Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55124 |
| ensemblid | ENSG00000197181.12 |
| hgncid | 17644 |
| symbol | PIWIL2 |
| name | piwi like RNA-mediated gene silencing 2 |
| refseq_nuc | NM_018068.5 |
| refseq_prot | NP_060538.2 |
| ensembl_nuc | ENST00000356766.11 |
| ensembl_prot | ENSP00000349208.6 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 22275316 |
| end | 22357568 |
| strand | + |
| ver | v1.2 |
| region | chr8:22275316-22357568 |
| region5000 | chr8:22270316-22362568 |
| regionname0 | PIWIL2_chr8_22275316_22357568 |
| regionname5000 | PIWIL2_chr8_22270316_22362568 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 973 | 274 | 87 | 60 | 92 | 6 | 28 | 75 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| a0002 | 0/0 | 973 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| a0003 | 0/0 | 973 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| a0004 | 0/0 | 973 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| a0005 | 0/0 | 973 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| a0006 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| a0007 | 0/0 | 973 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| a0008 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| a0009 | 0/0 | 973 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| a0010 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| a0011 | 0/1 | 973 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | MDPFR others(968): Show |
chr8 | 22270316 | 22362568 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2919 | 273 | 87 | 59 | 92 | 6 | 28 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0001c0010 | 0/0 | 2919 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0002c0003 | 0/0 | 2919 | 5 | 0 | 0 | 5 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0003c0002 | 0/0 | 2919 | 5 | 4 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0004c0004 | 0/0 | 2919 | 4 | 4 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0005c0005 | 0/0 | 2919 | 2 | 0 | 0 | 2 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0006c0011 | 0/0 | 2919 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0007c0008 | 0/0 | 2919 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0008c0007 | 0/0 | 2919 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0009c0012 | 0/0 | 2919 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0010c0006 | 0/0 | 2919 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 | ||
| a0011c0009 | 0/1 | 2919 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | ATGGA others(2914): Show |
chr8 | 22270316 | 22362568 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5114 | 66 | 52 | 6 | 6 | 1 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0002 | 1/0 | 5114 | 60 | 11 | 21 | 23 | 1 | 3 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0003 | 0/0 | 5114 | 43 | 1 | 9 | 22 | 1 | 10 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0004 | 0/0 | 5112 | 47 | 4 | 11 | 24 | 0 | 8 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5107): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0005 | 0/0 | 5114 | 10 | 0 | 6 | 4 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0006 | 0/0 | 5114 | 8 | 4 | 2 | 0 | 0 | 2 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0007 | 0/0 | 5114 | 5 | 5 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0008 | 0/0 | 5114 | 4 | 4 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0010 | 0/0 | 5113 | 4 | 0 | 0 | 3 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5108): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0011 | 0/0 | 5115 | 3 | 0 | 0 | 1 | 1 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5110): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0013 | 0/0 | 5115 | 3 | 0 | 0 | 3 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5110): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0014 | 0/0 | 5114 | 3 | 3 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0015 | 0/0 | 5114 | 2 | 1 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0016 | 0/0 | 5115 | 2 | 1 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5110): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0017 | 0/0 | 5114 | 2 | 0 | 0 | 0 | 2 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0018 | 0/0 | 5115 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5110): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0019 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0020 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0021 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0024 | 0/0 | 5114 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0025 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0026 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0027 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0028 | 0/0 | 5112 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5107): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0029 | 0/0 | 5112 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5107): Show |
chr8 | 22270316 | 22362568 |
| a0001c0001t0030 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5107): Show |
chr8 | 22270316 | 22362568 |
| a0001c0010t0003 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0002c0003t0003 | 0/0 | 5114 | 5 | 0 | 0 | 5 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0003c0002t0001 | 0/0 | 5114 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0003c0002t0012 | 0/0 | 5114 | 3 | 2 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0003c0002t0022 | 0/0 | 5114 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0004c0004t0009 | 0/0 | 5114 | 4 | 4 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0005c0005t0002 | 0/0 | 5114 | 2 | 0 | 0 | 2 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0006c0011t0003 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0007c0008t0004 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5107): Show |
chr8 | 22270316 | 22362568 |
| a0008c0007t0003 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0009c0012t0023 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5110): Show |
chr8 | 22270316 | 22362568 |
| a0010c0006t0002 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5109): Show |
chr8 | 22270316 | 22362568 |
| a0011c0009t0004 | 0/1 | 5112 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | GTGGG others(5107): Show |
chr8 | 22270316 | 22362568 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0006g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0010g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0010g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0011g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0011g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0013g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0013g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0013g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0014g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0014g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0014g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0015g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0015g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0016g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0017g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0017g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0018g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0019g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0020g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0021g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0024g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0025g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0026g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0027g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0028g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0029g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0001t0030g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0001c0010t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0002c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0002c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0002c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0002c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0002c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0003c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0003c0002t0012g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0003c0002t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0003c0002t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0003c0002t0022g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0004c0004t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0004c0004t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0004c0004t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0004c0004t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0005c0005t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0005c0005t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0006c0011t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0007c0008t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0008c0007t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0009c0012t0023g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0010c0006t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| a0011c0009t0004g0253 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00423 | hp1 | a0006 | c0011 | t0003 | g0281 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00597 | hp2 | a0002 | c0003 | t0003 | g0254 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00639 | hp1 | a0001 | c0001 | t0030 | g0187 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00735 | hp1 | a0001 | c0001 | t0021 | g0030 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG00741 | hp2 | a0001 | c0001 | t0019 | g0084 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0221 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01099 | hp2 | a0003 | c0002 | t0012 | g0017 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0259 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0213 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0214 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01243 | hp2 | a0007 | c0008 | t0004 | g0228 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0012 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01257 | hp2 | a0001 | c0010 | t0003 | g0172 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0183 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0222 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0199 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0218 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01516 | hp1 | a0001 | c0001 | t0011 | g0034 | EUR | IBS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01516 | hp2 | a0001 | c0001 | t0017 | g0282 | EUR | IBS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01517 | hp1 | a0001 | c0001 | t0017 | g0269 | EUR | IBS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0191 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01891 | hp1 | a0004 | c0004 | t0009 | g0176 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0038 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0236 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0211 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02027 | hp1 | a0008 | c0007 | t0003 | g0248 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02027 | hp2 | a0001 | c0001 | t0013 | g0238 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02055 | hp1 | a0001 | c0001 | t0016 | g0130 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02056 | hp2 | a0001 | c0001 | t0020 | g0088 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0086 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02145 | hp2 | a0003 | c0002 | t0001 | g0021 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0276 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0294 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02602 | hp2 | a0001 | c0001 | t0010 | g0182 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0160 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0179 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02723 | hp1 | a0003 | c0002 | t0012 | g0018 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0251 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02895 | hp1 | a0004 | c0004 | t0009 | g0178 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02922 | hp1 | a0004 | c0004 | t0009 | g0177 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0250 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03017 | hp1 | a0001 | c0001 | t0018 | g0081 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03139 | hp2 | a0001 | c0001 | t0024 | g0157 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03486 | hp1 | a0003 | c0002 | t0012 | g0020 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03486 | hp2 | a0001 | c0001 | t0014 | g0252 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0291 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0195 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03579 | hp2 | a0003 | c0002 | t0022 | g0019 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03654 | hp1 | a0001 | c0001 | t0011 | g0093 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0192 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0285 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0284 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0277 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0193 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0210 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0217 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0200 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0275 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0261 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG04204 | hp1 | a0001 | c0001 | t0015 | g0079 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0196 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0186 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0040 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | CHB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18959 | hp1 | a0001 | c0001 | t0013 | g0273 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18962 | hp1 | a0002 | c0003 | t0003 | g0256 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18962 | hp2 | a0005 | c0005 | t0002 | g0049 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18963 | hp1 | a0001 | c0001 | t0028 | g0189 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18972 | hp2 | a0005 | c0005 | t0002 | g0083 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18984 | hp1 | a0001 | c0001 | t0029 | g0194 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18985 | hp1 | a0001 | c0001 | t0016 | g0148 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18988 | hp2 | a0002 | c0003 | t0003 | g0255 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18989 | hp2 | a0001 | c0001 | t0010 | g0229 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19009 | hp2 | a0001 | c0001 | t0027 | g0006 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0173 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19056 | hp2 | a0002 | c0003 | t0003 | g0243 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19058 | hp1 | a0001 | c0001 | t0026 | g0147 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19064 | hp1 | a0001 | c0001 | t0013 | g0272 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19067 | hp2 | a0001 | c0001 | t0010 | g0230 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19080 | hp2 | a0001 | c0001 | t0010 | g0227 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19081 | hp1 | a0010 | c0006 | t0002 | g0072 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19081 | hp2 | a0002 | c0003 | t0003 | g0244 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19090 | hp2 | a0001 | c0001 | t0011 | g0095 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA20129 | hp1 | a0004 | c0004 | t0009 | g0174 | AFR | ASW | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | ASW | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0260 | EUR | TSI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01123 | hp1 | a0001 | c0001 | t0025 | g0171 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0159 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0121 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02486 | hp2 | a0001 | c0001 | t0014 | g0163 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03471 | hp1 | a0009 | c0012 | t0023 | g0246 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | USA | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | USA | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | USA | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| homoSapiens | chm13v2 | a0011 | c0009 | t0004 | g0253 | REF | REF | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0056 | REF | REF | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:22279558 | A | G | 1 | a0009 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.172A>G | p.Ser58Gly | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/23 | 301/5114 | 172/2922 | 58/973 | chr8 | 22279558 | |||
| chr8:22281440 | C | G | 1 | a0002 | 5 | HG00597.hp2 NA18962.hp1 NA18988.hp2 others(2): Show |
missense_variant | MODERATE | c.350C>G | p.Ser117Cys | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/23 | 479/5114 | 350/2922 | 117/973 | chr8 | 22281440 | |||
| chr8:22283138 | C | T | 1 | a0006 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.530C>T | p.Pro177Leu | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/23 | 659/5114 | 530/2922 | 177/973 | chr8 | 22283138 | |||
| chr8:22283143 | C | T | 1 | a0005 | 2 | NA18962.hp2 NA18972.hp2 |
missense_variant | MODERATE | c.535C>T | p.Arg179Trp | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/23 | 664/5114 | 535/2922 | 179/973 | chr8 | 22283143 | |||
| chr8:22287534 | T | G | 1 | a0010 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.750T>G | p.Asn250Lys | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/23 | 879/5114 | 750/2922 | 250/973 | chr8 | 22287534 | |||
| chr8:22289899 | A | G | 1 | a0005 | 2 | NA18962.hp2 NA18972.hp2 |
missense_variant | MODERATE | c.1039A>G | p.Thr347Ala | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 9/23 | 1168/5114 | 1039/2922 | 347/973 | chr8 | 22289899 | |||
| chr8:22308039 | G | A | 1 | a0008 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1652G>A | p.Arg551His | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/23 | 1781/5114 | 1652/2922 | 551/973 | chr8 | 22308039 | |||
| chr8:22308068 | C | T | 1 | a0003 | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
missense_variant | MODERATE | c.1681C>T | p.His561Tyr | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/23 | 1810/5114 | 1681/2922 | 561/973 | chr8 | 22308068 | |||
| chr8:22311155 | T | A | 1 | a0007 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1844T>A | p.Met615Lys | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/23 | 1973/5114 | 1844/2922 | 615/973 | chr8 | 22311155 | |||
| chr8:22311199 | G | A | 1 | a0004 | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.1888G>A | p.Gly630Ser | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/23 | 2017/5114 | 1888/2922 | 630/973 | chr8 | 22311199 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:22290314 | G | A | 1 | a0009c0012 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1149G>A | p.Lys383Lys | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/23 | 1278/5114 | 1149/2922 | 383/973 | chr8 | 22290314 | |||
| chr8:22307974 | T | C | 1 | a0006c0011 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.1587T>C | p.His529His | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/23 | 1716/5114 | 1587/2922 | 529/973 | chr8 | 22307974 | |||
| chr8:22311132 | A | C | 1 | a0001c0010 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.1821A>C | p.Ala607Ala | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/23 | 1950/5114 | 1821/2922 | 607/973 | chr8 | 22311132 | |||
| chr8:22316286 | C | T | 1 | a0009c0012 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2250C>T | p.Pro750Pro | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/23 | 2379/5114 | 2250/2922 | 750/973 | chr8 | 22316286 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:22275324 | C | T | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(25): Show |
215 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(212): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-121C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/23 | chr8 | 22275324 | |||||||
| chr8:22275351 | CCT | C | 6 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0028 others(3): Show |
55 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(52): Show |
5_prime_UTR_variant | MODIFIER | c.-93_-92delCT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/23 | 4034 | chr8 | 22275351 | ||||||
| chr8:22355748 | C | G | 1 | a0004c0004t0009 | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*243C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 243 | chr8 | 22355748 | ||||||
| chr8:22355788 | T | A | 1 | a0001c0001t0015 | 2 | HG02145.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*283T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 283 | chr8 | 22355788 | ||||||
| chr8:22355914 | T | C | 2 | a0003c0002t0012 a0003c0002t0022 |
4 | HG01099.hp2 HG02723.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*409T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 409 | chr8 | 22355914 | ||||||
| chr8:22355996 | C | T | 1 | a0001c0001t0007 | 5 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*491C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 491 | chr8 | 22355996 | ||||||
| chr8:22356062 | A | G | 1 | a0001c0001t0021 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*557A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 557 | chr8 | 22356062 | ||||||
| chr8:22356071 | C | CA | 6 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0013 others(3): Show |
14 | HG01516.hp1 HG02027.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*583dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 584 | INFO_REALIGN_3_PRIME | chr8 | 22356071 | |||||
| chr8:22356171 | C | T | 1 | a0001c0001t0020 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*666C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 666 | chr8 | 22356171 | ||||||
| chr8:22356246 | T | C | 1 | a0001c0001t0028 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*741T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 741 | chr8 | 22356246 | ||||||
| chr8:22356357 | G | A | 1 | a0001c0001t0024 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*852G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 852 | chr8 | 22356357 | ||||||
| chr8:22356376 | G | C | 1 | a0001c0001t0019 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*871G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 871 | chr8 | 22356376 | ||||||
| chr8:22356394 | G | A | 2 | a0004c0004t0009 a0009c0012t0023 |
5 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*889G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 889 | chr8 | 22356394 | ||||||
| chr8:22356698 | G | A | 1 | a0001c0001t0018 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1193G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1193 | chr8 | 22356698 | ||||||
| chr8:22356779 | A | G | 1 | a0003c0002t0022 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1274A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1274 | chr8 | 22356779 | ||||||
| chr8:22356840 | C | T | 1 | a0001c0001t0030 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1335C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1335 | chr8 | 22356840 | ||||||
| chr8:22356851 | G | C | 1 | a0001c0001t0024 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1346 | chr8 | 22356851 | ||||||
| chr8:22356853 | T | G | 2 | a0001c0001t0025 a0001c0001t0029 |
2 | HG01123.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1348T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1348 | chr8 | 22356853 | ||||||
| chr8:22356861 | C | T | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(14): Show |
124 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1356C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1356 | chr8 | 22356861 | ||||||
| chr8:22356995 | T | C | 8 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0016 others(5): Show |
81 | HG00597.hp1 HG00733.hp1 HG00738.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1490T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1490 | chr8 | 22356995 | ||||||
| chr8:22357043 | A | G | 1 | a0001c0001t0027 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1538A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1538 | chr8 | 22357043 | ||||||
| chr8:22357095 | A | G | 1 | a0001c0001t0017 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1590A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1590 | chr8 | 22357095 | ||||||
| chr8:22357156 | A | G | 1 | a0001c0001t0014 | 3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1651A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1651 | chr8 | 22357156 | ||||||
| chr8:22357178 | A | G | 1 | a0001c0001t0005 | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1673A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1673 | chr8 | 22357178 | ||||||
| chr8:22357487 | C | A | 1 | a0001c0001t0026 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1982C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1982 | chr8 | 22357487 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:22275410 | C | A | 1 | a0001c0001t0003g0003 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-47+12C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275410 | |||||||
| chr8:22275507 | T | C | 1 | a0001c0001t0004g0004 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-47+109T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275507 | |||||||
| chr8:22275668 | G | A | 2 | a0001c0001t0003g0005 a0001c0001t0027g0006 |
2 | NA19009.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-47+270G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275668 | |||||||
| chr8:22275802 | C | T | 1 | a0001c0001t0006g0294 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-47+404C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275802 | |||||||
| chr8:22275862 | C | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-47+464C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275862 | |||||||
| chr8:22275967 | G | A | 4 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+569G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275967 | |||||||
| chr8:22276018 | C | T | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+620C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276018 | |||||||
| chr8:22276102 | G | A | 1 | a0001c0001t0002g0026 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-47+704G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276102 | |||||||
| chr8:22276231 | C | T | 147 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0287 others(144): Show |
147 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.-47+833C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276231 | |||||||
| chr8:22276252 | G | C | 1 | a0001c0001t0002g0027 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-47+854G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276252 | |||||||
| chr8:22276391 | C | G | 7 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG00733.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+993C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276391 | |||||||
| chr8:22276509 | G | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-47+1111G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276509 | |||||||
| chr8:22276566 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-47+1168G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276566 | |||||||
| chr8:22276656 | T | C | 2 | a0003c0002t0012g0017 a0003c0002t0012g0018 |
2 | HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-47+1258T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276656 | |||||||
| chr8:22276711 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47+1313G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276711 | |||||||
| chr8:22276742 | T | C | 3 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0025g0171 |
3 | HG01070.hp1 HG01123.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-47+1344T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276742 | |||||||
