Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 89869 |
| ensemblid | ENSG00000139151.16 |
| hgncid | 19218 |
| symbol | PLCZ1 |
| name | phospholipase C zeta 1 |
| refseq_nuc | NM_033123.4 |
| refseq_prot | NP_149114.2 |
| ensembl_nuc | ENST00000266505.12 |
| ensembl_prot | ENSP00000266505.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 18683180 |
| end | 18738012 |
| strand | - |
| ver | v1.2 |
| region | chr12:18683180-18738012 |
| region5000 | chr12:18678180-18743012 |
| regionname0 | PLCZ1_chr12_18683180_18738012 |
| regionname5000 | PLCZ1_chr12_18678180_18743012 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 608 | 320 | 90 | 56 | 128 | 15 | 29 | 104 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | MEMRW others(603): Show |
chr12 | 18678180 | 18743012 |
| a0002 | 0/0 | 608 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | MEMRW others(603): Show |
chr12 | 18678180 | 18743012 |
| a0003 | 0/0 | 608 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | MEMRW others(603): Show |
chr12 | 18678180 | 18743012 |
| a0004 | 0/0 | 608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | MEMRW others(603): Show |
chr12 | 18678180 | 18743012 |
| a0005 | 0/0 | 608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | MEMRW others(603): Show |
chr12 | 18678180 | 18743012 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1824 | 317 | 90 | 56 | 125 | 15 | 29 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | ATGGA others(1819): Show |
chr12 | 18678180 | 18743012 | ||
| a0001c0002 | 0/0 | 1824 | 3 | 0 | 0 | 3 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | ATGGA others(1819): Show |
chr12 | 18678180 | 18743012 | ||
| a0002c0003 | 0/0 | 1824 | 2 | 0 | 0 | 0 | 1 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | ATGGA others(1819): Show |
chr12 | 18678180 | 18743012 | ||
| a0003c0006 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | ATGGA others(1819): Show |
chr12 | 18678180 | 18743012 | ||
| a0003c0007 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | ATGGA others(1819): Show |
chr12 | 18678180 | 18743012 | ||
| a0004c0005 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | ATGGA others(1819): Show |
chr12 | 18678180 | 18743012 | ||
| a0005c0004 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | ATGGA others(1819): Show |
chr12 | 18678180 | 18743012 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2105 | 308 | 82 | 55 | 125 | 15 | 29 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | AGTGT others(2100): Show |
chr12 | 18678180 | 18743012 |
| a0001c0001t0002 | 0/0 | 2105 | 4 | 4 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | AGTGT others(2100): Show |
chr12 | 18678180 | 18743012 |
| a0001c0001t0003 | 0/0 | 2105 | 4 | 4 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | AGTGT others(2100): Show |
chr12 | 18678180 | 18743012 |
| a0001c0001t0004 | 0/0 | 2105 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | AGTGT others(2100): Show |
chr12 | 18678180 | 18743012 |
| a0001c0002t0001 | 0/0 | 2105 | 3 | 0 | 0 | 3 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | AGTGT others(2100): Show |
chr12 | 18678180 | 18743012 |
| a0002c0003t0001 | 0/0 | 2105 | 2 | 0 | 0 | 0 | 1 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | AGTGT others(2100): Show |
chr12 | 18678180 | 18743012 |
| a0003c0006t0001 | 0/0 | 2105 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | AGTGT others(2100): Show |
chr12 | 18678180 | 18743012 |
| a0003c0007t0001 | 0/0 | 2105 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | AGTGT others(2100): Show |
chr12 | 18678180 | 18743012 |
| a0004c0005t0001 | 0/0 | 2105 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | AGTGT others(2100): Show |
chr12 | 18678180 | 18743012 |
| a0005c0004t0001 | 0/0 | 2105 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | AGTGT others(2100): Show |
chr12 | 18678180 | 18743012 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0003c0006t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0003c0007t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0004c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| a0005c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00099 | hp2 | a0002 | c0003 | t0001 | g0071 | EUR | GBR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0311 | EUR | GBR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | FIN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0323 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0310 | EUR | IBS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | IBS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0313 | EUR | IBS | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01884 | hp1 | a0003 | c0006 | t0001 | g0210 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03486 | hp2 | a0003 | c0007 | t0001 | g0188 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03927 | hp2 | a0002 | c0003 | t0001 | g0070 | SAS | BEB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | STU | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18969 | hp2 | a0004 | c0005 | t0001 | g0141 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | LWK | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | LWK | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19064 | hp2 | a0005 | c0004 | t0001 | g0291 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ASW | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | TSI | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | TSI | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | GIH | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | GIH | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | MSL | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | USA | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | USA | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | USA | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | USA | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | LWK | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0073 | REF | REF | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0015 | REF | REF | PLCZ1_chr12_18678180_18743012 | PLCZ1 | chr12 | 18678180 | 18743012 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:18688181 | G | A | 1 | a0002 | 2 | HG00099.hp2 HG03927.hp2 |
missense_variant | MODERATE | c.1499C>T | p.Ser500Leu | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/15 | 1718/2105 | 1499/1827 | 500/608 | chr12 | 18688181 | |||
| chr12:18701505 | T | C | 1 | a0004 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.1013A>G | p.Lys338Arg | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/15 | 1232/2105 | 1013/1827 | 338/608 | chr12 | 18701505 | |||
| chr12:18723318 | G | C | 1 | a0003 | 2 | HG01884.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.360C>G | p.Ile120Met | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/15 | 579/2105 | 360/1827 | 120/608 | chr12 | 18723318 | |||
| chr12:18723345 | A | C | 1 | a0005 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.333T>G | p.Phe111Leu | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/15 | 552/2105 | 333/1827 | 111/608 | chr12 | 18723345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:18684226 | A | G | 1 | a0001c0002 | 3 | NA18986.hp1 NA19063.hp2 NA19079.hp1 |
synonymous_variant | LOW | c.1645T>C | p.Leu549Leu | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 14/15 | 1864/2105 | 1645/1827 | 549/608 | chr12 | 18684226 | |||
| chr12:18699945 | C | T | 1 | a0003c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1023G>A | p.Arg341Arg | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/15 | 1242/2105 | 1023/1827 | 341/608 | chr12 | 18699945 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:18683238 | G | A | 1 | a0001c0001t0003 | 4 | HG02145.hp1 HG03209.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 15/15 | 1 | chr12 | 18683238 | ||||||
| chr12:18737419 | C | G | 1 | a0001c0001t0002 | 4 | HG02258.hp1 NA19030.hp2 NA20129.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-48G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/15 | 48 | chr12 | 18737419 | ||||||
| chr12:18737967 | T | C | 1 | a0001c0001t0004 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-174A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 1/15 | 596 | chr12 | 18737967 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:18683341 | A | G | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1742-17T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 14/14 | chr12 | 18683341 | |||||||
| chr12:18683437 | T | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1742-113A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 14/14 | chr12 | 18683437 | |||||||
| chr12:18683453 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1742-129G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 14/14 | chr12 | 18683453 | |||||||
| chr12:18683765 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0116 |
2 | HG00642.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1741+365A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 14/14 | chr12 | 18683765 | |||||||
| chr12:18683776 | C | T | 6 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0312 others(3): Show |
6 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1741+354G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 14/14 | chr12 | 18683776 | |||||||
| chr12:18683967 | A | G | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1741+163T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 14/14 | chr12 | 18683967 | |||||||
| chr12:18684758 | G | C | 1 | a0001c0001t0001g0174 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1592-479C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18684758 | |||||||
| chr12:18684817 | A | G | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1592-538T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18684817 | |||||||
| chr12:18684919 | C | T | 2 | a0001c0001t0001g0046 a0003c0007t0001g0188 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1592-640G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18684919 | |||||||
| chr12:18685148 | G | C | 17 | a0001c0001t0001g0035 a0001c0001t0001g0046 a0001c0001t0001g0050 others(14): Show |
17 | HG02145.hp2 HG02280.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1592-869C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685148 | |||||||
| chr12:18685238 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1592-959A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685238 | |||||||
| chr12:18685296 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1592-1017G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685296 | |||||||
| chr12:18685334 | C | G | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1592-1055G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685334 | |||||||
| chr12:18685376 | T | A | 1 | a0001c0001t0002g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1592-1097A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685376 | |||||||
| chr12:18685760 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0209 |
2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1592-1481A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685760 | |||||||
| chr12:18685819 | ATCTC | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0189 others(1): Show |
4 | HG01934.hp2 HG02818.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1592-1544_1592-154 others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685819 | |||||||
| chr12:18685842 | ACG | A | 26 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0077 others(23): Show |
26 | HG00642.hp2 HG00733.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.1592-1565_1592-156 others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685842 | |||||||
| chr12:18685844 | G | GCA | 17 | a0001c0001t0001g0035 a0001c0001t0001g0045 a0001c0001t0001g0047 others(14): Show |
17 | HG01069.hp1 HG01361.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.1592-1566_1592-156 others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685844 | |||||||
| chr12:18685844 | GCGCA | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1592-1569_1592-156 others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685844 | |||||||
| chr12:18685844 | GCGCACA | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0201 a0001c0001t0001g0203 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1592-1571_1592-156 others(10): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685844 | |||||||
| chr12:18685846 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0035 others(95): Show |
99 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.1592-1567C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685846 | |||||||
| chr12:18685846 | GCA | G | 25 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0022 others(22): Show |
25 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1592-1569_1592-156 others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685846 | |||||||
| chr12:18685846 | GCACA | G | 4 | a0001c0001t0003g0270 a0001c0001t0003g0282 a0001c0001t0003g0292 others(1): Show |
4 | HG02145.hp1 HG03209.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1592-1571_1592-156 others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685846 | |||||||
| chr12:18685850 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG00733.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1592-1571T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685850 | |||||||
| chr12:18685869 | CAT | C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | HG02559.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1592-1592_1592-159 others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685869 | |||||||
| chr12:18685871 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1592-1592A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685871 | |||||||
| chr12:18685892 | TAA | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.1592-1615_1592-161 others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685892 | |||||||
| chr12:18685902 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0048 others(122): Show |
126 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.1592-1623G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18685902 | |||||||
| chr12:18686013 | T | C | 19 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0050 others(16): Show |
19 | HG00642.hp2 HG00733.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1592-1734A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686013 | |||||||
| chr12:18686074 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0174 |
2 | NA18978.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1592-1795G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686074 | |||||||
| chr12:18686108 | G | A | 8 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0264 others(5): Show |
8 | NA18965.hp1 NA18971.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.1592-1829C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686108 | |||||||
| chr12:18686236 | G | A | 1 | a0001c0001t0001g0307 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1591+1853C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686236 | |||||||
| chr12:18686301 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1591+1788G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686301 | |||||||
| chr12:18686390 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1591+1699T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686390 | |||||||
| chr12:18686475 | CATGTTTA others(45): Show |
C | 1 | a0001c0001t0001g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1591+1562_1591+161 others(56): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686475 | |||||||
| chr12:18686545 | T | G | 1 | a0001c0001t0001g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1591+1544A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686545 | |||||||
| chr12:18686578 | G | A | 2 | a0001c0001t0001g0046 a0003c0007t0001g0188 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1591+1511C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686578 | |||||||
| chr12:18686629 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1591+1460C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686629 | |||||||
| chr12:18686709 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0065 others(96): Show |
100 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.1591+1380A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686709 | |||||||
| chr12:18686935 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1591+1154A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18686935 | |||||||
| chr12:18687166 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1591+923A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687166 | |||||||
| chr12:18687194 | G | A | 12 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(9): Show |
12 | HG01433.hp2 HG01952.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1591+895C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687194 | |||||||
| chr12:18687431 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0050 others(1): Show |
4 | HG02615.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1591+658T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687431 | |||||||
| chr12:18687449 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1591+640C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687449 | |||||||
| chr12:18687454 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1591+635A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687454 | |||||||
| chr12:18687518 | C | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1591+571G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687518 | |||||||
| chr12:18687548 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1591+541T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687548 | |||||||
| chr12:18687767 | A | C | 15 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0050 others(12): Show |
15 | HG00642.hp2 HG01099.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1591+322T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687767 | |||||||
| chr12:18687834 | A | T | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1591+255T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687834 | |||||||
| chr12:18687938 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0226 |
2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1591+151C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687938 | |||||||
| chr12:18687968 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1591+121T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687968 | |||||||
| chr12:18687977 | A | G | 34 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0050 others(31): Show |
34 | HG00099.hp2 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.1591+112T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 13/14 | chr12 | 18687977 | |||||||
| chr12:18688489 | T | A | 2 | a0001c0001t0001g0046 a0003c0007t0001g0188 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1462-271A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688489 | |||||||
| chr12:18688537 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1462-319C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688537 | |||||||
| chr12:18688548 | G | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1462-330C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688548 | |||||||
| chr12:18688553 | C | CAT | 16 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0046 others(13): Show |
16 | HG01346.hp2 HG01934.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.1462-337_1462-336d others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688553 | |||||||
| chr12:18688595 | G | T | 20 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0045 others(17): Show |
20 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.1462-377C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688595 | |||||||
| chr12:18688610 | A | T | 23 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0045 others(20): Show |
