| geneid | 4660 |
|---|---|
| ensemblid | ENSG00000077157.23 |
| hgncid | 7619 |
| symbol | PPP1R12B |
| name | protein phosphatase 1 regulatory subunit 12B |
| refseq_nuc | NM_002481.4 |
| refseq_prot | NP_002472.2 |
| ensembl_nuc | ENST00000608999.6 |
| ensembl_prot | ENSP00000476755.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 202348699 |
| end | 202592702 |
| strand | + |
| ver | v1.2 |
| region | chr1:202348699-202592702 |
| region5000 | chr1:202343699-202597702 |
| regionname0 | PPP1R12B_chr1_202348699_202592702 |
| regionname5000 | PPP1R12B_chr1_202343699_202597702 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 982 | 246 | 70 | 51 | 94 | 12 | 17 | 73 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0002 | 0/0 | 982 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0003 | 0/0 | 977 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0004 | 0/0 | 982 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0005 | 0/0 | 982 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0006 | 0/0 | 982 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0007 | 0/0 | 982 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0008 | 0/0 | 982 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2949 | 244 | 70 | 51 | 92 | 12 | 17 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| c0002 | 0/0 | 2949 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| c0003 | 0/0 | 2949 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| c0004 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| c0005 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| c0006 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| c0007 | 0/0 | 2949 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| c0008 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| c0009 | 0/0 | 2934 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 12308 | 22 | 4 | 2 | 15 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0002 | 0/0 | 12300 | 18 | 0 | 7 | 8 | 2 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0003 | 0/0 | 12296 | 16 | 1 | 6 | 5 | 3 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0004 | 0/0 | 12296 | 15 | 5 | 2 | 6 | 0 | 2 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0005 | 0/0 | 12312 | 13 | 0 | 4 | 7 | 1 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0006 | 0/0 | 12304 | 11 | 1 | 5 | 3 | 0 | 2 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0007 | 0/0 | 12304 | 7 | 0 | 4 | 1 | 0 | 2 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0008 | 0/0 | 12305 | 6 | 6 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0009 | 0/0 | 12304 | 6 | 3 | 1 | 1 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0010 | 0/0 | 12300 | 6 | 2 | 1 | 3 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0011 | 0/0 | 12301 | 5 | 1 | 1 | 3 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0012 | 0/0 | 12297 | 4 | 3 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0013 | 0/0 | 12305 | 4 | 0 | 1 | 3 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0014 | 0/0 | 12292 | 3 | 2 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0015 | 0/0 | 12308 | 3 | 0 | 3 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0016 | 0/0 | 12304 | 3 | 0 | 0 | 3 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0017 | 0/0 | 12303 | 3 | 3 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0018 | 0/0 | 12304 | 3 | 0 | 0 | 3 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0019 | 0/0 | 12320 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0020 | 0/0 | 12316 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0021 | 0/0 | 12288 | 2 | 0 | 1 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0022 | 0/0 | 12304 | 2 | 0 | 1 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0023 | 0/0 | 12299 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0024 | 0/0 | 12300 | 2 | 0 | 0 | 0 | 0 | 2 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0025 | 0/0 | 12300 | 2 | 1 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0026 | 0/0 | 12297 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0027 | 0/0 | 12305 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0028 | 0/0 | 12289 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0029 | 0/0 | 12297 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0030 | 0/0 | 12309 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0031 | 0/0 | 12297 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0032 | 0/0 | 12304 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0033 | 0/0 | 12289 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0034 | 0/0 | 12308 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0035 | 0/0 | 12300 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0036 | 0/0 | 12308 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0037 | 0/0 | 12304 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0038 | 0/0 | 12292 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0039 | 0/0 | 12280 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0040 | 0/0 | 12312 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0041 | 0/0 | 12312 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0042 | 0/0 | 12308 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0043 | 0/0 | 12308 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0044 | 0/0 | 12308 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0045 | 0/0 | 12308 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0046 | 0/0 | 12300 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0047 | 0/0 | 12296 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0048 | 0/0 | 12311 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0049 | 0/0 | 12304 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0050 | 0/0 | 12308 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0051 | 0/1 | 12308 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0052 | 0/0 | 12303 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0053 | 0/0 | 12300 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0054 | 0/0 | 12296 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0055 | 0/0 | 12287 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0056 | 0/0 | 12304 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0057 | 0/0 | 12312 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0058 | 0/0 | 12292 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0059 | 0/0 | 12288 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0060 | 0/0 | 12305 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0061 | 0/0 | 12297 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0062 | 0/0 | 12305 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0063 | 0/0 | 12312 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0064 | 0/0 | 12297 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0065 | 0/0 | 12296 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0066 | 0/0 | 12297 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0067 | 0/0 | 12300 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0068 | 0/0 | 12284 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0069 | 0/0 | 12297 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0070 | 0/0 | 12312 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0071 | 0/0 | 12304 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0072 | 0/0 | 12304 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0073 | 0/0 | 12300 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0074 | 0/0 | 12316 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0075 | 0/0 | 12312 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0076 | 0/0 | 12312 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0077 | 0/0 | 12308 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0078 | 0/0 | 12308 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0079 | 0/0 | 12304 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0080 | 0/0 | 12300 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0081 | 0/0 | 12300 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0082 | 0/0 | 12296 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0083 | 0/0 | 12296 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0084 | 0/0 | 12292 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0085 | 0/0 | 12292 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0086 | 0/0 | 12296 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0087 | 0/0 | 12304 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0088 | 0/0 | 12304 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0089 | 1/0 | 12296 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0090 | 0/0 | 12308 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0091 | 0/0 | 12308 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0092 | 0/0 | 12304 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0093 | 0/0 | 12304 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0094 | 0/0 | 12308 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0095 | 0/0 | 12304 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0096 | 0/0 | 12300 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0097 | 0/0 | 12296 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0098 | 0/0 | 12292 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0099 | 0/0 | 12323 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0100 | 0/0 | 12307 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0101 | 0/0 | 12307 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0102 | 0/0 | 12295 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0103 | 0/0 | 12304 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0104 | 0/0 | 12296 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0105 | 0/0 | 12304 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| t0106 | 0/0 | 12301 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2949 | 244 | 70 | 51 | 92 | 12 | 17 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0003 | 0/0 | 2949 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0002c0002 | 0/0 | 2949 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0003c0009 | 0/0 | 2934 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0004c0008 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0005c0007 | 0/0 | 2949 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0006c0004 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0007c0005 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0008c0006 | 0/0 | 2949 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 15256 | 21 | 4 | 2 | 14 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0002 | 0/0 | 15248 | 18 | 0 | 7 | 8 | 2 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0003 | 0/0 | 15244 | 16 | 1 | 6 | 5 | 3 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0004 | 0/0 | 15244 | 15 | 5 | 2 | 6 | 0 | 2 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0005 | 0/0 | 15260 | 13 | 0 | 4 | 7 | 1 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0006 | 0/0 | 15252 | 11 | 1 | 5 | 3 | 0 | 2 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0007 | 0/0 | 15252 | 4 | 0 | 1 | 1 | 0 | 2 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0008 | 0/0 | 15253 | 6 | 6 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0009 | 0/0 | 15252 | 5 | 3 | 1 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0010 | 0/0 | 15248 | 4 | 1 | 1 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0011 | 0/0 | 15249 | 5 | 1 | 1 | 3 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0012 | 0/0 | 15245 | 4 | 3 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0013 | 0/0 | 15253 | 4 | 0 | 1 | 3 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0014 | 0/0 | 15240 | 3 | 2 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0015 | 0/0 | 15256 | 3 | 0 | 3 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0016 | 0/0 | 15252 | 3 | 0 | 0 | 3 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0017 | 0/0 | 15251 | 3 | 3 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0018 | 0/0 | 15252 | 3 | 0 | 0 | 3 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0019 | 0/0 | 15268 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0020 | 0/0 | 15264 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0021 | 0/0 | 15236 | 2 | 0 | 1 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0022 | 0/0 | 15252 | 2 | 0 | 1 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0023 | 0/0 | 15247 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0024 | 0/0 | 15248 | 2 | 0 | 0 | 0 | 0 | 2 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0025 | 0/0 | 15248 | 2 | 1 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0026 | 0/0 | 15245 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0027 | 0/0 | 15253 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0029 | 0/0 | 15245 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0030 | 0/0 | 15257 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0031 | 0/0 | 15245 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0032 | 0/0 | 15252 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0033 | 0/0 | 15237 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0034 | 0/0 | 15256 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0035 | 0/0 | 15248 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0036 | 0/0 | 15256 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0037 | 0/0 | 15252 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0038 | 0/0 | 15240 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0039 | 0/0 | 15228 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0040 | 0/0 | 15260 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0041 | 0/0 | 15260 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0042 | 0/0 | 15256 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0043 | 0/0 | 15256 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0044 | 0/0 | 15256 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0045 | 0/0 | 15256 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0046 | 0/0 | 15248 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0047 | 0/0 | 15244 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0048 | 0/0 | 15259 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0049 | 0/0 | 15252 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0050 | 0/0 | 15256 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0051 | 0/1 | 15256 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0052 | 0/0 | 15251 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0053 | 0/0 | 15248 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0054 | 0/0 | 15244 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0055 | 0/0 | 15235 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0056 | 0/0 | 15252 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0057 | 0/0 | 15260 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0058 | 0/0 | 15240 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0059 | 0/0 | 15236 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0060 | 0/0 | 15253 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0061 | 0/0 | 15245 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0062 | 0/0 | 15253 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0063 | 0/0 | 15260 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0065 | 0/0 | 15244 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0066 | 0/0 | 15245 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0067 | 0/0 | 15248 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0068 | 0/0 | 15232 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0069 | 0/0 | 15245 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0070 | 0/0 | 15260 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0071 | 0/0 | 15252 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0072 | 0/0 | 15252 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0073 | 0/0 | 15248 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0074 | 0/0 | 15264 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0075 | 0/0 | 15260 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0076 | 0/0 | 15260 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0077 | 0/0 | 15256 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0078 | 0/0 | 15256 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0079 | 0/0 | 15252 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0080 | 0/0 | 15248 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0081 | 0/0 | 15248 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0082 | 0/0 | 15244 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0083 | 0/0 | 15244 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0084 | 0/0 | 15240 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0085 | 0/0 | 15240 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0086 | 0/0 | 15244 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0087 | 0/0 | 15252 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0088 | 0/0 | 15252 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0089 | 1/0 | 15244 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0090 | 0/0 | 15256 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0091 | 0/0 | 15256 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0092 | 0/0 | 15252 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0093 | 0/0 | 15252 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0094 | 0/0 | 15256 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0095 | 0/0 | 15252 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0096 | 0/0 | 15248 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0097 | 0/0 | 15244 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0098 | 0/0 | 15240 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0099 | 0/0 | 15271 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0100 | 0/0 | 15255 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0101 | 0/0 | 15255 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0102 | 0/0 | 15243 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0103 | 0/0 | 15252 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0104 | 0/0 | 15244 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0105 | 0/0 | 15252 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0001t0106 | 0/0 | 15249 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0001c0003t0028 | 0/0 | 15237 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0002c0002t0007 | 0/0 | 15252 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0003c0009t0007 | 0/0 | 15237 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0004c0008t0064 | 0/0 | 15245 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0005c0007t0009 | 0/0 | 15252 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0006c0004t0010 | 0/0 | 15248 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0007c0005t0010 | 0/0 | 15248 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| a0008c0006t0001 | 0/0 | 15256 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | copy fasta | chr1 | 202343699 | 202597702 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0009g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0009g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0010g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0011g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0013g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0013g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0013g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0014g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0014g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0014g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0015g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0015g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0015g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0016g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0016g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0016g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0017g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0017g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0017g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0018g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0018g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0018g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0019g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0019g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0020g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0020g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0021g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0021g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0022g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0022g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0023g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0023g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0024g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0024g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0025g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0025g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0026g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0026g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0027g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0027g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0029g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0029g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0030g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0030g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0031g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0031g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0032g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0032g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0033g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0033g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0034g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0034g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0035g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0035g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0036g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0036g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0037g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0038g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0039g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0040g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0041g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0042g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0043g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0044g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0045g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0046g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0047g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0048g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0049g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0050g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0051g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0052g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0053g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0054g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0055g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0056g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0057g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0058g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0059g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0060g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0061g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0062g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0063g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0065g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0066g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0067g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0068g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0069g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0070g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0071g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0072g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0073g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0074g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0075g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0076g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0077g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0078g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0079g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0080g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0081g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0082g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0083g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0084g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0085g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0086g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0087g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0088g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0089g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0090g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0091g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0092g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0093g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0094g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0095g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0096g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0097g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0098g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0099g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0100g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0101g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0102g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0103g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0104g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0105g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0001t0106g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0003t0028g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0001c0003t0028g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0002c0002t0007g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0002c0002t0007g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0003c0009t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0004c0008t0064g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0005c0007t0009g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0006c0004t0010g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0007c0005t0010g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| a0008c0006t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0235 | EUR | GBR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0032 | EUR | GBR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00280 | hp1 | a0001 | c0001 | t0022 | g0105 | EUR | FIN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | FIN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00323 | hp1 | a0001 | c0001 | t0055 | g0113 | EUR | FIN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0198 | EUR | FIN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | CHS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00408 | hp2 | a0001 | c0001 | t0010 | g0082 | EAS | CHS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00597 | hp1 | a0001 | c0001 | t0082 | g0097 | EAS | CHS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | CHS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | CHS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00639 | hp1 | a0001 | c0001 | t0015 | g0206 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00639 | hp2 | a0001 | c0001 | t0052 | g0128 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0114 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00673 | hp1 | a0001 | c0003 | t0028 | g0118 | EAS | CHS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00673 | hp2 | a0001 | c0001 | t0088 | g0085 | EAS | CHS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0207 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00733 | hp2 | a0001 | c0001 | t0022 | g0112 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00735 | hp1 | a0001 | c0001 | t0078 | g0050 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00738 | hp1 | a0001 | c0001 | t0023 | g0106 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG00738 | hp2 | a0001 | c0001 | t0050 | g0175 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01069 | hp1 | a0001 | c0001 | t0036 | g0017 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01069 | hp2 | a0001 | c0001 | t0025 | g0234 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01070 | hp1 | a0001 | c0001 | t0015 | g0208 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01071 | hp1 | a0001 | c0001 | t0015 | g0205 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01071 | hp2 | a0001 | c0001 | t0036 | g0074 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0199 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01074 | hp2 | a0001 | c0001 | t0083 | g0081 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01106 | hp1 | a0001 | c0001 | t0045 | g0189 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0194 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01169 | hp1 | a0001 | c0001 | t0023 | g0110 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01175 | hp2 | a0001 | c0001 | t0053 | g0109 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0236 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0148 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0062 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01256 | hp1 | a0002 | c0002 | t0007 | g0055 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01256 | hp2 | a0001 | c0001 | t0013 | g0116 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01258 | hp1 | a0002 | c0002 | t0007 | g0056 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0193 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0102 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0166 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0171 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01346 | hp2 | a0001 | c0001 | t0076 | g0051 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0237 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0035 | EUR | IBS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01515 | hp2 | a0001 | c0001 | t0048 | g0197 | EUR | IBS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0034 | EUR | IBS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0204 | EUR | IBS | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0156 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0238 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01934 | hp1 | a0001 | c0001 | t0010 | g0080 | AMR | PEL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0220 | AMR | PEL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PEL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02004 | hp2 | a0001 | c0001 | t0103 | g0026 | AMR | PEL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02027 | hp1 | a0008 | c0006 | t0001 | g0190 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02055 | hp1 | a0001 | c0001 | t0031 | g0001 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02055 | hp2 | a0001 | c0001 | t0032 | g0057 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02056 | hp1 | a0001 | c0001 | t0075 | g0018 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02056 | hp2 | a0001 | c0001 | t0020 | g0215 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02071 | hp1 | a0001 | c0001 | t0029 | g0123 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02074 | hp2 | a0001 | c0003 | t0028 | g0121 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02080 | hp1 | a0001 | c0001 | t0014 | g0251 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02080 | hp2 | a0001 | c0001 | t0087 | g0016 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02148 | hp1 | a0001 | c0001 | t0021 | g0254 | AMR | PEL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PEL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | CDX | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0107 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02257 | hp2 | a0001 | c0001 | t0084 | g0003 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02258 | hp1 | a0001 | c0001 | t0034 | g0045 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02280 | hp1 | a0001 | c0001 | t0031 | g0002 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02280 | hp2 | a0001 | c0001 | t0034 | g0044 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02300 | hp2 | a0001 | c0001 | t0085 | g0078 | AMR | PEL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02451 | hp1 | a0001 | c0001 | t0032 | g0058 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02451 | hp2 | a0001 | c0001 | t0038 | g0005 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02523 | hp1 | a0001 | c0001 | t0044 | g0252 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02523 | hp2 | a0001 | c0001 | t0016 | g0022 | EAS | KHV | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02572 | hp1 | a0001 | c0001 | t0033 | g0091 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0146 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0157 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0155 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02622 | hp1 | a0001 | c0001 | t0072 | g0012 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02622 | hp2 | a0001 | c0001 | t0077 | g0059 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0137 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02647 | hp2 | a0001 | c0001 | t0057 | g0241 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02698 | hp2 | a0001 | c0001 | t0056 | g0209 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02717 | hp2 | a0001 | c0001 | t0063 | g0159 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0103 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02738 | hp2 | a0001 | c0001 | t0059 | g0176 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02809 | hp1 | a0006 | c0004 | t0010 | g0063 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02809 | hp2 | a0001 | c0001 | t0062 | g0131 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02818 | hp1 | a0001 | c0001 | t0040 | g0247 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02818 | hp2 | a0001 | c0001 | t0027 | g0129 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02886 | hp1 | a0001 | c0001 | t0073 | g0010 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02896 | hp2 | a0001 | c0001 | t0026 | g0008 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02897 | hp1 | a0001 | c0001 | t0026 | g0009 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02897 | hp2 | a0001 | c0001 | t0105 | g0014 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02922 | hp1 | a0001 | c0001 | t0017 | g0143 | AFR | ESN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | ESN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02976 | hp1 | a0001 | c0001 | t0035 | g0135 | AFR | ESN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02976 | hp2 | a0001 | c0001 | t0067 | g0064 | AFR | ESN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03017 | hp1 | a0001 | c0001 | t0093 | g0047 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03017 | hp2 | a0001 | c0001 | t0024 | g0185 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0071 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03041 | hp2 | a0001 | c0001 | t0037 | g0006 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0141 | AFR | MSL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03098 | hp2 | a0001 | c0001 | t0086 | g0027 | AFR | MSL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0154 | AFR | ESN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0149 | AFR | ESN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03139 | hp2 | a0001 | c0001 | t0033 | g0090 | AFR | ESN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03239 | hp1 | a0005 | c0007 | t0009 | g0099 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0202 