Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81490 |
| ensemblid | ENSG00000174915.12 |
| hgncid | 15463 |
| symbol | PTDSS2 |
| name | phosphatidylserine synthase 2 |
| refseq_nuc | NM_030783.3 |
| refseq_prot | NP_110410.1 |
| ensembl_nuc | ENST00000308020.6 |
| ensembl_prot | ENSP00000308258.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 450279 |
| end | 491399 |
| strand | + |
| ver | v1.2 |
| region | chr11:450279-491399 |
| region5000 | chr11:445279-496399 |
| regionname0 | PTDSS2_chr11_450279_491399 |
| regionname5000 | PTDSS2_chr11_445279_496399 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 487 | 319 | 95 | 64 | 108 | 15 | 35 | 78 | PTDSS2_chr11_445279_496399 | PTDSS2 | MRRGE others(482): Show |
chr11 | 445279 | 496399 |
| a0002 | 0/0 | 487 | 17 | 0 | 16 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | MRRGE others(482): Show |
chr11 | 445279 | 496399 |
| a0003 | 0/0 | 487 | 8 | 0 | 5 | 2 | 0 | 1 | 2 | PTDSS2_chr11_445279_496399 | PTDSS2 | MRRGE others(482): Show |
chr11 | 445279 | 496399 |
| a0004 | 0/0 | 487 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | MRKGE others(482): Show |
chr11 | 445279 | 496399 |
| a0005 | 0/0 | 487 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | MRRGE others(482): Show |
chr11 | 445279 | 496399 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1461 | 264 | 87 | 51 | 81 | 13 | 30 | PTDSS2_chr11_445279_496399 | PTDSS2 | ATGCG others(1456): Show |
chr11 | 445279 | 496399 | ||
| a0001c0002 | 0/0 | 1461 | 42 | 3 | 8 | 27 | 0 | 4 | PTDSS2_chr11_445279_496399 | PTDSS2 | ATGCG others(1456): Show |
chr11 | 445279 | 496399 | ||
| a0001c0005 | 0/0 | 1461 | 7 | 0 | 5 | 0 | 2 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ATGCG others(1456): Show |
chr11 | 445279 | 496399 | ||
| a0001c0006 | 0/0 | 1461 | 4 | 4 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ATGCG others(1456): Show |
chr11 | 445279 | 496399 | ||
| a0001c0008 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ATGCG others(1456): Show |
chr11 | 445279 | 496399 | ||
| a0001c0010 | 0/0 | 1461 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | ATGCG others(1456): Show |
chr11 | 445279 | 496399 | ||
| a0002c0003 | 0/0 | 1461 | 17 | 0 | 16 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ATGCG others(1456): Show |
chr11 | 445279 | 496399 | ||
| a0003c0004 | 0/0 | 1461 | 8 | 0 | 5 | 2 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | ATGCG others(1456): Show |
chr11 | 445279 | 496399 | ||
| a0004c0007 | 0/0 | 1461 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ATGCG others(1456): Show |
chr11 | 445279 | 496399 | ||
| a0005c0009 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ATGCG others(1456): Show |
chr11 | 445279 | 496399 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2458 | 152 | 40 | 37 | 46 | 8 | 20 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0002 | 0/0 | 2468 | 69 | 28 | 13 | 19 | 5 | 4 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2463): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0003 | 0/0 | 2458 | 14 | 6 | 0 | 8 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0004 | 0/0 | 2458 | 11 | 11 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0006 | 0/1 | 2478 | 3 | 0 | 1 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2473): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0007 | 0/0 | 2468 | 4 | 0 | 0 | 1 | 0 | 3 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2463): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0009 | 0/0 | 2468 | 3 | 0 | 0 | 3 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2463): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0010 | 0/0 | 2480 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2475): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0011 | 0/0 | 2458 | 2 | 0 | 0 | 2 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0013 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0014 | 0/0 | 2458 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0015 | 0/0 | 2458 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0016 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2463): Show |
chr11 | 445279 | 496399 |
| a0001c0001t0017 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2463): Show |
chr11 | 445279 | 496399 |
| a0001c0002t0001 | 0/0 | 2458 | 41 | 2 | 8 | 27 | 0 | 4 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0002t0010 | 0/0 | 2480 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2475): Show |
chr11 | 445279 | 496399 |
| a0001c0005t0001 | 0/0 | 2458 | 7 | 0 | 5 | 0 | 2 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0006t0001 | 0/0 | 2458 | 4 | 4 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0008t0001 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0001c0010t0002 | 0/0 | 2468 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2463): Show |
chr11 | 445279 | 496399 |
| a0002c0003t0005 | 0/0 | 2478 | 11 | 0 | 10 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2473): Show |
chr11 | 445279 | 496399 |
| a0002c0003t0006 | 0/0 | 2478 | 2 | 0 | 2 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2473): Show |
chr11 | 445279 | 496399 |
| a0002c0003t0008 | 0/0 | 2480 | 4 | 0 | 4 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2475): Show |
chr11 | 445279 | 496399 |
| a0003c0004t0001 | 0/0 | 2458 | 8 | 0 | 5 | 2 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0004c0007t0012 | 0/0 | 2458 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| a0005c0009t0001 | 0/0 | 2458 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | ACAAT others(2453): Show |
chr11 | 445279 | 496399 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0004 | 1/0 | 4 | 0 | 3 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0006g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0009g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0009g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0010g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0011g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0014g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0015g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0016g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0001t0017g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0002t0010g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0005t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0005t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0005t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0005t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0005t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0005t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0006t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0006t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0006t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0008t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0001c0010t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0005g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0005g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0006g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0008g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0008g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0008g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0002c0003t0008g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0003c0004t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0003c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0003c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0003c0004t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0003c0004t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0003c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0004c0007t0012g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| a0005c0009t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0005 | g0021 | EUR | GBR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | FIN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | FIN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0079 | EUR | FIN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00323 | hp2 | a0001 | c0005 | t0001 | g0278 | EUR | FIN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | CHS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00544 | hp1 | a0001 | c0001 | t0009 | g0058 | EAS | CHS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00639 | hp1 | a0002 | c0003 | t0006 | g0192 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00733 | hp1 | a0002 | c0003 | t0008 | g0170 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00738 | hp2 | a0001 | c0005 | t0001 | g0214 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00741 | hp1 | a0002 | c0003 | t0006 | g0194 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01070 | hp2 | a0001 | c0005 | t0001 | g0181 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01081 | hp1 | a0002 | c0003 | t0008 | g0171 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01106 | hp1 | a0002 | c0003 | t0008 | g0172 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01109 | hp1 | a0004 | c0007 | t0012 | g0299 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01175 | hp2 | a0002 | c0003 | t0005 | g0193 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01257 | hp2 | a0002 | c0003 | t0005 | g0020 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01258 | hp1 | a0002 | c0003 | t0005 | g0020 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01346 | hp1 | a0002 | c0003 | t0005 | g0191 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | IBS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | IBS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0080 | EUR | IBS | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01928 | hp1 | a0002 | c0003 | t0005 | g0187 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01928 | hp2 | a0001 | c0005 | t0001 | g0182 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01934 | hp1 | a0002 | c0003 | t0005 | g0188 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01934 | hp2 | a0003 | c0004 | t0001 | g0179 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01952 | hp1 | a0001 | c0005 | t0001 | g0183 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01975 | hp1 | a0003 | c0004 | t0001 | g0006 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01975 | hp2 | a0002 | c0003 | t0005 | g0184 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01981 | hp2 | a0003 | c0004 | t0001 | g0180 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01993 | hp1 | a0002 | c0003 | t0008 | g0169 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01993 | hp2 | a0003 | c0004 | t0001 | g0006 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02004 | hp1 | a0003 | c0004 | t0001 | g0006 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02040 | hp2 | a0001 | c0001 | t0007 | g0057 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02148 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CDX | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | CDX | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02293 | hp1 | a0002 | c0003 | t0005 | g0189 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02300 | hp1 | a0002 | c0003 | t0005 | g0190 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02300 | hp2 | a0002 | c0003 | t0005 | g0021 | AMR | PEL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02572 | hp2 | a0001 | c0002 | t0010 | g0204 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0185 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02647 | hp2 | a0005 | c0009 | t0001 | g0024 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0019 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0062 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0064 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03139 | hp2 | a0001 | c0006 | t0001 | g0019 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0152 | AFR | ESN | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03688 | hp2 | a0001 | c0010 | t0002 | g0084 | SAS | STU | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03834 | hp1 | a0001 | c0001 | t0007 | g0066 | SAS | BEB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | BEB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | BEB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03927 | hp2 | a0001 | c0001 | t0015 | g0209 | SAS | BEB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03942 | hp2 | a0001 | c0001 | t0014 | g0258 | SAS | BEB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | BEB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG04184 | hp2 | a0003 | c0004 | t0001 | g0269 | SAS | BEB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | STU | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | STU | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | YRI | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | YRI | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CHB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | CHB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | YRI | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18942 | hp2 | a0003 | c0004 | t0001 | g0176 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0029 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18945 | hp1 | a0001 | c0001 | t0016 | g0107 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18974 | hp2 | a0001 | c0001 | t0011 | g0250 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19004 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19009 | hp2 | a0001 | c0001 | t0009 | g0034 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19010 | hp2 | a0001 | c0001 | t0009 | g0061 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | LWK | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | LWK | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19077 | hp2 | a0001 | c0001 | t0017 | g0060 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | YRI | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | ASW | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ASW | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA20752 | hp1 | a0001 | c0005 | t0001 | g0252 | EUR | TSI | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | GIH | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | CLM | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0167 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG02559 | hp2 | a0001 | c0006 | t0001 | g0166 | AFR | ACB | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0053 | AFR | MSL | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | USA | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | USA | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | USA | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | USA | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | LWK | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| NA21309 | hp2 | a0001 | c0008 | t0001 | g0289 | AFR | LWK | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0186 | REF | REF | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | PTDSS2_chr11_445279_496399 | PTDSS2 | chr11 | 445279 | 496399 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:450463 | G | A | 1 | a0004 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.8G>A | p.Arg3Lys | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/12 | 185/2458 | 8/1464 | 3/487 | chr11 | 450463 | |||
| chr11:490035 | C | T | 1 | a0002 | 17 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(14): Show |
missense_variant | MODERATE | c.1268C>T | p.Ala423Val | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 11/12 | 1445/2458 | 1268/1464 | 423/487 | chr11 | 490035 | |||
| chr11:490484 | A | G | 1 | a0003 | 8 | HG01934.hp2 HG01975.hp1 HG01981.hp2 others(5): Show |
missense_variant | MODERATE | c.1366A>G | p.Ser456Gly | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 1543/2458 | 1366/1464 | 456/487 | chr11 | 490484 | |||
| chr11:490490 | G | A | 1 | a0005 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1372G>A | p.Val458Ile | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 1549/2458 | 1372/1464 | 458/487 | chr11 | 490490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:450485 | A | G | 2 | a0001c0006 a0004c0007 |
5 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
synonymous_variant | LOW | c.30A>G | p.Gly10Gly | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/12 | 207/2458 | 30/1464 | 10/487 | chr11 | 450485 | |||
| chr11:460247 | G | A | 1 | a0001c0008 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.243G>A | p.Leu81Leu | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/12 | 420/2458 | 243/1464 | 81/487 | chr11 | 460247 | |||
| chr11:488609 | G | T | 1 | a0001c0005 | 7 | HG00323.hp2 HG00738.hp2 HG01070.hp2 others(4): Show |
synonymous_variant | LOW | c.816G>T | p.Thr272Thr | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/12 | 993/2458 | 816/1464 | 272/487 | chr11 | 488609 | |||
| chr11:489436 | G | A | 1 | a0004c0007 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.891G>A | p.Pro297Pro | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 9/12 | 1068/2458 | 891/1464 | 297/487 | chr11 | 489436 | |||
| chr11:490036 | G | A | 1 | a0001c0002 | 42 | HG00544.hp2 HG01123.hp2 HG01168.hp2 others(39): Show |
synonymous_variant | LOW | c.1269G>A | p.Ala423Ala | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 11/12 | 1446/2458 | 1269/1464 | 423/487 | chr11 | 490036 | |||
| chr11:490423 | C | T | 1 | a0001c0010 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.1305C>T | p.Asp435Asp | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 1482/2458 | 1305/1464 | 435/487 | chr11 | 490423 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:450319 | C | A | 1 | a0004c0007t0012 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-137C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/12 | 137 | chr11 | 450319 | ||||||
| chr11:450366 | C | G | 1 | a0004c0007t0012 | 1 | HG01109.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-90C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/12 | chr11 | 450366 | |||||||
| chr11:490591 | G | A | 1 | a0001c0001t0007 | 4 | HG02040.hp2 HG02738.hp2 HG03017.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 9 | chr11 | 490591 | ||||||
| chr11:490771 | C | CGTGTGTA others(13): Show |
2 | a0001c0001t0006 a0002c0003t0006 |
4 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*199_*218dupTGTGTA others(14): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 219 | INFO_REALIGN_3_PRIME | chr11 | 490771 | |||||
| chr11:490787 | T | TGCGTGTG others(13): Show |
1 | a0002c0003t0005 | 11 | HG00099.hp1 HG01175.hp2 HG01257.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*223_*224insACGCGT others(14): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 224 | INFO_REALIGN_3_PRIME | chr11 | 490787 | |||||
| chr11:490791 | T | C | 2 | a0001c0001t0004 a0001c0001t0013 |
12 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*209T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 209 | chr11 | 490791 | ||||||
| chr11:490791 | T | TGTGTGTA others(3): Show |
1 | a0001c0001t0009 | 3 | HG00544.hp1 NA19009.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*221_*230dupTGTGTA others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 231 | INFO_REALIGN_3_PRIME | chr11 | 490791 | |||||
| chr11:490809 | C | T | 1 | a0001c0001t0011 | 2 | NA18974.hp2 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*227C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 227 | chr11 | 490809 | ||||||
| chr11:490811 | C | CGTGTGTA others(3): Show |
5 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0016 others(2): Show |
76 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*230_*231insTGTGTA others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 231 | INFO_REALIGN_3_PRIME | chr11 | 490811 | |||||
| chr11:490811 | C | CGTGTGTG others(15): Show |
2 | a0001c0001t0010 a0001c0002t0010 |
2 | HG02572.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*230_*231insTGTGTG others(16): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 231 | INFO_REALIGN_3_PRIME | chr11 | 490811 | |||||
| chr11:490811 | C | CGTGTGTG others(15): Show |
1 | a0002c0003t0008 | 4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*230_*231insTGTGTG others(16): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 231 | INFO_REALIGN_3_PRIME | chr11 | 490811 | |||||
| chr11:490811 | C | T | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(2): Show |
40 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*229C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 229 | chr11 | 490811 | ||||||
| chr11:491067 | G | C | 1 | a0001c0001t0016 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 485 | chr11 | 491067 | ||||||
| chr11:491114 | C | T | 1 | a0001c0001t0015 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*532C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 532 | chr11 | 491114 | ||||||
| chr11:491135 | C | T | 1 | a0001c0001t0017 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 553 | chr11 | 491135 | ||||||
| chr11:491313 | C | T | 1 | a0001c0001t0014 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 731 | chr11 | 491313 | ||||||
| chr11:491334 | A | C | 4 | a0001c0001t0006 a0002c0003t0005 a0002c0003t0006 others(1): Show |
19 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*752A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 12/12 | 752 | chr11 | 491334 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:450683 | T | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.182+46T>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 450683 | |||||||
| chr11:450763 | T | G | 95 | a0001c0001t0001g0052 a0001c0001t0001g0119 a0001c0001t0001g0120 others(92): Show |
102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.182+126T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 450763 | |||||||
| chr11:450769 | G | A | 28 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(25): Show |
36 | HG00544.hp2 HG01168.hp2 HG01981.hp1 others(33): Show |
intron_variant | MODIFIER | c.182+132G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 450769 | |||||||
| chr11:450788 | C | G | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.182+151C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 450788 | |||||||
| chr11:450874 | C | G | 1 | a0001c0001t0002g0121 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.182+237C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 450874 | |||||||
| chr11:450987 | G | C | 89 | a0001c0001t0001g0052 a0001c0001t0002g0009 a0001c0001t0002g0011 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.182+350G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 450987 | |||||||