| chr8:22276904 | TA | T | 159 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0143 others(156): Show |
159 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.-47+1518delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 22276904 | ||||||
| chr8:22276989 | G | A | 7 | a0001c0001t0007g0173 a0001c0001t0008g0175 a0001c0001t0008g0179 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+1591G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276989 | |||||||
| chr8:22276997 | G | A | 7 | a0001c0001t0007g0173 a0001c0001t0008g0175 a0001c0001t0008g0179 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+1599G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276997 | |||||||
| chr8:22277018 | GAT | G | 6 | a0001c0001t0003g0249 a0003c0002t0001g0021 a0003c0002t0012g0017 others(3): Show |
6 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+1635_-47+1636d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 22277018 | ||||||
| chr8:22277028 | TA | T | 44 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(41): Show |
44 | HG00423.hp1 HG00558.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-47+1631delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277028 | |||||||
| chr8:22277029 | A | T | 1 | a0008c0007t0003g0248 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-47+1631A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277029 | |||||||
| chr8:22277030 | TA | T | 18 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0024 others(15): Show |
18 | HG00597.hp2 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+1633delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277030 | |||||||
| chr8:22277031 | A | AT | 17 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0100 others(14): Show |
18 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+1634dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 22277031 | ||||||
| chr8:22277031 | A | T | 52 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(49): Show |
52 | HG00423.hp1 HG00558.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-47+1633A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277031 | |||||||
| chr8:22277032 | TA | T | 18 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(15): Show |
18 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-47+1635delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277032 | |||||||
| chr8:22277033 | A | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(181): Show |
186 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.-47+1635A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277033 | |||||||
| chr8:22277033 | ATT | A | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+1645_-47+1646d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 22277033 | ||||||
| chr8:22277035 | T | A | 11 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0031 others(8): Show |
11 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47+1637T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277035 | |||||||
| chr8:22277037 | T | A | 1 | a0001c0001t0005g0007 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-47+1639T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277037 | |||||||
| chr8:22277049 | C | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(2): Show |
5 | HG02055.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+1651C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277049 | |||||||
| chr8:22277059 | T | C | 7 | a0001c0001t0001g0162 a0001c0001t0024g0157 a0003c0002t0001g0021 others(4): Show |
7 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+1661T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277059 | |||||||
| chr8:22277140 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-47+1742G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277140 | |||||||
| chr8:22277313 | T | C | 89 | a0001c0001t0001g0140 a0001c0001t0001g0162 a0001c0001t0001g0240 others(86): Show |
89 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.-47+1915T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277313 | |||||||
| chr8:22277568 | C | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG00733.hp1 HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-46-1773C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277568 | |||||||
| chr8:22277704 | A | G | 1 | a0001c0001t0004g0245 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-46-1637A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277704 | |||||||
| chr8:22277821 | A | C | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-1520A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277821 | |||||||
| chr8:22277852 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(46): Show |
51 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.-46-1489A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277852 | |||||||
| chr8:22277875 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-46-1466A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277875 | |||||||
| chr8:22277967 | G | C | 1 | a0001c0001t0001g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-46-1374G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277967 | |||||||
| chr8:22277998 | G | A | 1 | a0001c0001t0004g0180 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-46-1343G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277998 | |||||||
| chr8:22278066 | G | A | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-46-1275G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22278066 | |||||||
| chr8:22278177 | A | G | 59 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0287 others(56): Show |
59 | HG00423.hp1 HG00558.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.-46-1164A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22278177 | |||||||
| chr8:22278498 | C | T | 1 | a0001c0001t0004g0242 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-46-843C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22278498 | |||||||
| chr8:22278595 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-46-746T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22278595 | |||||||
| chr8:22278851 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-46-490C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22278851 | |||||||
| chr8:22279080 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-46-261C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22279080 | |||||||
| chr8:22279108 | TC | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46-231delC | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 22279108 | ||||||
| chr8:22279758 | G | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00597.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.198+174G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22279758 | |||||||
| chr8:22279812 | C | G | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.198+228C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22279812 | |||||||
| chr8:22279825 | C | T | 1 | a0001c0001t0003g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.198+241C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22279825 | |||||||
| chr8:22279897 | C | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+313C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22279897 | |||||||
| chr8:22279913 | C | T | 2 | a0001c0001t0002g0097 a0009c0012t0023g0246 |
2 | HG03471.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.198+329C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22279913 | |||||||
| chr8:22280002 | G | A | 121 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(118): Show |
121 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.198+418G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280002 | |||||||
| chr8:22280088 | G | C | 1 | a0001c0001t0002g0042 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.198+504G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280088 | |||||||
| chr8:22280164 | C | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(13): Show |
17 | HG00738.hp2 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+580C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280164 | |||||||
| chr8:22280212 | A | T | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.198+628A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280212 | |||||||
| chr8:22280366 | G | A | 1 | a0001c0001t0004g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.199-754G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280366 | |||||||
| chr8:22280498 | C | T | 1 | a0001c0001t0004g0004 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.199-622C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280498 | |||||||
| chr8:22280671 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199-449A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280671 | |||||||
| chr8:22280686 | T | G | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.199-434T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280686 | |||||||
| chr8:22280715 | A | G | 11 | a0001c0001t0001g0162 a0001c0001t0005g0007 a0001c0001t0005g0008 others(8): Show |
11 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.199-405A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280715 | |||||||
| chr8:22280771 | AGTTCTGT others(48): Show |
A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-302_199-248del others(55): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 22280771 | ||||||
| chr8:22280993 | G | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-127G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280993 | |||||||
| chr8:22281063 | C | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG00741.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.199-57C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22281063 | |||||||
| chr8:22281307 | A | T | 7 | a0001c0001t0008g0175 a0001c0001t0008g0179 a0001c0001t0014g0251 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-70A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 3/22 | chr8 | 22281307 | |||||||
| chr8:22281334 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.287-43G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 3/22 | chr8 | 22281334 | |||||||
| chr8:22281342 | C | T | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-35C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 3/22 | chr8 | 22281342 | |||||||
| chr8:22281657 | A | G | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.425+142A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22281657 | |||||||
| chr8:22281685 | T | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.425+170T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22281685 | |||||||
| chr8:22281767 | A | AT | 34 | a0001c0001t0001g0118 a0001c0001t0001g0140 a0001c0001t0001g0142 others(31): Show |
34 | HG00408.hp1 HG00597.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.425+274dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22281767 | ||||||
| chr8:22281767 | AT | A | 15 | a0001c0001t0001g0099 a0001c0001t0005g0007 a0001c0001t0005g0008 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.425+274delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22281767 | ||||||
| chr8:22281841 | G | C | 1 | a0001c0001t0002g0042 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.425+326G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22281841 | |||||||
| chr8:22281847 | C | T | 2 | a0001c0001t0014g0251 a0001c0001t0014g0252 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.425+332C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22281847 | |||||||
| chr8:22281876 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.425+361A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22281876 | |||||||
| chr8:22282074 | C | CT | 142 | a0001c0001t0001g0101 a0001c0001t0001g0140 a0001c0001t0001g0142 others(139): Show |
142 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.425+581dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282074 | ||||||
| chr8:22282074 | C | CTT | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(53): Show |
58 | HG00738.hp2 HG01175.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.425+580_425+581dup others(2): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282074 | ||||||
| chr8:22282074 | C | CTTTTT | 11 | a0001c0001t0005g0007 a0001c0001t0005g0009 a0001c0001t0005g0010 others(8): Show |
11 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.425+577_425+581dup others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282074 | ||||||
| chr8:22282191 | C | G | 1 | a0001c0001t0003g0286 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.425+676C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282191 | |||||||
| chr8:22282222 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.425+707A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282222 | |||||||
| chr8:22282229 | C | T | 2 | a0001c0001t0003g0247 a0001c0001t0003g0285 |
2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.425+714C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282229 | |||||||
| chr8:22282244 | C | CT | 33 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0142 others(30): Show |
34 | HG00408.hp1 HG00735.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.425+756dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282244 | ||||||
| chr8:22282244 | C | CTT | 9 | a0001c0001t0001g0154 a0001c0001t0002g0085 a0001c0001t0002g0094 others(6): Show |
9 | HG00741.hp2 HG01175.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.425+755_425+756dup others(2): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282244 | ||||||
| chr8:22282244 | CT | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0101 others(50): Show |
54 | HG00597.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.425+756delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282244 | ||||||
| chr8:22282244 | CTT | C | 32 | a0001c0001t0001g0241 a0001c0001t0003g0225 a0001c0001t0003g0237 others(29): Show |
32 | HG00423.hp1 HG00735.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.425+755_425+756del others(2): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282244 | ||||||
| chr8:22282244 | CTTT | C | 93 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(90): Show |
93 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.425+754_425+756del others(3): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282244 | ||||||
| chr8:22282316 | A | ATCTTGG | 4 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0075 others(1): Show |
4 | HG01099.hp1 HG01934.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-717_426-712dup others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282316 | ||||||
| chr8:22282320 | T | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.426-714T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282320 | |||||||
| chr8:22282470 | G | A | 4 | a0001c0001t0005g0009 a0001c0001t0005g0010 a0001c0001t0005g0011 others(1): Show |
4 | NA18942.hp1 NA18959.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-564G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282470 | |||||||
| chr8:22282473 | C | T | 1 | a0001c0001t0010g0230 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.426-561C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282473 | |||||||
| chr8:22282894 | C | T | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-140C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282894 | |||||||
| chr8:22283250 | G | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.632+10G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283250 | |||||||
| chr8:22283431 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.632+191C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283431 | |||||||
| chr8:22283448 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.632+208G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283448 | |||||||
| chr8:22283499 | C | T | 4 | a0001c0001t0004g0217 a0001c0001t0004g0218 a0001c0001t0004g0231 others(1): Show |
4 | HG01361.hp2 HG02056.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.632+259C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283499 | |||||||
| chr8:22283583 | G | C | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.632+343G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283583 | |||||||
| chr8:22283958 | A | C | 2 | a0001c0001t0003g0290 a0001c0001t0003g0291 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.633-204A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283958 | |||||||
| chr8:22284011 | G | GT | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.633-150dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr8 | 22284011 | ||||||
| chr8:22284098 | T | C | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.633-64T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22284098 | |||||||
| chr8:22284294 | A | G | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.743+22A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284294 | |||||||
| chr8:22284398 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.743+126C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284398 | |||||||
| chr8:22284468 | C | T | 1 | a0001c0001t0014g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.743+196C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284468 | |||||||
| chr8:22284498 | A | C | 5 | a0001c0001t0004g0213 a0001c0001t0004g0214 a0001c0001t0004g0215 others(2): Show |
5 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+226A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284498 | |||||||
| chr8:22284565 | C | G | 1 | a0001c0001t0024g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.743+293C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284565 | |||||||
| chr8:22284565 | C | T | 6 | a0001c0001t0008g0175 a0001c0001t0008g0179 a0004c0004t0009g0174 others(3): Show |
6 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+293C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284565 | |||||||
| chr8:22284582 | G | C | 1 | a0001c0001t0014g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.743+310G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284582 | |||||||
| chr8:22284665 | T | C | 4 | a0001c0001t0006g0038 a0001c0001t0006g0039 a0001c0001t0006g0040 others(1): Show |
4 | HG01496.hp1 HG01975.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+393T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284665 | |||||||
| chr8:22284685 | G | A | 6 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0012 others(3): Show |
6 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+413G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284685 | |||||||
| chr8:22284901 | G | A | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.743+629G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284901 | |||||||
| chr8:22284980 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.743+708A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284980 | |||||||
| chr8:22285248 | G | A | 4 | a0001c0001t0003g0258 a0001c0001t0003g0259 a0001c0001t0003g0260 others(1): Show |
4 | HG00735.hp2 HG01106.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+976G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22285248 | |||||||
| chr8:22285599 | T | C | 2 | a0001c0001t0002g0028 a0001c0001t0002g0029 |
2 | NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.743+1327T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22285599 | |||||||
| chr8:22285644 | C | A | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.743+1372C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22285644 | |||||||
| chr8:22285834 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.743+1562G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22285834 | |||||||
| chr8:22286197 | ATCT | A | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG02004.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.744-1327_744-1325d others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 22286197 | ||||||
| chr8:22286217 | C | T | 2 | a0001c0001t0014g0251 a0001c0001t0014g0252 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.744-1311C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22286217 | |||||||
| chr8:22286435 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.744-1093G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22286435 | |||||||
| chr8:22286438 | A | T | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.744-1090A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22286438 | |||||||
| chr8:22286804 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.744-724A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22286804 | |||||||
| chr8:22286999 | C | T | 6 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0012 others(3): Show |
6 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-529C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22286999 | |||||||
| chr8:22287084 | C | CA | 16 | a0001c0001t0003g0261 a0001c0001t0005g0007 a0001c0001t0005g0008 others(13): Show |
16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.744-433dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 22287084 | ||||||
| chr8:22287201 | G | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.744-327G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22287201 | |||||||
| chr8:22287428 | T | C | 4 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.744-100T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22287428 | |||||||
| chr8:22287806 | G | A | 25 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0108 others(22): Show |
25 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.861+161G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22287806 | |||||||
| chr8:22288059 | G | A | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.861+414G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22288059 | |||||||
| chr8:22288072 | G | A | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.861+427G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22288072 | |||||||
| chr8:22288175 | G | A | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.862-367G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22288175 | |||||||
| chr8:22288215 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.862-327G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22288215 | |||||||
| chr8:22288273 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.862-269G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22288273 | |||||||
| chr8:22288298 | C | CA | 24 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0135 others(21): Show |
24 | HG00639.hp2 HG00741.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.862-224dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr8 | 22288298 | ||||||
| chr8:22288298 | C | CAA | 115 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0047 others(112): Show |
115 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.862-225_862-224dup others(2): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr8 | 22288298 | ||||||
| chr8:22288298 | C | CAAA | 30 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0108 others(27): Show |
30 | HG00423.hp1 HG00597.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.862-226_862-224dup others(3): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr8 | 22288298 | ||||||
| chr8:22288872 | G | A | 118 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(115): Show |
118 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.986+206G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22288872 | |||||||
| chr8:22288922 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.986+256A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22288922 | |||||||
| chr8:22289099 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.986+433C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289099 | |||||||
| chr8:22289152 | C | CT | 15 | a0001c0001t0001g0100 a0001c0001t0001g0137 a0001c0001t0003g0235 others(12): Show |
15 | HG01074.hp2 HG01993.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.986+503dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr8 | 22289152 | ||||||
| chr8:22289152 | CT | C | 19 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(16): Show |
19 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.986+503delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr8 | 22289152 | ||||||
| chr8:22289168 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.986+502T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289168 | |||||||
| chr8:22289192 | C | T | 3 | a0001c0001t0003g0263 a0001c0001t0003g0286 a0001c0001t0003g0293 |
3 | NA18984.hp2 NA19060.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.986+526C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289192 | |||||||
| chr8:22289196 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.986+530A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289196 | |||||||
| chr8:22289213 | C | T | 1 | a0010c0006t0002g0072 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.986+547C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289213 | |||||||
| chr8:22289233 | A | G | 5 | a0001c0001t0002g0027 a0001c0001t0002g0068 a0001c0001t0002g0069 others(2): Show |
5 | HG01069.hp1 HG01255.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.986+567A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289233 | |||||||
| chr8:22289447 | G | A | 2 | a0001c0001t0005g0008 a0001c0001t0005g0016 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.987-400G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289447 | |||||||
| chr8:22289536 | A | T | 1 | a0001c0001t0004g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.987-311A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289536 | |||||||
| chr8:22289551 | A | G | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.987-296A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289551 | |||||||
| chr8:22289712 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.987-135T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289712 | |||||||
| chr8:22289731 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.987-116A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289731 | |||||||
| chr8:22289820 | A | G | 136 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(133): Show |
136 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.987-27A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289820 | |||||||
| chr8:22290572 | G | A | 125 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0047 others(122): Show |
125 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.1181+226G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290572 | |||||||
| chr8:22290583 | G | A | 1 | a0001c0001t0003g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1181+237G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290583 | |||||||
| chr8:22290613 | A | AT | 101 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(98): Show |
101 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1181+288dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290613 | ||||||
| chr8:22290613 | AT | A | 17 | a0001c0001t0002g0087 a0001c0001t0003g0293 a0001c0001t0005g0007 others(14): Show |
17 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1181+288delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290613 | ||||||
| chr8:22290613 | ATTTTTTT | A | 7 | a0001c0001t0001g0119 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
7 | HG00738.hp1 HG01255.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181+282_1181+288d others(9): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290613 | ||||||
| chr8:22290974 | A | ATATATAT others(49): Show |
1 | a0001c0001t0005g0015 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1181+629_1181+630i others(58): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | ||||||
| chr8:22290974 | A | ATATATAT others(45): Show |
1 | a0001c0001t0005g0011 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1181+629_1181+630i others(54): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | ||||||
| chr8:22290974 | A | ATATATAT others(44): Show |
1 | a0001c0001t0005g0009 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1181+629_1181+630i others(53): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | ||||||
| chr8:22290974 | A | ATATATAT others(38): Show |
1 | a0001c0001t0005g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1181+629_1181+630i others(47): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | ||||||
| chr8:22290974 | A | ATATATAT others(39): Show |
2 | a0001c0001t0005g0007 a0001c0001t0005g0013 |
2 | HG01258.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1181+629_1181+630i others(48): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | ||||||
