Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 257068 |
| ensemblid | ENSG00000240891.8 |
| hgncid | 26462 |
| symbol | PLCXD2 |
| name | phosphatidylinositol specific phospholipase C X domain containing 2 |
| refseq_nuc | NM_001413064.1 |
| refseq_prot | NP_001399993.1 |
| ensembl_nuc | ENST00000636933.2 |
| ensembl_prot | ENSP00000490816.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 111674676 |
| end | 111727007 |
| strand | + |
| ver | v1.2 |
| region | chr3:111674676-111727007 |
| region5000 | chr3:111669676-111732007 |
| regionname0 | PLCXD2_chr3_111674676_111727007 |
| regionname5000 | PLCXD2_chr3_111669676_111732007 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 341 | 312 | 83 | 61 | 112 | 14 | 40 | 91 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | MLAVR others(336): Show |
chr3 | 111669676 | 111732007 |
| a0002 | 0/0 | 341 | 8 | 0 | 0 | 8 | 0 | 0 | 8 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | MLAVR others(336): Show |
chr3 | 111669676 | 111732007 |
| a0003 | 0/0 | 341 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | MLAVR others(336): Show |
chr3 | 111669676 | 111732007 |
| a0004 | 0/0 | 341 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | MLAVR others(336): Show |
chr3 | 111669676 | 111732007 |
| a0005 | 0/0 | 341 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | MLAVR others(336): Show |
chr3 | 111669676 | 111732007 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1023 | 310 | 83 | 60 | 112 | 13 | 40 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | ATGCT others(1018): Show |
chr3 | 111669676 | 111732007 | ||
| a0001c0003 | 0/0 | 1023 | 2 | 0 | 1 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | ATGCT others(1018): Show |
chr3 | 111669676 | 111732007 | ||
| a0002c0002 | 0/0 | 1023 | 8 | 0 | 0 | 8 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | ATGCT others(1018): Show |
chr3 | 111669676 | 111732007 | ||
| a0003c0004 | 0/0 | 1023 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | ATGCT others(1018): Show |
chr3 | 111669676 | 111732007 | ||
| a0004c0005 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | ATGCT others(1018): Show |
chr3 | 111669676 | 111732007 | ||
| a0005c0006 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | ATGCT others(1018): Show |
chr3 | 111669676 | 111732007 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7738 | 76 | 3 | 17 | 44 | 4 | 8 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0002 | 0/0 | 7726 | 56 | 0 | 12 | 33 | 2 | 9 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0003 | 0/1 | 7730 | 47 | 33 | 7 | 1 | 1 | 4 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0004 | 0/0 | 7726 | 37 | 15 | 7 | 6 | 2 | 7 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0005 | 0/0 | 7729 | 12 | 0 | 1 | 10 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7724): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0006 | 0/0 | 7742 | 12 | 0 | 5 | 6 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7737): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0007 | 1/0 | 7721 | 8 | 2 | 4 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7716): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0008 | 0/0 | 7730 | 6 | 6 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0009 | 0/0 | 7738 | 5 | 0 | 0 | 0 | 0 | 5 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0010 | 0/0 | 7738 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0011 | 0/0 | 7726 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0012 | 0/0 | 7734 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7729): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0013 | 0/0 | 7734 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7729): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0014 | 0/0 | 7730 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0015 | 0/0 | 7730 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0016 | 0/0 | 7734 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7729): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0017 | 0/0 | 7738 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0019 | 0/0 | 7721 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7716): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0020 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0021 | 0/0 | 7725 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7720): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0022 | 0/0 | 7725 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7720): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0023 | 0/0 | 7726 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0024 | 0/0 | 7726 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0025 | 0/0 | 7726 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0026 | 0/0 | 7730 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0027 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0028 | 0/0 | 7730 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0029 | 0/0 | 7730 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0030 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0031 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0032 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7725): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0033 | 0/0 | 7734 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7729): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0034 | 0/0 | 7734 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7729): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0035 | 0/0 | 7734 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7729): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0036 | 0/0 | 7738 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0037 | 0/0 | 7738 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0038 | 0/0 | 7738 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0039 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0040 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0043 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0044 | 0/0 | 7738 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0045 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0046 | 0/0 | 7738 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0047 | 0/0 | 7738 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0048 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0049 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0050 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0051 | 0/0 | 7726 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0001c0001t0052 | 0/0 | 7726 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0001c0003t0011 | 0/0 | 7726 | 2 | 0 | 1 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0002c0002t0002 | 0/0 | 7726 | 7 | 0 | 0 | 7 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0002c0002t0042 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0003c0004t0002 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0003c0004t0041 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7721): Show |
chr3 | 111669676 | 111732007 |
| a0004c0005t0001 | 0/0 | 7738 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| a0005c0006t0018 | 0/0 | 7738 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | GCTGG others(7733): Show |
chr3 | 111669676 | 111732007 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 1 | 2 | 10 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0007g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0007g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0007g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0009g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0009g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0009g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0009g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0010g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0010g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0010g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0011g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0012g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0012g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0013g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0013g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0013g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0014g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0015g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0015g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0016g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0016g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0017g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0017g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0019g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0020g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0021g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0022g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0023g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0024g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0025g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0026g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0027g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0028g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0029g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0030g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0031g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0032g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0033g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0034g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0035g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0036g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0037g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0038g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0039g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0040g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0043g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0044g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0045g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0046g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0047g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0048g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0049g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0050g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0051g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0001t0052g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0003t0011g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0001c0003t0011g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0002c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0002c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0002c0002t0042g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0003c0004t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0003c0004t0041g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0004c0005t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| a0005c0006t0018g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00099 | hp2 | a0001 | c0001 | t0026 | g0018 | EUR | GBR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00140 | hp1 | a0001 | c0001 | t0040 | g0068 | EUR | GBR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00140 | hp2 | a0001 | c0003 | t0011 | g0166 | EUR | GBR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0006 | EUR | FIN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | FIN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00408 | hp1 | a0001 | c0001 | t0021 | g0218 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00609 | hp2 | a0003 | c0004 | t0041 | g0067 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0225 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00738 | hp2 | a0004 | c0005 | t0001 | g0019 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01081 | hp2 | a0001 | c0001 | t0028 | g0094 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01106 | hp1 | a0001 | c0001 | t0011 | g0226 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01168 | hp2 | a0001 | c0001 | t0013 | g0192 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0191 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01192 | hp2 | a0001 | c0003 | t0011 | g0167 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01243 | hp2 | a0001 | c0001 | t0029 | g0103 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0014 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0014 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0041 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0127 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0025 | EUR | IBS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0081 | EUR | IBS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0025 | EUR | IBS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01884 | hp2 | a0001 | c0001 | t0030 | g0246 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01934 | hp2 | a0001 | c0001 | t0013 | g0007 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0009 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0204 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01981 | hp2 | a0001 | c0001 | t0023 | g0004 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02027 | hp1 | a0001 | c0001 | t0046 | g0141 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02040 | hp2 | a0001 | c0001 | t0022 | g0190 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02055 | hp1 | a0001 | c0001 | t0025 | g0046 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0217 | EAS | CDX | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CDX | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02257 | hp1 | a0001 | c0001 | t0034 | g0052 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02258 | hp2 | a0001 | c0001 | t0014 | g0099 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02280 | hp2 | a0001 | c0001 | t0027 | g0244 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02300 | hp1 | a0001 | c0001 | t0007 | g0107 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02451 | hp2 | a0001 | c0001 | t0038 | g0232 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0243 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0188 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0111 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0197 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02647 | hp1 | a0001 | c0001 | t0031 | g0184 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02698 | hp1 | a0001 | c0001 | t0045 | g0210 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02717 | hp1 | a0001 | c0001 | t0036 | g0091 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02717 | hp2 | a0001 | c0001 | t0032 | g0185 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02735 | hp2 | a0001 | c0001 | t0052 | g0239 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02738 | hp2 | a0001 | c0001 | t0009 | g0123 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02809 | hp1 | a0005 | c0006 | t0018 | g0108 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02818 | hp2 | a0001 | c0001 | t0012 | g0181 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02886 | hp1 | a0001 | c0001 | t0017 | g0202 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02895 | hp1 | a0001 | c0001 | t0033 | g0247 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0050 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03041 | hp2 | a0001 | c0001 | t0035 | g0053 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03098 | hp2 | a0001 | c0001 | t0017 | g0095 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0037 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0207 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03209 | hp2 | a0001 | c0001 | t0019 | g0036 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03225 | hp2 | a0001 | c0001 | t0016 | g0235 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03239 | hp2 | a0001 | c0001 | t0051 | g0110 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03453 | hp1 | a0001 | c0001 | t0020 | g0049 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03486 | hp1 | a0001 | c0001 | t0016 | g0208 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0229 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03669 | hp2 | a0001 | c0001 | t0049 | g0153 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0170 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0189 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03834 | hp2 | a0001 | c0001 | t0009 | g0125 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0026 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0038 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03942 | hp1 | a0001 | c0001 | t0039 | g0203 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG04115 | hp2 | a0001 | c0001 | t0009 | g0100 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | YRI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | YRI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18945 | hp2 | a0001 | c0001 | t0010 | g0062 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18966 | hp1 | a0002 | c0002 | t0042 | g0066 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18968 | hp1 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18968 | hp2 | a0001 | c0001 | t0047 | g0146 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18975 | hp2 | a0001 | c0001 | t0010 | g0171 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18979 | hp2 | a0001 | c0001 | t0037 | g0159 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18988 | hp1 | a0001 | c0001 | t0044 | g0006 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19002 | hp2 | a0001 | c0001 | t0010 | g0071 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0129 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19081 | hp1 | a0001 | c0001 | t0010 | g0070 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19084 | hp1 | a0001 | c0001 | t0050 | g0193 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19084 | hp2 | a0001 | c0001 | t0043 | g0145 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | YRI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ASW | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ASW | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA20805 | hp1 | a0001 | c0001 | t0048 | g0117 | EUR | TSI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA20905 | hp1 | a0001 | c0001 | t0009 | g0209 | SAS | GIH | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0101 | SAS | GIH | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02109 | hp2 | a0001 | c0001 | t0015 | g0242 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0048 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0182 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0183 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | USA | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA18955 | hp2 | a0001 | c0001 | t0006 | g0213 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| NA21309 | hp2 | a0001 | c0001 | t0024 | g0178 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0043 | REF | REF | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0206 | REF | REF | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111675366 | C | G | 2 | a0002 a0003 |
10 | HG00609.hp2 NA18945.hp1 NA18955.hp1 others(7): Show |
missense_variant | MODERATE | c.121C>G | p.Pro41Ala | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/4 | 691/7721 | 121/1026 | 41/341 | chr3 | 111675366 | |||
| chr3:111708093 | C | T | 1 | a0004 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.331C>T | p.Arg111Cys | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/4 | 901/7721 | 331/1026 | 111/341 | chr3 | 111708093 | |||
| chr3:111713905 | T | C | 1 | a0002 | 8 | NA18945.hp1 NA18955.hp1 NA18966.hp1 others(5): Show |
missense_variant | MODERATE | c.643T>C | p.Cys215Arg | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/4 | 1213/7721 | 643/1026 | 215/341 | chr3 | 111713905 | |||
| chr3:111713957 | C | T | 1 | a0005 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.695C>T | p.Ala232Val | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/4 | 1265/7721 | 695/1026 | 232/341 | chr3 | 111713957 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111675401 | A | G | 1 | a0005c0006 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.156A>G | p.Ala52Ala | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/4 | 726/7721 | 156/1026 | 52/341 | chr3 | 111675401 | |||
| chr3:111713958 | G | A | 1 | a0001c0003 | 2 | HG00140.hp2 HG01192.hp2 |
synonymous_variant | LOW | c.696G>A | p.Ala232Ala | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/4 | 1266/7721 | 696/1026 | 232/341 | chr3 | 111713958 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111674834 | C | T | 1 | a0001c0001t0052 | 1 | HG02735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-412C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/4 | 412 | chr3 | 111674834 | ||||||
| chr3:111674954 | A | C | 1 | a0001c0001t0051 | 1 | HG03239.hp2 | 5_prime_UTR_variant | MODIFIER | c.-292A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/4 | 292 | chr3 | 111674954 | ||||||
| chr3:111720926 | G | A | 1 | a0005c0006t0018 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*44G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 44 | chr3 | 111720926 | ||||||
| chr3:111721030 | A | G | 1 | a0001c0001t0009 | 5 | HG02738.hp2 HG03704.hp1 HG03834.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*148A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 148 | chr3 | 111721030 | ||||||
| chr3:111721053 | G | C | 1 | a0001c0001t0010 | 4 | NA18945.hp2 NA18975.hp2 NA19002.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*171G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 171 | chr3 | 111721053 | ||||||
| chr3:111721107 | C | T | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(51): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*225C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 225 | chr3 | 111721107 | ||||||
| chr3:111721378 | A | G | 1 | a0001c0001t0050 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*496A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 496 | chr3 | 111721378 | ||||||
| chr3:111721629 | T | G | 1 | a0001c0001t0020 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*747T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 747 | chr3 | 111721629 | ||||||
| chr3:111721842 | C | T | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(17): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*960C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 960 | chr3 | 111721842 | ||||||
| chr3:111721979 | G | A | 1 | a0001c0001t0040 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1097G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1097 | chr3 | 111721979 | ||||||
| chr3:111722128 | AT | A | 3 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0022 |
14 | HG00408.hp1 HG01952.hp2 HG02040.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1256delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1256 | INFO_REALIGN_3_PRIME | chr3 | 111722128 | |||||
| chr3:111722141 | C | T | 1 | a0001c0001t0049 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1259C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1259 | chr3 | 111722141 | ||||||
| chr3:111722164 | G | A | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(51): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*1282G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1282 | chr3 | 111722164 | ||||||
| chr3:111722182 | G | GATTGACT others(1): Show |
6 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0016 others(3): Show |
11 | HG01168.hp2 HG01169.hp2 HG01934.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1303_*1304insGACT others(4): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1304 | INFO_REALIGN_3_PRIME | chr3 | 111722182 | |||||
| chr3:111722182 | G | GATTGACT others(5): Show |
17 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(14): Show |
100 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1303_*1304insGACT others(8): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1304 | INFO_REALIGN_3_PRIME | chr3 | 111722182 | |||||
| chr3:111722182 | G | GATTGACT others(9): Show |
1 | a0001c0001t0006 | 12 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1303_*1304insGACT others(12): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1304 | INFO_REALIGN_3_PRIME | chr3 | 111722182 | |||||
| chr3:111722184 | T | TTGAC | 13 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(10): Show |
76 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1303_*1304insGACT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1304 | INFO_REALIGN_3_PRIME | chr3 | 111722184 | |||||
| chr3:111722186 | T | G | 16 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(13): Show |
114 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1304T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1304 | chr3 | 111722186 | ||||||
| chr3:111722188 | T | C | 16 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(13): Show |
114 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1306T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1306 | chr3 | 111722188 | ||||||
| chr3:111722190 | T | G | 1 | a0001c0001t0022 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1308T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1308 | chr3 | 111722190 | ||||||
| chr3:111722192 | T | C | 1 | a0001c0001t0022 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1310T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1310 | chr3 | 111722192 | ||||||
| chr3:111722213 | T | G | 1 | a0001c0001t0044 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1331T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1331 | chr3 | 111722213 | ||||||
| chr3:111722227 | T | C | 1 | a0001c0001t0026 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1345T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1345 | chr3 | 111722227 | ||||||
| chr3:111722368 | C | G | 3 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0032 |
6 | HG02559.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1486C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1486 | chr3 | 111722368 | ||||||
| chr3:111722407 | A | G | 1 | a0001c0001t0025 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1525A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1525 | chr3 | 111722407 | ||||||
| chr3:111722477 | G | A | 3 | a0001c0001t0014 a0001c0001t0036 a0005c0006t0018 |
4 | HG02258.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1595G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1595 | chr3 | 111722477 | ||||||
| chr3:111722570 | T | G | 1 | a0001c0001t0023 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1688T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1688 | chr3 | 111722570 | ||||||
| chr3:111722825 | G | A | 11 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0016 others(8): Show |
68 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1943G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1943 | chr3 | 111722825 | ||||||
| chr3:111723213 | G | T | 1 | a0001c0001t0039 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2331G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 2331 | chr3 | 111723213 | ||||||
| chr3:111723467 | A | G | 1 | a0001c0001t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2585A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 2585 | chr3 | 111723467 | ||||||
| chr3:111723483 | C | G | 1 | a0001c0001t0038 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2601C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 2601 | chr3 | 111723483 | ||||||
| chr3:111723505 | G | A | 1 | a0001c0001t0027 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2623G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 2623 | chr3 | 111723505 | ||||||
| chr3:111723765 | G | A | 1 | a0001c0001t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2883G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 2883 | chr3 | 111723765 | ||||||
| chr3:111723949 | G | A | 1 | a0001c0001t0024 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3067G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3067 | chr3 | 111723949 | ||||||
| chr3:111723970 | C | T | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*3088C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3088 | chr3 | 111723970 | ||||||
| chr3:111724076 | T | A | 3 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0032 |
6 | HG02559.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3194T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3194 | chr3 | 111724076 | ||||||
| chr3:111724112 | A | G | 5 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0025 others(2): Show |
41 | HG00639.hp2 HG01071.hp2 HG01168.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3230A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3230 | chr3 | 111724112 | ||||||
| chr3:111724147 | G | A | 3 | a0001c0001t0014 a0001c0001t0036 a0005c0006t0018 |
4 | HG02258.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3265G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3265 | chr3 | 111724147 | ||||||
| chr3:111724156 | A | G | 34 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(31): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*3274A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3274 | chr3 | 111724156 | ||||||
| chr3:111724484 | T | C | 1 | a0001c0001t0028 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3602T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3602 | chr3 | 111724484 | ||||||
| chr3:111724801 | T | G | 1 | a0001c0001t0029 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3919T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3919 | chr3 | 111724801 | ||||||
| chr3:111724900 | T | C | 5 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0025 others(2): Show |
41 | HG00639.hp2 HG01071.hp2 HG01168.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4018T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4018 | chr3 | 111724900 | ||||||