| chr11:451012 | C | A | 1 | a0001c0001t0001g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.182+375C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 451012 | |||||||
| chr11:451210 | C | T | 1 | a0001c0001t0004g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.182+573C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 451210 | |||||||
| chr11:451490 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.182+853C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 451490 | |||||||
| chr11:451872 | A | T | 53 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(50): Show |
58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.182+1235A>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 451872 | |||||||
| chr11:451876 | C | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0293 others(3): Show |
8 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.182+1239C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 451876 | |||||||
| chr11:451934 | T | C | 1 | a0001c0001t0009g0034 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.182+1297T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 451934 | |||||||
| chr11:452052 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.182+1415G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452052 | |||||||
| chr11:452123 | G | C | 1 | a0001c0002t0001g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.182+1486G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452123 | |||||||
| chr11:452168 | T | C | 1 | a0001c0001t0002g0036 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.182+1531T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452168 | |||||||
| chr11:452282 | G | T | 17 | a0001c0001t0002g0036 a0001c0001t0002g0054 a0001c0001t0002g0055 others(14): Show |
17 | HG00544.hp1 HG01069.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.182+1645G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452282 | |||||||
| chr11:452310 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.182+1673G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452310 | |||||||
| chr11:452465 | C | T | 1 | a0001c0001t0004g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.182+1828C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452465 | |||||||
| chr11:452471 | A | G | 1 | a0001c0002t0001g0145 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.182+1834A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452471 | |||||||
| chr11:452672 | G | A | 5 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG02622.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.182+2035G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452672 | |||||||
| chr11:452714 | A | T | 2 | a0001c0001t0003g0037 a0001c0001t0010g0053 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.182+2077A>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452714 | |||||||
| chr11:452738 | G | C | 17 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0153 others(14): Show |
18 | HG01109.hp1 HG01884.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.182+2101G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452738 | |||||||
| chr11:452784 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG01261.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.182+2147A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452784 | |||||||
| chr11:452842 | T | G | 1 | a0001c0001t0001g0165 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.182+2205T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 452842 | |||||||
| chr11:453034 | G | T | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.182+2397G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453034 | |||||||
| chr11:453125 | G | A | 3 | a0001c0006t0001g0019 a0001c0006t0001g0166 a0001c0006t0001g0167 |
4 | HG02486.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.182+2488G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453125 | |||||||
| chr11:453139 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.182+2502G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453139 | |||||||
| chr11:453187 | CCTT | C | 7 | a0001c0001t0001g0168 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.182+2553_182+2555d others(5): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 453187 | ||||||
| chr11:453223 | A | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.182+2586A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453223 | |||||||
| chr11:453278 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG01243.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.182+2641C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453278 | |||||||
| chr11:453313 | T | G | 30 | a0001c0001t0001g0175 a0001c0002t0001g0002 a0001c0002t0001g0005 others(27): Show |
39 | HG00544.hp2 HG01123.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.182+2676T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453313 | |||||||
| chr11:453323 | A | G | 2 | a0001c0001t0003g0037 a0001c0001t0010g0053 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.182+2686A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453323 | |||||||
| chr11:453397 | C | T | 1 | a0001c0008t0001g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.182+2760C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453397 | |||||||
| chr11:453407 | C | T | 1 | a0001c0001t0004g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.182+2770C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453407 | |||||||
| chr11:453409 | C | T | 9 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.182+2772C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453409 | |||||||
| chr11:453519 | G | A | 1 | a0003c0004t0001g0176 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.182+2882G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453519 | |||||||
| chr11:453644 | T | G | 3 | a0001c0006t0001g0019 a0001c0006t0001g0166 a0001c0006t0001g0167 |
4 | HG02486.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.182+3007T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453644 | |||||||
| chr11:453868 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.182+3231G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453868 | |||||||
| chr11:453887 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.182+3250G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 453887 | |||||||
| chr11:454029 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.182+3392A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454029 | |||||||
| chr11:454054 | A | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.182+3417A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454054 | |||||||
| chr11:454067 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.182+3430C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454067 | |||||||
| chr11:454159 | G | A | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.182+3522G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454159 | |||||||
| chr11:454359 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.182+3722G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454359 | |||||||
| chr11:454363 | C | T | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.182+3726C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454363 | |||||||
| chr11:454582 | G | A | 4 | a0003c0004t0001g0006 a0003c0004t0001g0176 a0003c0004t0001g0179 others(1): Show |
6 | HG01934.hp2 HG01975.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.182+3945G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454582 | |||||||
| chr11:454673 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.182+4036C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454673 | |||||||
| chr11:454697 | T | C | 120 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.182+4060T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454697 | |||||||
| chr11:454737 | A | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.182+4100A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454737 | |||||||
| chr11:454743 | C | T | 87 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(84): Show |
93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.182+4106C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454743 | |||||||
| chr11:454744 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.182+4107G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454744 | |||||||
| chr11:454746 | G | A | 89 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.182+4109G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454746 | |||||||
| chr11:454775 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.182+4138C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454775 | |||||||
| chr11:454980 | A | G | 125 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(122): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.182+4343A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 454980 | |||||||
| chr11:455008 | G | A | 89 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.182+4371G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 455008 | |||||||
| chr11:455257 | C | T | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG00642.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.182+4620C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 455257 | |||||||
| chr11:455268 | C | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.182+4631C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 455268 | |||||||
| chr11:455321 | G | A | 87 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(84): Show |
93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.182+4684G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 455321 | |||||||
| chr11:455400 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.182+4763C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 455400 | |||||||
| chr11:455479 | G | A | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.183-4708G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 455479 | |||||||
| chr11:455815 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183-4372G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 455815 | |||||||
| chr11:455947 | G | T | 1 | a0001c0005t0001g0278 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.183-4240G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 455947 | |||||||
| chr11:456003 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.183-4184C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456003 | |||||||
| chr11:456012 | C | T | 9 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.183-4175C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456012 | |||||||
| chr11:456059 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.183-4128G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456059 | |||||||
| chr11:456064 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.183-4123G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456064 | |||||||
| chr11:456106 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.183-4081G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456106 | |||||||
| chr11:456170 | C | CT | 45 | a0001c0001t0001g0154 a0001c0001t0001g0270 a0001c0001t0001g0271 others(42): Show |
48 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.183-3997dupT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 456170 | ||||||
| chr11:456170 | C | CTT | 16 | a0001c0001t0002g0112 a0001c0001t0002g0297 a0001c0001t0004g0155 others(13): Show |
16 | HG00642.hp1 HG00733.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.183-3998_183-3997d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 456170 | ||||||
| chr11:456170 | C | CTTTT | 12 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(9): Show |
14 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.183-4000_183-3997d others(6): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 456170 | ||||||
| chr11:456170 | CT | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0032 others(12): Show |
19 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.183-3997delT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 456170 | ||||||
| chr11:456234 | G | A | 19 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0042 others(16): Show |
21 | HG00597.hp2 HG00609.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.183-3953G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456234 | |||||||
| chr11:456256 | C | A | 1 | a0002c0003t0005g0184 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.183-3931C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456256 | |||||||
| chr11:456341 | A | AT | 17 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0153 others(14): Show |
20 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.183-3831dupT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 456341 | ||||||
| chr11:456375 | CTA | C | 6 | a0001c0001t0001g0144 a0001c0002t0001g0137 a0001c0002t0001g0138 others(3): Show |
6 | NA18954.hp2 NA18995.hp2 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.183-3810_183-3809d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 456375 | ||||||
| chr11:456468 | T | C | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.183-3719T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456468 | |||||||
| chr11:456531 | G | A | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.183-3656G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456531 | |||||||
| chr11:456638 | G | A | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-3549G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456638 | |||||||
| chr11:456704 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.183-3483C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456704 | |||||||
| chr11:456804 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.183-3383G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 456804 | |||||||
| chr11:457122 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.183-3065A>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 457122 | |||||||
| chr11:457482 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.183-2705G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 457482 | |||||||
| chr11:457539 | G | A | 2 | a0001c0001t0004g0157 a0001c0001t0004g0158 |
2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.183-2648G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 457539 | |||||||
| chr11:457636 | C | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.183-2551C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 457636 | |||||||
| chr11:457732 | C | G | 1 | a0001c0001t0001g0292 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.183-2455C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 457732 | |||||||
| chr11:457755 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.183-2432G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 457755 | |||||||
| chr11:457854 | C | A | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-2333C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 457854 | |||||||
| chr11:457879 | C | T | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.183-2308C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 457879 | |||||||
| chr11:458206 | T | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG01243.hp2 HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.183-1981T>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458206 | |||||||
| chr11:458209 | T | C | 1 | a0001c0001t0002g0096 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.183-1978T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458209 | |||||||
| chr11:458210 | C | CT | 12 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(9): Show |
14 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.183-1965dupT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 458210 | ||||||
| chr11:458210 | CT | C | 13 | a0001c0001t0003g0070 a0001c0001t0004g0155 a0001c0001t0004g0156 others(10): Show |
13 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.183-1965delT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 458210 | ||||||
| chr11:458253 | G | A | 2 | a0001c0001t0003g0037 a0001c0001t0010g0053 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.183-1934G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458253 | |||||||
| chr11:458265 | C | T | 89 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.183-1922C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458265 | |||||||
| chr11:458266 | G | A | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-1921G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458266 | |||||||
| chr11:458368 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.183-1819G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458368 | |||||||
| chr11:458427 | G | A | 87 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(84): Show |
93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.183-1760G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458427 | |||||||
| chr11:458441 | G | C | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.183-1746G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458441 | |||||||
| chr11:458497 | G | A | 4 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0268 others(1): Show |
4 | HG01433.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-1690G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458497 | |||||||
| chr11:458507 | A | AT | 52 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0031 others(49): Show |
58 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.183-1657dupT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 458507 | ||||||
| chr11:458507 | A | ATT | 7 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0281 others(4): Show |
7 | HG00741.hp1 HG01943.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.183-1658_183-1657d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 458507 | ||||||
| chr11:458507 | AT | A | 77 | a0001c0001t0001g0206 a0001c0001t0002g0009 a0001c0001t0002g0011 others(74): Show |
81 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.183-1657delT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 458507 | ||||||
| chr11:458507 | ATTT | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.183-1659_183-1657d others(5): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 458507 | ||||||
| chr11:458595 | G | A | 12 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(9): Show |
14 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.183-1592G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458595 | |||||||
| chr11:458734 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.183-1453G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458734 | |||||||
| chr11:458737 | A | G | 1 | a0001c0001t0004g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.183-1450A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458737 | |||||||
| chr11:458784 | A | G | 13 | a0001c0001t0001g0279 a0001c0001t0004g0155 a0001c0001t0004g0156 others(10): Show |
13 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.183-1403A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 458784 | |||||||
| chr11:459025 | A | AGTGAATG others(33): Show |
1 | a0001c0001t0001g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.183-1159_183-1158i others(42): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459025 | ||||||
| chr11:459034 | A | AGGACCTG others(593): Show |
1 | a0001c0001t0002g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.183-1034_183-1033i others(602): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459034 | ||||||
| chr11:459034 | A | AGGACCTG others(593): Show |
1 | a0001c0001t0001g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.183-959_183-958ins others(600): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459034 | ||||||
| chr11:459034 | A | AGGACCTG others(73): Show |
1 | a0001c0001t0004g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.183-1125_183-1124i others(82): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459034 | ||||||
| chr11:459034 | A | AGGACCTG others(33): Show |
4 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0268 others(1): Show |
4 | HG01433.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-1132_183-1131i others(42): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459034 | ||||||
| chr11:459034 | A | C | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.183-1153A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459034 | |||||||
| chr11:459057 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.183-1130C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459057 | |||||||
| chr11:459057 | CACACTCC others(33): Show |
C | 1 | a0001c0001t0004g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.183-1118_183-1079d others(42): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459057 | ||||||
| chr11:459063 | C | G | 10 | a0001c0001t0001g0153 a0001c0001t0004g0155 a0001c0001t0004g0156 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.183-1124C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459063 | |||||||
| chr11:459064 | C | T | 5 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(2): Show |
5 | HG00323.hp2 HG01070.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.183-1123C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459064 | |||||||
| chr11:459069 | A | G | 21 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0268 others(18): Show |
22 | HG01433.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.183-1118A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459069 | |||||||
| chr11:459074 | A | AGGACCTG others(33): Show |
15 | a0001c0001t0006g0185 a0002c0003t0005g0021 a0002c0003t0005g0184 others(12): Show |
16 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.183-1092_183-1091i others(42): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459074 | ||||||
| chr11:459074 | A | AGGACCTG others(153): Show |
1 | a0001c0001t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.183-1092_183-1091i others(162): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459074 | ||||||
| chr11:459074 | A | AGGACCTG others(433): Show |
1 | a0001c0001t0002g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.183-1092_183-1091i others(442): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459074 | ||||||
| chr11:459074 | A | AGGACCTG others(353): Show |
1 | a0001c0001t0003g0069 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183-1092_183-1091i others(362): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459074 | ||||||
| chr11:459074 | A | AGGACCTG others(473): Show |