| chr8:22290974 | A | ATATATAT others(38): Show |
1 | a0001c0001t0005g0014 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1181+629_1181+630i others(47): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | ||||||
| chr8:22290974 | A | ATATATAT others(40): Show |
1 | a0001c0001t0005g0010 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1181+629_1181+630i others(49): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | ||||||
| chr8:22290974 | A | ATATATAT others(36): Show |
2 | a0001c0001t0005g0008 a0001c0001t0005g0016 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1181+629_1181+630i others(45): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | ||||||
| chr8:22290976 | T | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1181+630T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290976 | |||||||
| chr8:22290983 | A | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+637A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290983 | |||||||
| chr8:22290984 | A | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+638A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290984 | |||||||
| chr8:22290992 | A | G | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+646A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290992 | |||||||
| chr8:22291000 | A | G | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+654A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291000 | |||||||
| chr8:22291005 | A | G | 25 | a0001c0001t0001g0100 a0001c0001t0001g0140 a0001c0001t0001g0143 others(22): Show |
25 | HG00597.hp1 HG00639.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1181+659A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291005 | |||||||
| chr8:22291008 | A | G | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+662A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291008 | |||||||
| chr8:22291160 | T | C | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1181+814T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291160 | |||||||
| chr8:22291172 | A | G | 7 | a0001c0001t0008g0175 a0001c0001t0008g0179 a0004c0004t0009g0174 others(4): Show |
7 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181+826A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291172 | |||||||
| chr8:22291352 | T | C | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+1006T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291352 | |||||||
| chr8:22291497 | T | C | 1 | a0001c0001t0006g0294 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1181+1151T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291497 | |||||||
| chr8:22291551 | A | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | HG01167.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1181+1205A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291551 | |||||||
| chr8:22291609 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1181+1263A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291609 | |||||||
| chr8:22291727 | C | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1181+1381C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291727 | |||||||
| chr8:22291788 | A | G | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+1442A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291788 | |||||||
| chr8:22291927 | G | A | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+1581G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291927 | |||||||
| chr8:22291960 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1181+1614C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291960 | |||||||
| chr8:22291963 | A | G | 12 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0146 others(9): Show |
12 | HG00597.hp1 HG01109.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1181+1617A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291963 | |||||||
| chr8:22292030 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1181+1684G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292030 | |||||||
| chr8:22292059 | A | T | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+1713A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292059 | |||||||
| chr8:22292279 | GT | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1181+1935delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22292279 | ||||||
| chr8:22292380 | A | G | 1 | a0001c0001t0002g0087 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1181+2034A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292380 | |||||||
| chr8:22292394 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1181+2048G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292394 | |||||||
| chr8:22292403 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1181+2057G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292403 | |||||||
| chr8:22292467 | C | T | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1181+2121C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292467 | |||||||
| chr8:22292534 | A | G | 8 | a0001c0001t0001g0241 a0001c0001t0008g0175 a0001c0001t0008g0179 others(5): Show |
8 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1181+2188A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292534 | |||||||
| chr8:22292754 | G | A | 1 | a0001c0001t0014g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1181+2408G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292754 | |||||||
| chr8:22292974 | A | G | 1 | a0001c0001t0002g0032 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1181+2628A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292974 | |||||||
| chr8:22293008 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1181+2662G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293008 | |||||||
| chr8:22293017 | C | G | 6 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(3): Show |
6 | HG00733.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181+2671C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293017 | |||||||
| chr8:22293060 | A | G | 1 | a0001c0001t0004g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1181+2714A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293060 | |||||||
| chr8:22293337 | C | CAT | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1181+2991_1181+299 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293337 | |||||||
| chr8:22293338 | T | A | 137 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(134): Show |
137 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.1181+2992T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293338 | |||||||
| chr8:22293798 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1181+3452A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293798 | |||||||
| chr8:22294020 | G | A | 23 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0142 others(20): Show |
23 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1181+3674G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294020 | |||||||
| chr8:22294109 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1181+3763G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294109 | |||||||
| chr8:22294148 | G | T | 23 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0142 others(20): Show |
23 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1181+3802G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294148 | |||||||
| chr8:22294210 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0101 others(13): Show |
17 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1181+3864C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294210 | |||||||
| chr8:22294336 | T | TA | 124 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(121): Show |
124 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.1181+4012dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294336 | ||||||
| chr8:22294337 | A | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1181+3991A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294337 | |||||||
| chr8:22294363 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1181+4017C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294363 | |||||||
| chr8:22294421 | C | A | 1 | a0001c0001t0006g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1181+4075C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294421 | |||||||
| chr8:22294434 | G | A | 30 | a0001c0001t0001g0100 a0001c0001t0001g0143 a0001c0001t0001g0144 others(27): Show |
30 | HG00597.hp1 HG00639.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1181+4088G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294434 | |||||||
| chr8:22294502 | G | A | 1 | a0001c0001t0016g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1181+4156G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294502 | |||||||
| chr8:22294510 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1181+4164G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294510 | |||||||
| chr8:22294644 | C | CA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0118 others(38): Show |
42 | HG00408.hp2 HG00639.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1181+4322dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294644 | ||||||
| chr8:22294644 | CA | C | 30 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0107 others(27): Show |
30 | HG01069.hp1 HG01109.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1181+4322delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294644 | ||||||
| chr8:22294672 | A | G | 6 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0012 others(3): Show |
6 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181+4326A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294672 | |||||||
| chr8:22294805 | C | T | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+4459C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294805 | |||||||
| chr8:22294825 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1181+4479C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294825 | |||||||
| chr8:22294847 | G | A | 1 | a0001c0001t0006g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1181+4501G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294847 | |||||||
| chr8:22294898 | TG | T | 4 | a0001c0001t0001g0114 a0001c0001t0001g0127 a0004c0004t0009g0178 others(1): Show |
4 | HG02895.hp1 HG03041.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+4554delG | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294898 | ||||||
| chr8:22294899 | G | GA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(17): Show |
20 | HG01891.hp1 HG02004.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1181+4553_1181+455 others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | |||||||
| chr8:22294899 | G | GAA | 70 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0287 others(67): Show |
70 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1181+4553_1181+455 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | |||||||
| chr8:22294899 | G | GAAA | 49 | a0001c0001t0001g0288 a0001c0001t0003g0098 a0001c0001t0003g0225 others(46): Show |
49 | HG00558.hp1 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.1181+4553_1181+455 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | |||||||
| chr8:22294899 | G | GAAAA | 4 | a0001c0001t0003g0206 a0001c0001t0003g0237 a0001c0001t0003g0289 others(1): Show |
4 | HG01175.hp1 HG02027.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181+4553_1181+455 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | |||||||
| chr8:22294899 | GGA | G | 7 | a0001c0001t0001g0241 a0001c0001t0005g0007 a0001c0001t0005g0008 others(4): Show |
7 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181+4554_1181+455 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | |||||||
| chr8:22294899 | GGAAAAAA others(5): Show |
G | 1 | a0001c0001t0003g0278 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1181+4554_1181+456 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | |||||||
| chr8:22294899 | GGAAAAAA others(6): Show |
G | 2 | a0001c0001t0001g0116 a0001c0001t0008g0250 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1181+4554_1181+456 others(17): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | |||||||
| chr8:22294900 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(165): Show |
170 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.1181+4554G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294900 | |||||||
| chr8:22294900 | G | GA | 18 | a0001c0001t0001g0100 a0001c0001t0001g0115 a0001c0001t0001g0146 others(15): Show |
18 | HG01123.hp2 HG02074.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1181+4583dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294900 | ||||||
| chr8:22294900 | GAAAAAAA others(4): Show |
G | 2 | a0001c0001t0002g0051 a0001c0001t0002g0063 |
2 | NA18952.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1181+4573_1181+458 others(15): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294900 | ||||||
| chr8:22294900 | GAAAAAAA others(5): Show |
G | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1181+4572_1181+458 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294900 | ||||||
| chr8:22294900 | GAAAAAAA others(6): Show |
G | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1181+4571_1181+458 others(17): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294900 | ||||||
| chr8:22294901 | A | G | 1 | a0005c0005t0002g0049 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1181+4555A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294901 | |||||||
| chr8:22294954 | C | T | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1181+4608C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294954 | |||||||
| chr8:22294995 | C | T | 2 | a0001c0001t0003g0247 a0001c0001t0003g0285 |
2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1181+4649C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294995 | |||||||
| chr8:22295028 | G | A | 126 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(123): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1181+4682G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295028 | |||||||
| chr8:22295184 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1181+4838A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295184 | |||||||
| chr8:22295205 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1181+4859C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295205 | |||||||
| chr8:22295337 | C | CT | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(173): Show |
178 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.1181+5001dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22295337 | ||||||
| chr8:22295356 | G | A | 2 | a0001c0001t0001g0241 a0009c0012t0023g0246 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1181+5010G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295356 | |||||||
| chr8:22295472 | A | G | 3 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0025g0171 |
3 | HG01070.hp1 HG01123.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1181+5126A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295472 | |||||||
| chr8:22295580 | C | CT | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+5235dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22295580 | ||||||
| chr8:22295683 | C | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+5337C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295683 | |||||||
| chr8:22295723 | A | G | 126 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(123): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1181+5377A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295723 | |||||||
| chr8:22295750 | A | G | 1 | a0001c0001t0015g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1181+5404A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295750 | |||||||
| chr8:22295760 | G | C | 1 | a0001c0001t0024g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1181+5414G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295760 | |||||||
| chr8:22295868 | G | A | 126 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(123): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1181+5522G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295868 | |||||||
| chr8:22295916 | C | G | 1 | a0001c0001t0002g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1181+5570C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295916 | |||||||
| chr8:22295964 | G | T | 59 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(56): Show |
59 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1181+5618G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295964 | |||||||
| chr8:22296020 | C | CT | 20 | a0001c0001t0002g0041 a0001c0001t0002g0045 a0001c0001t0002g0048 others(17): Show |
20 | HG00733.hp2 HG00741.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1181+5712dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | ||||||
| chr8:22296020 | CT | C | 22 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0168 others(19): Show |
22 | HG00738.hp1 HG01099.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1181+5712delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | ||||||
| chr8:22296020 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0091 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1181+5702_1181+571 others(15): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | ||||||
| chr8:22296020 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0143 a0003c0002t0001g0021 |
2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1181+5700_1181+571 others(17): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | ||||||
| chr8:22296020 | CTTTTTTT others(7): Show |
C | 25 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(22): Show |
25 | HG00597.hp1 HG00639.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1181+5699_1181+571 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | ||||||
| chr8:22296020 | CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0005g0011 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181+5698_1181+571 others(19): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | ||||||
| chr8:22296020 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0003g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1181+5692_1181+571 others(25): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | ||||||
| chr8:22296020 | CTTTTTTT others(15): Show |
C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(163): Show |
168 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.1181+5691_1181+571 others(26): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | ||||||
| chr8:22296020 | CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0004g0211 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1181+5690_1181+571 others(27): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | ||||||
| chr8:22296022 | T | C | 1 | a0001c0001t0007g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1181+5676T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296022 | |||||||
| chr8:22296037 | TTTTTTTT others(15): Show |
T | 2 | a0001c0001t0001g0162 a0001c0001t0014g0252 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1181+5694_1181+571 others(26): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296037 | ||||||
| chr8:22296038 | TTTTTTTT others(14): Show |
T | 1 | a0001c0001t0014g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1181+5695_1181+571 others(25): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296038 | ||||||
| chr8:22296050 | T | G | 1 | a0001c0001t0002g0073 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1181+5704T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296050 | |||||||
| chr8:22296053 | T | G | 6 | a0001c0001t0001g0142 a0001c0001t0001g0166 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01934.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181+5707T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296053 | |||||||
| chr8:22296056 | T | G | 29 | a0001c0001t0001g0142 a0001c0001t0001g0164 a0001c0001t0001g0165 others(26): Show |
29 | HG00423.hp2 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1181+5710T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296056 | |||||||
| chr8:22296056 | T | TG | 6 | a0001c0001t0001g0167 a0001c0001t0002g0042 a0001c0001t0008g0179 others(3): Show |
6 | HG00733.hp1 HG01891.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181+5710_1181+571 others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296056 | |||||||
| chr8:22296059 | G | T | 1 | a0001c0001t0019g0084 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1181+5713G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296059 | |||||||
| chr8:22296083 | T | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(38): Show |
43 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1181+5737T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296083 | |||||||
| chr8:22296124 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1181+5778C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296124 | |||||||
| chr8:22296135 | A | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(168): Show |
173 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.1181+5789A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296135 | |||||||
| chr8:22296250 | T | A | 1 | a0001c0001t0004g0004 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1181+5904T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296250 | |||||||
| chr8:22296260 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(180): Show |
185 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.1181+5914C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296260 | |||||||
| chr8:22296319 | A | G | 1 | a0001c0001t0003g0277 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1181+5973A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296319 | |||||||
| chr8:22296337 | G | A | 4 | a0001c0001t0003g0266 a0001c0001t0003g0267 a0001c0001t0003g0268 others(1): Show |
4 | NA18940.hp1 NA18964.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+5991G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296337 | |||||||
| chr8:22296367 | A | G | 1 | a0001c0001t0025g0171 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1181+6021A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296367 | |||||||
| chr8:22296401 | T | A | 1 | a0001c0001t0003g0286 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1181+6055T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296401 | |||||||
| chr8:22296620 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(168): Show |
173 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.1181+6274T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296620 | |||||||
| chr8:22296933 | CA | C | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+6588delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296933 | |||||||
| chr8:22296981 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1181+6635T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296981 | |||||||
| chr8:22297100 | C | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1181+6754C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297100 | |||||||
| chr8:22297365 | T | C | 1 | a0001c0001t0002g0026 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1182-6656T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297365 | |||||||
| chr8:22297367 | T | G | 8 | a0001c0001t0001g0241 a0001c0001t0008g0175 a0001c0001t0008g0179 others(5): Show |
8 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1182-6654T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297367 | |||||||
| chr8:22297507 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1182-6514C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297507 | |||||||
| chr8:22297592 | A | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-6429A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297592 | |||||||
| chr8:22297608 | A | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-6413A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297608 | |||||||
| chr8:22297621 | C | T | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1182-6400C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297621 | |||||||
| chr8:22298169 | A | G | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1182-5852A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298169 | |||||||
| chr8:22298273 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(182): Show |
187 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(184): Show |
intron_variant | MODIFIER | c.1182-5748G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298273 | |||||||
| chr8:22298398 | G | A | 1 | a0001c0001t0004g0191 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1182-5623G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298398 | |||||||
| chr8:22298527 | A | G | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1182-5494A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298527 | |||||||
| chr8:22298572 | A | G | 1 | a0001c0001t0028g0189 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1182-5449A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298572 | |||||||
| chr8:22298680 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1182-5341C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298680 | |||||||
| chr8:22298803 | A | G | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1182-5218A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298803 | |||||||
| chr8:22298957 | G | C | 1 | a0001c0001t0015g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1182-5064G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298957 | |||||||
| chr8:22299013 | T | C | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1182-5008T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299013 | |||||||
| chr8:22299155 | G | T | 1 | a0001c0001t0004g0184 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1182-4866G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299155 | |||||||
| chr8:22299157 | A | T | 61 | a0001c0001t0002g0047 a0001c0001t0003g0206 a0001c0001t0003g0225 others(58): Show |
61 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1182-4864A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299157 | |||||||
| chr8:22299314 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-4707G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299314 | |||||||
| chr8:22299675 | C | T | 4 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0279 others(1): Show |
4 | HG01070.hp1 HG01074.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-4346C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299675 | |||||||
| chr8:22299755 | G | A | 4 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-4266G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299755 | |||||||
| chr8:22299825 | T | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1182-4196T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299825 | |||||||
| chr8:22299887 | A | T | 1 | a0001c0001t0004g0208 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1182-4134A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299887 | |||||||
| chr8:22299901 | G | A | 7 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182-4120G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299901 | |||||||
| chr8:22299954 | G | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02886.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1182-4067G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299954 | |||||||
| chr8:22300004 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1182-4017A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300004 | |||||||
| chr8:22300067 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(13): Show |
17 | HG00738.hp2 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1182-3954C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300067 | |||||||
| chr8:22300102 | A | AT | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-3911dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22300102 | ||||||
| chr8:22300178 | A | G | 1 | a0001c0001t0002g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1182-3843A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300178 | |||||||
| chr8:22300305 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1182-3716G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300305 | |||||||
| chr8:22300337 | G | C | 1 | a0001c0001t0004g0192 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1182-3684G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300337 | |||||||
| chr8:22300438 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1182-3583G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300438 | |||||||
