02165.hp2 HG02723.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-1032_1738-103 others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402045 | ||||||
| chr11:402045 | C | CCGCTCAC others(17): Show |
1 | a0001c0010t0001g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1738-1032_1738-103 others(28): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402045 | ||||||
| chr11:402045 | C | CGCTCACA | 2 | a0001c0002t0001g0172 a0006c0031t0001g0163 |
2 | HG01496.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1738-1033_1738-103 others(11): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402045 | |||||||
| chr11:402045 | C | CGCTCACC others(16): Show |
14 | a0001c0002t0001g0110 a0001c0002t0001g0132 a0001c0002t0001g0164 others(11): Show |
14 | HG00099.hp2 HG00642.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1738-1033_1738-103 others(27): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402045 | |||||||
| chr11:402046 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(51): Show |
57 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1738-1032C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402046 | |||||||
| chr11:402047 | C | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0008t0001g0093 |
3 | HG02723.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-1031C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402047 | |||||||
| chr11:402048 | G | C | 25 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0002t0001g0110 others(22): Show |
25 | HG00099.hp2 HG00642.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1738-1030G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402048 | |||||||
| chr11:402049 | G | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0002t0001g0104 others(12): Show |
15 | HG00673.hp1 HG01981.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.1738-1029G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402049 | |||||||
| chr11:402050 | C | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(56): Show |
62 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1738-1028C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402050 | |||||||
| chr11:402054 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1738-1024G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402054 | |||||||
| chr11:402057 | CACCCCCG others(186): Show |
C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0078 |
2 | HG01261.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1738-1011_1738-819 others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402057 | ||||||
| chr11:402058 | AC | A | 16 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0046 others(13): Show |
16 | HG00609.hp1 HG00621.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.1738-1015delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402058 | ||||||
| chr11:402059 | CCCCCGGC others(8): Show |
C | 24 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(21): Show |
25 | HG00544.hp1 HG00639.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.1738-1011_1738-997 others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402059 | ||||||
| chr11:402060 | C | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0002t0001g0130 others(1): Show |
4 | HG02723.hp1 HG02735.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-1018C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402060 | |||||||
| chr11:402062 | C | G | 5 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0004t0001g0176 others(2): Show |
5 | HG02717.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-1016C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402062 | |||||||
| chr11:402063 | C | A | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1738-1015C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402063 | |||||||
| chr11:402063 | C | G | 27 | a0001c0001t0001g0016 a0001c0001t0001g0177 a0001c0001t0001g0179 others(24): Show |
27 | HG00099.hp2 HG00642.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1738-1015C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402063 | |||||||
| chr11:402063 | CG | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0002t0001g0130 |
3 | HG02723.hp1 HG02735.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-1013delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402063 | ||||||
| chr11:402063 | CGGCTCCA others(187): Show |
C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0021t0001g0086 |
3 | HG02622.hp2 HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1738-1013_1738-820 others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402063 | ||||||
| chr11:402064 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0076 others(3): Show |
6 | HG00621.hp1 HG01192.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-1014G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402064 | |||||||
| chr11:402065 | G | A | 35 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0051 others(32): Show |
35 | HG00099.hp2 HG00642.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.1738-1013G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402065 | |||||||
| chr11:402065 | G | C | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1738-1013G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402065 | |||||||
| chr11:402065 | G | GCCCCCGC others(392): Show |
1 | a0001c0004t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1738-1012_1738-101 others(403): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402065 | ||||||
| chr11:402065 | G | GCCCCGCT others(70): Show |
1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1738-1012_1738-101 others(81): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402065 | ||||||
| chr11:402066 | CT | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0056 others(8): Show |
11 | HG01175.hp1 HG01981.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1738-1011delT | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402066 | |||||||
| chr11:402066 | CTCCACTG others(7): Show |
C | 1 | a0001c0003t0001g0161 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1738-1011_1738-998 others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402066 | |||||||
| chr11:402067 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(108): Show |
114 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.1738-1011T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402067 | |||||||
| chr11:402070 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(118): Show |
124 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1738-1008A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402070 | |||||||
| chr11:402073 | G | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(119): Show |
125 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.1738-1005G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402073 | |||||||
| chr11:402074 | A | AC | 24 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0002t0001g0110 others(21): Show |
24 | HG00099.hp2 HG00642.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1738-1000dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402074 | ||||||
| chr11:402074 | ACCCCGGC others(334): Show |
A | 5 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0007t0001g0208 others(2): Show |
5 | HG00733.hp2 HG02056.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-984_1738-644d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402074 | ||||||
| chr11:402075 | C | CA | 5 | a0001c0001t0001g0016 a0001c0007t0001g0010 a0001c0008t0001g0093 others(2): Show |
5 | HG01243.hp2 HG02129.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-1003_1738-100 others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402075 | |||||||
| chr11:402076 | C | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(64): Show |
70 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1738-1002C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402076 | |||||||
| chr11:402079 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0183 |
2 | HG02145.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1738-999G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402079 | |||||||
| chr11:402079 | G | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(70): Show |
76 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1738-999G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402079 | |||||||
| chr11:402079 | G | T | 2 | a0001c0008t0001g0189 a0001c0030t0001g0174 |
2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-999G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402079 | |||||||
| chr11:402080 | G | C | 2 | a0001c0007t0001g0010 a0001c0008t0001g0188 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1738-998G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402080 | |||||||
| chr11:402080 | G | GA | 2 | a0001c0001t0001g0029 a0001c0001t0001g0081 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-998_1738-997i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402080 | |||||||
| chr11:402081 | C | A | 6 | a0001c0001t0001g0056 a0001c0004t0001g0074 a0001c0005t0001g0023 others(3): Show |
6 | HG01175.hp1 HG02258.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-997C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402081 | |||||||
| chr11:402088 | C | G | 1 | a0001c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1738-990C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402088 | |||||||
| chr11:402091 | C | A | 17 | a0001c0001t0001g0029 a0001c0001t0001g0064 a0001c0001t0001g0081 others(14): Show |
17 | HG00609.hp1 HG01943.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.1738-987C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402091 | |||||||
| chr11:402093 | C | G | 3 | a0001c0003t0001g0114 a0001c0007t0001g0007 a0001c0012t0001g0120 |
3 | HG02027.hp1 HG03688.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1738-985C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402093 | |||||||
| chr11:402093 | CG | C | 53 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(50): Show |
54 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1738-983delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402093 | ||||||
| chr11:402094 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0051 |
2 | HG01981.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.1738-984G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402094 | |||||||
| chr11:402094 | G | C | 29 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(26): Show |
29 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1738-984G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402094 | |||||||
| chr11:402095 | G | A | 1 | a0010c0017t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1738-983G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402095 | |||||||
| chr11:402095 | G | C | 1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-983G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402095 | |||||||
| chr11:402095 | GA | G | 19 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0051 others(16): Show |
19 | HG00609.hp1 HG01175.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.1738-982delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402095 | |||||||
| chr11:402096 | A | C | 2 | a0001c0003t0001g0143 a0010c0017t0001g0106 |
2 | HG00673.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1738-982A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402096 | |||||||
| chr11:402096 | A | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0004t0001g0027 others(3): Show |
6 | HG00642.hp1 HG02622.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-982A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402096 | |||||||
| chr11:402096 | AC | A | 5 | a0001c0001t0001g0011 a0001c0002t0001g0130 a0001c0005t0001g0023 others(2): Show |
5 | HG02258.hp1 HG02735.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-978delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402096 | ||||||
| chr11:402097 | C | G | 2 | a0001c0001t0001g0056 a0004c0015t0001g0047 |
2 | HG01175.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1738-981C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402097 | |||||||
| chr11:402104 | CACCCCCG | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0076 others(2): Show |
5 | HG00621.hp1 HG01192.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-966_1738-960d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402104 | ||||||
| chr11:402105 | AC | A | 8 | a0001c0002t0001g0101 a0001c0002t0001g0118 a0001c0002t0001g0131 others(5): Show |
9 | HG00639.hp2 HG00733.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-968delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402105 | ||||||
| chr11:402106 | CCCCCGAC others(31): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1738-966_1738-929d others(40): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402106 | ||||||
| chr11:402106 | CCCCCGAC others(46): Show |
C | 1 | a0001c0011t0001g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1738-961_1738-909d others(55): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402106 | ||||||
| chr11:402106 | CCCCCGAC others(170): Show |
C | 1 | a0001c0004t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1738-966_1738-790d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402106 | ||||||
| chr11:402106 | CCCCCGAC others(403): Show |
C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0004t0001g0193 others(1): Show |
4 | HG02717.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-966_1738-557d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402106 | ||||||
| chr11:402107 | C | A | 16 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0034 others(13): Show |
16 | HG01496.hp1 HG01981.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1738-971C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402107 | |||||||
| chr11:402109 | C | G | 9 | a0001c0002t0001g0145 a0001c0002t0001g0170 a0001c0002t0001g0171 others(6): Show |
9 | HG00609.hp1 HG01943.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-969C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402109 | |||||||
| chr11:402110 | C | G | 31 | a0001c0001t0001g0064 a0001c0001t0001g0183 a0001c0002t0001g0110 others(28): Show |
31 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1738-968C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402110 | |||||||
| chr11:402110 | CGACCCCC others(1): Show |
C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0007t0001g0007 |
3 | HG01981.hp2 HG02056.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1738-966_1738-959d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402110 | ||||||
| chr11:402110 | CGACCCCC others(101): Show |
C | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1738-966_1738-859d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402110 | ||||||
| chr11:402111 | G | GACCCGCT others(1): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0046 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1738-963_1738-962i others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402111 | ||||||
| chr11:402111 | G | GCCCCGCT others(1): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0003t0001g0114 |
3 | HG02723.hp1 HG03579.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1738-967_1738-966i others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402111 | |||||||
| chr11:402112 | A | C | 3 | a0001c0002t0001g0172 a0006c0031t0001g0163 a0014c0034t0001g0157 |
3 | HG01496.hp1 HG02683.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1738-966A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402112 | |||||||
| chr11:402112 | A | G | 1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1738-966A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402112 | |||||||
| chr11:402112 | ACCCCCGG others(1): Show |
A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(58): Show |
64 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1738-962_1738-955d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402112 | ||||||
| chr11:402112 | ACCCCCGG others(32): Show |
A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0056 |
2 | HG00621.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1738-962_1738-924d others(41): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402112 | ||||||
| chr11:402113 | C | CCCCCGGC others(115): Show |
1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1738-944_1738-943i others(124): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402113 | ||||||
| chr11:402113 | CCCCCGGC others(17): Show |
C | 1 | a0015c0026t0004g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1738-962_1738-939d others(26): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402113 | ||||||
| chr11:402114 | C | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0076 a0001c0006t0001g0204 |
3 | HG00621.hp1 HG01192.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1738-964C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402114 | |||||||
| chr11:402115 | C | CCGCTCAC others(1): Show |
7 | a0001c0002t0001g0145 a0001c0002t0001g0170 a0001c0002t0001g0171 others(4): Show |
7 | HG00609.hp1 HG01943.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-962_1738-961i others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402115 | ||||||
| chr11:402115 | C | CCGCTCAC others(370): Show |
1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1738-962_1738-961i others(379): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402115 | ||||||
| chr11:402115 | C | CGCTCACA others(321): Show |
1 | a0001c0004t0001g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1738-963_1738-962i others(330): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402115 | |||||||
| chr11:402115 | C | CGCTCACA others(322): Show |
1 | a0014c0034t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1738-963_1738-962i others(331): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402115 | |||||||
| chr11:402115 | C | CGCTCACC others(16): Show |
2 | a0001c0002t0001g0172 a0006c0031t0001g0163 |
2 | HG01496.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1738-963_1738-962i others(25): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402115 | |||||||
| chr11:402117 | C | G | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-961C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402117 | |||||||
| chr11:402118 | G | C | 14 | a0001c0002t0001g0145 a0001c0002t0001g0170 a0001c0002t0001g0171 others(11): Show |
14 | HG00609.hp1 HG00642.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1738-960G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402118 | |||||||
| chr11:402118 | G | GGCCCCGC others(8): Show |
1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1738-949_1738-948i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402118 | ||||||