2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG00642.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.183-1092_183-1091i others(482): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459074 | ||||||
| chr11:459074 | A | AGGACCTG others(753): Show |
1 | a0001c0001t0004g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.183-1092_183-1091i others(762): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459074 | ||||||
| chr11:459074 | A | C | 13 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0268 others(10): Show |
14 | HG01109.hp1 HG01433.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.183-1113A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459074 | |||||||
| chr11:459074 | AGGACCTG others(33): Show |
A | 1 | a0001c0002t0001g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.183-1091_183-1052d others(42): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459074 | ||||||
| chr11:459095 | G | GACACACT others(111): Show |
1 | a0001c0001t0002g0112 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.183-1092_183-1091i others(120): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459095 | |||||||
| chr11:459095 | G | GACACACT others(591): Show |
1 | a0001c0001t0002g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.183-1092_183-1091i others(600): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459095 | |||||||
| chr11:459095 | G | GACACACT others(511): Show |
1 | a0001c0001t0002g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.183-1092_183-1091i others(520): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459095 | |||||||
| chr11:459095 | G | GACACACT others(31): Show |
2 | a0001c0001t0004g0158 a0001c0001t0004g0160 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.183-1092_183-1091i others(40): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459095 | |||||||
| chr11:459096 | G | A | 112 | a0001c0001t0001g0208 a0001c0001t0001g0279 a0001c0001t0002g0009 others(109): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.183-1091G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459096 | |||||||
| chr11:459097 | G | C | 111 | a0001c0001t0001g0208 a0001c0001t0001g0279 a0001c0001t0002g0009 others(108): Show |
119 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.183-1090G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459097 | |||||||
| chr11:459097 | G | CACACTCC others(153): Show |
1 | a0001c0001t0003g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.183-1090delGinsCAC others(158): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459097 | |||||||
| chr11:459097 | G | GAC | 3 | a0001c0001t0002g0110 a0001c0001t0002g0112 a0001c0001t0004g0158 |
3 | HG00642.hp1 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.183-1087_183-1086d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | G | GACACACT others(235): Show |
1 | a0001c0001t0004g0160 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.183-1086_183-1085i others(244): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | G | GACACTCC others(33): Show |
2 | a0001c0006t0001g0019 a0001c0006t0001g0167 |
3 | HG02486.hp2 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.183-1075_183-1074i others(42): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | G | GACACTCC others(233): Show |
1 | a0001c0006t0001g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.183-1075_183-1074i others(242): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | G | GACACTCC others(33): Show |
8 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0030 others(5): Show |
13 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.183-873_183-834dup others(40): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | G | GACACTCC others(73): Show |
12 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0032 others(9): Show |
15 | HG00140.hp2 HG00639.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.183-913_183-834dup others(80): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | G | GACACTCC others(633): Show |
1 | a0001c0001t0001g0281 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.183-959_183-958ins others(640): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | G | GACACTCC others(273): Show |
1 | a0001c0001t0001g0274 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.183-834_183-833ins others(280): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | G | GACACTCC others(473): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.183-834_183-833ins others(480): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | G | GACACTCC others(353): Show |
1 | a0001c0001t0001g0286 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.183-931_183-930ins others(360): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | G | GACACTCC others(233): Show |
1 | a0001c0001t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.183-1012_183-1011i others(242): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459097 | GACACTCC others(33): Show |
G | 3 | a0001c0001t0001g0253 a0001c0001t0002g0043 a0001c0001t0015g0209 |
3 | HG02486.hp1 HG03927.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.183-873_183-834del others(40): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459097 | ||||||
| chr11:459103 | C | G | 1 | a0001c0001t0004g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.183-1084C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459103 | |||||||
| chr11:459109 | G | GATGTCGG others(33): Show |
1 | a0001c0001t0004g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.183-1039_183-1038i others(42): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459109 | ||||||
| chr11:459114 | C | A | 1 | a0001c0001t0004g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.183-1073C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459114 | |||||||
| chr11:459114 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.183-1073C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459114 | |||||||
| chr11:459137 | C | CACACTCC others(113): Show |
1 | a0001c0001t0003g0089 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.183-931_183-930ins others(120): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459137 | ||||||
| chr11:459137 | C | CACACTCC others(73): Show |
2 | a0001c0001t0002g0011 a0001c0001t0002g0091 |
3 | HG02970.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.183-971_183-970ins others(80): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459137 | ||||||
| chr11:459143 | C | CCGGTGGA others(73): Show |
1 | a0001c0001t0004g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.183-965_183-964ins others(80): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459143 | ||||||
| chr11:459177 | C | CACACTCC others(593): Show |
1 | a0001c0001t0010g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.183-919_183-918ins others(600): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459177 | ||||||
| chr11:459177 | C | CACACTCC others(73): Show |
2 | a0001c0001t0002g0045 a0001c0001t0002g0108 |
2 | HG01192.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.183-931_183-930ins others(80): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459177 | ||||||
| chr11:459194 | C | CGGACCTG others(73): Show |
1 | a0001c0001t0003g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.183-919_183-918ins others(80): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459194 | ||||||
| chr11:459194 | C | CGGACCTG others(793): Show |
1 | a0001c0001t0001g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.183-931_183-930ins others(800): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459194 | ||||||
| chr11:459194 | C | CGGACCTG others(513): Show |
1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.183-964_183-963ins others(520): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459194 | ||||||
| chr11:459217 | C | CACACTCC others(33): Show |
1 | a0001c0001t0002g0067 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.183-946_183-945ins others(40): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459217 | ||||||
| chr11:459217 | C | CACACTCC others(713): Show |
1 | a0001c0001t0001g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.183-834_183-833ins others(720): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459217 | ||||||
| chr11:459217 | C | CACACTCC others(73): Show |
4 | a0001c0001t0002g0009 a0001c0001t0002g0041 a0001c0001t0002g0046 others(1): Show |
5 | HG02572.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.183-891_183-890ins others(80): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459217 | ||||||
| chr11:459217 | C | CACACTCC others(713): Show |
1 | a0001c0001t0002g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.183-891_183-890ins others(720): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459217 | ||||||
| chr11:459217 | C | CACACTCC others(33): Show |
59 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(56): Show |
63 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.183-931_183-930ins others(40): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459217 | ||||||
| chr11:459217 | C | T | 6 | a0001c0001t0002g0042 a0001c0001t0002g0048 a0001c0001t0002g0095 others(3): Show |
7 | HG02486.hp2 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.183-970C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459217 | |||||||
| chr11:459223 | C | CCGGTGGA others(33): Show |
4 | a0001c0001t0004g0156 a0001c0001t0004g0157 a0001c0001t0004g0161 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-925_183-924ins others(40): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459223 | ||||||
| chr11:459223 | C | G | 3 | a0001c0001t0004g0160 a0001c0001t0004g0163 a0001c0006t0001g0166 |
3 | HG02451.hp1 HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.183-964C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459223 | |||||||
| chr11:459224 | C | CGGTGGAT others(153): Show |
1 | a0001c0001t0001g0288 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.183-953_183-794dup others(160): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459224 | ||||||
| chr11:459234 | C | CGGACCTG others(513): Show |
1 | a0001c0001t0002g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.183-804_183-803ins others(520): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459234 | ||||||
| chr11:459234 | C | CGGACCTG others(73): Show |
1 | a0001c0001t0003g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.183-931_183-930ins others(80): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459234 | ||||||
| chr11:459234 | C | CGGACCTG others(313): Show |
1 | a0001c0001t0003g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.183-931_183-930ins others(320): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459234 | ||||||
| chr11:459257 | C | CACACTCC others(153): Show |
1 | a0001c0001t0001g0147 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.183-834_183-833ins others(160): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459257 | ||||||
| chr11:459257 | C | CACACTCC others(433): Show |
1 | a0001c0001t0002g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.183-834_183-833ins others(440): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459257 | ||||||
| chr11:459257 | C | T | 7 | a0001c0001t0001g0168 a0001c0001t0002g0043 a0001c0001t0002g0044 others(4): Show |
7 | HG00642.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.183-930C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459257 | |||||||
| chr11:459263 | C | G | 1 | a0001c0001t0004g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.183-924C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459263 | |||||||
| chr11:459264 | C | CGGTGGAT others(273): Show |
1 | a0001c0001t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.183-914_183-913ins others(280): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459264 | ||||||
| chr11:459264 | C | CGGTGGAT others(713): Show |
1 | a0001c0001t0002g0297 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.183-874_183-873ins others(720): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459264 | ||||||
| chr11:459274 | C | A | 1 | a0001c0001t0003g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.183-913C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459274 | |||||||
| chr11:459274 | C | CGGACCTG others(1313): Show |
1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.183-844_183-843ins others(1320): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459274 | ||||||
| chr11:459281 | G | GGGTTAGA others(33): Show |
4 | a0001c0001t0001g0200 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG01346.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-867_183-866ins others(40): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459281 | ||||||
| chr11:459281 | G | GGGTTAGA others(233): Show |
1 | a0001c0001t0001g0285 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.183-778_183-777ins others(240): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459281 | ||||||
| chr11:459290 | GTGAGGAC others(113): Show |
G | 1 | a0001c0001t0001g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.183-890_183-771del | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459290 | ||||||
| chr11:459297 | C | CACACTCC others(393): Show |
1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.183-834_183-833ins others(400): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459297 | ||||||
| chr11:459314 | C | A | 1 | a0001c0001t0002g0297 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.183-873C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459314 | |||||||
| chr11:459314 | C | CGGACCTG others(113): Show |
1 | a0001c0001t0002g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.183-834_183-833ins others(120): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459314 | ||||||
| chr11:459314 | C | CGGACCTG others(113): Show |
1 | a0001c0001t0001g0267 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.183-834_183-833ins others(120): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459314 | ||||||
| chr11:459314 | CGGACCTG others(73): Show |
C | 1 | a0001c0001t0001g0024 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.183-857_183-778del others(80): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459314 | ||||||
| chr11:459337 | C | CACACTCC others(73): Show |
1 | a0001c0006t0001g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.183-804_183-803ins others(80): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459337 | ||||||
| chr11:459337 | C | CACACTCC others(113): Show |
1 | a0001c0001t0002g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.183-834_183-833ins others(120): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459337 | ||||||
| chr11:459337 | C | CACACTCC others(153): Show |
1 | a0001c0001t0002g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.183-834_183-833ins others(160): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459337 | ||||||
| chr11:459344 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.183-843C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459344 | |||||||
| chr11:459349 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.183-838G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459349 | |||||||
| chr11:459354 | A | AGGACCTG others(113): Show |
1 | a0001c0001t0002g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.183-804_183-803ins others(120): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 459354 | ||||||
| chr11:459354 | A | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0147 a0001c0001t0002g0108 others(14): Show |
19 | HG00642.hp1 HG01109.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.183-833A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459354 | |||||||
| chr11:459376 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.183-811A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459376 | |||||||
| chr11:459377 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0091 |
3 | HG02970.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.183-810C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459377 | |||||||
| chr11:459384 | T | C | 15 | a0001c0001t0001g0149 a0001c0001t0001g0279 a0001c0001t0002g0011 others(12): Show |
16 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.183-803T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459384 | |||||||
| chr11:459391 | T | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.183-796T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459391 | |||||||
| chr11:459394 | A | C | 10 | a0001c0001t0001g0018 a0001c0001t0004g0155 a0001c0001t0004g0156 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.183-793A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459394 | |||||||
| chr11:459395 | G | C | 1 | a0001c0001t0002g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.183-792G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459395 | |||||||
| chr11:459410 | A | G | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.183-777A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459410 | |||||||
| chr11:459452 | G | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0030 others(16): Show |
24 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.183-735G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459452 | |||||||
| chr11:459461 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0295 others(1): Show |
6 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.183-726C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459461 | |||||||
| chr11:459507 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.183-680T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459507 | |||||||
| chr11:459564 | C | T | 4 | a0001c0001t0002g0063 a0001c0001t0007g0062 a0001c0001t0007g0064 others(1): Show |
4 | HG02738.hp2 HG03017.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-623C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459564 | |||||||
| chr11:459585 | G | C | 1 | a0001c0001t0007g0062 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.183-602G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 459585 | |||||||
| chr11:460011 | C | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.183-176C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 460011 | |||||||
| chr11:460025 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.183-162G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 460025 | |||||||
| chr11:460046 | C | T | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-141C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 460046 | |||||||
| chr11:460101 | G | A | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.183-86G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 1/11 | chr11 | 460101 | |||||||
| chr11:460303 | T | C | 123 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(120): Show |
131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.284+15T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460303 | |||||||
| chr11:460411 | G | T | 1 | a0001c0001t0016g0107 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.284+123G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460411 | |||||||
| chr11:460540 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.284+252G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460540 | |||||||
| chr11:460560 | T | C | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+272T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460560 | |||||||
| chr11:460607 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.284+319G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460607 | |||||||
| chr11:460667 | T | G | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+379T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460667 | |||||||
| chr11:460670 | C | T | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.284+382C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460670 | |||||||
| chr11:460671 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.284+383G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460671 | |||||||
| chr11:460697 | CAG | C | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+410_284+411del others(2): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460697 | |||||||
| chr11:460765 | A | G | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.284+477A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460765 | |||||||
| chr11:460818 | T | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0099 |
3 | NA18939.hp2 NA19077.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.284+530T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460818 | |||||||
| chr11:460932 | C | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.284+644C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 460932 | |||||||
| chr11:461269 | C | A | 8 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(5): Show |
8 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+981C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 461269 | |||||||
| chr11:461280 | G | A | 8 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(5): Show |
8 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+992G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 461280 | |||||||
| chr11:461512 | C | T | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+1224C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 461512 | |||||||
| chr11:461538 | C | T | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+1250C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 461538 | |||||||
| chr11:461546 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.284+1258C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 461546 | |||||||
| chr11:461748 | G | A | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+1460G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 461748 | |||||||
| chr11:462105 | A | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+1817A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462105 | |||||||
| chr11:462380 | G | T | 1 | a0001c0001t0011g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+2092G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462380 | |||||||
| chr11:462672 | C | T | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+2384C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462672 | |||||||
| chr11:462684 | C | T | 12 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(9): Show |
14 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.284+2396C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462684 | |||||||
| chr11:462833 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.284+2545A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462833 | |||||||
| chr11:462843 | G | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.284+2555G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462843 | |||||||
