Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5333 |
| ensemblid | ENSG00000187091.14 |
| hgncid | 9060 |
| symbol | PLCD1 |
| name | phospholipase C delta 1 |
| refseq_nuc | NM_006225.4 |
| refseq_prot | NP_006216.2 |
| ensembl_nuc | ENST00000334661.5 |
| ensembl_prot | ENSP00000335600.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 38007496 |
| end | 38029642 |
| strand | - |
| ver | v1.2 |
| region | chr3:38007496-38029642 |
| region5000 | chr3:38002496-38034642 |
| regionname0 | PLCD1_chr3_38007496_38029642 |
| regionname5000 | PLCD1_chr3_38002496_38034642 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 756 | 308 | 78 | 67 | 115 | 12 | 34 | 81 | PLCD1_chr3_38002496_38034642 | PLCD1 | MDSGR others(751): Show |
chr3 | 38002496 | 38034642 |
| a0002 | 0/0 | 756 | 33 | 1 | 0 | 30 | 0 | 2 | 25 | PLCD1_chr3_38002496_38034642 | PLCD1 | MDSGR others(751): Show |
chr3 | 38002496 | 38034642 |
| a0003 | 0/0 | 756 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | MDSGR others(751): Show |
chr3 | 38002496 | 38034642 |
| a0004 | 0/0 | 756 | 7 | 5 | 0 | 1 | 0 | 1 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | MDSGR others(751): Show |
chr3 | 38002496 | 38034642 |
| a0005 | 0/0 | 756 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | MDSGR others(751): Show |
chr3 | 38002496 | 38034642 |
| a0006 | 0/0 | 756 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | MDSGR others(751): Show |
chr3 | 38002496 | 38034642 |
| a0007 | 0/0 | 756 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | MDSGR others(751): Show |
chr3 | 38002496 | 38034642 |
| a0008 | 0/0 | 756 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | MDSGR others(751): Show |
chr3 | 38002496 | 38034642 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2268 | 240 | 44 | 54 | 108 | 10 | 22 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0003 | 0/0 | 2268 | 31 | 9 | 10 | 7 | 2 | 3 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0004 | 0/0 | 2268 | 10 | 9 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0006 | 0/0 | 2268 | 7 | 0 | 0 | 0 | 0 | 7 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0007 | 0/0 | 2268 | 6 | 5 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0009 | 0/0 | 2268 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0010 | 0/0 | 2268 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0011 | 0/0 | 2268 | 2 | 0 | 1 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0013 | 0/0 | 2268 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0015 | 0/0 | 2268 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0016 | 0/0 | 2268 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0017 | 0/0 | 2268 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0018 | 0/0 | 2268 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0001c0019 | 0/0 | 2268 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0002c0002 | 0/0 | 2268 | 33 | 1 | 0 | 30 | 0 | 2 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0003c0005 | 0/0 | 2268 | 7 | 7 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0003c0012 | 0/0 | 2268 | 2 | 0 | 2 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0004c0008 | 0/0 | 2268 | 5 | 5 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0004c0020 | 0/0 | 2268 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0004c0024 | 0/0 | 2268 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0005c0014 | 0/0 | 2268 | 2 | 0 | 0 | 2 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0006c0022 | 0/0 | 2268 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0007c0021 | 0/0 | 2268 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 | ||
| a0008c0023 | 0/0 | 2268 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATGGA others(2263): Show |
chr3 | 38002496 | 38034642 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2651 | 238 | 44 | 53 | 107 | 10 | 22 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0001c0001t0004 | 0/0 | 2651 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0001c0001t0005 | 0/0 | 2651 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0001c0003t0001 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0001c0003t0002 | 0/0 | 2650 | 30 | 8 | 10 | 7 | 2 | 3 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0001c0004t0002 | 0/0 | 2650 | 10 | 9 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0001c0006t0002 | 0/0 | 2650 | 7 | 0 | 0 | 0 | 0 | 7 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0001c0007t0002 | 0/0 | 2650 | 6 | 5 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0001c0009t0001 | 0/0 | 2651 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0001c0010t0002 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0001c0010t0003 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0001c0011t0001 | 0/0 | 2651 | 2 | 0 | 1 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0001c0013t0002 | 0/0 | 2650 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0001c0015t0002 | 0/0 | 2650 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0001c0016t0001 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0001c0017t0002 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0001c0018t0001 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0001c0019t0002 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0002c0002t0001 | 0/0 | 2651 | 33 | 1 | 0 | 30 | 0 | 2 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0003c0005t0001 | 0/0 | 2651 | 7 | 7 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0003c0012t0001 | 0/0 | 2651 | 2 | 0 | 2 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0004c0008t0002 | 0/0 | 2650 | 5 | 5 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0004c0020t0002 | 0/0 | 2650 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0004c0024t0001 | 0/0 | 2651 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0005c0014t0001 | 0/0 | 2651 | 2 | 0 | 0 | 2 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0006c0022t0001 | 0/0 | 2651 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2646): Show |
chr3 | 38002496 | 38034642 |
| a0007c0021t0002 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| a0008c0023t0002 | 0/0 | 2650 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | ATTCA others(2645): Show |
chr3 | 38002496 | 38034642 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 53 | 6 | 17 | 23 | 2 | 5 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0002 | 0/0 | 39 | 1 | 12 | 19 | 2 | 5 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0008 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0029 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0030 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0047 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0003 | 0/0 | 9 | 0 | 4 | 3 | 0 | 2 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0003t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0004t0002g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0004t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0004t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0004t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0004t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0004t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0006t0002g0018 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0006t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0006t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0007t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0007t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0007t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0007t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0009t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0010t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0010t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0011t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0011t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0013t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0015t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0015t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0016t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0017t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0018t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0001c0019t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0006 