| chr11:402119 | G | A | 22 | a0001c0002t0001g0110 a0001c0002t0001g0125 a0001c0002t0001g0132 others(19): Show |
22 | HG00099.hp2 HG00642.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1738-959G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402119 | |||||||
| chr11:402120 | C | A | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1738-958C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402120 | |||||||
| chr11:402124 | G | T | 2 | a0001c0008t0001g0189 a0001c0030t0001g0174 |
2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-954G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402124 | |||||||
| chr11:402128 | AC | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(50): Show |
56 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1738-945delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402128 | ||||||
| chr11:402129 | CCCCCGGC others(8): Show |
C | 3 | a0001c0001t0001g0064 a0001c0007t0001g0025 a0004c0015t0001g0047 |
3 | HG01175.hp1 HG03834.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1738-941_1738-927d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402129 | ||||||
| chr11:402130 | C | A | 4 | a0001c0001t0001g0089 a0001c0001t0001g0183 a0001c0008t0001g0189 others(1): Show |
4 | HG02145.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-948C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402130 | |||||||
| chr11:402130 | CCCCGGCT others(7): Show |
C | 2 | a0001c0003t0001g0116 a0001c0003t0001g0166 |
2 | HG02135.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1738-944_1738-931d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402130 | ||||||
| chr11:402133 | C | G | 16 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0082 others(13): Show |
16 | HG00642.hp1 HG01496.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.1738-945C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402133 | |||||||
| chr11:402133 | CGGCTCCA others(117): Show |
C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0076 a0001c0006t0001g0204 |
3 | HG00621.hp1 HG01192.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1738-943_1738-820d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402133 | ||||||
| chr11:402134 | G | C | 1 | a0001c0003t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1738-944G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402134 | |||||||
| chr11:402134 | GGCTCCAC others(7): Show |
G | 1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-942_1738-929d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402134 | ||||||
| chr11:402134 | GGCTCCAC others(45): Show |
G | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1738-942_1738-891d others(54): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402134 | ||||||
| chr11:402135 | G | A | 40 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0195 others(37): Show |
41 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1738-943G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402135 | |||||||
| chr11:402135 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1738-943G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402135 | |||||||
| chr11:402135 | GCTCCACT others(23): Show |
G | 2 | a0001c0005t0001g0023 a0001c0005t0001g0032 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1738-941_1738-912d others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402135 | ||||||
| chr11:402136 | C | A | 1 | a0001c0003t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1738-942C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402136 | |||||||
| chr11:402136 | CT | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0195 a0001c0002t0001g0004 others(25): Show |
29 | HG00544.hp1 HG00639.hp1 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.1738-941delT | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402136 | |||||||
| chr11:402137 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(88): Show |
94 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1738-941T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402137 | |||||||
| chr11:402140 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(92): Show |
98 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1738-938A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402140 | |||||||
| chr11:402143 | G | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(119): Show |
126 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1738-935G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402143 | |||||||
| chr11:402144 | A | AC | 13 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0002t0001g0145 others(10): Show |
13 | HG00609.hp1 HG01943.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1738-930dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402144 | ||||||
| chr11:402145 | C | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0064 |
2 | HG02004.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1738-933C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402145 | |||||||
| chr11:402145 | C | CA | 27 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0002t0001g0004 others(24): Show |
28 | HG00544.hp1 HG00639.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1738-933_1738-932i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402145 | |||||||
| chr11:402145 | C | CCCCGACC others(47): Show |
8 | a0001c0002t0001g0104 a0001c0002t0001g0126 a0001c0002t0001g0127 others(5): Show |
8 | HG01981.hp1 HG02273.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-929_1738-928i others(56): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402145 | ||||||
| chr11:402146 | C | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(4): Show |
7 | HG02129.hp1 HG02723.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-932C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402146 | |||||||
| chr11:402148 | C | CGACCCCG others(200): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1738-929_1738-928i others(209): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402148 | ||||||
| chr11:402149 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(44): Show |
50 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1738-929G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402149 | |||||||
| chr11:402149 | G | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0029 others(8): Show |
11 | HG02129.hp1 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1738-929G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402149 | |||||||
| chr11:402149 | G | T | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1738-929G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402149 | |||||||
| chr11:402150 | G | A | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-928G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402150 | |||||||
| chr11:402151 | C | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0029 others(5): Show |
8 | HG01515.hp1 HG02129.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-927C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402151 | |||||||
| chr11:402159 | A | AC | 5 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0183 others(2): Show |
5 | HG02129.hp2 HG02145.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-915dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402159 | ||||||
| chr11:402160 | C | CA | 3 | a0001c0004t0001g0094 a0001c0005t0001g0013 a0001c0008t0001g0093 |
3 | HG02145.hp2 HG03209.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1738-918_1738-917i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402160 | |||||||
| chr11:402161 | C | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(49): Show |
55 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1738-917C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402161 | |||||||
| chr11:402163 | C | CG | 3 | a0001c0002t0001g0130 a0001c0008t0001g0188 a0017c0027t0001g0107 |
3 | HG02622.hp1 HG02735.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1738-914dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402163 | ||||||
| chr11:402164 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0195 a0001c0009t0001g0122 others(1): Show |
4 | HG02027.hp2 HG02886.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-914G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402164 | |||||||
| chr11:402164 | G | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(91): Show |
98 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1738-914G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402164 | |||||||
| chr11:402165 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(115): Show |
122 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1738-913A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402165 | |||||||
| chr11:402166 | C | A | 1 | a0004c0015t0001g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1738-912C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402166 | |||||||
| chr11:402166 | C | G | 2 | a0001c0008t0001g0189 a0001c0030t0001g0174 |
2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-912C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402166 | |||||||
| chr11:402171 | C | T | 2 | a0001c0003t0001g0095 a0001c0003t0001g0098 |
2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1738-907C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402171 | |||||||
| chr11:402173 | CACCCCAG | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0029 others(7): Show |
10 | HG02004.hp1 HG02129.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738-899_1738-893d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402173 | ||||||
| chr11:402175 | CCCCAG | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0195 a0001c0009t0001g0122 others(1): Show |
4 | HG02027.hp2 HG02886.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-902_1738-898d others(7): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402175 | |||||||
| chr11:402175 | CCCCAGAC others(101): Show |
C | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1738-899_1738-792d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402175 | ||||||
| chr11:402176 | C | A | 2 | a0001c0008t0001g0093 a0001c0008t0001g0188 |
2 | HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-902C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402176 | |||||||
| chr11:402178 | C | G | 4 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0001c0005t0004g0006 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-900C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402178 | |||||||
| chr11:402179 | A | C | 76 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0001g0089 others(73): Show |
78 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.1738-899A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402179 | |||||||
| chr11:402179 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(64): Show |
70 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1738-899A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402179 | |||||||
| chr11:402179 | AGACCCCC others(1): Show |
A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0043 others(5): Show |
8 | HG00621.hp2 HG01884.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-897_1738-890d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402179 | ||||||
| chr11:402179 | AGACCCCC others(63): Show |
A | 1 | a0001c0006t0001g0005 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1738-804_1738-735d others(72): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402179 | ||||||
| chr11:402181 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1738-897A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402181 | |||||||
| chr11:402181 | ACCCCCGG | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(49): Show |
55 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1738-892_1738-886d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402181 | ||||||
| chr11:402183 | C | CCGCTCAC others(1): Show |
33 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(30): Show |
34 | HG00544.hp1 HG00639.hp1 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.1738-894_1738-893i others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402183 | ||||||
| chr11:402184 | C | CGCTCACA | 2 | a0001c0001t0001g0028 a0001c0001t0001g0046 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1738-894_1738-893i others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402184 | |||||||
| chr11:402184 | CCCG | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0195 a0001c0009t0001g0122 others(1): Show |
4 | HG02027.hp2 HG02886.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-893_1738-891d others(5): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402184 | |||||||
| chr11:402185 | C | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0005t0001g0023 others(2): Show |
5 | HG02258.hp1 HG02922.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-893C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402185 | |||||||
| chr11:402186 | CGGCCCCG others(40): Show |
C | 1 | a0001c0007t0001g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1738-890_1738-844d others(49): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402186 | ||||||
| chr11:402187 | G | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0001g0089 |
3 | HG02976.hp2 HG03453.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1738-891G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402187 | |||||||
| chr11:402188 | G | A | 15 | a0001c0002t0001g0145 a0001c0002t0001g0170 a0001c0002t0001g0171 others(12): Show |
15 | HG00609.hp1 HG00642.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.1738-890G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402188 | |||||||
| chr11:402189 | C | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0046 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-889C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402189 | |||||||
| chr11:402197 | AC | A | 36 | a0001c0001t0001g0089 a0001c0002t0001g0004 a0001c0002t0001g0100 others(33): Show |
37 | HG00544.hp1 HG00639.hp1 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.1738-876delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402197 | ||||||
| chr11:402198 | CCCCCGGC others(8): Show |
C | 3 | a0001c0001t0001g0016 a0001c0002t0001g0132 a0001c0003t0001g0003 |
4 | HG00099.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-872_1738-858d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402198 | ||||||
| chr11:402198 | CCCCCGGC others(78): Show |
C | 1 | a0001c0001t0001g0051 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1738-872_1738-788d others(87): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402198 | ||||||
| chr11:402199 | C | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(61): Show |
67 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.1738-879C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402199 | |||||||
| chr11:402201 | C | G | 2 | a0001c0001t0001g0195 a0015c0026t0004g0092 |
2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1738-877C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402201 | |||||||
| chr11:402202 | C | G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0195 a0001c0009t0001g0122 others(1): Show |
4 | HG02027.hp2 HG02886.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-876C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402202 | |||||||
| chr11:402202 | CG | C | 12 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0043 others(9): Show |
12 | HG00621.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-874delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402202 | ||||||
| chr11:402202 | CGGCTCCA others(9): Show |
C | 2 | a0001c0007t0001g0010 a0004c0015t0001g0047 |
2 | HG01175.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1738-874_1738-859d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402202 | ||||||
| chr11:402203 | G | A | 2 | a0001c0011t0001g0001 a0017c0027t0001g0107 |
2 | HG02486.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1738-875G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402203 | |||||||
| chr11:402203 | G | C | 3 | a0001c0003t0001g0143 a0001c0003t0001g0166 a0001c0008t0001g0188 |
3 | HG00673.hp1 HG02135.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1738-875G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402203 | |||||||
| chr11:402204 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0072 a0001c0001t0001g0081 others(5): Show |
8 | HG02027.hp2 HG02148.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-874G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402204 | |||||||
| chr11:402205 | C | A | 3 | a0001c0003t0001g0143 a0001c0003t0001g0166 a0001c0008t0001g0188 |
3 | HG00673.hp1 HG02135.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1738-873C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402205 | |||||||
| chr11:402205 | CT | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0003t0001g0116 others(1): Show |
4 | HG02148.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-872delT | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402205 | |||||||
| chr11:402206 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(143): Show |
150 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.1738-872T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402206 | |||||||
| chr11:402209 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(144): Show |
151 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.1738-869A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402209 | |||||||
| chr11:402212 | G | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(147): Show |
154 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1738-866G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402212 | |||||||
| chr11:402213 | A | ACACCCCG others(855): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1738-864_1738-863i others(864): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402213 | ||||||
| chr11:402213 | A | ACACCCGA others(24): Show |
1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1738-864_1738-863i others(33): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402213 | ||||||
| chr11:402214 | C | CA | 5 | a0001c0001t0001g0072 a0001c0003t0001g0116 a0001c0003t0001g0143 others(2): Show |
5 | HG00673.hp1 HG02027.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-864_1738-863i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402214 | |||||||
| chr11:402215 | C | A | 44 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0056 others(41): Show |
45 | HG00544.hp1 HG00639.hp1 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.1738-863C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402215 | |||||||
