Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84812 |
| ensemblid | ENSG00000115556.14 |
| hgncid | 9062 |
| symbol | PLCD4 |
| name | phospholipase C delta 4 |
| refseq_nuc | NM_032726.4 |
| refseq_prot | NP_116115.1 |
| ensembl_nuc | ENST00000450993.7 |
| ensembl_prot | ENSP00000388631.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 218607899 |
| end | 218637175 |
| strand | + |
| ver | v1.2 |
| region | chr2:218607899-218637175 |
| region5000 | chr2:218602899-218642175 |
| regionname0 | PLCD4_chr2_218607899_218637175 |
| regionname5000 | PLCD4_chr2_218602899_218642175 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 762 | 292 | 90 | 56 | 102 | 8 | 34 | 77 | PLCD4_chr2_218602899_218642175 | PLCD4 | MASLL others(757): Show |
chr2 | 218602899 | 218642175 |
| a0002 | 0/0 | 386 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | MASLL others(381): Show |
chr2 | 218602899 | 218642175 |
| a0003 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | MASLL others(757): Show |
chr2 | 218602899 | 218642175 |
| a0004 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | MASLL others(757): Show |
chr2 | 218602899 | 218642175 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2286 | 174 | 82 | 24 | 45 | 4 | 18 | PLCD4_chr2_218602899_218642175 | PLCD4 | ATGGC others(2281): Show |
chr2 | 218602899 | 218642175 | ||
| a0001c0002 | 0/1 | 2286 | 115 | 5 | 32 | 57 | 4 | 16 | PLCD4_chr2_218602899_218642175 | PLCD4 | ATGGC others(2281): Show |
chr2 | 218602899 | 218642175 | ||
| a0001c0003 | 0/0 | 2286 | 3 | 3 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | ATGGC others(2281): Show |
chr2 | 218602899 | 218642175 | ||
| a0002c0004 | 0/0 | 2286 | 3 | 3 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | ATGGC others(2281): Show |
chr2 | 218602899 | 218642175 | ||
| a0002c0007 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | ATGGC others(2281): Show |
chr2 | 218602899 | 218642175 | ||
| a0003c0006 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | ATGGC others(2281): Show |
chr2 | 218602899 | 218642175 | ||
| a0004c0005 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | ATGGC others(2281): Show |
chr2 | 218602899 | 218642175 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/0 | 3092 | 103 | 69 | 3 | 26 | 0 | 4 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0001c0001t0003 | 0/0 | 3092 | 54 | 1 | 20 | 15 | 4 | 14 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0001c0001t0004 | 0/0 | 3092 | 12 | 12 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0001c0001t0005 | 0/0 | 3092 | 4 | 0 | 0 | 4 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0001c0001t0007 | 0/0 | 3092 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0001c0002t0001 | 0/1 | 3092 | 112 | 4 | 32 | 56 | 4 | 15 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0001c0002t0006 | 0/0 | 3092 | 2 | 1 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0001c0002t0008 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0001c0003t0002 | 0/0 | 3092 | 3 | 3 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0002c0004t0002 | 0/0 | 3092 | 3 | 3 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0002c0007t0002 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0003c0006t0002 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| a0004c0005t0002 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | AGTCA others(3087): Show |
chr2 | 218602899 | 218642175 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0002 | 0/0 | 6 | 0 | 1 | 3 | 1 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0001 | 0/0 | 18 | 0 | 6 | 11 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0006g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0002t0008g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0001c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0002c0004t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0002c0004t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0002c0007t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0003c0006t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| a0004c0005t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0117 | EUR | GBR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0231 | EUR | GBR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0091 | EUR | FIN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0022 | EUR | FIN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | CHS | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | CHS | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | CHS | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | CHS | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00621 | hp1 | a0003 | c0006 | t0002 | g0062 | EAS | CHS | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0202 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0132 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0208 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | PEL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CDX | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | CDX | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0251 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02698 | hp1 | a0001 | c0002 | t0006 | g0114 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02896 | hp2 | a0002 | c0004 | t0002 | g0006 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02897 | hp1 | a0002 | c0004 | t0002 | g0006 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02922 | hp1 | a0001 | c0002 | t0006 | g0010 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03486 | hp1 | a0002 | c0007 | t0002 | g0020 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0250 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0081 | AFR | ESN | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | STU | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | STU | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | BEB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0150 | SAS | BEB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | BEB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0155 | SAS | BEB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0228 | SAS | BEB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | BEB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | BEB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0112 | SAS | STU | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | STU | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0219 | SAS | STU | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | STU | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | YRI | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | YRI | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | CHB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18906 | hp1 | a0002 | c0004 | t0002 | g0026 | AFR | YRI | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | YRI | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18951 | hp1 | a0004 | c0005 | t0002 | g0061 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18987 | hp2 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | LWK | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | LWK | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | LWK | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | LWK | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | YRI | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | YRI | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ASW | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | ASW | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0232 | EUR | TSI | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0144 | EUR | TSI | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | GIH | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | GIH | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | CLM | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | MSL | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | USA | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0249 | AFR | USA | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA18955 | hp2 | a0001 | c0002 | t0008 | g0096 | EAS | JPT | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | USA | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | USA | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | LWK | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | LWK | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0154 | REF | REF | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0198 | REF | REF | PLCD4_chr2_218602899_218642175 | PLCD4 | chr2 | 218602899 | 218642175 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218618746 | C | T | 1 | a0002 | 1 | HG03486.hp1 | stop_gained | HIGH | c.349C>T | p.Arg117* | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/16 | 554/3092 | 349/2289 | 117/762 | chr2 | 218618746 | |||
| chr2:218628174 | C | A | 1 | a0004 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.918C>A | p.Asn306Lys | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/16 | 1123/3092 | 918/2289 | 306/762 | chr2 | 218628174 | |||
| chr2:218630691 | C | A | 1 | a0002 | 3 | HG02896.hp2 HG02897.hp1 NA18906.hp1 |
stop_gained | HIGH | c.1161C>A | p.Cys387* | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 9/16 | 1366/3092 | 1161/2289 | 387/762 | chr2 | 218630691 | |||
| chr2:218635883 | G | A | 1 | a0003 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1984G>A | p.Val662Ile | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 14/16 | 2189/3092 | 1984/2289 | 662/762 | chr2 | 218635883 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218615745 | G | A | 1 | a0001c0003 | 3 | HG02257.hp2 HG03516.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.6G>A | p.Ala2Ala | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 2/16 | 211/3092 | 6/2289 | 2/762 | chr2 | 218615745 | |||
| chr2:218628201 | T | C | 1 | a0001c0002 | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
synonymous_variant | LOW | c.945T>C | p.Cys315Cys | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/16 | 1150/3092 | 945/2289 | 315/762 | chr2 | 218628201 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218608010 | C | T | 1 | a0001c0001t0004 | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-94C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/16 | chr2 | 218608010 | |||||||
| chr2:218608011 | G | A | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-93G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/16 | 7729 | chr2 | 218608011 | ||||||
| chr2:218636605 | G | A | 4 | a0001c0001t0005 a0001c0002t0001 a0001c0002t0006 others(1): Show |
118 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*28G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 16/16 | 28 | chr2 | 218636605 | ||||||