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0003c0005t0001g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0003c0012t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0004c0008t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0004c0008t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0004c0008t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0004c0020t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0004c0024t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0005c0014t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0006c0022t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0007c0021t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| a0008c0023t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00423 | hp2 | a0001 | c0003 | t0002 | g0051 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00642 | hp2 | a0001 | c0011 | t0001 | g0155 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00673 | hp1 | a0005 | c0014 | t0001 | g0038 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0134 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01074 | hp2 | a0003 | c0012 | t0001 | g0043 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0135 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01099 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01099 | hp2 | a0003 | c0012 | t0001 | g0043 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01109 | hp1 | a0001 | c0003 | t0002 | g0014 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01167 | hp2 | a0001 | c0004 | t0002 | g0152 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01192 | hp1 | a0001 | c0007 | t0002 | g0087 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01243 | hp2 | a0006 | c0022 | t0001 | g0148 | AMR | PUR | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01261 | hp1 | a0001 | c0003 | t0002 | g0119 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0065 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0068 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0034 | EUR | IBS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0034 | EUR | IBS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01884 | hp1 | a0001 | c0013 | t0002 | g0050 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01884 | hp2 | a0003 | c0005 | t0001 | g0005 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01891 | hp1 | a0001 | c0004 | t0002 | g0017 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0079 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01993 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0014 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02055 | hp2 | a0001 | c0007 | t0002 | g0088 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | CDX | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02165 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | CDX | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02257 | hp2 | a0003 | c0005 | t0001 | g0005 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02258 | hp1 | a0001 | c0009 | t0001 | g0024 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02258 | hp2 | a0003 | c0005 | t0001 | g0005 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02572 | hp1 | a0001 | c0007 | t0002 | g0089 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02602 | hp2 | a0001 | c0006 | t0002 | g0018 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02622 | hp1 | a0004 | c0008 | t0002 | g0019 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02622 | hp2 | a0001 | c0004 | t0002 | g0048 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02630 | hp1 | a0001 | c0003 | t0002 | g0156 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02630 | hp2 | a0003 | c0005 | t0001 | g0005 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02647 | hp2 | a0001 | c0018 | t0001 | g0086 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02698 | hp1 | a0001 | c0006 | t0002 | g0018 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02698 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02723 | hp1 | a0001 | c0013 | t0002 | g0050 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02723 | hp2 | a0001 | c0004 | t0002 | g0048 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0127 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0150 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02818 | hp2 | a0001 | c0015 | t0002 | g0083 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02895 | hp1 | a0001 | c0007 | t0002 | g0020 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02896 | hp1 | a0001 | c0010 | t0002 | g0052 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02896 | hp2 | a0001 | c0007 | t0002 | g0020 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0082 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02965 | hp2 | a0004 | c0008 | t0002 | g0019 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02970 | hp2 | a0001 | c0004 | t0002 | g0149 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02976 | hp1 | a0001 | c0003 | t0002 | g0014 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02976 | hp2 | a0001 | c0004 | t0002 | g0017 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03041 | hp2 | a0004 | c0008 | t0002 | g0142 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03130 | hp1 | a0001 | c0015 | t0002 | g0080 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03130 | hp2 | a0004 | c0008 | t0002 | g0019 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03139 | hp1 | a0007 | c0021 | t0002 | g0114 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03209 | hp2 | a0003 | c0005 | t0001 | g0005 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0014 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03239 | hp1 | a0001 | c0006 | t0002 | g0018 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03453 | hp1 | a0003 | c0005 | t0001 | g0005 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0157 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03491 | hp1 | a0001 | c0006 | t0002 | g0045 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03491 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03492 | hp1 | a0001 | c0006 | t0002 | g0045 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03516 | hp1 | a0001 | c0004 | t0002 | g0017 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03516 | hp2 | a0001 | c0004 | t0002 | g0151 | AFR | ESN | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03540 | hp1 | a0003 | c0005 | t0001 | g0005 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03540 | hp2 | a0001 | c0017 | t0002 | g0153 | AFR | GWD | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0121 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03579 | hp2 | a0001 | c0007 | t0002 | g0020 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03704 | hp1 | a0001 | c0006 | t0002 | g0018 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03704 | hp2 | a0001 | c0003 | t0002 | g0110 | SAS | PJL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03927 | hp1 | a0001 | c0016 | t0001 | g0116 | SAS | BEB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG04199 | hp1 | a0001 | c0006 | t0002 | g0094 | SAS | STU | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG04204 | hp2 | a0008 | c0023 | t0002 | g0131 | SAS | STU | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG04228 | hp1 | a0004 | c0020 | t0002 | g0054 | SAS | STU | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG04228 | hp2 | a0001 | c0011 | t0001 | g0154 | SAS | STU | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18522 | hp1 | a0004 | c0008 | t0002 | g0071 | AFR | YRI | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18522 | hp2 | a0001 | c0004 | t0002 | g0093 | AFR | YRI | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18948 | hp1 | a0004 | c0024 | t0001 | g0117 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18969 | hp2 | a0001 | c0003 | t0002 | g0095 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18997 | hp2 | a0001 | c0003 | t0002 | g0130 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0017 | AFR | LWK | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19062 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19085 | hp1 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19088 | hp1 | a0005 | c0014 | t0001 | g0038 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ASW | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA20129 | hp2 | a0001 | c0019 | t0002 | g0053 | AFR | ASW | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA20300 | hp1 | a0001 | c0010 | t0003 | g0077 | AFR | USA | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA21309 | hp1 | a0001 | c0009 | t0001 | g0024 | AFR | LWK | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | LWK | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0029 | REF | REF | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0030 | REF | REF | PLCD1_chr3_38002496_38034642 | PLCD1 | chr3 | 38002496 | 38034642 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38007819 | T | C | 1 | a0006 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.2225A>G | p.Gln742Arg | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 15/15 | 2328/2651 | 2225/2271 | 742/756 | chr3 | 38007819 | |||