| chr11:462854 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.284+2566G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462854 | |||||||
| chr11:462855 | G | A | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.284+2567G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462855 | |||||||
| chr11:462895 | G | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.284+2607G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462895 | |||||||
| chr11:462898 | G | T | 3 | a0001c0006t0001g0019 a0001c0006t0001g0166 a0001c0006t0001g0167 |
4 | HG02486.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+2610G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462898 | |||||||
| chr11:462939 | C | T | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+2651C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 462939 | |||||||
| chr11:463136 | C | T | 1 | a0001c0001t0004g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.284+2848C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463136 | |||||||
| chr11:463164 | CA | C | 13 | a0001c0001t0001g0248 a0001c0001t0004g0155 a0001c0001t0004g0156 others(10): Show |
13 | HG00733.hp2 HG01109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.284+2889delA | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 463164 | ||||||
| chr11:463288 | T | C | 92 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(89): Show |
98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.284+3000T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463288 | |||||||
| chr11:463290 | T | C | 92 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(89): Show |
98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.284+3002T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463290 | |||||||
| chr11:463291 | G | A | 91 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(88): Show |
97 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.284+3003G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463291 | |||||||
| chr11:463305 | G | A | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+3017G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463305 | |||||||
| chr11:463444 | A | AT | 28 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0277 others(25): Show |
28 | HG00438.hp2 HG01106.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.284+3172dupT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 463444 | ||||||
| chr11:463569 | C | A | 1 | a0001c0001t0011g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+3281C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463569 | |||||||
| chr11:463571 | G | A | 1 | a0001c0001t0011g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+3283G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463571 | |||||||
| chr11:463573 | C | A | 1 | a0001c0001t0011g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+3285C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463573 | |||||||
| chr11:463574 | T | A | 1 | a0001c0001t0011g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+3286T>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463574 | |||||||
| chr11:463575 | C | T | 1 | a0001c0001t0011g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+3287C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463575 | |||||||
| chr11:463576 | T | A | 1 | a0001c0001t0011g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+3288T>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463576 | |||||||
| chr11:463577 | C | A | 1 | a0001c0001t0011g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+3289C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463577 | |||||||
| chr11:463577 | C | T | 21 | a0001c0001t0002g0012 a0001c0001t0002g0075 a0001c0001t0002g0076 others(18): Show |
23 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.284+3289C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463577 | |||||||
| chr11:463587 | T | G | 1 | a0001c0001t0011g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+3299T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463587 | |||||||
| chr11:463610 | A | G | 14 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0004g0155 others(11): Show |
14 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.284+3322A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463610 | |||||||
| chr11:463632 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.284+3344C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463632 | |||||||
| chr11:463695 | C | T | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | HG01074.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.284+3407C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463695 | |||||||
| chr11:463703 | T | C | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+3415T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463703 | |||||||
| chr11:463779 | T | C | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+3491T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463779 | |||||||
| chr11:463820 | A | C | 1 | a0001c0001t0001g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.284+3532A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463820 | |||||||
| chr11:463826 | A | G | 132 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(129): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.284+3538A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463826 | |||||||
| chr11:463894 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.284+3606A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463894 | |||||||
| chr11:463913 | A | C | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+3625A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 463913 | |||||||
| chr11:464011 | G | A | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+3723G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464011 | |||||||
| chr11:464128 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.284+3840G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464128 | |||||||
| chr11:464148 | A | G | 1 | a0002c0003t0005g0190 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.284+3860A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464148 | |||||||
| chr11:464229 | C | G | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02622.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+3941C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464229 | |||||||
| chr11:464279 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.284+3991G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464279 | |||||||
| chr11:464291 | C | T | 119 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(116): Show |
127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.284+4003C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464291 | |||||||
| chr11:464307 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.284+4019G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464307 | |||||||
| chr11:464378 | G | A | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+4090G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464378 | |||||||
| chr11:464409 | G | T | 1 | a0001c0008t0001g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.284+4121G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464409 | |||||||
| chr11:464460 | C | A | 7 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0001c0001t0002g0041 others(4): Show |
8 | HG01074.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+4172C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464460 | |||||||
| chr11:464466 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284+4178G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464466 | |||||||
| chr11:464667 | T | C | 120 | a0001c0001t0001g0211 a0001c0001t0001g0282 a0001c0001t0002g0009 others(117): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.284+4379T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464667 | |||||||
| chr11:464971 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.284+4683C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464971 | |||||||
| chr11:464972 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0247 |
3 | HG00099.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.284+4684G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464972 | |||||||
| chr11:464976 | T | C | 6 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(3): Show |
6 | HG00323.hp2 HG00738.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.284+4688T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464976 | |||||||
| chr11:464977 | A | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.284+4689A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464977 | |||||||
| chr11:464994 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.284+4706G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 464994 | |||||||
| chr11:465006 | G | A | 1 | a0001c0005t0001g0182 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.284+4718G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 465006 | |||||||
| chr11:465183 | GC | G | 21 | a0001c0001t0002g0012 a0001c0001t0002g0075 a0001c0001t0002g0076 others(18): Show |
23 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.284+4896delC | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 465183 | |||||||
| chr11:465306 | T | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
6 | HG01884.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+5018T>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 465306 | |||||||
| chr11:465332 | C | T | 4 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0112 others(1): Show |
4 | HG00642.hp1 HG03927.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+5044C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 465332 | |||||||
| chr11:465453 | GTGAGCTA others(3): Show |
G | 1 | a0001c0002t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.284+5168_284+5177d others(12): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 465453 | ||||||
| chr11:465453 | GTGAGCTA others(28): Show |
G | 1 | a0001c0001t0001g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.284+5179_284+5213d others(37): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 465453 | ||||||
| chr11:465488 | C | T | 3 | a0001c0001t0003g0037 a0001c0001t0010g0053 a0001c0002t0010g0204 |
3 | HG02572.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.284+5200C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 465488 | |||||||
| chr11:465749 | G | A | 13 | a0001c0001t0001g0148 a0001c0001t0004g0155 a0001c0001t0004g0156 others(10): Show |
13 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.284+5461G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 465749 | |||||||
| chr11:465753 | A | AC | 77 | a0001c0001t0001g0028 a0001c0001t0001g0147 a0001c0001t0001g0149 others(74): Show |
83 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.284+5475dupC | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 465753 | ||||||
| chr11:465758 | C | CA | 6 | a0001c0001t0003g0010 a0001c0001t0003g0070 a0001c0001t0003g0073 others(3): Show |
7 | HG00438.hp2 NA18946.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+5470_284+5471i others(3): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 465758 | |||||||
| chr11:465759 | C | T | 1 | a0002c0003t0005g0193 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.284+5471C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 465759 | |||||||
| chr11:465763 | C | A | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.284+5475C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 465763 | |||||||
| chr11:465902 | A | G | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+5614A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 465902 | |||||||
| chr11:466025 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.284+5737C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466025 | |||||||
| chr11:466032 | A | T | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.284+5744A>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466032 | |||||||
| chr11:466048 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.284+5760C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466048 | |||||||
| chr11:466140 | G | A | 87 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(84): Show |
93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.284+5852G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466140 | |||||||
| chr11:466392 | A | G | 25 | a0001c0001t0001g0243 a0001c0001t0002g0036 a0001c0001t0002g0039 others(22): Show |
25 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.284+6104A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466392 | |||||||
| chr11:466401 | C | CT | 53 | a0001c0001t0001g0033 a0001c0001t0001g0148 a0001c0001t0001g0149 others(50): Show |
63 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.284+6135dupT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 466401 | ||||||
| chr11:466401 | C | CTT | 9 | a0001c0001t0001g0147 a0001c0002t0001g0129 a0001c0002t0001g0136 others(6): Show |
10 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.284+6134_284+6135d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 466401 | ||||||
| chr11:466468 | T | C | 150 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(147): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.284+6180T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466468 | |||||||
| chr11:466510 | C | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0072 a0001c0001t0002g0091 |
4 | HG02970.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+6222C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466510 | |||||||
| chr11:466580 | G | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.284+6292G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466580 | |||||||
| chr11:466843 | G | C | 2 | a0001c0001t0002g0055 a0001c0001t0002g0195 |
2 | HG01069.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.284+6555G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466843 | |||||||
| chr11:466857 | C | T | 88 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(85): Show |
94 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.284+6569C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466857 | |||||||
| chr11:466884 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.284+6596G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466884 | |||||||
| chr11:466966 | G | C | 7 | a0001c0001t0002g0012 a0001c0001t0002g0075 a0001c0001t0002g0079 others(4): Show |
8 | HG00280.hp1 HG00323.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+6678G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 466966 | |||||||
| chr11:467135 | G | A | 3 | a0001c0006t0001g0019 a0001c0006t0001g0166 a0001c0006t0001g0167 |
4 | HG02486.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-6760G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467135 | |||||||
| chr11:467188 | T | C | 4 | a0001c0001t0003g0089 a0001c0001t0003g0090 a0001c0001t0003g0092 others(1): Show |
4 | HG02559.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-6707T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467188 | |||||||
| chr11:467200 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-6695G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467200 | |||||||
| chr11:467339 | A | G | 117 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(114): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.285-6556A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467339 | |||||||
| chr11:467368 | A | G | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.285-6527A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467368 | |||||||
| chr11:467444 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.285-6451C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467444 | |||||||
| chr11:467585 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
6 | HG01884.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-6310G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467585 | |||||||
| chr11:467585 | G | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-6310G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467585 | |||||||
| chr11:467673 | C | T | 1 | a0001c0001t0004g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.285-6222C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467673 | |||||||
| chr11:467689 | C | A | 12 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(9): Show |
14 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.285-6206C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467689 | |||||||
| chr11:467710 | G | A | 1 | a0002c0003t0006g0192 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.285-6185G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467710 | |||||||
| chr11:467720 | G | A | 89 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.285-6175G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467720 | |||||||
| chr11:467801 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-6094G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 467801 | |||||||
| chr11:468134 | G | A | 2 | a0001c0002t0001g0124 a0001c0002t0001g0136 |
2 | HG02165.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.285-5761G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468134 | |||||||
| chr11:468252 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.285-5643C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468252 | |||||||
| chr11:468308 | C | T | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-5587C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468308 | |||||||
| chr11:468309 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.285-5586G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468309 | |||||||
| chr11:468322 | A | C | 2 | a0001c0001t0001g0237 a0001c0001t0001g0263 |
2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.285-5573A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468322 | |||||||
| chr11:468472 | T | TG | 26 | a0001c0001t0001g0119 a0001c0001t0001g0150 a0001c0001t0001g0168 others(23): Show |
26 | HG00733.hp1 HG01106.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.285-5418dupG | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 468472 | ||||||
| chr11:468531 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-5364G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468531 | |||||||
| chr11:468637 | G | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-5258G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468637 | |||||||
| chr11:468797 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.285-5098G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468797 | |||||||
| chr11:468810 | C | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-5085C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468810 | |||||||
| chr11:468864 | GTC | G | 19 | a0001c0001t0002g0036 a0001c0001t0002g0039 a0001c0001t0002g0054 others(16): Show |
19 | HG00280.hp2 HG00544.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.285-5027_285-5026d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 468864 | ||||||
| chr11:468909 | G | GGGAGGAG others(28): Show |
1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-4978_285-4977i others(37): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 468909 | ||||||
| chr11:468919 | G | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-4976G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468919 | |||||||
| chr11:468940 | A | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0268 |
3 | HG01433.hp2 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.285-4955A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468940 | |||||||
| chr11:468941 | AGAGGGGA others(121): Show |
A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0202 others(2): Show |
7 | HG01496.hp2 HG02004.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.285-4869_285-4742d others(2): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 468941 | ||||||
| chr11:468958 | T | C | 1 | a0001c0001t0004g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285-4937T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 468958 | |||||||
| chr11:469026 | CGGAAGGA others(121): Show |
C | 1 | a0001c0001t0001g0229 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285-4801_285-4674d others(2): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 469026 | ||||||
| chr11:469059 | AGAGGGAG others(313): Show |
A | 1 | a0001c0001t0001g0201 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.285-4813_285-4494d others(2): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 469059 | ||||||
| chr11:469154 | T | C | 16 | a0001c0001t0001g0248 a0001c0001t0001g0276 a0001c0001t0001g0291 others(13): Show |
16 | HG00733.hp2 HG01261.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.285-4741T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469154 | |||||||
| chr11:469164 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.285-4731A>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469164 | |||||||
| chr11:469265 | G | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-4630G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469265 | |||||||
| chr11:469267 | C | G | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-4628C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469267 | |||||||
| chr11:469267 | CAGTCTCT others(25): Show |
C | 1 | a0001c0001t0001g0280 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.285-4596_285-4565d others(34): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 469267 | ||||||
| chr11:469286 | G | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-4609G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469286 | |||||||
| chr11:469295 | AGGGGAGT others(101): Show |
A | 113 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(110): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.285-4583_285-4476d others(2): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 469295 | ||||||
| chr11:469299 | G | C | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-4596G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469299 | |||||||
| chr11:469327 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.285-4568A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469327 | |||||||
| chr11:469327 | AGGGCAGT others(69): Show |
A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-4564_285-4489d others(78): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 469327 | ||||||
| chr11:469435 | C | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.285-4460C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469435 | |||||||
| chr11:469503 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.285-4392C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469503 | |||||||