23 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1462-392T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688610 | |||||||
| chr12:18688743 | G | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG00642.hp2 HG01099.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.1462-525C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688743 | |||||||
| chr12:18688759 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1462-541A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688759 | |||||||
| chr12:18688792 | A | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1462-574T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688792 | |||||||
| chr12:18688869 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0045 others(21): Show |
24 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1462-651G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688869 | |||||||
| chr12:18688889 | C | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0203 |
2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1462-671G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688889 | |||||||
| chr12:18688998 | T | TAGAAG | 23 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0045 others(20): Show |
23 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1462-781_1462-780i others(7): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18688998 | |||||||
| chr12:18689154 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1462-936T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689154 | |||||||
| chr12:18689186 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1462-968T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689186 | |||||||
| chr12:18689197 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1462-979C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689197 | |||||||
| chr12:18689257 | C | T | 23 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0045 others(20): Show |
23 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1462-1039G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689257 | |||||||
| chr12:18689342 | G | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0045 a0001c0001t0001g0046 others(19): Show |
22 | HG00642.hp2 HG01099.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.1462-1124C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689342 | |||||||
| chr12:18689393 | C | T | 5 | a0001c0001t0001g0294 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1462-1175G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689393 | |||||||
| chr12:18689394 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0002g0040 |
2 | HG01433.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1462-1176C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689394 | |||||||
| chr12:18689402 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0100 others(1): Show |
5 | HG01257.hp1 HG01258.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1462-1184C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689402 | |||||||
| chr12:18689523 | G | A | 2 | a0001c0001t0001g0046 a0003c0007t0001g0188 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1462-1305C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689523 | |||||||
| chr12:18689632 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1462-1414C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689632 | |||||||
| chr12:18689885 | AG | A | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(10): Show |
13 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1462-1668delC | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689885 | |||||||
| chr12:18689972 | C | T | 8 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(5): Show |
8 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-1754G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18689972 | |||||||
| chr12:18690155 | T | C | 4 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1462-1937A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690155 | |||||||
| chr12:18690209 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0179 |
2 | HG01934.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1462-1991A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690209 | |||||||
| chr12:18690209 | T | TTTTG | 17 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0048 others(14): Show |
17 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1462-1995_1462-199 others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690209 | |||||||
| chr12:18690209 | TTTTG | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(6): Show |
9 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1462-1995_1462-199 others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690209 | |||||||
| chr12:18690237 | C | G | 4 | a0001c0001t0001g0301 a0001c0002t0001g0267 a0001c0002t0001g0295 others(1): Show |
4 | NA18612.hp2 NA18986.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462-2019G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690237 | |||||||
| chr12:18690293 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0095 |
2 | HG01346.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1462-2075C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690293 | |||||||
| chr12:18690326 | C | T | 4 | a0001c0001t0001g0100 a0001c0001t0001g0241 a0001c0001t0001g0277 others(1): Show |
4 | HG01928.hp1 NA18949.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462-2108G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690326 | |||||||
| chr12:18690350 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1462-2132T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690350 | |||||||
| chr12:18690544 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1462-2326C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690544 | |||||||
| chr12:18690614 | A | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0030 others(12): Show |
15 | HG00733.hp2 HG01891.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1462-2396T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690614 | |||||||
| chr12:18690640 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1462-2422G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690640 | |||||||
| chr12:18690676 | A | C | 3 | a0001c0001t0001g0244 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG02080.hp2 NA19001.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1462-2458T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690676 | |||||||
| chr12:18690783 | G | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1462-2565C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690783 | |||||||
| chr12:18690790 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1462-2572G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690790 | |||||||
| chr12:18690956 | A | T | 1 | a0001c0001t0002g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1462-2738T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18690956 | |||||||
| chr12:18691006 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1462-2788A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691006 | |||||||
| chr12:18691081 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1462-2863C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691081 | |||||||
| chr12:18691136 | T | C | 2 | a0001c0001t0001g0150 a0005c0004t0001g0291 |
2 | NA19064.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1462-2918A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691136 | |||||||
| chr12:18691168 | C | A | 1 | a0001c0001t0002g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1462-2950G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691168 | |||||||
| chr12:18691206 | T | C | 3 | a0001c0001t0001g0241 a0001c0001t0001g0277 a0001c0001t0001g0304 |
3 | NA18949.hp1 NA18951.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1462-2988A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691206 | |||||||
| chr12:18691212 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1462-2994G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691212 | |||||||
| chr12:18691261 | T | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0198 a0001c0001t0001g0199 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1462-3043A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691261 | |||||||
| chr12:18691268 | A | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0050 others(13): Show |
16 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1462-3050T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691268 | |||||||
| chr12:18691386 | C | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0050 others(13): Show |
16 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1462-3168G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691386 | |||||||
| chr12:18691403 | A | G | 18 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0050 others(15): Show |
18 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.1462-3185T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691403 | |||||||
| chr12:18691423 | T | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG00733.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-3205A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691423 | |||||||
| chr12:18691602 | T | C | 34 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0030 others(31): Show |
34 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1461+3308A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691602 | |||||||
| chr12:18691793 | T | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1461+3117A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691793 | |||||||
| chr12:18691901 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1461+3009C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691901 | |||||||
| chr12:18691917 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1461+2993G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691917 | |||||||
| chr12:18691980 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1461+2930G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691980 | |||||||
| chr12:18691998 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02257.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1461+2912C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18691998 | |||||||
| chr12:18692202 | A | G | 9 | a0001c0001t0001g0036 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
9 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1461+2708T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692202 | |||||||
| chr12:18692230 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1461+2680A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692230 | |||||||
| chr12:18692231 | G | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1461+2679C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692231 | |||||||
| chr12:18692316 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1461+2594C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692316 | |||||||
| chr12:18692342 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1461+2568C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692342 | |||||||
| chr12:18692359 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0134 |
2 | HG00733.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1461+2551C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692359 | |||||||
| chr12:18692410 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1461+2500T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692410 | |||||||
| chr12:18692555 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1461+2355C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692555 | |||||||
| chr12:18692577 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1461+2333T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692577 | |||||||
| chr12:18692668 | T | A | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1461+2242A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692668 | |||||||
| chr12:18692790 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1461+2120C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692790 | |||||||
| chr12:18692796 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1461+2114C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692796 | |||||||
| chr12:18692820 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1461+2090G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692820 | |||||||
| chr12:18692935 | C | A | 1 | a0001c0001t0001g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1461+1975G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692935 | |||||||
| chr12:18692935 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG00733.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1461+1975G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18692935 | |||||||
| chr12:18693017 | A | G | 2 | a0001c0001t0001g0046 a0003c0007t0001g0188 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1461+1893T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693017 | |||||||
| chr12:18693036 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0095 |
2 | HG01346.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1461+1874G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693036 | |||||||
| chr12:18693040 | T | TAGAAGAA others(1): Show |
3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0226 |
3 | HG02615.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1461+1862_1461+186 others(12): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693040 | |||||||
| chr12:18693087 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0177 |
2 | NA18946.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1461+1823C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693087 | |||||||
| chr12:18693113 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0180 a0001c0001t0001g0195 others(28): Show |
32 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1461+1797C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693113 | |||||||
| chr12:18693173 | C | T | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1461+1737G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693173 | |||||||
| chr12:18693174 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1461+1736T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693174 | |||||||
| chr12:18693193 | C | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1461+1717G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693193 | |||||||
| chr12:18693200 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1461+1710C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693200 | |||||||
| chr12:18693224 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1461+1686C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693224 | |||||||
| chr12:18693235 | A | G | 3 | a0001c0001t0001g0241 a0001c0001t0001g0277 a0001c0001t0001g0304 |
3 | NA18949.hp1 NA18951.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1461+1675T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693235 | |||||||
| chr12:18693262 | T | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0029 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1461+1648A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693262 | |||||||
| chr12:18693277 | T | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0029 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1461+1633A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693277 | |||||||
| chr12:18693318 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0029 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1461+1592G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693318 | |||||||
| chr12:18693435 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1461+1475T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693435 | |||||||
| chr12:18693579 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0203 |
2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1461+1331C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693579 | |||||||
| chr12:18693640 | C | T | 1 | a0001c0001t0002g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1461+1270G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693640 | |||||||
| chr12:18693712 | G | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0180 a0001c0001t0001g0220 others(5): Show |
9 | HG00140.hp1 HG01106.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1461+1198C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693712 | |||||||
| chr12:18693759 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(134): Show |
138 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.1461+1151A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693759 | |||||||
| chr12:18693796 | G | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0180 others(30): Show |
34 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1461+1114C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693796 | |||||||
| chr12:18693811 | C | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0029 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1461+1099G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693811 | |||||||
| chr12:18693847 | T | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0029 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1461+1063A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693847 | |||||||
| chr12:18693993 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1461+917G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18693993 | |||||||
| chr12:18694041 | C | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0029 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1461+869G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694041 | |||||||
| chr12:18694050 | A | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0029 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1461+860T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694050 | |||||||
| chr12:18694107 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0203 |
2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1461+803G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694107 | |||||||
| chr12:18694148 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1461+762A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694148 | |||||||
| chr12:18694168 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0179 |
2 | HG01934.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1461+742C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694168 | |||||||
| chr12:18694170 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1461+740C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694170 | |||||||
| chr12:18694304 | C | T | 15 | a0001c0001t0001g0048 a0001c0001t0001g0195 a0001c0001t0001g0204 others(12): Show |
15 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1461+606G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694304 | |||||||
| chr12:18694446 | T | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0029 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1461+464A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694446 | |||||||
| chr12:18694468 | T | G | 1 | a0001c0001t0001g0213 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1461+442A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694468 | |||||||
| chr12:18694598 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0180 a0001c0001t0001g0195 others(27): Show |
31 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1461+312G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694598 | |||||||
| chr12:18694609 | C | A | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1461+301G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694609 | |||||||
| chr12:18694664 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(138): Show |
142 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.1461+246A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694664 | |||||||
| chr12:18694723 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1461+187T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694723 | |||||||
| chr12:18694761 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0226 |