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0150 | AFR | MSL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03453 | hp2 | a0001 | c0001 | t0035 | g0028 | AFR | MSL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03486 | hp1 | a0001 | c0001 | t0100 | g0142 | AFR | MSL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03486 | hp2 | a0001 | c0001 | t0060 | g0007 | AFR | MSL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0173 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03516 | hp1 | a0001 | c0001 | t0061 | g0132 | AFR | ESN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0243 | AFR | ESN | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03540 | hp1 | a0001 | c0001 | t0065 | g0151 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03540 | hp2 | a0001 | c0001 | t0047 | g0240 | AFR | GWD | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0049 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0188 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03669 | hp2 | a0001 | c0001 | t0098 | g0060 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03710 | hp1 | a0001 | c0001 | t0046 | g0170 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03710 | hp2 | a0001 | c0001 | t0071 | g0073 | SAS | PJL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0087 | SAS | STU | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG04199 | hp2 | a0001 | c0001 | t0024 | g0164 | SAS | STU | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0147 | AFR | YRI | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18522 | hp2 | a0001 | c0001 | t0101 | g0144 | AFR | YRI | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18906 | hp1 | a0001 | c0001 | t0025 | g0233 | AFR | YRI | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0153 | AFR | YRI | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18943 | hp1 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18944 | hp1 | a0001 | c0001 | t0009 | g0100 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18944 | hp2 | a0001 | c0001 | t0042 | g0226 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18950 | hp2 | a0001 | c0001 | t0097 | g0019 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18952 | hp2 | a0001 | c0001 | t0010 | g0083 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18954 | hp2 | a0001 | c0001 | t0030 | g0122 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18956 | hp2 | a0001 | c0001 | t0081 | g0077 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18960 | hp1 | a0001 | c0001 | t0021 | g0249 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18961 | hp1 | a0001 | c0001 | t0011 | g0125 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18961 | hp2 | a0001 | c0001 | t0041 | g0227 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18962 | hp1 | a0001 | c0001 | t0016 | g0023 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18970 | hp1 | a0001 | c0001 | t0018 | g0041 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18970 | hp2 | a0001 | c0001 | t0049 | g0245 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18975 | hp1 | a0001 | c0001 | t0019 | g0167 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18975 | hp2 | a0001 | c0001 | t0096 | g0052 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18983 | hp1 | a0001 | c0001 | t0013 | g0126 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18984 | hp2 | a0001 | c0001 | t0092 | g0024 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18986 | hp1 | a0001 | c0001 | t0018 | g0042 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18991 | hp1 | a0001 | c0001 | t0094 | g0054 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18993 | hp1 | a0001 | c0001 | t0104 | g0101 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18993 | hp2 | a0001 | c0001 | t0091 | g0180 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19000 | hp2 | a0001 | c0001 | t0013 | g0093 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19002 | hp1 | a0001 | c0001 | t0016 | g0025 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19002 | hp2 | a0001 | c0001 | t0058 | g0250 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19005 | hp2 | a0001 | c0001 | t0066 | g0117 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19043 | hp1 | a0001 | c0001 | t0027 | g0130 | AFR | LWK | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0066 | AFR | LWK | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19056 | hp2 | a0001 | c0001 | t0018 | g0039 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19062 | hp1 | a0001 | c0001 | t0020 | g0217 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19062 | hp2 | a0001 | c0001 | t0030 | g0115 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19063 | hp2 | a0001 | c0001 | t0070 | g0136 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19064 | hp1 | a0001 | c0001 | t0029 | g0124 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19068 | hp1 | a0001 | c0001 | t0011 | g0119 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19074 | hp1 | a0001 | c0001 | t0080 | g0086 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19075 | hp2 | a0001 | c0001 | t0074 | g0088 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19078 | hp1 | a0001 | c0001 | t0043 | g0213 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19078 | hp2 | a0001 | c0001 | t0011 | g0120 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19079 | hp2 | a0007 | c0005 | t0010 | g0061 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19085 | hp1 | a0001 | c0001 | t0095 | g0038 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19090 | hp2 | a0001 | c0001 | t0013 | g0108 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19091 | hp1 | a0001 | c0001 | t0019 | g0218 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19091 | hp2 | a0001 | c0001 | t0090 | g0020 | EAS | JPT | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19240 | hp1 | a0001 | c0001 | t0102 | g0140 | AFR | YRI | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0065 | AFR | YRI | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA20129 | hp1 | a0004 | c0008 | t0064 | g0134 | AFR | ASW | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ASW | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA20805 | hp1 | a0001 | c0001 | t0079 | g0046 | EUR | TSI | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA20805 | hp2 | a0001 | c0001 | t0054 | g0111 | EUR | TSI | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0145 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG01123 | hp2 | a0003 | c0009 | t0007 | g0036 | AMR | CLM | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0152 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02109 | hp2 | a0001 | c0001 | t0069 | g0098 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02559 | hp1 | a0001 | c0001 | t0099 | g0138 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03471 | hp1 | a0001 | c0001 | t0068 | g0104 | AFR | MSL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG03471 | hp2 | a0001 | c0001 | t0106 | g0133 | AFR | MSL | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | USA | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | USA | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | USA | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| NA20300 | hp2 | a0001 | c0001 | t0039 | g0011 | AFR | USA | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0051 | g0232 | REF | REF | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0089 | g0139 | REF | REF | PPP1R12B_chr1_202343699_202597702 | PPP1R12B | chr1 | 202343699 | 202597702 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:202348989
|
GACCAGGC others(8): Show |
G | 1 | a0003 | 1 | HG01123.hp2 | conservative_inframe_deletion | MODERATE | c.139_153delACCAGGCG others(7): Show |
p.Thr47_Ser51del | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/24 | 292/15244 | 139/2949 | 47/982 | chr1 | 202348989 | ||
| chr1:202427060
|
A | G | 1 | a0004 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.722A>G | p.Tyr241Cys | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 5/24 | 875/15244 | 722/2949 | 241/982 | chr1 | 202427060 | ||
| chr1:202428903
|
G | C | 1 | a0002 | 2 | HG01256.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.895G>C | p.Glu299Gln | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 6/24 | 1048/15244 | 895/2949 | 299/982 | chr1 | 202428903 | ||
| chr1:202440718
|
A | G | 1 | a0005 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1471A>G | p.Lys491Glu | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/24 | 1624/15244 | 1471/2949 | 491/982 | chr1 | 202440718 | ||
| chr1:202562840
|
G | A | 1 | a0006 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2570G>A | p.Arg857Lys | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/24 | 2723/15244 | 2570/2949 | 857/982 | chr1 | 202562840 | ||
| chr1:202562858
|
G | A | 1 | a0007 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.2588G>A | p.Arg863Gln | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/24 | 2741/15244 | 2588/2949 | 863/982 | chr1 | 202562858 | ||
| chr1:202569187
|
A | G | 1 | a0008 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.2852A>G | p.Glu951Gly | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/24 | 3005/15244 | 2852/2949 | 951/982 | chr1 | 202569187 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:202422671
|
A | G | 1 | a0001c0003 | 2 | HG00673.hp1 HG02074.hp2 |
synonymous_variant | LOW | c.474A>G | p.Glu158Glu | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/24 | 627/15244 | 474/2949 | 158/982 | chr1 | 202422671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:202348766
|
G | T | 1 | a0001c0001t0106 | 1 | HG03471.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/24 | 86 | chr1 | 202348766 | |||||
| chr1:202580933
|
C | G | 1 | a0001c0001t0105 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 373 | chr1 | 202580933 | |||||
| chr1:202581144
|
G | A | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(54): Show | 148 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*584G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 584 | chr1 | 202581144 | |||||
| chr1:202581340
|
A | G | 1 | a0001c0001t0104 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*780A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 780 | chr1 | 202581340 | |||||
| chr1:202581419
|
G | A | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(34): Show | 107 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*859G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 859 | chr1 | 202581419 | |||||
| chr1:202581488
|
A | T | 1 | a0001c0001t0103 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*928A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 928 | chr1 | 202581488 | |||||
| chr1:202581507
|
T | C | 1 | a0001c0001t0069 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*947T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 947 | chr1 | 202581507 | |||||
| chr1:202581510
|
G | A | 2 | a0001c0001t0026a0001c0001t0060 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*950G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 950 | chr1 | 202581510 | |||||
| chr1:202581534
|
C | T | 1 | a0001c0001t0018 | 3 | NA18970.hp1 NA18986.hp1 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*974C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 974 | chr1 | 202581534 | |||||
| chr1:202581544
|
AC | A | 5 | a0001c0001t0017a0001c0001t0099a0001c0001t0100others(2): Show | 7 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*986delC | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 986 | INFO_REALIGN_3_PRIME | chr1 | 202581544 | ||||
| chr1:202581773
|
G | T | 1 | a0001c0001t0068 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1213G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 1213 | chr1 | 202581773 | |||||
| chr1:202581943
|
A | G | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(32): Show | 105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1383A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 1383 | chr1 | 202581943 | |||||
| chr1:202582236
|
C | T | 1 | a0001c0001t0097 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1676C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 1676 | chr1 | 202582236 | |||||
| chr1:202582337
|
T | G | 1 | a0001c0001t0068 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1777T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 1777 | chr1 | 202582337 | |||||
| chr1:202582388
|
G | C | 1 | a0001c0001t0061 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1828G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 1828 | chr1 | 202582388 | |||||
| chr1:202582547
|
C | T | 1 | a0001c0001t0059 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1987C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 1987 | chr1 | 202582547 | |||||
| chr1:202582693
|
G | T | 16 | a0001c0001t0003a0001c0001t0007a0001c0001t0016others(13): Show | 39 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2133G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2133 | chr1 | 202582693 | |||||
| chr1:202582729
|
C | T | 1 | a0001c0001t0031 | 2 | HG02055.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2169C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2169 | chr1 | 202582729 | |||||
| chr1:202582810
|
G | A | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(34): Show | 107 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2250G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2250 | chr1 | 202582810 | |||||
| chr1:202582928
|
G | T | 1 | a0001c0001t0106 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2368G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2368 | chr1 | 202582928 | |||||
| chr1:202582940
|
T | C | 2 | a0001c0001t0062a0001c0001t0063 | 2 | HG02717.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2380T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2380 | chr1 | 202582940 | |||||
| chr1:202582972
|
G | A | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(47): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*2412G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2412 | chr1 | 202582972 | |||||
| chr1:202583015
|
G | A | 1 | a0001c0001t0040 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2455G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2455 | chr1 | 202583015 | |||||
| chr1:202583174
|
T | C | 110 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(107): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*2614T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2614 | chr1 | 202583174 | |||||
| chr1:202583238
|
A | G | 4 | a0001c0001t0008a0001c0001t0012a0001c0001t0065others(1): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2678A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2678 | chr1 | 202583238 | |||||
| chr1:202583464
|
A | G | 1 | a0001c0001t0058 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2904A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2904 | chr1 | 202583464 | |||||
| chr1:202583540
|
A | G | 1 | a0001c0001t0088 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2980A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 2980 | chr1 | 202583540 | |||||
| chr1:202583711
|
T | C | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(35): Show | 108 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3151T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 3151 | chr1 | 202583711 | |||||
| chr1:202583765
|
T | A | 4 | a0001c0001t0016a0001c0001t0090a0001c0001t0091others(1): Show | 6 | HG02523.hp2 NA18962.hp1 NA18984.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3205T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 3205 | chr1 | 202583765 | |||||
| chr1:202584123
|
T | C | 1 | a0001c0001t0070 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3563T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 3563 | chr1 | 202584123 | |||||
| chr1:202584424
|
T | G | 2 | a0001c0001t0041a0001c0001t0042 | 2 | NA18944.hp2 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3864T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 3864 | chr1 | 202584424 | |||||
| chr1:202584768
|
A | G | 3 | a0001c0001t0015a0001c0001t0025a0001c0001t0057 | 6 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4208A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 4208 | chr1 | 202584768 | |||||
| chr1:202584819
|
C | T | 3 | a0001c0001t0037a0001c0001t0038a0001c0001t0039 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4259C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 4259 | chr1 | 202584819 | |||||
| chr1:202585053
|
G | A | 1 | a0001c0001t0061 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4493G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 4493 | chr1 | 202585053 | |||||
| chr1:202585101
|
A | C | 1 | a0001c0001t0067 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4541A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 4541 | chr1 | 202585101 | |||||
| chr1:202585133
|
C | T | 2 | a0001c0001t0024a0001c0001t0056 | 3 | HG02698.hp2 HG03017.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4573C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 4573 | chr1 | 202585133 | |||||
| chr1:202585182
|
A | G | 1 | a0001c0001t0087 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4622A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 4622 | chr1 | 202585182 | |||||
| chr1:202585802
|
T | C | 1 | a0001c0001t0093 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5242T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 5242 | chr1 | 202585802 | |||||
| chr1:202585809
|
T | C | 16 | a0001c0001t0003a0001c0001t0007a0001c0001t0016others(13): Show | 39 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*5249T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 5249 | chr1 | 202585809 | |||||
| chr1:202585916
|
C | G | 6 | a0001c0001t0022a0001c0001t0023a0001c0001t0052others(3): Show | 8 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5356C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 5356 | chr1 | 202585916 | |||||
| chr1:202585973
|
G | A | 1 | a0001c0001t0071 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5413G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 5413 | chr1 | 202585973 | |||||
| chr1:202586021
|
C | T | 1 | a0001c0001t0051 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5461C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 5461 | chr1 | 202586021 | |||||
| chr1:202586544
|
T | G | 1 | a0001c0001t0027 | 2 | HG02818.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5984T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 5984 | chr1 | 202586544 | |||||
| chr1:202587032
|
C | T | 1 | a0004c0008t0064 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6472C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 6472 | chr1 | 202587032 | |||||
| chr1:202587124
|
T | C | 1 | a0001c0001t0032 | 2 | HG02055.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6564T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 6564 | chr1 | 202587124 | |||||
| chr1:202587371
|
C | A | 3 | a0001c0001t0037a0001c0001t0038a0001c0001t0039 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6811C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 6811 | chr1 | 202587371 | |||||
| chr1:202587504
|
C | CTGTT | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(32): Show | 105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*6946_*6949dupGTTT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 6950 | INFO_REALIGN_3_PRIME | chr1 | 202587504 | ||||
| chr1:202587698
|
C | T | 2 | a0001c0001t0035a0001c0001t0086 | 3 | HG02976.hp1 HG03098.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7138C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 7138 | chr1 | 202587698 | |||||
| chr1:202587705
|
C | A | 1 | a0001c0001t0090 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7145C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 7145 | chr1 | 202587705 | |||||
| chr1:202587759
|
A | G | 1 | a0001c0001t0039 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7199A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 7199 | chr1 | 202587759 | |||||
| chr1:202587852
|
A | G | 3 | a0001c0001t0008a0001c0001t0012a0001c0001t0065 | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7292A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 7292 | chr1 | 202587852 | |||||
| chr1:202587889
|
C | T | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(31): Show | 104 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*7329C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 7329 | chr1 | 202587889 | |||||
| chr1:202587916
|
G | T | 1 | a0001c0001t0050 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7356G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 7356 | chr1 | 202587916 | |||||
| chr1:202588005
|
G | T | 1 | a0004c0008t0064 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7445G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 7445 | chr1 | 202588005 | |||||
| chr1:202588049
|
C | A | 2 | a0001c0001t0072a0001c0001t0073 | 2 | HG02622.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7489C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 7489 | chr1 | 202588049 | |||||
| chr1:202588235
|
C | T | 6 | a0001c0001t0011a0001c0001t0013a0001c0001t0029others(3): Show | 16 | HG00642.hp1 HG00673.hp1 HG01256.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*7675C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 7675 | chr1 | 202588235 | |||||
| chr1:202588307
|
C | T | 1 | a0001c0001t0049 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7747C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 7747 | chr1 | 202588307 | |||||
| chr1:202588738
|
C | T | 2 | a0001c0001t0035a0001c0001t0086 | 3 | HG02976.hp1 HG03098.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8178C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8178 | chr1 | 202588738 | |||||
| chr1:202588789
|
A | T | 1 | a0001c0001t0031 | 2 | HG02055.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8229A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8229 | chr1 | 202588789 | |||||
| chr1:202588809
|
G | A | 1 | a0001c0001t0027 | 2 | HG02818.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8249G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8249 | chr1 | 202588809 | |||||
| chr1:202588824
|
A | AAGAT | 14 | a0001c0001t0006a0001c0001t0010a0001c0001t0022others(11): Show | 29 | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*8310_*8313dupGATA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588824 | ||||
| chr1:202588824
|
A | AAGATAGA others(1): Show |
29 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(26): Show | 66 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*8306_*8313dupGATA others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588824 | ||||
| chr1:202588824
|
A | AAGATAGA others(5): Show |
13 | a0001c0001t0005a0001c0001t0034a0001c0001t0036others(10): Show | 27 | HG00323.hp2 HG00408.hp1 HG00735.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*8302_*8313dupGATA others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588824 | ||||
| chr1:202588824
|
A | AAGATAGA others(9): Show |
4 | a0001c0001t0020a0001c0001t0070a0001c0001t0075others(1): Show | 5 | HG01346.hp2 HG02056.hp1 HG02056.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8298_*8313dupGATA others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588824 | ||||
| chr1:202588824
|
A | AAGATAGA others(13): Show |
2 | a0001c0001t0019a0001c0001t0074 | 3 | NA18975.hp1 NA19075.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8294_*8313dupGATA others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588824 | ||||
| chr1:202588824
|
A | AAGATAGA others(21): Show |
1 | a0001c0001t0099 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8286_*8313dupGATA others(24): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588824 | ||||
| chr1:202588824
|
AAGAT | A | 6 | a0001c0001t0038a0001c0001t0047a0001c0001t0054others(3): Show | 6 | HG02257.hp2 HG02300.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8310_*8313delGATA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8310 | INFO_REALIGN_3_PRIME | chr1 | 202588824 | ||||
| chr1:202588824
|
AAGATAGA others(1): Show |
A | 2 | a0001c0001t0014a0001c0001t0058 | 4 | HG01891.hp2 HG02080.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8306_*8313delGATA others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8306 | INFO_REALIGN_3_PRIME | chr1 | 202588824 | ||||
| chr1:202588824
|
AAGATAGA others(5): Show |
A | 4 | a0001c0001t0021a0001c0001t0055a0001c0001t0059others(1): Show | 5 | HG00323.hp1 HG02148.hp1 HG02738.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8302_*8313delGATA others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8302 | INFO_REALIGN_3_PRIME | chr1 | 202588824 | ||||
| chr1:202588824
|
AAGATAGA others(9): Show |
A | 1 | a0001c0001t0039 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8298_*8313delGATA others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8298 | INFO_REALIGN_3_PRIME | chr1 | 202588824 | ||||
| chr1:202588841
|
A | AGATAGAT others(4): Show |
1 | a0001c0001t0048 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8282_*8292dupGATA others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8293 | INFO_REALIGN_3_PRIME | chr1 | 202588841 | ||||
| chr1:202588865
|
AGATAGAT | A | 2 | a0001c0001t0033a0001c0003t0028 | 4 | HG00673.hp1 HG02074.hp2 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8306_*8312delGATA others(3): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8306 | chr1 | 202588865 | |||||
| chr1:202588872
|
T | TA | 9 | a0001c0001t0012a0001c0001t0026a0001c0001t0029others(6): Show | 15 | HG01192.hp2 HG02055.hp1 HG02071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*8313dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588872 | ||||
| chr1:202588872
|
T | TAGATA | 1 | a0001c0001t0011 | 5 | HG00642.hp1 HG02257.hp1 NA18961.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8313_*8314insGATA others(1): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588872 | ||||
| chr1:202588872
|
T | TAGATAGA others(2): Show |
5 | a0001c0001t0008a0001c0001t0013a0001c0001t0027others(2): Show | 14 | HG01256.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*8313_*8314insGATA others(5): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588872 | ||||
| chr1:202588872
|
T | TAGATAGA others(6): Show |
1 | a0001c0001t0030 | 2 | NA18954.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8313_*8314insGATA others(9): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588872 | ||||
| chr1:202588872
|
T | TAGATAGA others(9): Show |
1 | a0001c0001t0063 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8313_*8314insGATA others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8314 | INFO_REALIGN_3_PRIME | chr1 | 202588872 | ||||
| chr1:202588898
|
C | G | 1 | a0001c0001t0045 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8338C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8338 | chr1 | 202588898 | |||||
| chr1:202589293
|
C | T | 1 | a0001c0001t0092 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8733C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8733 | chr1 | 202589293 | |||||
| chr1:202589342
|
C | T | 3 | a0001c0001t0037a0001c0001t0038a0001c0001t0039 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8782C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8782 | chr1 | 202589342 | |||||
| chr1:202589366
|
C | T | 1 | a0001c0001t0039 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8806C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 8806 | chr1 | 202589366 | |||||
| chr1:202589621
|
G | C | 1 | a0001c0001t0106 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9061G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 9061 | chr1 | 202589621 | |||||
| chr1:202589816
|
G | A | 5 | a0001c0001t0017a0001c0001t0099a0001c0001t0100others(2): Show | 7 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9256G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 9256 | chr1 | 202589816 | |||||
| chr1:202589987
|
G | A | 2 | a0001c0001t0039a0001c0001t0066 | 2 | NA19005.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9427G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 9427 | chr1 | 202589987 | |||||
| chr1:202590048
|
C | T | 1 | a0001c0001t0081 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9488C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 9488 | chr1 | 202590048 | |||||
| chr1:202590104
|
G | A | 4 | a0001c0001t0008a0001c0001t0012a0001c0001t0065others(1): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*9544G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 9544 | chr1 | 202590104 | |||||
| chr1:202590195
|
C | T | 3 | a0001c0001t0037a0001c0001t0038a0001c0001t0039 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9635C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 9635 | chr1 | 202590195 | |||||
| chr1:202590525
|
C | A | 2 | a0001c0001t0016a0001c0001t0090 | 4 | HG02523.hp2 NA18962.hp1 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9965C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 9965 | chr1 | 202590525 | |||||
| chr1:202590619
|
TA | T | 3 | a0001c0001t0023a0001c0001t0052a0001c0001t0055 | 4 | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10061delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10061 | INFO_REALIGN_3_PRIME | chr1 | 202590619 | ||||
| chr1:202590625
|
G | T | 18 | a0001c0001t0003a0001c0001t0007a0001c0001t0016others(15): Show | 41 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*10065G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10065 | chr1 | 202590625 | |||||
| chr1:202590643
|
A | G | 1 | a0001c0001t0061 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10083A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10083 | chr1 | 202590643 | |||||
| chr1:202591114
|
A | G | 1 | a0001c0001t0046 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10554A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10554 | chr1 | 202591114 | |||||
| chr1:202591163
|
C | T | 1 | a0001c0001t0027 | 2 | HG02818.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10603C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10603 | chr1 | 202591163 | |||||
| chr1:202591283
|
C | T | 2 | a0001c0001t0094a0001c0001t0095 | 2 | NA18991.hp1 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10723C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10723 | chr1 | 202591283 | |||||
| chr1:202591284
|
T | C | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(50): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*10724T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10724 | chr1 | 202591284 | |||||
| chr1:202591394
|
G | C | 1 | a0001c0001t0043 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10834G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10834 | chr1 | 202591394 | |||||
| chr1:202591395
|
C | A | 1 | a0001c0001t0043 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10835C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10835 | chr1 | 202591395 | |||||
| chr1:202591396
|
A | G | 1 | a0001c0001t0043 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10836A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10836 | chr1 | 202591396 | |||||
| chr1:202591401
|
G | T | 4 | a0001c0001t0076a0001c0001t0078a0001c0001t0079others(1): Show | 4 | HG00735.hp1 HG01346.hp2 HG02300.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10841G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10841 | chr1 | 202591401 | |||||
| chr1:202591450
|
C | A | 1 | a0001c0001t0031 | 2 | HG02055.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10890C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10890 | chr1 | 202591450 | |||||
| chr1:202591526
|
G | A | 1 | a0001c0001t0067 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10966G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10966 | chr1 | 202591526 | |||||
| chr1:202591530
|
A | G | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(37): Show | 111 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*10970A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10970 | chr1 | 202591530 | |||||
| chr1:202591552
|
C | T | 1 | a0001c0001t0044 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10992C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10992 | chr1 | 202591552 | |||||
| chr1:202591553
|
T | G | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(37): Show | 111 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*10993T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 10993 | chr1 | 202591553 | |||||
| chr1:202591693
|
G | A | 2 | a0001c0001t0080a0001c0001t0082 | 2 | HG00597.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11133G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 11133 | chr1 | 202591693 | |||||
| chr1:202591869
|
T | C | 4 | a0001c0001t0008a0001c0001t0012a0001c0001t0065others(1): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*11309T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 11309 | chr1 | 202591869 | |||||
| chr1:202591933
|
C | T | 1 | a0001c0001t0083 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11373C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 11373 | chr1 | 202591933 | |||||
| chr1:202591946
|
C | T | 1 | a0001c0001t0062 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11386C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 11386 | chr1 | 202591946 | |||||
| chr1:202591967
|
C | G | 3 | a0001c0001t0037a0001c0001t0038a0001c0001t0039 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11407C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 11407 | chr1 | 202591967 | |||||
| chr1:202592346
|
C | T | 3 | a0001c0001t0037a0001c0001t0038a0001c0001t0039 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11786C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 24/24 | 11786 | chr1 | 202592346 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:202349188
|
A | C | 96 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.291+46A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202349188 | ||||||
| chr1:202349205
|
G | C | 1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.291+63G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202349205 | ||||||
| chr1:202349422
|
G | A | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.291+280G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202349422 | ||||||
| chr1:202349622
|
C | T | 7 | a0001c0001t0002g0253a0001c0001t0005g0248a0001c0001t0014g0251others(4): Show | 7 | HG00597.hp2 HG02080.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.291+480C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202349622 | ||||||
| chr1:202350655
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.291+1513C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202350655 | ||||||
| chr1:202350856
|
G | A | 2 | a0001c0001t0004g0004a0001c0001t0084g0003 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.291+1714G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202350856 | ||||||
| chr1:202351051
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.291+1909G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202351051 | ||||||
| chr1:202351212
|
T | TTTG | 92 | a0001c0001t0002g0094a0001c0001t0003g0021a0001c0001t0003g0029others(89): Show | 92 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.291+2097_291+2099d others(5): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202351212 | |||||
| chr1:202351227
|
G | A | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+2085G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202351227 | ||||||
| chr1:202351242
|
T | A | 1 | a0001c0001t0003g0013 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.291+2100T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202351242 | ||||||
| chr1:202351242
|
TA | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+2114delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202351242 | |||||
| chr1:202351243
|
A | T | 3 | a0001c0001t0009g0157a0001c0001t0031g0001a0001c0001t0031g0002 | 3 | HG02055.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.291+2101A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202351243 | ||||||
| chr1:202351310
|
CTGCA | C | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.291+2173_291+2176d others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202351310 | |||||