| chr11:469538 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.285-4357C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469538 | |||||||
| chr11:469583 | A | G | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-4312A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469583 | |||||||
| chr11:469636 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.285-4259C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469636 | |||||||
| chr11:469682 | A | AG | 6 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0001c0001t0002g0041 others(3): Show |
7 | HG02451.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.285-4208dupG | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 469682 | ||||||
| chr11:469728 | C | A | 3 | a0001c0001t0003g0037 a0001c0001t0010g0053 a0001c0002t0010g0204 |
3 | HG02572.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.285-4167C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469728 | |||||||
| chr11:469787 | G | T | 1 | a0001c0001t0001g0008 | 3 | HG03017.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.285-4108G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469787 | |||||||
| chr11:469794 | C | G | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-4101C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469794 | |||||||
| chr11:469889 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.285-4006C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469889 | |||||||
| chr11:469892 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-4003C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 469892 | |||||||
| chr11:470007 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-3888G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470007 | |||||||
| chr11:470114 | C | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-3781C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470114 | |||||||
| chr11:470261 | C | T | 2 | a0001c0002t0001g0131 a0001c0002t0001g0132 |
2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.285-3634C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470261 | |||||||
| chr11:470296 | G | C | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02257.hp2 HG02723.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-3599G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470296 | |||||||
| chr11:470331 | A | G | 151 | a0001c0001t0001g0235 a0001c0001t0001g0262 a0001c0001t0001g0264 others(148): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.285-3564A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470331 | |||||||
| chr11:470407 | G | A | 2 | a0001c0002t0001g0035 a0001c0002t0001g0040 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.285-3488G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470407 | |||||||
| chr11:470617 | T | A | 1 | a0001c0001t0001g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.285-3278T>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470617 | |||||||
| chr11:470694 | A | G | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.285-3201A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470694 | |||||||
| chr11:470830 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.285-3065C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470830 | |||||||
| chr11:470847 | C | CA | 6 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(3): Show |
6 | HG00642.hp1 HG00642.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.285-3045dupA | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 470847 | ||||||
| chr11:470853 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.285-3042G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470853 | |||||||
| chr11:470906 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285-2989G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470906 | |||||||
| chr11:470963 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.285-2932C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 470963 | |||||||
| chr11:471065 | C | T | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.285-2830C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471065 | |||||||
| chr11:471097 | CT | C | 114 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(111): Show |
123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.285-2780delT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 471097 | ||||||
| chr11:471241 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.285-2654G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471241 | |||||||
| chr11:471269 | A | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.285-2626A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471269 | |||||||
| chr11:471300 | G | A | 1 | a0003c0004t0001g0269 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.285-2595G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471300 | |||||||
| chr11:471479 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-2416G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471479 | |||||||
| chr11:471557 | G | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-2338G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471557 | |||||||
| chr11:471670 | C | T | 89 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.285-2225C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471670 | |||||||
| chr11:471682 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.285-2213A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471682 | |||||||
| chr11:471683 | C | A | 1 | a0001c0001t0001g0234 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.285-2212C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471683 | |||||||
| chr11:471694 | C | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-2201C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471694 | |||||||
| chr11:471698 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
6 | HG01884.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-2197C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471698 | |||||||
| chr11:471749 | T | C | 3 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0079 |
3 | HG00323.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.285-2146T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471749 | |||||||
| chr11:471749 | T | TGGCCTGG others(15): Show |
1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-2137_285-2136i others(24): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 471749 | ||||||
| chr11:471787 | A | G | 11 | a0001c0001t0002g0082 a0001c0001t0002g0093 a0001c0001t0003g0010 others(8): Show |
13 | HG00280.hp1 HG00438.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.285-2108A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471787 | |||||||
| chr11:471793 | T | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0247 a0001c0001t0003g0037 others(2): Show |
6 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-2102T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471793 | |||||||
| chr11:471807 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.285-2088G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471807 | |||||||
| chr11:471815 | CGGCCTGG others(15): Show |
C | 1 | a0001c0001t0001g0243 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.285-2041_285-2020d others(24): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 471815 | ||||||
| chr11:471859 | T | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-2036T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471859 | |||||||
| chr11:471875 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0052 others(23): Show |
31 | HG00558.hp1 HG01175.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.285-2020G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471875 | |||||||
| chr11:471923 | A | G | 117 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(114): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.285-1972A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471923 | |||||||
| chr11:471943 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0246 a0001c0001t0001g0260 |
3 | NA18942.hp1 NA18984.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.285-1952G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471943 | |||||||
| chr11:471951 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285-1944C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 471951 | |||||||
| chr11:471967 | A | AGATGGCG others(15): Show |
12 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(9): Show |
14 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.285-1887_285-1866d others(24): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 471967 | ||||||
| chr11:471967 | AGATGGCG others(15): Show |
A | 13 | a0001c0001t0001g0033 a0001c0001t0001g0236 a0001c0001t0004g0155 others(10): Show |
13 | HG01361.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.285-1887_285-1866d others(24): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 471967 | ||||||
| chr11:472018 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0256 |
2 | HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.285-1877G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472018 | |||||||
| chr11:472035 | G | A | 1 | a0001c0001t0006g0185 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.285-1860G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472035 | |||||||
| chr11:472088 | A | G | 117 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(114): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.285-1807A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472088 | |||||||
| chr11:472149 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-1746G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472149 | |||||||
| chr11:472209 | T | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-1686T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472209 | |||||||
| chr11:472285 | G | T | 1 | a0001c0001t0004g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.285-1610G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472285 | |||||||
| chr11:472324 | T | C | 124 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(121): Show |
133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.285-1571T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472324 | |||||||
| chr11:472380 | C | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-1515C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472380 | |||||||
| chr11:472407 | A | G | 1 | a0001c0001t0003g0074 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.285-1488A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472407 | |||||||
| chr11:472480 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.285-1415G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472480 | |||||||
| chr11:472505 | G | T | 1 | a0001c0001t0001g0296 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.285-1390G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472505 | |||||||
| chr11:472576 | G | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(296): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.285-1319G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472576 | |||||||
| chr11:472661 | C | T | 7 | a0001c0001t0001g0168 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-1234C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472661 | |||||||
| chr11:472826 | CGT | C | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-1059_285-1058d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 472826 | ||||||
| chr11:472876 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.285-1019A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472876 | |||||||
| chr11:472997 | T | C | 124 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(121): Show |
133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.285-898T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 472997 | |||||||
| chr11:473039 | G | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-856G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 473039 | |||||||
| chr11:473208 | C | T | 3 | a0001c0006t0001g0019 a0001c0006t0001g0166 a0001c0006t0001g0167 |
4 | HG02486.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-687C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 473208 | |||||||
| chr11:473300 | G | T | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.285-595G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 473300 | |||||||
| chr11:473367 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-528G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 473367 | |||||||
| chr11:473373 | G | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-522G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 473373 | |||||||
| chr11:473573 | G | GCAGGGTG others(129): Show |
11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-298_285-163dup others(136): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 473573 | ||||||
| chr11:473638 | A | AGCCCAGG others(129): Show |
89 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.285-163_285-162ins others(136): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 473638 | ||||||
| chr11:473796 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-99G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 473796 | |||||||
| chr11:473850 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.285-45G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 2/11 | chr11 | 473850 | |||||||
| chr11:474033 | C | T | 86 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(83): Show |
92 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.367+56C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474033 | |||||||
| chr11:474151 | T | G | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+174T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474151 | |||||||
| chr11:474247 | C | T | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+270C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474247 | |||||||
| chr11:474388 | C | G | 1 | a0001c0001t0002g0096 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.367+411C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474388 | |||||||
| chr11:474389 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.367+412G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474389 | |||||||
| chr11:474405 | G | T | 2 | a0001c0001t0001g0018 a0001c0001t0013g0152 |
3 | HG01884.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.367+428G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474405 | |||||||
| chr11:474542 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.367+565C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474542 | |||||||
| chr11:474594 | C | G | 1 | a0001c0001t0002g0195 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.367+617C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474594 | |||||||
| chr11:474754 | GAAAATTT others(3): Show |
G | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+781_367+790del others(10): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 474754 | ||||||
| chr11:474794 | C | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+817C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474794 | |||||||
| chr11:474851 | T | G | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+874T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474851 | |||||||
| chr11:474860 | T | TGTGCGGA others(193): Show |
1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+883_367+884ins others(200): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474860 | |||||||
| chr11:474878 | T | C | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+901T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474878 | |||||||
| chr11:474889 | G | A | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+912G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474889 | |||||||
| chr11:474891 | G | A | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+914G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474891 | |||||||
| chr11:474903 | A | G | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+926A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474903 | |||||||
| chr11:474908 | C | T | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+931C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474908 | |||||||
| chr11:474912 | TACGG | T | 88 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(85): Show |
94 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.367+938_367+941del others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 474912 | ||||||
| chr11:474939 | C | T | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+962C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474939 | |||||||
| chr11:474951 | T | C | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+974T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474951 | |||||||
| chr11:474972 | G | GTTCACGT others(71): Show |
1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1001_367+1002i others(80): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 474972 | ||||||
| chr11:474978 | G | A | 1 | a0002c0003t0005g0188 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.367+1001G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474978 | |||||||
| chr11:474980 | G | T | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1003G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 474980 | |||||||
| chr11:474982 | TTGTGATA others(20): Show |
T | 85 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(82): Show |
91 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.367+1027_367+1053d others(29): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 474982 | ||||||
| chr11:475004 | A | C | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1027A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475004 | |||||||
| chr11:475004 | AGTTTGTG others(20): Show |
A | 2 | a0001c0001t0001g0241 a0001c0001t0006g0185 |
2 | HG01361.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.367+1047_367+1073d others(29): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475004 | ||||||
| chr11:475018 | G | A | 8 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(5): Show |
8 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.367+1041G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475018 | |||||||
| chr11:475020 | A | C | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1043A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475020 | |||||||
| chr11:475031 | T | C | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1054T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475031 | |||||||
| chr11:475094 | G | A | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1117G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475094 | |||||||
| chr11:475100 | T | C | 85 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(82): Show |
91 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.367+1123T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475100 | |||||||
| chr11:475104 | C | G | 1 | a0001c0001t0001g0293 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.367+1127C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475104 | |||||||
| chr11:475120 | A | ATGGACAT others(45): Show |
1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1143_367+1144i others(54): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475120 | |||||||
| chr11:475148 | C | T | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+1171C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475148 | |||||||
| chr11:475165 | T | G | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1188T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475165 | |||||||
| chr11:475176 | A | C | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1199A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475176 | |||||||
| chr11:475192 | A | G | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1215A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475192 | |||||||
| chr11:475198 | T | C | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1221T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475198 | |||||||
| chr11:475206 | A | T | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1229A>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475206 | |||||||
| chr11:475212 | T | C | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1235T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475212 | |||||||
| chr11:475213 | C | G | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1236C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475213 | |||||||
| chr11:475224 | T | TGGCCATA others(430): Show |
1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1249_367+1250i others(439): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475224 | ||||||
| chr11:475231 | G | A | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1254G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475231 | |||||||
| chr11:475238 | T | C | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.367+1261T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475238 | |||||||
| chr11:475247 | G | GTACGGAC others(847): Show |
1 | a0001c0001t0002g0096 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.367+1297_367+1298i others(856): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(846): Show |
1 | a0001c0001t0002g0059 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.367+1297_367+1298i others(855): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(821): Show |
1 | a0001c0001t0007g0064 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.367+1297_367+1298i others(830): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(846): Show |
23 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0042 others(20): Show |
25 | HG00597.hp2 HG00609.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.367+1297_367+1298i others(855): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(821): Show |
2 | a0001c0001t0002g0097 a0001c0001t0002g0098 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.367+1297_367+1298i others(830): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(821): Show |
1 | a0001c0001t0002g0054 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.367+1297_367+1298i others(830): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(821): Show |
46 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0036 others(43): Show |
49 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.367+1297_367+1298i others(830): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(844): Show |
1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.367+1297_367+1298i others(853): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(821): Show |