2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1461+149A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694761 | |||||||
| chr12:18694771 | C | T | 2 | a0001c0001t0001g0046 a0003c0007t0001g0188 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1461+139G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694771 | |||||||
| chr12:18694778 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0095 |
2 | HG01346.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1461+132G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694778 | |||||||
| chr12:18694794 | A | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0065 others(94): Show |
98 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1461+116T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694794 | |||||||
| chr12:18694798 | T | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0180 a0001c0001t0001g0201 others(10): Show |
14 | HG00140.hp1 HG01106.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1461+112A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 12/14 | chr12 | 18694798 | |||||||
| chr12:18695086 | G | T | 3 | a0001c0001t0001g0046 a0003c0006t0001g0210 a0003c0007t0001g0188 |
3 | HG01884.hp1 HG02922.hp1 HG03486.hp2 |
splice_region_variant&intron_variant | LOW | c.1292-7C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695086 | |||||||
| chr12:18695118 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1292-39T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695118 | |||||||
| chr12:18695197 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1292-118A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695197 | |||||||
| chr12:18695442 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0095 |
2 | HG01346.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1292-363G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695442 | |||||||
| chr12:18695611 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(132): Show |
136 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.1292-532A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695611 | |||||||
| chr12:18695632 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1291+518G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695632 | |||||||
| chr12:18695675 | G | A | 17 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0092 others(14): Show |
17 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+475C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695675 | |||||||
| chr12:18695705 | A | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0212 |
2 | HG01993.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1291+445T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695705 | |||||||
| chr12:18695716 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1291+434C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695716 | |||||||
| chr12:18695739 | G | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1291+411C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695739 | |||||||
| chr12:18695803 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1291+347C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695803 | |||||||
| chr12:18695840 | C | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0180 others(30): Show |
34 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1291+310G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695840 | |||||||
| chr12:18695964 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1291+186C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18695964 | |||||||
| chr12:18696010 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0095 |
2 | HG01346.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1291+140G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18696010 | |||||||
| chr12:18696039 | G | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0180 others(30): Show |
34 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1291+111C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18696039 | |||||||
| chr12:18696137 | G | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1291+13C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 11/14 | chr12 | 18696137 | |||||||
| chr12:18696322 | C | CTATA | 11 | a0001c0001t0001g0036 a0001c0001t0001g0195 a0001c0001t0001g0217 others(8): Show |
11 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.1175-60_1175-57dup others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATA | 11 | a0001c0001t0001g0045 a0001c0001t0001g0075 a0001c0001t0001g0095 others(8): Show |
11 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1175-62_1175-57dup others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(1): Show |
15 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0053 others(12): Show |
15 | HG00140.hp1 HG01106.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1175-64_1175-57dup others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(3): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0112 others(5): Show |
8 | HG00609.hp2 HG00735.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-66_1175-57dup others(10): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(5): Show |
4 | a0001c0001t0001g0033 a0001c0001t0001g0051 a0001c0001t0001g0233 others(1): Show |
4 | HG00099.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-68_1175-57dup others(12): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(7): Show |
8 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0189 others(5): Show |
8 | HG01934.hp2 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-70_1175-57dup others(14): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(9): Show |
8 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0038 others(5): Show |
8 | HG02572.hp1 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-72_1175-57dup others(16): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(11): Show |
14 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0020 others(11): Show |
14 | HG00673.hp1 HG01081.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.1175-74_1175-57dup others(18): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(13): Show |
29 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0021 others(26): Show |
29 | HG00642.hp2 HG01099.hp2 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1175-76_1175-57dup others(20): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(15): Show |
34 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
35 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1175-78_1175-57dup others(22): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(17): Show |
29 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0025 others(26): Show |
30 | HG01081.hp1 HG01256.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.1175-80_1175-57dup others(24): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(19): Show |
24 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(21): Show |
24 | HG01175.hp2 HG01928.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.1175-82_1175-57dup others(26): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(21): Show |
6 | a0001c0001t0001g0066 a0001c0001t0001g0129 a0001c0001t0001g0207 others(3): Show |
6 | HG00099.hp2 HG01358.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175-84_1175-57dup others(28): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(23): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0136 |
2 | HG02056.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1175-57_1175-56ins others(30): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | C | CTATATAT others(27): Show |
1 | a0001c0001t0001g0235 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1175-57_1175-56ins others(34): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | CTATATA | C | 6 | a0001c0001t0001g0065 a0001c0001t0001g0081 a0001c0001t0001g0101 others(3): Show |
6 | HG00733.hp1 HG02056.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175-62_1175-57del others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696322 | CTATATAT others(1): Show |
C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0068 others(90): Show |
94 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1175-64_1175-57del others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696322 | |||||||
| chr12:18696348 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0153 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1175-83_1175-82ins others(30): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696348 | |||||||
| chr12:18696348 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0155 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1175-83_1175-82ins others(28): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696348 | |||||||
| chr12:18696348 | A | ATATATAT others(17): Show |
4 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0001g0157 others(1): Show |
4 | NA18941.hp2 NA18944.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-83_1175-82ins others(24): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696348 | |||||||
| chr12:18696348 | A | ATATATAT others(13): Show |
6 | a0001c0001t0001g0126 a0001c0001t0001g0154 a0001c0001t0001g0161 others(3): Show |
6 | NA18982.hp1 NA18999.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175-83_1175-82ins others(20): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696348 | |||||||
| chr12:18696348 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0206 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1175-83_1175-82ins others(18): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696348 | |||||||
| chr12:18696501 | G | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1175-235C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696501 | |||||||
| chr12:18696659 | C | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1175-393G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696659 | |||||||
| chr12:18696692 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1175-426T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696692 | |||||||
| chr12:18696696 | C | T | 1 | a0001c0001t0002g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1175-430G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696696 | |||||||
| chr12:18696710 | C | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0180 others(30): Show |
34 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-444G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696710 | |||||||
| chr12:18696734 | T | A | 1 | a0001c0001t0001g0258 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1175-468A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696734 | |||||||
| chr12:18696756 | G | C | 3 | a0001c0001t0001g0244 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG02080.hp2 NA19001.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1175-490C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696756 | |||||||
| chr12:18696810 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG00733.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175-544G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696810 | |||||||
| chr12:18696847 | G | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1175-581C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696847 | |||||||
| chr12:18696919 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1175-653A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696919 | |||||||
| chr12:18696930 | A | C | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1175-664T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696930 | |||||||
| chr12:18696933 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1175-667G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696933 | |||||||
| chr12:18696934 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1175-668T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696934 | |||||||
| chr12:18696965 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1175-699A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18696965 | |||||||
| chr12:18697140 | A | G | 15 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0092 others(12): Show |
15 | HG00673.hp2 NA18941.hp2 NA18944.hp1 others(12): Show |
intron_variant | MODIFIER | c.1175-874T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697140 | |||||||
| chr12:18697155 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1175-889T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697155 | |||||||
| chr12:18697237 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1175-971A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697237 | |||||||
| chr12:18697355 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1175-1089C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697355 | |||||||
| chr12:18697472 | A | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0046 others(36): Show |
40 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.1175-1206T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697472 | |||||||
| chr12:18697544 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(133): Show |
137 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.1175-1278C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697544 | |||||||
| chr12:18697573 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0296 |
2 | HG02155.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1175-1307G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697573 | |||||||
| chr12:18697693 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1175-1427T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697693 | |||||||
| chr12:18697702 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(134): Show |
138 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.1175-1436T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697702 | |||||||
| chr12:18697737 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0075 others(33): Show |
37 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1175-1471C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697737 | |||||||
| chr12:18697802 | AT | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1175-1537delA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697802 | |||||||
| chr12:18697829 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0189 others(1): Show |
4 | HG01934.hp2 HG02818.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1563A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697829 | |||||||
| chr12:18697875 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1175-1609C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697875 | |||||||
| chr12:18697886 | A | AT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1175-1621dupA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697886 | |||||||
| chr12:18697886 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1175-1620T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697886 | |||||||
| chr12:18697980 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1175-1714T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18697980 | |||||||
| chr12:18698048 | T | TCCTGTCC others(43): Show |
1 | a0001c0001t0001g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1174+1745_1174+174 others(54): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698048 | |||||||
| chr12:18698060 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1734C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698060 | |||||||
| chr12:18698101 | C | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0180 others(17): Show |
21 | HG00140.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1174+1693G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698101 | |||||||
| chr12:18698185 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1174+1609G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698185 | |||||||
| chr12:18698242 | C | CTTCTA | 76 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(73): Show |
77 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1174+1547_1174+155 others(9): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698242 | |||||||
| chr12:18698242 | C | CTTCTATT others(3): Show |
71 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0047 others(68): Show |
71 | HG00140.hp1 HG00609.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.1174+1542_1174+155 others(14): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698242 | |||||||
| chr12:18698242 | C | CTTCTATT others(8): Show |
46 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0032 others(43): Show |
46 | HG00099.hp1 HG00621.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1174+1537_1174+155 others(19): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698242 | |||||||
| chr12:18698242 | C | CTTCTATT others(13): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(24): Show |
29 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1174+1532_1174+155 others(24): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698242 | |||||||
| chr12:18698242 | C | CTTCTATT others(18): Show |
2 | a0001c0001t0001g0287 a0002c0003t0001g0070 |
2 | HG01884.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1174+1527_1174+155 others(29): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698242 | |||||||
| chr12:18698242 | CTTCTA | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0319 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174+1547_1174+155 others(9): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698242 | |||||||
| chr12:18698282 | A | T | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1174+1512T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698282 | |||||||
| chr12:18698290 | C | A | 1 | a0005c0004t0001g0291 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1174+1504G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698290 | |||||||
| chr12:18698295 | C | T | 6 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0189 others(3): Show |
6 | HG01934.hp2 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174+1499G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698295 | |||||||
| chr12:18698394 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1174+1400G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698394 | |||||||
| chr12:18698394 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1400G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698394 | |||||||
| chr12:18698600 | G | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(123): Show |
127 | HG00099.hp1 HG00609.hp2 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.1174+1194C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698600 | |||||||
| chr12:18698630 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(145): Show |
149 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(146): Show |
intron_variant | MODIFIER | c.1174+1164T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698630 | |||||||
| chr12:18698889 | T | G | 10 | a0001c0001t0001g0157 a0001c0001t0001g0187 a0001c0001t0001g0258 others(7): Show |
10 | NA18944.hp1 NA18965.hp1 NA18971.hp2 others(7): Show |
intron_variant | MODIFIER | c.1174+905A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698889 | |||||||
| chr12:18698981 | G | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0214 a0001c0001t0001g0250 others(1): Show |
5 | HG01346.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174+813C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18698981 | |||||||
| chr12:18699000 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1174+794A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18699000 | |||||||
| chr12:18699327 | T | A | 1 | a0001c0001t0003g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1174+467A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18699327 | |||||||
| chr12:18699435 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1174+359G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18699435 | |||||||
| chr12:18699466 | C | T | 12 | a0001c0001t0001g0195 a0001c0001t0001g0217 a0001c0001t0001g0227 others(9): Show |
12 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174+328G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18699466 | |||||||