| chr3:38008524 | G | T | 1 | a0005 | 2 | HG00673.hp1 NA19088.hp1 |
missense_variant | MODERATE | c.1836C>A | p.Asn612Lys | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 12/15 | 1939/2651 | 1836/2271 | 612/756 | chr3 | 38008524 | |||
| chr3:38009720 | G | A | 1 | a0008 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1379C>T | p.Ser460Leu | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 9/15 | 1482/2651 | 1379/2271 | 460/756 | chr3 | 38009720 | |||
| chr3:38010458 | C | T | 1 | a0007 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.895G>A | p.Gly299Ser | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 6/15 | 998/2651 | 895/2271 | 299/756 | chr3 | 38010458 | |||
| chr3:38010476 | G | A | 1 | a0004 | 7 | HG02622.hp1 HG02965.hp2 HG03041.hp2 others(4): Show |
missense_variant | MODERATE | c.877C>T | p.Arg293Cys | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 6/15 | 980/2651 | 877/2271 | 293/756 | chr3 | 38010476 | |||
| chr3:38011234 | C | T | 1 | a0002 | 33 | HG00408.hp2 HG02056.hp1 HG02080.hp1 others(30): Show |
missense_variant | MODERATE | c.770G>A | p.Arg257His | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 5/15 | 873/2651 | 770/2271 | 257/756 | chr3 | 38011234 | |||
| chr3:38011313 | C | T | 1 | a0003 | 9 | HG01074.hp2 HG01099.hp2 HG01884.hp2 others(6): Show |
missense_variant | MODERATE | c.691G>A | p.Asp231Asn | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 5/15 | 794/2651 | 691/2271 | 231/756 | chr3 | 38011313 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38008506 | G | A | 1 | a0001c0004 | 10 | HG01167.hp2 HG01891.hp1 HG02622.hp2 others(7): Show |
synonymous_variant | LOW | c.1854C>T | p.Arg618Arg | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 12/15 | 1957/2651 | 1854/2271 | 618/756 | chr3 | 38008506 | |||
| chr3:38009716 | G | A | 2 | a0001c0015 a0001c0019 |
3 | HG02818.hp2 HG03130.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.1383C>T | p.Asp461Asp | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 9/15 | 1486/2651 | 1383/2271 | 461/756 | chr3 | 38009716 | |||
| chr3:38010450 | T | C | 15 | a0001c0003 a0001c0004 a0001c0006 others(12): Show |
79 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(76): Show |
synonymous_variant | LOW | c.903A>G | p.Pro301Pro | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 6/15 | 1006/2651 | 903/2271 | 301/756 | chr3 | 38010450 | |||
| chr3:38011269 | C | T | 2 | a0001c0013 a0001c0017 |
3 | HG01884.hp1 HG02723.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.735G>A | p.Ala245Ala | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 5/15 | 838/2651 | 735/2271 | 245/756 | chr3 | 38011269 | |||
| chr3:38016553 | C | T | 5 | a0001c0009 a0001c0010 a0001c0019 others(2): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
synonymous_variant | LOW | c.366G>A | p.Val122Val | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/15 | 469/2651 | 366/2271 | 122/756 | chr3 | 38016553 | |||
| chr3:38020201 | C | T | 3 | a0001c0007 a0001c0017 a0001c0018 |
8 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.186G>A | p.Pro62Pro | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/15 | 289/2651 | 186/2271 | 62/756 | chr3 | 38020201 | |||
| chr3:38020257 | A | G | 10 | a0001c0006 a0001c0007 a0001c0009 others(7): Show |
30 | HG00642.hp2 HG01192.hp1 HG01884.hp2 others(27): Show |
synonymous_variant | LOW | c.130T>C | p.Leu44Leu | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/15 | 233/2651 | 130/2271 | 44/756 | chr3 | 38020257 | |||
| chr3:38020288 | G | T | 1 | a0001c0016 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.99C>A | p.Ser33Ser | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/15 | 202/2651 | 99/2271 | 33/756 | chr3 | 38020288 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38007538 | TG | T | 13 | a0001c0003t0002 a0001c0004t0002 a0001c0006t0002 others(10): Show |
68 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*234delC | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 15/15 | 234 | chr3 | 38007538 | ||||||
| chr3:38007576 | C | T | 1 | a0001c0001t0005 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*197G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 15/15 | 197 | chr3 | 38007576 | ||||||
| chr3:38007734 | C | T | 1 | a0001c0001t0004 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 15/15 | 39 | chr3 | 38007734 | ||||||
| chr3:38007757 | A | G | 1 | a0001c0010t0003 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 15/15 | 16 | chr3 | 38007757 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:38007890 | A | G | 1 | a0001c0010t0003g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2186-32T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 14/14 | chr3 | 38007890 | |||||||
| chr3:38007919 | G | T | 1 | a0001c0010t0003g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2186-61C>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 14/14 | chr3 | 38007919 | |||||||
| chr3:38007931 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2186-73C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 14/14 | chr3 | 38007931 | |||||||
| chr3:38008668 | G | A | 13 | a0001c0003t0002g0003 a0001c0003t0002g0034 a0001c0003t0002g0051 others(10): Show |
23 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1724-32C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 11/14 | chr3 | 38008668 | |||||||
| chr3:38008684 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1724-48G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 11/14 | chr3 | 38008684 | |||||||
| chr3:38008822 | G | C | 2 | a0003c0005t0001g0005 a0003c0012t0001g0043 |
9 | HG01074.hp2 HG01099.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1724-186C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 11/14 | chr3 | 38008822 | |||||||
| chr3:38009177 | C | T | 1 | a0001c0003t0002g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1607-19G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 10/14 | chr3 | 38009177 | |||||||
| chr3:38009200 | G | A | 2 | a0003c0005t0001g0005 a0003c0012t0001g0043 |
9 | HG01074.hp2 HG01099.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1607-42C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 10/14 | chr3 | 38009200 | |||||||
| chr3:38009452 | C | A | 1 | a0004c0020t0002g0054 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1447-21G>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 9/14 | chr3 | 38009452 | |||||||
| chr3:38010070 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1138-17T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 7/14 | chr3 | 38010070 | |||||||
| chr3:38010586 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.791-24G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 5/14 | chr3 | 38010586 | |||||||
| chr3:38010840 | C | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0064 a0001c0001t0001g0066 others(2): Show |
9 | HG00609.hp1 HG02132.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.791-278G>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 5/14 | chr3 | 38010840 | |||||||
| chr3:38011122 | G | C | 44 | a0001c0003t0001g0133 a0001c0003t0002g0003 a0001c0003t0002g0014 others(41): Show |