| chr11:402216 | C | CG | 2 | a0001c0008t0001g0189 a0001c0030t0001g0174 |
2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-862_1738-861i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402216 | |||||||
| chr11:402218 | G | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(93): Show |
100 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1738-860G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402218 | |||||||
| chr11:402218 | G | GACCCCCG others(126): Show |
1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1738-860_1738-859i others(135): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402218 | |||||||
| chr11:402218 | G | T | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1738-860G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402218 | |||||||
| chr11:402219 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0053 others(27): Show |
30 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1738-859G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402219 | |||||||
| chr11:402219 | G | GA | 11 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0043 others(8): Show |
11 | HG00621.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1738-859_1738-858i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402219 | |||||||
| chr11:402220 | C | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0046 others(3): Show |
6 | HG02723.hp1 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-858C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402220 | |||||||
| chr11:402220 | C | G | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1738-858C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402220 | |||||||
| chr11:402227 | C | G | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-851C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402227 | |||||||
| chr11:402229 | C | CCCCCGAC others(196): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1738-846_1738-845i others(205): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402229 | ||||||
| chr11:402229 | C | CCCCCGAC others(108): Show |
1 | a0001c0028t0001g0128 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1738-846_1738-845i others(117): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402229 | ||||||
| chr11:402229 | C | CCCCCGAC others(107): Show |
4 | a0001c0002t0001g0101 a0001c0002t0001g0131 a0001c0002t0001g0135 others(1): Show |
4 | HG00639.hp2 HG01069.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-846_1738-845i others(116): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402229 | ||||||
| chr11:402230 | C | A | 12 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0041 others(9): Show |
12 | HG00621.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-848C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402230 | |||||||
| chr11:402232 | C | G | 1 | a0017c0027t0001g0107 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1738-846C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402232 | |||||||
| chr11:402232 | CG | C | 17 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0002t0001g0145 others(14): Show |
18 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1738-844delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402232 | ||||||
| chr11:402233 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(100): Show |
106 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.1738-845G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402233 | |||||||
| chr11:402234 | G | C | 1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1738-844G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402234 | |||||||
| chr11:402234 | GA | G | 3 | a0001c0001t0001g0072 a0001c0003t0001g0116 a0001c0009t0001g0122 |
3 | HG02027.hp2 HG02148.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1738-843delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402234 | |||||||
| chr11:402234 | GACCCCGC others(56): Show |
G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0064 |
3 | HG02004.hp1 HG02056.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1738-837_1738-775d others(65): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402234 | ||||||
| chr11:402235 | A | ACCCCCGG | 19 | a0001c0002t0001g0110 a0001c0002t0001g0118 a0001c0002t0001g0125 others(16): Show |
19 | HG00733.hp1 HG01256.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1738-839_1738-838i others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402235 | ||||||
| chr11:402235 | A | C | 1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-843A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402235 | |||||||
| chr11:402235 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(65): Show |
71 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1738-843A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402235 | |||||||
| chr11:402235 | AC | A | 3 | a0001c0001t0001g0016 a0001c0003t0001g0114 a0001c0008t0001g0188 |
3 | HG02129.hp1 HG02622.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1738-839delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402235 | ||||||
| chr11:402243 | CACCCCCG | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(19): Show |
22 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1738-827_1738-821d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402243 | ||||||
| chr11:402245 | CCCCCGAC others(31): Show |
C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(30): Show |
35 | HG00099.hp1 HG00609.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.1738-827_1738-790d others(40): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402245 | ||||||
| chr11:402246 | C | A | 5 | a0001c0001t0001g0089 a0001c0004t0001g0094 a0001c0008t0001g0093 others(2): Show |
5 | HG02486.hp1 HG03209.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-832C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402246 | |||||||
| chr11:402246 | CCCCGACC others(30): Show |
C | 3 | a0001c0001t0001g0082 a0001c0005t0001g0013 a0001c0006t0001g0049 |
3 | HG01175.hp2 HG02145.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1738-828_1738-792d others(39): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402246 | ||||||
| chr11:402249 | C | CCGGCCCC others(3): Show |
1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1738-829_1738-828i others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402249 | |||||||
| chr11:402249 | C | G | 2 | a0001c0007t0001g0007 a0007c0029t0001g0117 |
2 | HG01515.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1738-829C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402249 | |||||||
| chr11:402249 | CGACCCCC others(1): Show |
C | 11 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1738-827_1738-820d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402249 | ||||||
| chr11:402250 | G | C | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1738-828G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402250 | |||||||
| chr11:402250 | G | GACCCGCT others(1): Show |
2 | a0001c0001t0001g0089 a0001c0004t0001g0094 |
2 | HG03688.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1738-824_1738-823i others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402250 | ||||||
| chr11:402251 | A | G | 1 | a0001c0011t0001g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1738-827A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402251 | |||||||
| chr11:402252 | C | CCCGCTCA | 9 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0002t0001g0118 others(6): Show |
9 | HG00733.hp1 HG01175.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-824_1738-823i others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402252 | ||||||
| chr11:402253 | C | A | 1 | a0015c0026t0004g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1738-825C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402253 | |||||||
| chr11:402253 | C | CCACTCAC others(47): Show |
2 | a0001c0002t0001g0110 a0001c0010t0003g0021 |
2 | HG02723.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1738-824_1738-823i others(56): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402253 | ||||||
| chr11:402253 | C | CCGCTCAC others(146): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1738-824_1738-823i others(155): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402253 | ||||||
| chr11:402254 | C | CACTCACA others(185): Show |
1 | a0001c0010t0001g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1738-824_1738-823i others(194): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402254 | |||||||
| chr11:402254 | C | CACTCACA others(185): Show |
1 | a0001c0002t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1738-824_1738-823i others(194): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402254 | |||||||
| chr11:402254 | C | CACTCACA others(186): Show |
1 | a0001c0002t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1738-824_1738-823i others(195): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402254 | |||||||
| chr11:402254 | C | CACTCACA others(184): Show |
12 | a0001c0002t0001g0146 a0001c0003t0001g0095 a0001c0003t0001g0098 others(9): Show |
12 | HG01256.hp1 HG01952.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-824_1738-823i others(193): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402254 | |||||||
| chr11:402254 | C | CGCTCACC others(30): Show |
1 | a0019c0032t0001g0144 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1738-824_1738-823i others(39): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402254 | |||||||
| chr11:402254 | C | CGCTCACC others(62): Show |
2 | a0001c0003t0001g0096 a0001c0003t0001g0115 |
2 | HG01358.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1738-824_1738-823i others(71): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402254 | |||||||
| chr11:402254 | C | CGCTCACC others(61): Show |
29 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(26): Show |
30 | HG00544.hp1 HG00639.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1738-824_1738-823i others(70): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402254 | |||||||
| chr11:402255 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0046 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1738-823C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402255 | |||||||
| chr11:402256 | C | G | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1738-822C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402256 | |||||||
| chr11:402257 | G | C | 52 | a0001c0001t0001g0041 a0001c0001t0001g0070 a0001c0001t0001g0078 others(49): Show |
53 | HG00544.hp1 HG00621.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1738-821G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402257 | |||||||
| chr11:402257 | G | GGCCCCCG others(273): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1738-816_1738-815i others(282): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402257 | ||||||
| chr11:402258 | G | A | 4 | a0001c0002t0001g0118 a0001c0007t0001g0007 a0001c0007t0001g0025 others(1): Show |
4 | HG00733.hp1 HG01515.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-820G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402258 | |||||||
| chr11:402259 | C | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0046 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1738-819C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402259 | |||||||
| chr11:402266 | C | CACCCCCG | 2 | a0001c0004t0001g0073 a0001c0007t0001g0007 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1738-811_1738-805d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402266 | ||||||
| chr11:402266 | C | CACCCCCG others(107): Show |
1 | a0001c0003t0001g0003 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1738-805_1738-804i others(116): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402266 | ||||||
| chr11:402267 | AC | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0019 others(22): Show |
25 | HG00544.hp2 HG00673.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1738-806delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402267 | ||||||
| chr11:402268 | C | A | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1738-810C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402268 | |||||||
| chr11:402268 | C | CCCCAGCC others(54): Show |
1 | a0012c0020t0001g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1738-807_1738-806i others(63): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402268 | ||||||
| chr11:402268 | C | CCCCGACC others(107): Show |
1 | a0001c0036t0001g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1738-807_1738-806i others(116): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402268 | ||||||
| chr11:402268 | CCCCCGGC others(8): Show |
C | 7 | a0001c0001t0001g0072 a0001c0001t0001g0195 a0001c0002t0001g0130 others(4): Show |
7 | HG00609.hp1 HG01243.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-802_1738-788d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402268 | ||||||
| chr11:402269 | C | A | 3 | a0001c0002t0001g0168 a0001c0007t0001g0025 a0001c0008t0001g0093 |
3 | HG03209.hp2 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1738-809C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402269 | |||||||
| chr11:402269 | CCCCGGCT others(7): Show |
C | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1738-805_1738-792d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402269 | ||||||
| chr11:402271 | C | G | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1738-807C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402271 | |||||||
| chr11:402272 | C | G | 49 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(46): Show |
50 | HG00544.hp1 HG00639.hp1 HG01256.hp1 others(47): Show |
intron_variant | MODIFIER | c.1738-806C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402272 | |||||||
| chr11:402272 | CG | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0002t0001g0118 |
3 | HG00733.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-804delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402272 | ||||||
| chr11:402272 | CGGCTCCA others(9): Show |
C | 1 | a0001c0007t0001g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1738-804_1738-789d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402272 | ||||||
| chr11:402273 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0002t0001g0168 others(4): Show |
7 | HG01175.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-805G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402273 | |||||||
| chr11:402273 | G | C | 1 | a0001c0016t0001g0200 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1738-805G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402273 | |||||||
| chr11:402274 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(63): Show |
67 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1738-804G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402274 | |||||||
| chr11:402274 | G | T | 1 | a0015c0026t0004g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1738-804G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402274 | |||||||
| chr11:402275 | C | A | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1738-803C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402275 | |||||||
| chr11:402275 | CT | C | 3 | a0001c0002t0001g0132 a0001c0008t0001g0093 a0015c0026t0004g0092 |
3 | HG00099.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-802delT | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402275 | |||||||
| chr11:402276 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(124): Show |
129 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.1738-802T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402276 | |||||||
| chr11:402279 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0019 others(123): Show |
128 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.1738-799A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402279 | |||||||
| chr11:402282 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(127): Show |
132 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1738-796G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402282 | |||||||
| chr11:402283 | A | AC | 73 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0039 others(70): Show |
75 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1738-791dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402283 | ||||||
| chr11:402283 | A | ACACCCCG others(142): Show |
1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-794_1738-793i others(151): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402283 | ||||||
| chr11:402283 | A | ACCCCCGA others(179): Show |
1 | a0001c0016t0001g0200 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1738-791_1738-790i others(188): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402283 | ||||||
| chr11:402285 | C | A | 16 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0046 others(13): Show |
16 | HG01175.hp1 HG02148.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1738-793C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402285 | |||||||
| chr11:402285 | C | CCCCGCCC others(843): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1738-791_1738-790i others(852): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402285 | ||||||
| chr11:402288 | G | C | 25 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0029 others(22): Show |
25 | HG00639.hp2 HG01069.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1738-790G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402288 | |||||||
| chr11:402288 | G | T | 1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1738-790G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402288 | |||||||
| chr11:402289 | G | A | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG01496.hp1 HG01943.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-789G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402289 | |||||||
| chr11:402289 | G | C | 2 | a0001c0003t0001g0166 a0001c0004t0001g0027 |
2 | HG00642.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1738-789G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402289 | |||||||
| chr11:402289 | GCCCCGCT others(1): Show |
G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(11): Show |
14 | HG00544.hp2 HG00673.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.1738-788_1738-781d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402289 | |||||||
| chr11:402290 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0081 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-788C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402290 | |||||||
| chr11:402290 | C | G | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1738-788C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402290 | |||||||