| chr3:111724920 | A | C | 1 | a0002c0002t0042 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4038A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4038 | chr3 | 111724920 | ||||||
| chr3:111724937 | C | A | 1 | a0001c0001t0039 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4055C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4055 | chr3 | 111724937 | ||||||
| chr3:111724984 | G | C | 3 | a0001c0001t0014 a0001c0001t0036 a0005c0006t0018 |
4 | HG02258.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4102G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4102 | chr3 | 111724984 | ||||||
| chr3:111725216 | T | C | 1 | a0001c0001t0026 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4334T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4334 | chr3 | 111725216 | ||||||
| chr3:111725247 | C | G | 1 | a0001c0001t0030 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4365C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4365 | chr3 | 111725247 | ||||||
| chr3:111725470 | C | A | 1 | a0003c0004t0041 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4588C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4588 | chr3 | 111725470 | ||||||
| chr3:111725634 | C | T | 6 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0017 others(3): Show |
10 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4752C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4752 | chr3 | 111725634 | ||||||
| chr3:111725952 | G | A | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*5070G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5070 | chr3 | 111725952 | ||||||
| chr3:111726039 | C | T | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(12): Show |
113 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*5157C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5157 | chr3 | 111726039 | ||||||
| chr3:111726058 | T | TACCTG | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(51): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*5178_*5179insCTGA others(1): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5179 | INFO_REALIGN_3_PRIME | chr3 | 111726058 | |||||
| chr3:111726130 | C | A | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(11): Show |
112 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*5248C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5248 | chr3 | 111726130 | ||||||
| chr3:111726142 | C | T | 1 | a0001c0001t0047 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5260C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5260 | chr3 | 111726142 | ||||||
| chr3:111726188 | G | A | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(51): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*5306G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5306 | chr3 | 111726188 | ||||||
| chr3:111726325 | T | C | 1 | a0001c0001t0033 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5443T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5443 | chr3 | 111726325 | ||||||
| chr3:111726424 | G | C | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(49): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*5542G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5542 | chr3 | 111726424 | ||||||
| chr3:111726424 | G | T | 2 | a0001c0001t0008 a0001c0001t0035 |
7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5542G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5542 | chr3 | 111726424 | ||||||
| chr3:111726493 | G | C | 1 | a0001c0001t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5611G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5611 | chr3 | 111726493 | ||||||
| chr3:111726573 | G | A | 1 | a0001c0001t0045 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5691G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5691 | chr3 | 111726573 | ||||||
| chr3:111726699 | T | C | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(11): Show |
112 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*5817T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5817 | chr3 | 111726699 | ||||||
| chr3:111726820 | T | G | 5 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0022 others(2): Show |
16 | HG00408.hp1 HG01952.hp2 HG02027.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5938T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5938 | chr3 | 111726820 | ||||||
| chr3:111726865 | G | A | 1 | a0001c0001t0014 | 2 | HG02258.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5983G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5983 | chr3 | 111726865 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:111675559 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.163+151G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111675559 | |||||||
| chr3:111675694 | T | G | 1 | a0002c0002t0002g0035 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.163+286T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111675694 | |||||||
| chr3:111675772 | CACAA | C | 6 | a0001c0001t0004g0008 a0001c0001t0004g0245 a0001c0001t0008g0243 others(3): Show |
9 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+369_163+372del others(4): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111675772 | ||||||
| chr3:111675857 | A | G | 1 | a0001c0001t0015g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+449A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111675857 | |||||||
| chr3:111675882 | G | A | 6 | a0001c0001t0004g0008 a0001c0001t0004g0245 a0001c0001t0008g0243 others(3): Show |
9 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+474G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111675882 | |||||||
| chr3:111676130 | G | T | 3 | a0001c0001t0003g0033 a0001c0001t0003g0240 a0001c0001t0003g0241 |
4 | HG02922.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+722G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676130 | |||||||
| chr3:111676325 | A | T | 1 | a0001c0001t0052g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.163+917A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676325 | |||||||
| chr3:111676360 | G | A | 2 | a0001c0001t0014g0037 a0001c0001t0019g0036 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.163+952G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676360 | |||||||
| chr3:111676549 | C | T | 9 | a0001c0001t0003g0032 a0001c0001t0003g0231 a0001c0001t0003g0233 others(6): Show |
10 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+1141C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676549 | |||||||
| chr3:111676578 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.163+1170G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676578 | |||||||
| chr3:111676671 | T | G | 1 | a0001c0001t0006g0039 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.163+1263T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676671 | |||||||
| chr3:111676707 | A | G | 7 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0228 others(4): Show |
7 | HG00639.hp2 HG01106.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+1299A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676707 | |||||||
| chr3:111676721 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.163+1313T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676721 | |||||||
| chr3:111676761 | T | G | 1 | a0001c0001t0001g0017 | 2 | HG02080.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.163+1353T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676761 | |||||||
| chr3:111676864 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.163+1456G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676864 | |||||||
| chr3:111676999 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0006g0009 a0001c0001t0006g0041 |
4 | HG01358.hp1 HG01943.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+1591G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676999 | |||||||
| chr3:111677033 | G | A | 1 | a0001c0001t0003g0042 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.163+1625G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111677033 | |||||||
| chr3:111677378 | G | A | 4 | a0001c0001t0004g0008 a0001c0001t0004g0245 a0001c0001t0008g0243 others(1): Show |
7 | HG02280.hp2 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+1970G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111677378 | |||||||
| chr3:111677543 | G | T | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+2135G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111677543 | |||||||
| chr3:111677916 | G | A | 9 | a0001c0001t0003g0032 a0001c0001t0003g0231 a0001c0001t0003g0233 others(6): Show |
10 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+2508G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111677916 | |||||||
| chr3:111677920 | G | A | 4 | a0001c0001t0004g0008 a0001c0001t0004g0245 a0001c0001t0008g0243 others(1): Show |
7 | HG02280.hp2 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+2512G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111677920 | |||||||
| chr3:111678129 | C | T | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+2721C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111678129 | |||||||
| chr3:111678639 | G | A | 1 | a0001c0001t0003g0231 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.163+3231G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111678639 | |||||||
| chr3:111679075 | G | GT | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+3674dupT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111679075 | ||||||
| chr3:111679082 | T | TA | 5 | a0001c0001t0003g0018 a0001c0001t0004g0004 a0001c0001t0006g0044 others(2): Show |
8 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+3679dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111679082 | ||||||
| chr3:111679357 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.163+3949T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679357 | |||||||
| chr3:111679375 | G | T | 1 | a0001c0001t0002g0223 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.163+3967G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679375 | |||||||
| chr3:111679536 | A | T | 1 | a0001c0001t0002g0177 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.163+4128A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679536 | |||||||
| chr3:111679588 | G | A | 2 | a0001c0001t0005g0186 a0001c0001t0005g0187 |
2 | NA19003.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.163+4180G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679588 | |||||||
| chr3:111679774 | G | A | 10 | a0001c0001t0003g0032 a0001c0001t0003g0231 a0001c0001t0003g0233 others(7): Show |
11 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+4366G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679774 | |||||||
| chr3:111679777 | G | A | 12 | a0001c0001t0003g0018 a0001c0001t0003g0028 a0001c0001t0003g0179 others(9): Show |
19 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.163+4369G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679777 | |||||||
| chr3:111680021 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.163+4613G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680021 | |||||||
| chr3:111680041 | A | T | 14 | a0001c0001t0003g0018 a0001c0001t0003g0028 a0001c0001t0003g0179 others(11): Show |
21 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.163+4633A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680041 | |||||||
| chr3:111680228 | A | T | 2 | a0001c0001t0001g0175 a0001c0001t0003g0176 |
2 | HG01496.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.163+4820A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680228 | |||||||
| chr3:111680268 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(91): Show |
117 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.163+4860A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680268 | |||||||
| chr3:111680362 | C | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0054 others(80): Show |
110 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+4954C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680362 | |||||||
| chr3:111680457 | TG | T | 3 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 |
3 | HG02559.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.163+5050delG | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680457 | |||||||
| chr3:111680571 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.163+5163A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680571 | |||||||
| chr3:111680720 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.163+5312A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680720 | |||||||
| chr3:111680762 | T | C | 14 | a0001c0001t0003g0018 a0001c0001t0003g0028 a0001c0001t0003g0179 others(11): Show |
21 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.163+5354T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680762 | |||||||
| chr3:111680845 | T | A | 2 | a0001c0001t0030g0246 a0001c0001t0033g0247 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.163+5437T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680845 | |||||||
| chr3:111681010 | C | CA | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+5608dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111681010 | ||||||
| chr3:111681081 | A | G | 6 | a0001c0001t0002g0219 a0001c0001t0005g0217 a0001c0001t0005g0220 others(3): Show |
6 | HG00408.hp1 HG02040.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+5673A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681081 | |||||||
| chr3:111681096 | T | C | 1 | a0001c0001t0035g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163+5688T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681096 | |||||||
| chr3:111681178 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.163+5770C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681178 | |||||||
| chr3:111681315 | C | T | 13 | a0001c0001t0003g0018 a0001c0001t0003g0028 a0001c0001t0003g0179 others(10): Show |
20 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.163+5907C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681315 | |||||||
| chr3:111681440 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.163+6032T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681440 | |||||||
| chr3:111681548 | C | T | 1 | a0001c0001t0003g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.163+6140C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681548 | |||||||
| chr3:111681651 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(91): Show |
117 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.163+6243T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681651 | |||||||
| chr3:111681799 | T | C | 53 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0054 others(50): Show |
77 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.163+6391T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681799 | |||||||
| chr3:111681856 | C | T | 2 | a0001c0001t0001g0019 a0004c0005t0001g0019 |
2 | HG00738.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.163+6448C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681856 | |||||||
| chr3:111681933 | C | A | 2 | a0001c0001t0014g0037 a0001c0001t0019g0036 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.163+6525C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681933 | |||||||