| chr12:18699475 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1174+319G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18699475 | |||||||
| chr12:18699564 | C | G | 16 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(13): Show |
16 | HG01934.hp2 HG02451.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1174+230G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18699564 | |||||||
| chr12:18699570 | T | A | 1 | a0001c0001t0002g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1174+224A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 10/14 | chr12 | 18699570 | |||||||
| chr12:18700005 | A | T | 3 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02258.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1018-55T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700005 | |||||||
| chr12:18700006 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1018-56A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700006 | |||||||
| chr12:18700254 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1018-304C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700254 | |||||||
| chr12:18700512 | C | CA | 20 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
20 | HG01109.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1018-563dupT | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700512 | |||||||
| chr12:18700512 | C | CAA | 11 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1018-564_1018-563d others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700512 | |||||||
| chr12:18700512 | C | CAAA | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0046 others(63): Show |
67 | HG00609.hp1 HG00621.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.1018-565_1018-563d others(5): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700512 | |||||||
| chr12:18700512 | C | CAAAA | 41 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0060 others(38): Show |
42 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1018-566_1018-563d others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700512 | |||||||
| chr12:18700512 | C | CAAAAA | 15 | a0001c0001t0001g0157 a0001c0001t0001g0187 a0001c0001t0001g0198 others(12): Show |
15 | HG01106.hp1 HG01361.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1018-567_1018-563d others(7): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700512 | |||||||
| chr12:18700512 | C | CAAAAAA | 8 | a0001c0001t0001g0105 a0001c0001t0001g0135 a0001c0001t0001g0201 others(5): Show |
8 | HG02622.hp2 HG03195.hp1 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.1018-568_1018-563d others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700512 | |||||||
| chr12:18700512 | C | CAAAAAAA | 68 | a0001c0001t0001g0035 a0001c0001t0001g0059 a0001c0001t0001g0067 others(65): Show |
68 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1018-569_1018-563d others(9): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700512 | |||||||
| chr12:18700512 | C | CAAAAAAA others(1): Show |
40 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0064 others(37): Show |
41 | HG00673.hp1 HG00735.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1018-570_1018-563d others(10): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700512 | |||||||
| chr12:18700512 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0072 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1018-572_1018-563d others(12): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700512 | |||||||
| chr12:18700512 | CA | C | 12 | a0001c0001t0001g0195 a0001c0001t0001g0217 a0001c0001t0001g0227 others(9): Show |
12 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1018-563delT | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700512 | |||||||
| chr12:18700537 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1018-587A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700537 | |||||||
| chr12:18700538 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1018-588T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700538 | |||||||
| chr12:18700539 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1018-589C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700539 | |||||||
| chr12:18700801 | C | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG02818.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+700G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700801 | |||||||
| chr12:18700984 | ATT | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1017+515_1017+516d others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700984 | |||||||
| chr12:18700984 | ATTT | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(132): Show |
136 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.1017+514_1017+516d others(5): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700984 | |||||||
| chr12:18700986 | T | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG02818.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+515A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700986 | |||||||
| chr12:18700987 | T | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
120 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.1017+514A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700987 | |||||||
| chr12:18700988 | T | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(132): Show |
136 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.1017+513A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18700988 | |||||||
| chr12:18701051 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1017+450G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18701051 | |||||||
| chr12:18701317 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1017+184C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18701317 | |||||||
| chr12:18701449 | A | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017+52T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 9/14 | chr12 | 18701449 | |||||||
| chr12:18701606 | A | ATCC | 5 | a0001c0001t0001g0014 a0001c0001t0001g0162 a0001c0001t0001g0206 others(2): Show |
5 | HG00099.hp2 HG02723.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.950-41_950-39dupGG others(1): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 8/14 | chr12 | 18701606 | |||||||
| chr12:18701606 | A | ATCCTCC | 7 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0153 others(4): Show |
7 | HG00673.hp2 HG03516.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.950-44_950-39dupGG others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 8/14 | chr12 | 18701606 | |||||||
| chr12:18701606 | ATCC | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(7): Show |
10 | HG02148.hp2 HG02293.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.950-41_950-39delGG others(1): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 8/14 | chr12 | 18701606 | |||||||
| chr12:18701606 | ATCCTCC | A | 9 | a0001c0001t0001g0079 a0001c0001t0001g0164 a0001c0001t0001g0176 others(6): Show |
9 | HG00621.hp2 HG00642.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.950-44_950-39delGG others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 8/14 | chr12 | 18701606 | |||||||
| chr12:18701606 | ATCCTCCT others(2): Show |
A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(136): Show |
140 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.950-47_950-39delGG others(7): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 8/14 | chr12 | 18701606 | |||||||
| chr12:18701606 | ATCCTCCT others(5): Show |
A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
130 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.950-50_950-39delGG others(10): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 8/14 | chr12 | 18701606 | |||||||
| chr12:18701606 | ATCCTCCT others(8): Show |
A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.950-53_950-39delGG others(13): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 8/14 | chr12 | 18701606 | |||||||
| chr12:18701606 | ATCCTCCT others(11): Show |
A | 1 | a0003c0007t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.950-56_950-39delGG others(16): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 8/14 | chr12 | 18701606 | |||||||
| chr12:18701691 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp1 | splice_donor_variant&intron_variant | HIGH | c.949+1G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 8/14 | chr12 | 18701691 | |||||||
| chr12:18701898 | C | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.865-122G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18701898 | |||||||
| chr12:18701939 | T | C | 16 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(13): Show |
16 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(13): Show |
intron_variant | MODIFIER | c.865-163A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18701939 | |||||||
| chr12:18702418 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.865-642T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702418 | |||||||
| chr12:18702508 | G | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(111): Show |
115 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.865-732C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702508 | |||||||
| chr12:18702564 | C | G | 15 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(12): Show |
15 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(12): Show |
intron_variant | MODIFIER | c.865-788G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702564 | |||||||
| chr12:18702659 | A | C | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(15): Show |
18 | HG00733.hp2 HG01081.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.865-883T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702659 | |||||||
| chr12:18702770 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.865-994A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702770 | |||||||
| chr12:18702818 | C | CT | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
216 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.865-1043dupA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702818 | |||||||
| chr12:18702818 | C | CTT | 15 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0055 others(12): Show |
15 | HG00642.hp1 HG01934.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.865-1044_865-1043d others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702818 | |||||||
| chr12:18702818 | C | CTTT | 31 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(28): Show |
31 | HG00733.hp2 HG01081.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.865-1045_865-1043d others(5): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702818 | |||||||
| chr12:18702818 | C | CTTTTT | 15 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0154 others(12): Show |
15 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(12): Show |
intron_variant | MODIFIER | c.865-1047_865-1043d others(7): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702818 | |||||||
| chr12:18702843 | C | T | 5 | a0001c0001t0001g0189 a0001c0001t0001g0202 a0001c0001t0002g0040 others(2): Show |
5 | HG01884.hp1 HG01934.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.865-1067G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702843 | |||||||
| chr12:18702882 | A | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(118): Show |
122 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.865-1106T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702882 | |||||||
| chr12:18702907 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0168 |
2 | NA18952.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.865-1131C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18702907 | |||||||
| chr12:18703023 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02257.hp2 HG02647.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.865-1247T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703023 | |||||||
| chr12:18703128 | T | C | 7 | a0001c0001t0001g0189 a0001c0001t0001g0202 a0001c0001t0001g0319 others(4): Show |
7 | HG01934.hp2 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.865-1352A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703128 | |||||||
| chr12:18703217 | G | A | 15 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(12): Show |
15 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(12): Show |
intron_variant | MODIFIER | c.865-1441C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703217 | |||||||
| chr12:18703342 | A | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(115): Show |
119 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.865-1566T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703342 | |||||||
| chr12:18703596 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.864+1570A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703596 | |||||||
| chr12:18703705 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1461C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703705 | |||||||
| chr12:18703822 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0220 a0001c0001t0001g0246 others(3): Show |
7 | HG00140.hp1 HG01106.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.864+1344G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703822 | |||||||
| chr12:18703864 | A | C | 1 | a0003c0006t0001g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.864+1302T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703864 | |||||||
| chr12:18703867 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.864+1299T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703867 | |||||||
| chr12:18703880 | A | C | 15 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(12): Show |
15 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(12): Show |
intron_variant | MODIFIER | c.864+1286T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703880 | |||||||
| chr12:18703890 | C | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.864+1276G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703890 | |||||||
| chr12:18703942 | G | A | 14 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(11): Show |
14 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.864+1224C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18703942 | |||||||
| chr12:18704005 | C | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1161G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704005 | |||||||
| chr12:18704081 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0168 |
2 | NA18952.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.864+1085C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704081 | |||||||
| chr12:18704309 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.864+857G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704309 | |||||||
| chr12:18704419 | G | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(111): Show |
115 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.864+747C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704419 | |||||||
| chr12:18704429 | G | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.864+737C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704429 | |||||||
| chr12:18704485 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.864+681G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704485 | |||||||
| chr12:18704575 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.864+591G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704575 | |||||||
| chr12:18704621 | C | G | 3 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02258.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.864+545G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704621 | |||||||
| chr12:18704622 | G | A | 1 | a0001c0001t0004g0323 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.864+544C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704622 | |||||||
| chr12:18704766 | G | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG02818.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+400C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704766 | |||||||
| chr12:18704941 | T | A | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(15): Show |
18 | HG00733.hp2 HG01081.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.864+225A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18704941 | |||||||
| chr12:18705015 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.864+151A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18705015 | |||||||
| chr12:18705115 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.864+51A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 7/14 | chr12 | 18705115 | |||||||
| chr12:18705438 | C | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.715-123G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18705438 | |||||||
| chr12:18705483 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.715-168G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18705483 | |||||||
| chr12:18705664 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.715-349C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18705664 | |||||||
| chr12:18705931 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-616A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18705931 | |||||||
| chr12:18706047 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.715-732G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706047 | |||||||
| chr12:18706156 | C | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG00733.hp2 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-841G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706156 | |||||||
| chr12:18706188 | C | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
9 | HG02145.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-873G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706188 | |||||||
| chr12:18706214 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.715-899C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706214 | |||||||
| chr12:18706218 | T | C | 46 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(43): Show |
46 | HG00099.hp2 HG00323.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.715-903A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706218 | |||||||
| chr12:18706243 | TA | T | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
10 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-929delT | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706243 | |||||||
| chr12:18706297 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.715-982A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706297 | |||||||
| chr12:18706302 | G | A | 2 | a0002c0003t0001g0070 a0002c0003t0001g0071 |
2 | HG00099.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.715-987C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706302 | |||||||
| chr12:18706316 | G | C | 1 | a0001c0001t0001g0219 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.715-1001C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706316 | |||||||
| chr12:18706339 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.715-1024G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706339 | |||||||
| chr12:18706400 | A | G | 16 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(13): Show |
16 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(13): Show |
intron_variant | MODIFIER | c.715-1085T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706400 | |||||||
| chr12:18706416 | T | G | 1 | a0001c0001t0001g0290 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.715-1101A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706416 | |||||||
| chr12:18706544 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.715-1229C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706544 | |||||||
| chr12:18706577 | A | C | 4 | a0001c0001t0001g0183 a0001c0001t0002g0041 a0001c0001t0002g0042 others(1): Show |
4 | HG02258.hp1 HG03139.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1262T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706577 | |||||||