| chr1:202351676
|
T | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | HG01099.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.291+2534T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202351676 | ||||||
| chr1:202351715
|
A | G | 2 | a0001c0001t0007g0102a0001c0001t0007g0103 | 2 | HG01261.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.291+2573A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202351715 | ||||||
| chr1:202351969
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+2827G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202351969 | ||||||
| chr1:202351995
|
T | C | 97 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.291+2853T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202351995 | ||||||
| chr1:202352111
|
A | G | 1 | a0001c0001t0104g0101 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.291+2969A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202352111 | ||||||
| chr1:202352124
|
G | C | 1 | a0001c0001t0004g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.291+2982G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202352124 | ||||||
| chr1:202352534
|
G | A | 1 | a0001c0001t0006g0163 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.291+3392G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202352534 | ||||||
| chr1:202352892
|
A | AAAAAAG | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.291+3756_291+3761d others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202352892 | |||||
| chr1:202352924
|
T | C | 1 | a0001c0001t0087g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.291+3782T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202352924 | ||||||
| chr1:202352985
|
T | G | 94 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.291+3843T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202352985 | ||||||
| chr1:202353348
|
T | C | 25 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.291+4206T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202353348 | ||||||
| chr1:202353373
|
T | C | 1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.291+4231T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202353373 | ||||||
| chr1:202353586
|
T | TGTGTG | 3 | a0001c0001t0001g0165a0001c0001t0022g0105a0001c0001t0036g0017 | 3 | HG00280.hp1 HG01069.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.291+4444_291+4445i others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202353586 | ||||||
| chr1:202353586
|
T | TGTGTGTG | 3 | a0001c0001t0023g0106a0001c0001t0024g0164a0001c0001t0075g0018 | 3 | HG00738.hp1 HG02056.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.291+4444_291+4445i others(9): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202353586 | ||||||
| chr1:202353586
|
T | TTG | 16 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069others(13): Show | 16 | HG01106.hp2 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.291+4487_291+4488d others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353586 | |||||
| chr1:202353586
|
T | TTGTG | 41 | a0001c0001t0002g0158a0001c0001t0004g0015a0001c0001t0004g0075others(38): Show | 41 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.291+4485_291+4488d others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353586 | |||||
| chr1:202353586
|
T | TTGTGTG | 18 | a0001c0001t0002g0094a0001c0001t0004g0004a0001c0001t0004g0092others(15): Show | 18 | HG01175.hp1 HG01433.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.291+4483_291+4488d others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353586 | |||||
| chr1:202353586
|
T | TTGTGTGT others(1): Show |
6 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0014g0238others(3): Show | 6 | HG00597.hp1 HG00639.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.291+4481_291+4488d others(10): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353586 | |||||
| chr1:202353586
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0014g0243a0001c0001t0072g0012 | 2 | HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.291+4479_291+4488d others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353586 | |||||
| chr1:202353586
|
T | TTGTGTGT others(5): Show |
2 | a0001c0001t0038g0005a0001c0001t0069g0098 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.291+4477_291+4488d others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353586 | |||||
| chr1:202353586
|
T | TTGTGTGT others(7): Show |
3 | a0001c0001t0009g0100a0001c0001t0068g0104a0005c0007t0009g0099 | 3 | HG03239.hp1 HG03471.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.291+4475_291+4488d others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353586 | |||||
| chr1:202353586
|
TTG | T | 25 | a0001c0001t0003g0021a0001c0001t0003g0029a0001c0001t0003g0030others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.291+4487_291+4488d others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353586 | |||||
| chr1:202353586
|
TTGTGTGT others(3): Show |
T | 16 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0168others(13): Show | 16 | HG00738.hp2 HG01261.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.291+4479_291+4488d others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353586 | |||||
| chr1:202353586
|
TTGTGTGT others(5): Show |
T | 4 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0062g0131others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+4477_291+4488d others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353586 | |||||
| chr1:202353629
|
T | A | 18 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0001g0182others(15): Show | 18 | HG00738.hp2 HG01261.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.291+4487T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202353629 | ||||||
| chr1:202353629
|
T | TGA | 5 | a0001c0001t0005g0183a0001c0001t0005g0184a0001c0001t0009g0062others(2): Show | 5 | HG00408.hp1 HG01243.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.291+4488_291+4489d others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGAGA | 3 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0006g0187 | 3 | NA18945.hp1 NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.291+4489_291+4490i others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGTGA | 3 | a0001c0001t0002g0161a0001c0001t0005g0248a0001c0001t0006g0188 | 3 | HG01099.hp1 HG03654.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.291+4488_291+4489i others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGTGAGA | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0006g0193others(2): Show | 5 | HG00280.hp2 HG01106.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+4488_291+4489i others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGTGTGA | 23 | a0001c0001t0001g0160a0001c0001t0001g0195a0001c0001t0001g0201others(20): Show | 23 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.291+4488_291+4489i others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGTGTGAG others(1): Show |
18 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0001t0001g0219others(15): Show | 18 | HG01934.hp2 HG02056.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.291+4488_291+4489i others(10): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGTGTGTG others(1): Show |
12 | a0001c0001t0001g0230a0001c0001t0002g0162a0001c0001t0002g0228others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.291+4488_291+4489i others(10): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGTGTGTG others(3): Show |
3 | a0001c0001t0002g0239a0001c0001t0047g0240a0001c0001t0057g0241 | 3 | HG02647.hp2 HG03540.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.291+4488_291+4489i others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0001g0242 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.291+4488_291+4489i others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0001g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.291+4488_291+4489i others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0040g0247a0001c0001t0049g0245 | 2 | HG02818.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.291+4488_291+4489i others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353629
|
T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0246 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.291+4488_291+4489i others(22): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353629 | |||||
| chr1:202353791
|
T | C | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.291+4649T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202353791 | ||||||
| chr1:202353862
|
C | T | 1 | a0001c0001t0004g0096 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.291+4720C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202353862 | ||||||
| chr1:202353880
|
T | G | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.291+4738T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202353880 | ||||||
| chr1:202353921
|
A | G | 7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0181others(4): Show | 7 | HG02055.hp1 HG02280.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.291+4779A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202353921 | ||||||
| chr1:202353997
|
A | ATAGGCAA others(26): Show |
1 | a0001c0001t0041g0227 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.291+4856_291+4888d others(35): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202353997 | |||||
| chr1:202354168
|
G | A | 2 | a0001c0001t0027g0129a0001c0001t0027g0130 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.291+5026G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354168 | ||||||
| chr1:202354168
|
G | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.291+5026G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354168 | ||||||
| chr1:202354188
|
G | A | 52 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(49): Show | 52 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.291+5046G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354188 | ||||||
| chr1:202354254
|
T | C | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291+5112T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354254 | ||||||
| chr1:202354377
|
C | T | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.291+5235C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354377 | ||||||
| chr1:202354378
|
G | A | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.291+5236G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354378 | ||||||
| chr1:202354701
|
T | G | 1 | a0001c0001t0021g0249 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.291+5559T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354701 | ||||||
| chr1:202354716
|
C | T | 1 | a0001c0001t0062g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.291+5574C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354716 | ||||||
| chr1:202354747
|
A | G | 4 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0039g0011others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+5605A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354747 | ||||||
| chr1:202354820
|
TTTTTTGT others(5): Show |
T | 1 | a0001c0001t0005g0248 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.291+5684_291+5695d others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202354820 | |||||
| chr1:202354826
|
G | T | 96 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.291+5684G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354826 | ||||||
| chr1:202354829
|
G | GT | 98 | a0001c0001t0002g0094a0001c0001t0003g0013a0001c0001t0003g0021others(95): Show | 98 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.291+5689dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202354829 | |||||
| chr1:202354829
|
G | GTT | 5 | a0001c0001t0004g0072a0001c0001t0004g0087a0001c0001t0004g0089others(2): Show | 5 | HG02027.hp2 HG02155.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+5688_291+5689d others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202354829 | |||||
| chr1:202354832
|
G | T | 240 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.291+5690G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354832 | ||||||
| chr1:202354861
|
C | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.291+5719C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354861 | ||||||
| chr1:202354878
|
T | C | 1 | a0001c0001t0002g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.291+5736T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202354878 | ||||||
| chr1:202355017
|
C | T | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.291+5875C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202355017 | ||||||
| chr1:202355093
|
C | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.291+5951C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202355093 | ||||||
| chr1:202355131
|
T | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.291+5989T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202355131 | ||||||
| chr1:202355152
|
G | A | 1 | a0001c0001t0097g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.291+6010G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202355152 | ||||||
| chr1:202355368
|
A | C | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+6226A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202355368 | ||||||
| chr1:202355656
|
G | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+6514G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202355656 | ||||||
| chr1:202356123
|
G | A | 1 | a0001c0001t0062g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.291+6981G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202356123 | ||||||
| chr1:202356192
|
A | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.291+7050A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202356192 | ||||||
| chr1:202356436
|
A | G | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.291+7294A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202356436 | ||||||
| chr1:202356494
|
T | G | 5 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007others(2): Show | 5 | HG02622.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+7352T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202356494 | ||||||
| chr1:202356821
|
C | CT | 10 | a0001c0001t0009g0100a0001c0001t0011g0120a0001c0001t0042g0226others(7): Show | 10 | HG00597.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.291+7696dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202356821 | |||||
| chr1:202356908
|
G | A | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+7766G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202356908 | ||||||
| chr1:202356947
|
T | G | 130 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.291+7805T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202356947 | ||||||
| chr1:202356949
|
T | A | 130 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.291+7807T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202356949 | ||||||
| chr1:202357075
|
G | A | 1 | a0001c0001t0058g0250 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.291+7933G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202357075 | ||||||
| chr1:202357182
|
G | C | 8 | a0001c0001t0003g0021a0001c0001t0003g0043a0001c0001t0016g0022others(5): Show | 8 | HG02523.hp2 NA18950.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+8040G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202357182 | ||||||
| chr1:202357579
|
C | T | 1 | a0001c0001t0004g0089 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.291+8437C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202357579 | ||||||
| chr1:202358422
|
C | G | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.291+9280C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202358422 | ||||||
| chr1:202358475
|
G | A | 2 | a0001c0001t0036g0017a0001c0001t0036g0074 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.291+9333G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202358475 | ||||||
| chr1:202358539
|
G | A | 4 | a0001c0001t0001g0186a0001c0001t0001g0211a0001c0001t0001g0242others(1): Show | 4 | NA18945.hp1 NA18980.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+9397G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202358539 | ||||||
| chr1:202358565
|
C | T | 1 | a0001c0001t0010g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.291+9423C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202358565 | ||||||
| chr1:202358571
|
A | G | 3 | a0001c0001t0002g0253a0001c0001t0021g0249a0001c0001t0021g0254 | 3 | HG00597.hp2 HG02148.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.291+9429A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202358571 | ||||||
| chr1:202358681
|
C | CA | 10 | a0001c0001t0004g0087a0001c0001t0004g0096a0001c0001t0007g0102others(7): Show | 10 | HG01175.hp2 HG01261.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.291+9556dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202358681 | |||||
| chr1:202358681
|
CA | C | 100 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(97): Show | 100 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.291+9556delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202358681 | |||||
| chr1:202358698
|
A | C | 1 | a0001c0001t0014g0238 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.291+9556A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202358698 | ||||||
| chr1:202358700
|
T | G | 1 | a0001c0001t0090g0020 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.291+9558T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202358700 | ||||||
| chr1:202359103
|
A | T | 1 | a0001c0001t0090g0020 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.291+9961A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202359103 | ||||||
| chr1:202359145
|
AT | A | 5 | a0001c0001t0004g0072a0001c0001t0026g0008a0001c0001t0026g0009others(2): Show | 5 | HG02155.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.291+10014delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202359145 | |||||
| chr1:202359193
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.291+10051G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202359193 | ||||||
| chr1:202359272
|
A | T | 1 | a0001c0001t0004g0070 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.291+10130A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202359272 | ||||||
| chr1:202359372
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+10230A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202359372 | ||||||
| chr1:202359488
|
T | TA | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+10355dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202359488 | |||||
| chr1:202359606
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.291+10464C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202359606 | ||||||
| chr1:202359681
|
G | C | 2 | a0001c0001t0003g0021a0001c0001t0003g0043 | 2 | NA18963.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.291+10539G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202359681 | ||||||
| chr1:202359760
|
C | T | 1 | a0001c0001t0105g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.291+10618C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202359760 | ||||||
| chr1:202359818
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+10676A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202359818 | ||||||
| chr1:202359911
|
G | GGT | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.291+10784_291+1078 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202359911 | |||||
| chr1:202359911
|
GGT | G | 29 | a0001c0001t0002g0094a0001c0001t0004g0015a0001c0001t0004g0072others(26): Show | 29 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.291+10784_291+1078 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202359911 | |||||
| chr1:202359913
|
T | G | 1 | a0001c0001t0005g0166 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.291+10771T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202359913 | ||||||
| chr1:202360205
|
G | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+11063G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202360205 | ||||||
| chr1:202360382
|
C | T | 1 | a0001c0001t0011g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.291+11240C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202360382 | ||||||
| chr1:202360482
|
G | A | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.291+11340G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202360482 | ||||||
| chr1:202360636
|
G | C | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.291+11494G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202360636 | ||||||
| chr1:202360885
|
A | G | 1 | a0001c0003t0028g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.291+11743A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202360885 | ||||||
| chr1:202360892
|
CT | C | 230 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.291+11766delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202360892 | |||||
| chr1:202360917
|
G | A | 9 | a0001c0001t0002g0158a0001c0001t0022g0105a0001c0001t0022g0112others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.291+11775G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202360917 | ||||||
| chr1:202360990
|
A | C | 1 | a0001c0001t0002g0158 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.291+11848A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202360990 | ||||||
| chr1:202361139
|
C | T | 1 | a0001c0001t0007g0102 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.291+11997C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202361139 | ||||||
| chr1:202361145
|
G | A | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.291+12003G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202361145 | ||||||
| chr1:202361165
|
T | C | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+12023T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202361165 | ||||||
| chr1:202361198
|
T | G | 1 | a0001c0001t0103g0026 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.291+12056T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202361198 | ||||||
| chr1:202361484
|
C | T | 1 | a0001c0001t0032g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.291+12342C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202361484 | ||||||
| chr1:202361525
|
C | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.291+12383C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202361525 | ||||||
| chr1:202361526
|
T | G | 1 | a0001c0001t0037g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.291+12384T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202361526 | ||||||
| chr1:202362354
|
A | G | 2 | a0001c0001t0100g0142a0001c0001t0101g0144 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+13212A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202362354 | ||||||
| chr1:202362382
|
T | G | 25 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.291+13240T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202362382 | ||||||
| chr1:202362405
|
A | G | 1 | a0001c0001t0050g0175 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.291+13263A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202362405 | ||||||
| chr1:202362611
|
G | A | 4 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0062g0131others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+13469G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202362611 | ||||||
| chr1:202362653
|
G | GT | 81 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.291+13516dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202362653 | |||||
| chr1:202362653
|
G | GTT | 8 | a0001c0001t0001g0174a0001c0001t0001g0242a0001c0001t0005g0184others(5): Show | 8 | HG00408.hp1 HG01070.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+13515_291+1351 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202362653 | |||||
| chr1:202362658
|
TG | T | 5 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.291+13517delG | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202362658 | ||||||
| chr1:202362659
|
G | GT | 5 | a0001c0001t0011g0120a0001c0001t0027g0129a0001c0001t0027g0130others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+13529dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202362659 | |||||
| chr1:202362659
|
G | T | 99 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(96): Show | 99 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.291+13517G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202362659 | ||||||
| chr1:202362662
|
T | A | 2 | a0001c0001t0017g0137a0001c0001t0099g0138 | 2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.291+13520T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202362662 | ||||||
| chr1:202362811
|
G | A | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291+13669G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202362811 | ||||||
| chr1:202362822
|
G | GTTTA | 6 | a0001c0001t0007g0040a0001c0001t0018g0039a0001c0001t0018g0041others(3): Show | 6 | NA18943.hp1 NA18970.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.291+13702_291+1370 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202362822 | |||||
| chr1:202362877
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0006g0229 | 2 | NA18954.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.291+13735A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202362877 | ||||||
| chr1:202363048
|
G | T | 9 | a0001c0001t0002g0158a0001c0001t0022g0105a0001c0001t0022g0112others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.291+13906G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202363048 | ||||||
| chr1:202363194
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+14052A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202363194 | ||||||
| chr1:202363431
|
A | T | 25 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.291+14289A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202363431 | ||||||
| chr1:202363443
|
T | A | 5 | a0001c0001t0001g0230a0001c0001t0002g0161a0001c0001t0002g0162others(2): Show | 5 | HG00735.hp2 HG01099.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+14301T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202363443 | ||||||
| chr1:202363532
|
A | G | 4 | a0001c0001t0002g0235a0001c0001t0006g0207a0001c0001t0006g0236others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+14390A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202363532 | ||||||
| chr1:202363667
|
C | T | 1 | a0001c0001t0039g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291+14525C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202363667 | ||||||
| chr1:202363668
|
G | A | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.291+14526G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202363668 | ||||||
| chr1:202363736
|
T | C | 1 | a0001c0001t0013g0093 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.291+14594T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202363736 | ||||||
| chr1:202364101
|
A | G | 41 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(38): Show | 41 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.291+14959A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364101 | ||||||
| chr1:202364567
|
T | A | 94 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.291+15425T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364567 | ||||||
| chr1:202364586
|
A | T | 1 | a0001c0001t0017g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.291+15444A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364586 | ||||||
| chr1:202364590
|
T | A | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.291+15448T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364590 | ||||||
| chr1:202364726
|
G | A | 1 | a0001c0001t0004g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.291+15584G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364726 | ||||||
| chr1:202364727
|
C | A | 1 | a0001c0001t0004g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.291+15585C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364727 | ||||||
| chr1:202364817
|
G | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.291+15675G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364817 | ||||||
| chr1:202364818
|
G | T | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.291+15676G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364818 | ||||||
| chr1:202364822
|
C | T | 1 | a0001c0001t0005g0248 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.291+15680C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364822 | ||||||
| chr1:202364828
|
G | A | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.291+15686G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364828 | ||||||
| chr1:202364842
|
C | T | 6 | a0001c0001t0015g0205a0001c0001t0015g0206a0001c0001t0015g0208others(3): Show | 6 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.291+15700C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202364842 | ||||||
| chr1:202365146
|
T | C | 8 | a0001c0001t0022g0105a0001c0001t0022g0112a0001c0001t0023g0106others(5): Show | 8 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.291+16004T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202365146 | ||||||
| chr1:202365720
|
T | C | 1 | a0001c0001t0003g0021 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.291+16578T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202365720 | ||||||
| chr1:202365779
|
C | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+16637C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202365779 | ||||||
| chr1:202365952
|
T | C | 6 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0039g0011others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+16810T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202365952 | ||||||
| chr1:202365953
|
G | T | 6 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0039g0011others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+16811G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202365953 | ||||||
| chr1:202365992
|
C | T | 1 | a0001c0001t0008g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.291+16850C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202365992 | ||||||
| chr1:202365993
|
A | G | 243 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.291+16851A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202365993 | ||||||
| chr1:202365998
|
C | T | 1 | a0001c0001t0072g0012 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.291+16856C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202365998 | ||||||
| chr1:202366056
|
G | A | 1 | a0001c0001t0023g0110 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.291+16914G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202366056 | ||||||
| chr1:202366266
|
C | T | 5 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0181others(2): Show | 5 | NA18943.hp2 NA18962.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+17124C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202366266 | ||||||
| chr1:202366517
|
CA | C | 112 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.291+17399delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202366517 | |||||
| chr1:202366517
|
CAA | C | 126 | a0001c0001t0002g0158a0001c0001t0002g0181a0001c0001t0003g0013others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.291+17398_291+1739 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202366517 | |||||
| chr1:202366950
|
G | A | 3 | a0001c0001t0035g0028a0001c0001t0067g0064a0001c0001t0086g0027 | 3 | HG02976.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.291+17808G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202366950 | ||||||
| chr1:202367153
|
A | G | 1 | a0001c0001t0006g0173 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.291+18011A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202367153 | ||||||
| chr1:202367186
|
C | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.291+18044C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202367186 | ||||||
| chr1:202367578
|
A | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0037 | 2 | NA18960.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.291+18436A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202367578 | ||||||
| chr1:202367786
|
C | T | 1 | a0001c0001t0002g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.291+18644C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202367786 | ||||||
| chr1:202367868
|
G | A | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.291+18726G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202367868 | ||||||
| chr1:202367962
|
T | G | 1 | a0001c0001t0002g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.291+18820T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202367962 | ||||||
| chr1:202367969
|
T | G | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.291+18827T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202367969 | ||||||
| chr1:202367991
|
C | T | 52 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(49): Show | 52 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.291+18849C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202367991 | ||||||
| chr1:202368073
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.291+18931G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202368073 | ||||||
| chr1:202368308
|
C | A | 1 | a0001c0001t0016g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.291+19166C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202368308 | ||||||
| chr1:202368321
|
C | G | 4 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0062g0131others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+19179C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202368321 | ||||||
| chr1:202368406
|
A | G | 1 | a0001c0001t0030g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.291+19264A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202368406 | ||||||
| chr1:202368854
|
C | T | 9 | a0001c0001t0002g0158a0001c0001t0022g0105a0001c0001t0022g0112others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.291+19712C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202368854 | ||||||
| chr1:202369024
|
C | T | 1 | a0001c0001t0006g0237 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291+19882C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202369024 | ||||||
| chr1:202369127
|
G | A | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.291+19985G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202369127 | ||||||
| chr1:202369292
|
C | T | 2 | a0001c0001t0003g0068a0001c0001t0003g0069 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.291+20150C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202369292 | ||||||
| chr1:202369522
|
A | G | 1 | a0001c0001t0097g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.291+20380A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202369522 | ||||||
| chr1:202369548
|
A | G | 1 | a0001c0001t0062g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.291+20406A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202369548 | ||||||
| chr1:202369616
|
G | C | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.291+20474G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202369616 | ||||||
| chr1:202369780
|
A | G | 1 | a0001c0001t0002g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.291+20638A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202369780 | ||||||
| chr1:202369800
|
CT | C | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.291+20671delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202369800 | |||||
| chr1:202369859
|
G | A | 2 | a0001c0001t0003g0029a0001c0001t0003g0030 | 2 | HG01993.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.291+20717G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202369859 | ||||||
| chr1:202369985
|
G | A | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.291+20843G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202369985 | ||||||
| chr1:202370091
|
G | T | 1 | a0001c0001t0085g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.291+20949G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202370091 | ||||||
| chr1:202370341
|
A | C | 95 | a0001c0001t0002g0094a0001c0001t0003g0013a0001c0001t0003g0021others(92): Show | 95 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.291+21199A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202370341 | ||||||
| chr1:202370406
|