| chr11:402299 | C | CCCCCCGA others(264): Show |
1 | a0006c0031t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1738-776_1738-775i others(273): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402299 | ||||||
| chr11:402299 | C | CCCCCGGG others(9): Show |
1 | a0001c0002t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1738-776_1738-775i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402299 | ||||||
| chr11:402300 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0081 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-778C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402300 | |||||||
| chr11:402302 | CG | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(115): Show |
122 | HG00099.hp1 HG00544.hp1 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.1738-774delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402302 | ||||||
| chr11:402303 | G | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0019 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1738-775G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402303 | |||||||
| chr11:402303 | G | GGGACCCG others(8): Show |
4 | a0001c0002t0001g0101 a0001c0002t0001g0131 a0001c0002t0001g0137 others(1): Show |
4 | HG00639.hp2 HG01069.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-774_1738-773i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402303 | ||||||
| chr11:402304 | G | A | 3 | a0001c0001t0001g0082 a0001c0012t0001g0120 a0001c0021t0001g0086 |
3 | HG02027.hp1 HG02622.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1738-774G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402304 | |||||||
| chr11:402304 | GA | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0002t0001g0118 others(4): Show |
7 | HG00099.hp2 HG00733.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-773delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402304 | |||||||
| chr11:402305 | A | ACCCCCGG | 7 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(4): Show |
7 | HG01943.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-769_1738-768i others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402305 | ||||||
| chr11:402305 | A | C | 5 | a0001c0001t0001g0082 a0001c0004t0001g0027 a0001c0008t0001g0188 others(2): Show |
5 | HG00642.hp1 HG02027.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-773A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402305 | |||||||
| chr11:402305 | A | G | 3 | a0001c0007t0001g0007 a0001c0007t0001g0025 a0015c0026t0004g0092 |
3 | HG02886.hp2 HG03834.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1738-773A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402305 | |||||||
| chr11:402305 | AC | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0008t0001g0093 |
3 | HG02723.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-769delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402305 | ||||||
| chr11:402305 | ACCCCGCT others(16): Show |
A | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-734_1738-712d others(25): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402305 | ||||||
| chr11:402313 | C | G | 2 | a0001c0007t0001g0007 a0001c0007t0001g0025 |
2 | HG03834.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1738-765C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402313 | |||||||
| chr11:402313 | CACCCCCG | C | 6 | a0001c0001t0001g0011 a0001c0005t0001g0023 a0001c0005t0001g0032 others(3): Show |
6 | HG01175.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-757_1738-751d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402313 | ||||||
| chr11:402316 | C | A | 3 | a0001c0001t0001g0056 a0001c0008t0001g0189 a0001c0030t0001g0174 |
3 | HG03130.hp2 HG03579.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1738-762C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402316 | |||||||
| chr11:402319 | C | CGGCCCCG others(24): Show |
1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1738-758_1738-757i others(33): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402319 | ||||||
| chr11:402319 | C | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(116): Show |
122 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.1738-759C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402319 | |||||||
| chr11:402319 | CGACCCCC others(55): Show |
C | 1 | a0001c0008t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1738-757_1738-696d others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402319 | ||||||
| chr11:402321 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0002t0001g0118 others(1): Show |
4 | HG00733.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-757A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402321 | |||||||
| chr11:402322 | C | CCCGCTCA | 7 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0081 others(4): Show |
7 | HG02148.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-754_1738-753i others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402322 | ||||||
| chr11:402322 | C | CCCGCTCA others(15): Show |
1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1738-754_1738-753i others(24): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402322 | ||||||
| chr11:402323 | C | A | 5 | a0001c0001t0001g0011 a0001c0005t0001g0023 a0001c0005t0001g0032 others(2): Show |
5 | HG01175.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-755C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402323 | |||||||
| chr11:402323 | C | CCACTCAC others(1): Show |
8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG00642.hp1 HG01943.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-754_1738-753i others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402323 | ||||||
| chr11:402324 | C | CGCTCACA | 2 | a0001c0001t0001g0016 a0001c0001t0001g0089 |
2 | HG02129.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1738-754_1738-753i others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402324 | |||||||
| chr11:402327 | G | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0056 others(3): Show |
6 | HG02129.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-751G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402327 | |||||||
| chr11:402328 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(83): Show |
89 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1738-750G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402328 | |||||||
| chr11:402329 | C | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(1): Show |
4 | HG02129.hp1 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-749C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402329 | |||||||
| chr11:402329 | C | G | 1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1738-749C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402329 | |||||||
| chr11:402336 | CACCCCCG | C | 4 | a0001c0001t0001g0056 a0001c0008t0001g0093 a0001c0008t0001g0188 others(1): Show |
4 | HG02622.hp1 HG03209.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-734_1738-728d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402336 | ||||||
| chr11:402337 | A | C | 1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-741A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402337 | |||||||
| chr11:402338 | C | A | 1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-740C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402338 | |||||||
| chr11:402339 | C | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(14): Show |
17 | HG00544.hp2 HG00673.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.1738-739C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402339 | |||||||
| chr11:402341 | C | G | 1 | a0001c0030t0001g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1738-737C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402341 | |||||||
| chr11:402342 | C | A | 5 | a0001c0001t0001g0028 a0001c0002t0001g0110 a0001c0003t0001g0116 others(2): Show |
5 | HG02148.hp2 HG02723.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-736C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402342 | |||||||
| chr11:402342 | C | CGACCCGC others(1153): Show |
1 | a0001c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1738-731_1738-730i others(1162): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402342 | ||||||
| chr11:402342 | C | CGGCCCCG others(952): Show |
1 | a0001c0002t0001g0101 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1738-735_1738-734i others(961): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402342 | ||||||
| chr11:402342 | C | CGGCCCCG others(952): Show |
1 | a0001c0028t0001g0128 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1738-735_1738-734i others(961): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402342 | ||||||
| chr11:402342 | C | CGGCCCCG others(937): Show |
1 | a0001c0002t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1738-735_1738-734i others(946): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402342 | ||||||
| chr11:402342 | C | CGGCCCCG others(936): Show |
1 | a0001c0002t0001g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1738-735_1738-734i others(945): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402342 | ||||||
| chr11:402342 | C | CGGCCCCG others(956): Show |
1 | a0001c0002t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1738-735_1738-734i others(965): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402342 | ||||||
| chr11:402342 | C | G | 4 | a0001c0002t0001g0132 a0001c0002t0001g0136 a0001c0030t0001g0174 others(1): Show |
4 | HG00099.hp2 HG02886.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-736C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402342 | |||||||
| chr11:402342 | CGACCCCC others(1): Show |
C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0019 others(17): Show |
20 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1738-734_1738-727d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402342 | ||||||
| chr11:402343 | G | GACCCGCT others(17): Show |
1 | a0001c0004t0001g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1738-731_1738-730i others(26): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402343 | ||||||
| chr11:402343 | G | GCCCCGCT others(1): Show |
3 | a0001c0005t0001g0023 a0001c0005t0001g0032 a0004c0015t0001g0047 |
3 | HG01175.hp1 HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1738-735_1738-734i others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402343 | |||||||
| chr11:402343 | G | GCCCCGCT others(123): Show |
1 | a0001c0002t0001g0132 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1738-735_1738-734i others(132): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402343 | |||||||
| chr11:402343 | G | GCCCCGCT others(47): Show |
4 | a0001c0002t0001g0110 a0001c0003t0001g0116 a0001c0010t0003g0021 others(1): Show |
4 | HG02148.hp2 HG02723.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-735_1738-734i others(56): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402343 | |||||||
| chr11:402343 | G | GCCCCGCT others(16): Show |
1 | a0001c0003t0001g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1738-735_1738-734i others(25): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402343 | |||||||
| chr11:402343 | G | GCCCCGCT others(169): Show |
5 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-735_1738-734i others(178): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402343 | |||||||
| chr11:402343 | G | GGCCCCCG others(261): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1738-735_1738-734i others(270): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402343 | |||||||
| chr11:402343 | G | GGCCCGCT others(32): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0089 |
2 | HG02129.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1738-735_1738-734i others(41): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402343 | |||||||
| chr11:402344 | A | C | 1 | a0001c0001t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1738-734A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402344 | |||||||
| chr11:402345 | C | CCCACTCA others(199): Show |
4 | a0001c0002t0001g0145 a0001c0002t0001g0170 a0001c0003t0001g0003 others(1): Show |
5 | HG00609.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-731_1738-730i others(208): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402345 | ||||||
| chr11:402346 | C | A | 2 | a0001c0003t0001g0151 a0001c0008t0001g0188 |
2 | HG01943.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1738-732C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402346 | |||||||
| chr11:402348 | C | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(3): Show |
6 | HG02129.hp1 HG02723.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-730C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402348 | |||||||
| chr11:402349 | C | G | 11 | a0001c0002t0001g0110 a0001c0002t0001g0132 a0001c0002t0001g0171 others(8): Show |
11 | HG00099.hp2 HG01515.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1738-729C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402349 | |||||||
| chr11:402350 | G | C | 3 | a0001c0001t0001g0028 a0001c0003t0001g0140 a0001c0009t0001g0102 |
3 | HG01952.hp2 HG03453.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1738-728G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402350 | |||||||
| chr11:402351 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(135): Show |
141 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1738-727G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402351 | |||||||
| chr11:402351 | G | C | 3 | a0001c0003t0001g0143 a0001c0003t0001g0166 a0001c0008t0001g0188 |
3 | HG00673.hp1 HG02135.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1738-727G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402351 | |||||||
| chr11:402351 | G | GA | 4 | a0001c0002t0001g0145 a0001c0002t0001g0170 a0001c0003t0001g0003 others(1): Show |
5 | HG00609.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-727_1738-726i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402351 | |||||||
| chr11:402351 | G | GCCCCGCT others(177): Show |
2 | a0001c0004t0001g0027 a0014c0034t0001g0157 |
2 | HG00642.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1738-712_1738-711i others(186): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402351 | ||||||
| chr11:402352 | C | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(3): Show |
6 | HG02129.hp1 HG02723.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-726C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402352 | |||||||
| chr11:402361 | CCCCCGGC others(8): Show |
C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(14): Show |
17 | HG00544.hp2 HG00673.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.1738-709_1738-695d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402361 | ||||||
| chr11:402362 | C | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(120): Show |
126 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1738-716C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402362 | |||||||
| chr11:402363 | C | A | 1 | a0001c0009t0001g0121 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1738-715C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402363 | |||||||
| chr11:402365 | C | G | 2 | a0001c0001t0001g0028 a0001c0008t0001g0188 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1738-713C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402365 | |||||||
| chr11:402365 | CG | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(108): Show |
114 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.1738-711delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402365 | ||||||
| chr11:402365 | CGGCTCCA others(9): Show |
C | 1 | a0001c0030t0001g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1738-711_1738-696d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402365 | ||||||
| chr11:402365 | CGGCTCCA others(48): Show |
C | 2 | a0001c0011t0001g0001 a0001c0021t0001g0086 |
2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1738-711_1738-657d others(57): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402365 | ||||||
| chr11:402365 | CGGCTCCA others(118): Show |
C | 4 | a0001c0004t0001g0176 a0001c0004t0001g0196 a0003c0019t0001g0181 others(1): Show |
4 | HG03471.hp2 HG03540.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-711_1738-587d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402365 | ||||||
| chr11:402366 | G | C | 3 | a0001c0002t0001g0103 a0001c0009t0001g0121 a0001c0009t0001g0122 |
3 | HG03453.hp1 NA18994.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1738-712G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402366 | |||||||
| chr11:402366 | GGCTCCAC others(87): Show |
G | 1 | a0015c0026t0004g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1738-711_1738-618d others(96): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402366 | |||||||
| chr11:402367 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1738-711G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402367 | |||||||
| chr11:402367 | G | C | 3 | a0001c0001t0001g0048 a0001c0008t0001g0188 a0006c0031t0001g0163 |
3 | HG01496.hp1 HG02622.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1738-711G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402367 | |||||||
| chr11:402369 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.1738-709T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402369 | |||||||
| chr11:402372 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.1738-706A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402372 | |||||||
| chr11:402372 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1738-706A>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402372 | |||||||
| chr11:402374 | T | A | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1738-704T>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402374 | |||||||
| chr11:402375 | G | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.1738-703G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402375 | |||||||
| chr11:402376 | A | AC | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(108): Show |
114 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.1738-698dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402376 | ||||||
| chr11:402376 | ACCCCGGC others(32): Show |
A | 1 | a0001c0007t0001g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1738-682_1738-644d others(41): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402376 | ||||||
| chr11:402378 | C | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0046 others(5): Show |
8 | HG01943.hp2 HG02129.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-700C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402378 | |||||||
