Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9842 |
| ensemblid | ENSG00000225190.12 |
| hgncid | 29017 |
| symbol | PLEKHM1 |
| name | pleckstrin homology and RUN domain containing M1 |
| refseq_nuc | NM_014798.3 |
| refseq_prot | NP_055613.1 |
| ensembl_nuc | ENST00000430334.8 |
| ensembl_prot | ENSP00000389913.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 45435900 |
| end | 45490721 |
| strand | - |
| ver | v1.2 |
| region | chr17:45435900-45490721 |
| region5000 | chr17:45430900-45495721 |
| regionname0 | PLEKHM1_chr17_45435900_45490721 |
| regionname5000 | PLEKHM1_chr17_45430900_45495721 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1056 | 317 | 87 | 66 | 119 | 16 | 28 | 96 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | MLSVV others(1051): Show |
chr17 | 45430900 | 45495721 |
| a0002 | 0/0 | 1056 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | MLSVV others(1051): Show |
chr17 | 45430900 | 45495721 |
| a0003 | 0/0 | 1056 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | MLSVV others(1051): Show |
chr17 | 45430900 | 45495721 |
| a0004 | 0/0 | 1056 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | MLSVV others(1051): Show |
chr17 | 45430900 | 45495721 |
| a0005 | 0/0 | 1056 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | MLSVV others(1051): Show |
chr17 | 45430900 | 45495721 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3168 | 284 | 75 | 57 | 116 | 12 | 23 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0001c0002 | 0/0 | 3168 | 20 | 2 | 8 | 1 | 4 | 5 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0001c0004 | 0/0 | 3168 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0001c0005 | 0/0 | 3168 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0001c0008 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0001c0009 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0001c0010 | 0/0 | 3168 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0001c0011 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0001c0013 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0002c0003 | 0/0 | 3168 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0003c0012 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0004c0006 | 0/0 | 3168 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 | ||
| a0005c0007 | 0/0 | 3168 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATGCT others(3163): Show |
chr17 | 45430900 | 45495721 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5240 | 247 | 62 | 49 | 113 | 7 | 15 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0003 | 0/0 | 5240 | 15 | 0 | 5 | 0 | 4 | 6 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0004 | 0/0 | 5240 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0005 | 0/0 | 5240 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0006 | 0/0 | 5240 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0007 | 0/0 | 5240 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0008 | 0/0 | 5240 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0009 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0010 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0011 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0013 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0014 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0015 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0001t0016 | 0/0 | 5240 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0002t0001 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0002t0002 | 0/0 | 5240 | 19 | 1 | 8 | 1 | 4 | 5 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0004t0001 | 0/0 | 5240 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0005t0001 | 0/0 | 5240 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0008t0001 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0009t0012 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0010t0003 | 0/0 | 5240 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0011t0003 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0001c0013t0001 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0002c0003t0001 | 0/0 | 5240 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0003c0012t0001 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0004c0006t0002 | 0/0 | 5240 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| a0005c0007t0001 | 0/0 | 5240 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | ATCGT others(5235): Show |
chr17 | 45430900 | 45495721 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0002 | 0/0 | 9 | 1 | 3 | 5 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0003 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0005g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0007g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0011g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0013g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0014g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0015g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0001t0016g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0004t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0008t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0009t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0010t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0011t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0001c0013t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0002c0003t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0002c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0003c0012t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0004c0006t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| a0005c0007t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0016 | g0244 | EUR | GBR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0067 | EUR | GBR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0135 | EUR | FIN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0126 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00673 | hp2 | a0001 | c0001 | t0015 | g0207 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01099 | hp2 | a0001 | c0010 | t0003 | g0220 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0121 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0061 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0069 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0063 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0087 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0074 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0052 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02523 | hp1 | a0003 | c0012 | t0001 | g0179 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02602 | hp2 | a0004 | c0006 | t0002 | g0068 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0045 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02647 | hp2 | a0001 | c0009 | t0012 | g0058 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0088 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0050 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0073 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0051 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02922 | hp1 | a0001 | c0005 | t0001 | g0076 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0053 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0049 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0072 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03540 | hp1 | a0001 | c0001 | t0014 | g0086 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0243 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0039 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0020 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0066 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0062 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0039 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG04204 | hp2 | a0005 | c0007 | t0001 | g0080 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18942 | hp1 | a0001 | c0011 | t0003 | g0149 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18978 | hp1 | a0001 | c0008 | t0001 | g0196 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19005 | hp2 | a0001 | c0001 | t0013 | g0162 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0242 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19080 | hp1 | a0001 | c0001 | t0010 | g0177 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ASW | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0070 | EUR | TSI | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0137 | EUR | TSI | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02559 | hp1 | a0001 | c0013 | t0001 | g0079 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0055 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | USA | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | USA | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0189 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0183 | REF | REF | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45453891 | C | T | 1 | a0005 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1961G>A | p.Cys654Tyr | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/12 | 2072/5240 | 1961/3171 | 654/1056 | chr17 | 45453891 | |||
| chr17:45458385 | G | T | 1 | a0002 | 5 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
missense_variant | MODERATE | c.1363C>A | p.Pro455Thr | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/12 | 1474/5240 | 1363/3171 | 455/1056 | chr17 | 45458385 | |||
| chr17:45468456 | G | A | 1 | a0003 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1061C>T | p.Ala354Val | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/12 | 1172/5240 | 1061/3171 | 354/1056 | chr17 | 45468456 | |||
| chr17:45475377 | G | A | 1 | a0004 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.646C>T | p.Arg216Trp | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 757/5240 | 646/3171 | 216/1056 | chr17 | 45475377 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45437960 | C | T | 1 | a0001c0010 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.3069G>A | p.Glu1023Glu | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 3180/5240 | 3069/3171 | 1023/1056 | chr17 | 45437960 | |||
| chr17:45437969 | C | T | 1 | a0001c0005 | 3 | HG02922.hp1 HG03579.hp1 NA19030.hp2 |
splice_region_variant&synonymous_variant | LOW | c.3060G>A | p.Arg1020Arg | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 3171/5240 | 3060/3171 | 1020/1056 | chr17 | 45437969 | |||
| chr17:45439623 | C | T | 2 | a0001c0004 a0002c0003 |
10 | HG02257.hp2 HG02647.hp1 HG02717.hp2 others(7): Show |
synonymous_variant | LOW | c.2913G>A | p.Gly971Gly | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/12 | 3024/5240 | 2913/3171 | 971/1056 | chr17 | 45439623 | |||
| chr17:45445543 | G | T | 1 | a0001c0009 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.2764C>A | p.Arg922Arg | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/12 | 2875/5240 | 2764/3171 | 922/1056 | chr17 | 45445543 | |||
| chr17:45453575 | G | C | 1 | a0001c0011 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.2277C>G | p.Ala759Ala | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/12 | 2388/5240 | 2277/3171 | 759/1056 | chr17 | 45453575 | |||
| chr17:45453857 | C | T | 1 | a0001c0008 | 1 | NA18978.hp1 | synonymous_variant | LOW | c.1995G>A | p.Ala665Ala | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/12 | 2106/5240 | 1995/3171 | 665/1056 | chr17 | 45453857 | |||
| chr17:45468527 | T | C | 3 | a0001c0002 a0001c0013 a0004c0006 |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
synonymous_variant | LOW | c.990A>G | p.Thr330Thr | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/12 | 1101/5240 | 990/3171 | 330/1056 | chr17 | 45468527 | |||
| chr17:45475171 | G | A | 3 | a0001c0002 a0001c0013 a0004c0006 |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
synonymous_variant | LOW | c.852C>T | p.Cys284Cys | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 963/5240 | 852/3171 | 284/1056 | chr17 | 45475171 | |||
| chr17:45475351 | G | C | 3 | a0001c0002 a0001c0013 a0004c0006 |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
synonymous_variant | LOW | c.672C>G | p.Ser224Ser | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 783/5240 | 672/3171 | 224/1056 | chr17 | 45475351 | |||
| chr17:45475446 | A | G | 3 | a0001c0002 a0001c0013 a0004c0006 |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
synonymous_variant | LOW | c.577T>C | p.Leu193Leu | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 688/5240 | 577/3171 | 193/1056 | chr17 | 45475446 | |||
| chr17:45475555 | C | T | 3 | a0001c0002 a0001c0013 a0004c0006 |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
synonymous_variant | LOW | c.468G>A | p.Arg156Arg | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 579/5240 | 468/3171 | 156/1056 | chr17 | 45475555 | |||
| chr17:45475576 | G | A | 1 | a0001c0013 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.447C>T | p.Tyr149Tyr | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 558/5240 | 447/3171 | 149/1056 | chr17 | 45475576 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45435913 | C | G | 1 | a0001c0009t0012 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1945G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1945 | chr17 | 45435913 | ||||||
| chr17:45436075 | C | T | 3 | a0001c0001t0005 a0001c0002t0002 a0004c0006t0002 |
23 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1783G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1783 | chr17 | 45436075 | ||||||
| chr17:45436152 | C | T | 1 | a0001c0001t0005 | 3 | HG02886.hp2 HG03041.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1706G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1706 | chr17 | 45436152 | ||||||
| chr17:45436185 | C | G | 2 | a0001c0002t0002 a0004c0006t0002 |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1673G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1673 | chr17 | 45436185 | ||||||
| chr17:45436530 | C | T | 2 | a0001c0002t0002 a0004c0006t0002 |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1328G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1328 | chr17 | 45436530 | ||||||
| chr17:45436810 | C | T | 1 | a0001c0001t0008 | 2 | HG01891.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1048G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1048 | chr17 | 45436810 | ||||||
| chr17:45437026 | C | T | 2 | a0001c0001t0013 a0001c0009t0012 |
2 | HG02647.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*832G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 832 | chr17 | 45437026 | ||||||
| chr17:45437045 | G | C | 3 | a0001c0001t0003 a0001c0010t0003 a0001c0011t0003 |
17 | HG00280.hp1 HG01074.hp1 HG01099.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*813C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 813 | chr17 | 45437045 | ||||||
| chr17:45437171 | G | C | 1 | a0001c0001t0004 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*687C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 687 | chr17 | 45437171 | ||||||
| chr17:45437223 | G | C | 1 | a0001c0001t0006 | 3 | HG00642.hp2 HG01081.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*635C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 635 | chr17 | 45437223 | ||||||
| chr17:45437336 | G | A | 1 | a0001c0001t0014 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*522C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 522 | chr17 | 45437336 | ||||||