| chr3:111681993 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.163+6585C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681993 | |||||||
| chr3:111682091 | G | A | 2 | a0001c0001t0003g0087 a0001c0001t0004g0088 |
2 | HG00735.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.163+6683G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682091 | |||||||
| chr3:111682142 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.163+6734G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682142 | |||||||
| chr3:111682268 | A | G | 1 | a0001c0001t0005g0216 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.163+6860A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682268 | |||||||
| chr3:111682364 | T | A | 1 | a0001c0001t0012g0181 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.163+6956T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682364 | |||||||
| chr3:111682372 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.163+6964T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682372 | |||||||
| chr3:111682893 | C | T | 2 | a0001c0001t0002g0173 a0001c0001t0052g0239 |
2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.163+7485C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682893 | |||||||
| chr3:111682979 | A | T | 1 | a0001c0001t0034g0052 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.163+7571A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682979 | |||||||
| chr3:111682993 | C | T | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+7585C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682993 | |||||||
| chr3:111683002 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0003g0047 a0001c0001t0015g0048 others(3): Show |
6 | HG00738.hp2 HG01517.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+7594G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683002 | |||||||
| chr3:111683050 | C | T | 1 | a0001c0001t0020g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.163+7642C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683050 | |||||||
| chr3:111683088 | A | C | 1 | a0001c0001t0015g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+7680A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683088 | |||||||
| chr3:111683110 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.163+7702G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683110 | |||||||
| chr3:111683156 | A | G | 1 | a0001c0001t0003g0237 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163+7748A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683156 | |||||||
| chr3:111683184 | T | A | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.163+7776T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683184 | |||||||
| chr3:111683215 | T | C | 6 | a0001c0001t0001g0019 a0001c0001t0003g0047 a0001c0001t0015g0048 others(3): Show |
6 | HG00738.hp2 HG01517.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+7807T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683215 | |||||||
| chr3:111683218 | C | T | 1 | a0001c0001t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.163+7810C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683218 | |||||||
| chr3:111683531 | T | A | 1 | a0001c0001t0030g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.163+8123T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683531 | |||||||
| chr3:111683637 | A | G | 1 | a0001c0001t0003g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.163+8229A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683637 | |||||||
| chr3:111683715 | A | G | 5 | a0001c0001t0003g0045 a0001c0001t0003g0113 a0001c0001t0004g0112 others(2): Show |
5 | HG01192.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+8307A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683715 | |||||||
| chr3:111683753 | A | G | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+8345A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683753 | |||||||
| chr3:111683849 | C | T | 2 | a0001c0001t0014g0037 a0001c0001t0019g0036 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.163+8441C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683849 | |||||||
| chr3:111683851 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.163+8443C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683851 | |||||||
| chr3:111684056 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.163+8648G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684056 | |||||||
| chr3:111684175 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163+8767C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684175 | |||||||
| chr3:111684327 | T | TA | 19 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0173 others(16): Show |
26 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.163+8938dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111684327 | ||||||
| chr3:111684327 | TA | T | 9 | a0001c0001t0001g0083 a0001c0001t0001g0109 a0001c0001t0001g0118 others(6): Show |
9 | HG01515.hp2 HG02040.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+8938delA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111684327 | ||||||
| chr3:111684377 | G | A | 1 | a0001c0001t0032g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163+8969G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684377 | |||||||
| chr3:111684403 | C | G | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+8995C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684403 | |||||||
| chr3:111684451 | TGAGACTA others(90): Show |
T | 1 | a0001c0001t0002g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.163+9050_163+9146d others(99): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111684451 | ||||||
| chr3:111684527 | G | A | 6 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0150 others(3): Show |
6 | HG03017.hp1 HG03041.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+9119G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684527 | |||||||
| chr3:111684668 | T | A | 6 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(3): Show |
7 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+9260T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684668 | |||||||
| chr3:111684703 | A | C | 1 | a0001c0001t0005g0221 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.163+9295A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684703 | |||||||
| chr3:111685037 | G | T | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+9629G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685037 | |||||||
| chr3:111685120 | A | C | 1 | a0001c0001t0006g0172 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.163+9712A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685120 | |||||||
| chr3:111685164 | C | T | 2 | a0001c0001t0002g0214 a0001c0001t0006g0213 |
2 | HG01978.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.163+9756C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685164 | |||||||
| chr3:111685207 | A | T | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+9799A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685207 | |||||||
| chr3:111685263 | C | T | 1 | a0001c0001t0030g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.163+9855C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685263 | |||||||
| chr3:111685636 | A | G | 1 | a0001c0001t0016g0235 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.163+10228A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685636 | |||||||
| chr3:111685656 | T | C | 11 | a0001c0001t0003g0023 a0001c0001t0003g0089 a0001c0001t0003g0090 others(8): Show |
12 | HG01081.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+10248T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685656 | |||||||
| chr3:111685916 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.163+10508C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685916 | |||||||
| chr3:111685962 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.163+10554T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685962 | |||||||
| chr3:111686021 | C | T | 1 | a0001c0001t0010g0171 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.163+10613C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686021 | |||||||
| chr3:111686163 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.163+10755A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686163 | |||||||
| chr3:111686175 | T | C | 1 | a0001c0001t0033g0247 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.163+10767T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686175 | |||||||
| chr3:111686250 | C | T | 10 | a0001c0001t0003g0032 a0001c0001t0003g0231 a0001c0001t0003g0233 others(7): Show |
11 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+10842C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686250 | |||||||
| chr3:111686468 | T | G | 7 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0189 others(4): Show |
12 | HG01168.hp2 HG01169.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+11060T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686468 | |||||||
| chr3:111686504 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.163+11096T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686504 | |||||||
| chr3:111686560 | G | T | 100 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0022 others(97): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.163+11152G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686560 | |||||||
| chr3:111686769 | T | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(236): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.163+11361T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686769 | |||||||
| chr3:111686868 | A | C | 1 | a0001c0001t0005g0205 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.163+11460A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686868 | |||||||
| chr3:111686951 | G | A | 1 | a0001c0001t0021g0218 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.163+11543G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686951 | |||||||
| chr3:111687064 | C | T | 87 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0054 others(84): Show |
114 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.163+11656C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687064 | |||||||
| chr3:111687068 | G | A | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+11660G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687068 | |||||||
| chr3:111687097 | T | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(93): Show |
122 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.163+11689T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687097 | |||||||
| chr3:111687179 | T | A | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+11771T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687179 | |||||||
| chr3:111687241 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(80): Show |
105 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.163+11833A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687241 | |||||||
| chr3:111687449 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.163+12041G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687449 | |||||||
| chr3:111687570 | A | T | 1 | a0001c0001t0009g0170 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.163+12162A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687570 | |||||||
| chr3:111687661 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.163+12253A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687661 | |||||||
| chr3:111687665 | G | GT | 17 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0230 others(14): Show |
18 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.163+12263dupT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111687665 | ||||||
| chr3:111687684 | CT | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(94): Show |
123 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.163+12290delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111687684 | ||||||
| chr3:111687687 | T | TC | 3 | a0001c0001t0030g0246 a0001c0001t0031g0184 a0001c0001t0033g0247 |
3 | HG01884.hp2 HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.163+12279_163+1228 others(5): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687687 | |||||||
| chr3:111687688 | T | C | 19 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0109 others(16): Show |
21 | HG00735.hp1 HG01099.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.163+12280T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687688 | |||||||
| chr3:111687689 | T | C | 3 | a0001c0001t0003g0042 a0001c0001t0009g0125 a0001c0001t0009g0170 |
3 | HG01257.hp1 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.163+12281T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687689 | |||||||
| chr3:111687748 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.163+12340G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687748 | |||||||
| chr3:111687813 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.163+12405T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687813 | |||||||
| chr3:111688045 | G | C | 1 | a0001c0001t0003g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.163+12637G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688045 | |||||||
| chr3:111688317 | C | A | 1 | a0001c0001t0002g0126 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.163+12909C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688317 | |||||||
| chr3:111688335 | G | A | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+12927G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688335 | |||||||
| chr3:111688451 | G | A | 2 | a0001c0001t0030g0246 a0001c0001t0033g0247 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.163+13043G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688451 | |||||||
| chr3:111688463 | T | C | 2 | a0001c0001t0004g0024 a0001c0001t0004g0127 |
3 | HG01168.hp1 HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.163+13055T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688463 | |||||||
| chr3:111688646 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.163+13238C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688646 | |||||||
| chr3:111688719 | C | T | 1 | a0002c0002t0002g0013 | 3 | NA18945.hp1 NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.163+13311C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688719 | |||||||
| chr3:111688807 | C | T | 16 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0230 others(13): Show |
17 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.163+13399C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688807 | |||||||
| chr3:111688854 | CAAT | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0230 a0001c0001t0003g0047 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+13447_163+1344 others(7): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688854 | |||||||
| chr3:111688893 | T | TTA | 3 | a0001c0001t0001g0077 a0001c0001t0002g0078 a0001c0001t0003g0238 |
3 | HG01255.hp2 HG03098.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.163+13498_163+1349 others(6): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111688893 | ||||||