| chr12:18706605 | A | C | 16 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(13): Show |
16 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(13): Show |
intron_variant | MODIFIER | c.715-1290T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706605 | |||||||
| chr12:18706838 | A | T | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1523T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706838 | |||||||
| chr12:18706901 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.715-1586G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18706901 | |||||||
| chr12:18707062 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG00733.hp2 HG01891.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1747A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18707062 | |||||||
| chr12:18707113 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.715-1798G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18707113 | |||||||
| chr12:18707556 | G | C | 16 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(13): Show |
16 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(13): Show |
intron_variant | MODIFIER | c.715-2241C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18707556 | |||||||
| chr12:18707811 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.715-2496A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18707811 | |||||||
| chr12:18707915 | T | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
116 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.715-2600A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18707915 | |||||||
| chr12:18707927 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.715-2612G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18707927 | |||||||
| chr12:18707996 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(103): Show |
107 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.715-2681G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18707996 | |||||||
| chr12:18708065 | T | C | 54 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(51): Show |
54 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.715-2750A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708065 | |||||||
| chr12:18708129 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.715-2814C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708129 | |||||||
| chr12:18708159 | C | A | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.715-2844G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708159 | |||||||
| chr12:18708359 | A | AGAC | 16 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(13): Show |
16 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(13): Show |
intron_variant | MODIFIER | c.715-3047_715-3045d others(5): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708359 | |||||||
| chr12:18708421 | C | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(104): Show |
108 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.715-3106G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708421 | |||||||
| chr12:18708564 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.715-3249A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708564 | |||||||
| chr12:18708591 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.715-3276A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708591 | |||||||
| chr12:18708652 | C | T | 4 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0001g0272 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-3337G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708652 | |||||||
| chr12:18708799 | T | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.715-3484A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708799 | |||||||
| chr12:18708823 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA19006.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.715-3508C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708823 | |||||||
| chr12:18708854 | C | G | 1 | a0001c0001t0001g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.715-3539G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708854 | |||||||
| chr12:18708887 | T | C | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0109 others(6): Show |
9 | HG01981.hp1 HG02040.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-3572A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708887 | |||||||
| chr12:18708938 | A | AT | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-3624dupA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708938 | |||||||
| chr12:18708980 | T | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
9 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-3665A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18708980 | |||||||
| chr12:18709165 | T | A | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.714+3677A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18709165 | |||||||
| chr12:18709243 | G | GT | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.714+3598dupA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18709243 | |||||||
| chr12:18709382 | T | C | 1 | a0003c0007t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.714+3460A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18709382 | |||||||
| chr12:18709471 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0201 a0001c0001t0001g0202 others(8): Show |
12 | HG00140.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.714+3371G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18709471 | |||||||
| chr12:18709531 | C | CT | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.714+3310dupA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18709531 | |||||||
| chr12:18709572 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.714+3270A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18709572 | |||||||
| chr12:18709921 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.714+2921C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18709921 | |||||||
| chr12:18709950 | A | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(119): Show |
123 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.714+2892T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18709950 | |||||||
| chr12:18710008 | T | A | 1 | a0003c0007t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.714+2834A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710008 | |||||||
| chr12:18710037 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.714+2805A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710037 | |||||||
| chr12:18710156 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(110): Show |
114 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.714+2686A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710156 | |||||||
| chr12:18710232 | CAAGGCCT others(3): Show |
C | 1 | a0001c0001t0003g0270 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.714+2600_714+2609d others(12): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710232 | |||||||
| chr12:18710259 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(111): Show |
115 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.714+2583G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710259 | |||||||
| chr12:18710304 | T | C | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+2538A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710304 | |||||||
| chr12:18710463 | A | T | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+2379T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710463 | |||||||
| chr12:18710473 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.714+2369A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710473 | |||||||
| chr12:18710517 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.714+2325G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710517 | |||||||
| chr12:18710684 | A | G | 6 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+2158T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710684 | |||||||
| chr12:18710718 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(121): Show |
125 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.714+2124T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710718 | |||||||
| chr12:18710753 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.714+2089G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710753 | |||||||
| chr12:18710837 | C | A | 9 | a0001c0001t0001g0036 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
9 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+2005G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710837 | |||||||
| chr12:18710861 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.714+1981C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18710861 | |||||||
| chr12:18711089 | G | T | 6 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0201 others(3): Show |
6 | HG02280.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.714+1753C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711089 | |||||||
| chr12:18711171 | G | T | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+1671C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711171 | |||||||
| chr12:18711432 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG00733.hp2 HG01891.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+1410G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711432 | |||||||
| chr12:18711490 | A | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.714+1352T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711490 | |||||||
| chr12:18711529 | T | TATA | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.714+1310_714+1312d others(5): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711529 | |||||||
| chr12:18711529 | T | TATAATA | 30 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(27): Show |
30 | HG01257.hp2 HG01346.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.714+1307_714+1312d others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711529 | |||||||
| chr12:18711529 | T | TATAATAA others(2): Show |
3 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0190 |
3 | HG00323.hp2 HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.714+1304_714+1312d others(11): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711529 | |||||||
| chr12:18711529 | T | TATAATAA others(5): Show |
19 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(16): Show |
19 | HG00642.hp2 HG00733.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.714+1301_714+1312d others(14): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711529 | |||||||
| chr12:18711529 | T | TATAATAA others(8): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0201 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.714+1298_714+1312d others(17): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711529 | |||||||
| chr12:18711600 | G | T | 23 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0037 others(20): Show |
23 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.714+1242C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711600 | |||||||
| chr12:18711603 | C | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.714+1239G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711603 | |||||||
| chr12:18711619 | T | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(141): Show |
145 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(142): Show |
intron_variant | MODIFIER | c.714+1223A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711619 | |||||||
| chr12:18711675 | G | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+1167C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18711675 | |||||||
| chr12:18712054 | A | C | 20 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
20 | HG00323.hp2 HG00733.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.714+788T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18712054 | |||||||
| chr12:18712135 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.714+707C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18712135 | |||||||
| chr12:18712229 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0127 a0001c0001t0001g0285 |
3 | HG03942.hp1 NA18941.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.714+613C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18712229 | |||||||
| chr12:18712612 | C | T | 5 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0001t0001g0221 others(2): Show |
5 | NA18946.hp2 NA18953.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+230G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18712612 | |||||||
| chr12:18712710 | C | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0220 a0001c0001t0001g0246 others(2): Show |
6 | HG00140.hp1 HG01106.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+132G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 6/14 | chr12 | 18712710 | |||||||
| chr12:18713094 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570-108A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713094 | |||||||
| chr12:18713110 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.570-124A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713110 | |||||||
| chr12:18713174 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.570-188T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713174 | |||||||
| chr12:18713233 | G | A | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.570-247C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713233 | |||||||
| chr12:18713262 | T | A | 1 | a0001c0001t0001g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.570-276A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713262 | |||||||
| chr12:18713441 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.570-455T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713441 | |||||||
| chr12:18713462 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-476C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713462 | |||||||
| chr12:18713611 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02257.hp2 HG02647.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.570-625T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713611 | |||||||
| chr12:18713695 | T | G | 1 | a0001c0001t0001g0216 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.570-709A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713695 | |||||||
| chr12:18713706 | T | G | 28 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(25): Show |
28 | HG00323.hp2 HG00733.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.570-720A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713706 | |||||||
| chr12:18713722 | G | A | 3 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02258.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.570-736C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713722 | |||||||
| chr12:18713800 | T | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.570-814A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713800 | |||||||
| chr12:18713996 | C | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-1010G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18713996 | |||||||
| chr12:18714027 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.570-1041A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714027 | |||||||
| chr12:18714332 | T | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(114): Show |
118 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.570-1346A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714332 | |||||||
| chr12:18714603 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.570-1617A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714603 | |||||||
| chr12:18714628 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.570-1642A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714628 | |||||||
| chr12:18714655 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.570-1669G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714655 | |||||||
| chr12:18714675 | G | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
119 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.570-1689C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714675 | |||||||
| chr12:18714777 | A | G | 6 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.570-1791T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714777 | |||||||
| chr12:18714799 | T | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG02818.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.570-1813A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714799 | |||||||
| chr12:18714804 | C | G | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-1818G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714804 | |||||||
| chr12:18714808 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.570-1822T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714808 | |||||||
| chr12:18714879 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.570-1893T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18714879 | |||||||
| chr12:18715030 | C | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.570-2044G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715030 | |||||||
| chr12:18715077 | G | A | 14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(11): Show |
14 | HG00323.hp2 HG01081.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.570-2091C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715077 | |||||||
| chr12:18715112 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.570-2126A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715112 | |||||||
| chr12:18715156 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.570-2170T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715156 | |||||||
| chr12:18715168 | T | G | 4 | a0001c0001t0001g0138 a0001c0001t0001g0179 a0001c0001t0001g0217 others(1): Show |
4 | HG01934.hp1 HG02129.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-2182A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715168 | T | TG | 25 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0046 others(22): Show |
25 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.570-2183dupC | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715168 | T | TGG | 34 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0017 others(31): Show |
35 | HG00140.hp1 HG00642.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.570-2184_570-2183d others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715168 | T | TGGG | 37 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
38 | HG00140.hp2 HG01071.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.570-2185_570-2183d others(5): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715168 | T | TGGGG | 30 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0074 others(27): Show |
31 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.570-2186_570-2183d others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715168 | T | TGGGGG | 42 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0066 others(39): Show |
42 | HG00609.hp1 HG00735.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.570-2187_570-2183d others(7): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715168 | T | TGGGGGG | 30 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0064 others(27): Show |
30 | HG01255.hp1 HG01516.hp2 HG01928.hp2 others(27): Show |
intron_variant | MODIFIER | c.570-2188_570-2183d others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715168 | T | TGGGGGGG | 30 | a0001c0001t0001g0006 a0001c0001t0001g0065 a0001c0001t0001g0068 others(27): Show |
30 | HG00673.hp1 HG00673.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.570-2189_570-2183d others(9): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715168 | T | TGGGGGGG others(3): Show |
3 | a0001c0001t0001g0137 a0001c0001t0001g0146 a0001c0001t0001g0154 |
3 | HG02080.hp1 NA18953.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.570-2192_570-2183d others(12): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715168 | T | TGGGGGGG others(5): Show |
1 | a0001c0001t0001g0060 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.570-2194_570-2183d others(14): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715168 | T | TGGGGGGG others(6): Show |