| chr8:22300539 | C | G | 1 | a0001c0001t0002g0031 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1182-3482C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300539 | |||||||
| chr8:22300635 | A | G | 1 | a0001c0001t0003g0190 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1182-3386A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300635 | |||||||
| chr8:22300637 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(218): Show |
223 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(220): Show |
intron_variant | MODIFIER | c.1182-3384A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300637 | |||||||
| chr8:22300659 | A | G | 7 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG00733.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182-3362A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300659 | |||||||
| chr8:22300991 | CT | C | 181 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0108 others(178): Show |
181 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(178): Show |
intron_variant | MODIFIER | c.1182-3019delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22300991 | ||||||
| chr8:22300991 | CTT | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(36): Show |
41 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.1182-3020_1182-301 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22300991 | ||||||
| chr8:22301102 | C | T | 1 | a0001c0001t0004g0192 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1182-2919C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301102 | |||||||
| chr8:22301157 | T | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(180): Show |
185 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.1182-2864T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301157 | |||||||
| chr8:22301238 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1182-2783C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301238 | |||||||
| chr8:22301330 | G | T | 1 | a0003c0002t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1182-2691G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301330 | |||||||
| chr8:22301403 | C | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182-2618C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301403 | |||||||
| chr8:22301532 | G | T | 1 | a0001c0001t0002g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1182-2489G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301532 | |||||||
| chr8:22301589 | C | T | 3 | a0001c0001t0003g0235 a0001c0001t0003g0237 a0001c0001t0013g0238 |
3 | HG01175.hp1 HG02027.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1182-2432C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301589 | |||||||
| chr8:22301726 | G | GT | 133 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(130): Show |
133 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.1182-2284dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22301726 | ||||||
| chr8:22301770 | C | T | 6 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0001g0152 others(3): Show |
6 | NA18977.hp2 NA18985.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182-2251C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301770 | |||||||
| chr8:22301917 | A | G | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1182-2104A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301917 | |||||||
| chr8:22302081 | C | A | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1182-1940C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302081 | |||||||
| chr8:22302107 | A | C | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182-1914A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302107 | |||||||
| chr8:22302195 | T | C | 1 | a0001c0001t0015g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1182-1826T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302195 | |||||||
| chr8:22302214 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1182-1807G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302214 | |||||||
| chr8:22302242 | C | T | 1 | a0001c0001t0015g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1182-1779C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302242 | |||||||
| chr8:22302282 | A | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-1739A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302282 | |||||||
| chr8:22302430 | C | T | 3 | a0001c0001t0004g0191 a0001c0001t0010g0182 a0001c0001t0030g0187 |
3 | HG00639.hp1 HG01884.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1182-1591C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302430 | |||||||
| chr8:22302465 | T | C | 6 | a0001c0001t0001g0156 a0001c0001t0002g0037 a0004c0004t0009g0174 others(3): Show |
6 | HG00597.hp1 HG00741.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182-1556T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302465 | |||||||
| chr8:22302552 | C | T | 1 | a0003c0002t0012g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1182-1469C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302552 | |||||||
| chr8:22302553 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1182-1468G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302553 | |||||||
| chr8:22302693 | A | C | 1 | a0001c0001t0011g0093 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1182-1328A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302693 | |||||||
| chr8:22303086 | G | T | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1182-935G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303086 | |||||||
| chr8:22303257 | A | G | 1 | a0001c0001t0003g0261 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1182-764A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303257 | |||||||
| chr8:22303352 | A | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-669A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303352 | |||||||
| chr8:22303417 | G | C | 16 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(13): Show |
16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1182-604G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303417 | |||||||
| chr8:22303571 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1182-450T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303571 | |||||||
| chr8:22303666 | C | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(45): Show |
50 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.1182-355C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303666 | |||||||
| chr8:22303859 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1182-162G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303859 | |||||||
| chr8:22304669 | A | G | 6 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1371-115A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 11/22 | chr8 | 22304669 | |||||||
| chr8:22304758 | T | G | 3 | a0001c0001t0003g0235 a0001c0001t0003g0237 a0001c0001t0013g0238 |
3 | HG01175.hp1 HG02027.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1371-26T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 11/22 | chr8 | 22304758 | |||||||
| chr8:22304978 | A | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1455+110A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22304978 | |||||||
| chr8:22304999 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1455+131T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22304999 | |||||||
| chr8:22305082 | T | G | 1 | a0001c0001t0003g0003 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1455+214T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305082 | |||||||
| chr8:22305145 | G | A | 1 | a0001c0001t0006g0039 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1455+277G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305145 | |||||||
| chr8:22305168 | T | TATTC | 4 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455+304_1455+307d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305168 | ||||||
| chr8:22305172 | C | CATTT | 40 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(37): Show |
40 | HG00423.hp1 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1455+341_1455+344d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305172 | ||||||
| chr8:22305172 | C | CATTTATT others(1): Show |
50 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0140 others(47): Show |
50 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1455+337_1455+344d others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305172 | ||||||
| chr8:22305172 | C | CATTTATT others(5): Show |
46 | a0001c0001t0003g0005 a0001c0001t0003g0237 a0001c0001t0003g0247 others(43): Show |
46 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1455+333_1455+344d others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305172 | ||||||
| chr8:22305172 | C | CATTTATT others(9): Show |
11 | a0001c0001t0003g0235 a0001c0001t0003g0270 a0001c0001t0004g0183 others(8): Show |
11 | HG01261.hp2 HG01516.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1455+329_1455+344d others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305172 | ||||||
| chr8:22305172 | CATTT | C | 73 | a0001c0001t0001g0107 a0001c0001t0001g0142 a0001c0001t0001g0145 others(70): Show |
73 | HG00423.hp2 HG00597.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.1455+341_1455+344d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305172 | ||||||
| chr8:22305176 | T | C | 2 | a0001c0001t0001g0108 a0009c0012t0023g0246 |
2 | HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1455+308T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305176 | |||||||
| chr8:22305353 | C | T | 2 | a0001c0001t0002g0060 a0001c0001t0002g0064 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1455+485C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305353 | |||||||
| chr8:22305382 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1455+514C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305382 | |||||||
| chr8:22305438 | C | T | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1456-489C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305438 | |||||||
| chr8:22305589 | G | A | 1 | a0001c0001t0003g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1456-338G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305589 | |||||||
| chr8:22305599 | G | A | 131 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(128): Show |
131 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.1456-328G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305599 | |||||||
| chr8:22305662 | AT | A | 16 | a0001c0001t0003g0249 a0001c0001t0005g0007 a0001c0001t0005g0008 others(13): Show |
16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1456-254delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305662 | ||||||
| chr8:22305689 | C | T | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1456-238C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305689 | |||||||
| chr8:22305763 | A | G | 6 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456-164A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305763 | |||||||
| chr8:22305818 | C | T | 146 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(143): Show |
146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.1456-109C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305818 | |||||||
| chr8:22305911 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1456-16C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305911 | |||||||
| chr8:22306072 | T | A | 1 | a0001c0001t0025g0171 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1545+56T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306072 | |||||||
| chr8:22306106 | A | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1545+90A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306106 | |||||||
| chr8:22306258 | G | C | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1545+242G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306258 | |||||||
| chr8:22306284 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(171): Show |
176 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.1545+268A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306284 | |||||||
| chr8:22306463 | T | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00597.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1545+447T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306463 | |||||||
| chr8:22306538 | G | A | 1 | a0001c0001t0004g0234 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1545+522G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306538 | |||||||
| chr8:22306596 | T | A | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0007c0008t0004g0228 |
3 | HG01069.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1545+580T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306596 | |||||||
| chr8:22306622 | C | T | 1 | a0001c0001t0004g0224 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1545+606C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306622 | |||||||
| chr8:22306688 | G | A | 147 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(144): Show |
147 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.1545+672G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306688 | |||||||
| chr8:22306776 | C | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1545+760C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306776 | |||||||
| chr8:22307070 | A | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0100 others(14): Show |
18 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1546-863A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307070 | |||||||
| chr8:22307118 | G | A | 146 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(143): Show |
146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.1546-815G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307118 | |||||||
| chr8:22307276 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1546-657C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307276 | |||||||
| chr8:22307373 | C | G | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1546-560C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307373 | |||||||
| chr8:22307415 | T | G | 1 | a0001c0001t0002g0097 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1546-518T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307415 | |||||||
| chr8:22307473 | A | AT | 7 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0062 others(4): Show |
7 | HG01123.hp2 HG02293.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546-434dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | ||||||
| chr8:22307473 | AT | A | 15 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(12): Show |
15 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1546-434delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | ||||||
| chr8:22307473 | ATT | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(37): Show |
42 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1546-435_1546-434d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | ||||||
| chr8:22307473 | ATTT | A | 28 | a0001c0001t0001g0107 a0001c0001t0001g0119 a0001c0001t0001g0122 others(25): Show |
28 | HG00597.hp1 HG01099.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1546-436_1546-434d others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | ||||||
| chr8:22307473 | ATTTT | A | 11 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(8): Show |
11 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1546-437_1546-434d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | ||||||
| chr8:22307473 | ATTTTTT | A | 119 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(116): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1546-439_1546-434d others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | ||||||
| chr8:22307474 | T | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1546-459T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307474 | |||||||
| chr8:22307475 | T | A | 7 | a0001c0001t0014g0163 a0001c0001t0014g0251 a0001c0001t0014g0252 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546-458T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307475 | |||||||
| chr8:22307476 | T | A | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1546-457T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307476 | |||||||
| chr8:22307477 | T | A | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-456T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307477 | |||||||
| chr8:22307478 | T | A | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1546-455T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307478 | |||||||
| chr8:22307479 | T | A | 3 | a0001c0001t0001g0140 a0001c0001t0004g0004 a0001c0001t0004g0188 |
3 | HG00609.hp2 NA19001.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1546-454T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307479 | |||||||
| chr8:22307480 | T | A | 119 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(116): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1546-453T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307480 | |||||||
| chr8:22307481 | T | A | 1 | a0001c0001t0004g0216 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1546-452T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307481 | |||||||
| chr8:22307530 | T | C | 132 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(129): Show |
132 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1546-403T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307530 | |||||||
| chr8:22307828 | C | G | 3 | a0001c0001t0003g0263 a0001c0001t0003g0286 a0001c0001t0003g0293 |
3 | NA18984.hp2 NA19060.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1546-105C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307828 | |||||||
| chr8:22307878 | A | G | 1 | a0001c0001t0010g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1546-55A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307878 | |||||||
| chr8:22307925 | C | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.1546-8C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307925 | |||||||
| chr8:22308082 | A | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1686+9A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308082 | |||||||
| chr8:22308197 | G | GT | 16 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0044 others(13): Show |
16 | HG00639.hp2 HG00741.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1686+140dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 22308197 | ||||||
| chr8:22308215 | A | T | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1686+142A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308215 | |||||||
| chr8:22308327 | A | T | 24 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0108 others(21): Show |
24 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1686+254A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308327 | |||||||
| chr8:22308464 | C | G | 1 | a0001c0001t0002g0070 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1686+391C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308464 | |||||||
| chr8:22308588 | G | A | 24 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0108 others(21): Show |
24 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1686+515G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308588 | |||||||
| chr8:22308796 | A | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0113 a0001c0001t0001g0117 |
3 | HG02896.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1686+723A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308796 | |||||||
| chr8:22308837 | C | T | 2 | a0001c0001t0010g0227 a0001c0001t0010g0229 |
2 | NA18989.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1686+764C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308837 | |||||||
| chr8:22308923 | G | T | 144 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(141): Show |
144 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.1686+850G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308923 | |||||||
| chr8:22308942 | C | T | 6 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1686+869C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308942 | |||||||
| chr8:22309123 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1687-838G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309123 | |||||||
| chr8:22309174 | C | A | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687-787C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309174 | |||||||
| chr8:22309568 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00597.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1687-393A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309568 | |||||||
| chr8:22309633 | C | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1687-328C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309633 | |||||||
| chr8:22309634 | C | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1687-327C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309634 | |||||||
| chr8:22309758 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1687-203A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309758 | |||||||
| chr8:22309773 | A | G | 70 | a0001c0001t0001g0140 a0001c0001t0002g0047 a0001c0001t0003g0190 others(67): Show |
70 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1687-188A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309773 | |||||||
| chr8:22309873 | G | T | 7 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1687-88G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309873 | |||||||
| chr8:22310100 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(60): Show |
65 | HG00597.hp1 HG00733.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1800+26A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310100 | |||||||
| chr8:22310105 | A | G | 2 | a0001c0001t0014g0251 a0001c0001t0014g0252 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1800+31A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310105 | |||||||
| chr8:22310154 | T | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1800+80T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310154 | |||||||
| chr8:22310308 | A | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0087 |
2 | NA18950.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1800+234A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310308 | |||||||
| chr8:22310627 | TAATTA | T | 45 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0169 others(42): Show |
45 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1801-481_1801-477d others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr8 | 22310627 | ||||||
| chr8:22310636 | A | T | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0131 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1801-476A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310636 | |||||||
| chr8:22310637 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0131 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1801-475G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310637 | |||||||
| chr8:22310638 | A | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0131 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1801-474A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310638 | |||||||
| chr8:22310666 | A | G | 1 | a0003c0002t0012g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1801-446A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310666 | |||||||
| chr8:22310833 | C | A | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1801-279C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310833 | |||||||
| chr8:22310962 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1801-150T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310962 | |||||||
| chr8:22311379 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1989+79A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311379 | |||||||
| chr8:22311407 | A | G | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1989+107A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311407 | |||||||
| chr8:22311424 | G | A | 1 | a0001c0001t0016g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1989+124G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311424 | |||||||
| chr8:22311529 | G | A | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1989+229G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311529 | |||||||
| chr8:22311574 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(184): Show |
189 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.1989+274A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311574 | |||||||
| chr8:22311609 | G | A | 4 | a0001c0001t0007g0158 a0001c0001t0007g0159 a0001c0001t0007g0160 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1989+309G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311609 | |||||||
| chr8:22311739 | A | T | 1 | a0001c0001t0004g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1989+439A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311739 | |||||||
| chr8:22311751 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1989+451G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311751 | |||||||
| chr8:22311765 | AACTT | A | 4 | a0001c0001t0007g0158 a0001c0001t0007g0159 a0001c0001t0007g0160 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1989+467_1989+470d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr8 | 22311765 | ||||||
| chr8:22311813 | C | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(215): Show |
220 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(217): Show |
intron_variant | MODIFIER | c.1989+513C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311813 | |||||||
| chr8:22311836 | A | G | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1989+536A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311836 | |||||||
| chr8:22311943 | A | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1989+643A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311943 | |||||||
| chr8:22312022 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1989+722G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22312022 | |||||||
| chr8:22312265 | CA | C | 145 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0287 others(142): Show |
145 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.1989+982delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr8 | 22312265 | ||||||
| chr8:22312285 | A | T | 125 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(122): Show |
125 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.1989+985A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22312285 | |||||||
| chr8:22312347 | C | T | 1 | a0001c0001t0003g0292 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1989+1047C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22312347 | |||||||
| chr8:22312434 | A | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1989+1134A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22312434 | |||||||
| chr8:22312566 | G | A | 129 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(126): Show |
129 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.1989+1266G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22312566 | |||||||
| chr8:22313079 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1990-1249A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313079 | |||||||
| chr8:22313091 | C | G | 1 | a0001c0001t0003g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1990-1237C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313091 | |||||||
| chr8:22313163 | C | T | 7 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0149 others(4): Show |
7 | NA18977.hp2 NA18985.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.1990-1165C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313163 | |||||||
| chr8:22313323 | C | A | 4 | a0001c0001t0007g0158 a0001c0001t0007g0159 a0001c0001t0007g0160 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1990-1005C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313323 | |||||||
| chr8:22313353 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1990-975C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313353 | |||||||
| chr8:22313462 | T | C | 1 | a0001c0001t0014g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1990-866T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313462 | |||||||
| chr8:22313668 | G | A | 1 | a0001c0001t0007g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1990-660G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313668 | |||||||
| chr8:22313939 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(13): Show |
17 | HG00738.hp2 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1990-389A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313939 | |||||||
| chr8:22314044 | G | A | 1 | a0001c0001t0004g0004 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1990-284G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22314044 | |||||||