| chr11:402381 | G | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0046 others(6): Show |
9 | HG00733.hp1 HG01943.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-697G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402381 | |||||||
| chr11:402382 | G | A | 21 | a0001c0001t0001g0056 a0001c0002t0001g0110 a0001c0002t0001g0132 others(18): Show |
22 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1738-696G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402382 | |||||||
| chr11:402382 | G | C | 2 | a0001c0003t0001g0140 a0001c0009t0001g0102 |
2 | HG01952.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1738-696G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402382 | |||||||
| chr11:402390 | C | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(129): Show |
136 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1738-688C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402390 | |||||||
| chr11:402392 | CCCCGGAC others(47): Show |
C | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1738-682_1738-629d others(56): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402392 | ||||||
| chr11:402395 | C | G | 2 | a0001c0008t0001g0188 a0001c0008t0001g0189 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1738-683C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402395 | |||||||
| chr11:402395 | CG | C | 10 | a0001c0001t0001g0011 a0001c0002t0001g0101 a0001c0002t0001g0130 others(7): Show |
10 | HG00639.hp2 HG01069.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738-681delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402395 | ||||||
| chr11:402396 | G | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(130): Show |
137 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.1738-682G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402396 | |||||||
| chr11:402396 | G | GGACCCCC | 3 | a0001c0001t0001g0056 a0001c0005t0001g0023 a0001c0005t0001g0032 |
3 | HG02258.hp1 NA18966.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1738-676_1738-675i others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402396 | ||||||
| chr11:402396 | G | GGGACCCG others(8): Show |
1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1738-681_1738-680i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402396 | ||||||
| chr11:402397 | G | C | 2 | a0001c0002t0001g0103 a0001c0003t0001g0140 |
2 | HG01952.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1738-681G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402397 | |||||||
| chr11:402397 | GA | G | 2 | a0001c0001t0001g0028 a0001c0008t0001g0093 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1738-680delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402397 | |||||||
| chr11:402398 | A | ACCCCCGG | 17 | a0001c0002t0001g0110 a0001c0002t0001g0132 a0001c0002t0001g0145 others(14): Show |
18 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1738-676_1738-675i others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402398 | ||||||
| chr11:402398 | A | G | 2 | a0001c0002t0001g0103 a0001c0003t0001g0140 |
2 | HG01952.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1738-680A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402398 | |||||||
| chr11:402398 | AC | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(125): Show |
132 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1738-676delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402398 | ||||||
| chr11:402399 | C | A | 2 | a0001c0002t0001g0103 a0001c0003t0001g0140 |
2 | HG01952.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1738-679C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402399 | |||||||
| chr11:402406 | CACCCCCG | C | 2 | a0001c0001t0001g0028 a0001c0030t0001g0174 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-664_1738-658d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402406 | ||||||
| chr11:402409 | C | A | 4 | a0001c0001t0001g0046 a0001c0008t0001g0093 a0001c0008t0001g0188 others(1): Show |
4 | HG02622.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-669C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402409 | |||||||
| chr11:402412 | C | G | 2 | a0001c0001t0001g0011 a0001c0009t0001g0102 |
2 | HG02922.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1738-666C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402412 | |||||||
| chr11:402412 | CGACCCCC others(1): Show |
C | 3 | a0001c0008t0001g0093 a0001c0008t0001g0188 a0001c0008t0001g0189 |
3 | HG02622.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-664_1738-657d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402412 | ||||||
| chr11:402414 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1738-664A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402414 | |||||||
| chr11:402415 | C | CCCGCTCA | 5 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(2): Show |
5 | HG02129.hp1 HG02723.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-661_1738-660i others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402415 | ||||||
| chr11:402415 | C | CCCGCTCA others(76): Show |
1 | a0001c0003t0001g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1738-661_1738-660i others(85): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402415 | ||||||
| chr11:402419 | CGGCCCCG others(40): Show |
C | 1 | a0001c0009t0001g0102 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1738-657_1738-611d others(49): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402419 | ||||||
| chr11:402420 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1738-658G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402420 | |||||||
| chr11:402421 | G | A | 22 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0002t0001g0110 others(19): Show |
23 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1738-657G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402421 | |||||||
| chr11:402421 | G | C | 1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1738-657G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402421 | |||||||
| chr11:402430 | AC | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(3): Show |
6 | HG02129.hp1 HG02723.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-643delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402430 | ||||||
| chr11:402431 | CCCCCGGC others(8): Show |
C | 2 | a0001c0011t0001g0001 a0001c0021t0001g0086 |
2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1738-639_1738-625d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402431 | ||||||
| chr11:402431 | CCCCCGGC others(78): Show |
C | 6 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0007t0001g0025 others(3): Show |
6 | HG00733.hp2 HG02056.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-639_1738-555d others(87): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402431 | ||||||
| chr11:402432 | C | A | 21 | a0001c0001t0001g0056 a0001c0002t0001g0110 a0001c0002t0001g0132 others(18): Show |
22 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1738-646C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402432 | |||||||
| chr11:402432 | CCCCGGCT others(7): Show |
C | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-642_1738-629d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402432 | ||||||
| chr11:402435 | C | G | 2 | a0001c0008t0001g0188 a0001c0008t0001g0189 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1738-643C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402435 | |||||||
| chr11:402435 | CG | C | 20 | a0001c0001t0001g0056 a0001c0002t0001g0110 a0001c0002t0001g0132 others(17): Show |
21 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1738-641delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402435 | ||||||
| chr11:402436 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 |
3 | HG02129.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-642G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402436 | |||||||
| chr11:402436 | GGCTCCAC others(17): Show |
G | 1 | a0001c0001t0001g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1738-641_1738-618d others(26): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402436 | |||||||
| chr11:402437 | G | A | 3 | a0001c0008t0001g0188 a0001c0008t0001g0189 a0001c0030t0001g0174 |
3 | HG02622.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-641G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402437 | |||||||
| chr11:402437 | G | C | 1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1738-641G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402437 | |||||||
| chr11:402439 | T | C | 41 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(38): Show |
42 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1738-639T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402439 | |||||||
| chr11:402442 | A | G | 41 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(38): Show |
42 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1738-636A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402442 | |||||||
| chr11:402445 | G | C | 41 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(38): Show |
42 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1738-633G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402445 | |||||||
| chr11:402446 | A | AC | 24 | a0001c0001t0001g0046 a0001c0001t0001g0056 a0001c0002t0001g0110 others(21): Show |
25 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1738-628dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402446 | ||||||
| chr11:402446 | ACCCCGGC others(101): Show |
A | 10 | a0001c0001t0001g0048 a0001c0001t0001g0072 a0001c0001t0001g0078 others(7): Show |
10 | HG01243.hp1 HG01261.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738-612_1738-505d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402446 | ||||||
| chr11:402446 | ACCCCGGC others(155): Show |
A | 1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1738-612_1738-451d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402446 | ||||||
| chr11:402448 | C | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(3): Show |
6 | HG02129.hp1 HG02723.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-630C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402448 | |||||||
| chr11:402451 | G | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(4): Show |
7 | HG00733.hp1 HG02129.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-627G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402451 | |||||||
| chr11:402452 | G | A | 9 | a0001c0001t0001g0028 a0001c0002t0001g0101 a0001c0002t0001g0130 others(6): Show |
9 | HG00639.hp2 HG01069.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-626G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402452 | |||||||
| chr11:402452 | G | C | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1738-626G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402452 | |||||||
| chr11:402452 | GCCCCGCT others(132): Show |
G | 1 | a0001c0005t0001g0085 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1738-612_1738-474d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402452 | ||||||
| chr11:402460 | C | G | 23 | a0001c0001t0001g0056 a0001c0002t0001g0110 a0001c0002t0001g0132 others(20): Show |
24 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1738-618C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402460 | |||||||
| chr11:402460 | CACCCCGG others(139): Show |
C | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1738-612_1738-467d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402460 | ||||||
| chr11:402462 | CCCCGGAC others(47): Show |
C | 2 | a0001c0007t0001g0010 a0001c0012t0001g0120 |
2 | HG01243.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.1738-612_1738-559d others(56): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402462 | ||||||
| chr11:402462 | CCCCGGAC others(138): Show |
C | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1738-612_1738-468d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402462 | ||||||
| chr11:402462 | CCCCGGAC others(154): Show |
C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(55): Show |
61 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1738-612_1738-452d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402462 | ||||||
| chr11:402463 | CCCGGACC others(153): Show |
C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0064 a0001c0001t0001g0067 |
3 | HG01934.hp1 HG02056.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1738-612_1738-453d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402463 | ||||||
| chr11:402465 | C | G | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1738-613C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402465 | |||||||
| chr11:402465 | CG | C | 4 | a0001c0001t0001g0046 a0001c0003t0001g0114 a0001c0007t0001g0007 others(1): Show |
4 | HG02976.hp2 HG03130.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-611delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402465 | ||||||
| chr11:402466 | G | C | 34 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0002t0001g0101 others(31): Show |
35 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1738-612G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402466 | |||||||
| chr11:402466 | G | GGGACCCG others(901): Show |
1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1738-611_1738-610i others(910): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402466 | ||||||
| chr11:402468 | AC | A | 23 | a0001c0001t0001g0056 a0001c0002t0001g0110 a0001c0002t0001g0132 others(20): Show |
24 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1738-606delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402468 | ||||||
| chr11:402469 | C | CCCCCGGC others(354): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1738-606_1738-605i others(363): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402469 | ||||||
| chr11:402469 | C | CCCCCGGC others(353): Show |
6 | a0001c0002t0001g0101 a0001c0002t0001g0130 a0001c0002t0001g0131 others(3): Show |
6 | HG00639.hp2 HG01069.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-606_1738-605i others(362): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402469 | ||||||
| chr11:402469 | C | CCCCCGGC others(69): Show |
1 | a0001c0003t0001g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1738-606_1738-605i others(78): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402469 | ||||||
| chr11:402472 | C | T | 1 | a0005c0022t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1738-606C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402472 | |||||||
| chr11:402477 | AC | A | 54 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(51): Show |
55 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1738-596delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402477 | ||||||
| chr11:402478 | CCCCCGAC others(31): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1738-594_1738-557d others(40): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402478 | ||||||
| chr11:402479 | C | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0029 others(5): Show |
8 | HG02129.hp1 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-599C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402479 | |||||||
| chr11:402482 | C | G | 4 | a0001c0001t0001g0046 a0001c0002t0001g0118 a0001c0008t0001g0188 others(1): Show |
4 | HG00733.hp1 HG02622.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-596C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402482 | |||||||
| chr11:402482 | CGACCCCC others(1): Show |
C | 3 | a0001c0001t0001g0011 a0001c0008t0001g0093 a0015c0026t0004g0092 |
3 | HG02886.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-594_1738-587d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402482 | ||||||
| chr11:402483 | G | GCCCCGCT others(157): Show |
2 | a0001c0001t0001g0089 a0001c0004t0001g0094 |
2 | HG03688.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1738-595_1738-594i others(166): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402483 | |||||||
| chr11:402484 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 |
3 | HG02129.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-594A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402484 | |||||||
| chr11:402490 | G | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 |
3 | HG02129.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1738-588G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402490 | |||||||
| chr11:402491 | G | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0002t0001g0118 others(4): Show |
7 | HG00733.hp1 HG02622.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-587G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402491 | |||||||
| chr11:402493 | C | T | 5 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(2): Show |
5 | HG03471.hp1 NA18906.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-585C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402493 | |||||||
| chr11:402501 | CCCCCGGC others(8): Show |
C | 4 | a0001c0004t0001g0176 a0001c0004t0001g0196 a0003c0019t0001g0181 others(1): Show |
4 | HG03471.hp2 HG03540.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-569_1738-555d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402501 | ||||||
| chr11:402502 | C | A | 3 | a0001c0001t0001g0028 a0001c0009t0001g0102 a0001c0030t0001g0174 |
3 | HG03453.hp2 HG03579.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1738-576C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402502 | |||||||
| chr11:402505 | C | G | 1 | a0001c0008t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1738-573C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402505 | |||||||
| chr11:402505 | CGGCTCCA others(9): Show |
C | 2 | a0001c0007t0001g0007 a0001c0030t0001g0174 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1738-571_1738-556d others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402505 | ||||||
| chr11:402506 | G | C | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-572G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402506 | |||||||
| chr11:402506 | GGCTCCAC others(55): Show |
G | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1738-571_1738-510d others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402506 | |||||||
| chr11:402506 | GGCTCCAC others(361): Show |
G | 5 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(2): Show |
5 | HG03471.hp1 NA18906.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-571_1738-204d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402506 | |||||||
| chr11:402507 | G | A | 3 | a0001c0001t0001g0046 a0001c0008t0001g0093 a0001c0008t0001g0189 |
3 | HG02976.hp2 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-571G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402507 | |||||||