A | G | 1 | a0001c0001t0099g0138 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.291+21264A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202370406 | ||||||
| chr1:202370543
|
AT | A | 98 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.291+21413delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202370543 | |||||
| chr1:202370654
|
A | G | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.291+21512A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202370654 | ||||||
| chr1:202370758
|
G | A | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+21616G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202370758 | ||||||
| chr1:202370828
|
G | A | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.291+21686G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202370828 | ||||||
| chr1:202371000
|
T | G | 1 | a0001c0001t0002g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.291+21858T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202371000 | ||||||
| chr1:202371001
|
C | CT | 42 | a0001c0001t0001g0214a0001c0001t0002g0162a0001c0001t0004g0015others(39): Show | 42 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.291+21881dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202371001 | |||||
| chr1:202371037
|
T | A | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.291+21895T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202371037 | ||||||
| chr1:202371181
|
A | AT | 44 | a0001c0001t0001g0182a0001c0001t0001g0214a0001c0001t0001g0242others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.291+22059dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202371181 | |||||
| chr1:202371437
|
C | G | 1 | a0001c0001t0013g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.291+22295C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202371437 | ||||||
| chr1:202371481
|
A | AGT | 3 | a0001c0001t0002g0204a0001c0001t0068g0104a0001c0001t0106g0133 | 3 | HG01517.hp2 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.291+22358_291+2235 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202371481 | |||||
| chr1:202371858
|
C | CT | 10 | a0001c0001t0004g0127a0001c0001t0008g0152a0001c0001t0011g0119others(7): Show | 10 | HG00673.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.291+22738dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202371858 | |||||
| chr1:202371858
|
CT | C | 172 | a0001c0001t0001g0160a0001c0001t0001g0169a0001c0001t0001g0174others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.291+22738delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202371858 | |||||
| chr1:202371858
|
CTT | C | 7 | a0001c0001t0005g0216a0001c0001t0025g0233a0001c0001t0025g0234others(4): Show | 7 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.291+22737_291+2273 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202371858 | |||||
| chr1:202371858
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0075g0018 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.291+22726_291+2273 others(17): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202371858 | |||||
| chr1:202371895
|
G | T | 1 | a0001c0001t0031g0002 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.291+22753G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202371895 | ||||||
| chr1:202371918
|
C | G | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.291+22776C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202371918 | ||||||
| chr1:202372015
|
G | A | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+22873G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202372015 | ||||||
| chr1:202372375
|
G | A | 5 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007others(2): Show | 5 | HG02622.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+23233G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202372375 | ||||||
| chr1:202372501
|
C | CA | 12 | a0001c0001t0004g0089a0001c0001t0004g0095a0001c0001t0010g0083others(9): Show | 12 | HG00673.hp2 HG02027.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.291+23371dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202372501 | |||||
| chr1:202372510
|
A | T | 96 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.291+23368A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202372510 | ||||||
| chr1:202372607
|
A | G | 1 | a0001c0001t0002g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.291+23465A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202372607 | ||||||
| chr1:202372634
|
A | G | 1 | a0001c0001t0008g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.291+23492A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202372634 | ||||||
| chr1:202372783
|
A | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+23641A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202372783 | ||||||
| chr1:202372786
|
A | G | 95 | a0001c0001t0002g0094a0001c0001t0003g0013a0001c0001t0003g0021others(92): Show | 95 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.291+23644A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202372786 | ||||||
| chr1:202372835
|
A | G | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.291+23693A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202372835 | ||||||
| chr1:202373008
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.291+23866C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202373008 | ||||||
| chr1:202373226
|
G | A | 1 | a0001c0001t0033g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.291+24084G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202373226 | ||||||
| chr1:202373663
|
G | GT | 96 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.291+24531dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202373663 | |||||
| chr1:202373888
|
TTGGTCAA others(21): Show |
T | 5 | a0001c0001t0009g0065a0001c0001t0009g0066a0001c0001t0026g0008others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+24785_291+2481 others(32): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202373888 | |||||
| chr1:202373989
|
A | C | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.291+24847A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202373989 | ||||||
| chr1:202374493
|
C | CT | 30 | a0001c0001t0002g0158a0001c0001t0002g0181a0001c0001t0002g0239others(27): Show | 30 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.291+25373dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202374493 | |||||
| chr1:202374493
|
C | CTT | 170 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.291+25372_291+2537 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202374493 | |||||
| chr1:202374493
|
C | CTTT | 22 | a0001c0001t0003g0043a0001c0001t0003g0053a0001c0001t0004g0075others(19): Show | 22 | HG00597.hp1 HG01192.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.291+25371_291+2537 others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202374493 | |||||
| chr1:202374493
|
C | CTTTT | 5 | a0001c0001t0009g0065a0001c0001t0009g0066a0001c0001t0014g0238others(2): Show | 5 | HG01891.hp2 HG02809.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+25370_291+2537 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202374493 | |||||
| chr1:202374642
|
G | C | 1 | a0001c0001t0105g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.291+25500G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202374642 | ||||||
| chr1:202374660
|
A | G | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.291+25518A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202374660 | ||||||
| chr1:202374804
|
A | G | 1 | a0001c0001t0006g0193 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.291+25662A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202374804 | ||||||
| chr1:202374911
|
A | C | 3 | a0001c0001t0034g0044a0001c0001t0034g0045a0001c0001t0105g0014 | 3 | HG02258.hp1 HG02280.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.291+25769A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202374911 | ||||||
| chr1:202374984
|
C | T | 1 | a0001c0001t0002g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.291+25842C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202374984 | ||||||
| chr1:202375264
|
T | C | 1 | a0001c0001t0009g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.291+26122T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202375264 | ||||||
| chr1:202375314
|
G | T | 1 | a0001c0001t0035g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.291+26172G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202375314 | ||||||
| chr1:202375825
|
A | G | 25 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.291+26683A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202375825 | ||||||
| chr1:202377190
|
A | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+28048A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202377190 | ||||||
| chr1:202377329
|
T | TC | 3 | a0001c0001t0033g0090a0001c0001t0033g0091a0001c0001t0069g0098 | 3 | HG02109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.291+28187_291+2818 others(5): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202377329 | ||||||
| chr1:202377830
|
GTGTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.291+28690_291+2870 others(15): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202377830 | |||||
| chr1:202377832
|
G | GT | 83 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(80): Show | 83 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.291+28717dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202377832 | |||||
| chr1:202377832
|
G | GTT | 28 | a0001c0001t0002g0158a0001c0001t0003g0031a0001c0001t0003g0067others(25): Show | 28 | HG00642.hp1 HG00735.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.291+28716_291+2871 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202377832 | |||||
| chr1:202377832
|
GTTTTTTT others(2): Show |
G | 11 | a0001c0001t0001g0182a0001c0001t0001g0223a0001c0001t0002g0224others(8): Show | 11 | HG01070.hp1 HG01106.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.291+28709_291+2871 others(13): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202377832 | |||||
| chr1:202377832
|
GTTTTTTT others(3): Show |
G | 83 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.291+28708_291+2871 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202377832 | |||||
| chr1:202377832
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0060g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.291+28707_291+2871 others(15): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202377832 | |||||
| chr1:202377835
|
T | G | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.291+28693T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202377835 | ||||||
| chr1:202378079
|
C | G | 1 | a0001c0001t0085g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.291+28937C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202378079 | ||||||
| chr1:202378080
|
C | G | 1 | a0001c0001t0085g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.291+28938C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202378080 | ||||||
| chr1:202378247
|
C | CT | 29 | a0001c0001t0001g0223a0001c0001t0003g0030a0001c0001t0003g0043others(26): Show | 29 | HG00323.hp1 HG01243.hp1 HG01993.hp1 others(26): Show |
intron_variant | MODIFIER | c.291+29126dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202378247 | |||||
| chr1:202378247
|
C | CTT | 90 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(87): Show | 90 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.291+29125_291+2912 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202378247 | |||||
| chr1:202378247
|
C | CTTT | 9 | a0001c0001t0001g0182a0001c0001t0005g0183a0001c0001t0005g0184others(6): Show | 9 | HG00408.hp1 HG01069.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.291+29124_291+2912 others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202378247 | |||||
| chr1:202378247
|
CT | C | 16 | a0001c0001t0003g0029a0001c0001t0008g0150a0001c0001t0008g0152others(13): Show | 16 | HG01069.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.291+29126delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202378247 | |||||
| chr1:202378484
|
T | G | 1 | a0001c0001t0040g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.291+29342T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202378484 | ||||||
| chr1:202378636
|
C | A | 26 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.291+29494C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202378636 | ||||||
| chr1:202378738
|
A | G | 2 | a0001c0001t0080g0086a0001c0001t0082g0097 | 2 | HG00597.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.291+29596A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202378738 | ||||||
| chr1:202378855
|
T | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+29713T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202378855 | ||||||
| chr1:202378896
|
C | T | 91 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.291+29754C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202378896 | ||||||
| chr1:202379430
|
C | G | 1 | a0001c0001t0006g0173 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.291+30288C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202379430 | ||||||
| chr1:202379671
|
T | C | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG00099.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.291+30529T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202379671 | ||||||
| chr1:202380126
|
TCTTTGCT others(17): Show |
T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+30988_291+3101 others(28): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202380126 | |||||
| chr1:202380263
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.291+31121G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202380263 | ||||||
| chr1:202380326
|
C | T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291+31184C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202380326 | ||||||
| chr1:202380359
|
G | A | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.291+31217G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202380359 | ||||||
| chr1:202380484
|
A | G | 6 | a0001c0001t0001g0230a0001c0001t0002g0161a0001c0001t0002g0162others(3): Show | 6 | HG00735.hp2 HG01099.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+31342A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202380484 | ||||||
| chr1:202380485
|
T | A | 1 | a0001c0001t0001g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.291+31343T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202380485 | ||||||
| chr1:202380486
|
G | C | 1 | a0001c0001t0001g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.291+31344G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202380486 | ||||||
| chr1:202380561
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.291+31419C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202380561 | ||||||
| chr1:202380602
|
C | T | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.291+31460C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202380602 | ||||||
| chr1:202380775
|
T | A | 1 | a0001c0001t0001g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.291+31633T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202380775 | ||||||
| chr1:202381052
|
C | T | 95 | a0001c0001t0002g0094a0001c0001t0003g0013a0001c0001t0003g0021others(92): Show | 95 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.291+31910C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202381052 | ||||||
| chr1:202381143
|
C | T | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.291+32001C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202381143 | ||||||
| chr1:202381397
|
G | GGT | 4 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0099g0138others(1): Show | 4 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+32294_291+3229 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381397 | |||||
| chr1:202381397
|
G | GGTGTGTG others(5): Show |
20 | a0001c0001t0002g0200a0001c0001t0002g0204a0001c0001t0002g0228others(17): Show | 20 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.291+32265_291+3226 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381397 | |||||
| chr1:202381397
|
G | GGTGTGTG others(7): Show |
58 | a0001c0001t0001g0160a0001c0001t0001g0169a0001c0001t0001g0174others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.291+32265_291+3226 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381397 | |||||
| chr1:202381397
|
G | GGTGTGTG others(9): Show |
21 | a0001c0001t0001g0165a0001c0001t0001g0201a0001c0001t0001g0221others(18): Show | 21 | HG00639.hp1 HG00735.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.291+32265_291+3226 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381397 | |||||
| chr1:202381397
|
G | GGTGTGTG others(11): Show |
23 | a0001c0001t0002g0196a0001c0001t0004g0072a0001c0001t0008g0150others(20): Show | 23 | HG00735.hp1 HG00738.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.291+32265_291+3226 others(22): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381397 | |||||
| chr1:202381397
|
G | GGTGTGTG others(13): Show |
28 | a0001c0001t0003g0021a0001c0001t0004g0004a0001c0001t0004g0015others(25): Show | 28 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.291+32265_291+3226 others(24): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381397 | |||||
| chr1:202381397
|
G | GGTGTGTG others(15): Show |
38 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.291+32265_291+3226 others(26): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381397 | |||||
| chr1:202381397
|
G | GGTGTGTG others(17): Show |
42 | a0001c0001t0002g0094a0001c0001t0002g0158a0001c0001t0003g0013others(39): Show | 42 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.291+32265_291+3226 others(28): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381397 | |||||
| chr1:202381397
|
G | GGTGTGTG others(19): Show |
5 | a0001c0001t0003g0030a0001c0001t0003g0037a0001c0001t0013g0108others(2): Show | 5 | HG01993.hp1 HG03486.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+32265_291+3226 others(30): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381397 | |||||
| chr1:202381397
|
G | GGTGTGTG others(23): Show |
1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.291+32265_291+3226 others(34): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381397 | |||||
| chr1:202381398
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0040g0247a0001c0001t0061g0132 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.291+32265_291+3226 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381398 | |||||
| chr1:202381408
|
G | A | 4 | a0001c0001t0033g0090a0001c0001t0033g0091a0001c0001t0069g0098others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+32266G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202381408 | ||||||
| chr1:202381434
|
G | A | 239 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.291+32292G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202381434 | ||||||
| chr1:202381434
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0006g0163 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.291+32295_291+3229 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381434 | |||||
| chr1:202381434
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0051g0232 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.291+32295_291+3229 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381434 | |||||
| chr1:202381434
|
G | GTGTGTGT others(19): Show |
2 | a0001c0001t0033g0091a0001c0001t0069g0098 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.291+32295_291+3229 others(30): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381434 | |||||
| chr1:202381434
|
G | GTGTGTGT others(21): Show |
2 | a0001c0001t0033g0090a0006c0004t0010g0063 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.291+32295_291+3229 others(32): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202381434 | |||||
| chr1:202381513
|
C | T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291+32371C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202381513 | ||||||
| chr1:202381718
|
C | G | 2 | a0001c0001t0006g0163a0001c0001t0051g0232 | 2 | HG02258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.291+32576C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202381718 | ||||||
| chr1:202382096
|
A | G | 4 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0062g0131others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+32954A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202382096 | ||||||
| chr1:202382422
|
T | TA | 6 | a0001c0001t0006g0177a0001c0001t0027g0129a0001c0001t0027g0130others(3): Show | 6 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+33288dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202382422 | |||||
| chr1:202382429
|
A | T | 2 | a0001c0001t0056g0209a0001c0001t0068g0104 | 2 | HG02698.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.291+33287A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202382429 | ||||||
| chr1:202382431
|
T | A | 40 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0008g0150others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.291+33289T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202382431 | ||||||
| chr1:202382803
|
G | A | 1 | a0001c0001t0087g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.291+33661G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202382803 | ||||||
| chr1:202382875
|
CA | C | 6 | a0001c0001t0001g0160a0001c0001t0004g0087a0001c0001t0004g0096others(3): Show | 6 | HG00609.hp2 HG01074.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+33747delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202382875 | |||||
| chr1:202383169
|
C | T | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.292-33618C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202383169 | ||||||
| chr1:202383342
|
C | A | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-33445C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202383342 | ||||||
| chr1:202383417
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.292-33370A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202383417 | ||||||
| chr1:202383648
|
C | T | 6 | a0001c0001t0007g0040a0001c0001t0018g0039a0001c0001t0018g0041others(3): Show | 6 | NA18943.hp1 NA18970.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.292-33139C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202383648 | ||||||
| chr1:202383916
|
T | A | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.292-32871T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202383916 | ||||||
| chr1:202384303
|
T | C | 1 | a0005c0007t0009g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.292-32484T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202384303 | ||||||
| chr1:202384429
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-32358G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202384429 | ||||||
| chr1:202384848
|
C | T | 2 | a0001c0001t0009g0065a0001c0001t0009g0066 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.292-31939C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202384848 | ||||||
| chr1:202385335
|
T | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-31452T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202385335 | ||||||
| chr1:202385516
|
G | A | 2 | a0001c0001t0003g0034a0001c0001t0003g0035 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.292-31271G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202385516 | ||||||
| chr1:202385525
|
C | T | 1 | a0001c0001t0039g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.292-31262C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202385525 | ||||||
| chr1:202385939
|
C | CT | 5 | a0001c0001t0003g0043a0001c0001t0004g0070a0001c0001t0009g0062others(2): Show | 5 | HG01243.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-30836dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202385939 | |||||
| chr1:202386058
|
C | T | 1 | a0001c0001t0006g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.292-30729C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202386058 | ||||||
| chr1:202386082
|
C | T | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292-30705C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202386082 | ||||||
| chr1:202386114
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.292-30673C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202386114 | ||||||
| chr1:202386122
|
A | T | 4 | a0001c0001t0002g0235a0001c0001t0006g0207a0001c0001t0006g0236others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-30665A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202386122 | ||||||
| chr1:202386123
|
C | G | 1 | a0001c0001t0003g0021 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.292-30664C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202386123 | ||||||
| chr1:202386223
|
C | T | 1 | a0001c0001t0005g0184 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.292-30564C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202386223 | ||||||
| chr1:202386599
|
G | A | 1 | a0001c0001t0033g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.292-30188G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202386599 | ||||||
| chr1:202386691
|
G | A | 1 | a0001c0001t0033g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.292-30096G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202386691 | ||||||
| chr1:202386979
|
G | A | 1 | a0001c0001t0057g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.292-29808G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202386979 | ||||||
| chr1:202386995
|
T | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-29792T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202386995 | ||||||
| chr1:202387046
|
T | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.292-29741T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202387046 | ||||||
| chr1:202387219
|
G | A | 225 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.292-29568G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202387219 | ||||||
| chr1:202387245
|
G | A | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-29542G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202387245 | ||||||
| chr1:202387282
|
A | G | 1 | a0001c0001t0010g0082 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.292-29505A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202387282 | ||||||
| chr1:202387311
|
G | C | 1 | a0001c0001t0025g0234 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.292-29476G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202387311 | ||||||
| chr1:202387678
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-29109C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202387678 | ||||||
| chr1:202387807
|
T | G | 25 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.292-28980T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202387807 | ||||||
| chr1:202388118
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.292-28669G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202388118 | ||||||
| chr1:202388119
|
C | CA | 11 | a0001c0001t0001g0195a0001c0001t0013g0093a0001c0001t0027g0129others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-28653dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202388119 | |||||
| chr1:202388119
|
CA | C | 7 | a0001c0001t0003g0033a0001c0001t0006g0229a0001c0001t0010g0071others(4): Show | 7 | HG00642.hp1 HG01099.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-28653delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202388119 | |||||
| chr1:202389086
|
C | T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.292-27701C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389086 | ||||||
| chr1:202389240
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.292-27547A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389240 | ||||||
| chr1:202389460
|
C | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-27327C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389460 | ||||||
| chr1:202389472
|
G | A | 2 | a0001c0001t0006g0173a0001c0001t0050g0175 | 2 | HG00738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.292-27315G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389472 | ||||||
| chr1:202389536
|
C | T | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.292-27251C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389536 | ||||||
| chr1:202389670
|
G | T | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-27117G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389670 | ||||||
| chr1:202389736
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.292-27051G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389736 | ||||||
| chr1:202389810
|
C | T | 1 | a0001c0001t0047g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292-26977C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389810 | ||||||
| chr1:202389811
|
C | G | 7 | a0001c0001t0002g0253a0001c0001t0005g0248a0001c0001t0014g0251others(4): Show | 7 | HG00597.hp2 HG02080.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-26976C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389811 | ||||||
| chr1:202389819
|
C | T | 121 | a0001c0001t0002g0094a0001c0001t0002g0158a0001c0001t0003g0013others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.292-26968C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389819 | ||||||
| chr1:202389822
|
G | A | 121 | a0001c0001t0002g0094a0001c0001t0002g0158a0001c0001t0003g0013others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.292-26965G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389822 | ||||||
| chr1:202389878
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-26909G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389878 | ||||||
| chr1:202389926
|
C | CA | 11 | a0001c0001t0002g0253a0001c0001t0003g0031a0001c0001t0004g0072others(8): Show | 11 | HG00597.hp2 HG01243.hp1 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-26841dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202389926 | |||||
| chr1:202389926
|
CA | C | 116 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.292-26841delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202389926 | |||||
| chr1:202389977
|
G | A | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.292-26810G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202389977 | ||||||
| chr1:202390021
|
C | T | 1 | a0001c0001t0018g0039 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.292-26766C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202390021 | ||||||
| chr1:202390319
|
C | T | 1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.292-26468C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202390319 | ||||||
| chr1:202390421
|
G | A | 1 | a0001c0001t0085g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.292-26366G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202390421 | ||||||
| chr1:202390562
|
G | A | 1 | a0001c0001t0006g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.292-26225G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202390562 | ||||||
| chr1:202390639
|
C | A | 2 | a0001c0001t0014g0238a0001c0001t0014g0243 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.292-26148C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202390639 | ||||||
| chr1:202390661
|
G | C | 9 | a0001c0001t0002g0158a0001c0001t0022g0105a0001c0001t0022g0112others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.292-26126G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202390661 | ||||||
| chr1:202390662
|
CT | C | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.292-26108delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202390662 | |||||
| chr1:202390756
|
A | G | 1 | a0001c0001t0090g0020 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.292-26031A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202390756 | ||||||
| chr1:202390848
|
G | A | 121 | a0001c0001t0002g0094a0001c0001t0002g0158a0001c0001t0003g0013others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.292-25939G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202390848 | ||||||
| chr1:202390865
|
C | T | 1 | a0001c0001t0020g0217 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.292-25922C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202390865 | ||||||
| chr1:202390901
|
A | G | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.292-25886A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202390901 | ||||||
| chr1:202391118
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-25669A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202391118 | ||||||
| chr1:202391560
|
CTCAGGTG others(413): Show |
C | 4 | a0001c0001t0009g0062a0001c0001t0034g0044a0001c0001t0034g0045others(1): Show | 4 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-25217_292-2479 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391560 | |||||
| chr1:202391570
|
T | TTGAAGAT others(23): Show |
1 | a0001c0001t0014g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.292-24662_292-2463 others(34): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
T | TTGAAGAT others(53): Show |
1 | a0001c0001t0047g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292-24692_292-2463 others(64): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
T | TTGAAGAT others(143): Show |
1 | a0001c0001t0101g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.292-24782_292-2463 others(154): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
T | TTGAAGAT others(203): Show |
2 | a0001c0001t0004g0145a0001c0001t0017g0141 | 2 | HG01123.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.292-24842_292-2463 others(214): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
T | TTGAAGAT others(233): Show |
4 | a0001c0001t0017g0137a0001c0001t0017g0143a0001c0001t0099g0138others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-24872_292-2463 others(244): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
T | TTGAAGAT others(263): Show |
1 | a0001c0001t0102g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.292-24902_292-2463 others(274): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(23): Show |
T | 18 | a0001c0001t0001g0169a0001c0001t0001g0182a0001c0001t0001g0195others(15): Show | 18 | HG00408.hp1 HG00597.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.292-24662_292-2463 others(34): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(53): Show |
T | 34 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0191others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.292-24692_292-2463 others(64): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(83): Show |
T | 27 | a0001c0001t0001g0165a0001c0001t0001g0211a0001c0001t0001g0219others(24): Show | 27 | HG00639.hp1 HG00738.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.292-24722_292-2463 others(94): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(113): Show |
T | 3 | a0001c0001t0001g0186a0001c0001t0001g0230a0001c0001t0006g0173 | 3 | HG03490.hp2 NA18945.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.292-24752_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(173): Show |
T | 10 | a0001c0001t0002g0235a0001c0001t0006g0207a0001c0001t0006g0236others(7): Show | 10 | HG00099.hp1 HG00733.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.292-24812_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(203): Show |
T | 9 | a0001c0001t0031g0001a0001c0001t0031g0002a0001c0001t0038g0005others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.292-24842_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(233): Show |
T | 13 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(10): Show | 13 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.292-24872_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(263): Show |
T | 1 | a0001c0001t0012g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292-24902_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(293): Show |
T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-24932_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(323): Show |
T | 1 | a0001c0001t0035g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.292-24962_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(353): Show |
T | 1 | a0001c0001t0010g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.292-24992_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(383): Show |
T | 7 | a0001c0001t0004g0070a0001c0001t0013g0108a0001c0001t0016g0023others(4): Show | 7 | HG00673.hp2 HG01074.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-25022_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(413): Show |