| chr8:22314254 | A | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1990-74A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22314254 | |||||||
| chr8:22314437 | G | GGT | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091+11_2091+12dup others(2): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr8 | 22314437 | ||||||
| chr8:22314454 | C | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2091+25C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 17/22 | chr8 | 22314454 | |||||||
| chr8:22314831 | A | ATG | 4 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2092-182_2092-181d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr8 | 22314831 | ||||||
| chr8:22314894 | AATT | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0125 others(6): Show |
10 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2092-130_2092-128d others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr8 | 22314894 | ||||||
| chr8:22315189 | C | T | 58 | a0001c0001t0002g0047 a0001c0001t0004g0004 a0001c0001t0004g0180 others(55): Show |
58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.2208+44C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315189 | |||||||
| chr8:22315257 | A | G | 6 | a0001c0001t0001g0108 a0001c0001t0007g0158 a0001c0001t0007g0159 others(3): Show |
6 | HG02109.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2208+112A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315257 | |||||||
| chr8:22315452 | G | A | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2208+307G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315452 | |||||||
| chr8:22315491 | AT | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(30): Show |
35 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.2208+351delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 22315491 | ||||||
| chr8:22315498 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(30): Show |
35 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.2208+353G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315498 | |||||||
| chr8:22315533 | T | C | 1 | a0003c0002t0022g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2208+388T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315533 | |||||||
| chr8:22315566 | C | A | 124 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(121): Show |
124 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.2208+421C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315566 | |||||||
| chr8:22315666 | C | T | 1 | a0001c0001t0003g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2208+521C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315666 | |||||||
| chr8:22315885 | A | T | 2 | a0001c0001t0001g0241 a0002c0003t0003g0254 |
2 | HG00597.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2209-360A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315885 | |||||||
| chr8:22315906 | A | G | 1 | a0001c0001t0003g0003 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2209-339A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315906 | |||||||
| chr8:22315938 | A | G | 2 | a0001c0001t0006g0038 a0001c0001t0006g0039 |
2 | HG01496.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2209-307A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315938 | |||||||
| chr8:22315943 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2209-302G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315943 | |||||||
| chr8:22316462 | A | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2297+129A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22316462 | |||||||
| chr8:22316787 | A | G | 1 | a0001c0001t0018g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2297+454A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22316787 | |||||||
| chr8:22316869 | C | G | 1 | a0001c0001t0011g0034 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2297+536C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22316869 | |||||||
| chr8:22317013 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(256): Show |
261 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.2297+680T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317013 | |||||||
| chr8:22317106 | G | A | 1 | a0001c0001t0003g0262 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2297+773G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317106 | |||||||
| chr8:22317119 | C | T | 4 | a0001c0001t0007g0158 a0001c0001t0007g0159 a0001c0001t0007g0160 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2297+786C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317119 | |||||||
| chr8:22317210 | T | A | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2297+877T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317210 | |||||||
| chr8:22317248 | A | G | 1 | a0001c0001t0004g0004 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2297+915A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317248 | |||||||
| chr8:22317269 | G | C | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2298-901G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317269 | |||||||
| chr8:22317355 | C | A | 3 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0141 |
3 | NA18969.hp1 NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2298-815C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317355 | |||||||
| chr8:22317391 | A | AAC | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2298-765_2298-764d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 22317391 | ||||||
| chr8:22317507 | C | T | 1 | a0001c0001t0013g0238 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2298-663C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317507 | |||||||
| chr8:22317573 | A | G | 27 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0119 others(24): Show |
27 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.2298-597A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317573 | |||||||
| chr8:22317599 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2298-571A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317599 | |||||||
| chr8:22317649 | T | A | 6 | a0001c0001t0003g0263 a0003c0002t0001g0021 a0003c0002t0012g0017 others(3): Show |
6 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2298-521T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317649 | |||||||
| chr8:22317669 | A | T | 14 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0119 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2298-501A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317669 | |||||||
| chr8:22317669 | AT | A | 19 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.2298-493delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 22317669 | ||||||
| chr8:22317673 | T | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG00733.hp1 HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2298-497T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317673 | |||||||
| chr8:22317855 | G | T | 125 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(122): Show |
125 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.2298-315G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317855 | |||||||
| chr8:22317950 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0168 |
2 | HG02280.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2298-220C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317950 | |||||||
| chr8:22318020 | G | A | 161 | a0001c0001t0001g0107 a0001c0001t0001g0119 a0001c0001t0001g0122 others(158): Show |
161 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.2298-150G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22318020 | |||||||
| chr8:22318054 | C | T | 145 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(142): Show |
145 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.2298-116C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22318054 | |||||||
| chr8:22318071 | T | C | 1 | a0001c0001t0003g0279 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2298-99T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22318071 | |||||||
| chr8:22318357 | G | A | 1 | a0001c0001t0014g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2403+82G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318357 | |||||||
| chr8:22318474 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2403+199C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318474 | |||||||
| chr8:22318507 | G | T | 1 | a0001c0001t0015g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2403+232G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318507 | |||||||
| chr8:22318593 | C | T | 1 | a0001c0001t0004g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2403+318C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318593 | |||||||
| chr8:22318607 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0133 |
3 | HG00738.hp2 HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2403+332C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318607 | |||||||
| chr8:22318657 | T | C | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+382T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318657 | |||||||
| chr8:22318878 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2403+603T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318878 | |||||||
| chr8:22318897 | A | T | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2403+622A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318897 | |||||||
| chr8:22318955 | T | A | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2403+680T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318955 | |||||||
| chr8:22319190 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2403+915G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319190 | |||||||
| chr8:22319204 | T | C | 7 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG00733.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+929T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319204 | |||||||
| chr8:22319255 | C | T | 7 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+980C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319255 | |||||||
| chr8:22319337 | A | G | 4 | a0001c0001t0003g0258 a0001c0001t0003g0259 a0001c0001t0003g0260 others(1): Show |
4 | HG00735.hp2 HG01106.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2403+1062A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319337 | |||||||
| chr8:22319683 | C | A | 7 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+1408C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319683 | |||||||
| chr8:22319731 | A | T | 70 | a0001c0001t0001g0140 a0001c0001t0002g0047 a0001c0001t0003g0190 others(67): Show |
70 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.2403+1456A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319731 | |||||||
| chr8:22319816 | G | C | 6 | a0001c0001t0001g0108 a0001c0001t0007g0158 a0001c0001t0007g0159 others(3): Show |
6 | HG02109.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2403+1541G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319816 | |||||||
| chr8:22319860 | C | G | 2 | a0001c0001t0002g0089 a0001c0001t0002g0091 |
2 | HG00408.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2403+1585C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319860 | |||||||
| chr8:22319896 | G | C | 1 | a0001c0001t0004g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2403+1621G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319896 | |||||||
| chr8:22319956 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2403+1681T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319956 | |||||||
| chr8:22320163 | G | A | 3 | a0001c0001t0002g0044 a0001c0001t0002g0055 a0001c0001t0002g0059 |
3 | HG02818.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2403+1888G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320163 | |||||||
| chr8:22320259 | C | CT | 29 | a0001c0001t0001g0107 a0001c0001t0001g0128 a0001c0001t0001g0143 others(26): Show |
29 | HG00639.hp1 HG00639.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.2403+2006dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22320259 | ||||||
| chr8:22320259 | C | CTT | 63 | a0001c0001t0001g0140 a0001c0001t0002g0047 a0001c0001t0003g0190 others(60): Show |
63 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2403+2005_2403+200 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22320259 | ||||||
| chr8:22320259 | C | CTTT | 6 | a0001c0001t0004g0004 a0001c0001t0004g0183 a0001c0001t0004g0205 others(3): Show |
6 | HG01109.hp1 HG01261.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2403+2004_2403+200 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22320259 | ||||||
| chr8:22320399 | C | T | 56 | a0001c0001t0004g0004 a0001c0001t0004g0180 a0001c0001t0004g0181 others(53): Show |
56 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2403+2124C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320399 | |||||||
| chr8:22320471 | C | T | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2403+2196C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320471 | |||||||
| chr8:22320534 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2403+2259C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320534 | |||||||
| chr8:22320739 | C | T | 1 | a0001c0001t0006g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2403+2464C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320739 | |||||||
| chr8:22320839 | C | A | 1 | a0001c0001t0015g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2403+2564C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320839 | |||||||
| chr8:22320936 | GACTGTCT others(6): Show |
G | 1 | a0001c0001t0002g0090 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2403+2662_2403+267 others(17): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320936 | |||||||
| chr8:22320996 | G | A | 1 | a0001c0001t0024g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2403+2721G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320996 | |||||||
| chr8:22321043 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2403+2768G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321043 | |||||||
| chr8:22321229 | T | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(218): Show |
223 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(220): Show |
intron_variant | MODIFIER | c.2403+2954T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321229 | |||||||
| chr8:22321269 | C | A | 7 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+2994C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321269 | |||||||
| chr8:22321674 | T | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+3399T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321674 | |||||||
| chr8:22321823 | T | A | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2403+3548T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321823 | |||||||
| chr8:22321823 | T | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(284): Show |
289 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.2403+3548T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321823 | |||||||
| chr8:22321894 | C | A | 1 | a0001c0001t0004g0242 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2403+3619C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321894 | |||||||
| chr8:22322250 | C | T | 24 | a0001c0001t0001g0107 a0001c0001t0001g0119 a0001c0001t0001g0122 others(21): Show |
24 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2403+3975C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322250 | |||||||
| chr8:22322256 | C | G | 1 | a0001c0001t0015g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2403+3981C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322256 | |||||||
| chr8:22322331 | G | C | 127 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0047 others(124): Show |
127 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.2403+4056G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322331 | |||||||
| chr8:22322445 | G | T | 1 | a0001c0001t0004g0217 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2403+4170G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322445 | |||||||
| chr8:22322536 | G | A | 2 | a0001c0001t0001g0241 a0009c0012t0023g0246 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2403+4261G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322536 | |||||||
| chr8:22322580 | TGTCCCGT others(3): Show |
T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+4310_2403+431 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22322580 | ||||||
| chr8:22322691 | C | T | 1 | a0001c0001t0024g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2403+4416C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322691 | |||||||
| chr8:22322729 | C | T | 16 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(13): Show |
16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2403+4454C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322729 | |||||||
| chr8:22322821 | G | A | 130 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(127): Show |
130 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.2403+4546G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322821 | |||||||
| chr8:22322834 | C | T | 11 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0149 others(8): Show |
11 | HG00597.hp1 HG01109.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.2403+4559C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322834 | |||||||
| chr8:22322892 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2403+4617A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322892 | |||||||
| chr8:22323114 | G | A | 145 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(142): Show |
145 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.2403+4839G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323114 | |||||||
| chr8:22323114 | G | C | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2403+4839G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323114 | |||||||
| chr8:22323114 | G | T | 1 | a0001c0001t0015g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2403+4839G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323114 | |||||||
| chr8:22323143 | C | CT | 40 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0100 others(37): Show |
41 | HG00597.hp2 HG01070.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.2403+4890dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22323143 | ||||||
| chr8:22323143 | C | CTT | 129 | a0001c0001t0001g0115 a0001c0001t0001g0137 a0001c0001t0001g0140 others(126): Show |
129 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.2403+4889_2403+489 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22323143 | ||||||
| chr8:22323143 | C | CTTT | 31 | a0001c0001t0001g0107 a0001c0001t0001g0119 a0001c0001t0001g0123 others(28): Show |
31 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.2403+4888_2403+489 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22323143 | ||||||
| chr8:22323211 | A | G | 146 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(143): Show |
146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.2403+4936A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323211 | |||||||
| chr8:22323216 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2403+4941C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323216 | |||||||
| chr8:22323238 | C | G | 1 | a0001c0001t0004g0184 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2403+4963C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323238 | |||||||
| chr8:22323272 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0100 others(19): Show |
23 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.2403+4997C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323272 | |||||||
| chr8:22323315 | T | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0100 others(16): Show |
20 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.2403+5040T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323315 | |||||||
| chr8:22323327 | T | C | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2403+5052T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323327 | |||||||
| chr8:22323388 | C | T | 1 | a0001c0001t0006g0294 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2403+5113C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323388 | |||||||
| chr8:22323543 | T | A | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+5268T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323543 | |||||||
| chr8:22323642 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2403+5367T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323642 | |||||||
| chr8:22323815 | A | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0087 |
2 | NA18950.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.2403+5540A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323815 | |||||||
| chr8:22323850 | T | G | 172 | a0001c0001t0001g0107 a0001c0001t0001g0119 a0001c0001t0001g0122 others(169): Show |
172 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.2403+5575T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323850 | |||||||
| chr8:22324079 | T | A | 4 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2403+5804T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324079 | |||||||
| chr8:22324139 | G | A | 6 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0001t0001g0150 others(3): Show |
6 | HG00597.hp1 HG01109.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.2403+5864G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324139 | |||||||
| chr8:22324214 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2403+5939A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324214 | |||||||
| chr8:22324259 | C | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00597.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2403+5984C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324259 | |||||||
| chr8:22324263 | A | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2403+5988A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324263 | |||||||
| chr8:22324369 | T | C | 7 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+6094T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324369 | |||||||
| chr8:22324635 | A | C | 1 | a0001c0001t0002g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2403+6360A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324635 | |||||||
| chr8:22324703 | T | G | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+6428T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324703 | |||||||
| chr8:22324806 | AC | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(31): Show |
36 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(33): Show |
intron_variant | MODIFIER | c.2403+6532delC | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324806 | |||||||
| chr8:22324908 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2403+6633G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324908 | |||||||
| chr8:22325072 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+6797G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325072 | |||||||
| chr8:22325171 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2403+6896C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325171 | |||||||
| chr8:22325181 | A | G | 2 | a0001c0001t0014g0251 a0001c0001t0014g0252 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2403+6906A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325181 | |||||||
| chr8:22325481 | C | CT | 86 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0111 others(83): Show |
86 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.2403+7228dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22325481 | ||||||
| chr8:22325481 | C | CTT | 75 | a0001c0001t0001g0140 a0001c0001t0001g0151 a0001c0001t0001g0166 others(72): Show |
75 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.2403+7227_2403+722 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22325481 | ||||||
| chr8:22325481 | CT | C | 28 | a0001c0001t0001g0101 a0001c0001t0001g0125 a0001c0001t0001g0126 others(25): Show |
28 | HG00408.hp1 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.2403+7228delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22325481 | ||||||
| chr8:22325481 | CTTTTT | C | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+7224_2403+722 others(9): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22325481 | ||||||
| chr8:22325695 | C | T | 5 | a0001c0001t0004g0197 a0001c0001t0004g0198 a0001c0001t0004g0199 others(2): Show |
5 | HG01358.hp1 HG01978.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+7420C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325695 | |||||||
| chr8:22325759 | C | T | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2403+7484C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325759 | |||||||
| chr8:22325877 | G | T | 2 | a0001c0001t0002g0028 a0001c0001t0002g0029 |
2 | NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2403+7602G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325877 | |||||||
| chr8:22325927 | C | G | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+7652C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325927 | |||||||
| chr8:22325963 | T | C | 1 | a0001c0001t0004g0192 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2403+7688T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325963 | |||||||
| chr8:22326031 | A | G | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+7756A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326031 | |||||||
| chr8:22326053 | C | G | 2 | a0001c0001t0002g0028 a0001c0001t0002g0029 |
2 | NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2403+7778C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326053 | |||||||
| chr8:22326123 | A | C | 6 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0166 others(3): Show |
6 | HG00733.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2403+7848A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326123 | |||||||
| chr8:22326211 | TA | T | 16 | a0001c0001t0002g0141 a0001c0001t0005g0007 a0001c0001t0005g0008 others(13): Show |
16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2403+7950delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22326211 | ||||||
| chr8:22326304 | T | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG01109.hp2 HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2403+8029T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326304 | |||||||
| chr8:22326409 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(11): Show |
15 | HG00738.hp2 HG02004.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2403+8134G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326409 | |||||||
| chr8:22326535 | A | G | 2 | a0001c0001t0001g0107 a0009c0012t0023g0246 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2403+8260A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326535 | |||||||
| chr8:22326659 | G | A | 1 | a0001c0001t0014g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2403+8384G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326659 | |||||||
| chr8:22326661 | A | G | 4 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2403+8386A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326661 | |||||||
| chr8:22327024 | C | CT | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(173): Show |
178 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.2403+8770dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22327024 | ||||||
| chr8:22327024 | C | CTT | 34 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0119 others(31): Show |
34 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.2403+8769_2403+877 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22327024 | ||||||
| chr8:22327024 | C | CTTT | 12 | a0001c0001t0003g0275 a0001c0001t0005g0007 a0001c0001t0005g0008 others(9): Show |
12 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.2403+8768_2403+877 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22327024 | ||||||
| chr8:22327292 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2403+9017C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327292 | |||||||
| chr8:22327368 | C | T | 146 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(143): Show |
146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.2403+9093C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327368 | |||||||
| chr8:22327369 | G | GT | 37 | a0001c0001t0001g0100 a0001c0001t0001g0143 a0001c0001t0001g0144 others(34): Show |
37 | HG00597.hp1 HG00733.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.2403+9109dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22327369 | ||||||