| chr2:218636624 | A | C | 1 | a0001c0002t0008 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*47A>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 16/16 | 47 | chr2 | 218636624 | ||||||
| chr2:218636769 | C | T | 1 | a0001c0001t0007 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*192C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 16/16 | 192 | chr2 | 218636769 | ||||||
| chr2:218636874 | C | T | 1 | a0001c0002t0006 | 2 | HG02698.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*297C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 16/16 | 297 | chr2 | 218636874 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218608139 | C | G | 7 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34+69C>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218608139 | |||||||
| chr2:218608234 | C | T | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG02886.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+164C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218608234 | |||||||
| chr2:218608521 | T | G | 16 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(13): Show |
17 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34+451T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218608521 | |||||||
| chr2:218608695 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-34+625T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218608695 | |||||||
| chr2:218608815 | T | C | 7 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0042 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34+745T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218608815 | |||||||
| chr2:218608939 | C | G | 1 | a0001c0002t0001g0241 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-34+869C>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218608939 | |||||||
| chr2:218608966 | G | A | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG02886.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+896G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218608966 | |||||||
| chr2:218609014 | T | C | 162 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(159): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.-34+944T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218609014 | |||||||
| chr2:218609035 | G | A | 7 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0159 others(4): Show |
9 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34+965G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218609035 | |||||||
| chr2:218609127 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-34+1057C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218609127 | |||||||
| chr2:218609140 | C | CA | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(49): Show |
57 | HG00558.hp2 HG00621.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.-34+1087dupA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 218609140 | ||||||
| chr2:218609191 | A | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0005 others(75): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-34+1121A>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218609191 | |||||||
| chr2:218609193 | C | T | 16 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(13): Show |
17 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34+1123C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218609193 | |||||||
| chr2:218609259 | C | A | 1 | a0001c0002t0001g0090 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-34+1189C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218609259 | |||||||
| chr2:218609277 | T | G | 10 | a0001c0001t0002g0164 a0001c0001t0002g0167 a0001c0001t0002g0168 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34+1207T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218609277 | |||||||
| chr2:218609433 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-34+1363A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218609433 | |||||||
| chr2:218609494 | C | G | 7 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0042 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34+1424C>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218609494 | |||||||
| chr2:218609961 | G | T | 1 | a0001c0002t0001g0158 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-34+1891G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218609961 | |||||||
| chr2:218610020 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-34+1950G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610020 | |||||||
| chr2:218610058 | G | A | 1 | a0001c0001t0003g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-34+1988G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610058 | |||||||
| chr2:218610133 | T | A | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
40 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.-34+2063T>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610133 | |||||||
| chr2:218610134 | A | T | 1 | a0001c0001t0003g0240 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-34+2064A>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610134 | |||||||
| chr2:218610141 | A | T | 1 | a0001c0001t0002g0075 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-34+2071A>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610141 | |||||||
| chr2:218610142 | T | A | 13 | a0001c0001t0002g0164 a0001c0001t0002g0167 a0001c0001t0002g0168 others(10): Show |
13 | HG00280.hp2 HG01257.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-34+2072T>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610142 | |||||||
| chr2:218610153 | G | C | 1 | a0001c0001t0002g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-34+2083G>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610153 | |||||||
| chr2:218610277 | C | A | 7 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34+2207C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610277 | |||||||
| chr2:218610396 | T | C | 1 | a0001c0001t0002g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-34+2326T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610396 | |||||||
| chr2:218610446 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-34+2376T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610446 | |||||||
| chr2:218610487 | G | A | 1 | a0001c0002t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-34+2417G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610487 | |||||||
| chr2:218610507 | C | CA | 15 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0177 others(12): Show |
15 | HG01975.hp2 HG02723.hp2 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34+2446dupA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 218610507 | ||||||
| chr2:218610507 | CA | C | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
40 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.-34+2446delA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 218610507 | ||||||
| chr2:218610575 | G | A | 1 | a0001c0001t0002g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-34+2505G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610575 | |||||||
| chr2:218610685 | T | C | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.-34+2615T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218610685 | |||||||
| chr2:218611723 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-34+3653C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218611723 | |||||||
| chr2:218611887 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-34+3817C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218611887 | |||||||
| chr2:218612144 | G | C | 1 | a0001c0001t0002g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-33-3563G>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218612144 | |||||||
| chr2:218612246 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-33-3461T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218612246 | |||||||
| chr2:218612491 | T | G | 1 | a0001c0001t0002g0074 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-33-3216T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218612491 | |||||||
| chr2:218612600 | C | T | 11 | a0001c0001t0002g0164 a0001c0001t0002g0167 a0001c0001t0002g0168 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33-3107C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218612600 | |||||||
| chr2:218612904 | G | T | 1 | a0001c0001t0002g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-33-2803G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218612904 | |||||||
| chr2:218612922 | G | A | 7 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33-2785G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218612922 | |||||||
| chr2:218613252 | G | A | 1 | a0001c0001t0003g0190 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-33-2455G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218613252 | |||||||
| chr2:218613301 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-33-2406C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218613301 | |||||||
| chr2:218613392 | C | CA | 9 | a0001c0001t0002g0047 a0001c0001t0002g0168 a0001c0001t0003g0039 others(6): Show |
9 | HG00741.hp1 HG02080.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-2294dupA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 218613392 | ||||||
| chr2:218613392 | CA | C | 25 | a0001c0001t0002g0073 a0001c0001t0002g0246 a0001c0001t0002g0248 others(22): Show |
27 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-33-2294delA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 218613392 | ||||||
| chr2:218613392 | CAA | C | 101 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(98): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-33-2295_-33-2294d others(4): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 218613392 | ||||||
| chr2:218613445 | T | G | 1 | a0001c0001t0002g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-33-2262T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218613445 | |||||||
| chr2:218613470 | C | T | 162 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(159): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.-33-2237C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218613470 | |||||||
| chr2:218613570 | T | G | 1 | a0001c0002t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-33-2137T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218613570 | |||||||
| chr2:218613571 | G | T | 1 | a0001c0002t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-33-2136G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218613571 | |||||||
| chr2:218613625 | G | A | 2 | a0001c0001t0002g0020 a0002c0007t0002g0020 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-33-2082G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218613625 | |||||||