| chr3:111689044 | A | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0230 others(12): Show |
16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.163+13636A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111689044 | |||||||
| chr3:111689623 | G | A | 1 | a0001c0001t0002g0057 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.163+14215G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111689623 | |||||||
| chr3:111689708 | G | A | 2 | a0001c0001t0008g0050 a0001c0001t0008g0051 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.163+14300G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111689708 | |||||||
| chr3:111690119 | A | G | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+14711A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111690119 | |||||||
| chr3:111690134 | T | TA | 121 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(118): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.163+14731dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111690134 | ||||||
| chr3:111690251 | G | A | 3 | a0001c0001t0003g0033 a0001c0001t0003g0240 a0001c0001t0003g0241 |
4 | HG02922.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+14843G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111690251 | |||||||
| chr3:111690478 | G | A | 1 | a0001c0001t0004g0127 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163+15070G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111690478 | |||||||
| chr3:111690631 | C | A | 3 | a0001c0001t0001g0034 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.163+15223C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111690631 | |||||||
| chr3:111690727 | C | T | 4 | a0001c0001t0004g0008 a0001c0001t0004g0245 a0001c0001t0014g0037 others(1): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+15319C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111690727 | |||||||
| chr3:111691050 | T | A | 2 | a0001c0001t0001g0121 a0001c0001t0006g0039 |
2 | NA19057.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.163+15642T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691050 | |||||||
| chr3:111691072 | AAAG | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0230 a0001c0001t0003g0047 others(3): Show |
6 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+15668_163+1567 others(7): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111691072 | ||||||
| chr3:111691177 | C | T | 3 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 |
4 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+15769C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691177 | |||||||
| chr3:111691200 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.163+15792T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691200 | |||||||
| chr3:111691214 | G | C | 3 | a0001c0001t0001g0034 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.163+15806G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691214 | |||||||
| chr3:111691235 | A | G | 1 | a0001c0001t0032g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163+15827A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691235 | |||||||
| chr3:111691690 | A | G | 1 | a0001c0001t0002g0012 | 3 | HG00733.hp1 HG00735.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.164-16236A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691690 | |||||||
| chr3:111691902 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.164-16024A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691902 | |||||||
| chr3:111691962 | C | A | 1 | a0001c0001t0003g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-15964C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691962 | |||||||
| chr3:111691976 | A | C | 3 | a0001c0001t0001g0034 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164-15950A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691976 | |||||||
| chr3:111692041 | G | T | 3 | a0001c0001t0001g0034 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164-15885G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692041 | |||||||
| chr3:111692187 | A | G | 15 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0230 others(12): Show |
16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-15739A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692187 | |||||||
| chr3:111692294 | C | T | 2 | a0001c0001t0003g0238 a0001c0001t0007g0107 |
2 | HG02300.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.164-15632C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692294 | |||||||
| chr3:111692337 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.164-15589G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692337 | |||||||
| chr3:111692420 | A | G | 1 | a0001c0001t0003g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-15506A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692420 | |||||||
| chr3:111692543 | G | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.164-15383G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692543 | |||||||
| chr3:111692677 | A | C | 1 | a0001c0001t0003g0106 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.164-15249A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692677 | |||||||
| chr3:111692965 | C | T | 15 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0230 others(12): Show |
16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-14961C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692965 | |||||||
| chr3:111693015 | G | A | 5 | a0001c0001t0001g0055 a0001c0001t0002g0010 a0001c0001t0002g0058 others(2): Show |
7 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-14911G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693015 | |||||||
| chr3:111693300 | T | C | 1 | a0001c0001t0019g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.164-14626T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693300 | |||||||
| chr3:111693419 | C | T | 1 | a0001c0001t0009g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.164-14507C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693419 | |||||||
| chr3:111693426 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(80): Show |
105 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.164-14500C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693426 | |||||||
| chr3:111693678 | T | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0230 others(12): Show |
16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-14248T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693678 | |||||||
| chr3:111693691 | C | T | 10 | a0001c0001t0003g0032 a0001c0001t0003g0231 a0001c0001t0003g0233 others(7): Show |
11 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-14235C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693691 | |||||||
| chr3:111693942 | A | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(232): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.164-13984A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693942 | |||||||
| chr3:111694011 | G | A | 1 | a0001c0001t0004g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.164-13915G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694011 | |||||||
| chr3:111694085 | A | G | 1 | a0001c0001t0006g0163 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.164-13841A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694085 | |||||||
| chr3:111694130 | C | A | 1 | a0001c0001t0006g0009 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.164-13796C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694130 | |||||||
| chr3:111694168 | C | G | 15 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0230 others(12): Show |
16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-13758C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694168 | |||||||
| chr3:111694241 | G | A | 1 | a0001c0001t0031g0184 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.164-13685G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694241 | |||||||
| chr3:111694423 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0230 a0001c0001t0003g0047 others(3): Show |
6 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-13503G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694423 | |||||||
| chr3:111694471 | C | CT | 19 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0054 others(16): Show |
20 | HG00738.hp2 HG01099.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.164-13442dupT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111694471 | ||||||
| chr3:111694471 | CT | C | 9 | a0001c0001t0002g0165 a0001c0001t0003g0018 a0001c0001t0004g0004 others(6): Show |
15 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.164-13442delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111694471 | ||||||
| chr3:111694832 | T | G | 1 | a0001c0001t0024g0178 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164-13094T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694832 | |||||||
| chr3:111695073 | C | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0230 a0001c0001t0003g0047 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-12853C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695073 | |||||||
| chr3:111695090 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.164-12836A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695090 | |||||||
| chr3:111695142 | AT | A | 16 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0109 others(13): Show |
18 | HG00735.hp1 HG01099.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.164-12777delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111695142 | ||||||
| chr3:111695160 | T | TA | 198 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.164-12745dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111695160 | ||||||
| chr3:111695160 | T | TAA | 16 | a0001c0001t0001g0056 a0001c0001t0001g0077 a0001c0001t0001g0083 others(13): Show |
17 | HG01981.hp1 HG02080.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.164-12746_164-1274 others(6): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111695160 | ||||||
| chr3:111695486 | T | G | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-12440T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695486 | |||||||
| chr3:111695524 | C | T | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-12402C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695524 | |||||||
| chr3:111695559 | A | G | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-12367A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695559 | |||||||
| chr3:111695613 | C | A | 4 | a0001c0001t0003g0028 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-12313C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695613 | |||||||
| chr3:111695651 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.164-12275A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695651 | |||||||
| chr3:111695726 | A | G | 15 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0230 others(12): Show |
16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-12200A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695726 | |||||||
| chr3:111695737 | G | C | 14 | a0001c0001t0003g0032 a0001c0001t0003g0231 a0001c0001t0003g0233 others(11): Show |
18 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-12189G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695737 | |||||||
| chr3:111695765 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.164-12161G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695765 | |||||||
| chr3:111695996 | T | C | 1 | a0001c0001t0003g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164-11930T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695996 | |||||||
| chr3:111696092 | A | G | 13 | a0001c0001t0001g0019 a0001c0001t0001g0230 a0001c0001t0003g0028 others(10): Show |
14 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.164-11834A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696092 | |||||||
| chr3:111696108 | G | A | 2 | a0001c0001t0004g0024 a0001c0001t0004g0127 |
3 | HG01168.hp1 HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.164-11818G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696108 | |||||||
| chr3:111696126 | G | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(249): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.164-11800G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696126 | |||||||
| chr3:111696200 | G | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0230 a0001c0001t0003g0047 others(4): Show |
7 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-11726G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696200 | |||||||
| chr3:111696252 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.164-11674G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696252 | |||||||
| chr3:111696336 | T | G | 3 | a0001c0001t0001g0130 a0001c0001t0002g0156 a0001c0001t0006g0129 |
3 | HG00621.hp2 NA18953.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.164-11590T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696336 | |||||||
| chr3:111696379 | G | T | 1 | a0001c0001t0050g0193 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.164-11547G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696379 | |||||||
| chr3:111696464 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.164-11462A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696464 | |||||||
| chr3:111696600 | A | G | 9 | a0001c0001t0001g0019 a0001c0001t0001g0230 a0001c0001t0003g0047 others(6): Show |
9 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-11326A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696600 | |||||||
| chr3:111696632 | T | C | 1 | a0001c0001t0010g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.164-11294T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696632 | |||||||
| chr3:111696749 | C | A | 4 | a0001c0001t0003g0106 a0001c0001t0009g0100 a0001c0001t0009g0209 others(1): Show |
4 | HG02698.hp1 HG04115.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-11177C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696749 | |||||||
| chr3:111696749 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.164-11177C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696749 | |||||||
| chr3:111697208 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.164-10718G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697208 | |||||||
| chr3:111697293 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0230 a0001c0001t0003g0047 others(3): Show |
6 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-10633G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697293 | |||||||
| chr3:111697307 | A | T | 10 | a0001c0001t0003g0032 a0001c0001t0003g0231 a0001c0001t0003g0233 others(7): Show |
11 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-10619A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697307 | |||||||
| chr3:111697406 | A | G | 1 | a0001c0001t0004g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.164-10520A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697406 | |||||||
| chr3:111697415 | G | C | 4 | a0001c0001t0004g0008 a0001c0001t0004g0245 a0001c0001t0014g0037 others(1): Show |
7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-10511G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697415 | |||||||