1 | a0001c0001t0009g0058 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.367+1297_367+1298i others(830): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(821): Show |
4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+1297_367+1298i others(830): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(821): Show |
3 | a0001c0001t0002g0045 a0001c0001t0002g0049 a0001c0001t0002g0050 |
3 | HG02109.hp1 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.367+1297_367+1298i others(830): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(821): Show |
1 | a0001c0001t0002g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.367+1297_367+1298i others(830): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(821): Show |
7 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0001c0001t0002g0041 others(4): Show |
8 | HG01074.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.367+1297_367+1298i others(830): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(846): Show |
1 | a0001c0001t0002g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.367+1297_367+1298i others(855): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(432): Show |
1 | a0001c0001t0004g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.367+1297_367+1298i others(441): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(432): Show |
10 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.367+1297_367+1298i others(441): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475247 | G | GTACGGAC others(818): Show |
12 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(9): Show |
14 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.367+1296_367+1297i others(827): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475247 | ||||||
| chr11:475257 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.367+1280A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475257 | |||||||
| chr11:475272 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.367+1295A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475272 | |||||||
| chr11:475278 | C | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+1301C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475278 | |||||||
| chr11:475289 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
6 | HG01884.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.367+1312C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475289 | |||||||
| chr11:475392 | C | T | 1 | a0001c0001t0006g0185 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.367+1415C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475392 | |||||||
| chr11:475461 | A | G | 1 | a0001c0001t0004g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.367+1484A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475461 | |||||||
| chr11:475480 | A | G | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+1503A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475480 | |||||||
| chr11:475537 | CATTCACG others(18): Show |
C | 1 | a0001c0001t0001g0225 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.367+1580_367+1604d others(27): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 475537 | ||||||
| chr11:475588 | T | C | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02622.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.367+1611T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475588 | |||||||
| chr11:475634 | C | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.367+1657C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475634 | |||||||
| chr11:475651 | T | G | 1 | a0001c0001t0007g0057 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.367+1674T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475651 | |||||||
| chr11:475655 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.367+1678C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475655 | |||||||
| chr11:475959 | C | G | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+1982C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 475959 | |||||||
| chr11:476014 | C | A | 32 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0015 others(29): Show |
41 | HG00544.hp2 HG01123.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.367+2037C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 476014 | |||||||
| chr11:476158 | G | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+2181G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 476158 | |||||||
| chr11:476233 | G | C | 1 | a0001c0001t0001g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.367+2256G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 476233 | |||||||
| chr11:476274 | G | A | 117 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(114): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.367+2297G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 476274 | |||||||
| chr11:476394 | G | A | 4 | a0002c0003t0005g0020 a0002c0003t0005g0021 a0002c0003t0005g0189 others(1): Show |
6 | HG00099.hp1 HG01175.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.367+2417G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 476394 | |||||||
| chr11:476568 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.368-2517G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 476568 | |||||||
| chr11:476724 | G | A | 1 | a0001c0002t0001g0136 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.368-2361G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 476724 | |||||||
| chr11:476782 | G | T | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-2303G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 476782 | |||||||
| chr11:476828 | C | T | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-2257C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 476828 | |||||||
| chr11:476957 | T | C | 117 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(114): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.368-2128T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 476957 | |||||||
| chr11:477007 | C | T | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-2078C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477007 | |||||||
| chr11:477093 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.368-1992G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477093 | |||||||
| chr11:477130 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.368-1955G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477130 | |||||||
| chr11:477162 | A | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.368-1923A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477162 | |||||||
| chr11:477181 | C | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.368-1904C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477181 | |||||||
| chr11:477246 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.368-1839G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477246 | |||||||
| chr11:477495 | C | G | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-1590C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477495 | |||||||
| chr11:477616 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.368-1469G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477616 | |||||||
| chr11:477623 | C | T | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.368-1462C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477623 | |||||||
| chr11:477746 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.368-1339G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477746 | |||||||
| chr11:477846 | C | G | 2 | a0001c0002t0001g0016 a0001c0002t0001g0122 |
3 | NA18941.hp2 NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.368-1239C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 477846 | |||||||
| chr11:478050 | C | T | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.368-1035C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478050 | |||||||
| chr11:478070 | G | A | 1 | a0001c0001t0002g0121 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.368-1015G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478070 | |||||||
| chr11:478110 | T | C | 1 | a0001c0001t0003g0094 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.368-975T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478110 | |||||||
| chr11:478122 | A | T | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-963A>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478122 | |||||||
| chr11:478147 | A | C | 12 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(9): Show |
14 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.368-938A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478147 | |||||||
| chr11:478267 | A | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.368-818A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478267 | |||||||
| chr11:478287 | C | CA | 16 | a0001c0001t0003g0073 a0001c0001t0006g0185 a0001c0002t0001g0117 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.368-784dupA | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 478287 | ||||||
| chr11:478287 | CA | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0154 others(8): Show |
13 | HG01109.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.368-784delA | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 478287 | ||||||
| chr11:478401 | G | A | 89 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.368-684G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478401 | |||||||
| chr11:478419 | C | G | 1 | a0001c0001t0001g0221 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.368-666C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478419 | |||||||
| chr11:478427 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.368-658G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478427 | |||||||
| chr11:478451 | C | CA | 9 | a0001c0001t0001g0024 a0001c0001t0001g0226 a0001c0001t0001g0235 others(6): Show |
9 | HG00741.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.368-623dupA | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 478451 | ||||||
| chr11:478629 | A | T | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-456A>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478629 | |||||||
| chr11:478730 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.368-355C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478730 | |||||||
| chr11:478767 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.368-318C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478767 | |||||||
| chr11:478847 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.368-238T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478847 | |||||||
| chr11:478856 | A | C | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02622.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-229A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478856 | |||||||
| chr11:478911 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
6 | HG01884.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-174G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 478911 | |||||||
| chr11:479057 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.368-28A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 479057 | |||||||
| chr11:479063 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.368-22G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 3/11 | chr11 | 479063 | |||||||
| chr11:479175 | A | T | 1 | a0001c0001t0001g0262 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.435+23A>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479175 | |||||||
| chr11:479240 | GC | G | 21 | a0001c0001t0002g0012 a0001c0001t0002g0075 a0001c0001t0002g0076 others(18): Show |
23 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.435+91delC | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 479240 | ||||||
| chr11:479245 | C | T | 21 | a0001c0001t0002g0012 a0001c0001t0002g0075 a0001c0001t0002g0076 others(18): Show |
23 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.435+93C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479245 | |||||||
| chr11:479246 | G | T | 21 | a0001c0001t0002g0012 a0001c0001t0002g0075 a0001c0001t0002g0076 others(18): Show |
23 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.435+94G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479246 | |||||||
| chr11:479273 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.435+121C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479273 | |||||||
| chr11:479281 | AGTAGGCC others(75): Show |
A | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.435+150_435+231del others(82): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 479281 | ||||||
| chr11:479331 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0244 |
2 | HG02155.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.435+179T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479331 | |||||||
| chr11:479383 | G | C | 9 | a0001c0001t0002g0038 a0001c0001t0004g0155 a0001c0001t0004g0156 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.435+231G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479383 | |||||||
| chr11:479444 | G | GGAGGGCA others(113): Show |
3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.435+344_435+345ins others(120): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 479444 | ||||||
| chr11:479633 | C | T | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.435+481C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479633 | |||||||
| chr11:479695 | T | G | 2 | a0001c0001t0001g0018 a0001c0001t0013g0152 |
3 | HG01884.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.435+543T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479695 | |||||||
| chr11:479708 | C | A | 1 | a0001c0010t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.435+556C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479708 | |||||||
| chr11:479723 | C | T | 9 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.435+571C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479723 | |||||||
| chr11:479729 | G | GA | 81 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(78): Show |
87 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.435+578dupA | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 479729 | ||||||
| chr11:479794 | T | C | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.435+642T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479794 | |||||||
| chr11:479858 | G | C | 1 | a0001c0001t0004g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.435+706G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479858 | |||||||
| chr11:479937 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.435+785G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 479937 | |||||||
| chr11:480016 | G | A | 17 | a0001c0001t0002g0036 a0001c0001t0002g0039 a0001c0001t0002g0054 others(14): Show |
17 | HG00280.hp2 HG01069.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.435+864G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480016 | |||||||
| chr11:480099 | T | C | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.435+947T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480099 | |||||||
| chr11:480129 | G | A | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG01261.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.435+977G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480129 | |||||||
| chr11:480156 | A | ACCCTGCA others(221): Show |
1 | a0001c0001t0002g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.435+1104_435+1331d others(230): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 480156 | ||||||
| chr11:480199 | GGCAGCCT others(50): Show |
G | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.435+1104_435+1160d others(59): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 480199 | ||||||
| chr11:480256 | T | TGCAGCCT others(50): Show |
1 | a0001c0001t0001g0267 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.435+1315_435+1371d others(59): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 480256 | ||||||
| chr11:480256 | T | TGCAGCCT others(107): Show |
14 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(11): Show |
14 | HG00544.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.435+1258_435+1371d others(116): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 480256 | ||||||
| chr11:480256 | TGCAGCCT others(50): Show |
T | 3 | a0001c0006t0001g0019 a0001c0006t0001g0166 a0001c0006t0001g0167 |
4 | HG02486.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1315_435+1371d others(59): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 480256 | ||||||
| chr11:480269 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02630.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.435+1117C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480269 | |||||||
| chr11:480333 | C | T | 4 | a0001c0002t0001g0127 a0001c0002t0001g0137 a0001c0002t0001g0141 others(1): Show |
4 | NA18954.hp2 NA18970.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+1181C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480333 | |||||||
| chr11:480441 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0083 a0001c0001t0002g0085 |
3 | NA18939.hp1 NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.435+1289G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480441 | |||||||
| chr11:480506 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.435+1354C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480506 | |||||||
| chr11:480582 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.435+1430G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480582 | |||||||
| chr11:480583 | A | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.435+1431A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480583 | |||||||
| chr11:480606 | T | C | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02622.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+1454T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480606 | |||||||
| chr11:480610 | G | A | 1 | a0002c0003t0005g0184 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.435+1458G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480610 | |||||||
| chr11:480870 | C | T | 89 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.435+1718C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480870 | |||||||
| chr11:480950 | C | G | 125 | a0001c0001t0001g0018 a0001c0001t0001g0147 a0001c0001t0001g0148 others(122): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.435+1798C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 480950 | |||||||
| chr11:481083 | C | CA | 7 | a0001c0001t0001g0174 a0001c0001t0001g0208 a0001c0001t0001g0270 others(4): Show |
7 | HG01243.hp1 HG01243.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+1947dupA | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 481083 | ||||||
| chr11:481083 | CA | C | 13 | a0001c0001t0001g0231 a0001c0001t0004g0155 a0001c0001t0004g0156 others(10): Show |
13 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.435+1947delA | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 481083 | ||||||
| chr11:481156 | G | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.435+2004G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 481156 | |||||||
| chr11:481158 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.435+2006G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 481158 | |||||||
| chr11:481227 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.435+2075C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 481227 | |||||||
| chr11:481375 | A | G | 17 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0063 others(14): Show |
19 | HG00597.hp2 HG00609.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.435+2223A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 481375 | |||||||
| chr11:481509 | G | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0297 |
2 | HG01192.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.435+2357G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 481509 | |||||||
| chr11:481603 | G | A | 117 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(114): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.435+2451G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 481603 | |||||||
| chr11:481837 | A | G | 2 | a0001c0002t0001g0016 a0001c0002t0001g0122 |
3 | NA18941.hp2 NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.435+2685A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 481837 | |||||||
| chr11:481846 | CT | C | 8 | a0001c0001t0001g0229 a0001c0001t0001g0248 a0001c0001t0001g0249 others(5): Show |
8 | HG00733.hp2 HG01099.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.435+2708delT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 481846 | ||||||
| chr11:482005 | G | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.435+2853G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482005 | |||||||
| chr11:482089 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.435+2937G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482089 | |||||||
| chr11:482133 | A | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0268 |
3 | HG01433.hp2 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.435+2981A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482133 | |||||||
| chr11:482136 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0143 a0001c0001t0001g0215 others(1): Show |
5 | HG03540.hp1 NA18948.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.435+2984G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482136 | |||||||
| chr11:482141 | C | T | 4 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0049 others(1): Show |
4 | HG02109.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+2989C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482141 | |||||||
| chr11:482166 | G | A | 86 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(83): Show |
92 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.435+3014G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482166 | |||||||
| chr11:482223 | C | CT | 8 | a0001c0001t0001g0197 a0001c0002t0001g0126 a0001c0005t0001g0214 others(5): Show |
8 | HG00733.hp1 HG00738.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.435+3088dupT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482223 | ||||||
| chr11:482223 | C | CTTT | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.435+3086_435+3088d others(5): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482223 | ||||||
| chr11:482223 | CT | C | 86 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(83): Show |
92 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.435+3088delT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482223 | ||||||