T | 106 | a0001c0001t0002g0094a0001c0001t0002g0158a0001c0001t0003g0013others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.292-25052_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391570
|
TTGAAGAT others(443): Show |
T | 1 | a0001c0001t0009g0100 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.292-25082_292-2463 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391570 | |||||
| chr1:202391727
|
TAAATGAA others(410): Show |
T | 1 | a0001c0001t0033g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.292-25059_292-2464 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202391727 | ||||||
| chr1:202391732
|
GAATTATC others(144): Show |
G | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.292-25053_292-2490 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202391732 | |||||
| chr1:202392222
|
A | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.292-24565A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202392222 | ||||||
| chr1:202392473
|
G | A | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.292-24314G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202392473 | ||||||
| chr1:202392575
|
G | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-24212G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202392575 | ||||||
| chr1:202392612
|
C | A | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.292-24175C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202392612 | ||||||
| chr1:202392727
|
A | G | 1 | a0001c0001t0011g0107 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.292-24060A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202392727 | ||||||
| chr1:202392894
|
A | G | 1 | a0001c0001t0073g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.292-23893A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202392894 | ||||||
| chr1:202392909
|
A | T | 1 | a0001c0001t0104g0101 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.292-23878A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202392909 | ||||||
| chr1:202392952
|
T | C | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-23835T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202392952 | ||||||
| chr1:202392965
|
A | C | 3 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069 | 3 | HG01106.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.292-23822A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202392965 | ||||||
| chr1:202392985
|
G | A | 26 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.292-23802G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202392985 | ||||||
| chr1:202393255
|
A | G | 2 | a0001c0001t0011g0125a0001c0001t0013g0126 | 2 | NA18961.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.292-23532A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202393255 | ||||||
| chr1:202393793
|
G | A | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.292-22994G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202393793 | ||||||
| chr1:202393916
|
A | C | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-22871A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202393916 | ||||||
| chr1:202394005
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-22782C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202394005 | ||||||
| chr1:202394248
|
G | A | 1 | a0001c0001t0049g0245 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.292-22539G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202394248 | ||||||
| chr1:202394529
|
C | T | 1 | a0001c0001t0035g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.292-22258C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202394529 | ||||||
| chr1:202394856
|
T | C | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.292-21931T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202394856 | ||||||
| chr1:202394858
|
T | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-21929T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202394858 | ||||||
| chr1:202394966
|
A | G | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.292-21821A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202394966 | ||||||
| chr1:202395001
|
C | T | 3 | a0001c0001t0004g0070a0001c0001t0010g0071a0001c0001t0077g0059 | 3 | HG02622.hp2 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.292-21786C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202395001 | ||||||
| chr1:202395094
|
G | A | 4 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0062g0131others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-21693G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202395094 | ||||||
| chr1:202395114
|
C | CA | 204 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.292-21653dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202395114 | |||||
| chr1:202395114
|
C | CAA | 9 | a0001c0001t0001g0186a0001c0001t0003g0067a0001c0001t0006g0237others(6): Show | 9 | HG01106.hp2 HG01243.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-21654_292-2165 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202395114 | |||||
| chr1:202395377
|
C | T | 95 | a0001c0001t0002g0094a0001c0001t0003g0013a0001c0001t0003g0021others(92): Show | 95 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.292-21410C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202395377 | ||||||
| chr1:202395389
|
G | A | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292-21398G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202395389 | ||||||
| chr1:202395393
|
C | T | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.292-21394C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202395393 | ||||||
| chr1:202395439
|
A | T | 1 | a0001c0001t0012g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.292-21348A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202395439 | ||||||
| chr1:202395572
|
C | T | 2 | a0001c0001t0011g0114a0001c0001t0013g0116 | 2 | HG00642.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.292-21215C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202395572 | ||||||
| chr1:202395599
|
C | T | 2 | a0001c0001t0080g0086a0001c0001t0082g0097 | 2 | HG00597.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.292-21188C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202395599 | ||||||
| chr1:202395607
|
A | G | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.292-21180A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202395607 | ||||||
| chr1:202395781
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.292-21006A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202395781 | ||||||
| chr1:202396074
|
A | G | 2 | a0001c0001t0032g0057a0001c0001t0032g0058 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.292-20713A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202396074 | ||||||
| chr1:202396204
|
A | G | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.292-20583A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202396204 | ||||||
| chr1:202396229
|
A | G | 5 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007others(2): Show | 5 | HG02622.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-20558A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202396229 | ||||||
| chr1:202396294
|
G | A | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.292-20493G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202396294 | ||||||
| chr1:202396474
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-20313G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202396474 | ||||||
| chr1:202396638
|
T | G | 1 | a0001c0001t0062g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.292-20149T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202396638 | ||||||
| chr1:202397233
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.292-19554T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202397233 | ||||||
| chr1:202397296
|
C | T | 1 | a0001c0001t0008g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.292-19491C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202397296 | ||||||
| chr1:202398026
|
C | T | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-18761C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202398026 | ||||||
| chr1:202398134
|
T | A | 93 | a0001c0001t0002g0094a0001c0001t0003g0013a0001c0001t0003g0029others(90): Show | 93 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.292-18653T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202398134 | ||||||
| chr1:202398138
|
G | T | 1 | a0001c0001t0010g0083 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.292-18649G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202398138 | ||||||
| chr1:202398225
|
C | T | 3 | a0001c0001t0033g0090a0001c0001t0033g0091a0001c0001t0069g0098 | 3 | HG02109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.292-18562C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202398225 | ||||||
| chr1:202398370
|
T | C | 1 | a0001c0001t0004g0089 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.292-18417T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202398370 | ||||||
| chr1:202398484
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.292-18303T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202398484 | ||||||
| chr1:202398703
|
G | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-18084G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202398703 | ||||||
| chr1:202398816
|
T | C | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.292-17971T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202398816 | ||||||
| chr1:202398981
|
A | T | 1 | a0001c0001t0097g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.292-17806A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202398981 | ||||||
| chr1:202399015
|
A | G | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.292-17772A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202399015 | ||||||
| chr1:202399033
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0005g0166a0001c0001t0006g0171 | 3 | HG01261.hp2 HG01346.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.292-17754A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202399033 | ||||||
| chr1:202399324
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0168others(4): Show | 7 | HG01261.hp2 HG01346.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-17463G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202399324 | ||||||
| chr1:202399339
|
G | A | 1 | a0001c0001t0030g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.292-17448G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202399339 | ||||||
| chr1:202399529
|
C | T | 1 | a0001c0001t0040g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.292-17258C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202399529 | ||||||
| chr1:202399536
|
G | A | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.292-17251G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202399536 | ||||||
| chr1:202399579
|
C | G | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.292-17208C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202399579 | ||||||
| chr1:202399785
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.292-17002T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202399785 | ||||||
| chr1:202399871
|
CA | C | 4 | a0001c0001t0004g0087a0001c0001t0004g0096a0001c0001t0010g0080others(1): Show | 4 | HG01074.hp2 HG01433.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-16915delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202399871 | ||||||
| chr1:202400093
|
T | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-16694T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202400093 | ||||||
| chr1:202400094
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.292-16693A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202400094 | ||||||
| chr1:202400205
|
T | C | 1 | a0001c0001t0039g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.292-16582T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202400205 | ||||||
| chr1:202400228
|
A | G | 9 | a0001c0001t0004g0004a0001c0001t0004g0070a0001c0001t0004g0075others(6): Show | 9 | HG01243.hp1 HG02257.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.292-16559A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202400228 | ||||||
| chr1:202400356
|
C | G | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.292-16431C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202400356 | ||||||
| chr1:202400757
|
A | C | 1 | a0001c0001t0005g0199 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.292-16030A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202400757 | ||||||
| chr1:202400839
|
TA | T | 4 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0062g0131others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-15946delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202400839 | |||||
| chr1:202401046
|
G | A | 1 | a0001c0001t0087g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.292-15741G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202401046 | ||||||
| chr1:202401249
|
G | A | 1 | a0001c0001t0098g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.292-15538G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202401249 | ||||||
| chr1:202401327
|
C | G | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.292-15460C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202401327 | ||||||
| chr1:202401361
|
A | AT | 27 | a0001c0001t0002g0094a0001c0001t0003g0013a0001c0001t0003g0037others(24): Show | 27 | HG00323.hp2 HG00597.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.292-15397dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202401361 | |||||
| chr1:202401361
|
A | ATT | 65 | a0001c0001t0001g0160a0001c0001t0001g0169a0001c0001t0001g0174others(62): Show | 65 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.292-15398_292-1539 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202401361 | |||||
| chr1:202401361
|
A | ATTT | 36 | a0001c0001t0001g0182a0001c0001t0001g0230a0001c0001t0002g0158others(33): Show | 36 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.292-15399_292-1539 others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202401361 | |||||
| chr1:202401361
|
A | ATTTT | 8 | a0001c0001t0002g0253a0001c0001t0004g0127a0001c0001t0005g0248others(5): Show | 8 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-15400_292-1539 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202401361 | |||||
| chr1:202401361
|
ATTTTTTT | A | 6 | a0001c0001t0001g0225a0001c0001t0027g0129a0001c0001t0027g0130others(3): Show | 6 | HG02280.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.292-15403_292-1539 others(11): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202401361 | |||||
| chr1:202401361
|
ATTTTTTT others(2): Show |
A | 25 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0191others(22): Show | 25 | HG00280.hp2 HG01106.hp1 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.292-15405_292-1539 others(13): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202401361 | |||||
| chr1:202401546
|
ATTTTG | A | 121 | a0001c0001t0002g0094a0001c0001t0002g0158a0001c0001t0003g0013others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.292-15236_292-1523 others(9): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202401546 | |||||
| chr1:202401869
|
C | T | 26 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.292-14918C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202401869 | ||||||
| chr1:202402437
|
A | T | 1 | a0001c0001t0017g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.292-14350A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202402437 | ||||||
| chr1:202402494
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.292-14293T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202402494 | ||||||
| chr1:202402505
|
C | A | 242 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.292-14282C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202402505 | ||||||
| chr1:202402624
|
C | T | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.292-14163C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202402624 | ||||||
| chr1:202402684
|
A | G | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.292-14103A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202402684 | ||||||
| chr1:202402833
|
C | T | 1 | a0001c0001t0008g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.292-13954C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202402833 | ||||||
| chr1:202402837
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.292-13950G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202402837 | ||||||
| chr1:202403505
|
A | G | 2 | a0001c0001t0006g0163a0001c0001t0051g0232 | 2 | HG02258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.292-13282A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202403505 | ||||||
| chr1:202403547
|
G | A | 25 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.292-13240G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202403547 | ||||||
| chr1:202403655
|
T | A | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.292-13132T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202403655 | ||||||
| chr1:202403694
|
T | G | 1 | a0001c0001t0062g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.292-13093T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202403694 | ||||||
| chr1:202403836
|
T | C | 97 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.292-12951T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202403836 | ||||||
| chr1:202403952
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-12835G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202403952 | ||||||
| chr1:202404074
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.292-12713C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202404074 | ||||||
| chr1:202404221
|
C | T | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.292-12566C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202404221 | ||||||
| chr1:202404237
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0006g0177 | 2 | NA18943.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.292-12550T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202404237 | ||||||
| chr1:202404266
|
A | G | 44 | a0001c0001t0002g0094a0001c0001t0004g0004a0001c0001t0004g0015others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.292-12521A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202404266 | ||||||
| chr1:202404590
|
T | C | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.292-12197T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202404590 | ||||||
| chr1:202404677
|
T | A | 5 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-12110T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202404677 | ||||||
| chr1:202404781
|
G | A | 28 | a0001c0001t0002g0094a0001c0001t0004g0015a0001c0001t0004g0072others(25): Show | 28 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.292-12006G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202404781 | ||||||
| chr1:202404974
|
A | G | 3 | a0001c0001t0018g0039a0001c0001t0018g0041a0001c0001t0018g0042 | 3 | NA18970.hp1 NA18986.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.292-11813A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202404974 | ||||||
| chr1:202405053
|
T | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0006g0163others(1): Show | 4 | HG02258.hp2 HG06807.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-11734T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202405053 | ||||||
| chr1:202405524
|
C | A | 1 | a0001c0001t0014g0251 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.292-11263C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202405524 | ||||||
| chr1:202405575
|
A | G | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.292-11212A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202405575 | ||||||
| chr1:202405597
|
T | C | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.292-11190T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202405597 | ||||||
| chr1:202405809
|
C | T | 1 | a0001c0001t0008g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.292-10978C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202405809 | ||||||
| chr1:202405918
|
A | G | 3 | a0001c0001t0003g0032a0001c0001t0003g0033a0003c0009t0007g0036 | 3 | HG00099.hp2 HG01099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.292-10869A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202405918 | ||||||
| chr1:202406085
|
A | G | 1 | a0001c0001t0007g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.292-10702A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202406085 | ||||||
| chr1:202406835
|
A | G | 5 | a0001c0001t0001g0230a0001c0001t0002g0161a0001c0001t0002g0162others(2): Show | 5 | HG00735.hp2 HG01099.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-9952A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202406835 | ||||||
| chr1:202407067
|
T | A | 2 | a0001c0001t0032g0057a0001c0001t0032g0058 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.292-9720T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407067 | ||||||
| chr1:202407093
|
A | C | 4 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0202others(1): Show | 4 | HG00323.hp2 HG01074.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-9694A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407093 | ||||||
| chr1:202407237
|
G | A | 1 | a0001c0001t0024g0185 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.292-9550G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407237 | ||||||
| chr1:202407241
|
G | A | 2 | a0001c0001t0026g0008a0001c0001t0026g0009 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.292-9546G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407241 | ||||||
| chr1:202407242
|
G | T | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-9545G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407242 | ||||||
| chr1:202407259
|
T | C | 2 | a0001c0001t0009g0065a0001c0001t0009g0066 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.292-9528T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407259 | ||||||
| chr1:202407267
|
A | G | 1 | a0001c0001t0024g0185 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.292-9520A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407267 | ||||||
| chr1:202407342
|
T | C | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.292-9445T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407342 | ||||||
| chr1:202407450
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-9337G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407450 | ||||||
| chr1:202407542
|
A | T | 2 | a0001c0001t0027g0129a0001c0001t0027g0130 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.292-9245A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407542 | ||||||
| chr1:202407672
|
G | T | 95 | a0001c0001t0002g0094a0001c0001t0003g0013a0001c0001t0003g0021others(92): Show | 95 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.292-9115G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407672 | ||||||
| chr1:202407700
|
A | G | 1 | a0001c0001t0024g0185 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.292-9087A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202407700 | ||||||
| chr1:202408298
|
CAT | C | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.292-8488_292-8487d others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202408298 | ||||||
| chr1:202408409
|
T | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.292-8378T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202408409 | ||||||
| chr1:202408464
|
A | G | 6 | a0001c0001t0001g0230a0001c0001t0002g0161a0001c0001t0002g0162others(3): Show | 6 | HG00735.hp2 HG01099.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-8323A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202408464 | ||||||
| chr1:202408617
|
C | T | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.292-8170C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202408617 | ||||||
| chr1:202408735
|
G | C | 1 | a0001c0001t0048g0197 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.292-8052G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202408735 | ||||||
| chr1:202408835
|
A | C | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.292-7952A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202408835 | ||||||
| chr1:202408843
|
C | CT | 30 | a0001c0001t0002g0158a0001c0001t0004g0089a0001c0001t0004g0127others(27): Show | 30 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.292-7924dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202408843 | |||||
| chr1:202408843
|
CT | C | 101 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.292-7924delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202408843 | |||||
| chr1:202408843
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0037g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292-7933_292-7924d others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202408843 | |||||
| chr1:202409000
|
G | T | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.292-7787G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202409000 | ||||||
| chr1:202409086
|
G | T | 2 | a0001c0001t0027g0129a0001c0001t0027g0130 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.292-7701G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202409086 | ||||||
| chr1:202409160
|
C | T | 1 | a0001c0001t0004g0089 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.292-7627C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202409160 | ||||||
| chr1:202409326
|
C | CT | 8 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(5): Show | 8 | HG00642.hp1 HG01256.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.292-7447dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202409326 | |||||
| chr1:202409326
|
CT | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.292-7447delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202409326 | |||||
| chr1:202409362
|
A | T | 1 | a0001c0001t0093g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.292-7425A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202409362 | ||||||
| chr1:202409478
|
C | T | 1 | a0001c0001t0046g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.292-7309C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202409478 | ||||||
| chr1:202410235
|
C | T | 1 | a0001c0001t0005g0248 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.292-6552C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202410235 | ||||||
| chr1:202410279
|
T | C | 1 | a0001c0001t0040g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.292-6508T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202410279 | ||||||
| chr1:202410589
|
G | A | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.292-6198G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202410589 | ||||||
| chr1:202411270
|
C | CA | 7 | a0001c0001t0004g0084a0001c0001t0013g0108a0001c0001t0043g0213others(4): Show | 7 | HG00609.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-5499dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202411270 | |||||
| chr1:202411471
|
C | T | 1 | a0001c0001t0031g0001 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-5316C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202411471 | ||||||
| chr1:202411477
|
A | G | 6 | a0001c0001t0007g0040a0001c0001t0018g0039a0001c0001t0018g0041others(3): Show | 6 | NA18943.hp1 NA18970.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.292-5310A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202411477 | ||||||
| chr1:202411598
|
T | G | 29 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0191others(26): Show | 29 | HG00280.hp2 HG01106.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.292-5189T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202411598 | ||||||
| chr1:202411620
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-5167G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202411620 | ||||||
| chr1:202411844
|
T | G | 1 | a0001c0001t0001g0242 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.292-4943T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202411844 | ||||||
| chr1:202411866
|
G | T | 5 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-4921G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202411866 | ||||||
| chr1:202411888
|
C | T | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.292-4899C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202411888 | ||||||
| chr1:202412087
|
A | G | 1 | a0001c0001t0052g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.292-4700A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202412087 | ||||||
| chr1:202412151
|
C | T | 5 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-4636C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202412151 | ||||||
| chr1:202412403
|
A | C | 44 | a0001c0001t0002g0094a0001c0001t0004g0004a0001c0001t0004g0015others(41): Show | 44 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.292-4384A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202412403 | ||||||
| chr1:202412405
|
G | A | 1 | a0001c0001t0014g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.292-4382G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202412405 | ||||||
| chr1:202412445
|
C | T | 1 | a0001c0001t0004g0145 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.292-4342C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202412445 | ||||||
| chr1:202412544
|
C | T | 1 | a0001c0001t0019g0167 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.292-4243C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202412544 | ||||||
| chr1:202412601
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.292-4186G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202412601 | ||||||
| chr1:202412637
|
C | CT | 3 | a0001c0001t0003g0031a0001c0001t0003g0034a0001c0001t0003g0035 | 3 | HG01515.hp1 HG01517.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.292-4149dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202412637 | |||||
| chr1:202412700
|
G | A | 4 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0062g0131others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-4087G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202412700 | ||||||
| chr1:202412953
|
T | C | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.292-3834T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202412953 | ||||||
| chr1:202413047
|
C | T | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.292-3740C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202413047 | ||||||
| chr1:202413182
|
G | T | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.292-3605G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202413182 | ||||||
| chr1:202413279
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-3508C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202413279 | ||||||
| chr1:202413450
|
T | C | 1 | a0001c0001t0096g0052 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.292-3337T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202413450 | ||||||
| chr1:202413842
|
A | G | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.292-2945A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202413842 | ||||||
| chr1:202413880
|
T | C | 1 | a0001c0001t0037g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292-2907T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202413880 | ||||||
| chr1:202413911
|
C | G | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.292-2876C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202413911 | ||||||
| chr1:202413990
|
T | C | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.292-2797T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202413990 | ||||||
| chr1:202414087
|
A | T | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.292-2700A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202414087 | ||||||
| chr1:202414721
|
G | T | 5 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-2066G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202414721 | ||||||
| chr1:202414772
|
G | C | 4 | a0001c0001t0002g0235a0001c0001t0006g0207a0001c0001t0006g0236others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-2015G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202414772 | ||||||
| chr1:202414930
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-1857G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202414930 | ||||||
| chr1:202415260
|
T | A | 1 | a0001c0001t0053g0109 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.292-1527T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202415260 | ||||||
| chr1:202415541
|
C | T | 1 | a0001c0001t0005g0220 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.292-1246C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202415541 | ||||||
| chr1:202415905
|
T | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-882T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202415905 | ||||||
| chr1:202416111
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292-676A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | chr1 | 202416111 | ||||||
| chr1:202416525
|
T | TA | 188 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.292-241dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202416525 | |||||
| chr1:202416525
|
T | TAA | 6 | a0001c0001t0026g0008a0001c0001t0037g0006a0001c0001t0038g0005others(3): Show | 6 | HG02451.hp2 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-242_292-241dup others(2): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr1 | 202416525 | |||||
| chr1:202416922
|
G | A | 1 | a0001c0001t0054g0111 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.422+5G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202416922 | ||||||
| chr1:202416947
|
T | C | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.422+30T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202416947 | ||||||
| chr1:202417662
|
A | C | 1 | a0001c0001t0090g0020 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.422+745A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202417662 | ||||||
| chr1:202418472
|
CT | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.422+1567delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202418472 | |||||
| chr1:202418507
|
T | G | 1 | a0001c0001t0049g0245 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.422+1590T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202418507 | ||||||
| chr1:202418858
|
C | G | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.422+1941C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202418858 | ||||||
| chr1:202419046
|
T | A | 1 | a0001c0001t0024g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.422+2129T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202419046 | ||||||
| chr1:202419196
|
A | G | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.422+2279A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202419196 | ||||||
| chr1:202419516
|
T | C | 94 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.422+2599T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202419516 | ||||||
| chr1:202419543
|
A | G | 1 | a0001c0001t0003g0033 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.422+2626A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202419543 | ||||||
| chr1:202419996
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.423-2624C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202419996 | ||||||
| chr1:202420085
|
A | G | 1 | a0001c0001t0027g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.423-2535A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202420085 | ||||||
| chr1:202420283
|
G | T | 3 | a0001c0001t0024g0164a0001c0001t0024g0185a0001c0001t0056g0209 | 3 | HG02698.hp2 HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.423-2337G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202420283 | ||||||
| chr1:202420420
|
A | G | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.423-2200A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202420420 | ||||||
| chr1:202420483
|
G | A | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.423-2137G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202420483 | ||||||
| chr1:202420613
|
G | T | 8 | a0001c0001t0004g0004a0001c0001t0004g0070a0001c0001t0004g0075others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.423-2007G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202420613 | ||||||