| chr3:111697463 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(103): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.164-10463A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697463 | |||||||
| chr3:111697604 | A | C | 16 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0109 others(13): Show |
18 | HG00735.hp1 HG01099.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.164-10322A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697604 | |||||||
| chr3:111697841 | C | T | 2 | a0001c0001t0030g0246 a0001c0001t0033g0247 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.164-10085C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697841 | |||||||
| chr3:111697843 | G | GTATT | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.164-10077_164-1007 others(8): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111697843 | ||||||
| chr3:111698867 | C | G | 1 | a0001c0001t0031g0184 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.164-9059C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111698867 | |||||||
| chr3:111698916 | A | G | 3 | a0001c0001t0004g0011 a0001c0001t0004g0073 a0001c0001t0035g0053 |
5 | HG02145.hp1 HG02647.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-9010A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111698916 | |||||||
| chr3:111698942 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.164-8984T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111698942 | |||||||
| chr3:111698946 | A | G | 1 | a0001c0001t0031g0184 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.164-8980A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111698946 | |||||||
| chr3:111699258 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.164-8668T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699258 | |||||||
| chr3:111699282 | G | A | 1 | a0001c0001t0024g0178 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164-8644G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699282 | |||||||
| chr3:111699356 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.164-8570G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699356 | |||||||
| chr3:111699524 | A | G | 1 | a0001c0001t0025g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164-8402A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699524 | |||||||
| chr3:111699678 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.164-8248G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699678 | |||||||
| chr3:111699720 | A | T | 1 | a0001c0001t0003g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.164-8206A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699720 | |||||||
| chr3:111699777 | A | G | 1 | a0001c0001t0004g0245 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-8149A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699777 | |||||||
| chr3:111699891 | T | C | 1 | a0001c0001t0005g0217 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.164-8035T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699891 | |||||||
| chr3:111700126 | G | A | 1 | a0001c0001t0038g0232 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164-7800G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700126 | |||||||
| chr3:111700143 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.164-7783T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700143 | |||||||
| chr3:111700154 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.164-7772C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700154 | |||||||
| chr3:111700213 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.164-7713A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700213 | |||||||
| chr3:111700288 | G | A | 1 | a0001c0001t0032g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.164-7638G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700288 | |||||||
| chr3:111700483 | T | C | 1 | a0001c0001t0002g0174 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.164-7443T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700483 | |||||||
| chr3:111700610 | GA | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
110 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.164-7306delA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111700610 | ||||||
| chr3:111700639 | G | T | 48 | a0001c0001t0003g0016 a0001c0001t0003g0032 a0001c0001t0003g0033 others(45): Show |
68 | HG00408.hp1 HG00639.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.164-7287G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700639 | |||||||
| chr3:111700668 | G | A | 12 | a0001c0001t0001g0133 a0001c0001t0002g0002 a0001c0001t0002g0021 others(9): Show |
21 | HG00438.hp2 HG00621.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.164-7258G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700668 | |||||||
| chr3:111700697 | A | C | 1 | a0001c0001t0046g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.164-7229A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700697 | |||||||
| chr3:111700845 | C | T | 1 | a0001c0001t0002g0061 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.164-7081C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700845 | |||||||
| chr3:111700851 | G | T | 2 | a0001c0001t0013g0191 a0001c0001t0013g0192 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.164-7075G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700851 | |||||||
| chr3:111700883 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0124 a0001c0001t0001g0131 others(4): Show |
8 | HG01071.hp1 HG01109.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-7043C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700883 | |||||||
| chr3:111700970 | G | A | 2 | a0001c0001t0007g0111 a0001c0001t0007g0197 |
2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.164-6956G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700970 | |||||||
| chr3:111701531 | C | T | 1 | a0001c0001t0015g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-6395C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111701531 | |||||||
| chr3:111701564 | C | T | 3 | a0001c0001t0002g0021 a0001c0001t0002g0057 a0001c0001t0002g0074 |
4 | NA18952.hp2 NA18970.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-6362C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111701564 | |||||||
| chr3:111701671 | T | C | 1 | a0001c0001t0019g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.164-6255T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111701671 | |||||||
| chr3:111701714 | A | G | 45 | a0001c0001t0002g0137 a0001c0001t0003g0018 a0001c0001t0003g0023 others(42): Show |
48 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.164-6212A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111701714 | |||||||
| chr3:111701972 | T | C | 3 | a0001c0001t0002g0059 a0001c0001t0002g0064 a0001c0001t0002g0065 |
3 | HG02015.hp1 HG02080.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.164-5954T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111701972 | |||||||
| chr3:111702486 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.164-5440T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702486 | |||||||
| chr3:111702567 | C | T | 5 | a0001c0001t0003g0016 a0001c0001t0003g0030 a0001c0001t0003g0195 others(2): Show |
8 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-5359C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702567 | |||||||
| chr3:111702651 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-5275C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702651 | |||||||
| chr3:111702663 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.164-5263T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702663 | |||||||
| chr3:111702840 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.164-5086A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702840 | |||||||
| chr3:111702858 | C | T | 39 | a0001c0001t0003g0023 a0001c0001t0003g0028 a0001c0001t0003g0030 others(36): Show |
42 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.164-5068C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702858 | |||||||
| chr3:111702958 | T | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.164-4968T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702958 | |||||||
| chr3:111703047 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.164-4879T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111703047 | |||||||
| chr3:111703216 | G | A | 3 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0158 |
3 | HG00741.hp1 HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.164-4710G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111703216 | |||||||
| chr3:111703516 | A | G | 1 | a0001c0001t0004g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.164-4410A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111703516 | |||||||
| chr3:111703855 | C | A | 1 | a0001c0001t0009g0209 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.164-4071C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111703855 | |||||||
| chr3:111704189 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.164-3737G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704189 | |||||||
| chr3:111704202 | G | GGGGTAGT others(15): Show |
3 | a0001c0001t0003g0016 a0001c0001t0003g0195 a0001c0001t0004g0196 |
5 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-3723_164-3702d others(24): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111704202 | ||||||
| chr3:111704246 | A | G | 1 | a0001c0001t0004g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.164-3680A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704246 | |||||||
| chr3:111704282 | G | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.164-3644G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704282 | |||||||
| chr3:111704337 | C | T | 1 | a0001c0001t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.164-3589C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704337 | |||||||
| chr3:111704495 | A | C | 48 | a0001c0001t0003g0018 a0001c0001t0003g0023 a0001c0001t0003g0028 others(45): Show |
51 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.164-3431A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704495 | |||||||
| chr3:111704566 | T | G | 45 | a0001c0001t0003g0018 a0001c0001t0003g0023 a0001c0001t0003g0028 others(42): Show |
48 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.164-3360T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704566 | |||||||
| chr3:111704783 | A | G | 30 | a0001c0001t0003g0016 a0001c0001t0003g0032 a0001c0001t0003g0033 others(27): Show |
49 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.164-3143A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704783 | |||||||
| chr3:111704817 | A | AT | 49 | a0001c0001t0002g0065 a0001c0001t0003g0018 a0001c0001t0003g0023 others(46): Show |
52 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.164-3094dupT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111704817 | ||||||
| chr3:111704922 | C | A | 1 | a0001c0001t0003g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.164-3004C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704922 | |||||||
| chr3:111704936 | C | T | 4 | a0001c0001t0003g0045 a0001c0001t0003g0047 a0001c0001t0003g0113 others(1): Show |
4 | HG01192.hp1 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-2990C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704936 | |||||||
| chr3:111705055 | G | T | 1 | a0003c0004t0041g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.164-2871G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705055 | |||||||
| chr3:111705064 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.164-2862G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705064 | |||||||
| chr3:111705066 | C | T | 30 | a0001c0001t0003g0016 a0001c0001t0003g0032 a0001c0001t0003g0033 others(27): Show |
49 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.164-2860C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705066 | |||||||
| chr3:111705257 | T | C | 2 | a0001c0001t0003g0045 a0001c0001t0003g0047 |
2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.164-2669T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705257 | |||||||
| chr3:111705318 | C | T | 1 | a0001c0001t0015g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-2608C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705318 | |||||||
| chr3:111705377 | G | T | 1 | a0001c0001t0015g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.164-2549G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705377 | |||||||
| chr3:111705481 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.164-2445G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705481 | |||||||
| chr3:111705682 | G | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.164-2244G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705682 | |||||||
| chr3:111706050 | G | T | 1 | a0001c0001t0002g0115 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.164-1876G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706050 | |||||||
| chr3:111706185 | A | G | 1 | a0001c0001t0032g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.164-1741A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706185 | |||||||
| chr3:111706530 | A | G | 1 | a0001c0001t0015g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-1396A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706530 | |||||||
| chr3:111706558 | G | T | 1 | a0001c0001t0002g0165 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.164-1368G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706558 | |||||||
| chr3:111706754 | C | A | 1 | a0001c0001t0001g0027 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.164-1172C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706754 | |||||||
| chr3:111706754 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.164-1172C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706754 | |||||||
| chr3:111706812 | C | CA | 4 | a0001c0001t0001g0015 a0001c0001t0001g0116 a0001c0001t0001g0194 others(1): Show |
6 | HG02300.hp1 NA18963.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-1099dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111706812 | ||||||
| chr3:111706812 | C | CAAA | 6 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-1101_164-1099d others(5): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111706812 | ||||||
| chr3:111706812 | CA | C | 108 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(105): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.164-1099delA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111706812 | ||||||
| chr3:111706812 | CAA | C | 7 | a0001c0001t0002g0074 a0001c0001t0003g0241 a0001c0001t0004g0038 others(4): Show |
7 | HG01358.hp2 HG02602.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-1100_164-1099d others(4): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111706812 | ||||||
| chr3:111706918 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.164-1008C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706918 | |||||||
| chr3:111707141 | G | A | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-785G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707141 | |||||||