| chr11:482246 | G | A | 86 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
91 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.435+3094G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482246 | |||||||
| chr11:482568 | C | T | 89 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.435+3416C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482568 | |||||||
| chr11:482609 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.435+3457T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482609 | |||||||
| chr11:482660 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
6 | HG01884.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+3508A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482660 | |||||||
| chr11:482740 | T | C | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.435+3588T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482740 | |||||||
| chr11:482766 | A | AGTTCTGT others(35): Show |
9 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.435+3657_435+3698d others(44): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482766 | ||||||
| chr11:482766 | AGTTCTGT others(329): Show |
A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.435+3699_436-3753d others(2): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482766 | ||||||
| chr11:482851 | T | G | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.435+3699T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482851 | |||||||
| chr11:482880 | C | CCGAGTGC others(77): Show |
2 | a0001c0001t0001g0225 a0001c0001t0001g0293 |
2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.435+3811_435+3812i others(86): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482880 | ||||||
| chr11:482887 | C | G | 2 | a0001c0001t0004g0159 a0001c0001t0004g0161 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.435+3735C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482887 | |||||||
| chr11:482892 | A | G | 2 | a0001c0001t0004g0159 a0001c0001t0004g0161 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.435+3740A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482892 | |||||||
| chr11:482923 | C | T | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.435+3771C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482923 | |||||||
| chr11:482927 | T | G | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.435+3775T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482927 | |||||||
| chr11:482929 | G | C | 2 | a0001c0001t0004g0159 a0001c0001t0004g0161 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.435+3777G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482929 | |||||||
| chr11:482934 | G | A | 2 | a0001c0001t0004g0159 a0001c0001t0004g0161 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.435+3782G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482934 | |||||||
| chr11:482934 | GGTTCTGT others(35): Show |
G | 1 | a0001c0001t0002g0114 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.435+3819_435+3860d others(44): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482934 | ||||||
| chr11:482957 | C | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0030 others(15): Show |
23 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.435+3805C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482957 | |||||||
| chr11:482971 | C | G | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.435+3819C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482971 | |||||||
| chr11:482976 | A | AGTTCTGT others(35): Show |
2 | a0001c0001t0001g0232 a0001c0001t0001g0277 |
2 | NA18954.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.436-3632_436-3591d others(44): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482976 | ||||||
| chr11:482976 | A | G | 14 | a0001c0001t0001g0198 a0001c0001t0001g0256 a0001c0001t0001g0266 others(11): Show |
14 | HG01175.hp1 HG02056.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.435+3824A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 482976 | |||||||
| chr11:482976 | AGTTCTGT others(35): Show |
A | 2 | a0001c0001t0001g0206 a0001c0002t0001g0139 |
2 | HG01192.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.436-3632_436-3591d others(44): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482976 | ||||||
| chr11:482976 | AGTTCTGT others(77): Show |
A | 8 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
9 | HG02486.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.436-3674_436-3591d others(86): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482976 | ||||||
| chr11:482976 | AGTTCTGT others(161): Show |
A | 104 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(101): Show |
112 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.436-3758_436-3591d others(2): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 482976 | ||||||
| chr11:483007 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.435+3855C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483007 | |||||||
| chr11:483019 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.435+3867G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483019 | |||||||
| chr11:483055 | G | C | 1 | a0001c0001t0002g0114 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.436-3884G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483055 | |||||||
| chr11:483060 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.436-3879G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483060 | |||||||
| chr11:483062 | TTCTGTG | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0030 others(15): Show |
23 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.436-3876_436-3871d others(8): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483062 | |||||||
| chr11:483069 | A | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0030 others(15): Show |
23 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.436-3870A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483069 | |||||||
| chr11:483092 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02622.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-3847G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483092 | |||||||
| chr11:483139 | G | C | 1 | a0001c0001t0002g0114 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.436-3800G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483139 | |||||||
| chr11:483144 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.436-3795G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483144 | |||||||
| chr11:483187 | G | T | 9 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.436-3752G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483187 | |||||||
| chr11:483223 | G | C | 10 | a0001c0001t0001g0219 a0001c0001t0004g0155 a0001c0001t0004g0156 others(7): Show |
10 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-3716G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483223 | |||||||
| chr11:483228 | G | A | 10 | a0001c0001t0001g0219 a0001c0001t0004g0155 a0001c0001t0004g0156 others(7): Show |
10 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-3711G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483228 | |||||||
| chr11:483228 | G | GTTTCTGT others(35): Show |
2 | a0001c0001t0004g0159 a0001c0001t0004g0161 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.436-3711_436-3710i others(44): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483228 | |||||||
| chr11:483307 | G | C | 150 | a0001c0001t0001g0018 a0001c0001t0001g0146 a0001c0001t0001g0147 others(147): Show |
169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.436-3632G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483307 | |||||||
| chr11:483312 | G | A | 148 | a0001c0001t0001g0018 a0001c0001t0001g0146 a0001c0001t0001g0147 others(145): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.436-3627G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483312 | |||||||
| chr11:483313 | G | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436-3626G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483313 | |||||||
| chr11:483427 | T | C | 13 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(10): Show |
13 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.436-3512T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483427 | |||||||
| chr11:483467 | T | G | 11 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0001c0001t0002g0041 others(8): Show |
12 | HG01074.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-3472T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483467 | |||||||
| chr11:483581 | GT | G | 4 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0049 others(1): Show |
4 | HG02109.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-3353delT | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 483581 | ||||||
| chr11:483767 | A | G | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-3172A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483767 | |||||||
| chr11:483782 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.436-3157C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483782 | |||||||
| chr11:483805 | G | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436-3134G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483805 | |||||||
| chr11:483815 | A | ATG | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-3122_436-3121d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 483815 | ||||||
| chr11:483838 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.436-3101T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483838 | |||||||
| chr11:483854 | G | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.436-3085G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483854 | |||||||
| chr11:483855 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0206 a0001c0001t0001g0213 others(2): Show |
6 | HG00140.hp1 HG01192.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-3084C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483855 | |||||||
| chr11:483888 | C | T | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-3051C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483888 | |||||||
| chr11:483996 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436-2943G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 483996 | |||||||
| chr11:484158 | G | T | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.436-2781G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484158 | |||||||
| chr11:484159 | C | T | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.436-2780C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484159 | |||||||
| chr11:484204 | A | G | 181 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0022 others(178): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.436-2735A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484204 | |||||||
| chr11:484469 | C | T | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.436-2470C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484469 | |||||||
| chr11:484490 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.436-2449A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484490 | |||||||
| chr11:484527 | G | A | 76 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(73): Show |
81 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.436-2412G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484527 | |||||||
| chr11:484545 | TGCACGGG others(1): Show |
T | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.436-2391_436-2384d others(10): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 484545 | ||||||
| chr11:484566 | A | G | 1 | a0001c0008t0001g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.436-2373A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484566 | |||||||
| chr11:484688 | GTGC | G | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.436-2248_436-2246d others(5): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 484688 | ||||||
| chr11:484706 | C | T | 7 | a0001c0001t0003g0010 a0001c0001t0003g0070 a0001c0001t0003g0073 others(4): Show |
8 | HG00438.hp2 NA18946.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.436-2233C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484706 | |||||||
| chr11:484729 | C | CGT | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-2206_436-2205d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 484729 | ||||||
| chr11:484738 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.436-2201A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484738 | |||||||
| chr11:484778 | C | CTG | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-2158_436-2157d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 484778 | ||||||
| chr11:484784 | G | A | 2 | a0001c0006t0001g0019 a0001c0006t0001g0167 |
3 | HG02486.hp2 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.436-2155G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484784 | |||||||
| chr11:484805 | G | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.436-2134G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484805 | |||||||
| chr11:484810 | CGT | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0030 others(15): Show |
23 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.436-2125_436-2124d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 484810 | ||||||
| chr11:484811 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436-2128G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484811 | |||||||
| chr11:484821 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0196 |
4 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-2118C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484821 | |||||||
| chr11:484853 | G | A | 1 | a0001c0002t0001g0141 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.436-2086G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484853 | |||||||
| chr11:484866 | C | CTG | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-2070_436-2069d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 484866 | ||||||
| chr11:484872 | G | A | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.436-2067G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484872 | |||||||
| chr11:484925 | TGTAAACT others(39): Show |
T | 1 | a0001c0001t0001g0052 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.436-1998_436-1953d others(48): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 484925 | ||||||
| chr11:484940 | C | T | 2 | a0001c0001t0001g0154 a0003c0004t0001g0006 |
2 | HG01993.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.436-1999C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484940 | |||||||
| chr11:484961 | C | G | 1 | a0001c0001t0004g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.436-1978C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484961 | |||||||
| chr11:484961 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.436-1978C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484961 | |||||||
| chr11:484962 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.436-1977G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484962 | |||||||
| chr11:484977 | C | CAG | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-1962_436-1961i others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 484977 | |||||||
| chr11:485024 | C | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436-1915C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485024 | |||||||
| chr11:485042 | CTG | C | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-1892_436-1891d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485042 | ||||||
| chr11:485050 | G | GCAGGCGA others(35): Show |
1 | a0001c0001t0001g0281 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.436-1873_436-1832d others(44): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485050 | ||||||
| chr11:485065 | CTGCACGG others(37): Show |
C | 86 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(83): Show |
92 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.436-1864_436-1821d others(46): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485065 | ||||||
| chr11:485075 | A | G | 1 | a0001c0001t0002g0099 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.436-1864A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485075 | |||||||
| chr11:485075 | ACGTGTGC others(253): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.436-1857_436-1598d others(2): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485075 | ||||||
| chr11:485084 | T | C | 1 | a0001c0001t0002g0099 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.436-1855T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485084 | |||||||
| chr11:485092 | A | G | 1 | a0001c0001t0002g0099 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.436-1847A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485092 | |||||||
| chr11:485120 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.436-1819C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485120 | |||||||
| chr11:485130 | CTG | C | 13 | a0001c0001t0002g0043 a0001c0001t0004g0155 a0001c0001t0004g0156 others(10): Show |
13 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.436-1804_436-1803d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485130 | ||||||
| chr11:485198 | A | G | 1 | a0001c0001t0002g0099 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.436-1741A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485198 | |||||||
| chr11:485236 | C | CAG | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-1703_436-1702i others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485236 | |||||||
| chr11:485241 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.436-1698C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485241 | |||||||
| chr11:485288 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.436-1651G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485288 | |||||||
| chr11:485289 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.436-1650C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485289 | |||||||
| chr11:485303 | CTG | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0220 |
3 | HG01168.hp1 HG01169.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.436-1631_436-1630d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485303 | ||||||
| chr11:485330 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.436-1609C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485330 | |||||||
| chr11:485352 | G | A | 3 | a0001c0001t0002g0112 a0001c0001t0010g0053 a0001c0002t0010g0204 |
3 | HG00642.hp1 HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.436-1587G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485352 | |||||||
| chr11:485374 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.436-1565T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485374 | |||||||
| chr11:485379 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.436-1560A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485379 | |||||||
| chr11:485380 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.436-1559T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485380 | |||||||
| chr11:485424 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.436-1515C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485424 | |||||||
| chr11:485466 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0001c0001t0002g0041 others(3): Show |
7 | HG02451.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-1473C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485466 | |||||||
| chr11:485481 | A | G | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-1458A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485481 | |||||||
| chr11:485545 | CAG | C | 4 | a0002c0003t0008g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-1393_436-1392d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485545 | |||||||
| chr11:485547 | GTGCACGG others(35): Show |
G | 87 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(84): Show |
93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.436-1370_436-1329d others(44): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485547 | ||||||
| chr11:485552 | C | T | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-1387C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485552 | |||||||
| chr11:485570 | G | A | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.436-1369G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485570 | |||||||
| chr11:485581 | C | CGA | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-1357_436-1356i others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485581 | ||||||
| chr11:485600 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.436-1339C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485600 | |||||||
| chr11:485624 | G | GTAAGCAG others(39): Show |
1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436-1312_436-1311i others(48): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485624 | ||||||
| chr11:485628 | A | G | 12 | a0001c0001t0001g0153 a0001c0001t0004g0155 a0001c0001t0004g0156 others(9): Show |
12 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-1311A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485628 | |||||||
| chr11:485632 | T | C | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436-1307T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485632 | |||||||
| chr11:485640 | C | CGCGTGTG others(39): Show |
10 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.436-1270_436-1269i others(48): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485640 | ||||||
| chr11:485670 | T | G | 2 | a0001c0001t0001g0153 a0001c0001t0004g0298 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.436-1269T>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485670 | |||||||
| chr11:485678 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.436-1261C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485678 | |||||||
| chr11:485686 | C | T | 1 | a0001c0001t0004g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.436-1253C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485686 | |||||||
| chr11:485690 | TGTGTGCT others(33): Show |
T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0206 a0001c0001t0001g0213 others(2): Show |
6 | HG00140.hp1 HG01192.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-1226_436-1187d others(42): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485690 | ||||||
| chr11:485704 | G | A | 1 | a0001c0002t0001g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.436-1235G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485704 | |||||||
| chr11:485714 | G | T | 1 | a0001c0001t0004g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.436-1225G>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485714 | |||||||