69 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.790+92C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 5/14 | chr3 | 38011122 | |||||||
| chr3:38011458 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.559-13C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 4/14 | chr3 | 38011458 | |||||||
| chr3:38011715 | T | C | 43 | a0001c0003t0002g0003 a0001c0003t0002g0014 a0001c0003t0002g0034 others(40): Show |
68 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.429-42A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38011715 | |||||||
| chr3:38011790 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG00408.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.429-117A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38011790 | |||||||
| chr3:38011831 | T | TGTTACGT others(3): Show |
43 | a0001c0003t0002g0003 a0001c0003t0002g0014 a0001c0003t0002g0034 others(40): Show |
68 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.429-159_429-158ins others(10): Show |
PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38011831 | |||||||
| chr3:38011878 | T | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0070 others(2): Show |
5 | HG01070.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.429-205A>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38011878 | |||||||
| chr3:38011942 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02738.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.429-269T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38011942 | |||||||
| chr3:38012031 | C | CT | 6 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
8 | HG02004.hp1 HG02970.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.429-359dupA | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012031 | |||||||
| chr3:38012031 | C | CTTTT | 32 | a0001c0003t0002g0003 a0001c0003t0002g0014 a0001c0003t0002g0034 others(29): Show |
51 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.429-362_429-359dup others(4): Show |
PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012031 | |||||||
| chr3:38012031 | C | CTTTTT | 6 | a0001c0003t0002g0130 a0001c0006t0002g0018 a0001c0006t0002g0094 others(3): Show |
11 | HG01192.hp1 HG02055.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.429-363_429-359dup others(5): Show |
PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012031 | |||||||
| chr3:38012031 | CT | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0109 others(4): Show |
8 | HG01256.hp2 HG01993.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.429-359delA | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012031 | |||||||
| chr3:38012062 | C | T | 3 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 |
5 | HG01192.hp1 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-389G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012062 | |||||||
| chr3:38012103 | T | C | 2 | a0003c0005t0001g0005 a0003c0012t0001g0043 |
9 | HG01074.hp2 HG01099.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-430A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012103 | |||||||
| chr3:38012162 | C | T | 1 | a0001c0003t0002g0034 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.429-489G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012162 | |||||||
| chr3:38012166 | G | C | 1 | a0004c0008t0002g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.429-493C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012166 | |||||||
| chr3:38012172 | C | CT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0059 others(4): Show |
11 | HG01192.hp1 HG02055.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.429-500dupA | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012172 | |||||||
| chr3:38012187 | T | C | 3 | a0001c0003t0002g0121 a0003c0005t0001g0005 a0003c0012t0001g0043 |
10 | HG01074.hp2 HG01099.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.429-514A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012187 | |||||||
| chr3:38012189 | G | T | 1 | a0001c0001t0001g0025 | 2 | NA19066.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.429-516C>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012189 | |||||||
| chr3:38012210 | A | G | 1 | a0001c0003t0002g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.429-537T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012210 | |||||||
| chr3:38012249 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.429-576T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012249 | |||||||
| chr3:38012322 | T | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0091 others(2): Show |
15 | HG01074.hp2 HG01099.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.429-649A>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012322 | |||||||
| chr3:38012462 | C | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0091 others(5): Show |
21 | HG01074.hp2 HG01099.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.429-789G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012462 | |||||||
| chr3:38012516 | G | GT | 12 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0061 others(9): Show |
22 | HG01074.hp2 HG01099.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.429-844dupA | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012516 | |||||||
| chr3:38012516 | GT | G | 7 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0084 others(4): Show |
10 | HG01070.hp1 HG01192.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.429-844delA | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012516 | |||||||
| chr3:38012585 | C | T | 1 | a0002c0002t0001g0060 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.429-912G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012585 | |||||||
| chr3:38012612 | A | G | 2 | a0001c0003t0002g0121 a0001c0007t0002g0089 |
2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.429-939T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012612 | |||||||
| chr3:38012768 | T | C | 8 | a0001c0001t0001g0040 a0001c0001t0001g0084 a0001c0001t0001g0122 others(5): Show |
11 | HG01192.hp1 HG02055.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.429-1095A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012768 | |||||||
| chr3:38012784 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0090 others(1): Show |
8 | HG01358.hp2 HG02015.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.429-1111C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012784 | |||||||
| chr3:38012805 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.429-1132G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012805 | |||||||
| chr3:38012885 | AT | A | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.429-1213delA | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012885 | |||||||
| chr3:38012926 | C | T | 5 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0019t0002g0053 others(2): Show |
12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.429-1253G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38012926 | |||||||
| chr3:38013072 | G | T | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.429-1399C>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013072 | |||||||
| chr3:38013091 | C | T | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.429-1418G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013091 | |||||||
| chr3:38013109 | C | T | 1 | a0001c0010t0002g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.429-1436G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013109 | |||||||
| chr3:38013128 | G | A | 1 | a0002c0002t0001g0060 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.429-1455C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013128 | |||||||
| chr3:38013177 | G | A | 7 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(4): Show |
14 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.429-1504C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013177 | |||||||
| chr3:38013194 | T | C | 2 | a0002c0002t0001g0100 a0002c0002t0001g0101 |
2 | NA18947.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.429-1521A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013194 | |||||||
| chr3:38013208 | C | CT | 6 | a0001c0001t0001g0059 a0001c0001t0001g0111 a0001c0001t0001g0128 others(3): Show |