1 | a0001c0001t0001g0286 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.570-2195_570-2183d others(15): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715168 | |||||||
| chr12:18715173 | G | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02280.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.570-2187C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715173 | |||||||
| chr12:18715174 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0184 |
2 | HG00733.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.570-2188C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715174 | |||||||
| chr12:18715179 | G | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.570-2193C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715179 | |||||||
| chr12:18715182 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.570-2196C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715182 | |||||||
| chr12:18715183 | C | G | 45 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(42): Show |
45 | HG01071.hp2 HG01081.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.570-2197G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715183 | |||||||
| chr12:18715186 | A | G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(45): Show |
48 | HG01071.hp2 HG01081.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.570-2200T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715186 | |||||||
| chr12:18715187 | G | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(29): Show |
32 | HG01071.hp2 HG01106.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.570-2201C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715187 | |||||||
| chr12:18715187 | G | GC | 8 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(5): Show |
8 | HG01081.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.570-2202_570-2201i others(3): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715187 | |||||||
| chr12:18715187 | G | GGC | 4 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0051 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.570-2202_570-2201i others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715187 | |||||||
| chr12:18715190 | A | AG | 4 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0001c0001t0001g0088 others(1): Show |
4 | HG03927.hp1 HG03942.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.570-2205dupC | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715190 | |||||||
| chr12:18715190 | A | AGG | 13 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0081 others(10): Show |
13 | HG01109.hp2 HG01256.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.570-2206_570-2205d others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715190 | |||||||
| chr12:18715190 | A | G | 3 | a0001c0001t0001g0033 a0003c0006t0001g0210 a0003c0007t0001g0188 |
3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570-2204T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715190 | |||||||
| chr12:18715191 | G | C | 3 | a0001c0001t0001g0033 a0003c0006t0001g0210 a0003c0007t0001g0188 |
3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570-2205C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715191 | |||||||
| chr12:18715192 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.570-2206C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715192 | |||||||
| chr12:18715192 | G | GGA | 6 | a0001c0001t0001g0184 a0001c0001t0001g0200 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.570-2208_570-2207d others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715192 | |||||||
| chr12:18715192 | G | GGAGA | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-2210_570-2207d others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715192 | |||||||
| chr12:18715192 | G | GGAGAGA | 3 | a0001c0001t0001g0039 a0001c0001t0001g0318 a0001c0001t0002g0041 |
3 | HG02717.hp1 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.570-2212_570-2207d others(8): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715192 | |||||||
| chr12:18715192 | GGA | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.570-2208_570-2207d others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715192 | |||||||
| chr12:18715194 | A | AGG | 26 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(23): Show |
26 | HG01071.hp2 HG01106.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.570-2209_570-2208i others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715194 | |||||||
| chr12:18715194 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(111): Show |
115 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.570-2208T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715194 | |||||||
| chr12:18715196 | A | G | 25 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(22): Show |
25 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.570-2210T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715196 | |||||||
| chr12:18715198 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0296 |
2 | NA18984.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.570-2212T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715198 | |||||||
| chr12:18715200 | A | G | 3 | a0001c0001t0001g0033 a0003c0006t0001g0210 a0003c0007t0001g0188 |
3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570-2214T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715200 | |||||||
| chr12:18715298 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-2312T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715298 | |||||||
| chr12:18715399 | G | GT | 15 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0044 others(12): Show |
15 | HG01109.hp2 HG01928.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.570-2414dupA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715399 | |||||||
| chr12:18715551 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570-2565T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715551 | |||||||
| chr12:18715558 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.570-2572G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715558 | |||||||
| chr12:18715563 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0002g0040 |
2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.570-2577C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715563 | |||||||
| chr12:18715734 | G | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
104 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.570-2748C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715734 | |||||||
| chr12:18715804 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570-2818A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715804 | |||||||
| chr12:18715957 | C | G | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-2971G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18715957 | |||||||
| chr12:18716007 | C | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA18957.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.570-3021G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716007 | |||||||
| chr12:18716065 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
3 | HG01891.hp1 HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.570-3079A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716065 | |||||||
| chr12:18716083 | A | G | 13 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(10): Show |
13 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(10): Show |
intron_variant | MODIFIER | c.570-3097T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716083 | |||||||
| chr12:18716097 | A | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
15 | HG00323.hp2 HG01081.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.570-3111T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716097 | |||||||
| chr12:18716209 | G | A | 1 | a0003c0007t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.569+3222C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716209 | |||||||
| chr12:18716253 | G | GA | 8 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0198 others(5): Show |
8 | HG02109.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.569+3177dupT | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716253 | |||||||
| chr12:18716272 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.569+3159T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716272 | |||||||
| chr12:18716308 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.569+3123G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716308 | |||||||
| chr12:18716353 | G | A | 5 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.569+3078C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716353 | |||||||
| chr12:18716373 | A | T | 1 | a0001c0001t0001g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.569+3058T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716373 | |||||||
| chr12:18716386 | A | G | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG02818.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.569+3045T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716386 | |||||||
| chr12:18716441 | C | G | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.569+2990G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716441 | |||||||
| chr12:18716445 | C | T | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.569+2986G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716445 | |||||||
| chr12:18716461 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0203 |
2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.569+2970T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716461 | |||||||
| chr12:18716496 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.569+2935C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716496 | |||||||
| chr12:18716797 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.569+2634A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716797 | |||||||
| chr12:18716808 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.569+2623T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716808 | |||||||
| chr12:18716955 | T | A | 17 | a0001c0001t0001g0183 a0001c0001t0001g0191 a0001c0001t0001g0192 others(14): Show |
17 | HG00642.hp2 HG01099.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.569+2476A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716955 | |||||||
| chr12:18716974 | A | T | 12 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(9): Show |
12 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.569+2457T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716974 | |||||||
| chr12:18716990 | A | G | 12 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(9): Show |
12 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.569+2441T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18716990 | |||||||
| chr12:18717030 | C | A | 1 | a0001c0001t0001g0167 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.569+2401G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717030 | |||||||
| chr12:18717083 | A | C | 5 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.569+2348T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717083 | |||||||
| chr12:18717214 | T | C | 1 | a0003c0007t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.569+2217A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717214 | |||||||
| chr12:18717285 | T | G | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
16 | HG00323.hp2 HG01081.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.569+2146A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717285 | |||||||
| chr12:18717386 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.569+2045T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717386 | |||||||
| chr12:18717518 | T | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG00733.hp2 HG01891.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.569+1913A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717518 | |||||||
| chr12:18717529 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.569+1902C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717529 | |||||||
| chr12:18717573 | C | A | 1 | a0001c0001t0001g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.569+1858G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717573 | |||||||
| chr12:18717698 | T | G | 1 | a0001c0001t0001g0284 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.569+1733A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717698 | |||||||
| chr12:18717741 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.569+1690G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717741 | |||||||
| chr12:18717787 | C | G | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.569+1644G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717787 | |||||||
| chr12:18717852 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.569+1579A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717852 | |||||||
| chr12:18717865 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.569+1566G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717865 | |||||||
| chr12:18717944 | G | A | 10 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0143 others(7): Show |
10 | NA18946.hp1 NA18946.hp2 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.569+1487C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717944 | |||||||
| chr12:18717972 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.569+1459C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18717972 | |||||||
| chr12:18718016 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.569+1415T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18718016 | |||||||
| chr12:18718080 | G | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG00733.hp2 HG01891.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.569+1351C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18718080 | |||||||
| chr12:18718113 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.569+1318A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18718113 | |||||||
| chr12:18718215 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.569+1216C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18718215 | |||||||
| chr12:18718248 | A | G | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
15 | HG00323.hp2 HG01081.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.569+1183T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18718248 | |||||||
| chr12:18718328 | T | C | 13 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0153 others(10): Show |
13 | HG00099.hp2 HG00673.hp2 HG03927.hp2 others(10): Show |
intron_variant | MODIFIER | c.569+1103A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18718328 | |||||||
| chr12:18718425 | A | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0175 |
2 | HG01069.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.569+1006T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18718425 | |||||||
| chr12:18718442 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.569+989A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18718442 | |||||||
| chr12:18718450 | A | G | 8 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(5): Show |
8 | HG00642.hp2 HG01099.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+981T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18718450 | |||||||
| chr12:18718792 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.569+639G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18718792 | |||||||
| chr12:18719005 | T | A | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.569+426A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18719005 | |||||||
| chr12:18719167 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.569+264C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18719167 | |||||||
| chr12:18719189 | G | A | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.569+242C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18719189 | |||||||
| chr12:18719391 | G | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(123): Show |
127 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(124): Show |
intron_variant | MODIFIER | c.569+40C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 5/14 | chr12 | 18719391 | |||||||
| chr12:18719641 | AT | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-10delA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18719641 | |||||||
| chr12:18719649 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.368-17T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18719649 | |||||||
| chr12:18719651 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.368-19T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18719651 | |||||||
| chr12:18719793 | T | G | 1 | a0001c0001t0001g0284 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.368-161A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18719793 | |||||||
| chr12:18720050 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(113): Show |
117 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.368-418G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18720050 | |||||||
| chr12:18720079 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.368-447C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18720079 | |||||||
| chr12:18720267 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0168 |
2 | NA18952.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.368-635C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18720267 | |||||||
| chr12:18720405 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.368-773A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18720405 | |||||||
| chr12:18720532 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.368-900C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18720532 | |||||||
| chr12:18720804 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.368-1172T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18720804 | |||||||
| chr12:18720820 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.368-1188T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18720820 | |||||||
| chr12:18720849 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(126): Show |
130 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(127): Show |
intron_variant | MODIFIER | c.368-1217T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18720849 | |||||||
| chr12:18721155 | C | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.368-1523G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18721155 | |||||||
| chr12:18721276 | C | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-1644G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18721276 | |||||||
| chr12:18721287 | C | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(145): Show |
149 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(146): Show |
intron_variant | MODIFIER | c.368-1655G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18721287 | |||||||
| chr12:18721290 | A | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(128): Show |
132 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.368-1658T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18721290 | |||||||
| chr12:18721381 | T | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG00733.hp2 HG02280.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-1749A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18721381 | |||||||
| chr12:18721416 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(127): Show |
131 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.368-1784C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18721416 | |||||||
| chr12:18721472 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0180 |
2 | HG03688.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.367+1839A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18721472 | |||||||
| chr12:18721513 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.367+1798A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18721513 | |||||||
| chr12:18721715 | TA | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(108): Show |