| chr17:45437366 | T | C | 1 | a0001c0001t0015 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 492 | chr17 | 45437366 | ||||||
| chr17:45437496 | G | T | 1 | a0001c0001t0011 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*362C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 362 | chr17 | 45437496 | ||||||
| chr17:45437555 | C | T | 1 | a0001c0001t0010 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*303G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 303 | chr17 | 45437555 | ||||||
| chr17:45437588 | G | A | 2 | a0001c0002t0002 a0004c0006t0002 |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*270C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 270 | chr17 | 45437588 | ||||||
| chr17:45437839 | C | T | 1 | a0001c0001t0007 | 2 | HG03669.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*19G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 19 | chr17 | 45437839 | ||||||
| chr17:45490678 | G | C | 1 | a0001c0001t0016 | 1 | HG00099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/12 | 8194 | chr17 | 45490678 | ||||||
| chr17:45490707 | C | T | 2 | a0001c0001t0004 a0001c0001t0009 |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/12 | 8223 | chr17 | 45490707 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45437993 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0129 |
4 | HG00099.hp2 HG00597.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.3060-24G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45437993 | |||||||
| chr17:45438116 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3060-147C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438116 | |||||||
| chr17:45438300 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3060-331C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438300 | |||||||
| chr17:45438398 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3060-429C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438398 | |||||||
| chr17:45438457 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3060-488C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438457 | |||||||
| chr17:45438480 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.3060-511G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438480 | |||||||
| chr17:45438519 | A | G | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.3060-550T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438519 | |||||||
| chr17:45438547 | A | T | 1 | a0001c0001t0001g0160 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3060-578T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438547 | |||||||
| chr17:45438561 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.3060-592G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438561 | |||||||
| chr17:45438619 | C | A | 2 | a0001c0001t0003g0135 a0001c0001t0003g0144 |
2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.3060-650G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438619 | |||||||
| chr17:45438760 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3059+717A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438760 | |||||||
| chr17:45438809 | G | A | 2 | a0001c0002t0002g0010 a0001c0002t0002g0062 |
4 | HG01074.hp2 HG01123.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3059+668C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438809 | |||||||
| chr17:45438812 | C | T | 4 | a0001c0004t0001g0049 a0001c0004t0001g0050 a0001c0004t0001g0051 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3059+665G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438812 | |||||||
| chr17:45438839 | G | C | 1 | a0001c0013t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3059+638C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438839 | |||||||
| chr17:45438854 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3059+623C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438854 | |||||||
| chr17:45438909 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3059+568G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438909 | |||||||
| chr17:45438923 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3059+554G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438923 | |||||||
| chr17:45439036 | A | G | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.3059+441T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439036 | |||||||
| chr17:45439108 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3059+369G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439108 | |||||||
| chr17:45439178 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3059+299G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439178 | |||||||
| chr17:45439231 | T | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0239 |
2 | NA18967.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.3059+246A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439231 | |||||||
| chr17:45439372 | A | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(171): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.3059+105T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439372 | |||||||
| chr17:45439373 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.3059+104C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439373 | |||||||
| chr17:45439688 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2902-54C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 10/11 | chr17 | 45439688 | |||||||
| chr17:45439768 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2902-134G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 10/11 | chr17 | 45439768 | |||||||
| chr17:45439886 | T | C | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2902-252A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 10/11 | chr17 | 45439886 | |||||||
| chr17:45440366 | C | T | 1 | a0001c0001t0003g0027 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2838-140G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45440366 | |||||||
| chr17:45440490 | A | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0056 |
3 | HG02280.hp2 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2838-264T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45440490 | |||||||
| chr17:45440608 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2838-382C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45440608 | |||||||
| chr17:45440786 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(166): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2838-560T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45440786 | |||||||
| chr17:45440962 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2838-736G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45440962 | |||||||
| chr17:45441034 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2838-808C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45441034 | |||||||
| chr17:45441538 | G | A | 4 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(1): Show |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2838-1312C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45441538 | |||||||
| chr17:45441780 | G | A | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2838-1554C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45441780 | |||||||
| chr17:45441870 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2838-1644A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45441870 | |||||||
| chr17:45442086 | A | G | 16 | a0001c0001t0001g0024 a0001c0001t0001g0083 a0001c0001t0001g0092 others(13): Show |
17 | HG00735.hp1 HG01884.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2838-1860T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442086 | |||||||
| chr17:45442185 | G | A | 4 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(1): Show |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2838-1959C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442185 | |||||||
| chr17:45442198 | C | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2838-1972G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442198 | |||||||
| chr17:45442261 | A | G | 1 | a0001c0001t0003g0027 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2838-2035T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442261 | |||||||
| chr17:45442370 | A | T | 3 | a0001c0005t0001g0076 a0001c0005t0001g0242 a0001c0005t0001g0243 |
3 | HG02922.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2838-2144T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442370 | |||||||
| chr17:45442394 | G | T | 2 | a0001c0001t0003g0135 a0001c0001t0003g0144 |
2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2838-2168C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442394 | |||||||
| chr17:45442593 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG01243.hp2 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2838-2367G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442593 | |||||||
| chr17:45442723 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2838-2497G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442723 | |||||||
| chr17:45442752 | A | G | 26 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(23): Show |
31 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.2838-2526T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442752 | |||||||
| chr17:45442906 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2837+2564C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442906 | |||||||
| chr17:45443032 | G | T | 14 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0033 others(11): Show |
17 | HG00280.hp1 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.2837+2438C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443032 | |||||||
| chr17:45443092 | C | G | 4 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(1): Show |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2837+2378G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443092 | |||||||
| chr17:45443147 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2837+2323A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443147 | |||||||
| chr17:45443188 | A | G | 1 | a0001c0001t0003g0146 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2837+2282T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443188 | |||||||
| chr17:45443309 | T | C | 26 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(23): Show |
31 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.2837+2161A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443309 | |||||||
| chr17:45443494 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18966.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2837+1976C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443494 | |||||||
| chr17:45443623 | G | A | 1 | a0001c0005t0001g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2837+1847C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443623 | |||||||
| chr17:45443628 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0082 a0001c0001t0001g0102 others(6): Show |
12 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2837+1842C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443628 | |||||||
| chr17:45443795 | C | G | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2837+1675G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443795 | |||||||
| chr17:45443827 | A | G | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2837+1643T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443827 | |||||||
| chr17:45444028 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2837+1442C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444028 | |||||||
| chr17:45444069 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2837+1401C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444069 | |||||||
| chr17:45444096 | C | T | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2837+1374G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444096 | |||||||
| chr17:45444097 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2837+1373C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444097 | |||||||
| chr17:45444185 | G | A | 1 | a0001c0001t0006g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2837+1285C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444185 | |||||||
| chr17:45444219 | G | T | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2837+1251C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444219 | |||||||
| chr17:45444304 | C | T | 1 | a0001c0005t0001g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2837+1166G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444304 | |||||||
| chr17:45444557 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2837+913C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444557 | |||||||
| chr17:45444876 | AGATGGAG others(42): Show |
A | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2837+545_2837+593d others(51): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444876 | |||||||
| chr17:45444974 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0209 |
3 | NA18747.hp1 NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2837+496C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444974 | |||||||
| chr17:45444995 | T | C | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2837+475A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444995 | |||||||
| chr17:45445027 | G | A | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2837+443C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445027 | |||||||
| chr17:45445080 | C | G | 2 | a0001c0001t0001g0059 a0001c0002t0001g0075 |
2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2837+390G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445080 | |||||||
| chr17:45445112 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2837+358T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445112 | |||||||
| chr17:45445201 | C | G | 3 | a0001c0005t0001g0076 a0001c0005t0001g0242 a0001c0005t0001g0243 |
3 | HG02922.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2837+269G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445201 | |||||||
| chr17:45445240 | G | A | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2837+230C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445240 | |||||||
| chr17:45445245 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2837+225C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445245 | |||||||
| chr17:45445409 | TTGTG | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2837+57_2837+60del others(4): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445409 | |||||||
| chr17:45445434 | C | T | 2 | a0001c0001t0001g0059 a0001c0002t0001g0075 |
2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2837+36G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445434 | |||||||
| chr17:45445446 | C | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2837+24G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445446 | |||||||
| chr17:45446019 | T | TC | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2644-357dupG | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446019 | |||||||
| chr17:45446080 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2644-417C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446080 | |||||||
| chr17:45446241 | A | G | 1 | a0001c0005t0001g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2644-578T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446241 | |||||||