6 | HG02572.hp1 HG02735.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-1536dupA | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013208 | |||||||
| chr3:38013208 | CT | C | 15 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0140 others(12): Show |
21 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.429-1536delA | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013208 | |||||||
| chr3:38013208 | CTT | C | 7 | a0001c0004t0002g0152 a0001c0009t0001g0024 a0001c0010t0002g0052 others(4): Show |
14 | HG01167.hp2 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.429-1537_429-1536d others(4): Show |
PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013208 | |||||||
| chr3:38013212 | T | C | 2 | a0001c0003t0002g0034 a0001c0003t0002g0135 |
3 | HG01081.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.429-1539A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013212 | |||||||
| chr3:38013237 | G | A | 2 | a0001c0003t0002g0157 a0001c0013t0002g0050 |
3 | HG01884.hp1 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.429-1564C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013237 | |||||||
| chr3:38013241 | C | G | 1 | a0001c0001t0001g0107 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.429-1568G>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013241 | |||||||
| chr3:38013273 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0085 |
11 | HG03834.hp1 NA18945.hp1 NA18955.hp1 others(8): Show |
intron_variant | MODIFIER | c.429-1600G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013273 | |||||||
| chr3:38013305 | C | T | 2 | a0001c0003t0002g0156 a0001c0007t0002g0089 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.429-1632G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013305 | |||||||
| chr3:38013369 | C | G | 5 | a0001c0006t0002g0018 a0001c0006t0002g0045 a0001c0006t0002g0094 others(2): Show |
9 | HG00642.hp2 HG02602.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.429-1696G>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013369 | |||||||
| chr3:38013453 | T | C | 5 | a0001c0006t0002g0018 a0001c0006t0002g0045 a0001c0006t0002g0094 others(2): Show |
9 | HG00642.hp2 HG02602.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.429-1780A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013453 | |||||||
| chr3:38013465 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.429-1792C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013465 | |||||||
| chr3:38013513 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.429-1840G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013513 | |||||||
| chr3:38013559 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.429-1886A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013559 | |||||||
| chr3:38013791 | G | T | 1 | a0001c0003t0002g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.429-2118C>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013791 | |||||||
| chr3:38013901 | C | T | 1 | a0002c0002t0001g0098 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.429-2228G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38013901 | |||||||
| chr3:38014020 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.429-2347A>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014020 | |||||||
| chr3:38014095 | T | G | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+2396A>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014095 | |||||||
| chr3:38014123 | C | T | 1 | a0007c0021t0002g0114 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.428+2368G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014123 | |||||||
| chr3:38014272 | G | GA | 7 | a0001c0001t0001g0081 a0001c0003t0002g0014 a0001c0003t0002g0082 others(4): Show |
11 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.428+2218dupT | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014272 | |||||||
| chr3:38014272 | G | GAA | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+2217_428+2218d others(4): Show |
PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014272 | |||||||
| chr3:38014336 | T | C | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+2155A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014336 | |||||||
| chr3:38014415 | A | G | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+2076T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014415 | |||||||
| chr3:38014417 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.428+2074G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014417 | |||||||
| chr3:38014418 | G | A | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+2073C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014418 | |||||||
| chr3:38014446 | T | C | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+2045A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014446 | |||||||
| chr3:38014578 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0124 others(2): Show |
14 | HG00609.hp2 HG00741.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.428+1913T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014578 | |||||||
| chr3:38014589 | G | A | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+1902C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014589 | |||||||
| chr3:38014629 | G | A | 2 | a0001c0003t0002g0157 a0001c0013t0002g0050 |
3 | HG01884.hp1 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.428+1862C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014629 | |||||||
| chr3:38014785 | T | TAA | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+1704_428+1705d others(4): Show |
PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014785 | |||||||
| chr3:38014797 | A | T | 12 | a0001c0001t0001g0140 a0001c0004t0002g0017 a0001c0004t0002g0048 others(9): Show |
18 | HG01167.hp2 HG01192.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.428+1694T>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014797 | |||||||
| chr3:38014798 | T | A | 1 | a0002c0002t0001g0106 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.428+1693A>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014798 | |||||||
| chr3:38014947 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.428+1544T>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38014947 | |||||||
| chr3:38015073 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.428+1418T>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015073 | |||||||
| chr3:38015139 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.428+1352G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015139 | |||||||
| chr3:38015157 | T | C | 1 | a0001c0010t0003g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.428+1334A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015157 | |||||||
| chr3:38015241 | A | AT | 6 | a0001c0001t0001g0081 a0001c0003t0002g0014 a0001c0003t0002g0079 others(3): Show |
9 | HG01109.hp1 HG01934.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.428+1249dupA | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015241 | |||||||
| chr3:38015298 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
282 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.428+1193A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015298 | |||||||
| chr3:38015312 | C | T | 1 | a0002c0002t0001g0102 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.428+1179G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015312 | |||||||
| chr3:38015503 | T | C | 1 | a0001c0007t0002g0088 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.428+988A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015503 | |||||||
| chr3:38015615 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0122 |
3 | HG02559.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.428+876T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015615 | |||||||
| chr3:38015671 | A | C | 1 | a0001c0003t0002g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.428+820T>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015671 | |||||||
| chr3:38015943 | G | A | 2 | a0001c0003t0002g0156 a0001c0007t0002g0089 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.428+548C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015943 | |||||||
| chr3:38015944 | G | C | 1 | a0001c0006t0002g0094 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.428+547C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38015944 | |||||||