| chr11:485720 | T | C | 1 | a0001c0001t0004g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.436-1219T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485720 | |||||||
| chr11:485726 | G | GGC | 10 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.436-1209_436-1208d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485726 | ||||||
| chr11:485731 | G | A | 6 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(3): Show |
6 | HG00642.hp1 HG00642.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-1208G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485731 | |||||||
| chr11:485740 | C | CCGTG | 5 | a0001c0001t0004g0157 a0001c0001t0004g0160 a0001c0001t0004g0161 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-1199_436-1198i others(6): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485740 | |||||||
| chr11:485740 | C | CCGTGCGC others(45): Show |
5 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0158 others(2): Show |
5 | HG02280.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-1199_436-1198i others(54): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485740 | |||||||
| chr11:485741 | T | C | 10 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.436-1198T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485741 | |||||||
| chr11:485741 | T | TGCGCAGG others(41): Show |
26 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0153 others(23): Show |
34 | HG00544.hp2 HG00733.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.436-989_436-942dup others(48): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485741 | ||||||
| chr11:485741 | T | TGCGCAGG others(89): Show |
2 | a0001c0001t0001g0274 a0001c0002t0001g0134 |
2 | HG02257.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.436-1037_436-942du others(97): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485741 | ||||||
| chr11:485741 | T | TGCGCAGG others(137): Show |
1 | a0001c0002t0001g0125 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.436-1085_436-942du others(145): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485741 | ||||||
| chr11:485741 | TGCGCAGG others(41): Show |
T | 88 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(85): Show |
94 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.436-989_436-942del others(48): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485741 | ||||||
| chr11:485741 | TGCGCAGG others(89): Show |
T | 6 | a0001c0002t0001g0016 a0001c0002t0001g0122 a0002c0003t0008g0169 others(3): Show |
7 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-1037_436-942de others(97): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485741 | ||||||
| chr11:485741 | TGCGCAGG others(137): Show |
T | 14 | a0001c0001t0001g0023 a0001c0001t0001g0247 a0001c0001t0006g0185 others(11): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.436-1085_436-942de others(1): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485741 | ||||||
| chr11:485743 | C | TGCAGGCG others(41): Show |
3 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0135 |
3 | HG01168.hp2 HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.436-1197_436-1196i others(50): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485743 | |||||||
| chr11:485753 | C | T | 3 | a0001c0001t0004g0298 a0001c0001t0010g0053 a0001c0002t0010g0204 |
3 | HG02572.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.436-1186C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485753 | |||||||
| chr11:485757 | AAC | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0268 |
3 | HG01433.hp2 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.436-1180_436-1179d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485757 | ||||||
| chr11:485759 | CAG | C | 3 | a0001c0001t0004g0298 a0001c0001t0010g0053 a0001c0002t0010g0204 |
3 | HG02572.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.436-1179_436-1178d others(4): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485759 | |||||||
| chr11:485784 | CCGTGCGC others(93): Show |
C | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.436-1152_436-1053d others(102): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485784 | ||||||
| chr11:485840 | G | GCAGGCGA others(41): Show |
2 | a0001c0002t0001g0139 a0001c0002t0001g0140 |
2 | NA18995.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.436-1052_436-1051i others(50): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485840 | ||||||
| chr11:485862 | C | CGGGCGCG others(42): Show |
1 | a0001c0002t0001g0130 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.436-1074_436-1026d others(51): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485862 | ||||||
| chr11:485864 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.436-1075G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485864 | |||||||
| chr11:485885 | C | T | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.436-1054C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485885 | |||||||
| chr11:485929 | C | T | 1 | a0001c0002t0001g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.436-1010C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485929 | |||||||
| chr11:485934 | G | A | 16 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0001c0001t0002g0041 others(13): Show |
17 | HG01074.hp2 HG01346.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.436-1005G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485934 | |||||||
| chr11:485950 | A | ACAGTGCA others(41): Show |
1 | a0001c0002t0001g0017 | 2 | NA18747.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.436-969_436-922dup others(48): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 485950 | ||||||
| chr11:485950 | A | G | 5 | a0001c0001t0001g0150 a0002c0003t0008g0169 a0002c0003t0008g0170 others(2): Show |
5 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-989A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485950 | |||||||
| chr11:485990 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.436-949G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485990 | |||||||
| chr11:485998 | G | A | 12 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-941G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 485998 | |||||||
| chr11:486006 | C | T | 11 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0001c0001t0002g0041 others(8): Show |
12 | HG01074.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-933C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486006 | |||||||
| chr11:486014 | C | CGT | 6 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0158 others(3): Show |
6 | HG02280.hp2 HG03471.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-923_436-922dup others(2): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 486014 | ||||||
| chr11:486014 | C | CGTGTGCT others(43): Show |
5 | a0001c0001t0004g0157 a0001c0001t0004g0160 a0001c0001t0004g0161 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-922_436-921ins others(50): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 486014 | ||||||
| chr11:486014 | C | CGTGTGCT others(187): Show |
1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436-922_436-921ins others(194): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 486014 | ||||||
| chr11:486018 | C | T | 16 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(13): Show |
16 | HG00733.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.436-921C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486018 | |||||||
| chr11:486027 | T | C | 23 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(20): Show |
25 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.436-912T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486027 | |||||||
| chr11:486039 | T | C | 16 | a0001c0001t0003g0037 a0001c0001t0004g0155 a0001c0001t0004g0156 others(13): Show |
17 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.436-900T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486039 | |||||||
| chr11:486044 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0153 others(3): Show |
7 | HG01884.hp2 HG02630.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-895A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486044 | |||||||
| chr11:486076 | G | A | 12 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(9): Show |
14 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.436-863G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486076 | |||||||
| chr11:486321 | A | G | 3 | a0001c0006t0001g0019 a0001c0006t0001g0166 a0001c0006t0001g0167 |
4 | HG02486.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-618A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486321 | |||||||
| chr11:486341 | C | T | 1 | a0002c0003t0005g0184 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.436-598C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486341 | |||||||
| chr11:486397 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.436-542A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486397 | |||||||
| chr11:486407 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436-532G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486407 | |||||||
| chr11:486414 | G | A | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.436-525G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486414 | |||||||
| chr11:486510 | C | T | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.436-429C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486510 | |||||||
| chr11:486535 | G | A | 5 | a0001c0001t0001g0230 a0001c0001t0001g0237 a0001c0001t0001g0243 others(2): Show |
5 | HG00609.hp2 HG02071.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-404G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486535 | |||||||
| chr11:486720 | C | T | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436-219C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486720 | |||||||
| chr11:486826 | C | T | 116 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(113): Show |
124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.436-113C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486826 | |||||||
| chr11:486835 | G | A | 116 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(113): Show |
124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.436-104G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486835 | |||||||
| chr11:486843 | A | G | 116 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(113): Show |
124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.436-96A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486843 | |||||||
| chr11:486855 | T | A | 114 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(111): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.436-84T>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486855 | |||||||
| chr11:486874 | T | C | 87 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(84): Show |
93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.436-65T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486874 | |||||||
| chr11:486898 | C | A | 1 | a0001c0002t0001g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.436-41C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486898 | |||||||
| chr11:486914 | G | A | 1 | a0001c0002t0001g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.436-25G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 4/11 | chr11 | 486914 | |||||||
| chr11:487087 | G | A | 1 | a0004c0007t0012g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.570+14G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 5/11 | chr11 | 487087 | |||||||
| chr11:487101 | C | T | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.570+28C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 5/11 | chr11 | 487101 | |||||||
| chr11:487135 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.570+62C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 5/11 | chr11 | 487135 | |||||||
| chr11:487136 | G | A | 13 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(10): Show |
15 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+63G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 5/11 | chr11 | 487136 | |||||||
| chr11:487201 | T | C | 15 | a0001c0001t0006g0185 a0002c0003t0005g0021 a0002c0003t0005g0184 others(12): Show |
16 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.570+128T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 5/11 | chr11 | 487201 | |||||||
| chr11:487229 | A | G | 11 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.570+156A>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 5/11 | chr11 | 487229 | |||||||
| chr11:487257 | G | C | 87 | a0001c0001t0001g0197 a0001c0001t0002g0009 a0001c0001t0002g0011 others(84): Show |
93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.571-163G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 5/11 | chr11 | 487257 | |||||||
| chr11:487411 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.571-9C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 5/11 | chr11 | 487411 | |||||||
| chr11:487534 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.621+64C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 487534 | |||||||
| chr11:487666 | C | T | 9 | a0001c0001t0002g0012 a0001c0001t0002g0075 a0001c0001t0002g0076 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+196C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 487666 | |||||||
| chr11:487671 | C | T | 32 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0015 others(29): Show |
41 | HG00544.hp2 HG01123.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.621+201C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 487671 | |||||||
| chr11:487688 | C | T | 3 | a0001c0001t0002g0063 a0001c0001t0002g0071 a0001c0001t0002g0101 |
3 | HG01167.hp2 HG01169.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.621+218C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 487688 | |||||||
| chr11:487878 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.622-321G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 487878 | |||||||
| chr11:487935 | C | T | 90 | a0001c0001t0001g0274 a0001c0001t0002g0009 a0001c0001t0002g0011 others(87): Show |
96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.622-264C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 487935 | |||||||
| chr11:487969 | TGCTGCCA others(63): Show |
T | 1 | a0001c0001t0017g0060 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.622-216_622-147del others(70): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 487969 | ||||||
| chr11:487979 | C | T | 30 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0015 others(27): Show |
37 | HG00544.hp2 HG01123.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.622-220C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 487979 | |||||||
| chr11:487980 | GGGGTGGG others(62): Show |
G | 86 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(83): Show |
92 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.622-175_622-107del others(69): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 487980 | ||||||
| chr11:488049 | CGGGTGGG others(63): Show |
C | 1 | a0001c0001t0001g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.622-113_622-44delC others(69): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 488049 | ||||||
| chr11:488070 | C | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0001c0001t0002g0048 |
3 | HG02451.hp2 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.622-129C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 488070 | |||||||
| chr11:488086 | CGTGGCCG others(63): Show |
C | 2 | a0001c0001t0004g0164 a0001c0002t0001g0122 |
2 | NA18941.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.622-86_622-17delCC others(68): Show |
PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 488086 | ||||||
| chr11:488099 | C | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0229 |
2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.622-100C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 488099 | |||||||
| chr11:488118 | CG | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0010g0053 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.622-77delG | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 488118 | ||||||
| chr11:488119 | G | A | 4 | a0001c0001t0007g0057 a0001c0001t0007g0062 a0001c0001t0007g0064 others(1): Show |
4 | HG02040.hp2 HG02738.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-80G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 488119 | |||||||
| chr11:488135 | G | A | 98 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(95): Show |
104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.622-64G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 488135 | |||||||
| chr11:488140 | C | T | 88 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(85): Show |
94 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.622-59C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 6/11 | chr11 | 488140 | |||||||
| chr11:488333 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0264 |
2 | HG00741.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.735+21C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 7/11 | chr11 | 488333 | |||||||
| chr11:488389 | C | A | 90 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0268 others(87): Show |
96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.735+77C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 7/11 | chr11 | 488389 | |||||||
| chr11:488456 | T | A | 4 | a0001c0006t0001g0019 a0001c0006t0001g0166 a0001c0006t0001g0167 others(1): Show |
5 | HG02486.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.736-73T>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 7/11 | chr11 | 488456 | |||||||
| chr11:488655 | G | A | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
splice_region_variant&intron_variant | LOW | c.854+8G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 488655 | |||||||
| chr11:488711 | C | T | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02622.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.854+64C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 488711 | |||||||
| chr11:488714 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0274 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.854+67G>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 488714 | |||||||
| chr11:488771 | G | A | 17 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0063 others(14): Show |
19 | HG00597.hp2 HG00609.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.854+124G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 488771 | |||||||
| chr11:488798 | T | C | 32 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0015 others(29): Show |
41 | HG00544.hp2 HG01123.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.854+151T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 488798 | |||||||
| chr11:488877 | C | T | 89 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0002g0009 others(86): Show |
95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.854+230C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 488877 | |||||||
| chr11:488878 | T | C | 28 | a0001c0001t0001g0213 a0001c0001t0004g0155 a0001c0001t0004g0156 others(25): Show |
30 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.854+231T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 488878 | |||||||
| chr11:489098 | G | A | 11 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0001c0001t0002g0041 others(8): Show |
12 | HG01074.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.855-302G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 489098 | |||||||
| chr11:489102 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.855-298C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 489102 | |||||||
| chr11:489149 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.855-251C>G | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 489149 | |||||||
| chr11:489292 | C | T | 1 | a0001c0001t0002g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.855-108C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 489292 | |||||||
| chr11:489382 | C | T | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.855-18C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 489382 | |||||||
| chr11:489386 | T | C | 88 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(85): Show |
94 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.855-14T>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 8/11 | chr11 | 489386 | |||||||
| chr11:489537 | C | T | 16 | a0001c0001t0006g0185 a0002c0003t0005g0020 a0002c0003t0005g0021 others(13): Show |
18 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.969+23C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 9/11 | chr11 | 489537 | |||||||
| chr11:489541 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.969+27G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 9/11 | chr11 | 489541 | |||||||
| chr11:489570 | C | T | 2 | a0001c0001t0010g0053 a0001c0002t0010g0204 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.970-18C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 9/11 | chr11 | 489570 | |||||||
| chr11:489737 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG02257.hp1 | splice_region_variant&intron_variant | LOW | c.1115+4A>C | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 10/11 | chr11 | 489737 | |||||||
| chr11:489799 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1115+66G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 10/11 | chr11 | 489799 | |||||||
| chr11:489829 | C | A | 88 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(85): Show |
94 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1116-54C>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 10/11 | chr11 | 489829 | |||||||
| chr11:489857 | C | T | 1 | a0001c0002t0001g0136 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1116-26C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 10/11 | chr11 | 489857 | |||||||
| chr11:490114 | C | T | 4 | a0001c0001t0002g0114 a0001c0002t0001g0125 a0001c0002t0001g0128 others(1): Show |
4 | HG00642.hp2 HG01981.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+46C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 11/11 | chr11 | 490114 | |||||||
| chr11:490196 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1301+128C>T | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 11/11 | chr11 | 490196 | |||||||
| chr11:490254 | G | A | 4 | a0001c0001t0001g0200 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG01346.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302-166G>A | PTDSS2 | ENSG00000174915.12 | transcript | ENST00000308020.6 | protein_coding | 11/11 | chr11 | 490254 |