| chr17:45446372 | C | T | 1 | a0001c0002t0002g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2644-709G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446372 | |||||||
| chr17:45446396 | G | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0136 others(1): Show |
4 | HG01106.hp2 HG01175.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.2644-733C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446396 | |||||||
| chr17:45446520 | G | A | 2 | a0001c0005t0001g0076 a0001c0005t0001g0243 |
2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2644-857C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446520 | |||||||
| chr17:45446654 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0011g0189 |
2 | HG01358.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2644-991G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446654 | |||||||
| chr17:45446772 | T | C | 2 | a0001c0002t0002g0065 a0001c0002t0002g0067 |
2 | HG00140.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2644-1109A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446772 | |||||||
| chr17:45446979 | C | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0104 others(6): Show |
10 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2644-1316G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446979 | |||||||
| chr17:45447079 | G | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0153 |
3 | HG02683.hp2 NA18951.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2644-1416C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447079 | |||||||
| chr17:45447160 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2644-1497G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447160 | |||||||
| chr17:45447361 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2644-1698C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447361 | |||||||
| chr17:45447382 | G | C | 1 | a0001c0005t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2644-1719C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447382 | |||||||
| chr17:45447589 | C | CCAGCCAG others(18): Show |
1 | a0001c0001t0008g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2644-1951_2644-192 others(29): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447589 | |||||||
| chr17:45447589 | CCAGCCAG others(18): Show |
C | 1 | a0001c0013t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2644-1951_2644-192 others(29): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447589 | |||||||
| chr17:45447656 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2644-1993C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447656 | |||||||
| chr17:45447710 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2644-2047G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447710 | |||||||
| chr17:45447800 | C | CT | 19 | a0001c0001t0001g0228 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.2644-2138dupA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447800 | |||||||
| chr17:45447800 | CT | C | 5 | a0001c0001t0001g0113 a0001c0001t0004g0018 a0001c0001t0004g0041 others(2): Show |
6 | HG02818.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2644-2138delA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447800 | |||||||
| chr17:45447839 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2644-2176G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447839 | |||||||
| chr17:45447883 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2644-2220G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447883 | |||||||
| chr17:45447922 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2644-2259C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447922 | |||||||
| chr17:45447945 | C | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2644-2282G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447945 | |||||||
| chr17:45447980 | TAG | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2644-2319_2644-231 others(6): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447980 | |||||||
| chr17:45447999 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2644-2336G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447999 | |||||||
| chr17:45448331 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0225 |
5 | HG02074.hp1 NA18948.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.2643+2287C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45448331 | |||||||
| chr17:45448353 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2643+2265G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45448353 | |||||||
| chr17:45448888 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2643+1730G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45448888 | |||||||
| chr17:45449225 | C | CAGCTCG | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2643+1392_2643+139 others(10): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449225 | |||||||
| chr17:45449286 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2643+1332G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449286 | |||||||
| chr17:45449289 | TCCACCCA others(69): Show |
T | 1 | a0001c0001t0001g0231 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2643+1253_2643+132 others(80): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449289 | |||||||
| chr17:45449485 | G | A | 4 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(1): Show |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2643+1133C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449485 | |||||||
| chr17:45449581 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0048 others(18): Show |
25 | HG00642.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2643+1037G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449581 | |||||||
| chr17:45449659 | C | T | 18 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(15): Show |
21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.2643+959G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449659 | |||||||
| chr17:45449753 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2643+865G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449753 | |||||||
| chr17:45449781 | C | T | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2643+837G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449781 | |||||||
| chr17:45449821 | C | A | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2643+797G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449821 | |||||||
| chr17:45449947 | C | A | 1 | a0001c0001t0001g0023 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2643+671G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449947 | |||||||
| chr17:45449957 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2643+661G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449957 | |||||||
| chr17:45450170 | C | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2643+448G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45450170 | |||||||
| chr17:45450234 | C | T | 1 | a0001c0001t0008g0087 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2643+384G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45450234 | |||||||
| chr17:45450311 | T | TTATC | 2 | a0002c0003t0001g0009 a0002c0003t0001g0055 |
4 | HG02896.hp2 HG02897.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2643+303_2643+306d others(6): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45450311 | |||||||
| chr17:45450818 | T | C | 1 | a0001c0001t0004g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2498-55A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45450818 | |||||||
| chr17:45451215 | G | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0104 others(7): Show |
11 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2498-452C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451215 | |||||||
| chr17:45451526 | C | T | 8 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2498-763G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451526 | |||||||
| chr17:45451583 | A | G | 1 | a0001c0001t0011g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2498-820T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451583 | |||||||
| chr17:45451790 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2498-1027C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451790 | |||||||
| chr17:45451899 | C | T | 1 | a0001c0002t0002g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2498-1136G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451899 | |||||||
| chr17:45451927 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2498-1164C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451927 | |||||||
| chr17:45451957 | A | G | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2498-1194T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451957 | |||||||
| chr17:45451975 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG01192.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.2498-1212C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451975 | |||||||
| chr17:45452042 | G | A | 1 | a0001c0005t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2498-1279C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452042 | |||||||
| chr17:45452055 | C | T | 1 | a0001c0001t0008g0087 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2498-1292G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452055 | |||||||
| chr17:45452290 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2497+1065T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452290 | |||||||
| chr17:45452306 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2497+1049T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452306 | |||||||
| chr17:45452321 | T | C | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2497+1034A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452321 | |||||||
| chr17:45452327 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2497+1028A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452327 | |||||||
| chr17:45452349 | T | C | 3 | a0001c0001t0001g0235 a0001c0001t0008g0087 a0001c0001t0008g0088 |
3 | HG01891.hp1 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2497+1006A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452349 | |||||||
| chr17:45452362 | A | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2497+993T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452362 | |||||||
| chr17:45452403 | G | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2497+952C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452403 | |||||||
| chr17:45452567 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2497+788C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452567 | |||||||
| chr17:45452728 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2497+627C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452728 | |||||||
| chr17:45452791 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2497+564A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452791 | |||||||
| chr17:45452792 | G | T | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2497+563C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452792 | |||||||
| chr17:45452937 | A | G | 4 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(1): Show |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2497+418T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452937 | |||||||
| chr17:45453184 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2497+171C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45453184 | |||||||
| chr17:45454402 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0241 a0001c0013t0001g0079 |
5 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-130G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454402 | |||||||
| chr17:45454458 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1580-186C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454458 | |||||||
| chr17:45454526 | C | T | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1580-254G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454526 | |||||||
| chr17:45454560 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1580-288G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454560 | |||||||
| chr17:45454594 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1580-322C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454594 | |||||||
| chr17:45454691 | C | G | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1580-419G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454691 | |||||||
| chr17:45454693 | C | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1580-421G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454693 | |||||||
| chr17:45454724 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1580-452G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454724 | |||||||
| chr17:45454886 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1580-614G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454886 | |||||||
| chr17:45454908 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1580-636G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454908 | |||||||
| chr17:45454947 | G | A | 1 | a0001c0005t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1580-675C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454947 | |||||||
| chr17:45455049 | C | T | 2 | a0001c0001t0001g0059 a0001c0002t0001g0075 |
2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1580-777G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455049 | |||||||
| chr17:45455050 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG00609.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1580-778C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455050 | |||||||
| chr17:45455173 | T | G | 2 | a0001c0001t0008g0087 a0001c0001t0008g0088 |
2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1580-901A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455173 | |||||||
| chr17:45455212 | C | T | 3 | a0002c0003t0001g0009 a0002c0003t0001g0045 a0002c0003t0001g0055 |
5 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580-940G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455212 | |||||||
| chr17:45455313 | C | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1580-1041G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455313 | |||||||
| chr17:45455320 | C | T | 1 | a0001c0001t0008g0087 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1580-1048G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455320 | |||||||
| chr17:45455409 | G | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1580-1137C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455409 | |||||||
| chr17:45455438 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1580-1166G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455438 | |||||||
| chr17:45455593 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1580-1321G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455593 | |||||||
| chr17:45455702 | C | T | 1 | a0001c0001t0001g0038 | 2 | NA18985.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1580-1430G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455702 | |||||||
| chr17:45455921 | G | T | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1580-1649C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455921 | |||||||
| chr17:45455956 | C | T | 1 | a0002c0003t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1580-1684G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455956 | |||||||
| chr17:45456166 | A | G | 2 | a0001c0001t0008g0087 a0001c0001t0008g0088 |