112 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.367+1595delT | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18721715 | |||||||
| chr12:18721756 | T | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+1555A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18721756 | |||||||
| chr12:18722003 | A | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0091 |
2 | NA19007.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.367+1308T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722003 | |||||||
| chr12:18722214 | C | A | 1 | a0001c0001t0001g0296 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.367+1097G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722214 | |||||||
| chr12:18722217 | T | TC | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.367+1093dupG | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722217 | |||||||
| chr12:18722219 | T | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.367+1092A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722219 | |||||||
| chr12:18722219 | T | TC | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.367+1091_367+1092i others(3): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722219 | |||||||
| chr12:18722228 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.367+1083C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722228 | |||||||
| chr12:18722253 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.367+1058A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722253 | |||||||
| chr12:18722385 | T | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
18 | HG00323.hp2 HG01081.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.367+926A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722385 | |||||||
| chr12:18722420 | G | T | 9 | a0001c0001t0001g0200 a0001c0001t0001g0308 a0001c0001t0001g0309 others(6): Show |
9 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.367+891C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722420 | |||||||
| chr12:18722784 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.367+527C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722784 | |||||||
| chr12:18722786 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.367+525C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722786 | |||||||
| chr12:18722852 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0178 |
2 | NA19010.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.367+459A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722852 | |||||||
| chr12:18722982 | G | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.367+329C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18722982 | |||||||
| chr12:18723001 | G | A | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0207 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.367+310C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18723001 | |||||||
| chr12:18723067 | G | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0034 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.367+244C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18723067 | |||||||
| chr12:18723124 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.367+187G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18723124 | |||||||
| chr12:18723180 | T | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
18 | HG00323.hp2 HG01081.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.367+131A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18723180 | |||||||
| chr12:18723197 | C | T | 21 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(18): Show |
21 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.367+114G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 4/14 | chr12 | 18723197 | |||||||
| chr12:18723563 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.136-21C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18723563 | |||||||
| chr12:18723704 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.136-162G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18723704 | |||||||
| chr12:18723754 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.136-212C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18723754 | |||||||
| chr12:18723770 | G | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0021 |
3 | HG02895.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.136-228C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18723770 | |||||||
| chr12:18724042 | T | C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG00621.hp2 HG02040.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-500A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18724042 | |||||||
| chr12:18724196 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.136-654A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18724196 | |||||||
| chr12:18724325 | C | A | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-783G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18724325 | |||||||
| chr12:18724359 | C | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-817G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18724359 | |||||||
| chr12:18724520 | G | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.136-978C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18724520 | |||||||
| chr12:18724573 | A | T | 7 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(4): Show |
7 | HG00642.hp2 HG01099.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-1031T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18724573 | |||||||
| chr12:18724644 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.136-1102C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18724644 | |||||||
| chr12:18725041 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.136-1499A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725041 | |||||||
| chr12:18725082 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0052 others(139): Show |
143 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(140): Show |
intron_variant | MODIFIER | c.136-1540A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725082 | |||||||
| chr12:18725238 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.136-1696C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725238 | |||||||
| chr12:18725262 | G | A | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.136-1720C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725262 | |||||||
| chr12:18725452 | A | C | 1 | a0001c0001t0001g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.136-1910T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725452 | |||||||
| chr12:18725535 | C | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-1993G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725535 | |||||||
| chr12:18725567 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.136-2025T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725567 | |||||||
| chr12:18725600 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.136-2058C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725600 | |||||||
| chr12:18725714 | G | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.136-2172C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725714 | |||||||
| chr12:18725803 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0052 others(135): Show |
139 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(136): Show |
intron_variant | MODIFIER | c.136-2261C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725803 | |||||||
| chr12:18725868 | T | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-2326A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18725868 | |||||||
| chr12:18726162 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.136-2620G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18726162 | |||||||
| chr12:18726204 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02257.hp2 HG02647.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-2662A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18726204 | |||||||
| chr12:18726237 | C | G | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.136-2695G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18726237 | |||||||
| chr12:18726617 | G | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0059 others(127): Show |
131 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(128): Show |
intron_variant | MODIFIER | c.136-3075C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18726617 | |||||||
| chr12:18726650 | AT | A | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-3109delA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18726650 | |||||||
| chr12:18726665 | T | C | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-3123A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18726665 | |||||||
| chr12:18726839 | T | C | 14 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0191 others(11): Show |
14 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-3297A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18726839 | |||||||
| chr12:18726956 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.136-3414C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18726956 | |||||||
| chr12:18726999 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.136-3457T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18726999 | |||||||
| chr12:18727027 | G | C | 11 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-3485C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727027 | |||||||
| chr12:18727048 | G | A | 1 | a0001c0001t0003g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.136-3506C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727048 | |||||||
| chr12:18727072 | A | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(13): Show |
17 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.136-3530T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727072 | |||||||
| chr12:18727141 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.136-3599G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727141 | |||||||
| chr12:18727163 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.136-3621C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727163 | |||||||
| chr12:18727184 | T | TA | 15 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0191 others(12): Show |
15 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.136-3643dupT | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727184 | |||||||
| chr12:18727212 | T | C | 2 | a0003c0006t0001g0210 a0003c0007t0001g0188 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136-3670A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727212 | |||||||
| chr12:18727350 | A | AT | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-3809dupA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727350 | |||||||
| chr12:18727401 | T | A | 1 | a0001c0001t0001g0079 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.136-3859A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727401 | |||||||
| chr12:18727410 | T | C | 13 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(10): Show |
13 | HG01884.hp1 HG01934.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.136-3868A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727410 | |||||||
| chr12:18727453 | A | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-3911T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727453 | |||||||
| chr12:18727502 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.136-3960G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727502 | |||||||
| chr12:18727524 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.136-3982C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727524 | |||||||
| chr12:18727556 | A | G | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0003c0006t0001g0210 others(1): Show |
4 | HG01884.hp1 HG01934.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-4014T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727556 | |||||||
| chr12:18727611 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.136-4069G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727611 | |||||||
| chr12:18727703 | T | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0207 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.136-4161A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727703 | |||||||
| chr12:18727741 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.136-4199G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727741 | |||||||
| chr12:18727856 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.136-4314A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727856 | |||||||
| chr12:18727991 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.136-4449T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18727991 | |||||||
| chr12:18728052 | A | C | 11 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
11 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-4510T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728052 | |||||||
| chr12:18728162 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.136-4620C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728162 | |||||||
| chr12:18728190 | G | T | 1 | a0003c0007t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136-4648C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728190 | |||||||
| chr12:18728195 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.136-4653A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728195 | |||||||
| chr12:18728446 | C | T | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-4904G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728446 | |||||||
| chr12:18728463 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0019 |
2 | HG02056.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.136-4921C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728463 | |||||||
| chr12:18728568 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.136-5026T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728568 | |||||||
| chr12:18728570 | G | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.136-5028C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728570 | |||||||
| chr12:18728671 | CAG | C | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-5131_136-5130d others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728671 | |||||||
| chr12:18728720 | G | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0207 others(96): Show |
100 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.136-5178C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728720 | |||||||
| chr12:18728731 | G | A | 16 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(13): Show |
16 | HG00642.hp2 HG01099.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-5189C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728731 | |||||||
| chr12:18728821 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.136-5279T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728821 | |||||||
| chr12:18728894 | A | C | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | NA18952.hp2 NA18981.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-5352T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728894 | |||||||
| chr12:18728962 | T | G | 4 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(1): Show |
4 | HG02109.hp2 HG02257.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-5420A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18728962 | |||||||
| chr12:18729035 | T | C | 16 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(13): Show |
16 | HG00642.hp2 HG01099.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-5493A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729035 | |||||||
| chr12:18729174 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.136-5632G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729174 | |||||||
| chr12:18729200 | C | T | 1 | a0001c0001t0003g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.136-5658G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729200 | |||||||
| chr12:18729237 | T | C | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-5695A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729237 | |||||||
| chr12:18729287 | T | G | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-5745A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729287 | |||||||
| chr12:18729288 | C | G | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-5746G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729288 | |||||||
| chr12:18729289 | T | A | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-5747A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729289 | |||||||
| chr12:18729290 | T | C | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-5748A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729290 | |||||||
| chr12:18729291 | A | C | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-5749T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729291 | |||||||
| chr12:18729292 | T | A | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-5750A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729292 | |||||||
| chr12:18729294 | T | A | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-5752A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729294 | |||||||
| chr12:18729295 | A | C | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-5753T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729295 | |||||||
| chr12:18729416 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.136-5874C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729416 | |||||||
| chr12:18729425 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.136-5883C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729425 | |||||||
| chr12:18729475 | A | G | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0003c0006t0001g0210 others(1): Show |
4 | HG01884.hp1 HG01934.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-5933T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729475 | |||||||
| chr12:18729503 | C | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.136-5961G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729503 | |||||||
| chr12:18729547 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-6005A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729547 | |||||||
| chr12:18729551 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-6009T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729551 | |||||||
| chr12:18729654 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.136-6112A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729654 | |||||||
| chr12:18729763 | G | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0207 others(93): Show |
97 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.136-6221C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729763 | |||||||
| chr12:18729829 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0034 others(96): Show |
100 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.136-6287G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729829 | |||||||
| chr12:18729904 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.135+6317G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729904 | |||||||
| chr12:18729945 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.135+6276T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18729945 | |||||||
| chr12:18730072 | T | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.135+6149A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730072 | |||||||
| chr12:18730147 | C | T | 5 | a0001c0001t0001g0065 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG02056.hp1 NA18980.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+6074G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730147 | |||||||
| chr12:18730250 | TA | T | 16 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(13): Show |
16 | HG00642.hp2 HG01099.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+5970delT | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730250 | |||||||
| chr12:18730289 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.135+5932G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730289 | |||||||