| chr2:218613786 | C | T | 2 | a0001c0001t0002g0175 a0001c0002t0001g0157 |
2 | HG02135.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-33-1921C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218613786 | |||||||
| chr2:218613997 | A | G | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
40 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.-33-1710A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218613997 | |||||||
| chr2:218614018 | C | CT | 53 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(50): Show |
58 | HG00558.hp2 HG00621.hp1 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.-33-1676dupT | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 218614018 | ||||||
| chr2:218614089 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-33-1618G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614089 | |||||||
| chr2:218614221 | A | G | 13 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0242 others(10): Show |
13 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33-1486A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614221 | |||||||
| chr2:218614236 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0197 |
3 | HG02630.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-33-1471G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614236 | |||||||
| chr2:218614315 | A | G | 249 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(246): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.-33-1392A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614315 | |||||||
| chr2:218614403 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-33-1304G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614403 | |||||||
| chr2:218614442 | T | C | 37 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(34): Show |
41 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.-33-1265T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614442 | |||||||
| chr2:218614478 | C | T | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-33-1229C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614478 | |||||||
| chr2:218614481 | G | A | 7 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0042 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33-1226G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614481 | |||||||
| chr2:218614524 | C | G | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-33-1183C>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614524 | |||||||
| chr2:218614540 | C | T | 6 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(3): Show |
6 | HG02257.hp2 HG03516.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-1167C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614540 | |||||||
| chr2:218614600 | C | A | 2 | a0001c0001t0002g0246 a0001c0001t0002g0248 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-33-1107C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614600 | |||||||
| chr2:218614601 | C | A | 2 | a0001c0001t0002g0246 a0001c0001t0002g0248 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-33-1106C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614601 | |||||||
| chr2:218614674 | C | A | 1 | a0001c0001t0002g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-33-1033C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614674 | |||||||
| chr2:218614864 | T | C | 11 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0177 others(8): Show |
11 | HG02723.hp2 HG02886.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-33-843T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614864 | |||||||
| chr2:218614962 | C | T | 1 | a0001c0002t0001g0090 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-33-745C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218614962 | |||||||
| chr2:218615057 | T | A | 1 | a0001c0001t0003g0199 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-33-650T>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218615057 | |||||||
| chr2:218615163 | T | C | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
40 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.-33-544T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218615163 | |||||||
| chr2:218615207 | G | A | 14 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0177 others(11): Show |
14 | HG02723.hp2 HG02886.hp2 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33-500G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218615207 | |||||||
| chr2:218615284 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-33-423A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218615284 | |||||||
| chr2:218615362 | G | T | 1 | a0001c0001t0003g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-33-345G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218615362 | |||||||
| chr2:218615397 | T | G | 1 | a0001c0002t0001g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-33-310T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218615397 | |||||||
| chr2:218615423 | G | A | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
40 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.-33-284G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 1/15 | chr2 | 218615423 | |||||||
| chr2:218615897 | G | A | 1 | a0001c0001t0003g0200 | 1 | HG01943.hp1 | splice_region_variant&intron_variant | LOW | c.23-7G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 2/15 | chr2 | 218615897 | |||||||
| chr2:218616081 | G | C | 115 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(112): Show |
144 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.181+19G>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616081 | |||||||
| chr2:218616625 | G | A | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
40 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.181+563G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616625 | |||||||
| chr2:218616726 | T | TATAC | 4 | a0001c0001t0002g0020 a0001c0002t0001g0080 a0001c0002t0001g0087 others(1): Show |
4 | HG03486.hp1 HG03654.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.181+691_181+694dup others(4): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616726 | ||||||
| chr2:218616726 | T | TATACATA others(1): Show |
54 | a0001c0001t0002g0072 a0001c0001t0002g0164 a0001c0001t0002g0167 others(51): Show |
59 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.181+687_181+694dup others(8): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616726 | ||||||
| chr2:218616726 | T | TATACATA others(5): Show |
110 | a0001c0001t0002g0024 a0001c0001t0002g0036 a0001c0001t0002g0071 others(107): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.181+683_181+694dup others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616726 | ||||||
| chr2:218616726 | T | TATACATA others(9): Show |
74 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(71): Show |
83 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.181+679_181+694dup others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616726 | ||||||
| chr2:218616726 | T | TATACATA others(13): Show |
9 | a0001c0001t0002g0021 a0001c0001t0002g0047 a0001c0001t0002g0049 others(6): Show |
10 | HG00642.hp1 HG02083.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+675_181+694dup others(20): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616726 | ||||||
| chr2:218616898 | T | A | 1 | a0001c0002t0001g0108 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.181+836T>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616898 | |||||||
| chr2:218616898 | T | TATATATA others(6): Show |
1 | a0001c0001t0003g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.181+836_181+837ins others(13): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616898 | |||||||
| chr2:218616898 | T | TATATATA others(12): Show |
1 | a0001c0001t0003g0207 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.181+836_181+837ins others(19): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616898 | |||||||
| chr2:218616898 | T | TTA | 11 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0172 others(8): Show |
11 | HG00280.hp2 HG01243.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.181+865_181+866dup others(2): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATA | 22 | a0001c0001t0002g0033 a0001c0001t0002g0056 a0001c0001t0002g0167 others(19): Show |
23 | HG00733.hp2 HG01106.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.181+863_181+866dup others(4): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATA | 10 | a0001c0001t0002g0034 a0001c0001t0002g0164 a0001c0001t0003g0222 others(7): Show |
10 | HG01070.hp2 HG01106.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+861_181+866dup others(6): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(1): Show |
12 | a0001c0001t0002g0057 a0001c0001t0003g0223 a0001c0002t0001g0011 others(9): Show |
13 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.181+859_181+866dup others(8): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(3): Show |
9 | a0001c0001t0002g0047 a0001c0001t0002g0058 a0001c0001t0003g0176 others(6): Show |
9 | HG02683.hp1 HG03239.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.181+857_181+866dup others(10): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(5): Show |
14 | a0001c0001t0002g0008 a0001c0001t0002g0035 a0001c0001t0002g0059 others(11): Show |
15 | HG00597.hp1 HG01070.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.181+855_181+866dup others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(7): Show |
8 | a0001c0001t0002g0060 a0001c0001t0002g0175 a0001c0001t0002g0181 others(5): Show |
9 | HG00741.hp2 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+853_181+866dup others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(9): Show |
10 | a0001c0001t0002g0168 a0001c0001t0003g0196 a0001c0001t0003g0199 others(7): Show |
12 | HG01081.hp2 HG01952.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.181+851_181+866dup others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(11): Show |
7 | a0001c0001t0002g0248 a0001c0001t0003g0229 a0001c0001t0003g0230 others(4): Show |
8 | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.181+849_181+866dup others(18): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(13): Show |
6 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0072 others(3): Show |
7 | HG01993.hp1 HG02976.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+847_181+866dup others(20): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(15): Show |
7 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0003g0232 others(4): Show |
8 | HG02083.hp2 NA18939.hp2 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+845_181+866dup others(22): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(17): Show |