2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1580-1894T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456166 | |||||||
| chr17:45456201 | T | C | 2 | a0001c0001t0001g0059 a0001c0002t0001g0075 |
2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1580-1929A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456201 | |||||||
| chr17:45456595 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1579+1574C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456595 | |||||||
| chr17:45456733 | A | G | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1579+1436T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456733 | |||||||
| chr17:45456956 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1579+1213A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456956 | |||||||
| chr17:45456987 | T | C | 34 | a0001c0001t0001g0024 a0001c0001t0001g0083 a0001c0001t0001g0092 others(31): Show |
38 | HG00140.hp1 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1579+1182A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456987 | |||||||
| chr17:45457172 | G | GA | 26 | a0001c0001t0001g0085 a0001c0001t0001g0112 a0001c0001t0001g0116 others(23): Show |
29 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.1579+996dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457172 | |||||||
| chr17:45457172 | GA | G | 7 | a0001c0001t0001g0109 a0001c0001t0001g0180 a0001c0001t0001g0193 others(4): Show |
7 | HG01168.hp2 HG01993.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579+996delT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457172 | |||||||
| chr17:45457195 | A | C | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1579+974T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457195 | |||||||
| chr17:45457328 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1579+841G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457328 | |||||||
| chr17:45457366 | C | T | 1 | a0003c0012t0001g0179 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1579+803G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457366 | |||||||
| chr17:45457560 | CA | C | 6 | a0001c0001t0001g0160 a0001c0001t0001g0214 a0001c0001t0008g0087 others(3): Show |
6 | HG01891.hp1 HG02922.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+608delT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457560 | |||||||
| chr17:45457681 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0192 a0001c0001t0001g0193 others(5): Show |
10 | HG01168.hp2 HG01169.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1579+488A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457681 | |||||||
| chr17:45458067 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1579+102G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45458067 | |||||||
| chr17:45458586 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(166): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1309-147G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45458586 | |||||||
| chr17:45458618 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1309-179G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45458618 | |||||||
| chr17:45458881 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1309-442G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45458881 | |||||||
| chr17:45459024 | A | C | 2 | a0001c0005t0001g0076 a0001c0005t0001g0243 |
2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1309-585T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459024 | |||||||
| chr17:45459042 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-603G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459042 | |||||||
| chr17:45459076 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0170 |
2 | HG01433.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1309-637G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459076 | |||||||
| chr17:45459282 | C | A | 1 | a0001c0004t0001g0052 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1309-843G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459282 | |||||||
| chr17:45459372 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1309-933G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459372 | |||||||
| chr17:45459377 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-938G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459377 | |||||||
| chr17:45459407 | A | C | 1 | a0001c0002t0002g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1309-968T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459407 | |||||||
| chr17:45459604 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-1165C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459604 | |||||||
| chr17:45459716 | C | T | 2 | a0001c0001t0008g0087 a0001c0001t0008g0088 |
2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1309-1277G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459716 | |||||||
| chr17:45459802 | G | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1309-1363C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459802 | |||||||
| chr17:45459915 | T | G | 15 | a0001c0001t0001g0024 a0001c0001t0001g0083 a0001c0001t0001g0092 others(12): Show |
16 | HG00735.hp1 HG01884.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1309-1476A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459915 | |||||||
| chr17:45460103 | T | C | 1 | a0001c0001t0003g0137 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1309-1664A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460103 | |||||||
| chr17:45460195 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1309-1756C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460195 | |||||||
| chr17:45460345 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-1906G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460345 | |||||||
| chr17:45460384 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1309-1945G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460384 | |||||||
| chr17:45460395 | G | A | 2 | a0001c0001t0008g0087 a0001c0001t0008g0088 |
2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1309-1956C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460395 | |||||||
| chr17:45460420 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1309-1981G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460420 | |||||||
| chr17:45460652 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1309-2213C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460652 | |||||||
| chr17:45460731 | A | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0190 a0001c0001t0011g0189 |
3 | HG01358.hp1 HG03654.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1309-2292T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460731 | |||||||
| chr17:45460947 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1309-2508G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460947 | |||||||
| chr17:45461157 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-2718C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461157 | |||||||
| chr17:45461163 | A | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1309-2724T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461163 | |||||||
| chr17:45461340 | T | C | 2 | a0001c0001t0001g0141 a0005c0007t0001g0080 |
2 | HG00735.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1309-2901A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461340 | |||||||
| chr17:45461441 | T | G | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-3002A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461441 | |||||||
| chr17:45461625 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-3186C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461625 | |||||||
| chr17:45461627 | G | C | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-3188C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461627 | |||||||
| chr17:45461669 | G | A | 19 | a0001c0001t0001g0234 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1309-3230C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461669 | |||||||
| chr17:45461705 | T | C | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1309-3266A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461705 | |||||||
| chr17:45461716 | C | T | 2 | a0001c0001t0001g0059 a0001c0002t0001g0075 |
2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1309-3277G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461716 | |||||||
| chr17:45461737 | A | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1309-3298T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461737 | |||||||
| chr17:45461839 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0232 |
2 | NA18960.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1309-3400A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461839 | |||||||
| chr17:45462010 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1309-3571A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462010 | |||||||
| chr17:45462045 | C | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1309-3606G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462045 | |||||||
| chr17:45462071 | C | G | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-3632G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462071 | |||||||
| chr17:45462095 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0001g0123 |
4 | NA18964.hp2 NA18966.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-3656C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462095 | |||||||
| chr17:45462250 | C | T | 2 | a0001c0001t0001g0059 a0001c0002t0001g0075 |
2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1309-3811G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462250 | |||||||
| chr17:45462357 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-3918G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462357 | |||||||
| chr17:45462505 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1309-4066G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462505 | |||||||
| chr17:45462585 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1309-4146C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462585 | |||||||
| chr17:45462598 | T | G | 1 | a0001c0001t0001g0216 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1309-4159A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462598 | |||||||
| chr17:45462602 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-4163C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462602 | |||||||
| chr17:45462678 | G | A | 1 | a0001c0001t0008g0087 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1309-4239C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462678 | |||||||
| chr17:45462907 | C | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-4468G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462907 | |||||||
| chr17:45463071 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(186): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1309-4632T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463071 | |||||||
| chr17:45463083 | G | C | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-4644C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463083 | |||||||
| chr17:45463085 | C | CA | 8 | a0001c0001t0001g0138 a0001c0001t0001g0193 a0001c0001t0001g0203 others(5): Show |
8 | HG01168.hp1 HG01168.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309-4647dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463085 | |||||||
| chr17:45463085 | CA | C | 19 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0092 others(16): Show |
22 | HG00609.hp2 HG01884.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1309-4647delT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463085 | |||||||
| chr17:45463106 | A | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-4667T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463106 | |||||||
| chr17:45463192 | C | T | 1 | a0001c0001t0001g0035 | 2 | NA18973.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1309-4753G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463192 | |||||||
| chr17:45463223 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1309-4784A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463223 | |||||||
| chr17:45463314 | C | T | 1 | a0001c0004t0001g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1309-4875G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463314 | |||||||
| chr17:45463345 | G | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0117 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1308+4864C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463345 | |||||||
| chr17:45463366 | T | C | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1308+4843A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463366 | |||||||
| chr17:45463515 | C | T | 1 | a0001c0001t0006g0142 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1308+4694G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463515 | |||||||
| chr17:45463519 | A | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0232 |
2 | NA18960.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1308+4690T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463519 | |||||||
| chr17:45463705 | T | C | 2 | a0001c0004t0001g0050 a0001c0004t0001g0051 |
2 | HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1308+4504A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463705 | |||||||
| chr17:45463718 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1308+4491G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463718 | |||||||
| chr17:45463763 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(170): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1308+4446G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463763 | |||||||
| chr17:45463793 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG00673.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1308+4416G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463793 | |||||||
| chr17:45463850 | G | A | 1 | a0001c0004t0001g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1308+4359C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463850 | |||||||
| chr17:45463853 | A | G | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1308+4356T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463853 | |||||||
| chr17:45463854 | C | T | 2 | a0001c0001t0001g0234 a0001c0009t0012g0058 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1308+4355G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463854 | |||||||
| chr17:45463954 | A | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0128 a0001c0001t0001g0129 |
5 | HG00099.hp2 HG00597.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1308+4255T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463954 | |||||||
| chr17:45464219 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1308+3990C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464219 | |||||||
| chr17:45464261 | C | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1308+3948G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464261 | |||||||
| chr17:45464290 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1308+3919G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464290 | |||||||
| chr17:45464448 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1308+3761C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464448 | |||||||
| chr17:45464468 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1308+3741G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464468 | |||||||