| chr1:202420635
|
C | G | 1 | a0001c0001t0002g0181 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.423-1985C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202420635 | ||||||
| chr1:202420741
|
G | A | 1 | a0001c0001t0062g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.423-1879G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202420741 | ||||||
| chr1:202420967
|
C | CTTTTTT | 84 | a0001c0001t0001g0160a0001c0001t0001g0186a0001c0001t0001g0191others(81): Show | 84 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.423-1637_423-1632d others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202420967 | |||||
| chr1:202420967
|
C | CTTTTTTT | 15 | a0001c0001t0001g0165a0001c0001t0001g0169a0001c0001t0001g0174others(12): Show | 15 | HG01074.hp1 HG01106.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.423-1638_423-1632d others(9): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202420967 | |||||
| chr1:202420967
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0061g0132a0001c0001t0062g0131a0001c0001t0063g0159 | 3 | HG02717.hp2 HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.423-1641_423-1632d others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202420967 | |||||
| chr1:202420967
|
C | CTTTTTTT others(4): Show |
8 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(5): Show | 8 | HG01192.hp2 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.423-1642_423-1632d others(13): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202420967 | |||||
| chr1:202420967
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0008g0154a0001c0001t0008g0156a0001c0001t0027g0129others(1): Show | 4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-1643_423-1632d others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202420967 | |||||
| chr1:202420967
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0008g0155a0001c0001t0031g0002a0004c0008t0064g0134 | 3 | HG02280.hp1 HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423-1644_423-1632d others(15): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202420967 | |||||
| chr1:202420967
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0031g0001a0001c0001t0106g0133 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.423-1645_423-1632d others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202420967 | |||||
| chr1:202420967
|
CTTTTTTT | C | 120 | a0001c0001t0002g0094a0001c0001t0002g0158a0001c0001t0003g0013others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.423-1638_423-1632d others(9): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202420967 | |||||
| chr1:202421031
|
C | T | 2 | a0001c0001t0007g0102a0001c0001t0007g0103 | 2 | HG01261.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.423-1589C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202421031 | ||||||
| chr1:202421047
|
C | T | 1 | a0001c0001t0003g0013 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.423-1573C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202421047 | ||||||
| chr1:202421117
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.423-1503G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202421117 | ||||||
| chr1:202421301
|
C | CT | 6 | a0001c0001t0026g0008a0001c0001t0037g0006a0001c0001t0039g0011others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-1300dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202421301 | |||||
| chr1:202421301
|
CT | C | 18 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0002g0158others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.423-1300delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202421301 | |||||
| chr1:202421348
|
T | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.423-1272T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202421348 | ||||||
| chr1:202421418
|
C | T | 2 | a0001c0001t0037g0006a0001c0001t0038g0005 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.423-1202C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202421418 | ||||||
| chr1:202421651
|
CA | C | 7 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0033g0090others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.423-959delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr1 | 202421651 | |||||
| chr1:202421654
|
A | C | 8 | a0001c0001t0022g0105a0001c0001t0022g0112a0001c0001t0023g0106others(5): Show | 8 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.423-966A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202421654 | ||||||
| chr1:202421661
|
A | G | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.423-959A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202421661 | ||||||
| chr1:202421683
|
G | T | 3 | a0001c0001t0004g0015a0001c0001t0004g0079a0001c0001t0004g0084 | 3 | HG00609.hp1 HG03490.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.423-937G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202421683 | ||||||
| chr1:202422214
|
T | G | 3 | a0001c0001t0003g0031a0001c0001t0003g0034a0001c0001t0003g0035 | 3 | HG01515.hp1 HG01517.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.423-406T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202422214 | ||||||
| chr1:202422276
|
A | G | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.423-344A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202422276 | ||||||
| chr1:202422291
|
G | A | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.423-329G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202422291 | ||||||
| chr1:202422338
|
T | G | 4 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0062g0131others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-282T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 2/23 | chr1 | 202422338 | ||||||
| chr1:202422945
|
C | A | 1 | a0001c0001t0093g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.541+207C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202422945 | ||||||
| chr1:202422998
|
G | T | 2 | a0001c0001t0004g0075a0001c0001t0004g0076 | 2 | HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.541+260G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202422998 | ||||||
| chr1:202423287
|
C | G | 1 | a0001c0001t0008g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.541+549C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202423287 | ||||||
| chr1:202423304
|
C | G | 2 | a0001c0001t0014g0238a0001c0001t0014g0243 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.541+566C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202423304 | ||||||
| chr1:202423323
|
C | A | 1 | a0001c0001t0007g0049 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.541+585C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202423323 | ||||||
| chr1:202423952
|
C | T | 1 | a0001c0001t0087g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.541+1214C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202423952 | ||||||
| chr1:202424326
|
C | CT | 9 | a0001c0001t0009g0062a0001c0001t0034g0044a0001c0001t0034g0045others(6): Show | 9 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.542-1225dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr1 | 202424326 | |||||
| chr1:202424385
|
G | T | 1 | a0001c0001t0076g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.542-1181G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202424385 | ||||||
| chr1:202424757
|
C | T | 1 | a0001c0001t0072g0012 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.542-809C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202424757 | ||||||
| chr1:202424990
|
C | T | 1 | a0001c0001t0009g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.542-576C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202424990 | ||||||
| chr1:202425071
|
A | G | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.542-495A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202425071 | ||||||
| chr1:202425159
|
C | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.542-407C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202425159 | ||||||
| chr1:202425187
|
A | G | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.542-379A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 3/23 | chr1 | 202425187 | ||||||
| chr1:202425755
|
G | T | 3 | a0001c0001t0001g0182a0001c0001t0005g0183a0001c0001t0005g0184 | 3 | HG00408.hp1 HG02071.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.701+30G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 4/23 | chr1 | 202425755 | ||||||
| chr1:202425901
|
C | G | 1 | a0001c0001t0102g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.701+176C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 4/23 | chr1 | 202425901 | ||||||
| chr1:202426311
|
G | A | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.701+586G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 4/23 | chr1 | 202426311 | ||||||
| chr1:202426635
|
G | T | 245 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.702-405G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 4/23 | chr1 | 202426635 | ||||||
| chr1:202426919
|
G | T | 1 | a0001c0001t0013g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.702-121G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 4/23 | chr1 | 202426919 | ||||||
| chr1:202427501
|
T | G | 46 | a0001c0001t0001g0165a0001c0001t0001g0169a0001c0001t0001g0174others(43): Show | 46 | HG00280.hp2 HG00738.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.846+317T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 5/23 | chr1 | 202427501 | ||||||
| chr1:202427638
|
A | T | 1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.846+454A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 5/23 | chr1 | 202427638 | ||||||
| chr1:202427794
|
G | A | 1 | a0001c0001t0092g0024 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.846+610G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 5/23 | chr1 | 202427794 | ||||||
| chr1:202427796
|
C | T | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.846+612C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 5/23 | chr1 | 202427796 | ||||||
| chr1:202427914
|
C | T | 2 | a0001c0001t0003g0067a0001c0001t0011g0107 | 2 | HG01106.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.846+730C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 5/23 | chr1 | 202427914 | ||||||
| chr1:202427943
|
C | A | 1 | a0001c0001t0007g0102 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.846+759C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 5/23 | chr1 | 202427943 | ||||||
| chr1:202427971
|
AT | A | 98 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.846+802delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr1 | 202427971 | |||||
| chr1:202428051
|
T | TC | 253 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.847-801dupC | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr1 | 202428051 | |||||
| chr1:202428305
|
G | A | 2 | a0001c0001t0034g0044a0001c0001t0034g0045 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.847-550G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 5/23 | chr1 | 202428305 | ||||||
| chr1:202429295
|
T | A | 1 | a0001c0001t0080g0086 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.921+366T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 6/23 | chr1 | 202429295 | ||||||
| chr1:202429307
|
G | T | 2 | a0002c0002t0007g0055a0002c0002t0007g0056 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.921+378G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 6/23 | chr1 | 202429307 | ||||||
| chr1:202429555
|
C | T | 1 | a0001c0001t0039g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.921+626C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 6/23 | chr1 | 202429555 | ||||||
| chr1:202429673
|
T | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.921+744T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 6/23 | chr1 | 202429673 | ||||||
| chr1:202430262
|
T | C | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.922-469T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 6/23 | chr1 | 202430262 | ||||||
| chr1:202430461
|
C | CT | 102 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.922-260dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr1 | 202430461 | |||||
| chr1:202430525
|
C | T | 1 | a0001c0001t0059g0176 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.922-206C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 6/23 | chr1 | 202430525 | ||||||
| chr1:202430841
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1001+31A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 7/23 | chr1 | 202430841 | ||||||
| chr1:202431133
|
AT | A | 3 | a0001c0001t0035g0028a0001c0001t0035g0135a0001c0001t0086g0027 | 3 | HG02976.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1001+327delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr1 | 202431133 | |||||
| chr1:202431304
|
G | A | 2 | a0001c0001t0003g0048a0001c0001t0096g0052 | 2 | NA18975.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1002-176G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 7/23 | chr1 | 202431304 | ||||||
| chr1:202431649
|
C | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1141+30C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202431649 | ||||||
| chr1:202431682
|
G | A | 2 | a0001c0001t0037g0006a0001c0001t0038g0005 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1141+63G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202431682 | ||||||
| chr1:202431815
|
C | T | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1141+196C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202431815 | ||||||
| chr1:202431889
|
G | T | 1 | a0001c0001t0004g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1141+270G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202431889 | ||||||
| chr1:202432620
|
T | G | 1 | a0001c0001t0013g0093 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1141+1001T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202432620 | ||||||
| chr1:202432965
|
T | G | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1141+1346T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202432965 | ||||||
| chr1:202433181
|
A | G | 3 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0063g0159 | 3 | HG02717.hp2 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1142-1475A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202433181 | ||||||
| chr1:202433654
|
G | A | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1142-1002G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202433654 | ||||||
| chr1:202434380
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1142-276T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202434380 | ||||||
| chr1:202434466
|
A | T | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1142-190A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202434466 | ||||||
| chr1:202434514
|
G | C | 1 | a0001c0001t0003g0033 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1142-142G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202434514 | ||||||
| chr1:202434559
|
A | G | 1 | a0001c0001t0062g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1142-97A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 8/23 | chr1 | 202434559 | ||||||
| chr1:202434930
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0203 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1254+162A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202434930 | ||||||
| chr1:202435149
|
G | C | 132 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1254+381G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202435149 | ||||||
| chr1:202435300
|
A | G | 1 | a0001c0001t0005g0248 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1254+532A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202435300 | ||||||
| chr1:202435570
|
T | C | 1 | a0001c0001t0049g0245 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1254+802T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202435570 | ||||||
| chr1:202435938
|
C | G | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1254+1170C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202435938 | ||||||
| chr1:202435986
|
G | T | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1254+1218G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202435986 | ||||||
| chr1:202436268
|
A | AAAC | 15 | a0001c0001t0002g0200a0001c0001t0002g0204a0001c0001t0006g0163others(12): Show | 15 | HG01192.hp2 HG01517.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1254+1526_1255-152 others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr1 | 202436268 | |||||
| chr1:202436437
|
A | C | 1 | a0001c0001t0005g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1255-1384A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202436437 | ||||||
| chr1:202436543
|
A | G | 160 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1255-1278A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202436543 | ||||||
| chr1:202436613
|
A | T | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1255-1208A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202436613 | ||||||
| chr1:202436836
|
C | G | 1 | a0001c0001t0006g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1255-985C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202436836 | ||||||
| chr1:202436935
|
A | C | 1 | a0001c0001t0075g0018 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1255-886A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202436935 | ||||||
| chr1:202437052
|
C | A | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1255-769C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202437052 | ||||||
| chr1:202437193
|
A | C | 1 | a0001c0001t0021g0249 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1255-628A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202437193 | ||||||
| chr1:202437312
|
TAA | T | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1255-508_1255-507d others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202437312 | ||||||
| chr1:202437512
|
A | G | 1 | a0001c0001t0046g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1255-309A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202437512 | ||||||
| chr1:202437580
|
G | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1255-241G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202437580 | ||||||
| chr1:202437591
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1255-230G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 9/23 | chr1 | 202437591 | ||||||
| chr1:202438085
|
A | G | 1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1458+61A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202438085 | ||||||
| chr1:202438225
|
A | T | 5 | a0001c0001t0001g0186a0001c0001t0001g0211a0001c0001t0001g0242others(2): Show | 5 | NA18945.hp1 NA18980.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1458+201A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202438225 | ||||||
| chr1:202438382
|
G | A | 1 | a0001c0001t0075g0018 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1458+358G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202438382 | ||||||
| chr1:202438894
|
A | G | 1 | a0001c0001t0003g0053 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1458+870A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202438894 | ||||||
| chr1:202439045
|
C | T | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1458+1021C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202439045 | ||||||
| chr1:202439350
|
A | G | 1 | a0001c0001t0048g0197 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1458+1326A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202439350 | ||||||
| chr1:202439390
|
C | T | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1459-1316C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202439390 | ||||||
| chr1:202439466
|
C | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1459-1240C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202439466 | ||||||
| chr1:202439623
|
A | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1459-1083A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202439623 | ||||||
| chr1:202439672
|
T | C | 132 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1459-1034T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202439672 | ||||||
| chr1:202439751
|
C | T | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1459-955C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202439751 | ||||||
| chr1:202439760
|
AG | A | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1459-941delG | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr1 | 202439760 | |||||
| chr1:202439933
|
T | C | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1459-773T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202439933 | ||||||
| chr1:202439936
|
T | A | 1 | a0001c0001t0040g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1459-770T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202439936 | ||||||
| chr1:202440035
|
A | T | 41 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(38): Show | 41 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.1459-671A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202440035 | ||||||
| chr1:202440036
|
T | A | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1459-670T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202440036 | ||||||
| chr1:202440122
|
A | C | 2 | a0001c0001t0014g0238a0001c0001t0014g0243 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1459-584A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202440122 | ||||||
| chr1:202440129
|
A | C | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1459-577A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202440129 | ||||||
| chr1:202440273
|
C | T | 2 | a0001c0001t0041g0227a0001c0001t0042g0226 | 2 | NA18944.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1459-433C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202440273 | ||||||
| chr1:202440299
|
T | C | 2 | a0001c0001t0011g0114a0001c0001t0013g0116 | 2 | HG00642.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1459-407T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202440299 | ||||||
| chr1:202440671
|
A | G | 4 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0062g0131others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459-35A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 10/23 | chr1 | 202440671 | ||||||
| chr1:202440812
|
A | G | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1541+24A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/23 | chr1 | 202440812 | ||||||
| chr1:202441226
|
A | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1541+438A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/23 | chr1 | 202441226 | ||||||
| chr1:202441301
|
C | T | 94 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1541+513C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/23 | chr1 | 202441301 | ||||||
| chr1:202441359
|
G | C | 4 | a0001c0001t0016g0022a0001c0001t0016g0023a0001c0001t0016g0025others(1): Show | 4 | HG02523.hp2 NA18962.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1541+571G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/23 | chr1 | 202441359 | ||||||
| chr1:202441606
|
G | T | 6 | a0001c0001t0004g0127a0001c0001t0011g0125a0001c0001t0013g0126others(3): Show | 6 | HG02071.hp1 NA18954.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1541+818G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/23 | chr1 | 202441606 | ||||||
| chr1:202441618
|
A | C | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1542-829A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/23 | chr1 | 202441618 | ||||||
| chr1:202441930
|
C | T | 1 | a0001c0001t0012g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1542-517C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/23 | chr1 | 202441930 | ||||||
| chr1:202442285
|
T | A | 4 | a0001c0001t0002g0235a0001c0001t0006g0207a0001c0001t0006g0236others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1542-162T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/23 | chr1 | 202442285 | ||||||
| chr1:202442316
|
G | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1542-131G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/23 | chr1 | 202442316 | ||||||
| chr1:202442410
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1542-37G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 11/23 | chr1 | 202442410 | ||||||
| chr1:202442610
|
C | T | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1667+38C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202442610 | ||||||
| chr1:202442618
|
A | G | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1667+46A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202442618 | ||||||
| chr1:202442807
|
C | T | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1667+235C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202442807 | ||||||
| chr1:202443274
|
TG | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1667+703delG | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202443274 | ||||||
| chr1:202443905
|
A | C | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1667+1333A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202443905 | ||||||
| chr1:202444252
|
C | T | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1667+1680C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202444252 | ||||||
| chr1:202444410
|
G | T | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1667+1838G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202444410 | ||||||
| chr1:202444712
|
C | A | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1667+2140C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202444712 | ||||||
| chr1:202444855
|
C | A | 1 | a0001c0001t0025g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1667+2283C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202444855 | ||||||
| chr1:202445558
|
A | G | 1 | a0001c0001t0098g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1667+2986A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202445558 | ||||||
| chr1:202445818
|
T | C | 14 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(11): Show | 14 | HG01123.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1668-3171T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202445818 | ||||||
| chr1:202445951
|
A | G | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1668-3038A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202445951 | ||||||
| chr1:202446213
|
A | ACTCTCTC others(3): Show |
8 | a0001c0001t0002g0200a0001c0001t0002g0228a0001c0001t0005g0183others(5): Show | 8 | HG00408.hp1 HG00642.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1668-2761_1668-275 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446213 | |||||
| chr1:202446213
|
A | ACTCTCTC others(5): Show |
12 | a0001c0001t0001g0165a0001c0001t0001g0201a0001c0001t0001g0221others(9): Show | 12 | HG01258.hp2 HG01515.hp2 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.1668-2763_1668-275 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446213 | |||||
| chr1:202446213
|
A | ACTCTCTC others(9): Show |
1 | a0001c0001t0050g0175 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1668-2767_1668-275 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446213 | |||||
| chr1:202446213
|
A | T | 1 | a0001c0001t0049g0245 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1668-2776A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446213 | ||||||
| chr1:202446213
|
ACT | A | 14 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(11): Show | 14 | HG00639.hp2 HG00738.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1668-2753_1668-275 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446213 | |||||
| chr1:202446230
|
C | A | 4 | a0001c0001t0001g0174a0001c0001t0002g0168a0001c0001t0005g0166others(1): Show | 4 | HG01261.hp2 HG01346.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1668-2759C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446230 | ||||||
| chr1:202446232
|
C | A | 36 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0158others(33): Show | 36 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1668-2757C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446232 | ||||||
| chr1:202446234
|
C | A | 71 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0094others(68): Show | 71 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.1668-2755C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446234 | ||||||
| chr1:202446236
|
C | A | 112 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0094others(109): Show | 112 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.1668-2753C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446236 | ||||||
| chr1:202446236
|
C | CTCTCTAT others(3): Show |
1 | a0001c0001t0006g0229 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1668-2752_1668-275 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTAT others(5): Show |
5 | a0001c0001t0001g0160a0001c0001t0001g0195a0001c0001t0002g0161others(2): Show | 5 | HG00609.hp2 HG01099.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(3): Show |
3 | a0001c0001t0014g0251a0001c0001t0044g0252a0001c0001t0058g0250 | 3 | HG02080.hp1 HG02523.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(5): Show |
10 | a0001c0001t0002g0239a0001c0001t0005g0194a0001c0001t0015g0205others(7): Show | 10 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(7): Show |
2 | a0001c0001t0001g0244a0001c0001t0025g0234 | 2 | HG01069.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(9): Show |
1 | a0001c0001t0006g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1668-2752_1668-275 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(3): Show |
9 | a0001c0001t0001g0203a0001c0001t0002g0204a0001c0001t0002g0253others(6): Show | 9 | HG00597.hp2 HG01517.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(5): Show |
2 | a0001c0001t0001g0211a0001c0001t0024g0185 | 2 | HG03017.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(7): Show |
2 | a0001c0001t0056g0209a0008c0006t0001g0190 | 2 | HG02027.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(5): Show |
11 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(8): Show | 11 | HG00280.hp2 HG01106.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(7): Show |
3 | a0001c0001t0002g0179a0001c0001t0006g0177a0001c0001t0019g0218 | 3 | NA18943.hp2 NA19064.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(7): Show |
7 | a0001c0001t0001g0182a0001c0001t0001g0246a0001c0001t0002g0181others(4): Show | 7 | HG01934.hp2 HG02071.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(9): Show |
2 | a0001c0001t0002g0178a0001c0001t0005g0198 | 2 | HG00323.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1668-2752_1668-275 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0214 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1668-2752_1668-275 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446236
|
CTA | C | 4 | a0001c0001t0003g0021a0001c0001t0003g0032a0001c0001t0003g0033others(1): Show | 4 | HG00099.hp2 HG01099.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668-2733_1668-273 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446236 | |||||
| chr1:202446238
|
A | C | 17 | a0001c0001t0001g0230a0001c0001t0002g0196a0001c0001t0002g0231others(14): Show | 17 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1668-2751A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446238 | ||||||
| chr1:202446240
|
A | C | 8 | a0001c0001t0004g0089a0001c0001t0004g0095a0001c0001t0010g0083others(5): Show | 8 | HG00673.hp2 HG02027.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1668-2749A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446240 | ||||||
| chr1:202446249
|
TATA | T | 11 | a0001c0001t0004g0145a0001c0001t0013g0108a0001c0001t0017g0137others(8): Show | 11 | HG01123.hp1 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1668-2739_1668-273 others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446249 | ||||||
| chr1:202446250
|
A | T | 3 | a0001c0001t0008g0150a0001c0001t0062g0131a0001c0001t0063g0159 | 3 | HG02717.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1668-2739A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446250 | ||||||
| chr1:202446251
|
TATA | T | 12 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0168others(9): Show | 12 | HG01261.hp2 HG01346.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.1668-2737_1668-273 others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446251 | ||||||
| chr1:202446252
|
A | T | 16 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(13): Show | 16 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1668-2737A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446252 | ||||||
| chr1:202446253
|
TATA | T | 68 | a0001c0001t0002g0158a0001c0001t0003g0013a0001c0001t0003g0029others(65): Show | 68 | HG00280.hp1 HG00673.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.1668-2735_1668-273 others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446253 | ||||||
| chr1:202446254
|
A | T | 35 | a0001c0001t0001g0182a0001c0001t0004g0145a0001c0001t0008g0150others(32): Show | 35 | HG01123.hp1 HG01192.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1668-2735A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446254 | ||||||
| chr1:202446254
|
ATAT | A | 10 | a0001c0001t0003g0037a0001c0001t0004g0070a0001c0001t0007g0102others(7): Show | 10 | HG00323.hp1 HG00642.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1668-2733_1668-273 others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446254 | |||||
| chr1:202446256
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0230 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1668-2732_1668-273 others(22): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446256 | |||||
| chr1:202446256
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0002g0196a0001c0001t0002g0231 | 2 | HG00735.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1668-2732_1668-273 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446256 | |||||
| chr1:202446256
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0002g0235a0001c0001t0006g0236 | 2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1668-2732_1668-273 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446256 | |||||
| chr1:202446256
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0006g0207 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1668-2732_1668-273 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446256 | |||||
| chr1:202446256
|
A | ATTT | 10 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0181others(7): Show | 10 | HG01168.hp2 HG02647.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1668-2720_1668-271 others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446256 | |||||
| chr1:202446256
|
A | ATTTT | 32 | a0001c0001t0001g0160a0001c0001t0001g0195a0001c0001t0001g0203others(29): Show | 32 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1668-2721_1668-271 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446256 | |||||
| chr1:202446256
|
A | ATTTTT | 7 | a0001c0001t0001g0214a0001c0001t0001g0246a0001c0001t0005g0216others(4): Show | 7 | HG02027.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1668-2722_1668-271 others(9): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446256 | |||||
| chr1:202446256
|
A | ATTTTTT | 22 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0192others(19): Show | 22 | HG00280.hp2 HG01106.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1668-2723_1668-271 others(10): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446256 | |||||
| chr1:202446256
|
A | ATTTTTTT | 6 | a0001c0001t0001g0165a0001c0001t0002g0253a0001c0001t0005g0248others(3): Show | 6 | HG00597.hp2 HG02056.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1668-2724_1668-271 others(11): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr1 | 202446256 | |||||
| chr1:202446256
|
A | T | 52 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0001g0182others(49): Show | 52 | HG00738.hp2 HG01123.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.1668-2733A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446256 | ||||||
| chr1:202446258
|
T | A | 1 | a0001c0001t0088g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1668-2731T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446258 | ||||||
| chr1:202446285
|
G | T | 52 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(49): Show | 52 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.1668-2704G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446285 | ||||||