| chr3:38016020 | T | A | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+471A>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38016020 | |||||||
| chr3:38016115 | T | C | 13 | a0001c0003t0002g0157 a0001c0006t0002g0018 a0001c0006t0002g0045 others(10): Show |
25 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.428+376A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38016115 | |||||||
| chr3:38016156 | G | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02738.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.428+335C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38016156 | |||||||
| chr3:38016371 | T | C | 1 | a0002c0002t0001g0106 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.428+120A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38016371 | |||||||
| chr3:38016384 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.428+107A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38016384 | |||||||
| chr3:38016407 | A | G | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.428+84T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 3/14 | chr3 | 38016407 | |||||||
| chr3:38016750 | G | C | 6 | a0001c0001t0001g0081 a0001c0003t0002g0014 a0001c0003t0002g0079 others(3): Show |
9 | HG01109.hp1 HG01934.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.200-31C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38016750 | |||||||
| chr3:38016803 | G | C | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-84C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38016803 | |||||||
| chr3:38016894 | G | C | 1 | a0001c0016t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.200-175C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38016894 | |||||||
| chr3:38016894 | G | T | 6 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0010t0003g0077 others(3): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-175C>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38016894 | |||||||
| chr3:38016902 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.200-183T>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38016902 | |||||||
| chr3:38016975 | C | T | 7 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(4): Show |
9 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.200-256G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38016975 | |||||||
| chr3:38016976 | A | G | 12 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(9): Show |
21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.200-257T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38016976 | |||||||
| chr3:38016993 | G | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(84): Show |
217 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.200-274C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38016993 | |||||||
| chr3:38017009 | G | A | 7 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(4): Show |
9 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.200-290C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017009 | |||||||
| chr3:38017055 | G | A | 1 | a0001c0010t0003g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.200-336C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017055 | |||||||
| chr3:38017204 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
228 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.200-485G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017204 | |||||||
| chr3:38017279 | C | T | 12 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(9): Show |
21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.200-560G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017279 | |||||||
| chr3:38017303 | C | T | 12 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(9): Show |
21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.200-584G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017303 | |||||||
| chr3:38017346 | C | T | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | NA18949.hp1 NA18969.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-627G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017346 | |||||||
| chr3:38017347 | G | A | 17 | a0001c0006t0002g0018 a0001c0006t0002g0045 a0001c0006t0002g0094 others(14): Show |
30 | HG00642.hp2 HG01192.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.200-628C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017347 | |||||||
| chr3:38017581 | C | A | 1 | a0007c0021t0002g0114 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.200-862G>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017581 | |||||||
| chr3:38017864 | G | T | 1 | a0001c0010t0003g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.200-1145C>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017864 | |||||||
| chr3:38017865 | G | C | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | NA18949.hp1 NA18969.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-1146C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017865 | |||||||
| chr3:38017866 | G | A | 5 | a0001c0009t0001g0024 a0001c0010t0002g0052 a0001c0019t0002g0053 others(2): Show |
12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.200-1147C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017866 | |||||||
| chr3:38017925 | C | T | 1 | a0001c0003t0002g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.200-1206G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38017925 | |||||||
| chr3:38018040 | C | A | 1 | a0001c0001t0001g0041 | 2 | HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.200-1321G>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018040 | |||||||
| chr3:38018052 | A | G | 2 | a0001c0007t0002g0020 a0001c0007t0002g0087 |
4 | HG01192.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-1333T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018052 | |||||||
| chr3:38018116 | A | C | 1 | a0001c0010t0003g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.200-1397T>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018116 | |||||||
| chr3:38018174 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.200-1455C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018174 | |||||||
| chr3:38018285 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.200-1566G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018285 | |||||||
| chr3:38018286 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.200-1567C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018286 | |||||||
| chr3:38018294 | C | T | 12 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(9): Show |
21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.200-1575G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018294 | |||||||
| chr3:38018455 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG01433.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.199+1733G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018455 | |||||||
| chr3:38018512 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.199+1676T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018512 | |||||||
| chr3:38018529 | C | T | 1 | a0001c0003t0002g0034 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.199+1659G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018529 | |||||||
| chr3:38018576 | T | C | 1 | a0001c0011t0001g0155 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.199+1612A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38018576 | |||||||
| chr3:38019421 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.199+767A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38019421 | |||||||
| chr3:38019447 | G | A | 1 | a0001c0001t0001g0042 | 2 | NA18973.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.199+741C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38019447 | |||||||
| chr3:38019670 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.199+518T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38019670 | |||||||
| chr3:38019841 | C | T | 7 | a0001c0001t0001g0140 a0001c0003t0002g0150 a0001c0004t0002g0017 others(4): Show |
11 | HG01167.hp2 HG01891.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.199+347G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38019841 | |||||||