5 | a0001c0001t0002g0049 a0001c0001t0002g0067 a0001c0001t0002g0068 others(2): Show |
5 | HG00558.hp2 HG02083.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.181+843_181+866dup others(24): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(19): Show |
3 | a0001c0001t0002g0070 a0001c0001t0003g0233 a0001c0003t0002g0250 |
3 | HG03516.hp1 NA18960.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.181+841_181+866dup others(26): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTATATAT others(27): Show |
1 | a0001c0001t0003g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(34): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616898 | T | TTTTATAT others(5): Show |
1 | a0001c0002t0001g0155 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.181+837_181+838ins others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616898 | ||||||
| chr2:218616921 | TATATATA others(5): Show |
T | 1 | a0001c0001t0002g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.181+861_181+872del others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616921 | ||||||
| chr2:218616923 | T | G | 1 | a0001c0001t0003g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.181+861T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616923 | |||||||
| chr2:218616923 | T | TAGAGAGA others(9): Show |
1 | a0001c0001t0003g0211 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.181+862_181+863ins others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616923 | ||||||
| chr2:218616923 | TATATAGA others(5): Show |
T | 1 | a0001c0001t0002g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.181+863_181+874del others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616923 | ||||||
| chr2:218616925 | T | G | 3 | a0001c0001t0003g0023 a0001c0001t0003g0211 a0002c0004t0002g0026 |
3 | HG00735.hp1 NA18906.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.181+863T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616925 | |||||||
| chr2:218616925 | T | TAGAGAGA others(5): Show |
1 | a0001c0001t0003g0212 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.181+864_181+865ins others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616925 | ||||||
| chr2:218616925 | T | TAGAGAGA others(9): Show |
1 | a0001c0001t0003g0193 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.181+864_181+865ins others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616925 | ||||||
| chr2:218616925 | TATAGAGA others(5): Show |
T | 2 | a0001c0001t0002g0018 a0001c0001t0002g0021 |
2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.181+865_181+876del others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616925 | ||||||
| chr2:218616925 | TATAGAGA others(7): Show |
T | 1 | a0001c0001t0002g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.181+865_181+878del others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616925 | ||||||
| chr2:218616925 | TATAGAGA others(9): Show |
T | 1 | a0001c0001t0002g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.181+865_181+880del others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616925 | ||||||
| chr2:218616925 | TATAGAGA others(11): Show |
T | 1 | a0001c0001t0002g0007 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.181+865_181+882del others(18): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616925 | ||||||
| chr2:218616927 | T | G | 5 | a0001c0001t0003g0023 a0001c0001t0003g0193 a0001c0001t0003g0211 others(2): Show |
5 | HG00735.hp1 NA18906.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.181+865T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616927 | |||||||
| chr2:218616927 | T | TAGAGAGA others(7): Show |
1 | a0001c0002t0001g0001 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.181+911_181+924dup others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATAGAGA others(3): Show |
1 | a0001c0002t0001g0012 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(10): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATAGAGA others(7): Show |
1 | a0001c0001t0003g0002 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATAGAGA others(9): Show |
1 | a0001c0001t0002g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATAGAGA others(11): Show |
1 | a0001c0002t0001g0001 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(18): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATAGA others(5): Show |
1 | a0001c0001t0002g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATAGA others(7): Show |
1 | a0001c0002t0008g0096 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATAGA others(9): Show |
1 | a0001c0001t0002g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(3): Show |
2 | a0001c0001t0002g0076 a0001c0001t0003g0190 |
2 | HG01891.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(10): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(5): Show |
1 | a0001c0001t0003g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(7): Show |
1 | a0001c0002t0001g0001 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(9): Show |
1 | a0001c0001t0002g0052 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(11): Show |
1 | a0001c0001t0004g0081 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(18): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(13): Show |
1 | a0001c0002t0001g0116 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(20): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(17): Show |
1 | a0001c0001t0004g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(24): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(21): Show |
1 | a0001c0002t0001g0001 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(28): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(3): Show |
2 | a0001c0002t0001g0001 a0001c0002t0001g0004 |
3 | HG01167.hp1 HG01169.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.181+866_181+867ins others(10): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(7): Show |
3 | a0001c0001t0003g0002 a0001c0001t0003g0216 a0001c0002t0006g0114 |
3 | HG00280.hp1 HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(9): Show |
4 | a0001c0001t0002g0003 a0001c0002t0001g0001 a0001c0002t0001g0113 others(1): Show |
4 | HG02165.hp2 NA18977.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.181+866_181+867ins others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(11): Show |
1 | a0001c0001t0002g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(18): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(19): Show |
1 | a0001c0001t0003g0022 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(26): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(5): Show |
1 | a0001c0001t0002g0038 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(7): Show |
3 | a0001c0001t0003g0023 a0001c0001t0003g0194 a0002c0007t0002g0020 |
3 | HG01952.hp1 HG03486.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(9): Show |
2 | a0001c0001t0002g0003 a0001c0001t0004g0009 |
2 | HG03540.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.181+866_181+867ins others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(11): Show |
2 | a0001c0001t0004g0009 a0001c0002t0001g0001 |
2 | HG00621.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(18): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(13): Show |
1 | a0001c0002t0001g0001 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(20): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(7): Show |
3 | a0001c0001t0002g0238 a0001c0001t0003g0210 a0001c0001t0003g0215 |
3 | HG02630.hp2 NA18953.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(9): Show |
3 | a0001c0001t0002g0078 a0001c0001t0003g0237 a0001c0002t0001g0012 |
3 | HG01099.hp2 NA19062.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.181+866_181+867ins others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(11): Show |
2 | a0001c0001t0002g0074 a0001c0001t0003g0022 |
2 | HG00323.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(18): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(13): Show |
2 | a0001c0001t0002g0050 a0001c0002t0001g0001 |
2 | NA19011.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(20): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(15): Show |
2 | a0001c0001t0002g0003 a0001c0001t0002g0073 |
2 | NA18981.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(22): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(17): Show |
1 | a0001c0001t0003g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(24): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(21): Show |
1 | a0001c0001t0005g0192 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(28): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(9): Show |
2 | a0001c0001t0003g0200 a0001c0002t0001g0090 |
2 | HG01943.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.181+866_181+867ins others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(11): Show |
2 | a0001c0001t0003g0002 a0001c0002t0001g0001 |
2 | NA18940.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.181+866_181+867ins others(18): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(13): Show |
1 | a0001c0002t0001g0001 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(20): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(15): Show |
2 | a0001c0001t0002g0053 a0001c0002t0001g0001 |
2 | HG01255.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.181+866_181+867ins others(22): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(11): Show |
1 | a0001c0002t0001g0001 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(18): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(13): Show |
2 | a0001c0001t0002g0079 a0001c0002t0001g0001 |
2 | NA19055.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(20): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(15): Show |
1 | a0001c0002t0001g0108 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(22): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(17): Show |
3 | a0001c0001t0002g0246 a0001c0002t0001g0112 a0001c0002t0001g0117 |
3 | HG00140.hp1 HG04204.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(24): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(19): Show |
2 | a0001c0001t0003g0002 a0001c0002t0001g0121 |
2 | HG00597.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.181+866_181+867ins others(26): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(21): Show |
1 | a0001c0002t0001g0001 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(28): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(27): Show |
1 | a0001c0001t0005g0213 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(34): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(17): Show |
1 | a0001c0002t0001g0241 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(24): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(25): Show |