| chr1:202446346
|
C | T | 3 | a0001c0001t0004g0070a0001c0001t0010g0071a0001c0001t0077g0059 | 3 | HG02622.hp2 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1668-2643C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446346 | ||||||
| chr1:202446537
|
G | A | 2 | a0001c0001t0027g0129a0001c0001t0027g0130 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1668-2452G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446537 | ||||||
| chr1:202446622
|
A | G | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1668-2367A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446622 | ||||||
| chr1:202446655
|
A | G | 1 | a0001c0001t0066g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1668-2334A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446655 | ||||||
| chr1:202446739
|
C | T | 1 | a0001c0001t0037g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1668-2250C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446739 | ||||||
| chr1:202446866
|
T | C | 3 | a0001c0001t0005g0198a0001c0001t0005g0202a0001c0001t0048g0197 | 3 | HG00323.hp2 HG01515.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1668-2123T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202446866 | ||||||
| chr1:202447763
|
A | G | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1668-1226A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202447763 | ||||||
| chr1:202447870
|
T | C | 2 | a0001c0001t0032g0057a0001c0001t0032g0058 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1668-1119T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202447870 | ||||||
| chr1:202447925
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1668-1064C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202447925 | ||||||
| chr1:202447936
|
G | A | 1 | a0001c0001t0079g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1668-1053G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202447936 | ||||||
| chr1:202447994
|
A | G | 28 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0191others(25): Show | 28 | HG00280.hp2 HG01106.hp1 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1668-995A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202447994 | ||||||
| chr1:202448305
|
T | C | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1668-684T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202448305 | ||||||
| chr1:202448435
|
A | G | 26 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1668-554A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202448435 | ||||||
| chr1:202448599
|
C | G | 3 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069 | 3 | HG01106.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1668-390C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202448599 | ||||||
| chr1:202448917
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0020g0217 | 2 | NA19062.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1668-72T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202448917 | ||||||
| chr1:202448927
|
A | G | 1 | a0001c0001t0073g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1668-62A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 12/23 | chr1 | 202448927 | ||||||
| chr1:202449220
|
C | T | 1 | a0001c0001t0104g0101 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1850+49C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202449220 | ||||||
| chr1:202449234
|
G | A | 1 | a0001c0001t0086g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1850+63G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202449234 | ||||||
| chr1:202449368
|
C | T | 1 | a0001c0001t0004g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1850+197C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202449368 | ||||||
| chr1:202449493
|
G | T | 28 | a0001c0001t0004g0145a0001c0001t0008g0150a0001c0001t0008g0152others(25): Show | 28 | HG01123.hp1 HG01192.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1850+322G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202449493 | ||||||
| chr1:202449568
|
G | A | 9 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(6): Show | 9 | HG00735.hp1 HG01346.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1850+397G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202449568 | ||||||
| chr1:202449976
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1850+805G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202449976 | ||||||
| chr1:202449981
|
C | T | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1850+810C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202449981 | ||||||
| chr1:202450430
|
G | A | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1850+1259G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202450430 | ||||||
| chr1:202451094
|
A | G | 1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1850+1923A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451094 | ||||||
| chr1:202451130
|
C | CT | 117 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(114): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1850+1969dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202451130 | |||||
| chr1:202451205
|
G | A | 3 | a0001c0001t0034g0044a0001c0001t0034g0045a0001c0001t0105g0014 | 3 | HG02258.hp1 HG02280.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1850+2034G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451205 | ||||||
| chr1:202451210
|
C | T | 132 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1850+2039C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451210 | ||||||
| chr1:202451225
|
T | G | 2 | a0001c0001t0001g0195a0001c0001t0006g0229 | 2 | NA18954.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1850+2054T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451225 | ||||||
| chr1:202451342
|
C | G | 158 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1850+2171C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451342 | ||||||
| chr1:202451781
|
C | T | 1 | a0001c0001t0006g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1850+2610C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451781 | ||||||
| chr1:202451784
|
C | T | 2 | a0001c0001t0007g0102a0001c0001t0007g0103 | 2 | HG01261.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1850+2613C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451784 | ||||||
| chr1:202451869
|
C | G | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1850+2698C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451869 | ||||||
| chr1:202451904
|
CCAGACGG others(33): Show |
C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850+2743_1850+278 others(44): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202451904 | |||||
| chr1:202451953
|
G | T | 1 | a0001c0001t0087g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1850+2782G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451953 | ||||||
| chr1:202451965
|
C | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1850+2794C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451965 | ||||||
| chr1:202451994
|
C | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1850+2823C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202451994 | ||||||
| chr1:202452072
|
G | A | 42 | a0001c0001t0001g0160a0001c0001t0001g0182a0001c0001t0001g0195others(39): Show | 42 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1850+2901G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202452072 | ||||||
| chr1:202452081
|
G | T | 25 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1850+2910G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202452081 | ||||||
| chr1:202452083
|
G | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850+2912G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202452083 | ||||||
| chr1:202452154
|
C | T | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1850+2983C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202452154 | ||||||
| chr1:202452560
|
G | A | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1850+3389G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202452560 | ||||||
| chr1:202452569
|
C | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0037 | 2 | NA18960.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1850+3398C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202452569 | ||||||
| chr1:202452728
|
G | A | 5 | a0001c0001t0001g0230a0001c0001t0002g0161a0001c0001t0002g0162others(2): Show | 5 | HG00735.hp2 HG01099.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1850+3557G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202452728 | ||||||
| chr1:202452832
|
CT | C | 5 | a0001c0001t0002g0161a0001c0001t0002g0178a0001c0001t0003g0069others(2): Show | 5 | HG01099.hp1 HG01168.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1850+3674delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202452832 | |||||
| chr1:202452946
|
C | T | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1850+3775C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202452946 | ||||||
| chr1:202452964
|
G | A | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1850+3793G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202452964 | ||||||
| chr1:202453408
|
T | C | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1850+4237T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202453408 | ||||||
| chr1:202453533
|
G | A | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1850+4362G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202453533 | ||||||
| chr1:202453574
|
G | A | 1 | a0001c0001t0005g0216 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1850+4403G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202453574 | ||||||
| chr1:202453613
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1850+4442A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202453613 | ||||||
| chr1:202453678
|
A | G | 1 | a0001c0001t0013g0093 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1850+4507A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202453678 | ||||||
| chr1:202453707
|
CT | C | 114 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(111): Show | 114 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1850+4550delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202453707 | |||||
| chr1:202453824
|
T | G | 1 | a0001c0001t0013g0093 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1850+4653T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202453824 | ||||||
| chr1:202454082
|
A | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850+4911A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202454082 | ||||||
| chr1:202454419
|
C | T | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1850+5248C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202454419 | ||||||
| chr1:202454482
|
C | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0168others(4): Show | 7 | HG01261.hp2 HG01346.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1850+5311C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202454482 | ||||||
| chr1:202454848
|
G | A | 6 | a0001c0001t0010g0083a0001c0001t0013g0093a0001c0001t0070g0136others(3): Show | 6 | HG00673.hp2 NA18952.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1850+5677G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202454848 | ||||||
| chr1:202454869
|
C | T | 1 | a0001c0001t0004g0145 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1850+5698C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202454869 | ||||||
| chr1:202454871
|
A | G | 1 | a0006c0004t0010g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1850+5700A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202454871 | ||||||
| chr1:202454914
|
C | G | 1 | a0001c0001t0024g0185 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1850+5743C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202454914 | ||||||
| chr1:202455089
|
G | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850+5918G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202455089 | ||||||
| chr1:202455193
|
C | CAT | 8 | a0001c0001t0003g0021a0001c0001t0003g0043a0001c0001t0016g0022others(5): Show | 8 | HG02523.hp2 NA18950.hp2 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.1850+6034_1850+603 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202455193 | |||||
| chr1:202455203
|
T | G | 1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1850+6032T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202455203 | ||||||
| chr1:202455205
|
T | G | 12 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0026g0008others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1850+6034T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202455205 | ||||||
| chr1:202455205
|
TAGAG | T | 91 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(88): Show | 91 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1850+6048_1850+605 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202455205 | |||||
| chr1:202455207
|
G | T | 68 | a0001c0001t0002g0094a0001c0001t0002g0158a0001c0001t0002g0235others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1850+6036G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202455207 | ||||||
| chr1:202455209
|
G | T | 6 | a0001c0001t0004g0127a0001c0001t0011g0114a0001c0001t0030g0122others(3): Show | 6 | HG00642.hp1 HG02451.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1850+6038G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202455209 | ||||||
| chr1:202455211
|
G | T | 76 | a0001c0001t0001g0160a0001c0001t0001g0169a0001c0001t0001g0174others(73): Show | 76 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1850+6040G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202455211 | ||||||
| chr1:202455213
|
G | T | 36 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0195others(33): Show | 36 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1850+6042G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202455213 | ||||||
| chr1:202455236
|
A | G | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1850+6065A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202455236 | ||||||
| chr1:202455318
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850+6147A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202455318 | ||||||
| chr1:202455423
|
A | G | 1 | a0001c0001t0039g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1850+6252A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202455423 | ||||||
| chr1:202456183
|
C | T | 1 | a0001c0001t0030g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1850+7012C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202456183 | ||||||
| chr1:202456224
|
G | A | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1850+7053G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202456224 | ||||||
| chr1:202456264
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0211 | 2 | NA18945.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1850+7093G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202456264 | ||||||
| chr1:202456368
|
C | G | 4 | a0001c0001t0076g0051a0001c0001t0078g0050a0001c0001t0079g0046others(1): Show | 4 | HG00735.hp1 HG01346.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1850+7197C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202456368 | ||||||
| chr1:202456731
|
C | T | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1850+7560C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202456731 | ||||||
| chr1:202456785
|
A | G | 1 | a0001c0001t0046g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1850+7614A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202456785 | ||||||
| chr1:202457245
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0168others(4): Show | 7 | HG01261.hp2 HG01346.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1850+8074G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202457245 | ||||||
| chr1:202457264
|
T | G | 1 | a0001c0001t0009g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1850+8093T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202457264 | ||||||
| chr1:202457334
|
G | A | 1 | a0001c0001t0037g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1850+8163G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202457334 | ||||||
| chr1:202457347
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850+8176C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202457347 | ||||||
| chr1:202457457
|
G | A | 1 | a0001c0001t0019g0218 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1850+8286G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202457457 | ||||||
| chr1:202457648
|
T | C | 253 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1850+8477T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202457648 | ||||||
| chr1:202457658
|
G | A | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1850+8487G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202457658 | ||||||
| chr1:202457736
|
A | G | 4 | a0001c0001t0076g0051a0001c0001t0078g0050a0001c0001t0079g0046others(1): Show | 4 | HG00735.hp1 HG01346.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1850+8565A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202457736 | ||||||
| chr1:202457786
|
T | C | 1 | a0001c0001t0039g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1850+8615T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202457786 | ||||||
| chr1:202458119
|
A | AGTTTTGT others(281): Show |
3 | a0001c0001t0016g0022a0001c0001t0016g0025a0001c0001t0090g0020 | 3 | HG02523.hp2 NA19002.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1850+9112_1850+939 others(292): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202458119 | |||||
| chr1:202458119
|
AGTTTTGT others(281): Show |
A | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1850+9112_1850+939 others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202458119 | |||||
| chr1:202458154
|
C | G | 2 | a0001c0001t0009g0065a0001c0001t0009g0066 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1850+8983C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202458154 | ||||||
| chr1:202458645
|
C | A | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1850+9474C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202458645 | ||||||
| chr1:202459051
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850+9880G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202459051 | ||||||
| chr1:202459732
|
T | C | 210 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1850+10561T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202459732 | ||||||
| chr1:202459894
|
C | T | 2 | a0001c0001t0034g0044a0001c0001t0034g0045 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1850+10723C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202459894 | ||||||
| chr1:202460016
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1850+10845T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202460016 | ||||||
| chr1:202460509
|
G | A | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1850+11338G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202460509 | ||||||
| chr1:202460632
|
G | GT | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1850+11467dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202460632 | |||||
| chr1:202460665
|
T | C | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1850+11494T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202460665 | ||||||
| chr1:202461296
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1850+12125G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202461296 | ||||||
| chr1:202461374
|
C | T | 1 | a0001c0001t0098g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1850+12203C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202461374 | ||||||
| chr1:202461809
|
C | A | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1850+12638C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202461809 | ||||||
| chr1:202461846
|
T | C | 1 | a0001c0001t0004g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1850+12675T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202461846 | ||||||
| chr1:202462315
|
C | T | 5 | a0001c0001t0004g0087a0001c0001t0004g0096a0001c0001t0010g0080others(2): Show | 5 | HG01074.hp2 HG01433.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.1850+13144C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202462315 | ||||||
| chr1:202462336
|
G | A | 6 | a0001c0001t0001g0230a0001c0001t0002g0161a0001c0001t0002g0162others(3): Show | 6 | HG00735.hp2 HG01099.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1850+13165G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202462336 | ||||||
| chr1:202462874
|
A | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1850+13703A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202462874 | ||||||
| chr1:202463032
|
T | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1850+13861T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202463032 | ||||||
| chr1:202463320
|
G | A | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1850+14149G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202463320 | ||||||
| chr1:202463382
|
C | G | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1850+14211C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202463382 | ||||||
| chr1:202463395
|
T | A | 1 | a0001c0003t0028g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1850+14224T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202463395 | ||||||
| chr1:202463718
|
C | T | 1 | a0001c0001t0040g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1850+14547C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202463718 | ||||||
| chr1:202463802
|
G | A | 1 | a0001c0001t0074g0088 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1850+14631G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202463802 | ||||||
| chr1:202463863
|
A | G | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1850+14692A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202463863 | ||||||
| chr1:202464383
|
C | T | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1850+15212C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202464383 | ||||||
| chr1:202464485
|
A | G | 2 | a0001c0001t0041g0227a0001c0001t0042g0226 | 2 | NA18944.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1850+15314A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202464485 | ||||||
| chr1:202464795
|
C | T | 2 | a0001c0001t0035g0028a0001c0001t0086g0027 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1850+15624C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202464795 | ||||||
| chr1:202464850
|
G | A | 1 | a0001c0001t0006g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1850+15679G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202464850 | ||||||
| chr1:202465154
|
T | C | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1850+15983T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202465154 | ||||||
| chr1:202465322
|
G | C | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1850+16151G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202465322 | ||||||
| chr1:202465453
|
C | G | 1 | a0001c0001t0047g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1850+16282C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202465453 | ||||||
| chr1:202465794
|
G | A | 1 | a0001c0001t0033g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1850+16623G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202465794 | ||||||
| chr1:202465823
|
T | C | 1 | a0001c0001t0090g0020 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1850+16652T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202465823 | ||||||
| chr1:202466027
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850+16856A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202466027 | ||||||
| chr1:202466100
|
A | T | 102 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1850+16929A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202466100 | ||||||
| chr1:202466480
|
C | A | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1850+17309C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202466480 | ||||||
| chr1:202466632
|
T | G | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1850+17461T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202466632 | ||||||
| chr1:202466813
|
C | T | 5 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1850+17642C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202466813 | ||||||
| chr1:202467083
|
A | C | 2 | a0001c0001t0014g0238a0001c0001t0014g0243 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1850+17912A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202467083 | ||||||
| chr1:202467445
|
A | G | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1850+18274A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202467445 | ||||||
| chr1:202467498
|
G | A | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1850+18327G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202467498 | ||||||
| chr1:202467595
|
C | G | 1 | a0001c0001t0012g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1850+18424C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202467595 | ||||||
| chr1:202467650
|
T | A | 1 | a0001c0001t0104g0101 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1850+18479T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202467650 | ||||||
| chr1:202467682
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1850+18511A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202467682 | ||||||
| chr1:202467915
|
T | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850+18744T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202467915 | ||||||
| chr1:202468006
|
G | T | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1850+18835G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202468006 | ||||||
| chr1:202468303
|
C | T | 1 | a0001c0001t0088g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1850+19132C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202468303 | ||||||
| chr1:202468529
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1850+19358C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202468529 | ||||||
| chr1:202468725
|
G | A | 1 | a0006c0004t0010g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1850+19554G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202468725 | ||||||
| chr1:202468783
|
G | T | 1 | a0001c0001t0070g0136 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1850+19612G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202468783 | ||||||
| chr1:202468911
|
T | G | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1851-19622T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202468911 | ||||||
| chr1:202469093
|
A | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1851-19440A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202469093 | ||||||
| chr1:202469238
|
G | A | 2 | a0001c0001t0004g0127a0001c0001t0030g0122 | 2 | NA18954.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1851-19295G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202469238 | ||||||
| chr1:202469257
|
T | G | 2 | a0001c0001t0034g0044a0001c0001t0034g0045 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1851-19276T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202469257 | ||||||
| chr1:202469322
|
C | T | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1851-19211C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202469322 | ||||||
| chr1:202469822
|
G | A | 3 | a0001c0001t0024g0164a0001c0001t0024g0185a0001c0001t0056g0209 | 3 | HG02698.hp2 HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1851-18711G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202469822 | ||||||
| chr1:202470129
|
G | A | 1 | a0001c0001t0003g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1851-18404G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202470129 | ||||||
| chr1:202470159
|
G | A | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1851-18374G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202470159 | ||||||
| chr1:202470160
|
G | A | 5 | a0001c0001t0017g0141a0001c0001t0017g0143a0001c0001t0100g0142others(2): Show | 5 | HG02922.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1851-18373G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202470160 | ||||||
| chr1:202470241
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1851-18292A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202470241 | ||||||
| chr1:202470515
|
G | A | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1851-18018G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202470515 | ||||||
| chr1:202470905
|
C | CA | 5 | a0001c0001t0003g0033a0001c0001t0004g0089a0001c0001t0017g0143others(2): Show | 5 | HG01099.hp2 HG02027.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1851-17612dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202470905 | |||||
| chr1:202470923
|
G | GAA | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1851-17609_1851-17 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202470923 | |||||
| chr1:202471228
|
C | G | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1851-17305C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202471228 | ||||||
| chr1:202471291
|
C | T | 8 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(5): Show | 8 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1851-17242C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202471291 | ||||||
| chr1:202471575
|
G | GT | 47 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(44): Show | 47 | HG00099.hp2 HG00597.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1851-16940dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202471575 | |||||
| chr1:202471575
|
G | GTT | 5 | a0001c0001t0007g0040a0001c0001t0061g0132a0001c0001t0072g0012others(2): Show | 5 | HG01346.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1851-16941_1851-16 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202471575 | |||||
| chr1:202471575
|
GT | G | 127 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1851-16940delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202471575 | |||||
| chr1:202471641
|
A | T | 2 | a0001c0001t0001g0225a0001c0001t0006g0187 | 2 | NA18994.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1851-16892A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202471641 | ||||||
| chr1:202471700
|
C | G | 1 | a0001c0001t0002g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1851-16833C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202471700 | ||||||
| chr1:202471795
|
GT | G | 7 | a0001c0001t0007g0040a0001c0001t0018g0039a0001c0001t0018g0041others(4): Show | 7 | NA18943.hp1 NA18970.hp1 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.1851-16725delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202471795 | |||||
| chr1:202471808
|
T | A | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1851-16725T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202471808 | ||||||
| chr1:202471994
|
T | C | 2 | a0001c0001t0009g0065a0001c0001t0009g0066 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1851-16539T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202471994 | ||||||
| chr1:202472355
|
G | A | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1851-16178G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202472355 | ||||||
| chr1:202472550
|
A | G | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1851-15983A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202472550 | ||||||
| chr1:202472954
|
G | A | 132 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1851-15579G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202472954 | ||||||
| chr1:202472960
|
T | C | 1 | a0001c0001t0004g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1851-15573T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202472960 | ||||||
| chr1:202472985
|
A | G | 1 | a0001c0001t0012g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1851-15548A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202472985 | ||||||
| chr1:202473257
|
A | G | 94 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1851-15276A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202473257 | ||||||
| chr1:202473446
|
G | A | 16 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0168others(13): Show | 16 | HG00738.hp2 HG01261.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.1851-15087G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202473446 | ||||||
| chr1:202473655
|
A | G | 1 | a0001c0001t0004g0084 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1851-14878A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202473655 | ||||||
| chr1:202473801
|
T | G | 1 | a0001c0003t0028g0121 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1851-14732T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202473801 | ||||||
| chr1:202473872
|
C | A | 25 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1851-14661C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202473872 | ||||||
| chr1:202474241
|
G | C | 1 | a0001c0001t0098g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1851-14292G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202474241 | ||||||
| chr1:202474304
|
T | C | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1851-14229T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202474304 | ||||||
| chr1:202474327
|
G | A | 51 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(48): Show | 51 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.1851-14206G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202474327 | ||||||
| chr1:202474393
|
G | A | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1851-14140G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202474393 | ||||||
| chr1:202474535
|
C | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1851-13998C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202474535 | ||||||
| chr1:202474701
|
T | C | 2 | a0001c0001t0037g0006a0001c0001t0038g0005 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1851-13832T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202474701 | ||||||
| chr1:202475258
|
A | C | 253 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1851-13275A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202475258 | ||||||
| chr1:202475295
|
T | C | 25 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1851-13238T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202475295 | ||||||
| chr1:202475337
|
C | T | 1 | a0001c0001t0087g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1851-13196C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202475337 | ||||||
| chr1:202476058
|
G | A | 1 | a0001c0001t0062g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1851-12475G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202476058 | ||||||
| chr1:202476204
|
C | CA | 48 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(45): Show | 48 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.1851-12312dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202476204 | |||||
| chr1:202476204
|
CA | C | 9 | a0001c0001t0001g0225a0001c0001t0011g0119a0001c0001t0026g0008others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1851-12312delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202476204 | |||||
| chr1:202476632
|
G | A | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1851-11901G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202476632 | ||||||
| chr1:202476640
|
G | A | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1851-11893G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202476640 | ||||||
| chr1:202476697
|
A | T | 2 | a0001c0001t0072g0012a0001c0001t0090g0020 | 2 | HG02622.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1851-11836A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202476697 | ||||||
| chr1:202476728
|
T | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1851-11805T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202476728 | ||||||
| chr1:202476866
|
G | A | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1851-11667G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202476866 | ||||||
| chr1:202476959
|
G | A | 4 | a0001c0001t0002g0235a0001c0001t0006g0207a0001c0001t0006g0236others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1851-11574G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202476959 | ||||||
| chr1:202477190
|