| chr3:111707445 | A | G | 1 | a0001c0001t0004g0245 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-481A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707445 | |||||||
| chr3:111707479 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.164-447A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707479 | |||||||
| chr3:111707819 | A | G | 9 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(6): Show |
9 | HG02559.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-107A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707819 | |||||||
| chr3:111707843 | T | G | 24 | a0001c0001t0003g0023 a0001c0001t0003g0028 a0001c0001t0003g0042 others(21): Show |
26 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.164-83T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707843 | |||||||
| chr3:111707860 | A | T | 4 | a0001c0001t0008g0031 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
5 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-66A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707860 | |||||||
| chr3:111708447 | G | C | 1 | a0001c0001t0004g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.624+61G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708447 | |||||||
| chr3:111708512 | T | A | 1 | a0001c0001t0002g0065 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.624+126T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708512 | |||||||
| chr3:111708523 | C | T | 1 | a0005c0006t0018g0108 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.624+137C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708523 | |||||||
| chr3:111708583 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.624+197T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708583 | |||||||
| chr3:111708608 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0002g0002 a0001c0001t0002g0003 others(49): Show |
72 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.624+222G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708608 | |||||||
| chr3:111708876 | G | A | 7 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(4): Show |
7 | HG02559.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+490G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708876 | |||||||
| chr3:111708988 | C | T | 1 | a0001c0001t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.624+602C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708988 | |||||||
| chr3:111708994 | G | GGAAGAGG others(3): Show |
15 | a0001c0001t0003g0030 a0001c0001t0003g0180 a0001c0001t0003g0215 others(12): Show |
16 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.624+610_624+619dup others(10): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 111708994 | ||||||
| chr3:111709090 | TG | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
119 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.624+706delG | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 111709090 | ||||||
| chr3:111709091 | G | GA | 50 | a0001c0001t0001g0135 a0001c0001t0002g0002 a0001c0001t0002g0003 others(47): Show |
69 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.624+705_624+706ins others(1): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709091 | |||||||
| chr3:111709091 | GGA | G | 4 | a0001c0001t0001g0116 a0001c0001t0010g0071 a0001c0001t0012g0181 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+706_624+707del others(2): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709091 | |||||||
| chr3:111709092 | G | A | 134 | a0001c0001t0001g0135 a0001c0001t0002g0002 a0001c0001t0002g0003 others(131): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.624+706G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709092 | |||||||
| chr3:111709290 | A | T | 1 | a0001c0001t0003g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.624+904A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709290 | |||||||
| chr3:111709467 | T | TAC | 77 | a0001c0001t0003g0016 a0001c0001t0003g0018 a0001c0001t0003g0023 others(74): Show |
99 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.624+1096_624+1097d others(4): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 111709467 | ||||||
| chr3:111709531 | C | T | 1 | a0001c0001t0004g0029 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.624+1145C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709531 | |||||||
| chr3:111709620 | A | G | 1 | a0001c0001t0015g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.624+1234A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709620 | |||||||
| chr3:111709680 | G | C | 85 | a0001c0001t0003g0016 a0001c0001t0003g0018 a0001c0001t0003g0023 others(82): Show |
107 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.624+1294G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709680 | |||||||
| chr3:111709733 | A | G | 7 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(4): Show |
7 | HG02559.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+1347A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709733 | |||||||
| chr3:111709919 | A | G | 135 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(132): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.624+1533A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709919 | |||||||
| chr3:111709944 | G | A | 2 | a0001c0001t0004g0029 a0001c0001t0004g0189 |
3 | HG02735.hp1 HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.624+1558G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709944 | |||||||
| chr3:111710021 | C | T | 1 | a0001c0001t0039g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.624+1635C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710021 | |||||||
| chr3:111710064 | C | T | 6 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(3): Show |
6 | HG02559.hp2 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+1678C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710064 | |||||||
| chr3:111710098 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.624+1712G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710098 | |||||||
| chr3:111710163 | C | T | 2 | a0001c0003t0011g0166 a0001c0003t0011g0167 |
2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.624+1777C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710163 | |||||||
| chr3:111710168 | G | A | 1 | a0001c0001t0015g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.624+1782G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710168 | |||||||
| chr3:111710514 | C | T | 2 | a0001c0003t0011g0166 a0001c0003t0011g0167 |
2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.624+2128C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710514 | |||||||
| chr3:111710570 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.624+2184C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710570 | |||||||
| chr3:111710606 | C | T | 2 | a0001c0001t0004g0008 a0001c0001t0004g0245 |
5 | HG02809.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+2220C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710606 | |||||||
| chr3:111710685 | G | A | 50 | a0001c0001t0003g0018 a0001c0001t0003g0023 a0001c0001t0003g0028 others(47): Show |
53 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.624+2299G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710685 | |||||||
| chr3:111710746 | G | C | 2 | a0001c0001t0003g0238 a0001c0001t0003g0240 |
2 | HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.624+2360G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710746 | |||||||
| chr3:111710835 | T | G | 3 | a0001c0001t0014g0037 a0001c0001t0036g0091 a0005c0006t0018g0108 |
3 | HG02717.hp1 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.624+2449T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710835 | |||||||
| chr3:111711009 | A | G | 30 | a0001c0001t0003g0016 a0001c0001t0003g0032 a0001c0001t0003g0033 others(27): Show |
49 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.624+2623A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711009 | |||||||
| chr3:111711220 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.625-2667G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711220 | |||||||
| chr3:111711277 | G | A | 5 | a0001c0001t0003g0045 a0001c0001t0003g0047 a0001c0001t0003g0113 others(2): Show |
5 | HG01192.hp1 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-2610G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711277 | |||||||
| chr3:111711400 | G | A | 1 | a0001c0001t0006g0172 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.625-2487G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711400 | |||||||
| chr3:111711532 | A | T | 2 | a0001c0001t0010g0070 a0001c0001t0010g0071 |
2 | NA19002.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.625-2355A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711532 | |||||||
| chr3:111711788 | A | T | 1 | a0001c0001t0019g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.625-2099A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711788 | |||||||
| chr3:111711874 | A | G | 2 | a0001c0001t0003g0028 a0001c0001t0003g0179 |
3 | HG02055.hp2 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625-2013A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711874 | |||||||
| chr3:111712122 | G | C | 49 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(46): Show |
69 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.625-1765G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712122 | |||||||
| chr3:111712218 | C | A | 1 | a0001c0001t0002g0173 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.625-1669C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712218 | |||||||
| chr3:111712350 | A | G | 1 | a0001c0001t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-1537A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712350 | |||||||
| chr3:111712399 | C | A | 1 | a0001c0001t0004g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.625-1488C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712399 | |||||||
| chr3:111712432 | CT | C | 6 | a0001c0001t0008g0031 a0001c0001t0008g0050 a0001c0001t0008g0051 others(3): Show |
7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-1454delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712432 | |||||||
| chr3:111712475 | C | T | 1 | a0001c0001t0032g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.625-1412C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712475 | |||||||
| chr3:111712505 | C | T | 44 | a0001c0001t0002g0060 a0001c0001t0003g0023 a0001c0001t0003g0028 others(41): Show |
47 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.625-1382C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712505 | |||||||
| chr3:111712577 | G | A | 1 | a0001c0001t0039g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.625-1310G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712577 | |||||||
| chr3:111712601 | C | G | 1 | a0001c0001t0032g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.625-1286C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712601 | |||||||
| chr3:111712630 | A | G | 1 | a0001c0001t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-1257A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712630 | |||||||
| chr3:111712646 | C | A | 6 | a0001c0001t0008g0031 a0001c0001t0008g0050 a0001c0001t0008g0051 others(3): Show |
7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-1241C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712646 | |||||||
| chr3:111712744 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
105 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.625-1143G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712744 | |||||||
| chr3:111712764 | C | T | 1 | a0001c0001t0004g0198 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.625-1123C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712764 | |||||||
| chr3:111712772 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.625-1115T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712772 | |||||||
| chr3:111712971 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
104 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.625-916G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712971 | |||||||
| chr3:111713042 | G | T | 1 | a0001c0001t0001g0072 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.625-845G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713042 | |||||||
| chr3:111713053 | C | T | 24 | a0001c0001t0003g0023 a0001c0001t0003g0028 a0001c0001t0003g0042 others(21): Show |
26 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.625-834C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713053 | |||||||
| chr3:111713355 | A | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0150 a0001c0001t0001g0161 others(1): Show |
4 | NA18964.hp2 NA18988.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-532A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713355 | |||||||
| chr3:111713391 | G | A | 46 | a0001c0001t0003g0018 a0001c0001t0003g0023 a0001c0001t0003g0028 others(43): Show |
49 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.625-496G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713391 | |||||||
| chr3:111713467 | T | A | 2 | a0001c0003t0011g0166 a0001c0003t0011g0167 |
2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.625-420T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713467 | |||||||
| chr3:111713652 | A | G | 4 | a0001c0001t0014g0037 a0001c0001t0014g0099 a0001c0001t0024g0178 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-235A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713652 | |||||||
| chr3:111713816 | G | A | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-71G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713816 | |||||||
| chr3:111713824 | C | T | 5 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-63C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713824 | |||||||
| chr3:111714201 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.866+73C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714201 | |||||||
| chr3:111714205 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.866+77G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714205 | |||||||
| chr3:111714449 | G | A | 1 | a0001c0001t0015g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.866+321G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714449 | |||||||
| chr3:111714481 | T | G | 1 | a0001c0001t0006g0172 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.866+353T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714481 | |||||||
| chr3:111714579 | C | T | 48 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(45): Show |
68 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.866+451C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714579 | |||||||
| chr3:111714647 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.866+519T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714647 | |||||||
| chr3:111714775 | C | T | 1 | a0001c0001t0038g0232 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.866+647C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714775 | |||||||
| chr3:111714823 | C | CAT | 6 | a0001c0001t0008g0031 a0001c0001t0008g0050 a0001c0001t0008g0051 others(3): Show |