| chr12:18730469 | T | G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02818.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.135+5752A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730469 | |||||||
| chr12:18730486 | T | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02818.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.135+5735A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730486 | |||||||
| chr12:18730490 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.135+5731T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730490 | |||||||
| chr12:18730585 | C | A | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+5636G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730585 | |||||||
| chr12:18730634 | A | C | 1 | a0001c0001t0001g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+5587T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730634 | |||||||
| chr12:18730645 | T | C | 1 | a0005c0004t0001g0291 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.135+5576A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730645 | |||||||
| chr12:18730779 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.135+5442G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730779 | |||||||
| chr12:18730936 | T | TAAAAACT others(274): Show |
1 | a0001c0001t0003g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.135+5284_135+5285i others(283): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18730936 | |||||||
| chr12:18731006 | T | C | 1 | a0003c0007t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.135+5215A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731006 | |||||||
| chr12:18731056 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.135+5165C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731056 | |||||||
| chr12:18731066 | G | GA | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0003c0006t0001g0210 others(1): Show |
4 | HG01884.hp1 HG01934.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+5154dupT | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731066 | |||||||
| chr12:18731113 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02818.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.135+5108A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731113 | |||||||
| chr12:18731173 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.135+5048C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731173 | |||||||
| chr12:18731261 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(4): Show |
7 | HG02280.hp1 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+4960C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731261 | |||||||
| chr12:18731445 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02818.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.135+4776C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731445 | |||||||
| chr12:18731482 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0189 others(101): Show |
105 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.135+4739C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731482 | |||||||
| chr12:18731533 | C | CT | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(208): Show |
213 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(210): Show |
intron_variant | MODIFIER | c.135+4687dupA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731533 | |||||||
| chr12:18731533 | C | CTT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0068 others(18): Show |
21 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+4686_135+4687d others(4): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731533 | |||||||
| chr12:18731533 | CT | C | 17 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0048 others(14): Show |
17 | HG00323.hp2 HG01069.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+4687delA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731533 | |||||||
| chr12:18731559 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.135+4662T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731559 | |||||||
| chr12:18731560 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.135+4661G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731560 | |||||||
| chr12:18731722 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0059 others(125): Show |
129 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.135+4499C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731722 | |||||||
| chr12:18731736 | T | C | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.135+4485A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731736 | |||||||
| chr12:18731877 | T | C | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.135+4344A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731877 | |||||||
| chr12:18731962 | C | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(133): Show |
137 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.135+4259G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18731962 | |||||||
| chr12:18732178 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.135+4043C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732178 | |||||||
| chr12:18732246 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(100): Show |
104 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.135+3975T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732246 | |||||||
| chr12:18732309 | G | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.135+3912C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732309 | |||||||
| chr12:18732443 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(148): Show |
152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.135+3778G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732443 | |||||||
| chr12:18732484 | C | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+3737G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732484 | |||||||
| chr12:18732567 | G | A | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.135+3654C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732567 | |||||||
| chr12:18732651 | T | C | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.135+3570A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732651 | |||||||
| chr12:18732728 | T | C | 1 | a0001c0001t0001g0298 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.135+3493A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732728 | |||||||
| chr12:18732824 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA19006.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.135+3397T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732824 | |||||||
| chr12:18732897 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.135+3324C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732897 | |||||||
| chr12:18732904 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.135+3317T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732904 | |||||||
| chr12:18732930 | G | T | 1 | a0001c0001t0001g0211 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.135+3291C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732930 | |||||||
| chr12:18732993 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.135+3228A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18732993 | |||||||
| chr12:18733161 | G | T | 1 | a0001c0001t0001g0019 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.135+3060C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733161 | |||||||
| chr12:18733165 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.135+3056A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733165 | |||||||
| chr12:18733177 | T | A | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+3044A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733177 | |||||||
| chr12:18733195 | G | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.135+3026C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733195 | |||||||
| chr12:18733250 | T | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+2971A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733250 | |||||||
| chr12:18733416 | G | C | 2 | a0003c0006t0001g0210 a0003c0007t0001g0188 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.135+2805C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733416 | |||||||
| chr12:18733512 | CT | C | 4 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(1): Show |
4 | HG02258.hp1 NA19030.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+2708delA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733512 | |||||||
| chr12:18733575 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.135+2646G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733575 | |||||||
| chr12:18733576 | T | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+2645A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733576 | |||||||
| chr12:18733581 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.135+2640A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733581 | |||||||
| chr12:18733826 | T | G | 14 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
14 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.135+2395A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733826 | |||||||
| chr12:18733965 | A | G | 2 | a0003c0006t0001g0210 a0003c0007t0001g0188 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.135+2256T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18733965 | |||||||
| chr12:18734046 | G | C | 1 | a0001c0001t0001g0206 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.135+2175C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734046 | |||||||
| chr12:18734100 | G | C | 1 | a0001c0001t0001g0299 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.135+2121C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734100 | |||||||
| chr12:18734123 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.135+2098A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734123 | |||||||
| chr12:18734209 | G | T | 1 | a0003c0007t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.135+2012C>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734209 | |||||||
| chr12:18734290 | T | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+1931A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734290 | |||||||
| chr12:18734328 | G | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+1893C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734328 | |||||||
| chr12:18734343 | T | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG00733.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.135+1878A>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734343 | |||||||
| chr12:18734343 | T | TTTG | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0300 |
3 | HG02809.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.135+1875_135+1877d others(5): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734343 | |||||||
| chr12:18734412 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.135+1809C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734412 | |||||||
| chr12:18734414 | A | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(156): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.135+1807T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734414 | |||||||
| chr12:18734508 | G | A | 1 | a0003c0007t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.135+1713C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734508 | |||||||
| chr12:18734540 | G | A | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.135+1681C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734540 | |||||||
| chr12:18734564 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.135+1657A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734564 | |||||||
| chr12:18734609 | C | A | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.135+1612G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734609 | |||||||
| chr12:18734718 | G | C | 1 | a0001c0001t0001g0301 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.135+1503C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734718 | |||||||
| chr12:18734849 | T | A | 1 | a0001c0001t0003g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.135+1372A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734849 | |||||||
| chr12:18734937 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.135+1284A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734937 | |||||||
| chr12:18734996 | A | G | 8 | a0001c0001t0001g0036 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+1225T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734996 | |||||||
| chr12:18734997 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+1224A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18734997 | |||||||
| chr12:18735008 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.135+1213A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735008 | |||||||
| chr12:18735344 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.135+877G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735344 | |||||||
| chr12:18735377 | CCTGGGCT others(20): Show |
C | 1 | a0001c0001t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.135+817_135+843del others(27): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735377 | |||||||
| chr12:18735392 | G | A | 11 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
11 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+829C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735392 | |||||||
| chr12:18735417 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.135+804T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735417 | |||||||
| chr12:18735425 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.135+796T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735425 | |||||||
| chr12:18735509 | G | C | 1 | a0001c0001t0001g0304 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.135+712C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735509 | |||||||
| chr12:18735522 | A | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0034 others(126): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.135+699T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735522 | |||||||
| chr12:18735538 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.135+683G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735538 | |||||||
| chr12:18735596 | G | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(12): Show |
16 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+625C>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735596 | |||||||
| chr12:18735695 | A | G | 1 | a0001c0001t0001g0307 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.135+526T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735695 | |||||||
| chr12:18735749 | T | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0034 others(126): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.135+472A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735749 | |||||||
| chr12:18735763 | G | A | 17 | a0001c0001t0001g0036 a0001c0001t0001g0191 a0001c0001t0001g0192 others(14): Show |
17 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.135+458C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735763 | |||||||
| chr12:18735825 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.135+396T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735825 | |||||||
| chr12:18735840 | A | C | 11 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
11 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+381T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735840 | |||||||
| chr12:18735855 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
3 | HG01891.hp1 HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.135+366C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735855 | |||||||
| chr12:18735906 | A | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG01109.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.135+315T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735906 | |||||||
| chr12:18735936 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.135+285G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18735936 | |||||||
| chr12:18736192 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.135+29C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18736192 | |||||||
| chr12:18736215 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(102): Show |
106 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(103): Show |
splice_region_variant&intron_variant | LOW | c.135+6A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 3/14 | chr12 | 18736215 | |||||||
| chr12:18736387 | T | C | 1 | a0001c0001t0001g0306 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.12-43A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18736387 | |||||||
| chr12:18736583 | A | AAATTTGA others(1): Show |
142 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0059 others(139): Show |
143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.12-247_12-240dupCT others(6): Show |
PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18736583 | |||||||
| chr12:18736613 | C | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0189 others(119): Show |
123 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.12-269G>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18736613 | |||||||
| chr12:18736631 | A | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(120): Show |
124 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.12-287T>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18736631 | |||||||
| chr12:18736952 | C | CA | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.11+408_11+409insT | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18736952 | |||||||
| chr12:18736953 | G | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.11+408C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18736953 | |||||||
| chr12:18736961 | T | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0187 others(120): Show |
124 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.11+400A>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18736961 | |||||||
| chr12:18736969 | A | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
9 | HG01109.hp1 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.11+392T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18736969 | |||||||
| chr12:18737029 | C | G | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
6 | NA18959.hp2 NA18964.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.11+332G>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18737029 | |||||||
| chr12:18737044 | A | G | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+317T>C | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18737044 | |||||||
| chr12:18737053 | A | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(4): Show |
7 | HG02280.hp1 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+308T>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 2/14 | chr12 | 18737053 | |||||||
| chr12:18737538 | GT | G | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-138-30delA | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 1/14 | chr12 | 18737538 | |||||||
| chr12:18737593 | T | C | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-138-84A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 1/14 | chr12 | 18737593 | |||||||
| chr12:18737830 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-139+102G>A | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 1/14 | chr12 | 18737830 | |||||||
| chr12:18737853 | T | C | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(5): Show |
8 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-139+79A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 1/14 | chr12 | 18737853 | |||||||
| chr12:18737879 | T | C | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-139+53A>G | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 1/14 | chr12 | 18737879 | |||||||
| chr12:18737900 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139+32C>T | PLCZ1 | ENSG00000139151.16 | transcript | ENST00000266505.12 | protein_coding | 1/14 | chr12 | 18737900 |