1 | a0001c0001t0002g0051 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(32): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(19): Show |
1 | a0001c0002t0001g0004 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(26): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(21): Show |
1 | a0001c0001t0003g0002 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(28): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(19): Show |
1 | a0001c0002t0001g0098 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(26): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(21): Show |
1 | a0001c0002t0001g0001 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(28): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(25): Show |
1 | a0001c0002t0001g0111 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(32): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(35): Show |
1 | a0001c0001t0002g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(42): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(21): Show |
1 | a0001c0002t0001g0101 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(28): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(31): Show |
1 | a0001c0001t0003g0204 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(38): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(27): Show |
1 | a0001c0002t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.181+866_181+867ins others(34): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(33): Show |
1 | a0001c0001t0002g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(40): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | T | TATATATA others(29): Show |
1 | a0001c0001t0003g0002 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.181+866_181+867ins others(36): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | TAG | T | 9 | a0001c0001t0002g0055 a0001c0001t0002g0165 a0001c0001t0002g0187 others(6): Show |
9 | HG00639.hp2 HG00741.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+923_181+924del others(2): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | TAGAG | T | 6 | a0001c0001t0002g0243 a0001c0002t0001g0001 a0001c0002t0001g0103 others(3): Show |
6 | HG01978.hp1 HG03041.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.181+921_181+924del others(4): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | TAGAGAG | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0036 a0001c0001t0002g0166 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.181+919_181+924del others(6): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | TAGAGAGA others(1): Show |
T | 3 | a0001c0001t0002g0159 a0001c0001t0002g0183 a0001c0001t0002g0184 |
3 | HG02723.hp2 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.181+917_181+924del others(8): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | TAGAGAGA others(3): Show |
T | 7 | a0001c0001t0002g0029 a0001c0001t0002g0088 a0001c0001t0002g0089 others(4): Show |
7 | HG02257.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+915_181+924del others(10): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | TAGAGAGA others(5): Show |
T | 4 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0161 others(1): Show |
5 | HG02602.hp1 HG03041.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.181+913_181+924del others(12): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | TAGAGAGA others(7): Show |
T | 1 | a0001c0001t0002g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.181+911_181+924del others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | TAGAGAGA others(9): Show |
T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0054 a0001c0001t0002g0179 others(1): Show |
4 | HG01891.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+909_181+924del others(16): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | TAGAGAGA others(13): Show |
T | 1 | a0001c0001t0002g0186 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.181+905_181+924del others(20): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616927 | TAGAGAGA others(17): Show |
T | 1 | a0001c0001t0002g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.181+901_181+924del others(24): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616927 | ||||||
| chr2:218616929 | G | T | 108 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0031 others(105): Show |
112 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.181+867G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616929 | |||||||
| chr2:218616931 | G | T | 89 | a0001c0001t0002g0031 a0001c0001t0002g0033 a0001c0001t0002g0034 others(86): Show |
89 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.181+869G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616931 | |||||||
| chr2:218616933 | G | T | 74 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0055 others(71): Show |
74 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.181+871G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616933 | |||||||
| chr2:218616935 | G | T | 65 | a0001c0001t0002g0030 a0001c0001t0002g0033 a0001c0001t0002g0034 others(62): Show |
65 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.181+873G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616935 | |||||||
| chr2:218616937 | G | T | 50 | a0001c0001t0002g0030 a0001c0001t0002g0033 a0001c0001t0002g0055 others(47): Show |
50 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.181+875G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616937 | |||||||
| chr2:218616939 | G | T | 45 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0055 others(42): Show |
45 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.181+877G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616939 | |||||||
| chr2:218616941 | G | T | 34 | a0001c0001t0002g0019 a0001c0001t0002g0029 a0001c0001t0002g0030 others(31): Show |
35 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.181+879G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616941 | |||||||
| chr2:218616943 | G | T | 22 | a0001c0001t0002g0019 a0001c0001t0002g0029 a0001c0001t0002g0048 others(19): Show |
23 | HG00280.hp2 HG00735.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.181+881G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616943 | |||||||
| chr2:218616945 | G | T | 16 | a0001c0001t0002g0029 a0001c0001t0002g0048 a0001c0001t0002g0054 others(13): Show |
16 | HG00280.hp2 HG00735.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.181+883G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616945 | |||||||
| chr2:218616947 | G | T | 9 | a0001c0001t0002g0029 a0001c0001t0002g0048 a0001c0001t0002g0054 others(6): Show |
9 | HG02886.hp2 HG02965.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+885G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616947 | |||||||
| chr2:218616949 | G | T | 6 | a0001c0001t0002g0048 a0001c0001t0002g0054 a0001c0001t0002g0179 others(3): Show |
6 | HG02886.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.181+887G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616949 | |||||||
| chr2:218616951 | G | T | 3 | a0001c0001t0002g0048 a0001c0001t0002g0185 a0001c0001t0002g0186 |
3 | HG02886.hp2 HG02965.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.181+889G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616951 | |||||||
| chr2:218616953 | G | T | 2 | a0001c0001t0002g0048 a0001c0001t0002g0186 |
2 | HG02965.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.181+891G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616953 | |||||||
| chr2:218616955 | G | T | 1 | a0001c0001t0002g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.181+893G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616955 | |||||||
| chr2:218616957 | G | T | 1 | a0001c0001t0002g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.181+895G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616957 | |||||||
| chr2:218616959 | G | T | 1 | a0001c0001t0002g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.181+897G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616959 | |||||||
| chr2:218616960 | A | AGAGAGAG others(12): Show |
1 | a0001c0001t0004g0083 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.181+916_181+917ins others(19): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218616960 | ||||||
| chr2:218616960 | A | AT | 8 | a0001c0001t0004g0009 a0001c0001t0004g0042 a0001c0001t0004g0043 others(5): Show |
9 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+898_181+899ins others(1): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616960 | |||||||
| chr2:218616987 | T | A | 1 | a0002c0004t0002g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.181+925T>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218616987 | |||||||
| chr2:218617028 | GATCTC | G | 13 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0242 others(10): Show |
13 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.181+968_181+972del others(5): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218617028 | ||||||
| chr2:218617075 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.181+1013T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617075 | |||||||
| chr2:218617095 | G | A | 2 | a0001c0001t0003g0220 a0001c0001t0003g0222 |
2 | HG01070.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.181+1033G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617095 | |||||||
| chr2:218617104 | A | G | 1 | a0001c0002t0001g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.181+1042A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617104 | |||||||
| chr2:218617253 | T | C | 2 | a0001c0002t0001g0109 a0001c0002t0001g0124 |
2 | HG00735.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.181+1191T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617253 | |||||||
| chr2:218617294 | C | T | 126 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(123): Show |
156 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.181+1232C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617294 | |||||||
| chr2:218617295 | G | A | 15 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0177 others(12): Show |
15 | HG01975.hp2 HG02723.hp2 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.181+1233G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617295 | |||||||
| chr2:218617325 | C | T | 5 | a0001c0001t0002g0025 a0001c0001t0002g0028 a0001c0001t0002g0029 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-1254C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617325 | |||||||
| chr2:218617364 | A | G | 251 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(248): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.182-1215A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617364 | |||||||