7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.866+696_866+697dup others(2): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111714823 | ||||||
| chr3:111714968 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.866+840C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714968 | |||||||
| chr3:111715047 | A | G | 1 | a0002c0002t0002g0013 | 3 | NA18945.hp1 NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.866+919A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715047 | |||||||
| chr3:111715209 | T | C | 1 | a0001c0001t0003g0106 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.866+1081T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715209 | |||||||
| chr3:111715269 | C | G | 29 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0241 others(26): Show |
46 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.866+1141C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715269 | |||||||
| chr3:111715286 | T | C | 1 | a0001c0001t0006g0041 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.866+1158T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715286 | |||||||
| chr3:111715396 | A | G | 1 | a0001c0001t0037g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.866+1268A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715396 | |||||||
| chr3:111715459 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.866+1331G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715459 | |||||||
| chr3:111715597 | G | A | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+1469G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715597 | |||||||
| chr3:111715960 | T | C | 2 | a0001c0001t0006g0044 a0001c0001t0038g0232 |
2 | HG01081.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.866+1832T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715960 | |||||||
| chr3:111715964 | G | C | 1 | a0001c0001t0040g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.866+1836G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715964 | |||||||
| chr3:111716022 | G | A | 1 | a0001c0001t0030g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.866+1894G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716022 | |||||||
| chr3:111716023 | C | T | 1 | a0001c0001t0034g0052 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.866+1895C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716023 | |||||||
| chr3:111716141 | A | T | 2 | a0001c0003t0011g0166 a0001c0003t0011g0167 |
2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.866+2013A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716141 | |||||||
| chr3:111716148 | C | T | 4 | a0001c0001t0014g0037 a0001c0001t0014g0099 a0001c0001t0036g0091 others(1): Show |
4 | HG02258.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+2020C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716148 | |||||||
| chr3:111716190 | G | A | 1 | a0002c0002t0042g0066 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.866+2062G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716190 | |||||||
| chr3:111716271 | C | G | 1 | a0001c0001t0015g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.866+2143C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716271 | |||||||
| chr3:111716276 | G | A | 29 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0241 others(26): Show |
46 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.866+2148G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716276 | |||||||
| chr3:111716571 | T | C | 52 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(49): Show |
72 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.866+2443T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716571 | |||||||
| chr3:111716629 | C | G | 2 | a0001c0001t0017g0095 a0001c0001t0032g0185 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.866+2501C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716629 | |||||||
| chr3:111716635 | G | T | 1 | a0001c0001t0019g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.866+2507G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716635 | |||||||
| chr3:111716700 | A | C | 29 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0241 others(26): Show |
46 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.866+2572A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716700 | |||||||
| chr3:111716738 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.866+2610C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716738 | |||||||
| chr3:111716956 | C | T | 2 | a0001c0001t0014g0037 a0001c0001t0014g0099 |
2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.866+2828C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716956 | |||||||
| chr3:111716969 | G | A | 1 | a0001c0001t0031g0184 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.866+2841G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716969 | |||||||
| chr3:111716993 | C | T | 41 | a0001c0001t0003g0016 a0001c0001t0003g0023 a0001c0001t0003g0028 others(38): Show |
46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.866+2865C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716993 | |||||||
| chr3:111717110 | C | T | 41 | a0001c0001t0003g0016 a0001c0001t0003g0023 a0001c0001t0003g0028 others(38): Show |
46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.866+2982C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717110 | |||||||
| chr3:111717212 | T | C | 1 | a0001c0001t0006g0213 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.866+3084T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717212 | |||||||
| chr3:111717323 | G | T | 4 | a0001c0001t0014g0037 a0001c0001t0014g0099 a0001c0001t0036g0091 others(1): Show |
4 | HG02258.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+3195G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717323 | |||||||
| chr3:111717401 | C | T | 1 | a0001c0001t0015g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.866+3273C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717401 | |||||||
| chr3:111717507 | G | T | 1 | a0001c0001t0038g0232 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.867-3216G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717507 | |||||||
| chr3:111717772 | A | C | 3 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 |
3 | HG02559.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.867-2951A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717772 | |||||||
| chr3:111717793 | A | G | 1 | a0001c0001t0038g0232 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.867-2930A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717793 | |||||||
| chr3:111717990 | CT | C | 86 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(83): Show |
123 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.867-2722delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111717990 | ||||||
| chr3:111718231 | G | A | 1 | a0001c0001t0004g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867-2492G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718231 | |||||||
| chr3:111718281 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.867-2442G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718281 | |||||||
| chr3:111718325 | C | A | 2 | a0001c0001t0014g0037 a0001c0001t0014g0099 |
2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.867-2398C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718325 | |||||||
| chr3:111718329 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.867-2394G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718329 | |||||||
| chr3:111718357 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.867-2366C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718357 | |||||||
| chr3:111718397 | G | A | 6 | a0001c0001t0003g0023 a0001c0001t0003g0089 a0001c0001t0003g0090 others(3): Show |
7 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.867-2326G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718397 | |||||||
| chr3:111718403 | T | C | 1 | a0001c0001t0038g0232 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.867-2320T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718403 | |||||||
| chr3:111718443 | G | C | 1 | a0001c0001t0002g0081 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.867-2280G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718443 | |||||||
| chr3:111718449 | A | G | 1 | a0001c0001t0039g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.867-2274A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718449 | |||||||
| chr3:111718491 | T | TGATA | 17 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0001g0072 others(14): Show |
17 | HG00140.hp2 HG01106.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.867-2192_867-2189d others(6): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718491 | ||||||
| chr3:111718491 | T | TGATAGAT others(1): Show |
6 | a0001c0001t0001g0121 a0001c0001t0001g0161 a0001c0001t0001g0201 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.867-2196_867-2189d others(10): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718491 | ||||||
| chr3:111718491 | TGATA | T | 5 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0012g0181 others(2): Show |
5 | HG01109.hp2 HG02698.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.867-2192_867-2189d others(6): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718491 | ||||||
| chr3:111718519 | AGATAGAT others(9): Show |
A | 2 | a0001c0001t0003g0140 a0001c0001t0015g0242 |
2 | HG02109.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.867-2200_867-2185d others(18): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718519 | ||||||
| chr3:111718523 | AGATAGAT others(5): Show |
A | 10 | a0001c0001t0002g0002 a0001c0001t0003g0028 a0001c0001t0003g0138 others(7): Show |
15 | HG00741.hp1 HG01256.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.867-2196_867-2185d others(14): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718523 | ||||||
| chr3:111718523 | AGATAGAT others(9): Show |
A | 1 | a0001c0001t0039g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.867-2196_867-2181d others(18): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718523 | ||||||
| chr3:111718527 | AGATAGAT others(1): Show |
A | 46 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0150 others(43): Show |
57 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.867-2192_867-2185d others(10): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718527 | ||||||
| chr3:111718529 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.867-2194A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718529 | |||||||
| chr3:111718531 | AGATT | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0022 others(62): Show |
78 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.867-2183_867-2180d others(6): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718531 | ||||||
| chr3:111718535 | T | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.867-2188T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718535 | |||||||
| chr3:111718539 | T | A | 2 | a0001c0001t0002g0084 a0001c0001t0003g0097 |
2 | HG04199.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.867-2184T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718539 | |||||||
| chr3:111718606 | G | A | 2 | a0001c0001t0024g0178 a0001c0001t0030g0246 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.867-2117G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718606 | |||||||
| chr3:111718842 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.867-1881A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718842 | |||||||
| chr3:111718871 | T | A | 6 | a0001c0001t0008g0031 a0001c0001t0008g0050 a0001c0001t0008g0051 others(3): Show |
7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.867-1852T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718871 | |||||||
| chr3:111718907 | C | T | 3 | a0001c0001t0011g0226 a0001c0003t0011g0166 a0001c0003t0011g0167 |
3 | HG00140.hp2 HG01106.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.867-1816C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718907 | |||||||
| chr3:111719030 | C | T | 1 | a0001c0001t0022g0190 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.867-1693C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719030 | |||||||
| chr3:111719031 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0227 |
2 | HG01256.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.867-1692G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719031 | |||||||
| chr3:111719250 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.867-1473T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719250 | |||||||
| chr3:111719268 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.867-1455C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719268 | |||||||
| chr3:111719273 | C | T | 4 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(1): Show |
4 | HG02559.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.867-1450C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719273 | |||||||
| chr3:111719524 | G | T | 1 | a0001c0001t0032g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.867-1199G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719524 | |||||||
| chr3:111719572 | C | T | 2 | a0001c0001t0007g0014 a0001c0001t0007g0107 |
4 | HG01256.hp1 HG01258.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-1151C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719572 | |||||||
| chr3:111719596 | G | A | 48 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(45): Show |
68 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.867-1127G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719596 | |||||||
| chr3:111719797 | T | C | 1 | a0001c0001t0050g0193 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.867-926T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719797 | |||||||
| chr3:111719887 | C | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.867-836C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719887 | |||||||
| chr3:111719907 | A | G | 1 | a0001c0001t0006g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.867-816A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719907 | |||||||
| chr3:111720150 | G | A | 7 | a0001c0001t0008g0031 a0001c0001t0008g0050 a0001c0001t0008g0051 others(4): Show |
8 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.867-573G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111720150 | |||||||
| chr3:111720278 | G | A | 10 | a0001c0001t0012g0181 a0001c0001t0012g0182 a0001c0001t0012g0183 others(7): Show |
10 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.867-445G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111720278 | |||||||
| chr3:111720291 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.867-432T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111720291 | |||||||
| chr3:111720311 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.867-412C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111720311 | |||||||
| chr3:111720696 | C | T | 17 | a0001c0001t0003g0030 a0001c0001t0003g0032 a0001c0001t0003g0033 others(14): Show |
20 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.867-27C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111720696 |