| chr11:402508 | C | A | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-570C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402508 | |||||||
| chr11:402509 | T | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(9): Show |
12 | HG02129.hp1 HG02723.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-569T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402509 | |||||||
| chr11:402512 | A | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(7): Show |
10 | HG02129.hp1 HG02723.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1738-566A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402512 | |||||||
| chr11:402515 | G | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(7): Show |
10 | HG02129.hp1 HG02723.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1738-563G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402515 | |||||||
| chr11:402516 | A | AC | 9 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(6): Show |
9 | HG00673.hp1 HG02129.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-558dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402516 | ||||||
| chr11:402517 | CCCCGGCC others(7): Show |
C | 2 | a0001c0001t0001g0011 a0015c0026t0004g0092 |
2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1738-557_1738-544d others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402517 | ||||||
| chr11:402518 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1738-560C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402518 | |||||||
| chr11:402521 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1738-557G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402521 | |||||||
| chr11:402522 | G | A | 1 | a0001c0008t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1738-556G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402522 | |||||||
| chr11:402522 | G | C | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-556G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402522 | |||||||
| chr11:402523 | C | A | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1738-555C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402523 | |||||||
| chr11:402530 | C | G | 2 | a0001c0001t0001g0028 a0001c0009t0001g0102 |
2 | HG03453.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1738-548C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402530 | |||||||
| chr11:402531 | A | AC | 5 | a0001c0001t0001g0046 a0001c0001t0001g0202 a0001c0003t0001g0166 others(2): Show |
5 | HG01261.hp1 HG01496.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-543dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402531 | ||||||
| chr11:402532 | CCCCGACC others(84): Show |
C | 5 | a0001c0001t0001g0056 a0001c0005t0001g0023 a0001c0005t0001g0032 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-542_1738-452d others(93): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402532 | ||||||
| chr11:402533 | C | A | 5 | a0001c0004t0001g0176 a0001c0004t0001g0196 a0001c0008t0001g0189 others(2): Show |
5 | HG03130.hp2 HG03471.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-545C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402533 | |||||||
| chr11:402535 | C | CG | 24 | a0001c0002t0001g0101 a0001c0002t0001g0110 a0001c0002t0001g0130 others(21): Show |
25 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1738-542dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402535 | ||||||
| chr11:402536 | G | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0089 a0001c0003t0001g0114 others(8): Show |
11 | HG01175.hp1 HG03130.hp2 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.1738-542G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402536 | |||||||
| chr11:402537 | A | G | 13 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0001g0089 others(10): Show |
13 | HG01175.hp1 HG02976.hp2 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.1738-541A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402537 | |||||||
| chr11:402538 | C | A | 2 | a0001c0001t0001g0028 a0001c0009t0001g0102 |
2 | HG03453.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1738-540C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402538 | |||||||
| chr11:402538 | C | G | 1 | a0004c0015t0001g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1738-540C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402538 | |||||||
| chr11:402540 | CCGCTCAC others(83): Show |
C | 1 | a0004c0015t0001g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1738-536_1738-447d others(92): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402540 | ||||||
| chr11:402545 | C | G | 2 | a0001c0001t0001g0046 a0001c0030t0001g0174 |
2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-533C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402545 | |||||||
| chr11:402545 | CACCCCCG | C | 4 | a0001c0004t0001g0176 a0001c0004t0001g0196 a0003c0019t0001g0181 others(1): Show |
4 | HG03471.hp2 HG03540.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-525_1738-519d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402545 | ||||||
| chr11:402545 | CACCCCCG others(54): Show |
C | 1 | a0001c0008t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1738-525_1738-465d others(63): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402545 | ||||||
| chr11:402546 | AC | A | 24 | a0001c0002t0001g0101 a0001c0002t0001g0110 a0001c0002t0001g0130 others(21): Show |
25 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1738-527delC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402546 | ||||||
| chr11:402551 | C | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0081 others(6): Show |
9 | HG02129.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-527C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402551 | |||||||
| chr11:402551 | C | T | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-527C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402551 | |||||||
| chr11:402551 | CGACCCCC others(17): Show |
C | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1738-525_1738-502d others(26): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402551 | ||||||
| chr11:402552 | G | GACCCGCT others(232): Show |
2 | a0001c0001t0001g0089 a0001c0004t0001g0094 |
2 | HG03688.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1738-522_1738-521i others(241): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402552 | ||||||
| chr11:402557 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1738-521C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402557 | |||||||
| chr11:402558 | C | G | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-520C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402558 | |||||||
| chr11:402559 | G | GACCCCGC others(31): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0081 |
2 | HG02129.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1738-519_1738-518i others(40): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402559 | |||||||
| chr11:402560 | G | A | 7 | a0001c0001t0001g0029 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-518G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402560 | |||||||
| chr11:402560 | G | C | 1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1738-518G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402560 | |||||||
| chr11:402560 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1738-518G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402560 | |||||||
| chr11:402562 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1738-516C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402562 | |||||||
| chr11:402565 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1738-513G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402565 | |||||||
| chr11:402567 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1738-511T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402567 | |||||||
| chr11:402568 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1738-510C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402568 | |||||||
| chr11:402570 | C | CCCCCGGC others(8): Show |
24 | a0001c0002t0001g0101 a0001c0002t0001g0110 a0001c0002t0001g0130 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1738-501_1738-500i others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402570 | ||||||
| chr11:402574 | CG | C | 8 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0007t0001g0010 others(5): Show |
8 | HG00733.hp2 HG01243.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-502delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402574 | ||||||
| chr11:402576 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
8 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-502G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402576 | |||||||
| chr11:402576 | G | C | 1 | a0001c0002t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1738-502G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402576 | |||||||
| chr11:402576 | G | GCTCCACT others(9): Show |
1 | a0001c0002t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1738-501_1738-500i others(18): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402576 | ||||||
| chr11:402577 | C | A | 8 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0007t0001g0010 others(5): Show |
8 | HG00733.hp2 HG01243.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-501C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402577 | |||||||
| chr11:402577 | CCCCGCTC others(1): Show |
C | 6 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-497_1738-490d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402577 | ||||||
| chr11:402577 | CCCCGCTC others(46): Show |
C | 4 | a0001c0001t0001g0072 a0001c0005t0001g0090 a0001c0005t0001g0091 others(1): Show |
4 | HG01884.hp1 HG02027.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-418_1738-366d others(55): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402577 | ||||||
| chr11:402578 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0009t0001g0102 others(1): Show |
4 | HG02886.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-500C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402578 | |||||||
| chr11:402581 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0009t0001g0102 others(1): Show |
4 | HG02886.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-497G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402581 | |||||||
| chr11:402584 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(3): Show |
6 | HG02129.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-494C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402584 | |||||||
| chr11:402585 | A | AC | 6 | a0001c0002t0001g0145 a0001c0002t0001g0172 a0001c0003t0001g0114 others(3): Show |
6 | HG00609.hp1 HG00673.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-489dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402585 | ||||||
| chr11:402585 | A | ACACCCGC others(47): Show |
1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1738-492_1738-491i others(56): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402585 | ||||||
| chr11:402587 | C | A | 1 | a0001c0008t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1738-491C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402587 | |||||||
| chr11:402590 | G | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0081 a0001c0004t0001g0176 others(4): Show |
7 | HG02129.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-488G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402590 | |||||||
| chr11:402590 | G | T | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1738-488G>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402590 | |||||||
| chr11:402591 | A | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0028 others(10): Show |
13 | HG02129.hp1 HG02622.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1738-487A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402591 | |||||||
| chr11:402592 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0081 |
2 | HG02129.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1738-486C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402592 | |||||||
| chr11:402592 | CCCCGCTC others(45): Show |
C | 1 | a0001c0001t0001g0078 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1738-482_1738-431d others(54): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402592 | ||||||
| chr11:402595 | C | G | 2 | a0001c0001t0001g0046 a0001c0030t0001g0174 |
2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-483C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402595 | |||||||
| chr11:402599 | CACCCCCG | C | 3 | a0001c0007t0001g0007 a0001c0008t0001g0188 a0001c0012t0001g0120 |
3 | HG02027.hp1 HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1738-471_1738-465d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402599 | ||||||
| chr11:402602 | C | A | 6 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-476C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402602 | |||||||
| chr11:402603 | C | A | 2 | a0001c0001t0001g0046 a0001c0030t0001g0174 |
2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-475C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402603 | |||||||
| chr11:402605 | C | G | 6 | a0001c0001t0001g0089 a0001c0004t0001g0094 a0001c0004t0001g0176 others(3): Show |
6 | HG03471.hp2 HG03540.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-473C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402605 | |||||||
| chr11:402605 | C | T | 2 | a0001c0001t0001g0046 a0001c0030t0001g0174 |
2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-473C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402605 | |||||||
| chr11:402605 | CGACCCCC others(1): Show |
C | 12 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(9): Show |
12 | HG00733.hp2 HG01243.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-471_1738-464d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402605 | ||||||
| chr11:402606 | G | GCCCCGCT others(16): Show |
1 | a0001c0003t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1738-472_1738-471i others(25): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402606 | |||||||
| chr11:402606 | GACCCCCG others(15): Show |
G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0005t0001g0085 others(2): Show |
5 | HG02886.hp2 HG02922.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-471_1738-450d others(24): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402606 | |||||||
| chr11:402606 | GACCCCCG others(98): Show |
G | 4 | a0001c0004t0001g0176 a0001c0004t0001g0196 a0003c0019t0001g0181 others(1): Show |
4 | HG03471.hp2 HG03540.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-471_1738-367d others(2): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402606 | |||||||
| chr11:402607 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1738-471A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402607 | |||||||
| chr11:402612 | C | G | 1 | a0001c0003t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1738-466C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402612 | |||||||
| chr11:402613 | G | C | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1738-465G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402613 | |||||||
| chr11:402614 | G | A | 3 | a0001c0001t0001g0089 a0001c0004t0001g0094 a0001c0008t0001g0192 |
3 | HG03516.hp1 HG03688.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1738-464G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402614 | |||||||
| chr11:402615 | CCCCGCTC others(8): Show |
C | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1738-450_1738-436d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402615 | ||||||
| chr11:402622 | C | G | 3 | a0001c0008t0001g0093 a0001c0008t0001g0188 a0001c0008t0001g0189 |
3 | HG02622.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-456C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402622 | |||||||
| chr11:402625 | C | A | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-453C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402625 | |||||||
| chr11:402628 | C | CG | 35 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0082 others(32): Show |
36 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1738-449dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402628 | ||||||
| chr11:402628 | C | CGGCTCCA others(25): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0081 |
2 | HG02129.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1738-449_1738-448i others(34): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402628 | ||||||
| chr11:402628 | C | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(63): Show |
69 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1738-450C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402628 | |||||||
| chr11:402628 | C | T | 8 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0007t0001g0010 others(5): Show |
8 | HG00733.hp2 HG01243.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-450C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402628 | |||||||
| chr11:402630 | A | AC | 3 | a0001c0002t0001g0124 a0001c0003t0001g0166 a0001c0030t0001g0174 |
3 | HG02109.hp2 HG02135.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1738-445dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402630 | ||||||
| chr11:402630 | A | ACCCACTC others(502): Show |
1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1738-445_1738-444i others(511): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402630 | ||||||
| chr11:402630 | A | ACCCCCGA others(117): Show |
2 | a0001c0001t0001g0089 a0001c0004t0001g0094 |
2 | HG03688.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1738-445_1738-444i others(126): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402630 | ||||||
| chr11:402630 | A | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(115): Show |
122 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1738-448A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402630 | |||||||
| chr11:402630 | ACCCGCTC others(31): Show |
A | 2 | a0001c0005t0001g0013 a0001c0005t0001g0014 |
2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1738-435_1738-398d others(40): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402630 | ||||||
| chr11:402637 | CACCCCGA others(15): Show |
C | 6 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0007t0001g0025 others(3): Show |
6 | HG00733.hp2 HG02056.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-435_1738-414d others(24): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402637 | ||||||
| chr11:402638 | A | AC | 6 | a0001c0002t0001g0134 a0001c0003t0001g0166 a0001c0008t0001g0093 others(3): Show |