| chr2:218617433 | C | T | 2 | a0001c0002t0001g0122 a0001c0002t0001g0129 |
2 | HG01106.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.182-1146C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617433 | |||||||
| chr2:218617491 | C | T | 1 | a0001c0001t0002g0053 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.182-1088C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617491 | |||||||
| chr2:218617594 | CA | C | 114 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(111): Show |
143 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.182-975delA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218617594 | ||||||
| chr2:218617857 | C | T | 3 | a0001c0001t0003g0216 a0001c0001t0003g0220 a0001c0001t0003g0240 |
3 | HG01175.hp2 HG01255.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.182-722C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218617857 | |||||||
| chr2:218618052 | A | C | 9 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0021 others(6): Show |
12 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.182-527A>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218618052 | |||||||
| chr2:218618089 | A | AAAAC | 31 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0021 others(28): Show |
34 | HG00639.hp1 HG01884.hp1 HG01975.hp2 others(31): Show |
intron_variant | MODIFIER | c.182-461_182-458dup others(4): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218618089 | ||||||
| chr2:218618089 | AAAAC | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0022 a0001c0001t0003g0023 others(46): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.182-461_182-458del others(4): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 218618089 | ||||||
| chr2:218618497 | G | T | 1 | a0001c0001t0002g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.182-82G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218618497 | |||||||
| chr2:218618567 | C | A | 5 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0180 others(2): Show |
5 | HG02897.hp2 HG02922.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-12C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 3/15 | chr2 | 218618567 | |||||||
| chr2:218619158 | T | A | 86 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0005 others(83): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.410+351T>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218619158 | |||||||
| chr2:218619266 | CAT | C | 43 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0021 others(40): Show |
48 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.410+482_410+483del others(2): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 218619266 | ||||||
| chr2:218619266 | CATAT | C | 190 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(187): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.410+480_410+483del others(4): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 218619266 | ||||||
| chr2:218619286 | T | C | 1 | a0001c0002t0001g0112 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.410+479T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218619286 | |||||||
| chr2:218619354 | C | G | 59 | a0001c0001t0002g0168 a0001c0001t0002g0170 a0001c0001t0002g0171 others(56): Show |
66 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.410+547C>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218619354 | |||||||
| chr2:218619495 | A | G | 2 | a0001c0001t0003g0194 a0001c0001t0003g0215 |
2 | NA18950.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.410+688A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218619495 | |||||||
| chr2:218619918 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.410+1111C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218619918 | |||||||
| chr2:218620150 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.411-1320G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218620150 | |||||||
| chr2:218620444 | G | A | 2 | a0001c0002t0001g0091 a0001c0002t0001g0092 |
2 | HG00280.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.411-1026G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218620444 | |||||||
| chr2:218620466 | A | G | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG02886.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-1004A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218620466 | |||||||
| chr2:218620552 | TAATA | T | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
40 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.411-907_411-904del others(4): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 218620552 | ||||||
| chr2:218620632 | C | G | 1 | a0001c0001t0002g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.411-838C>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218620632 | |||||||
| chr2:218620703 | G | T | 1 | a0001c0002t0001g0121 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.411-767G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218620703 | |||||||
| chr2:218620760 | G | C | 6 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(3): Show |
6 | HG02257.hp2 HG03516.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-710G>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218620760 | |||||||
| chr2:218620893 | C | CA | 25 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0159 others(22): Show |
27 | HG00733.hp1 HG00741.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.411-552dupA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 218620893 | ||||||
| chr2:218620893 | CA | C | 56 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0025 others(53): Show |
60 | HG00558.hp2 HG01070.hp1 HG01261.hp1 others(57): Show |
intron_variant | MODIFIER | c.411-552delA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 218620893 | ||||||
| chr2:218620893 | CAA | C | 103 | a0001c0001t0002g0024 a0001c0001t0002g0027 a0001c0001t0002g0029 others(100): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.411-553_411-552del others(2): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 218620893 | ||||||
| chr2:218621067 | C | T | 1 | a0001c0002t0001g0120 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.411-403C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218621067 | |||||||
| chr2:218621108 | T | A | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
40 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.411-362T>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218621108 | |||||||
| chr2:218621200 | T | C | 1 | a0001c0001t0002g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.411-270T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218621200 | |||||||
| chr2:218621213 | C | T | 249 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(246): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.411-257C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218621213 | |||||||
| chr2:218621221 | C | T | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
40 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.411-249C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | chr2 | 218621221 | |||||||
| chr2:218621427 | CACAA | C | 7 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0042 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.411-39_411-36delAA others(2): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 218621427 | ||||||
| chr2:218621718 | GCTAGGCT others(7): Show |
G | 4 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 others(1): Show |
4 | HG01975.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+132_540+145del others(14): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 218621718 | ||||||
| chr2:218621808 | A | C | 1 | a0001c0002t0001g0147 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.540+209A>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | chr2 | 218621808 | |||||||
| chr2:218621903 | C | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0201 a0001c0001t0003g0239 |
4 | HG00323.hp1 HG02602.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+304C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | chr2 | 218621903 | |||||||
| chr2:218621904 | C | A | 126 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(123): Show |
156 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.540+305C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | chr2 | 218621904 | |||||||
| chr2:218622079 | C | CA | 6 | a0001c0001t0002g0166 a0001c0001t0002g0174 a0001c0001t0003g0039 others(3): Show |
6 | HG00741.hp1 HG01261.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+501dupA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 218622079 | ||||||
| chr2:218622079 | CA | C | 28 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0024 others(25): Show |
31 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.540+501delA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 218622079 | ||||||
| chr2:218622079 | CAA | C | 100 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(97): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.540+500_540+501del others(2): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 218622079 | ||||||
| chr2:218622079 | CAAA | C | 6 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0002t0001g0100 others(3): Show |
6 | HG01256.hp1 HG02165.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+499_540+501del others(3): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 218622079 | ||||||
| chr2:218622098 | AAAG | A | 34 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(31): Show |
38 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.540+502_540+504del others(3): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 218622098 | ||||||
| chr2:218622306 | C | T | 2 | a0001c0001t0003g0223 a0001c0001t0003g0228 |
2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.541-341C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | chr2 | 218622306 | |||||||
| chr2:218622507 | A | G | 1 | a0001c0001t0002g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.541-140A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | chr2 | 218622507 | |||||||
| chr2:218622567 | T | A | 9 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0021 others(6): Show |
12 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.541-80T>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | chr2 | 218622567 | |||||||
| chr2:218622576 | A | T | 86 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0005 others(83): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.541-71A>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | chr2 | 218622576 | |||||||
| chr2:218622587 | T | G | 1 | a0001c0002t0001g0135 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.541-60T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | chr2 | 218622587 | |||||||