| chr8:22327374 | T | G | 1 | a0001c0001t0004g0004 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2403+9099T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327374 | |||||||
| chr8:22327424 | A | G | 131 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(128): Show |
131 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.2403+9149A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327424 | |||||||
| chr8:22327429 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+9154G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327429 | |||||||
| chr8:22327592 | C | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2403+9317C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327592 | |||||||
| chr8:22327979 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2403+9704T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327979 | |||||||
| chr8:22327986 | C | T | 1 | a0001c0001t0004g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2403+9711C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327986 | |||||||
| chr8:22328055 | T | G | 1 | a0003c0002t0022g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2403+9780T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328055 | |||||||
| chr8:22328448 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2403+10173G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328448 | |||||||
| chr8:22328463 | G | A | 1 | a0001c0001t0024g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2403+10188G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328463 | |||||||
| chr8:22328465 | A | G | 3 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0007c0008t0004g0228 |
3 | HG01069.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2403+10190A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328465 | |||||||
| chr8:22328593 | T | C | 1 | a0004c0004t0009g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2403+10318T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328593 | |||||||
| chr8:22328634 | T | A | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+10359T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328634 | |||||||
| chr8:22328818 | G | GT | 11 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0120 others(8): Show |
11 | HG01516.hp1 HG01891.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2403+10562dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22328818 | ||||||
| chr8:22328818 | G | GTT | 127 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(124): Show |
127 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.2403+10561_2403+10 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22328818 | ||||||
| chr8:22328818 | G | T | 3 | a0001c0001t0004g0181 a0001c0001t0008g0250 a0001c0001t0028g0189 |
3 | HG02976.hp2 NA18612.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.2403+10543G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328818 | |||||||
| chr8:22328818 | GT | G | 19 | a0001c0001t0001g0125 a0001c0001t0002g0041 a0001c0001t0002g0059 others(16): Show |
19 | HG00639.hp2 HG01069.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.2403+10562delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22328818 | ||||||
| chr8:22328820 | T | C | 1 | a0001c0001t0015g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2403+10545T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328820 | |||||||
| chr8:22328825 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2403+10550T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328825 | |||||||
| chr8:22328916 | T | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG01109.hp2 HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2403+10641T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328916 | |||||||
| chr8:22329022 | C | G | 1 | a0001c0001t0002g0085 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2403+10747C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329022 | |||||||
| chr8:22329095 | C | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(225): Show |
230 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(227): Show |
intron_variant | MODIFIER | c.2403+10820C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329095 | |||||||
| chr8:22329105 | C | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(225): Show |
230 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(227): Show |
intron_variant | MODIFIER | c.2403+10830C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329105 | |||||||
| chr8:22329391 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2403+11116G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329391 | |||||||
| chr8:22329502 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(268): Show |
273 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.2403+11227C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329502 | |||||||
| chr8:22329539 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2403+11264T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329539 | |||||||
| chr8:22329574 | C | G | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+11299C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329574 | |||||||
| chr8:22329620 | A | G | 2 | a0001c0001t0004g0217 a0001c0001t0004g0218 |
2 | HG01361.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2403+11345A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329620 | |||||||
| chr8:22329915 | A | T | 1 | a0001c0001t0024g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2403+11640A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329915 | |||||||
| chr8:22329985 | C | G | 135 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(132): Show |
135 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.2403+11710C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329985 | |||||||
| chr8:22330261 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2403+11986A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330261 | |||||||
| chr8:22330342 | A | G | 133 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(130): Show |
133 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.2403+12067A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330342 | |||||||
| chr8:22330421 | G | A | 1 | a0001c0001t0003g0263 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2403+12146G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330421 | |||||||
| chr8:22330546 | C | A | 156 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(153): Show |
156 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.2403+12271C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330546 | |||||||
| chr8:22330557 | C | G | 1 | a0001c0001t0002g0075 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2403+12282C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330557 | |||||||
| chr8:22330697 | A | AAAAT | 71 | a0001c0001t0001g0107 a0001c0001t0001g0119 a0001c0001t0001g0122 others(68): Show |
71 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.2403+12466_2403+12 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | ||||||
| chr8:22330697 | A | AAAATAAA others(1): Show |
26 | a0001c0001t0001g0154 a0001c0001t0002g0032 a0001c0001t0002g0047 others(23): Show |
26 | HG00738.hp1 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.2403+12462_2403+12 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | ||||||
| chr8:22330697 | A | AAAATAAA others(5): Show |
6 | a0001c0001t0002g0035 a0001c0001t0003g0190 a0001c0001t0003g0206 others(3): Show |
6 | HG00609.hp1 HG01517.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2403+12458_2403+12 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | ||||||
| chr8:22330697 | A | AAAATAAA others(9): Show |
1 | a0001c0001t0003g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2403+12454_2403+12 others(22): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | ||||||
| chr8:22330697 | AAAAT | A | 55 | a0001c0001t0001g0167 a0001c0001t0002g0026 a0001c0001t0002g0027 others(52): Show |
55 | HG00408.hp1 HG00423.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2403+12466_2403+12 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | ||||||
| chr8:22330697 | AAAATAAA others(1): Show |
A | 5 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
5 | HG02280.hp2 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+12462_2403+12 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | ||||||
| chr8:22330697 | AAAATAAA others(5): Show |
A | 6 | a0001c0001t0001g0100 a0001c0001t0001g0113 a0001c0001t0001g0144 others(3): Show |
6 | HG03516.hp1 NA18906.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.2403+12458_2403+12 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | ||||||
| chr8:22330697 | AAAATAAA others(9): Show |
A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(43): Show |
48 | HG00597.hp1 HG00738.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.2403+12454_2403+12 others(22): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | ||||||
| chr8:22330741 | T | TAAATAAA others(1): Show |
3 | a0001c0001t0004g0207 a0001c0001t0006g0040 a0001c0001t0006g0294 |
3 | HG02602.hp1 HG04228.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2403+12469_2403+12 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330741 | ||||||
| chr8:22330745 | A | T | 5 | a0001c0001t0001g0140 a0001c0001t0003g0258 a0001c0001t0004g0198 others(2): Show |
5 | HG01358.hp1 HG01358.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+12470A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330745 | |||||||
| chr8:22330817 | T | C | 140 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(137): Show |
140 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.2403+12542T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330817 | |||||||
| chr8:22330865 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2403+12590A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330865 | |||||||
| chr8:22330932 | T | C | 1 | a0001c0001t0003g0259 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2403+12657T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330932 | |||||||
| chr8:22330945 | C | T | 1 | a0003c0002t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2403+12670C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330945 | |||||||
| chr8:22330983 | T | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+12708T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330983 | |||||||
| chr8:22331004 | G | A | 1 | a0001c0001t0004g0215 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2403+12729G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331004 | |||||||
| chr8:22331107 | T | C | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2403+12832T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331107 | |||||||
| chr8:22331130 | T | C | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2403+12855T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331130 | |||||||
| chr8:22331303 | C | G | 1 | a0001c0001t0004g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2403+13028C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331303 | |||||||
| chr8:22331447 | A | G | 1 | a0001c0001t0004g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2403+13172A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331447 | |||||||
| chr8:22331483 | T | C | 1 | a0001c0001t0004g0211 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2403+13208T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331483 | |||||||
| chr8:22331797 | T | C | 1 | a0001c0001t0007g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2403+13522T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331797 | |||||||
| chr8:22331862 | A | G | 2 | a0001c0001t0002g0060 a0001c0001t0002g0064 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2403+13587A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331862 | |||||||
| chr8:22332217 | A | G | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2403+13942A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332217 | |||||||
| chr8:22332472 | C | G | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+14197C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332472 | |||||||
| chr8:22332617 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0139 |
2 | HG01517.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.2403+14342A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332617 | |||||||
| chr8:22332726 | A | G | 3 | a0001c0001t0014g0163 a0001c0001t0014g0251 a0001c0001t0014g0252 |
3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2403+14451A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332726 | |||||||
| chr8:22332887 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2403+14612G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332887 | |||||||
| chr8:22332967 | G | A | 1 | a0001c0001t0018g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2403+14692G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332967 | |||||||
| chr8:22333113 | T | C | 1 | a0001c0001t0014g0251 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2403+14838T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333113 | |||||||
| chr8:22333139 | T | C | 4 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2403+14864T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333139 | |||||||
| chr8:22333314 | G | A | 16 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(13): Show |
16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2403+15039G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333314 | |||||||
| chr8:22333540 | A | G | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+15265A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333540 | |||||||
| chr8:22333600 | G | A | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+15325G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333600 | |||||||
| chr8:22333648 | T | C | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2403+15373T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333648 | |||||||
| chr8:22333990 | G | C | 131 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0031 others(128): Show |
131 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.2403+15715G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333990 | |||||||
| chr8:22334057 | T | A | 1 | a0001c0001t0002g0075 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2403+15782T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334057 | |||||||
| chr8:22334059 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2403+15784C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334059 | |||||||
| chr8:22334323 | A | G | 156 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(153): Show |
156 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.2403+16048A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334323 | |||||||
| chr8:22334335 | C | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+16060C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334335 | |||||||
| chr8:22334437 | G | A | 2 | a0001c0001t0002g0089 a0001c0001t0002g0091 |
2 | HG00408.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2403+16162G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334437 | |||||||
| chr8:22334519 | C | CA | 140 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(137): Show |
140 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.2403+16257dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22334519 | ||||||
| chr8:22334519 | CA | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+16257delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22334519 | ||||||
| chr8:22334668 | A | G | 1 | a0001c0001t0018g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2403+16393A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334668 | |||||||
| chr8:22334865 | G | C | 1 | a0001c0001t0001g0113 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2403+16590G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334865 | |||||||
| chr8:22335072 | A | AT | 139 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(136): Show |
139 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.2403+16797_2403+16 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335072 | |||||||
| chr8:22335072 | A | T | 13 | a0001c0001t0002g0139 a0001c0001t0004g0191 a0001c0001t0004g0197 others(10): Show |
13 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.2403+16797A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335072 | |||||||
| chr8:22335101 | A | G | 23 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0119 others(20): Show |
23 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2403+16826A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335101 | |||||||
| chr8:22335163 | A | G | 1 | a0001c0001t0005g0011 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2403+16888A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335163 | |||||||
| chr8:22335179 | A | G | 157 | a0001c0001t0001g0140 a0001c0001t0001g0287 a0001c0001t0001g0288 others(154): Show |
157 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.2403+16904A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335179 | |||||||
| chr8:22335189 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2403+16914A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335189 | |||||||
| chr8:22335259 | C | T | 4 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2403+16984C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335259 | |||||||
| chr8:22335292 | C | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+17017C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335292 | |||||||
| chr8:22335325 | T | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0101 others(17): Show |
21 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.2403+17050T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335325 | |||||||
| chr8:22335334 | A | G | 24 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0119 others(21): Show |
24 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2403+17059A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335334 | |||||||
| chr8:22335419 | T | C | 1 | a0001c0001t0003g0190 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2403+17144T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335419 | |||||||
| chr8:22335427 | TCATA | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(285): Show |
290 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.2403+17157_2403+17 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22335427 | ||||||
| chr8:22335543 | C | CT | 13 | a0001c0001t0001g0135 a0001c0001t0001g0143 a0001c0001t0001g0152 others(10): Show |
13 | HG01074.hp1 HG01175.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2403+17290dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22335543 | ||||||
| chr8:22335543 | CT | C | 145 | a0001c0001t0001g0101 a0001c0001t0001g0119 a0001c0001t0001g0122 others(142): Show |
145 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.2403+17290delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22335543 | ||||||
| chr8:22335543 | CTT | C | 10 | a0001c0001t0001g0123 a0001c0001t0001g0287 a0001c0001t0003g0289 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+17289_2403+17 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22335543 | ||||||
| chr8:22335567 | A | G | 1 | a0001c0001t0004g0226 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2403+17292A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335567 | |||||||
| chr8:22335575 | T | C | 1 | a0001c0001t0007g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2403+17300T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335575 | |||||||
| chr8:22335643 | G | C | 5 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(2): Show |
5 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404-17316G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335643 | |||||||
| chr8:22335672 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2404-17287C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335672 | |||||||
| chr8:22335802 | A | G | 13 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0154 others(10): Show |
13 | HG00733.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2404-17157A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335802 | |||||||
| chr8:22335839 | G | A | 1 | a0001c0001t0029g0194 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2404-17120G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335839 | |||||||
| chr8:22335848 | T | C | 1 | a0001c0001t0003g0262 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2404-17111T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335848 | |||||||
| chr8:22336012 | A | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2404-16947A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336012 | |||||||
| chr8:22336187 | C | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-16772C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336187 | |||||||
| chr8:22336210 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2404-16749G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336210 | |||||||
| chr8:22336255 | T | C | 7 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2404-16704T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336255 | |||||||
| chr8:22336424 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-16535G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336424 | |||||||
| chr8:22336510 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2404-16449G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336510 | |||||||
| chr8:22336568 | A | G | 2 | a0001c0001t0003g0005 a0001c0001t0027g0006 |
2 | NA19009.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2404-16391A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336568 | |||||||
| chr8:22336703 | C | T | 1 | a0001c0001t0003g0270 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2404-16256C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336703 | |||||||
| chr8:22336974 | A | G | 1 | a0001c0001t0004g0183 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2404-15985A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336974 | |||||||
| chr8:22337070 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2404-15889C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337070 | |||||||
| chr8:22337324 | A | G | 2 | a0001c0001t0014g0163 a0001c0001t0014g0251 |
2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2404-15635A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337324 | |||||||
| chr8:22337341 | A | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2404-15618A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337341 | |||||||
| chr8:22337355 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-15604G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337355 | |||||||
| chr8:22337486 | T | C | 4 | a0001c0001t0003g0266 a0001c0001t0003g0267 a0001c0001t0003g0268 others(1): Show |
4 | NA18940.hp1 NA18964.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-15473T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337486 | |||||||
| chr8:22337510 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2404-15449C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337510 | |||||||
| chr8:22337570 | TA | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-15377delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22337570 | ||||||
| chr8:22337943 | T | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-15016T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337943 | |||||||
| chr8:22338092 | C | CA | 6 | a0001c0001t0001g0099 a0001c0001t0006g0022 a0001c0001t0006g0023 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404-14856dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22338092 | ||||||
| chr8:22338168 | A | G | 1 | a0001c0001t0005g0011 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2404-14791A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338168 | |||||||
| chr8:22338172 | C | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(283): Show |
288 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.2404-14787C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338172 | |||||||
| chr8:22338225 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-14734G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338225 | |||||||
| chr8:22338337 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2404-14622A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338337 | |||||||
| chr8:22338445 | C | G | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-14514C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338445 | |||||||
| chr8:22338691 | A | AAAAT | 23 | a0001c0001t0001g0100 a0001c0001t0001g0119 a0001c0001t0001g0122 others(20): Show |
23 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2404-14237_2404-14 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22338691 | ||||||
| chr8:22338691 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0016g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2404-14245_2404-14 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22338691 | ||||||
| chr8:22338691 | AAAAT | A | 129 | a0001c0001t0001g0140 a0001c0001t0003g0003 a0001c0001t0003g0005 others(126): Show |
129 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.2404-14237_2404-14 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22338691 | ||||||
| chr8:22338691 | AAAATAAA others(1): Show |
A | 11 | a0001c0001t0001g0107 a0001c0001t0005g0007 a0001c0001t0005g0008 others(8): Show |
11 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.2404-14241_2404-14 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22338691 | ||||||
| chr8:22338811 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0128 a0001c0001t0001g0133 |
4 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-14148G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338811 | |||||||
| chr8:22338915 | C | G | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-14044C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338915 | |||||||
| chr8:22338970 | A | G | 1 | a0001c0001t0007g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2404-13989A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338970 | |||||||
| chr8:22339034 | A | G | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-13925A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339034 | |||||||
| chr8:22339248 | C | T | 1 | a0001c0001t0024g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2404-13711C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339248 | |||||||
| chr8:22339331 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2404-13628C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339331 | |||||||
| chr8:22339376 | C | T | 121 | a0001c0001t0001g0140 a0001c0001t0003g0003 a0001c0001t0003g0005 others(118): Show |
121 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.2404-13583C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339376 | |||||||
| chr8:22339380 | C | T | 8 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(5): Show |
8 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2404-13579C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339380 | |||||||
| chr8:22339393 | A | G | 1 | a0004c0004t0009g0178 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2404-13566A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339393 | |||||||
| chr8:22339416 | G | C | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG02004.hp1 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-13543G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339416 | |||||||
| chr8:22339466 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2404-13493C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339466 | |||||||
| chr8:22339506 | C | CA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(62): Show |
67 | HG00597.hp1 HG00733.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2404-13443dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22339506 | ||||||
| chr8:22339581 | C | G | 145 | a0001c0001t0001g0140 a0001c0001t0003g0003 a0001c0001t0003g0005 others(142): Show |
145 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.2404-13378C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339581 | |||||||
| chr8:22339599 | C | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-13360C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339599 | |||||||
| chr8:22339600 | G | A | 3 | a0001c0001t0002g0048 a0001c0001t0002g0054 a0001c0001t0002g0065 |
3 | HG00733.hp2 HG01123.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2404-13359G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339600 | |||||||
| chr8:22339637 | A | G | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-13322A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339637 | |||||||