6 | HG02027.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-436dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402638 | ||||||
| chr11:402639 | CCCCGACC others(14): Show |
C | 1 | a0001c0007t0001g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1738-435_1738-415d others(23): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402639 | ||||||
| chr11:402640 | C | A | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
5 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-438C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402640 | |||||||
| chr11:402643 | G | C | 6 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-435G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402643 | |||||||
| chr11:402644 | A | G | 11 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(8): Show |
11 | HG02027.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1738-434A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402644 | |||||||
| chr11:402652 | CACCCCCG | C | 10 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(7): Show |
10 | HG02027.hp1 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1738-418_1738-412d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402652 | ||||||
| chr11:402654 | CCCCCGAC others(45): Show |
C | 1 | a0001c0011t0001g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1738-419_1738-368d others(54): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402654 | ||||||
| chr11:402655 | C | A | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-423C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402655 | |||||||
| chr11:402658 | C | CCGCCCCG others(19): Show |
1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-420_1738-419i others(28): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402658 | |||||||
| chr11:402658 | C | CCGCCCCG others(17): Show |
2 | a0001c0002t0001g0134 a0001c0003t0001g0155 |
2 | HG02074.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1738-420_1738-419i others(26): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402658 | |||||||
| chr11:402658 | C | G | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-420C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402658 | |||||||
| chr11:402658 | CGACCCCC others(1): Show |
C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0209 a0001c0008t0001g0192 |
3 | HG02647.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1738-418_1738-411d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402658 | ||||||
| chr11:402659 | G | C | 3 | a0001c0002t0001g0134 a0001c0003t0001g0143 a0001c0003t0001g0155 |
3 | HG00673.hp1 HG02074.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1738-419G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402659 | |||||||
| chr11:402659 | G | GCCCCGCT others(17): Show |
1 | a0001c0002t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1738-419_1738-418i others(26): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402659 | |||||||
| chr11:402659 | G | GCCCCGCT others(16): Show |
1 | a0019c0032t0001g0144 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1738-419_1738-418i others(25): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402659 | |||||||
| chr11:402659 | G | GCCCCGCT others(18): Show |
1 | a0001c0003t0001g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1738-419_1738-418i others(27): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402659 | |||||||
| chr11:402659 | G | GCCCCGCT others(17): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1738-419_1738-418i others(26): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402659 | |||||||
| chr11:402659 | G | GCCCCGCT others(16): Show |
46 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0104 others(43): Show |
47 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1738-419_1738-418i others(25): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402659 | |||||||
| chr11:402659 | GACCCCCG others(31): Show |
G | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1738-418_1738-381d others(40): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402659 | |||||||
| chr11:402665 | C | G | 53 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0104 others(50): Show |
54 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1738-413C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402665 | |||||||
| chr11:402665 | CGGCCCCG others(69): Show |
C | 1 | a0001c0030t0001g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1738-395_1738-320d others(78): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402665 | ||||||
| chr11:402666 | G | C | 1 | a0001c0002t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1738-412G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402666 | |||||||
| chr11:402667 | G | A | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-411G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402667 | |||||||
| chr11:402667 | G | C | 1 | a0001c0003t0001g0116 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1738-411G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402667 | |||||||
| chr11:402668 | C | G | 1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1738-410C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402668 | |||||||
| chr11:402669 | C | T | 3 | a0001c0008t0001g0093 a0001c0008t0001g0188 a0001c0008t0001g0189 |
3 | HG02622.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-409C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402669 | |||||||
| chr11:402672 | G | A | 3 | a0001c0008t0001g0093 a0001c0008t0001g0188 a0001c0008t0001g0189 |
3 | HG02622.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-406G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402672 | |||||||
| chr11:402675 | C | G | 3 | a0001c0008t0001g0093 a0001c0008t0001g0188 a0001c0008t0001g0189 |
3 | HG02622.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-403C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402675 | |||||||
| chr11:402681 | C | CG | 64 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(61): Show |
65 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1738-396dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402681 | ||||||
| chr11:402681 | C | G | 4 | a0001c0008t0001g0093 a0001c0008t0001g0188 a0001c0008t0001g0189 others(1): Show |
4 | HG02027.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-397C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402681 | |||||||
| chr11:402681 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0209 a0001c0002t0001g0103 |
3 | HG02647.hp1 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1738-397C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402681 | |||||||
| chr11:402681 | CGACCCGC others(53): Show |
C | 1 | a0001c0007t0001g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1738-395_1738-336d others(62): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402681 | ||||||
| chr11:402682 | G | A | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1738-396G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402682 | |||||||
| chr11:402683 | A | C | 74 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(71): Show |
75 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.1738-395A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402683 | |||||||
| chr11:402695 | C | CG | 6 | a0001c0001t0001g0195 a0001c0001t0001g0209 a0001c0002t0001g0103 others(3): Show |
6 | HG02622.hp1 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-382dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402695 | ||||||
| chr11:402696 | G | C | 6 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
6 | HG01358.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-382G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402696 | |||||||
| chr11:402697 | A | AC | 4 | a0001c0001t0001g0078 a0001c0003t0001g0155 a0001c0005t0001g0032 others(1): Show |
4 | HG01261.hp2 HG01515.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-377dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402697 | ||||||
| chr11:402697 | A | G | 11 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(8): Show |
11 | HG01358.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1738-381A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402697 | |||||||
| chr11:402706 | A | AC | 7 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0001g0186 others(4): Show |
7 | HG00642.hp1 HG01243.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-367dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402706 | ||||||
| chr11:402708 | C | A | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-370C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402708 | |||||||
| chr11:402710 | C | CG | 4 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0004t0001g0193 others(1): Show |
4 | HG02717.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-368_1738-367i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402710 | |||||||
| chr11:402711 | C | CCCGACCC others(5): Show |
1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-367_1738-366i others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402711 | |||||||
| chr11:402711 | C | CCGACCCC others(3): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1738-367_1738-366i others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402711 | |||||||
| chr11:402711 | C | CG | 4 | a0001c0001t0001g0195 a0001c0002t0001g0103 a0001c0003t0001g0114 others(1): Show |
4 | HG02027.hp1 HG03453.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-366dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402711 | ||||||
| chr11:402711 | C | CGACCCCC others(1): Show |
48 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0104 others(45): Show |
49 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.1738-366_1738-365i others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402711 | ||||||
| chr11:402711 | C | G | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(6): Show |
9 | HG01358.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-367C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402711 | |||||||
| chr11:402711 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1738-367C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402711 | |||||||
| chr11:402712 | G | A | 3 | a0001c0008t0001g0093 a0001c0008t0001g0188 a0001c0008t0001g0189 |
3 | HG02622.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-366G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402712 | |||||||
| chr11:402713 | C | A | 16 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0004t0001g0176 others(13): Show |
16 | HG00733.hp2 HG01243.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1738-365C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402713 | |||||||
| chr11:402714 | CCCGCTCA | C | 7 | a0001c0007t0001g0008 a0001c0007t0001g0009 a0001c0007t0001g0010 others(4): Show |
7 | HG00733.hp2 HG01243.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-361_1738-355d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402714 | ||||||
| chr11:402719 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1738-359T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402719 | |||||||
| chr11:402721 | A | AC | 55 | a0001c0001t0001g0183 a0001c0002t0001g0004 a0001c0002t0001g0100 others(52): Show |
56 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1738-353dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402721 | ||||||
| chr11:402722 | CCCCTGCC others(3): Show |
C | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1738-354_1738-345d others(12): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402722 | ||||||
| chr11:402726 | T | C | 4 | a0001c0003t0001g0114 a0001c0008t0001g0093 a0001c0008t0001g0188 others(1): Show |
4 | HG02622.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-352T>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402726 | |||||||
| chr11:402726 | T | G | 76 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(73): Show |
77 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.1738-352T>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402726 | |||||||
| chr11:402727 | G | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(11): Show |
14 | HG01358.hp2 HG02630.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1738-351G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402727 | |||||||
| chr11:402727 | GCCCCGCT others(1): Show |
G | 3 | a0001c0008t0001g0093 a0001c0008t0001g0188 a0001c0008t0001g0189 |
3 | HG02622.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1738-350_1738-343d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402727 | |||||||
| chr11:402735 | C | CACCCCCG | 2 | a0001c0002t0001g0103 a0001c0003t0001g0115 |
2 | HG01358.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1738-338_1738-337i others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402735 | ||||||
| chr11:402740 | CG | C | 49 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0104 others(46): Show |
50 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1738-335delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402740 | ||||||
| chr11:402741 | G | C | 19 | a0001c0001t0001g0195 a0001c0001t0001g0209 a0001c0002t0001g0103 others(16): Show |
19 | HG00733.hp2 HG01243.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1738-337G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402741 | |||||||
| chr11:402742 | G | C | 53 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0104 others(50): Show |
54 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1738-336G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402742 | |||||||
| chr11:402743 | G | A | 10 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(7): Show |
10 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738-335G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402743 | |||||||
| chr11:402744 | C | A | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-334C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402744 | |||||||
| chr11:402753 | CCCCCGGC others(8): Show |
C | 1 | a0001c0012t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1738-319_1738-305d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402753 | ||||||
| chr11:402757 | C | G | 52 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0104 others(49): Show |
53 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1738-321C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402757 | |||||||
| chr11:402757 | CG | C | 10 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(7): Show |
10 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738-319delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402757 | ||||||
| chr11:402758 | G | C | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-320G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402758 | |||||||
| chr11:402759 | G | A | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-319G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402759 | |||||||
| chr11:402760 | C | A | 52 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0104 others(49): Show |
53 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1738-318C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402760 | |||||||
| chr11:402765 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(87): Show |
93 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.1738-313C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402765 | |||||||
| chr11:402768 | A | AC | 5 | a0001c0001t0001g0195 a0001c0002t0001g0125 a0001c0003t0001g0116 others(2): Show |
5 | HG00673.hp1 HG02148.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-306dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402768 | ||||||
| chr11:402772 | C | CG | 12 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(9): Show |
12 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(9): Show |
intron_variant | MODIFIER | c.1738-305dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402772 | ||||||
| chr11:402773 | G | C | 2 | a0001c0002t0001g0103 a0001c0003t0001g0115 |
2 | HG01358.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1738-305G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402773 | |||||||
| chr11:402774 | A | G | 5 | a0001c0001t0001g0195 a0001c0001t0001g0209 a0001c0002t0001g0103 others(2): Show |
5 | HG01358.hp2 HG02647.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-304A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402774 | |||||||
| chr11:402775 | C | A | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-303C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402775 | |||||||
| chr11:402782 | CACCCCCG | C | 2 | a0001c0001t0001g0209 a0001c0003t0001g0115 |
2 | HG01358.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1738-288_1738-282d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402782 | ||||||
| chr11:402788 | C | G | 1 | a0001c0002t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1738-290C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402788 | |||||||
| chr11:402788 | CGACCCCC others(1): Show |
C | 2 | a0001c0001t0001g0195 a0001c0003t0001g0114 |
2 | HG03688.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1738-288_1738-281d others(10): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402788 | ||||||
| chr11:402795 | C | G | 1 | a0001c0003t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1738-283C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402795 | |||||||
| chr11:402796 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1738-282G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402796 | |||||||
| chr11:402797 | G | A | 2 | a0001c0002t0001g0103 a0001c0008t0001g0192 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1738-281G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402797 | |||||||
| chr11:402798 | C | A | 1 | a0001c0003t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1738-280C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402798 | |||||||
| chr11:402799 | C | T | 10 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(7): Show |
10 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738-279C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402799 | |||||||
| chr11:402806 | A | AC | 7 | a0001c0001t0001g0053 a0001c0001t0001g0082 a0001c0003t0001g0097 others(4): Show |
7 | HG01243.hp2 HG01515.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-267dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402806 | ||||||
| chr11:402811 | C | G | 2 | a0001c0003t0001g0114 a0001c0008t0001g0192 |
2 | HG03516.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1738-267C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402811 | |||||||
| chr11:402811 | CG | C | 8 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(5): Show |