| chr2:218622619 | T | C | 36 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
40 | HG00558.hp2 HG00621.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.541-28T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 5/15 | chr2 | 218622619 | |||||||
| chr2:218622911 | T | C | 7 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0159 others(4): Show |
9 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.772+33T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218622911 | |||||||
| chr2:218623314 | C | T | 34 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0047 others(31): Show |
37 | HG00558.hp2 HG00621.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.772+436C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218623314 | |||||||
| chr2:218623903 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.772+1025G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218623903 | |||||||
| chr2:218623975 | G | A | 120 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(117): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.772+1097G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218623975 | |||||||
| chr2:218624254 | T | C | 162 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(159): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.772+1376T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624254 | |||||||
| chr2:218624268 | A | G | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG02886.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.772+1390A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624268 | |||||||
| chr2:218624301 | G | C | 1 | a0001c0001t0002g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.772+1423G>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624301 | |||||||
| chr2:218624591 | C | T | 9 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0246 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.772+1713C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624591 | |||||||
| chr2:218624645 | G | A | 4 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 others(1): Show |
4 | HG01975.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.772+1767G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624645 | |||||||
| chr2:218624657 | C | G | 42 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
46 | HG00558.hp2 HG00621.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.772+1779C>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624657 | |||||||
| chr2:218624735 | G | A | 1 | a0001c0001t0003g0233 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.772+1857G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624735 | |||||||
| chr2:218624816 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.772+1938G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624816 | |||||||
| chr2:218624836 | C | T | 2 | a0001c0001t0003g0227 a0001c0001t0003g0237 |
2 | NA18977.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.772+1958C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624836 | |||||||
| chr2:218624864 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.772+1986A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624864 | |||||||
| chr2:218624946 | A | G | 1 | a0001c0001t0005g0213 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.772+2068A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624946 | |||||||
| chr2:218624967 | C | T | 5 | a0001c0001t0002g0025 a0001c0001t0002g0028 a0001c0001t0002g0029 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.772+2089C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218624967 | |||||||
| chr2:218625050 | TGCA | T | 162 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(159): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.772+2177_772+2179d others(5): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 218625050 | ||||||
| chr2:218625114 | C | CA | 14 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0244 others(11): Show |
14 | HG02965.hp1 HG02976.hp1 HG03195.hp2 others(11): Show |
intron_variant | MODIFIER | c.772+2254dupA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 218625114 | ||||||
| chr2:218625114 | CA | C | 77 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(74): Show |
87 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.772+2254delA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 218625114 | ||||||
| chr2:218625130 | AAAGAAAG others(8): Show |
A | 1 | a0001c0002t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.772+2255_772+2269d others(17): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 218625130 | ||||||
| chr2:218625132 | AG | A | 45 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(42): Show |
50 | HG00558.hp2 HG00621.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.772+2255delG | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218625132 | |||||||
| chr2:218625133 | G | A | 117 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(114): Show |
145 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.772+2255G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218625133 | |||||||
| chr2:218625145 | G | A | 118 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0028 others(115): Show |
148 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.772+2267G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218625145 | |||||||
| chr2:218625388 | C | A | 120 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(117): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.772+2510C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218625388 | |||||||
| chr2:218625708 | C | T | 4 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 others(1): Show |
4 | HG01975.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.773-2321C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218625708 | |||||||
| chr2:218625732 | G | A | 7 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0042 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.773-2297G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218625732 | |||||||
| chr2:218626040 | G | A | 1 | a0001c0002t0001g0144 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.773-1989G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218626040 | |||||||
| chr2:218626137 | T | G | 1 | a0001c0001t0002g0051 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.773-1892T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218626137 | |||||||
| chr2:218626200 | G | A | 42 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
46 | HG00558.hp2 HG00621.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.773-1829G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218626200 | |||||||
| chr2:218626258 | CA | C | 7 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(4): Show |
8 | HG01261.hp1 HG01261.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.773-1755delA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 218626258 | ||||||
| chr2:218626258 | CAA | C | 156 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(153): Show |
189 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.773-1756_773-1755d others(4): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 218626258 | ||||||
| chr2:218626317 | A | C | 1 | a0001c0001t0003g0196 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.773-1712A>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218626317 | |||||||
| chr2:218626792 | A | G | 1 | a0001c0002t0001g0121 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.773-1237A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218626792 | |||||||
| chr2:218626837 | C | T | 3 | a0001c0001t0004g0009 a0001c0001t0004g0081 a0001c0001t0004g0083 |
4 | HG02723.hp1 HG03139.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.773-1192C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218626837 | |||||||
| chr2:218626982 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.773-1047G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218626982 | |||||||
| chr2:218627028 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.773-1001C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218627028 | |||||||
| chr2:218627036 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0030 |
2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.773-993G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218627036 | |||||||
| chr2:218627153 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.773-876C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218627153 | |||||||
| chr2:218627169 | G | C | 1 | a0001c0001t0002g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.773-860G>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218627169 | |||||||
| chr2:218627178 | G | A | 1 | a0001c0001t0002g0052 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.773-851G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218627178 | |||||||
| chr2:218627242 | C | T | 1 | a0001c0001t0003g0232 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.773-787C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218627242 | |||||||
| chr2:218627455 | TA | T | 11 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(8): Show |
12 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.773-563delA | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 218627455 | ||||||
| chr2:218627643 | G | T | 4 | a0001c0001t0002g0164 a0001c0001t0002g0167 a0001c0001t0002g0169 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.773-386G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218627643 | |||||||
| chr2:218627663 | C | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0054 |
3 | HG01891.hp1 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.773-366C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218627663 | |||||||
| chr2:218627703 | G | GGGGTTTC others(3): Show |
11 | a0001c0001t0004g0009 a0001c0001t0004g0040 a0001c0001t0004g0041 others(8): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.773-324_773-315dup others(10): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 218627703 | ||||||
| chr2:218627713 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.773-316C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218627713 | |||||||
| chr2:218627804 | G | A | 1 | a0001c0002t0008g0096 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.773-225G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 6/15 | chr2 | 218627804 | |||||||
| chr2:218628432 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.974+202C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/15 | chr2 | 218628432 | |||||||
| chr2:218628620 | T | G | 42 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