| chr3:38019884 | G | T | 5 | a0001c0006t0002g0018 a0001c0006t0002g0045 a0001c0006t0002g0094 others(2): Show |
9 | HG00642.hp2 HG02602.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.199+304C>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38019884 | |||||||
| chr3:38019960 | A | T | 1 | a0004c0024t0001g0117 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.199+228T>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38019960 | |||||||
| chr3:38019982 | T | G | 1 | a0003c0012t0001g0043 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.199+206A>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38019982 | |||||||
| chr3:38020049 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
283 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.199+139T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 2/14 | chr3 | 38020049 | |||||||
| chr3:38020489 | C | T | 1 | a0001c0004t0002g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.35-137G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38020489 | |||||||
| chr3:38020619 | C | T | 3 | a0002c0002t0001g0099 a0002c0002t0001g0100 a0002c0002t0001g0101 |
3 | NA18947.hp1 NA18970.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.35-267G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38020619 | |||||||
| chr3:38020654 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.35-302T>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38020654 | |||||||
| chr3:38020833 | G | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0047 a0001c0001t0001g0091 others(2): Show |
7 | HG00099.hp1 HG01168.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-481C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38020833 | |||||||
| chr3:38020857 | A | G | 1 | a0001c0010t0003g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.35-505T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38020857 | |||||||
| chr3:38020901 | G | A | 1 | a0007c0021t0002g0114 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.35-549C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38020901 | |||||||
| chr3:38020904 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
227 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.35-552G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38020904 | |||||||
| chr3:38020921 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): Show |
253 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.35-569T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38020921 | |||||||
| chr3:38020926 | G | A | 1 | a0007c0021t0002g0114 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.35-574C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38020926 | |||||||
| chr3:38021059 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
262 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.35-707T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021059 | |||||||
| chr3:38021342 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
6 | HG01516.hp1 HG01517.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.35-990G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021342 | |||||||
| chr3:38021343 | G | A | 1 | a0001c0006t0002g0045 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.35-991C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021343 | |||||||
| chr3:38021407 | C | G | 1 | a0001c0018t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.35-1055G>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021407 | |||||||
| chr3:38021450 | C | T | 1 | a0001c0003t0002g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.35-1098G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021450 | |||||||
| chr3:38021537 | T | C | 6 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(3): Show |
8 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.35-1185A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021537 | |||||||
| chr3:38021586 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
274 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.35-1234G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021586 | |||||||
| chr3:38021722 | C | G | 1 | a0001c0003t0002g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.35-1370G>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021722 | |||||||
| chr3:38021792 | T | C | 1 | a0002c0002t0001g0141 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.35-1440A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021792 | |||||||
| chr3:38021804 | C | A | 5 | a0001c0006t0002g0018 a0001c0006t0002g0045 a0001c0006t0002g0094 others(2): Show |
9 | HG00642.hp2 HG02602.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.35-1452G>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021804 | |||||||
| chr3:38021881 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
265 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.35-1529G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38021881 | |||||||
| chr3:38022017 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
265 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.35-1665C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38022017 | |||||||
| chr3:38022311 | G | A | 2 | a0002c0002t0001g0022 a0002c0002t0001g0098 |
4 | NA18957.hp2 NA18991.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-1959C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38022311 | |||||||
| chr3:38022366 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
265 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.35-2014G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38022366 | |||||||
| chr3:38022777 | T | C | 1 | a0001c0001t0001g0012 | 5 | HG03834.hp1 NA19005.hp1 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-2425A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38022777 | |||||||
| chr3:38022952 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0036 others(1): Show |
11 | HG01255.hp2 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.35-2600A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38022952 | |||||||
| chr3:38023022 | T | G | 1 | a0001c0017t0002g0153 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.35-2670A>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38023022 | |||||||
| chr3:38023093 | C | T | 6 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(3): Show |
8 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.35-2741G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38023093 | |||||||
| chr3:38023183 | G | A | 6 | a0001c0001t0001g0081 a0001c0003t0002g0014 a0001c0003t0002g0079 others(3): Show |
9 | HG01109.hp1 HG01934.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.35-2831C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38023183 | |||||||
| chr3:38023244 | A | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(17): Show |
48 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.35-2892T>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38023244 | |||||||
| chr3:38023435 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
265 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.35-3083T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38023435 | |||||||
| chr3:38023478 | C | T | 1 | a0001c0003t0002g0079 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.35-3126G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38023478 | |||||||
| chr3:38023514 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.35-3162G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38023514 | |||||||
| chr3:38023686 | TG | T | 2 | a0002c0002t0001g0022 a0002c0002t0001g0098 |
4 | NA18957.hp2 NA18991.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-3335delC | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38023686 | |||||||
| chr3:38024045 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.35-3693G>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38024045 | |||||||
| chr3:38024350 | A | C | 1 | a0002c0002t0001g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.35-3998T>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38024350 | |||||||
| chr3:38024570 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.35-4218G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38024570 | |||||||