| chr17:45464514 | C | T | 3 | a0001c0005t0001g0076 a0001c0005t0001g0242 a0001c0005t0001g0243 |
3 | HG02922.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1308+3695G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464514 | |||||||
| chr17:45464552 | G | C | 3 | a0001c0005t0001g0076 a0001c0005t0001g0242 a0001c0005t0001g0243 |
3 | HG02922.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1308+3657C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464552 | |||||||
| chr17:45464671 | T | C | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1308+3538A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464671 | |||||||
| chr17:45464761 | T | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0022 others(9): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1308+3448A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464761 | |||||||
| chr17:45464859 | G | A | 8 | a0001c0004t0001g0049 a0001c0004t0001g0050 a0001c0004t0001g0051 others(5): Show |
10 | HG02257.hp2 HG02647.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1308+3350C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464859 | |||||||
| chr17:45464871 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1308+3338G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464871 | |||||||
| chr17:45464910 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1308+3299G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464910 | |||||||
| chr17:45464935 | C | T | 18 | a0001c0001t0001g0234 a0001c0002t0002g0010 a0001c0002t0002g0020 others(15): Show |
21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1308+3274G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464935 | |||||||
| chr17:45464940 | T | C | 2 | a0001c0005t0001g0242 a0001c0005t0001g0243 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1308+3269A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464940 | |||||||
| chr17:45464993 | G | A | 1 | a0001c0004t0001g0052 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1308+3216C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464993 | |||||||
| chr17:45465042 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1308+3167G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465042 | |||||||
| chr17:45465046 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1308+3163A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465046 | |||||||
| chr17:45465282 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1308+2927A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465282 | |||||||
| chr17:45465430 | C | T | 8 | a0001c0001t0001g0054 a0001c0004t0001g0049 a0001c0004t0001g0050 others(5): Show |
10 | HG02257.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1308+2779G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465430 | |||||||
| chr17:45465625 | A | G | 1 | a0001c0001t0003g0033 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1308+2584T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465625 | |||||||
| chr17:45465698 | A | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(56): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1308+2511T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465698 | |||||||
| chr17:45465709 | C | CA | 16 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0083 others(13): Show |
19 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1308+2499dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465709 | |||||||
| chr17:45465716 | A | AT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1308+2492dupA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465716 | |||||||
| chr17:45465717 | T | A | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1308+2492A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465717 | |||||||
| chr17:45465841 | T | C | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1308+2368A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465841 | |||||||
| chr17:45466122 | C | A | 1 | a0001c0001t0009g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1308+2087G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466122 | |||||||
| chr17:45466132 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1308+2077C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466132 | |||||||
| chr17:45466206 | A | G | 4 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(1): Show |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1308+2003T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466206 | |||||||
| chr17:45466299 | T | C | 2 | a0001c0009t0012g0058 a0001c0013t0001g0079 |
2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1308+1910A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466299 | |||||||
| chr17:45466306 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1308+1903A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466306 | |||||||
| chr17:45466464 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(168): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1308+1745A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466464 | |||||||
| chr17:45466840 | G | C | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1308+1369C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466840 | |||||||
| chr17:45466888 | A | G | 1 | a0001c0005t0001g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1308+1321T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466888 | |||||||
| chr17:45467004 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | NA18966.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1308+1205A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467004 | |||||||
| chr17:45467013 | G | A | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1308+1196C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467013 | |||||||
| chr17:45467090 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1308+1119C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467090 | |||||||
| chr17:45467459 | C | T | 1 | a0001c0001t0015g0207 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1308+750G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467459 | |||||||
| chr17:45467587 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1308+622G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467587 | |||||||
| chr17:45467734 | C | T | 1 | a0001c0001t0008g0087 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1308+475G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467734 | |||||||
| chr17:45467770 | C | A | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0077 others(10): Show |
16 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1308+439G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467770 | |||||||
| chr17:45467934 | C | T | 13 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0047 others(10): Show |
16 | HG01243.hp1 HG02257.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.1308+275G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467934 | |||||||
| chr17:45468631 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.924-38C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468631 | |||||||
| chr17:45468691 | G | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.924-98C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468691 | |||||||
| chr17:45468817 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.924-224C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468817 | |||||||
| chr17:45468858 | G | A | 2 | a0001c0005t0001g0242 a0001c0005t0001g0243 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.924-265C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468858 | |||||||
| chr17:45468931 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.924-338G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468931 | |||||||
| chr17:45468956 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.924-363C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468956 | |||||||
| chr17:45469024 | C | CTG | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.924-433_924-432dup others(2): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469024 | |||||||
| chr17:45469076 | A | G | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.924-483T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469076 | |||||||
| chr17:45469297 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.924-704G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469297 | |||||||
| chr17:45469474 | T | G | 1 | a0001c0001t0008g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.924-881A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469474 | |||||||
| chr17:45469487 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.924-894C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469487 | |||||||
| chr17:45469612 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.924-1019G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469612 | |||||||
| chr17:45469839 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.924-1246A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469839 | |||||||
| chr17:45469871 | A | G | 15 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0083 others(12): Show |
18 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.924-1278T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469871 | |||||||
| chr17:45469911 | A | G | 1 | a0001c0001t0003g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.924-1318T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469911 | |||||||
| chr17:45470115 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.924-1522T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470115 | |||||||
| chr17:45470193 | G | A | 4 | a0001c0001t0003g0146 a0001c0001t0003g0147 a0001c0001t0003g0148 others(1): Show |
4 | HG01123.hp1 HG01192.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-1600C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470193 | |||||||
| chr17:45470343 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0083 others(12): Show |
18 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.924-1750G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470343 | |||||||
| chr17:45470424 | T | C | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.924-1831A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470424 | |||||||
| chr17:45470448 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.924-1855C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470448 | |||||||
| chr17:45470544 | AC | A | 12 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0093 others(9): Show |
13 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.924-1952delG | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470544 | |||||||
| chr17:45470558 | C | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(169): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.924-1965G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470558 | |||||||
| chr17:45470558 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.924-1965G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470558 | |||||||
| chr17:45470658 | G | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0098 a0001c0005t0001g0242 |
4 | HG01167.hp1 HG01169.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.924-2065C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470658 | |||||||
| chr17:45470682 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(132): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.924-2089A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470682 | |||||||
| chr17:45470690 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(132): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.924-2097T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470690 | |||||||
| chr17:45470781 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.924-2188G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470781 | |||||||
| chr17:45470955 | T | C | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.924-2362A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470955 | |||||||
| chr17:45471022 | TG | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(132): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.924-2430delC | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471022 | |||||||
| chr17:45471058 | A | G | 18 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(15): Show |
21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.924-2465T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471058 | |||||||
| chr17:45471073 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.924-2480A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471073 | |||||||
| chr17:45471115 | A | G | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.924-2522T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471115 | |||||||
| chr17:45471305 | A | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(172): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.924-2712T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471305 | |||||||
| chr17:45471367 | C | G | 1 | a0001c0013t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.924-2774G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471367 | |||||||
| chr17:45471412 | G | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(105): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.924-2819C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471412 | |||||||
| chr17:45471537 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
4 | HG00609.hp1 NA18973.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-2944G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471537 | |||||||
| chr17:45471584 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0077 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.924-2991A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471584 | |||||||
| chr17:45471762 | T | C | 1 | a0001c0013t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.924-3169A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471762 | |||||||
| chr17:45471833 | G | A | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.924-3240C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471833 | |||||||
| chr17:45471925 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.923+3175G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471925 | |||||||
| chr17:45471992 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.923+3108G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471992 | |||||||
| chr17:45471993 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.923+3107C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471993 | |||||||
| chr17:45472000 | A | G | 1 | a0001c0013t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.923+3100T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472000 | |||||||
| chr17:45472009 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.923+3091A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472009 | |||||||
| chr17:45472031 | T | C | 1 | a0001c0002t0002g0071 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.923+3069A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472031 | |||||||
| chr17:45472097 | G | A | 1 | a0001c0010t0003g0220 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.923+3003C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472097 | |||||||
| chr17:45472133 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.923+2967A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472133 | |||||||