| chr8:22339721 | C | T | 4 | a0001c0001t0002g0044 a0001c0001t0002g0055 a0001c0001t0002g0059 others(1): Show |
4 | HG02486.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-13238C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339721 | |||||||
| chr8:22339818 | C | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0101 others(14): Show |
18 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2404-13141C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339818 | |||||||
| chr8:22339839 | G | A | 145 | a0001c0001t0001g0140 a0001c0001t0003g0003 a0001c0001t0003g0005 others(142): Show |
145 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.2404-13120G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339839 | |||||||
| chr8:22339971 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-12988G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339971 | |||||||
| chr8:22340045 | A | AT | 51 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0102 others(48): Show |
52 | HG00423.hp2 HG00735.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2404-12890dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340045 | ||||||
| chr8:22340045 | A | ATT | 14 | a0001c0001t0001g0107 a0001c0001t0001g0128 a0001c0001t0001g0166 others(11): Show |
14 | HG00733.hp1 HG00741.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.2404-12891_2404-12 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340045 | ||||||
| chr8:22340045 | A | ATTT | 87 | a0001c0001t0001g0140 a0001c0001t0002g0047 a0001c0001t0003g0003 others(84): Show |
87 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.2404-12892_2404-12 others(9): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340045 | ||||||
| chr8:22340045 | A | ATTTT | 33 | a0001c0001t0003g0005 a0001c0001t0003g0237 a0001c0001t0003g0247 others(30): Show |
33 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.2404-12893_2404-12 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340045 | ||||||
| chr8:22340045 | ATT | A | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2404-12891_2404-12 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340045 | ||||||
| chr8:22340130 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-12829G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340130 | |||||||
| chr8:22340139 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2404-12820G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340139 | |||||||
| chr8:22340146 | G | A | 3 | a0001c0001t0003g0235 a0001c0001t0004g0004 a0001c0001t0013g0238 |
3 | HG02027.hp2 NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2404-12813G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340146 | |||||||
| chr8:22340197 | CAT | C | 9 | a0001c0001t0001g0107 a0001c0001t0001g0119 a0001c0001t0001g0122 others(6): Show |
9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2404-12761_2404-12 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340197 | |||||||
| chr8:22340235 | T | C | 1 | a0001c0001t0025g0171 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2404-12724T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340235 | |||||||
| chr8:22340478 | A | G | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2404-12481A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340478 | |||||||
| chr8:22340501 | T | TAG | 21 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
22 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.2404-12455_2404-12 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340501 | ||||||
| chr8:22340548 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2404-12411G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340548 | |||||||
| chr8:22340623 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2404-12336G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340623 | |||||||
| chr8:22340900 | A | G | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-12059A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340900 | |||||||
| chr8:22341299 | TA | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-11646delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341299 | ||||||
| chr8:22341377 | C | T | 1 | a0001c0001t0024g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2404-11582C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341377 | |||||||
| chr8:22341429 | C | T | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-11530C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341429 | |||||||
| chr8:22341468 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(216): Show |
221 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(218): Show |
intron_variant | MODIFIER | c.2404-11491A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341468 | |||||||
| chr8:22341478 | C | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0125 others(5): Show |
9 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404-11481C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341478 | |||||||
| chr8:22341595 | C | CA | 138 | a0001c0001t0001g0140 a0001c0001t0001g0146 a0001c0001t0001g0150 others(135): Show |
138 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.2404-11346dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341595 | ||||||
| chr8:22341595 | C | CAA | 6 | a0001c0001t0003g0237 a0002c0003t0003g0244 a0004c0004t0009g0174 others(3): Show |
6 | HG01175.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404-11347_2404-11 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341595 | ||||||
| chr8:22341611 | A | AG | 4 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0113 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-11348_2404-11 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341611 | |||||||
| chr8:22341754 | A | G | 1 | a0001c0001t0003g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2404-11205A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341754 | |||||||
| chr8:22341757 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0021g0030 |
2 | HG00735.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2404-11202A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341757 | |||||||
| chr8:22341832 | A | G | 3 | a0001c0001t0014g0163 a0001c0001t0014g0251 a0001c0001t0014g0252 |
3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2404-11127A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341832 | |||||||
| chr8:22341977 | T | TA | 25 | a0001c0001t0001g0145 a0001c0001t0001g0152 a0001c0001t0002g0028 others(22): Show |
25 | HG00741.hp1 HG01167.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.2404-10964dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341977 | ||||||
| chr8:22341977 | TA | T | 19 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0126 others(16): Show |
19 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.2404-10964delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341977 | ||||||
| chr8:22341977 | TAA | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0107 a0001c0001t0001g0119 others(7): Show |
11 | HG00738.hp2 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2404-10965_2404-10 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341977 | ||||||
| chr8:22342000 | A | C | 1 | a0001c0001t0004g0231 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2404-10959A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342000 | |||||||
| chr8:22342157 | C | CA | 131 | a0001c0001t0001g0155 a0001c0001t0002g0047 a0001c0001t0003g0003 others(128): Show |
131 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.2404-10799dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22342157 | ||||||
| chr8:22342393 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-10566G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342393 | |||||||
| chr8:22342542 | A | G | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2404-10417A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342542 | |||||||
| chr8:22342546 | T | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG01891.hp2 HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2404-10413T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342546 | |||||||
| chr8:22342552 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2404-10407T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342552 | |||||||
| chr8:22342567 | C | T | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10392C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342567 | |||||||
| chr8:22342568 | C | A | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10391C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342568 | |||||||
| chr8:22342570 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10389G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342570 | |||||||
| chr8:22342575 | C | T | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10384C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342575 | |||||||
| chr8:22342576 | A | G | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10383A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342576 | |||||||
| chr8:22342578 | A | T | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10381A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342578 | |||||||
| chr8:22342579 | A | G | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10380A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342579 | |||||||
| chr8:22342580 | A | T | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10379A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342580 | |||||||
| chr8:22342581 | A | T | 1 | a0001c0001t0002g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10378A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342581 | |||||||
| chr8:22342613 | A | C | 1 | a0001c0001t0004g0226 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2404-10346A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342613 | |||||||
| chr8:22342635 | A | G | 123 | a0001c0001t0001g0155 a0001c0001t0002g0047 a0001c0001t0003g0003 others(120): Show |
123 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.2404-10324A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342635 | |||||||
| chr8:22342717 | G | T | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-10242G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342717 | |||||||
| chr8:22342721 | T | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-10238T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342721 | |||||||
| chr8:22343002 | C | T | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404-9957C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343002 | |||||||
| chr8:22343170 | C | T | 122 | a0001c0001t0001g0155 a0001c0001t0002g0047 a0001c0001t0003g0003 others(119): Show |
122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.2404-9789C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343170 | |||||||
| chr8:22343171 | G | A | 1 | a0001c0001t0016g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2404-9788G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343171 | |||||||
| chr8:22343233 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(55): Show |
60 | HG00597.hp1 HG00733.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.2404-9726C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343233 | |||||||
| chr8:22343261 | G | A | 1 | a0008c0007t0003g0248 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2404-9698G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343261 | |||||||
| chr8:22343313 | A | G | 2 | a0002c0003t0003g0243 a0002c0003t0003g0244 |
2 | NA19056.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2404-9646A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343313 | |||||||
| chr8:22343422 | C | T | 1 | a0001c0001t0007g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2404-9537C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343422 | |||||||
| chr8:22343435 | C | CA | 7 | a0001c0001t0002g0085 a0001c0001t0008g0250 a0003c0002t0001g0021 others(4): Show |
7 | HG01099.hp2 HG02074.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2404-9511dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22343435 | ||||||
| chr8:22343450 | T | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-9509T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343450 | |||||||
| chr8:22343470 | T | C | 142 | a0001c0001t0001g0155 a0001c0001t0002g0047 a0001c0001t0003g0003 others(139): Show |
142 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.2404-9489T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343470 | |||||||
| chr8:22343487 | A | G | 3 | a0001c0001t0014g0163 a0001c0001t0014g0251 a0001c0001t0014g0252 |
3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2404-9472A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343487 | |||||||
| chr8:22343609 | G | A | 6 | a0001c0001t0001g0241 a0004c0004t0009g0174 a0004c0004t0009g0176 others(3): Show |
6 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404-9350G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343609 | |||||||
| chr8:22343610 | A | G | 126 | a0001c0001t0001g0155 a0001c0001t0002g0047 a0001c0001t0003g0003 others(123): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.2404-9349A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343610 | |||||||
| chr8:22343770 | G | A | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2404-9189G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343770 | |||||||
| chr8:22343789 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2404-9170G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343789 | |||||||
| chr8:22343914 | C | T | 1 | a0001c0010t0003g0172 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2404-9045C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343914 | |||||||
| chr8:22344191 | A | G | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2404-8768A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344191 | |||||||
| chr8:22344206 | T | C | 126 | a0001c0001t0001g0155 a0001c0001t0002g0047 a0001c0001t0003g0003 others(123): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.2404-8753T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344206 | |||||||
| chr8:22344427 | A | G | 1 | a0001c0001t0004g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2404-8532A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344427 | |||||||
| chr8:22344501 | A | G | 5 | a0001c0001t0004g0213 a0001c0001t0004g0214 a0001c0001t0004g0215 others(2): Show |
5 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404-8458A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344501 | |||||||
| chr8:22344545 | G | A | 1 | a0001c0001t0007g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2404-8414G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344545 | |||||||
| chr8:22344555 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-8404G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344555 | |||||||
| chr8:22344665 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2404-8294T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344665 | |||||||
| chr8:22344803 | G | T | 1 | a0001c0001t0007g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2404-8156G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344803 | |||||||
| chr8:22344889 | A | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | HG01167.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2404-8070A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344889 | |||||||
| chr8:22345274 | TTGTGTAC others(19): Show |
T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-7684_2404-765 others(30): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345274 | |||||||
| chr8:22345292 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2404-7667T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345292 | |||||||
| chr8:22345300 | C | T | 123 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0098 others(120): Show |
123 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.2404-7659C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345300 | |||||||
| chr8:22345320 | T | C | 4 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0149 others(1): Show |
4 | HG02976.hp2 NA19060.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-7639T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345320 | |||||||
| chr8:22345333 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0133 |
3 | HG00738.hp2 HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2404-7626G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345333 | |||||||
| chr8:22345490 | A | G | 12 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0146 others(9): Show |
12 | HG00597.hp1 HG01109.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.2404-7469A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345490 | |||||||
| chr8:22345671 | T | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(215): Show |
220 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(217): Show |
intron_variant | MODIFIER | c.2404-7288T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345671 | |||||||
| chr8:22345786 | C | T | 1 | a0001c0001t0004g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2404-7173C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345786 | |||||||
| chr8:22345853 | T | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-7106T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345853 | |||||||
| chr8:22345863 | A | T | 1 | a0001c0001t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2404-7096A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345863 | |||||||
| chr8:22345884 | C | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-7075C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345884 | |||||||
| chr8:22345921 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(215): Show |
220 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(217): Show |
intron_variant | MODIFIER | c.2404-7038A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345921 | |||||||
| chr8:22346034 | T | A | 4 | a0001c0001t0002g0044 a0001c0001t0002g0055 a0001c0001t0002g0059 others(1): Show |
4 | HG02486.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-6925T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346034 | |||||||
| chr8:22346049 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2404-6910T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346049 | |||||||
| chr8:22346251 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2404-6708A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346251 | |||||||
| chr8:22346380 | G | A | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2404-6579G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346380 | |||||||
| chr8:22346568 | T | G | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-6391T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346568 | |||||||
| chr8:22346664 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2404-6295C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346664 | |||||||
| chr8:22346793 | G | T | 141 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(138): Show |
141 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.2404-6166G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346793 | |||||||
| chr8:22346831 | G | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-6128G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346831 | |||||||
| chr8:22346994 | A | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0125 others(5): Show |
9 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404-5965A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346994 | |||||||
| chr8:22347161 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2404-5798C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347161 | |||||||
| chr8:22347169 | C | CA | 21 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
21 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.2404-5772dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347169 | ||||||
| chr8:22347169 | CA | C | 18 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(15): Show |
18 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.2404-5772delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347169 | ||||||
| chr8:22347213 | A | AT | 24 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(21): Show |
24 | HG00597.hp2 HG01099.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.2404-5729dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347213 | ||||||
| chr8:22347269 | G | A | 126 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(123): Show |
126 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.2404-5690G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347269 | |||||||
| chr8:22347281 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2404-5678C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347281 | |||||||
| chr8:22347316 | G | A | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2404-5643G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347316 | |||||||
| chr8:22347514 | G | T | 1 | a0001c0001t0002g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2404-5445G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347514 | |||||||
| chr8:22347516 | C | CT | 13 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0001c0001t0001g0144 others(10): Show |
13 | HG00597.hp1 HG00735.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2404-5419dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347516 | ||||||
| chr8:22347516 | CT | C | 122 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0067 others(119): Show |
122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.2404-5419delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347516 | ||||||
| chr8:22347516 | CTT | C | 15 | a0001c0001t0003g0265 a0001c0001t0004g0184 a0001c0001t0005g0007 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-5420_2404-541 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347516 | ||||||
| chr8:22347578 | G | T | 6 | a0001c0001t0003g0265 a0001c0001t0004g0202 a0001c0001t0004g0204 others(3): Show |
6 | NA18950.hp2 NA18952.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404-5381G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347578 | |||||||
| chr8:22347776 | C | T | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-5183C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347776 | |||||||
| chr8:22347885 | C | T | 1 | a0001c0001t0014g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2404-5074C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347885 | |||||||
| chr8:22348051 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2404-4908C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348051 | |||||||
| chr8:22348088 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(30): Show |
35 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.2404-4871G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348088 | |||||||
| chr8:22348125 | A | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2404-4834A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348125 | |||||||
| chr8:22348155 | G | A | 7 | a0001c0001t0003g0265 a0001c0001t0004g0202 a0001c0001t0004g0204 others(4): Show |
7 | NA18950.hp2 NA18952.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.2404-4804G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348155 | |||||||
| chr8:22348226 | G | A | 2 | a0001c0001t0003g0247 a0001c0001t0003g0285 |
2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2404-4733G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348226 | |||||||
| chr8:22348463 | G | C | 6 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2404-4496G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348463 | |||||||
| chr8:22348512 | C | T | 1 | a0001c0001t0004g0245 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2404-4447C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348512 | |||||||
| chr8:22348525 | G | A | 127 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(124): Show |
127 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.2404-4434G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348525 | |||||||
| chr8:22348922 | C | T | 1 | a0001c0001t0029g0194 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2404-4037C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348922 | |||||||
| chr8:22349051 | C | CT | 135 | a0001c0001t0001g0100 a0001c0001t0001g0143 a0001c0001t0001g0144 others(132): Show |
135 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.2404-3893dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349051 | ||||||
| chr8:22349051 | C | CTT | 15 | a0001c0001t0004g0185 a0001c0001t0005g0007 a0001c0001t0005g0008 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.2404-3894_2404-389 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349051 | ||||||
| chr8:22349118 | T | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-3841T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349118 | |||||||
| chr8:22349250 | G | A | 127 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(124): Show |
127 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.2404-3709G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349250 | |||||||
| chr8:22349409 | A | ATG | 33 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0101 others(30): Show |
34 | HG00597.hp1 HG01109.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.2404-3540_2404-353 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349409 | ||||||
| chr8:22349409 | ATG | A | 5 | a0001c0001t0004g0191 a0001c0001t0004g0231 a0001c0001t0010g0182 others(2): Show |
5 | HG00597.hp2 HG00639.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404-3540_2404-353 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349409 | ||||||
| chr8:22349415 | G | GTA | 7 | a0001c0001t0003g0264 a0001c0001t0004g0004 a0001c0001t0004g0201 others(4): Show |
7 | HG00558.hp1 HG00558.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.2404-3543_2404-354 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | ||||||
| chr8:22349415 | G | GTATA | 32 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(29): Show |
32 | HG00423.hp1 HG01257.hp2 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.2404-3543_2404-354 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | ||||||
| chr8:22349415 | G | GTATATA | 19 | a0001c0001t0003g0098 a0001c0001t0003g0169 a0001c0001t0003g0190 others(16): Show |
19 | HG00609.hp1 HG01070.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.2404-3543_2404-354 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | ||||||
| chr8:22349415 | G | GTATATAT others(1): Show |
7 | a0001c0001t0003g0225 a0001c0001t0003g0274 a0001c0001t0025g0171 others(4): Show |
7 | HG01123.hp1 HG02145.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2404-3543_2404-354 others(12): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | ||||||
| chr8:22349415 | G | GTATATAT others(3): Show |
1 | a0001c0001t0004g0188 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2404-3543_2404-354 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | ||||||
| chr8:22349415 | G | GTATATAT others(7): Show |
1 | a0003c0002t0012g0017 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2404-3543_2404-354 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | ||||||
| chr8:22349415 | GTGTGTAT others(5): Show |
G | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0271 others(1): Show |
4 | NA18940.hp1 NA18964.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-3542_2404-353 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | ||||||
| chr8:22349417 | G | A | 128 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(125): Show |
128 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.2404-3542G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349417 | |||||||
| chr8:22349417 | G | GTATATAT others(5): Show |
2 | a0001c0001t0003g0257 a0001c0001t0003g0259 |
2 | HG01106.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2404-3541_2404-354 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349417 | ||||||
| chr8:22349417 | G | GTATATAT others(9): Show |
1 | a0001c0001t0003g0280 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2404-3541_2404-354 others(20): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349417 | ||||||
| chr8:22349419 | G | A | 137 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0003g0003 others(134): Show |
137 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.2404-3540G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349419 | |||||||
| chr8:22349419 | G | GTA | 9 | a0001c0001t0001g0164 a0001c0001t0002g0036 a0001c0001t0002g0037 others(6): Show |
9 | HG00741.hp1 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404-3515_2404-351 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349419 | ||||||