| chr3:38024579 | G | T | 1 | a0001c0001t0001g0032 | 2 | HG01346.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.35-4227C>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38024579 | |||||||
| chr3:38024835 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0085 others(3): Show |
21 | HG00408.hp2 HG02056.hp1 HG03834.hp1 others(18): Show |
intron_variant | MODIFIER | c.35-4483G>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38024835 | |||||||
| chr3:38025033 | C | A | 1 | a0001c0003t0002g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.34+4473G>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025033 | |||||||
| chr3:38025096 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.34+4410C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025096 | |||||||
| chr3:38025099 | G | A | 6 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(3): Show |
8 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.34+4407C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025099 | |||||||
| chr3:38025131 | G | A | 2 | a0003c0005t0001g0005 a0004c0008t0002g0142 |
8 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.34+4375C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025131 | |||||||
| chr3:38025233 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0046 others(11): Show |
23 | HG00099.hp1 HG01074.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.34+4273C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025233 | |||||||
| chr3:38025286 | C | G | 1 | a0001c0001t0001g0021 | 3 | HG02155.hp2 HG02523.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.34+4220G>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025286 | |||||||
| chr3:38025383 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
268 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.34+4123A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025383 | |||||||
| chr3:38025415 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(154): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.34+4091T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025415 | |||||||
| chr3:38025456 | C | T | 6 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(3): Show |
8 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.34+4050G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025456 | |||||||
| chr3:38025713 | C | T | 1 | a0001c0004t0002g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.34+3793G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025713 | |||||||
| chr3:38025717 | AACAGTGG others(12): Show |
A | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.34+3770_34+3788del others(19): Show |
PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38025717 | |||||||
| chr3:38026028 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.34+3478T>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026028 | |||||||
| chr3:38026342 | C | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
284 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.34+3164G>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026342 | |||||||
| chr3:38026355 | C | T | 1 | a0001c0001t0001g0025 | 2 | NA19066.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.34+3151G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026355 | |||||||
| chr3:38026517 | CATAA | C | 6 | a0001c0007t0002g0020 a0001c0007t0002g0087 a0001c0007t0002g0088 others(3): Show |
8 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.34+2985_34+2988del others(4): Show |
PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026517 | |||||||
| chr3:38026767 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0091 |
3 | HG02145.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.34+2739T>C | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026767 | |||||||
| chr3:38026785 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.34+2721G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026785 | |||||||
| chr3:38026791 | C | T | 3 | a0001c0006t0002g0018 a0001c0011t0001g0154 a0001c0011t0001g0155 |
6 | HG00642.hp2 HG02602.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.34+2715G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026791 | |||||||
| chr3:38026838 | G | A | 4 | a0001c0006t0002g0018 a0001c0010t0003g0077 a0001c0011t0001g0154 others(1): Show |
7 | HG00642.hp2 HG02602.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+2668C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026838 | |||||||
| chr3:38026858 | G | A | 1 | a0001c0004t0002g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.34+2648C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026858 | |||||||
| chr3:38026938 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
270 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.34+2568G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026938 | |||||||
| chr3:38026953 | G | A | 2 | a0001c0004t0002g0048 a0001c0004t0002g0152 |
3 | HG01167.hp2 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.34+2553C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38026953 | |||||||
| chr3:38027045 | G | T | 9 | a0001c0006t0002g0018 a0001c0007t0002g0020 a0001c0007t0002g0087 others(6): Show |
14 | HG00642.hp2 HG01192.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.34+2461C>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38027045 | |||||||
| chr3:38027054 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0049 |
5 | HG02004.hp1 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+2452G>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38027054 | |||||||
| chr3:38027181 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.34+2325G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38027181 | |||||||
| chr3:38027260 | A | C | 1 | a0001c0001t0001g0055 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.34+2246T>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38027260 | |||||||
| chr3:38027267 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
284 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.34+2239G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38027267 | |||||||
| chr3:38027612 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
284 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.34+1894G>A | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38027612 | |||||||
| chr3:38027693 | G | A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0003t0002g0014 others(6): Show |
13 | HG01109.hp1 HG01884.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.34+1813C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38027693 | |||||||
| chr3:38027731 | T | C | 1 | a0001c0010t0003g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.34+1775A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38027731 | |||||||
| chr3:38027777 | C | A | 1 | a0001c0017t0002g0153 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.34+1729G>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38027777 | |||||||
| chr3:38027957 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.34+1549A>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38027957 | |||||||
| chr3:38028755 | G | A | 12 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0003t0002g0014 others(9): Show |
19 | HG00642.hp2 HG01109.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.34+751C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38028755 | |||||||
| chr3:38029249 | T | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
257 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.34+257A>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38029249 | |||||||
| chr3:38029256 | G | A | 3 | a0001c0003t0002g0156 a0001c0003t0002g0157 a0001c0013t0002g0050 |
4 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+250C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38029256 | |||||||
| chr3:38029303 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.34+203C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38029303 | |||||||
| chr3:38029371 | G | A | 1 | a0001c0001t0001g0009 | 7 | HG01891.hp2 HG02559.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+135C>T | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38029371 | |||||||
| chr3:38029406 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.34+100C>G | PLCD1 | ENSG00000187091.14 | transcript | ENST00000334661.5 | protein_coding | 1/14 | chr3 | 38029406 |