| chr17:45472137 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.923+2963C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472137 | |||||||
| chr17:45472160 | A | G | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+2940T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472160 | |||||||
| chr17:45472164 | C | CGGTGAGA others(37): Show |
5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0089 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+2892_923+2935d others(46): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472164 | |||||||
| chr17:45472207 | C | G | 1 | a0001c0005t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.923+2893G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472207 | |||||||
| chr17:45472242 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.923+2858C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472242 | |||||||
| chr17:45472331 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | NA18980.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.923+2769A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472331 | |||||||
| chr17:45472430 | C | T | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0077 others(10): Show |
16 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.923+2670G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472430 | |||||||
| chr17:45472467 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0180 |
2 | HG00609.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.923+2633C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472467 | |||||||
| chr17:45472741 | A | G | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+2359T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472741 | |||||||
| chr17:45472744 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.923+2356T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472744 | |||||||
| chr17:45472920 | C | T | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.923+2180G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472920 | |||||||
| chr17:45472984 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.923+2116A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472984 | |||||||
| chr17:45473145 | G | C | 1 | a0001c0005t0001g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.923+1955C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473145 | |||||||
| chr17:45473155 | G | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(145): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.923+1945C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473155 | |||||||
| chr17:45473220 | C | T | 3 | a0001c0001t0006g0121 a0001c0001t0006g0126 a0001c0001t0006g0142 |
3 | HG00642.hp2 HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.923+1880G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473220 | |||||||
| chr17:45473221 | C | A | 1 | a0001c0001t0001g0169 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.923+1879G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473221 | |||||||
| chr17:45473346 | T | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.923+1754A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473346 | |||||||
| chr17:45473415 | C | A | 1 | a0001c0011t0003g0149 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.923+1685G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473415 | |||||||
| chr17:45473563 | AT | A | 20 | a0001c0001t0001g0023 a0001c0002t0001g0075 a0001c0002t0002g0010 others(17): Show |
24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.923+1536delA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473563 | |||||||
| chr17:45473575 | T | C | 1 | a0001c0001t0001g0017 | 3 | NA18988.hp1 NA18989.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.923+1525A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473575 | |||||||
| chr17:45473644 | C | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0104 others(7): Show |
11 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.923+1456G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473644 | |||||||
| chr17:45473653 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.923+1447C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473653 | |||||||
| chr17:45473717 | C | T | 18 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(15): Show |
21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+1383G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473717 | |||||||
| chr17:45473720 | G | A | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(5): Show |
10 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.923+1380C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473720 | |||||||
| chr17:45473731 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.923+1369A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473731 | |||||||
| chr17:45473780 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.923+1320C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473780 | |||||||
| chr17:45473785 | C | G | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+1315G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473785 | |||||||
| chr17:45473809 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.923+1291G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473809 | |||||||
| chr17:45473838 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.923+1262C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473838 | |||||||
| chr17:45473955 | G | C | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+1145C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473955 | |||||||
| chr17:45474062 | A | T | 15 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0047 others(12): Show |
18 | HG01243.hp1 HG01256.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.923+1038T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474062 | |||||||
| chr17:45474062 | AT | A | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+1037delA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474062 | |||||||
| chr17:45474066 | T | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(24): Show |
45 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.923+1034A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474066 | |||||||
| chr17:45474157 | T | C | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+943A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474157 | |||||||
| chr17:45474180 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.923+920G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474180 | |||||||
| chr17:45474247 | C | T | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+853G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474247 | |||||||
| chr17:45474306 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(132): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.923+794G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474306 | |||||||
| chr17:45474358 | C | CA | 13 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0047 others(10): Show |
16 | HG01243.hp1 HG02257.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.923+741dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474358 | |||||||
| chr17:45474582 | C | T | 1 | a0001c0013t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.923+518G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474582 | |||||||
| chr17:45474740 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(132): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.923+360G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474740 | |||||||
| chr17:45474823 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0198 |
5 | HG01891.hp2 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+277G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474823 | |||||||
| chr17:45474888 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.923+212C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474888 | |||||||
| chr17:45475019 | T | C | 2 | a0001c0005t0001g0242 a0001c0005t0001g0243 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.923+81A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45475019 | |||||||
| chr17:45475086 | G | A | 1 | a0001c0001t0006g0142 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.923+14C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45475086 | |||||||
| chr17:45475784 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(119): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.297-58A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45475784 | |||||||
| chr17:45476064 | T | C | 1 | a0001c0001t0003g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.297-338A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476064 | |||||||
| chr17:45476130 | AAT | A | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.297-406_297-405del others(2): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476130 | |||||||
| chr17:45476145 | A | T | 2 | a0001c0005t0001g0242 a0001c0005t0001g0243 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.297-419T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476145 | |||||||
| chr17:45476162 | A | C | 1 | a0001c0013t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.297-436T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476162 | |||||||
| chr17:45476198 | TTA | T | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.297-474_297-473del others(2): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476198 | |||||||
| chr17:45476223 | T | C | 1 | a0001c0001t0009g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.297-497A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476223 | |||||||
| chr17:45476345 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.297-619C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476345 | |||||||
| chr17:45476362 | T | C | 1 | a0001c0001t0001g0040 | 2 | HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.297-636A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476362 | |||||||
| chr17:45476691 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297-965G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476691 | |||||||
| chr17:45476787 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.297-1061G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476787 | |||||||
| chr17:45476872 | C | A | 2 | a0001c0002t0002g0063 a0001c0002t0002g0069 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.296+1028G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476872 | |||||||
| chr17:45477035 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.296+865C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477035 | |||||||
| chr17:45477337 | G | C | 10 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0094 others(7): Show |
11 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.296+563C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477337 | |||||||
| chr17:45477429 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(172): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.296+471T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477429 | |||||||
| chr17:45477433 | C | CAAA | 15 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(12): Show |
18 | HG00140.hp1 HG01074.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.296+464_296+466dup others(3): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477433 | |||||||
| chr17:45477434 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.296+466T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477434 | |||||||
| chr17:45477438 | A | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(2): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.296+462T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477438 | |||||||
| chr17:45477536 | T | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(171): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.296+364A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477536 | |||||||
| chr17:45477766 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.296+134G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477766 | |||||||
| chr17:45477887 | A | G | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.296+13T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477887 | |||||||
| chr17:45478236 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.49-89C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478236 | |||||||
| chr17:45478395 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0199 a0001c0001t0001g0200 |
4 | HG00738.hp1 HG01943.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-248A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478395 | |||||||
| chr17:45478659 | T | C | 2 | a0001c0002t0002g0070 a0001c0002t0002g0071 |
2 | NA19085.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.49-512A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478659 | |||||||
| chr17:45478777 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.49-630C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478777 | |||||||
| chr17:45478826 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.49-679C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478826 | |||||||
| chr17:45478898 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.49-751A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478898 | |||||||
| chr17:45478901 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.49-754C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478901 | |||||||
| chr17:45479026 | CT | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.49-880delA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479026 | |||||||
| chr17:45479208 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.49-1061A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479208 | |||||||
| chr17:45479286 | G | A | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.49-1139C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479286 | |||||||
| chr17:45479315 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0212 |
2 | HG01069.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.49-1168G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479315 | |||||||
| chr17:45479368 | A | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(119): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.49-1221T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479368 | |||||||
| chr17:45479441 | T | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(26): Show |
34 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.49-1294A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479441 | |||||||
| chr17:45479496 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.49-1349G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479496 | |||||||
| chr17:45479512 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(105): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.49-1365G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479512 | |||||||
| chr17:45479517 | C | CA | 23 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0001g0099 others(20): Show |
25 | HG00738.hp2 HG02027.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.49-1371dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479517 | |||||||
| chr17:45479517 | CA | C | 32 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0035 others(29): Show |
42 | HG00140.hp1 HG00609.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.49-1371delT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479517 | |||||||
| chr17:45479538 | T | A | 1 | a0001c0001t0001g0223 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.49-1391A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479538 | |||||||