8 | HG02630.hp2 HG03209.hp1 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-265delG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402811 | ||||||
| chr11:402812 | G | C | 1 | a0001c0004t0001g0197 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1738-266G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402812 | |||||||
| chr11:402812 | GGCCCCGC others(8): Show |
G | 4 | a0001c0005t0001g0023 a0001c0008t0001g0188 a0001c0008t0001g0189 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-236_1738-222d others(17): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402812 | ||||||
| chr11:402812 | GGCCCCGC others(55): Show |
G | 1 | a0003c0019t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1738-265_1738-204d others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402812 | |||||||
| chr11:402813 | G | A | 4 | a0001c0001t0001g0195 a0001c0001t0001g0209 a0001c0003t0001g0115 others(1): Show |
4 | HG01358.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-265G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402813 | |||||||
| chr11:402822 | A | AC | 8 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0064 others(5): Show |
8 | HG00621.hp1 HG01243.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-251dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402822 | ||||||
| chr11:402827 | C | CCGCCCCG others(41): Show |
2 | a0001c0002t0001g0164 a0001c0003t0001g0098 |
2 | HG00642.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1738-251_1738-250i others(50): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402827 | |||||||
| chr11:402827 | C | CGCCCCGC others(63): Show |
9 | a0001c0002t0001g0110 a0001c0002t0001g0170 a0001c0002t0001g0171 others(6): Show |
9 | HG02451.hp1 HG02486.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-237_1738-236i others(72): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402827 | ||||||
| chr11:402827 | C | G | 3 | a0001c0001t0001g0018 a0001c0003t0001g0114 a0001c0003t0001g0115 |
3 | HG01358.hp2 HG03688.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1738-251C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402827 | |||||||
| chr11:402828 | G | A | 3 | a0001c0002t0001g0164 a0001c0003t0001g0098 a0001c0003t0001g0114 |
3 | HG00642.hp2 HG01975.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1738-250G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402828 | |||||||
| chr11:402828 | G | C | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1738-250G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402828 | |||||||
| chr11:402828 | G | GCCCCCCC others(54): Show |
1 | a0001c0003t0001g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1738-246_1738-245i others(63): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | G | GCCCCGCT others(126): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1738-240_1738-239i others(135): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | G | GCCCCGCT others(127): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1738-237_1738-236i others(136): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | G | GCCCCGCT others(126): Show |
2 | a0001c0002t0001g0145 a0001c0004t0001g0073 |
2 | HG00609.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1738-237_1738-236i others(135): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | G | GCCCCGCT others(41): Show |
1 | a0001c0003t0001g0141 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1738-237_1738-236i others(50): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | G | GCCCCGCT others(41): Show |
2 | a0001c0002t0001g0125 a0006c0031t0001g0163 |
2 | HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1738-237_1738-236i others(50): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | G | GCCCCGCT others(126): Show |
1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1738-237_1738-236i others(135): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | G | GCCCCGCT others(126): Show |
1 | a0001c0002t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1738-237_1738-236i others(135): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | G | GCCCCGCT others(125): Show |
9 | a0001c0002t0001g0101 a0001c0002t0001g0130 a0001c0002t0001g0131 others(6): Show |
10 | HG00099.hp2 HG00639.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1738-237_1738-236i others(134): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | G | GCCCCGCT others(124): Show |
1 | a0001c0002t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1738-237_1738-236i others(133): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | G | GCCCCGCT others(40): Show |
45 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0104 others(42): Show |
46 | HG00544.hp1 HG00639.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.1738-237_1738-236i others(49): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402828 | GCCCCGCT others(55): Show |
G | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(6): Show |
9 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-219_1738-158d others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402828 | ||||||
| chr11:402837 | A | AC | 8 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0061 others(5): Show |
8 | HG00621.hp2 HG01192.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-236dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402837 | ||||||
| chr11:402837 | A | ACCCCGGG others(130): Show |
1 | a0001c0003t0001g0116 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1738-237_1738-236i others(139): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402837 | ||||||
| chr11:402837 | A | ACCCCGGG others(41): Show |
2 | a0001c0002t0001g0134 a0017c0027t0001g0107 |
2 | HG02074.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1738-237_1738-236i others(50): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402837 | ||||||
| chr11:402842 | C | G | 2 | a0001c0003t0001g0114 a0001c0008t0001g0192 |
2 | HG03516.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1738-236C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402842 | |||||||
| chr11:402843 | G | GA | 2 | a0001c0003t0001g0114 a0001c0008t0001g0192 |
2 | HG03516.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1738-235_1738-234i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402843 | |||||||
| chr11:402853 | C | CA | 2 | a0001c0001t0001g0018 a0001c0002t0001g0145 |
2 | HG00609.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1738-225_1738-224i others(3): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402853 | |||||||
| chr11:402856 | C | T | 1 | a0001c0003t0001g0112 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1738-222C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402856 | |||||||
| chr11:402858 | G | C | 2 | a0001c0003t0001g0114 a0001c0008t0001g0192 |
2 | HG03516.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1738-220G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402858 | |||||||
| chr11:402860 | A | AC | 6 | a0001c0001t0001g0060 a0001c0002t0001g0136 a0001c0002t0001g0148 others(3): Show |
6 | HG00544.hp1 HG01175.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738-215dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402860 | ||||||
| chr11:402860 | A | C | 1 | a0001c0003t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1738-218A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402860 | |||||||
| chr11:402874 | A | G | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-204A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402874 | |||||||
| chr11:402876 | C | T | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-202C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402876 | |||||||
| chr11:402888 | G | C | 8 | a0001c0003t0001g0114 a0001c0004t0001g0012 a0001c0004t0001g0190 others(5): Show |
8 | HG03471.hp1 HG03516.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-190G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402888 | |||||||
| chr11:402889 | G | C | 1 | a0003c0019t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1738-189G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402889 | |||||||
| chr11:402889 | GA | G | 6 | a0001c0004t0001g0012 a0001c0004t0001g0190 a0001c0008t0001g0191 others(3): Show |
6 | HG03471.hp1 HG03516.hp1 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-188delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402889 | |||||||
| chr11:402890 | A | G | 1 | a0003c0019t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1738-188A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402890 | |||||||
| chr11:402899 | A | AC | 8 | a0001c0001t0001g0018 a0001c0001t0001g0064 a0001c0001t0001g0072 others(5): Show |
8 | HG00544.hp1 HG02027.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1738-174dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402899 | ||||||
| chr11:402913 | CACCCCGG others(16): Show |
C | 15 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(12): Show |
15 | HG02630.hp2 HG02717.hp2 HG03209.hp1 others(12): Show |
intron_variant | MODIFIER | c.1738-159_1738-137d others(25): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402913 | ||||||
| chr11:402919 | G | C | 2 | a0001c0003t0001g0114 a0001c0008t0001g0192 |
2 | HG03516.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1738-159G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402919 | |||||||
| chr11:402920 | G | C | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-158G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402920 | |||||||
| chr11:402921 | A | G | 1 | a0001c0008t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1738-157A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402921 | |||||||
| chr11:402929 | CACCCCCG | C | 2 | a0001c0003t0001g0114 a0001c0008t0001g0192 |
2 | HG03516.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1738-141_1738-135d others(9): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402929 | ||||||
| chr11:402936 | G | GACCCCCG others(55): Show |
1 | a0001c0002t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1738-133_1738-132i others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402936 | ||||||
| chr11:402936 | G | GACCCCCG others(39): Show |
2 | a0001c0003t0001g0003 a0014c0034t0001g0157 |
3 | HG01256.hp2 HG01258.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1738-133_1738-132i others(48): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402936 | ||||||
| chr11:402936 | G | GACCCCCG others(54): Show |
13 | a0001c0002t0001g0101 a0001c0002t0001g0130 a0001c0002t0001g0131 others(10): Show |
13 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1738-133_1738-132i others(63): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402936 | ||||||
| chr11:402937 | A | ACCCCCGG others(55): Show |
1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1738-133_1738-132i others(64): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402937 | ||||||
| chr11:402943 | G | GGCTCCGC others(31): Show |
1 | a0001c0002t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1738-133_1738-132i others(40): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402943 | ||||||
| chr11:402946 | C | T | 63 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(60): Show |
64 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1738-132C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402946 | |||||||
| chr11:402953 | A | AC | 12 | a0001c0001t0001g0078 a0001c0002t0001g0168 a0001c0003t0001g0114 others(9): Show |
12 | HG01175.hp1 HG01243.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-120dupC | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402953 | ||||||
| chr11:402973 | G | A | 1 | a0018c0023t0002g0037 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1738-105G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402973 | |||||||
| chr11:402973 | G | C | 64 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(61): Show |
65 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1738-105G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402973 | |||||||
| chr11:402974 | G | C | 4 | a0001c0002t0001g0168 a0001c0003t0001g0166 a0006c0031t0001g0163 others(1): Show |
4 | HG01496.hp1 HG02135.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-104G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402974 | |||||||
| chr11:402974 | GA | G | 59 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(56): Show |
60 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1738-103delA | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402974 | |||||||
| chr11:402975 | A | G | 5 | a0001c0002t0001g0159 a0001c0002t0001g0168 a0001c0003t0001g0166 others(2): Show |
5 | HG01496.hp1 HG01891.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-103A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402975 | |||||||
| chr11:402989 | C | CG | 20 | a0001c0003t0001g0095 a0001c0003t0001g0096 a0001c0003t0001g0097 others(17): Show |
20 | HG01358.hp2 HG01496.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.1738-88dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 402989 | ||||||
| chr11:402995 | A | G | 64 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(61): Show |
65 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1738-83A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 402995 | |||||||
| chr11:403001 | A | C | 64 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(61): Show |
65 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1738-77A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 403001 | |||||||
| chr11:403001 | ACCCGACC others(7): Show |
A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(132): Show |
139 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1738-40_1738-27del others(14): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 403001 | ||||||
| chr11:403004 | C | CG | 40 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(37): Show |
41 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1738-73dupG | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 403004 | ||||||
| chr11:403004 | C | G | 1 | a0001c0002t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1738-74C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 403004 | |||||||
| chr11:403006 | A | C | 63 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(60): Show |
64 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1738-72A>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 403006 | |||||||
| chr11:403015 | C | CCCCCCGC others(41): Show |
2 | a0001c0002t0001g0125 a0001c0003t0001g0139 |
2 | NA18971.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1738-60_1738-59ins others(48): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 403015 | ||||||
| chr11:403015 | C | CCCCCGCC others(9): Show |
1 | a0001c0002t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1738-60_1738-59ins others(16): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 403015 | ||||||
| chr11:403015 | C | CCCCCGCC others(40): Show |
39 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0103 others(36): Show |
40 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1738-60_1738-59ins others(47): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 403015 | ||||||
| chr11:403015 | C | CCCCCGGA others(26): Show |
1 | a0001c0003t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1738-60_1738-59ins others(33): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 403015 | ||||||
| chr11:403015 | C | CCCCGGAC others(25): Show |
21 | a0001c0002t0001g0168 a0001c0003t0001g0095 a0001c0003t0001g0096 others(18): Show |
21 | HG01358.hp2 HG01496.hp1 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.1738-59_1738-58ins others(32): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 403015 | ||||||
| chr11:403015 | CCCCGACC others(6): Show |
C | 2 | a0001c0005t0001g0014 a0007c0029t0001g0117 |
2 | HG01243.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1738-59_1738-47del others(13): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 403015 | ||||||
| chr11:403020 | ACCCGCTC others(8): Show |
A | 1 | a0001c0001t0001g0018 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1738-55_1738-41del others(15): Show |
PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 403020 | ||||||
| chr11:403029 | C | A | 1 | a0007c0029t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1738-49C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 403029 | |||||||
| chr11:403046 | C | T | 83 | a0001c0001t0001g0062 a0001c0002t0001g0004 a0001c0002t0001g0100 others(80): Show |
85 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1738-32C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 8/12 | chr11 | 403046 | |||||||
| chr11:403484 | G | C | 79 | a0001c0002t0001g0004 a0001c0002t0001g0100 a0001c0002t0001g0101 others(76): Show |
81 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1924-134G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 9/12 | chr11 | 403484 | |||||||
| chr11:403545 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(102): Show |
108 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1924-73C>T | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 9/12 | chr11 | 403545 | |||||||
| chr11:403795 | C | G | 2 | a0001c0008t0001g0192 a0001c0008t0001g0194 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2077+24C>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 10/12 | chr11 | 403795 | |||||||
| chr11:403880 | G | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(88): Show |
94 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2078-63G>C | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 10/12 | chr11 | 403880 | |||||||
| chr11:403939 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
208 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(205): Show |
splice_region_variant&intron_variant | LOW | c.2078-4A>G | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 10/12 | chr11 | 403939 | |||||||
| chr11:404154 | G | A | 2 | a0001c0004t0001g0190 a0001c0008t0001g0191 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2270+19G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 11/12 | chr11 | 404154 | |||||||
| chr11:404188 | C | A | 1 | a0001c0004t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2271-48C>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 11/12 | chr11 | 404188 | |||||||
| chr11:404468 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(87): Show |
93 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.2359-66G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 12/12 | chr11 | 404468 | |||||||
| chr11:404478 | G | A | 1 | a0001c0005t0004g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2359-56G>A | PKP3 | ENSG00000184363.10 | transcript | ENST00000331563.7 | protein_coding | 12/12 | chr11 | 404478 |