| chr8:22349419 | G | GTATGTAT others(27): Show |
1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-3537_2404-353 others(38): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349419 | ||||||
| chr8:22349419 | G | GTGTA | 3 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0016g0148 |
3 | HG03516.hp1 NA18985.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2404-3539_2404-353 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349419 | ||||||
| chr8:22349419 | GTA | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0241 a0001c0001t0002g0069 others(1): Show |
4 | HG01099.hp1 HG01258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-3515_2404-351 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349419 | ||||||
| chr8:22349421 | A | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(19): Show |
23 | HG00738.hp2 HG01243.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2404-3538A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349421 | |||||||
| chr8:22349423 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2404-3536A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349423 | |||||||
| chr8:22349430 | T | A | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-3529T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349430 | |||||||
| chr8:22349445 | A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0199 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2404-3514_2404-351 others(19): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349445 | |||||||
| chr8:22349601 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2404-3358C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349601 | |||||||
| chr8:22349644 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2404-3315T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349644 | |||||||
| chr8:22349857 | T | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-3102T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349857 | |||||||
| chr8:22350018 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2404-2941G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350018 | |||||||
| chr8:22350098 | A | C | 3 | a0001c0001t0004g0191 a0001c0001t0010g0182 a0001c0001t0030g0187 |
3 | HG00639.hp1 HG01884.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2404-2861A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350098 | |||||||
| chr8:22350107 | G | A | 1 | a0001c0001t0004g0236 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2404-2852G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350107 | |||||||
| chr8:22350286 | C | CA | 16 | a0001c0001t0002g0071 a0001c0001t0005g0007 a0001c0001t0005g0008 others(13): Show |
16 | HG00639.hp2 HG01069.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.2404-2665dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22350286 | ||||||
| chr8:22350295 | T | A | 1 | a0001c0001t0002g0075 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2404-2664T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350295 | |||||||
| chr8:22350541 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2404-2418G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350541 | |||||||
| chr8:22350572 | C | T | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-2387C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350572 | |||||||
| chr8:22350582 | A | G | 149 | a0001c0001t0001g0241 a0001c0001t0001g0287 a0001c0001t0001g0288 others(146): Show |
149 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.2404-2377A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350582 | |||||||
| chr8:22350886 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(248): Show |
253 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.2404-2073G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350886 | |||||||
| chr8:22350915 | C | T | 1 | a0001c0001t0007g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2404-2044C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350915 | |||||||
| chr8:22350988 | A | T | 7 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2404-1971A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350988 | |||||||
| chr8:22351048 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2404-1911G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351048 | |||||||
| chr8:22351079 | T | A | 148 | a0001c0001t0001g0241 a0001c0001t0001g0287 a0001c0001t0001g0288 others(145): Show |
148 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.2404-1880T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351079 | |||||||
| chr8:22351146 | G | A | 2 | a0001c0001t0004g0221 a0007c0008t0004g0228 |
2 | HG01069.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2404-1813G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351146 | |||||||
| chr8:22351160 | T | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(30): Show |
35 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.2404-1799T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351160 | |||||||
| chr8:22351179 | C | T | 1 | a0001c0001t0004g0004 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2404-1780C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351179 | |||||||
| chr8:22351345 | A | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0100 others(14): Show |
18 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2404-1614A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351345 | |||||||
| chr8:22351432 | C | CATATATA others(3): Show |
1 | a0001c0001t0003g0286 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2404-1524_2404-152 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351432 | ||||||
| chr8:22351432 | C | CATATATA others(13): Show |
1 | a0002c0003t0003g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2404-1524_2404-152 others(24): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351432 | ||||||
| chr8:22351435 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0003g0293 |
2 | HG03139.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2404-1524A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351435 | |||||||
| chr8:22351436 | C | CAT | 10 | a0001c0001t0001g0114 a0001c0001t0003g0169 a0001c0001t0003g0170 others(7): Show |
10 | HG01069.hp2 HG01070.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-1521_2404-152 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATAT | 7 | a0001c0001t0002g0047 a0001c0001t0003g0264 a0001c0001t0003g0275 others(4): Show |
7 | HG00558.hp1 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATAT | 10 | a0001c0001t0001g0134 a0001c0001t0003g0276 a0001c0001t0003g0280 others(7): Show |
10 | HG00423.hp1 HG00735.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATATA others(1): Show |
13 | a0001c0001t0003g0260 a0001c0001t0003g0277 a0001c0001t0004g0004 others(10): Show |
13 | HG00408.hp2 HG00609.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(12): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATATA others(3): Show |
14 | a0001c0001t0003g0270 a0001c0001t0004g0200 a0001c0001t0004g0202 others(11): Show |
14 | HG01169.hp2 HG01346.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATATA others(5): Show |
12 | a0001c0001t0001g0135 a0001c0001t0003g0259 a0001c0001t0003g0263 others(9): Show |
12 | HG01074.hp2 HG01106.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATATA others(7): Show |
12 | a0001c0001t0003g0257 a0001c0001t0003g0271 a0001c0001t0003g0274 others(9): Show |
12 | HG01257.hp2 HG01975.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATATA others(9): Show |
5 | a0001c0001t0001g0287 a0001c0001t0003g0003 a0001c0001t0003g0261 others(2): Show |
5 | HG02622.hp2 HG03017.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(20): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATATA others(11): Show |
7 | a0001c0001t0001g0166 a0001c0001t0003g0005 a0001c0001t0003g0262 others(4): Show |
7 | HG00558.hp2 HG01978.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(22): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATATA others(13): Show |
4 | a0001c0001t0003g0235 a0001c0001t0003g0247 a0001c0001t0004g0205 others(1): Show |
4 | HG02027.hp2 HG04199.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(24): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATATA others(15): Show |
4 | a0001c0001t0003g0278 a0001c0001t0003g0289 a0001c0001t0004g0196 others(1): Show |
4 | HG04204.hp2 NA19009.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(26): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATATA others(19): Show |
2 | a0001c0001t0003g0249 a0001c0001t0027g0006 |
2 | NA18942.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(30): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | CATATATA others(21): Show |
2 | a0001c0001t0003g0290 a0001c0001t0003g0291 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(32): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | C | T | 2 | a0001c0001t0003g0286 a0002c0003t0003g0254 |
2 | HG00597.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2404-1523C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351436 | |||||||
| chr8:22351436 | CATACATA others(3): Show |
C | 5 | a0001c0001t0003g0268 a0001c0001t0006g0022 a0001c0001t0006g0023 others(2): Show |
5 | HG02717.hp1 HG03130.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404-1519_2404-151 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | CATACATA others(5): Show |
C | 3 | a0001c0001t0001g0288 a0001c0001t0003g0258 a0001c0001t0014g0163 |
3 | HG01358.hp2 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2404-1519_2404-150 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | CATACATA others(7): Show |
C | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2404-1519_2404-150 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | CATACATA others(11): Show |
C | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2404-1519_2404-150 others(22): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | CATACATA others(13): Show |
C | 2 | a0001c0001t0004g0201 a0009c0012t0023g0246 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2404-1519_2404-150 others(24): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | CATACATA others(15): Show |
C | 19 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.2404-1519_2404-149 others(26): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | CATACATA others(21): Show |
C | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-1519_2404-149 others(32): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351436 | CATACATA others(25): Show |
C | 4 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-1519_2404-148 others(36): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | ||||||
| chr8:22351438 | TAC | T | 3 | a0001c0001t0001g0116 a0001c0001t0003g0225 a0001c0001t0003g0267 |
3 | HG02630.hp1 NA18964.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2404-1519_2404-151 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351438 | ||||||
| chr8:22351440 | C | CAT | 6 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0105 others(3): Show |
6 | HG01516.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404-1477_2404-147 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | C | CATAT | 10 | a0001c0001t0001g0113 a0001c0001t0002g0026 a0001c0001t0002g0032 others(7): Show |
10 | HG00609.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-1479_2404-147 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | C | CATATATA others(1): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0106 a0001c0001t0001g0128 others(5): Show |
9 | HG00738.hp2 HG01255.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2404-1483_2404-147 others(12): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | C | CATATATA others(3): Show |
2 | a0001c0001t0002g0041 a0001c0001t0011g0093 |
2 | HG03654.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2404-1485_2404-147 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | C | CATATATA others(5): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0168 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2404-1487_2404-147 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | C | CATATATA others(7): Show |
2 | a0001c0001t0001g0120 a0001c0001t0001g0131 |
2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2404-1489_2404-147 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | C | CATATATA others(9): Show |
2 | a0001c0001t0010g0182 a0001c0001t0015g0086 |
2 | HG02145.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2404-1491_2404-147 others(20): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | C | CATATATA others(15): Show |
3 | a0001c0001t0001g0138 a0001c0001t0001g0165 a0001c0001t0003g0293 |
3 | HG02630.hp2 HG03209.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2404-1497_2404-147 others(26): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | C | CATATATA others(17): Show |
1 | a0001c0001t0001g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2404-1499_2404-147 others(28): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | C | T | 110 | a0001c0001t0001g0114 a0001c0001t0001g0134 a0001c0001t0001g0135 others(107): Show |
110 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.2404-1519C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351440 | |||||||
| chr8:22351440 | CAT | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0108 a0001c0001t0002g0037 others(16): Show |
19 | HG00408.hp1 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.2404-1477_2404-147 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | CATAT | C | 14 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0042 others(11): Show |
14 | HG01074.hp1 HG01258.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2404-1479_2404-147 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | CATATAT | C | 3 | a0001c0001t0001g0162 a0001c0001t0002g0057 a0001c0001t0002g0090 |
3 | HG02135.hp2 NA18612.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2404-1481_2404-147 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | CATATATA others(1): Show |
C | 21 | a0001c0001t0002g0027 a0001c0001t0002g0045 a0001c0001t0002g0048 others(18): Show |
21 | HG00423.hp2 HG00733.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.2404-1483_2404-147 others(12): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | CATATATA others(3): Show |
C | 4 | a0001c0001t0002g0044 a0001c0001t0002g0046 a0001c0001t0002g0055 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-1485_2404-147 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | CATATATA others(7): Show |
C | 1 | a0001c0001t0002g0073 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2404-1489_2404-147 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | CATATATA others(9): Show |
C | 1 | a0001c0001t0030g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2404-1491_2404-147 others(20): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0167 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2404-1499_2404-147 others(28): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351440 | CATATATA others(19): Show |
C | 28 | a0001c0001t0001g0101 a0001c0001t0001g0107 a0001c0001t0001g0117 others(25): Show |
28 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.2404-1501_2404-147 others(30): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | ||||||
| chr8:22351461 | A | C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-1498A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351461 | |||||||
| chr8:22351482 | T | A | 4 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-1477T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351482 | |||||||
| chr8:22351525 | G | GT | 6 | a0001c0001t0001g0133 a0001c0001t0002g0044 a0001c0001t0003g0235 others(3): Show |
6 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2404-1424dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351525 | ||||||
| chr8:22351534 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2404-1425T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351534 | |||||||
| chr8:22351536 | G | T | 7 | a0001c0001t0001g0241 a0003c0002t0001g0021 a0004c0004t0009g0174 others(4): Show |
7 | HG01891.hp1 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2404-1423G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351536 | |||||||
| chr8:22351536 | GT | G | 14 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
14 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2404-1416delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351536 | ||||||
| chr8:22351537 | T | G | 1 | a0003c0002t0001g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2404-1422T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351537 | |||||||
| chr8:22351538 | T | G | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-1421T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351538 | |||||||
| chr8:22351539 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2404-1420T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351539 | |||||||
| chr8:22351540 | T | G | 4 | a0004c0004t0009g0174 a0004c0004t0009g0176 a0004c0004t0009g0177 others(1): Show |
4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-1419T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351540 | |||||||
| chr8:22351608 | G | A | 4 | a0001c0001t0004g0185 a0001c0001t0004g0193 a0001c0001t0004g0195 others(1): Show |
4 | HG01106.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-1351G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351608 | |||||||
| chr8:22351726 | C | T | 1 | a0001c0001t0024g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2404-1233C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351726 | |||||||
| chr8:22351739 | A | G | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-1220A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351739 | |||||||
| chr8:22351796 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0125 others(5): Show |
9 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404-1163C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351796 | |||||||
| chr8:22351804 | G | T | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-1155G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351804 | |||||||
| chr8:22351806 | T | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0100 others(14): Show |
18 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2404-1153T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351806 | |||||||
| chr8:22351829 | G | A | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-1130G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351829 | |||||||
| chr8:22351861 | A | G | 1 | a0001c0001t0003g0279 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2404-1098A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351861 | |||||||
| chr8:22352161 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2404-798T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352161 | |||||||
| chr8:22352383 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-576G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352383 | |||||||
| chr8:22352399 | C | G | 2 | a0001c0001t0004g0188 a0001c0001t0004g0203 |
2 | HG00558.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.2404-560C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352399 | |||||||
| chr8:22352417 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2404-542G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352417 | |||||||
| chr8:22352451 | T | C | 1 | a0001c0001t0003g0275 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2404-508T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352451 | |||||||
| chr8:22352603 | A | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-356A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352603 | |||||||
| chr8:22352721 | A | G | 149 | a0001c0001t0001g0241 a0001c0001t0001g0287 a0001c0001t0001g0288 others(146): Show |
149 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.2404-238A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352721 | |||||||
| chr8:22352739 | T | G | 1 | a0001c0001t0002g0141 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2404-220T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352739 | |||||||
| chr8:22352911 | C | T | 1 | a0001c0001t0004g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2404-48C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352911 | |||||||
| chr8:22352945 | C | T | 1 | a0001c0001t0016g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2404-14C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352945 | |||||||
| chr8:22353292 | GT | G | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2657+83delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353292 | ||||||
| chr8:22353315 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2657+103G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353315 | |||||||
| chr8:22353540 | C | G | 1 | a0001c0001t0004g0192 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2657+328C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353540 | |||||||
| chr8:22353607 | C | T | 1 | a0001c0001t0004g0180 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2657+395C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353607 | |||||||
| chr8:22353723 | G | A | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2657+511G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353723 | |||||||
| chr8:22353743 | A | G | 5 | a0003c0002t0001g0021 a0003c0002t0012g0017 a0003c0002t0012g0018 others(2): Show |
5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2658-528A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353743 | |||||||
| chr8:22353764 | C | CT | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0099 others(50): Show |
55 | HG00423.hp2 HG00733.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.2658-479dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | C | CTT | 22 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0133 others(19): Show |
22 | HG00597.hp1 HG01109.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.2658-480_2658-479d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | C | CTTTT | 7 | a0001c0001t0001g0100 a0001c0001t0001g0144 a0001c0001t0003g0291 others(4): Show |
7 | HG02109.hp1 HG02970.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.2658-482_2658-479d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | C | CTTTTT | 26 | a0001c0001t0003g0247 a0001c0001t0003g0249 a0001c0001t0003g0260 others(23): Show |
26 | HG00558.hp1 HG01257.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.2658-483_2658-479d others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | C | CTTTTTT | 16 | a0001c0001t0003g0098 a0001c0001t0003g0170 a0001c0001t0003g0259 others(13): Show |
16 | HG00423.hp1 HG00597.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.2658-484_2658-479d others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | C | CTTTTTTT others(2): Show |
10 | a0001c0001t0001g0241 a0001c0001t0003g0266 a0001c0001t0004g0214 others(7): Show |
10 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2658-487_2658-479d others(11): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | C | CTTTTTTT others(3): Show |
25 | a0001c0001t0003g0005 a0001c0001t0004g0184 a0001c0001t0004g0185 others(22): Show |
25 | HG00609.hp2 HG00639.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2658-488_2658-479d others(12): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | C | CTTTTTTT others(4): Show |
29 | a0001c0001t0003g0225 a0001c0001t0003g0258 a0001c0001t0004g0004 others(26): Show |
29 | HG00408.hp2 HG00558.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.2658-489_2658-479d others(13): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | C | CTTTTTTT others(5): Show |
10 | a0001c0001t0003g0190 a0001c0001t0003g0206 a0001c0001t0003g0212 others(7): Show |
10 | HG00609.hp1 HG02027.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.2658-490_2658-479d others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0006g0022 a0001c0001t0010g0230 a0001c0001t0014g0163 others(1): Show |
4 | HG02486.hp2 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2658-491_2658-479d others(15): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0237 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2658-492_2658-479d others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353764 | CTTTTTTT others(4): Show |
C | 15 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(12): Show |
15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2658-489_2658-479d others(13): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | ||||||
| chr8:22353916 | T | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0101 others(17): Show |
21 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.2658-355T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353916 | |||||||
| chr8:22353964 | C | T | 1 | a0001c0001t0024g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2658-307C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353964 | |||||||
| chr8:22353985 | A | G | 1 | a0001c0001t0003g0237 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2658-286A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353985 | |||||||
| chr8:22354073 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG01891.hp2 HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2658-198G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22354073 | |||||||
| chr8:22354144 | T | C | 2 | a0001c0001t0010g0227 a0001c0001t0010g0229 |
2 | NA18989.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2658-127T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22354144 | |||||||
| chr8:22354243 | T | A | 146 | a0001c0001t0001g0241 a0001c0001t0002g0047 a0001c0001t0003g0003 others(143): Show |
146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.2658-28T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22354243 | |||||||
| chr8:22354430 | C | CTAG | 8 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(5): Show |
8 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2765+53_2765+55dup others(3): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr8 | 22354430 | ||||||
| chr8:22354614 | C | T | 1 | a0003c0002t0012g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2765+236C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22354614 | |||||||
| chr8:22354629 | A | T | 1 | a0001c0001t0003g0258 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2765+251A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22354629 | |||||||
| chr8:22354690 | A | G | 1 | a0009c0012t0023g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2765+312A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22354690 | |||||||
| chr8:22354773 | C | T | 1 | a0001c0001t0028g0189 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2765+395C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22354773 | |||||||
| chr8:22354798 | G | A | 123 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0169 others(120): Show |
123 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.2765+420G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22354798 | |||||||
| chr8:22355067 | CA | C | 16 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(13): Show |
16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2766-270delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr8 | 22355067 | ||||||
| chr8:22355086 | A | G | 10 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0009 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2766-263A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355086 | |||||||
| chr8:22355089 | AAAC | A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG02004.hp1 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2766-248_2766-246d others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr8 | 22355089 | ||||||
| chr8:22355101 | C | A | 16 | a0001c0001t0002g0073 a0001c0001t0005g0007 a0001c0001t0005g0008 others(13): Show |
16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2766-248C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355101 | |||||||
| chr8:22355104 | A | C | 6 | a0001c0001t0003g0275 a0001c0001t0004g0198 a0004c0004t0009g0174 others(3): Show |
6 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2766-245A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355104 | |||||||
| chr8:22355245 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2766-104G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355245 | |||||||
| chr8:22355265 | A | G | 1 | a0001c0001t0008g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2766-84A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355265 | |||||||
| chr8:22355319 | T | C | 1 | a0001c0001t0004g0188 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2766-30T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355319 |