| chr17:45479616 | G | A | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.49-1469C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479616 | |||||||
| chr17:45479688 | A | AAAAAC | 4 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG01993.hp1 NA18747.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-1546_49-1542dup others(5): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479688 | |||||||
| chr17:45479688 | A | AAAAACAA others(3): Show |
19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.49-1551_49-1542dup others(10): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479688 | |||||||
| chr17:45479688 | AAAAAC | A | 5 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(2): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-1546_49-1542del others(5): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479688 | |||||||
| chr17:45479995 | T | A | 1 | a0001c0001t0001g0206 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49-1848A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479995 | |||||||
| chr17:45479996 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49-1849T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479996 | |||||||
| chr17:45480246 | G | A | 19 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(16): Show |
22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.49-2099C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480246 | |||||||
| chr17:45480321 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(169): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.48+2116G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480321 | |||||||
| chr17:45480341 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0089 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+2096C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480341 | |||||||
| chr17:45480438 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.48+1999A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480438 | |||||||
| chr17:45480439 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(150): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.48+1998C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480439 | |||||||
| chr17:45480479 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.48+1958C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480479 | |||||||
| chr17:45480482 | TCAAAAAA others(1): Show |
T | 23 | a0001c0001t0001g0100 a0001c0001t0001g0104 a0001c0001t0001g0105 others(20): Show |
26 | HG00140.hp1 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.48+1947_48+1954del others(8): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480482 | |||||||
| chr17:45480498 | A | C | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.48+1939T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480498 | |||||||
| chr17:45480511 | A | C | 2 | a0001c0002t0002g0062 a0001c0002t0002g0063 |
2 | HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.48+1926T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480511 | |||||||
| chr17:45480519 | C | CA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(5): Show |
9 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+1917dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480519 | |||||||
| chr17:45480726 | C | T | 18 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(15): Show |
21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.48+1711G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480726 | |||||||
| chr17:45480766 | T | C | 1 | a0001c0013t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.48+1671A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480766 | |||||||
| chr17:45480793 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.48+1644A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480793 | |||||||
| chr17:45480850 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.48+1587G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480850 | |||||||
| chr17:45480901 | A | G | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.48+1536T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480901 | |||||||
| chr17:45481034 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.48+1403G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481034 | |||||||
| chr17:45481369 | G | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.48+1068C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481369 | |||||||
| chr17:45481483 | G | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0083 others(12): Show |
18 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.48+954C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481483 | |||||||
| chr17:45481647 | C | T | 5 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(2): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+790G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481647 | |||||||
| chr17:45481662 | G | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(8): Show |
13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.48+775C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481662 | |||||||
| chr17:45481834 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.48+603C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481834 | |||||||
| chr17:45481860 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.48+577T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481860 | |||||||
| chr17:45481904 | T | G | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.48+533A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481904 | |||||||
| chr17:45481917 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.48+520T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481917 | |||||||
| chr17:45481929 | G | C | 1 | a0001c0005t0001g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.48+508C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481929 | |||||||
| chr17:45481974 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.48+463A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481974 | |||||||
| chr17:45482133 | C | A | 1 | a0001c0011t0003g0149 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.48+304G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482133 | |||||||
| chr17:45482332 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0001g0123 |
4 | NA18964.hp2 NA18966.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+105T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482332 | |||||||
| chr17:45482360 | A | ATTCATT | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(164): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.48+76_48+77insAATG others(2): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482360 | |||||||
| chr17:45482361 | A | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(164): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.48+76T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482361 | |||||||
| chr17:45482362 | G | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(164): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.48+75C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482362 | |||||||
| chr17:45482377 | C | A | 2 | a0001c0005t0001g0242 a0001c0005t0001g0243 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.48+60G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482377 | |||||||
| chr17:45482392 | C | T | 2 | a0001c0005t0001g0242 a0001c0005t0001g0243 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.48+45G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482392 | |||||||
| chr17:45482589 | C | T | 1 | a0001c0002t0002g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-41-64G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482589 | |||||||
| chr17:45482647 | C | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(8): Show |
13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-122G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482647 | |||||||
| chr17:45482829 | T | C | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(8): Show |
13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-304A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482829 | |||||||
| chr17:45482850 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-41-325C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482850 | |||||||
| chr17:45482882 | C | A | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-41-357G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482882 | |||||||
| chr17:45482885 | G | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(8): Show |
13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-360C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482885 | |||||||
| chr17:45482919 | A | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(172): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-41-394T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482919 | |||||||
| chr17:45482922 | G | T | 1 | a0001c0013t0001g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-41-397C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482922 | |||||||
| chr17:45483108 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(8): Show |
13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-583G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483108 | |||||||
| chr17:45483146 | T | G | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-41-621A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483146 | |||||||
| chr17:45483224 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-41-699C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483224 | |||||||
| chr17:45483324 | C | T | 3 | a0001c0005t0001g0242 a0001c0005t0001g0243 a0001c0013t0001g0079 |
3 | HG02559.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-41-799G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483324 | |||||||
| chr17:45483335 | T | A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(9): Show |
16 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-41-810A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483335 | |||||||
| chr17:45483414 | T | TGGGTG | 3 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0047 |
4 | HG01243.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-894_-41-890dup others(5): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483414 | |||||||
| chr17:45483414 | TGGGTGGG others(8): Show |
T | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(10): Show |
17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-41-904_-41-890del others(15): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483414 | |||||||
| chr17:45483449 | G | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(22): Show |
38 | HG00099.hp1 HG00323.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.-41-924C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483449 | |||||||
| chr17:45483550 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-41-1025G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483550 | |||||||
| chr17:45483692 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-41-1167G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483692 | |||||||
| chr17:45483761 | T | C | 1 | a0001c0001t0009g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-41-1236A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483761 | |||||||
| chr17:45484364 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-41-1839G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484364 | |||||||
| chr17:45484399 | T | C | 1 | a0001c0001t0014g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-41-1874A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484399 | |||||||
| chr17:45484499 | C | T | 1 | a0001c0004t0001g0052 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-41-1974G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484499 | |||||||
| chr17:45484678 | C | T | 1 | a0001c0001t0006g0121 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-41-2153G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484678 | |||||||
| chr17:45484845 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-41-2320C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484845 | |||||||
| chr17:45484866 | C | T | 1 | a0002c0003t0001g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-41-2341G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484866 | |||||||
| chr17:45484890 | G | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG02559.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-41-2365C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484890 | |||||||
| chr17:45485092 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-41-2567A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485092 | |||||||
| chr17:45485184 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0239 |
2 | NA18967.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.-41-2659C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485184 | |||||||
| chr17:45485194 | G | GAAAAGGG others(6): Show |
2 | a0001c0005t0001g0242 a0001c0005t0001g0243 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-41-2682_-41-2670d others(15): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485194 | |||||||
| chr17:45485512 | T | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0093 others(8): Show |
12 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41-2987A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485512 | |||||||
| chr17:45485612 | A | T | 1 | a0001c0001t0015g0207 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-41-3087T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485612 | |||||||
| chr17:45485727 | A | G | 21 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(18): Show |
24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3202T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485727 | |||||||
| chr17:45485736 | T | TA | 7 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0004t0001g0049 others(4): Show |
7 | HG02257.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41-3212dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485736 | |||||||
| chr17:45485775 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-41-3250A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485775 | |||||||
| chr17:45485816 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
16 | HG00597.hp2 HG00609.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-41-3291C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485816 | |||||||
| chr17:45485832 | C | T | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-41-3307G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485832 | |||||||
| chr17:45485938 | A | C | 21 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(18): Show |
24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3413T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485938 | |||||||
| chr17:45485939 | T | G | 21 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(18): Show |
24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3414A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485939 | |||||||
| chr17:45485983 | G | A | 21 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(18): Show |
24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3458C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485983 | |||||||
| chr17:45485992 | G | A | 36 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0029 others(33): Show |