46 | HG00558.hp2 HG00621.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.974+390T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/15 | chr2 | 218628620 | |||||||
| chr2:218628691 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.974+461A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/15 | chr2 | 218628691 | |||||||
| chr2:218628756 | G | C | 4 | a0001c0001t0003g0208 a0001c0001t0003g0209 a0001c0001t0003g0217 others(1): Show |
4 | HG01256.hp2 HG01261.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.974+526G>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/15 | chr2 | 218628756 | |||||||
| chr2:218628771 | A | G | 1 | a0001c0002t0001g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.974+541A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/15 | chr2 | 218628771 | |||||||
| chr2:218629131 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0054 |
3 | HG01891.hp1 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.975-388G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/15 | chr2 | 218629131 | |||||||
| chr2:218629275 | G | A | 7 | a0001c0001t0002g0003 a0001c0001t0002g0049 a0001c0001t0002g0050 others(4): Show |
9 | HG02083.hp1 NA18939.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.975-244G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/15 | chr2 | 218629275 | |||||||
| chr2:218629290 | A | G | 1 | a0001c0001t0003g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.975-229A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/15 | chr2 | 218629290 | |||||||
| chr2:218629314 | G | A | 86 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0005 others(83): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.975-205G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/15 | chr2 | 218629314 | |||||||
| chr2:218629496 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.975-23C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 7/15 | chr2 | 218629496 | |||||||
| chr2:218629821 | T | C | 11 | a0001c0001t0004g0009 a0001c0001t0004g0040 a0001c0001t0004g0041 others(8): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1119+158T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 8/15 | chr2 | 218629821 | |||||||
| chr2:218629863 | A | G | 7 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0159 others(4): Show |
9 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1119+200A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 8/15 | chr2 | 218629863 | |||||||
| chr2:218629915 | T | C | 175 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(172): Show |
212 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1119+252T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 8/15 | chr2 | 218629915 | |||||||
| chr2:218630004 | C | A | 7 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+341C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 8/15 | chr2 | 218630004 | |||||||
| chr2:218630007 | G | A | 7 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+344G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 8/15 | chr2 | 218630007 | |||||||
| chr2:218630133 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1119+470G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 8/15 | chr2 | 218630133 | |||||||
| chr2:218630312 | A | C | 7 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1120-338A>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 8/15 | chr2 | 218630312 | |||||||
| chr2:218630358 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1120-292C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 8/15 | chr2 | 218630358 | |||||||
| chr2:218630469 | G | A | 10 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(7): Show |
11 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1120-181G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 8/15 | chr2 | 218630469 | |||||||
| chr2:218630581 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1120-69G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 8/15 | chr2 | 218630581 | |||||||
| chr2:218631141 | C | A | 1 | a0001c0002t0001g0011 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1272+339C>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 9/15 | chr2 | 218631141 | |||||||
| chr2:218631159 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1272+357C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 9/15 | chr2 | 218631159 | |||||||
| chr2:218631337 | G | A | 4 | a0001c0002t0001g0004 a0001c0002t0001g0110 a0001c0002t0001g0136 others(1): Show |
6 | HG00323.hp2 HG00639.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1272+535G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 9/15 | chr2 | 218631337 | |||||||
| chr2:218631419 | C | T | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG02886.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272+617C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 9/15 | chr2 | 218631419 | |||||||
| chr2:218631526 | T | C | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0067 |
3 | HG02559.hp1 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1273-610T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 9/15 | chr2 | 218631526 | |||||||
| chr2:218631543 | T | TCCCAGCA others(70): Show |
9 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0246 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1273-588_1273-512d others(79): Show |
PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 218631543 | ||||||
| chr2:218631779 | G | A | 1 | a0001c0002t0001g0148 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1273-357G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 9/15 | chr2 | 218631779 | |||||||
| chr2:218632325 | T | G | 42 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
46 | HG00558.hp2 HG00621.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.1449+13T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | chr2 | 218632325 | |||||||
| chr2:218632447 | A | AG | 9 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0246 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1449+136dupG | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 218632447 | ||||||
| chr2:218632542 | A | T | 1 | a0001c0002t0001g0241 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1449+230A>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | chr2 | 218632542 | |||||||
| chr2:218632556 | C | G | 42 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
46 | HG00558.hp2 HG00621.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.1449+244C>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | chr2 | 218632556 | |||||||
| chr2:218632557 | G | A | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1449+245G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | chr2 | 218632557 | |||||||
| chr2:218632587 | T | C | 2 | a0001c0001t0002g0007 a0001c0001t0002g0054 |
3 | HG01891.hp1 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1449+275T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | chr2 | 218632587 | |||||||
| chr2:218632792 | G | A | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1449+480G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | chr2 | 218632792 | |||||||
| chr2:218633113 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1450-492T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | chr2 | 218633113 | |||||||
| chr2:218633205 | A | C | 47 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(44): Show |
51 | HG00140.hp1 HG00621.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.1450-400A>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | chr2 | 218633205 | |||||||
| chr2:218633272 | A | G | 1 | a0001c0002t0001g0116 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1450-333A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | chr2 | 218633272 | |||||||
| chr2:218633356 | G | T | 42 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
46 | HG00558.hp2 HG00621.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.1450-249G>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 10/15 | chr2 | 218633356 | |||||||
| chr2:218634036 | T | G | 185 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(182): Show |
222 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1607-69T>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 11/15 | chr2 | 218634036 | |||||||
| chr2:218634248 | A | C | 21 | a0001c0001t0002g0164 a0001c0001t0002g0167 a0001c0001t0002g0168 others(18): Show |
22 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1723+27A>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 12/15 | chr2 | 218634248 | |||||||
| chr2:218634711 | A | T | 1 | a0001c0003t0002g0251 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1896+81A>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 13/15 | chr2 | 218634711 | |||||||
| chr2:218634996 | T | C | 143 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0021 others(140): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1896+366T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 13/15 | chr2 | 218634996 | |||||||
| chr2:218635125 | A | G | 4 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0183 others(1): Show |
4 | HG02723.hp2 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1896+495A>G | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 13/15 | chr2 | 218635125 | |||||||
| chr2:218635323 | T | A | 21 | a0001c0001t0002g0164 a0001c0001t0002g0167 a0001c0001t0002g0168 others(18): Show |
22 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1897-473T>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 13/15 | chr2 | 218635323 | |||||||
| chr2:218635458 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1897-338C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 13/15 | chr2 | 218635458 | |||||||
| chr2:218635463 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1897-333C>T | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 13/15 | chr2 | 218635463 | |||||||
| chr2:218635473 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1897-323G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 13/15 | chr2 | 218635473 | |||||||
| chr2:218636156 | T | C | 14 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0027 others(11): Show |
15 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2033-87T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 14/15 | chr2 | 218636156 | |||||||
| chr2:218636410 | G | A | 127 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0021 others(124): Show |
158 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.2182+18G>A | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 15/15 | chr2 | 218636410 | |||||||
| chr2:218636431 | T | C | 1 | a0001c0001t0007g0202 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2182+39T>C | PLCD4 | ENSG00000115556.14 | transcript | ENST00000450993.7 | protein_coding | 15/15 | chr2 | 218636431 |