42 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-41-3467C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485992 | |||||||
| chr17:45486029 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-41-3504T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486029 | |||||||
| chr17:45486060 | C | CA | 5 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(2): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41-3536dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486060 | |||||||
| chr17:45486078 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0187 |
4 | NA18942.hp2 NA18980.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-3553C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486078 | |||||||
| chr17:45486114 | G | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0059 others(6): Show |
13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-3589C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486114 | |||||||
| chr17:45486125 | G | A | 1 | a0001c0002t0002g0060 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-41-3600C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486125 | |||||||
| chr17:45486134 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-41-3609C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486134 | |||||||
| chr17:45486149 | G | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0190 a0001c0001t0011g0189 |
3 | HG01358.hp1 HG03654.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-41-3624C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486149 | |||||||
| chr17:45486160 | T | G | 1 | a0001c0005t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-41-3635A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486160 | |||||||
| chr17:45486183 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-41-3658G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486183 | |||||||
| chr17:45486226 | AAGATAAA others(10): Show |
A | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-41-3718_-41-3702d others(19): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486226 | |||||||
| chr17:45486227 | AG | A | 3 | a0001c0002t0002g0061 a0001c0002t0002g0066 a0001c0002t0002g0073 |
3 | HG01433.hp2 HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-41-3703delC | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486227 | |||||||
| chr17:45486228 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(169): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.-41-3703C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486228 | |||||||
| chr17:45486230 | T | A | 21 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(18): Show |
24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3705A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486230 | |||||||
| chr17:45486235 | T | A | 21 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(18): Show |
24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3710A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486235 | |||||||
| chr17:45486237 | A | T | 1 | a0001c0002t0002g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-41-3712T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486237 | |||||||
| chr17:45486240 | A | T | 25 | a0001c0001t0001g0016 a0001c0001t0001g0111 a0001c0001t0001g0192 others(22): Show |
30 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.-41-3715T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486240 | |||||||
| chr17:45486243 | T | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.-41-3718A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486243 | |||||||
| chr17:45486246 | T | A | 18 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0092 others(15): Show |
19 | HG00639.hp2 HG00735.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-41-3721A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486246 | |||||||
| chr17:45486316 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-41-3791G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486316 | |||||||
| chr17:45486353 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-41-3828G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486353 | |||||||
| chr17:45486441 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-41-3916C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486441 | |||||||
| chr17:45486504 | G | A | 1 | a0001c0005t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-41-3979C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486504 | |||||||
| chr17:45486528 | T | C | 21 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(18): Show |
24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-4003A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486528 | |||||||
| chr17:45486560 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-41-4035G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486560 | |||||||
| chr17:45486573 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-41-4048G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486573 | |||||||
| chr17:45486583 | A | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18966.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-41-4058T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486583 | |||||||
| chr17:45486585 | T | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-41-4060A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486585 | |||||||
| chr17:45486586 | T | A | 4 | a0001c0001t0003g0146 a0001c0001t0003g0147 a0001c0001t0003g0148 others(1): Show |
4 | HG01123.hp1 HG01192.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-4061A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486586 | |||||||
| chr17:45486856 | T | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(23): Show |
30 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.-42+3796A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486856 | |||||||
| chr17:45486991 | C | T | 21 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(18): Show |
24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-42+3661G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486991 | |||||||
| chr17:45487131 | G | A | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-42+3521C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45487131 | |||||||
| chr17:45487160 | A | T | 1 | a0001c0005t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-42+3492T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45487160 | |||||||
| chr17:45487193 | C | T | 3 | a0001c0004t0001g0049 a0001c0004t0001g0050 a0001c0004t0001g0051 |
3 | HG02717.hp2 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-42+3459G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45487193 | |||||||
| chr17:45487411 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-42+3241C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45487411 | |||||||
| chr17:45487744 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-42+2908C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45487744 | |||||||
| chr17:45488057 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-42+2595C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488057 | |||||||
| chr17:45488233 | T | C | 21 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(18): Show |
24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-42+2419A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488233 | |||||||
| chr17:45488324 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(44): Show |
69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-42+2328A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488324 | |||||||
| chr17:45488409 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-42+2243T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488409 | |||||||
| chr17:45488474 | G | A | 22 | a0001c0001t0001g0077 a0001c0002t0001g0075 a0001c0002t0002g0010 others(19): Show |
25 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-42+2178C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488474 | |||||||
| chr17:45488495 | T | G | 1 | a0001c0002t0002g0074 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-42+2157A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488495 | |||||||
| chr17:45488540 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-42+2112T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488540 | |||||||
| chr17:45488565 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0199 a0001c0001t0001g0200 |
4 | HG00738.hp1 HG01943.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+2087T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488565 | |||||||
| chr17:45488631 | C | T | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-42+2021G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488631 | |||||||
| chr17:45488640 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.-42+2012A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488640 | |||||||
| chr17:45488669 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-42+1983G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488669 | |||||||
| chr17:45488680 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-42+1972G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488680 | |||||||
| chr17:45488704 | C | T | 1 | a0001c0002t0002g0060 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-42+1948G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488704 | |||||||
| chr17:45488796 | G | A | 1 | a0001c0001t0003g0033 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-42+1856C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488796 | |||||||
| chr17:45488939 | A | C | 1 | a0001c0001t0009g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-42+1713T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488939 | |||||||
| chr17:45489042 | A | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0192 a0001c0001t0001g0193 others(5): Show |
10 | HG01168.hp2 HG01169.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42+1610T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489042 | |||||||
| chr17:45489063 | GACTTGGG others(3): Show |
G | 1 | a0005c0007t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-42+1579_-42+1588d others(12): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489063 | |||||||
| chr17:45489276 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-42+1376T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489276 | |||||||
| chr17:45489322 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-42+1330A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489322 | |||||||
| chr17:45489328 | G | A | 3 | a0001c0005t0001g0242 a0001c0005t0001g0243 a0001c0013t0001g0079 |
3 | HG02559.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-42+1324C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489328 | |||||||
| chr17:45489565 | A | G | 23 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0002t0001g0075 others(20): Show |
26 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.-42+1087T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489565 | |||||||
| chr17:45489600 | G | A | 4 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(1): Show |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+1052C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489600 | |||||||
| chr17:45489603 | G | C | 6 | a0001c0001t0001g0054 a0001c0004t0001g0049 a0001c0004t0001g0050 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+1049C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489603 | |||||||
| chr17:45489618 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-42+1034C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489618 | |||||||
| chr17:45489622 | C | T | 2 | a0001c0005t0001g0242 a0001c0005t0001g0243 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-42+1030G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489622 | |||||||
| chr17:45489623 | C | G | 2 | a0001c0005t0001g0242 a0001c0005t0001g0243 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-42+1029G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489623 | |||||||
| chr17:45489692 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-42+960T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489692 | |||||||
| chr17:45489775 | G | T | 1 | a0001c0005t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-42+877C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489775 | |||||||
| chr17:45489781 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-42+871C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489781 | |||||||
| chr17:45489809 | T | G | 17 | a0001c0002t0002g0010 a0001c0002t0002g0020 a0001c0002t0002g0060 others(14): Show |
20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.-42+843A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489809 | |||||||
| chr17:45489828 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-42+824C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489828 | |||||||
| chr17:45489855 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-42+797C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489855 | |||||||
| chr17:45489941 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-42+711C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489941 | |||||||
| chr17:45489961 | T | A | 2 | a0001c0001t0001g0190 a0001c0001t0011g0189 |
2 | HG01358.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-42+691A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489961 | |||||||
| chr17:45489971 | C | G | 18 | a0001c0002t0001g0075 a0001c0002t0002g0010 a0001c0002t0002g0020 others(15): Show |
21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-42+681G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489971 | |||||||
| chr17:45490030 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-42+622G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490030 | |||||||
| chr17:45490118 | G | C | 3 | a0001c0001t0001g0056 a0002c0003t0001g0009 a0002c0003t0001g0055 |
5 | HG02896.hp2 HG02897.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+534C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490118 | |||||||
| chr17:45490140 | G | T | 4 | a0001c0001t0004g0018 a0001c0001t0004g0041 a0001c0001t0004g0042 others(1): Show |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+512C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490140 | |||||||
| chr17:45490179 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(176): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-42+473T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490179 | |||||||
| chr17:45490259 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-42+393C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490259 | |||||||
| chr17:45490329 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-42+323C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490329 | |||||||
| chr17:45490341 | G | C | 2 | a0001c0005t0001g0242 a0001c0005t0001g0243 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-42+311C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490341 | |||||||
| chr17:45490360 | A | C | 1 | a0001c0009t0012g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-42+292T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490360 | |||||||
| chr17:45490372 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-42+280T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490372 | |||||||
| chr17:45490641 | C | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0047 others(11): Show |
17 | HG01243.hp1 HG02257.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42+11G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490641 |