G | A | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1851-11343G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202477190 | ||||||
| chr1:202477426
|
T | C | 1 | a0001c0001t0003g0021 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1851-11107T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202477426 | ||||||
| chr1:202477466
|
G | A | 1 | a0001c0001t0008g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1851-11067G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202477466 | ||||||
| chr1:202477898
|
A | G | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1851-10635A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202477898 | ||||||
| chr1:202478166
|
C | A | 101 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1851-10367C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202478166 | ||||||
| chr1:202478168
|
A | C | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1851-10365A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202478168 | ||||||
| chr1:202478225
|
G | A | 1 | a0001c0001t0079g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1851-10308G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202478225 | ||||||
| chr1:202478320
|
G | A | 3 | a0001c0001t0003g0031a0001c0001t0003g0034a0001c0001t0003g0035 | 3 | HG01515.hp1 HG01517.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1851-10213G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202478320 | ||||||
| chr1:202478369
|
G | A | 1 | a0001c0001t0017g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1851-10164G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202478369 | ||||||
| chr1:202478427
|
G | A | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1851-10106G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202478427 | ||||||
| chr1:202478428
|
C | A | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1851-10105C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202478428 | ||||||
| chr1:202478548
|
A | G | 1 | a0001c0001t0081g0077 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1851-9985A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202478548 | ||||||
| chr1:202479188
|
G | T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1851-9345G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202479188 | ||||||
| chr1:202479458
|
C | T | 1 | a0001c0001t0020g0215 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1851-9075C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202479458 | ||||||
| chr1:202479523
|
G | A | 2 | a0001c0001t0034g0044a0001c0001t0034g0045 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1851-9010G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202479523 | ||||||
| chr1:202479766
|
T | C | 1 | a0001c0001t0004g0004 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1851-8767T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202479766 | ||||||
| chr1:202479871
|
A | C | 1 | a0001c0001t0009g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1851-8662A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202479871 | ||||||
| chr1:202479886
|
T | C | 2 | a0001c0001t0009g0065a0001c0001t0009g0066 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1851-8647T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202479886 | ||||||
| chr1:202480274
|
A | C | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1851-8259A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202480274 | ||||||
| chr1:202480458
|
T | C | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1851-8075T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202480458 | ||||||
| chr1:202480536
|
T | C | 1 | a0001c0001t0006g0207 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1851-7997T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202480536 | ||||||
| chr1:202480578
|
A | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1851-7955A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202480578 | ||||||
| chr1:202480691
|
A | G | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1851-7842A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202480691 | ||||||
| chr1:202480757
|
T | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1851-7776T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202480757 | ||||||
| chr1:202480988
|
G | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1851-7545G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202480988 | ||||||
| chr1:202481024
|
A | G | 1 | a0001c0001t0013g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1851-7509A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202481024 | ||||||
| chr1:202481281
|
C | T | 1 | a0001c0001t0049g0245 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1851-7252C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202481281 | ||||||
| chr1:202481550
|
A | AT | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1851-6983_1851-698 others(5): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202481550 | ||||||
| chr1:202481616
|
A | G | 1 | a0001c0001t0073g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1851-6917A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202481616 | ||||||
| chr1:202481736
|
A | G | 1 | a0001c0001t0002g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1851-6797A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202481736 | ||||||
| chr1:202481884
|
C | T | 12 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(9): Show | 12 | HG01123.hp1 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1851-6649C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202481884 | ||||||
| chr1:202482046
|
C | T | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1851-6487C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202482046 | ||||||
| chr1:202482310
|
C | T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1851-6223C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202482310 | ||||||
| chr1:202482410
|
T | C | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1851-6123T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202482410 | ||||||
| chr1:202482431
|
T | C | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1851-6102T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202482431 | ||||||
| chr1:202482522
|
A | G | 1 | a0001c0001t0101g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1851-6011A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202482522 | ||||||
| chr1:202482622
|
T | A | 2 | a0001c0001t0006g0173a0001c0001t0050g0175 | 2 | HG00738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1851-5911T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202482622 | ||||||
| chr1:202482675
|
T | G | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1851-5858T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202482675 | ||||||
| chr1:202482701
|
C | G | 1 | a0001c0001t0105g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1851-5832C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202482701 | ||||||
| chr1:202483019
|
G | C | 2 | a0001c0001t0006g0173a0001c0001t0050g0175 | 2 | HG00738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1851-5514G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202483019 | ||||||
| chr1:202483278
|
C | CT | 13 | a0001c0001t0001g0182a0001c0001t0001g0246a0001c0001t0005g0183others(10): Show | 13 | HG00408.hp1 HG00408.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1851-5236dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202483278 | |||||
| chr1:202483278
|
C | CTT | 86 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(83): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1851-5237_1851-523 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202483278 | |||||
| chr1:202483367
|
G | T | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1851-5166G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202483367 | ||||||
| chr1:202483642
|
G | A | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1851-4891G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202483642 | ||||||
| chr1:202484027
|
G | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1851-4506G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202484027 | ||||||
| chr1:202484800
|
C | T | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1851-3733C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202484800 | ||||||
| chr1:202484835
|
G | A | 3 | a0001c0001t0033g0090a0001c0001t0033g0091a0001c0001t0069g0098 | 3 | HG02109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1851-3698G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202484835 | ||||||
| chr1:202484925
|
G | A | 8 | a0001c0001t0004g0089a0001c0001t0004g0095a0001c0001t0010g0083others(5): Show | 8 | HG00673.hp2 HG02027.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1851-3608G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202484925 | ||||||
| chr1:202485123
|
T | C | 1 | a0001c0001t0071g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1851-3410T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202485123 | ||||||
| chr1:202485140
|
G | GT | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1851-3390dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202485140 | |||||
| chr1:202485285
|
A | G | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1851-3248A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202485285 | ||||||
| chr1:202485304
|
A | G | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1851-3229A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202485304 | ||||||
| chr1:202485316
|
A | G | 2 | a0001c0001t0004g0079a0001c0001t0004g0084 | 2 | HG00609.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1851-3217A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202485316 | ||||||
| chr1:202485365
|
G | T | 1 | a0001c0001t0044g0252 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1851-3168G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202485365 | ||||||
| chr1:202485405
|
A | T | 1 | a0001c0001t0039g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1851-3128A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202485405 | ||||||
| chr1:202485530
|
G | A | 1 | a0001c0001t0059g0176 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1851-3003G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202485530 | ||||||
| chr1:202486007
|
G | A | 4 | a0001c0001t0008g0152a0001c0001t0008g0153a0001c0001t0008g0154others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-2526G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202486007 | ||||||
| chr1:202486129
|
G | A | 1 | a0001c0001t0013g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1851-2404G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202486129 | ||||||
| chr1:202486340
|
C | T | 3 | a0001c0001t0004g0070a0001c0001t0010g0071a0001c0001t0077g0059 | 3 | HG02622.hp2 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1851-2193C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202486340 | ||||||
| chr1:202486380
|
G | C | 1 | a0001c0001t0033g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1851-2153G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202486380 | ||||||
| chr1:202486412
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1851-2121A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202486412 | ||||||
| chr1:202486565
|
G | A | 4 | a0001c0001t0035g0028a0001c0001t0035g0135a0001c0001t0071g0073others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-1968G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202486565 | ||||||
| chr1:202486913
|
T | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1851-1620T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202486913 | ||||||
| chr1:202487134
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1851-1399A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202487134 | ||||||
| chr1:202487150
|
G | A | 133 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(130): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1851-1383G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202487150 | ||||||
| chr1:202487392
|
C | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1851-1141C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202487392 | ||||||
| chr1:202487603
|
C | CT | 53 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(50): Show | 53 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1851-918dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202487603 | |||||
| chr1:202487616
|
C | CT | 12 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(9): Show | 12 | HG00673.hp1 HG01123.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1851-909dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr1 | 202487616 | |||||
| chr1:202487625
|
G | T | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1851-908G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202487625 | ||||||
| chr1:202487661
|
T | A | 1 | a0001c0001t0093g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1851-872T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202487661 | ||||||
| chr1:202487693
|
C | T | 2 | a0001c0001t0006g0163a0001c0001t0051g0232 | 2 | HG02258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1851-840C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202487693 | ||||||
| chr1:202487861
|
G | A | 1 | a0001c0001t0014g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1851-672G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202487861 | ||||||
| chr1:202487887
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1851-646C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202487887 | ||||||
| chr1:202488049
|
C | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1851-484C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202488049 | ||||||
| chr1:202488219
|
C | T | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1851-314C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 13/23 | chr1 | 202488219 | ||||||
| chr1:202488656
|
T | A | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1941+33T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202488656 | ||||||
| chr1:202488745
|
T | C | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1941+122T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202488745 | ||||||
| chr1:202489017
|
C | T | 1 | a0001c0001t0030g0115 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1941+394C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202489017 | ||||||
| chr1:202489493
|
A | T | 2 | a0001c0001t0006g0173a0001c0001t0050g0175 | 2 | HG00738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1941+870A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202489493 | ||||||
| chr1:202489669
|
A | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1941+1046A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202489669 | ||||||
| chr1:202489986
|
A | G | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1941+1363A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202489986 | ||||||
| chr1:202490170
|
C | T | 1 | a0001c0001t0016g0023 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1941+1547C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202490170 | ||||||
| chr1:202490435
|
C | A | 1 | a0001c0001t0002g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1941+1812C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202490435 | ||||||
| chr1:202490691
|
T | C | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1941+2068T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202490691 | ||||||
| chr1:202490871
|
G | A | 158 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1942-2243G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202490871 | ||||||
| chr1:202490989
|
G | T | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1942-2125G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202490989 | ||||||
| chr1:202491051
|
C | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1942-2063C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202491051 | ||||||
| chr1:202491129
|
T | C | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1942-1985T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202491129 | ||||||
| chr1:202491208
|
TCTGCCTC others(18): Show |
T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1942-1871_1942-184 others(29): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr1 | 202491208 | |||||
| chr1:202491279
|
G | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1942-1835G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202491279 | ||||||
| chr1:202491494
|
C | T | 25 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1942-1620C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202491494 | ||||||
| chr1:202491677
|
T | C | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1942-1437T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202491677 | ||||||
| chr1:202491767
|
T | C | 3 | a0001c0001t0035g0028a0001c0001t0035g0135a0001c0001t0086g0027 | 3 | HG02976.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1942-1347T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202491767 | ||||||
| chr1:202491975
|
T | C | 14 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0001g0203others(11): Show | 14 | HG00323.hp2 HG00408.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1942-1139T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202491975 | ||||||
| chr1:202492025
|
A | G | 1 | a0001c0001t0004g0084 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1942-1089A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492025 | ||||||
| chr1:202492073
|
C | G | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1942-1041C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492073 | ||||||
| chr1:202492100
|
C | G | 1 | a0001c0001t0040g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1942-1014C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492100 | ||||||
| chr1:202492199
|
C | T | 2 | a0001c0001t0004g0075a0001c0001t0004g0076 | 2 | HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1942-915C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492199 | ||||||
| chr1:202492200
|
G | A | 1 | a0001c0001t0104g0101 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1942-914G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492200 | ||||||
| chr1:202492435
|
A | G | 5 | a0001c0001t0001g0186a0001c0001t0001g0211a0001c0001t0001g0242others(2): Show | 5 | NA18945.hp1 NA18980.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1942-679A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492435 | ||||||
| chr1:202492578
|
C | T | 1 | a0001c0001t0013g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1942-536C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492578 | ||||||
| chr1:202492612
|
T | C | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1942-502T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492612 | ||||||
| chr1:202492719
|
A | T | 223 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1942-395A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492719 | ||||||
| chr1:202492854
|
G | A | 133 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(130): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1942-260G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492854 | ||||||
| chr1:202492895
|
G | A | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1942-219G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202492895 | ||||||
| chr1:202493007
|
A | G | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1942-107A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202493007 | ||||||
| chr1:202493085
|
A | G | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1942-29A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 14/23 | chr1 | 202493085 | ||||||
| chr1:202493411
|
A | G | 6 | a0001c0001t0004g0127a0001c0001t0011g0125a0001c0001t0013g0126others(3): Show | 6 | HG02071.hp1 NA18954.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.2145+94A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | chr1 | 202493411 | ||||||
| chr1:202494484
|
A | G | 2 | a0001c0001t0027g0129a0001c0001t0027g0130 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2146-809A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | chr1 | 202494484 | ||||||
| chr1:202494582
|
TA | T | 56 | a0001c0001t0001g0160a0001c0001t0001g0182a0001c0001t0001g0195others(53): Show | 56 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.2146-693delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr1 | 202494582 | |||||
| chr1:202494692
|
C | G | 2 | a0001c0001t0005g0183a0001c0001t0005g0184 | 2 | HG00408.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2146-601C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | chr1 | 202494692 | ||||||
| chr1:202494712
|
A | G | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2146-581A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | chr1 | 202494712 | ||||||
| chr1:202494798
|
C | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2146-495C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | chr1 | 202494798 | ||||||
| chr1:202494865
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2146-428G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | chr1 | 202494865 | ||||||
| chr1:202495032
|
G | A | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2146-261G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | chr1 | 202495032 | ||||||
| chr1:202495098
|
G | GT | 12 | a0001c0001t0002g0178a0001c0001t0021g0249a0001c0001t0033g0091others(9): Show | 12 | HG01256.hp1 HG01258.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2146-181dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr1 | 202495098 | |||||
| chr1:202495152
|
G | A | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2146-141G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | chr1 | 202495152 | ||||||
| chr1:202495220
|
T | G | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2146-73T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | chr1 | 202495220 | ||||||
| chr1:202495222
|
G | A | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2146-71G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 15/23 | chr1 | 202495222 | ||||||
| chr1:202496278
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2449-503A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 17/23 | chr1 | 202496278 | ||||||
| chr1:202496551
|
T | C | 1 | a0001c0001t0039g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2449-230T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 17/23 | chr1 | 202496551 | ||||||
| chr1:202497378
|
C | G | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2490+556C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202497378 | ||||||
| chr1:202497563
|
T | C | 1 | a0001c0001t0066g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2490+741T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202497563 | ||||||
| chr1:202497732
|
G | A | 1 | a0001c0001t0031g0002 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2490+910G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202497732 | ||||||
| chr1:202498065
|
CT | C | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2490+1247delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202498065 | |||||
| chr1:202498273
|
A | G | 2 | a0001c0001t0003g0048a0001c0001t0096g0052 | 2 | NA18975.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2490+1451A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202498273 | ||||||
| chr1:202498299
|
G | A | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2490+1477G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202498299 | ||||||
| chr1:202498699
|
A | G | 4 | a0001c0001t0035g0028a0001c0001t0035g0135a0001c0001t0071g0073others(1): Show | 4 | HG02976.hp1 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490+1877A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202498699 | ||||||
| chr1:202498974
|
A | G | 12 | a0001c0001t0004g0127a0001c0001t0011g0119a0001c0001t0011g0120others(9): Show | 12 | HG00673.hp1 HG02071.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.2490+2152A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202498974 | ||||||
| chr1:202499179
|
G | A | 5 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2490+2357G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202499179 | ||||||
| chr1:202499271
|
T | C | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2490+2449T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202499271 | ||||||
| chr1:202499397
|
G | A | 1 | a0001c0001t0079g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2490+2575G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202499397 | ||||||
| chr1:202499583
|
G | A | 1 | a0001c0001t0005g0220 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2490+2761G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202499583 | ||||||
| chr1:202499593
|
C | T | 1 | a0001c0001t0097g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2490+2771C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202499593 | ||||||
| chr1:202499594
|
G | A | 1 | a0001c0001t0009g0100 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2490+2772G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202499594 | ||||||
| chr1:202500218
|
G | GCT | 62 | a0001c0001t0001g0165a0001c0001t0001g0169a0001c0001t0001g0174others(59): Show | 62 | HG00280.hp2 HG00738.hp2 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.2490+3422_2490+342 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202500218 | |||||
| chr1:202500218
|
G | GCTCT | 43 | a0001c0001t0001g0160a0001c0001t0001g0182a0001c0001t0001g0195others(40): Show | 43 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.2490+3420_2490+342 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202500218 | |||||
| chr1:202500218
|
GCTCT | G | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2490+3420_2490+342 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202500218 | |||||
| chr1:202500420
|
A | T | 1 | a0001c0001t0006g0237 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2490+3598A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202500420 | ||||||
| chr1:202500599
|
C | T | 1 | a0001c0001t0005g0199 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2490+3777C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202500599 | ||||||
| chr1:202500634
|
G | A | 1 | a0001c0001t0013g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2490+3812G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202500634 | ||||||
| chr1:202500842
|
T | C | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2490+4020T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202500842 | ||||||
| chr1:202501445
|
C | T | 1 | a0001c0001t0085g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2490+4623C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202501445 | ||||||
| chr1:202501475
|
T | A | 3 | a0001c0001t0005g0198a0001c0001t0005g0202a0001c0001t0048g0197 | 3 | HG00323.hp2 HG01515.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2490+4653T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202501475 | ||||||
| chr1:202501711
|
G | T | 2 | a0001c0001t0027g0129a0001c0001t0027g0130 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2490+4889G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202501711 | ||||||
| chr1:202502032
|
A | G | 1 | a0001c0001t0073g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2490+5210A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502032 | ||||||
| chr1:202502095
|
C | G | 2 | a0001c0001t0085g0078a0001c0001t0098g0060 | 2 | HG02300.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2490+5273C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502095 | ||||||
| chr1:202502111
|
T | C | 2 | a0001c0001t0027g0129a0001c0001t0027g0130 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2490+5289T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502111 | ||||||
| chr1:202502187
|
G | A | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2490+5365G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502187 | ||||||
| chr1:202502248
|
T | C | 29 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0191others(26): Show | 29 | HG00280.hp2 HG01106.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.2490+5426T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502248 | ||||||
| chr1:202502276
|
G | T | 2 | a0001c0001t0006g0173a0001c0001t0050g0175 | 2 | HG00738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.2490+5454G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502276 | ||||||
| chr1:202502538
|
T | G | 2 | a0001c0001t0100g0142a0001c0001t0101g0144 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2490+5716T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502538 | ||||||
| chr1:202502564
|
T | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2490+5742T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502564 | ||||||
| chr1:202502588
|
G | T | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2490+5766G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502588 | ||||||
| chr1:202502752
|
G | A | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2490+5930G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502752 | ||||||
| chr1:202502800
|
G | A | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2490+5978G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502800 | ||||||
| chr1:202502938
|
C | A | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2490+6116C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202502938 | ||||||
| chr1:202503055
|
G | T | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2490+6233G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202503055 | ||||||
| chr1:202503241
|
G | A | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2490+6419G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202503241 | ||||||
| chr1:202503725
|
C | T | 1 | a0001c0001t0049g0245 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2490+6903C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202503725 | ||||||
| chr1:202503754
|
G | A | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2490+6932G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202503754 | ||||||
| chr1:202504104
|
G | A | 1 | a0001c0001t0066g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2490+7282G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202504104 | ||||||
| chr1:202504198
|
C | T | 1 | a0001c0001t0071g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2490+7376C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202504198 | ||||||
| chr1:202504224
|
C | A | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2490+7402C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202504224 | ||||||
| chr1:202504254
|
G | T | 1 | a0001c0001t0003g0043 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2490+7432G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202504254 | ||||||
| chr1:202504364
|
G | T | 1 | a0001c0001t0010g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2490+7542G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202504364 | ||||||
| chr1:202504397
|
A | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2490+7575A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202504397 | ||||||
| chr1:202504485
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2490+7663G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202504485 | ||||||
| chr1:202504645
|
A | G | 6 | a0001c0001t0001g0230a0001c0001t0002g0161a0001c0001t0002g0162others(3): Show | 6 | HG00735.hp2 HG01099.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2490+7823A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202504645 | ||||||
| chr1:202504774
|
C | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2490+7952C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202504774 | ||||||
| chr1:202505055
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2490+8233G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202505055 | ||||||
| chr1:202505081
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2490+8259A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202505081 | ||||||
| chr1:202505132
|
G | A | 1 | a0001c0001t0010g0082 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2490+8310G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202505132 | ||||||
| chr1:202505388
|
A | G | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2490+8566A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202505388 | ||||||
| chr1:202505671
|
T | A | 132 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.2490+8849T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202505671 | ||||||
| chr1:202505911
|
G | A | 1 | a0001c0001t0071g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2490+9089G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202505911 | ||||||
| chr1:202505946
|
G | A | 2 | a0001c0001t0011g0114a0001c0001t0013g0116 | 2 | HG00642.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2490+9124G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202505946 | ||||||
| chr1:202506016
|
G | T | 2 | a0001c0001t0033g0090a0001c0001t0033g0091 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2490+9194G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202506016 | ||||||
| chr1:202506079
|
A | T | 2 | a0001c0001t0002g0172a0001c0001t0019g0167 | 2 | NA18975.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2490+9257A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202506079 | ||||||
| chr1:202506207
|
G | A | 1 | a0001c0001t0009g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2490+9385G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202506207 | ||||||
| chr1:202506362
|
C | A | 1 | a0001c0001t0102g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2490+9540C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202506362 | ||||||
| chr1:202506481
|
G | T | 1 | a0007c0005t0010g0061 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2490+9659G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202506481 | ||||||
| chr1:202506682
|
G | A | 4 | a0001c0001t0002g0235a0001c0001t0006g0207a0001c0001t0006g0236others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.2490+9860G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202506682 | ||||||
| chr1:202506754
|
T | A | 1 | a0001c0001t0070g0136 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2490+9932T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202506754 | ||||||
| chr1:202507135
|
T | G | 1 | a0001c0001t0004g0072 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2490+10313T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202507135 | ||||||
| chr1:202507140
|
A | G | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2490+10318A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202507140 | ||||||
| chr1:202507199
|
C | T | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2490+10377C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202507199 | ||||||
| chr1:202507411
|
C | G | 1 | a0001c0001t0076g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2490+10589C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202507411 | ||||||
| chr1:202507426
|
C | A | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2490+10604C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202507426 | ||||||
| chr1:202507594
|
A | G | 2 | a0002c0002t0007g0055a0002c0002t0007g0056 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2490+10772A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202507594 | ||||||
| chr1:202507730
|
T | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2490+10908T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202507730 | ||||||
| chr1:202507796
|
G | A | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2490+10974G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202507796 | ||||||
| chr1:202508243
|
T | C | 1 | a0001c0001t0033g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2490+11421T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202508243 | ||||||
| chr1:202508849
|
A | T | 2 | a0001c0001t0036g0017a0001c0001t0036g0074 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2490+12027A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202508849 | ||||||
| chr1:202508913
|
A | G | 3 | a0001c0001t0033g0090a0001c0001t0033g0091a0001c0001t0069g0098 | 3 | HG02109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2490+12091A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202508913 | ||||||
| chr1:202509196
|
G | C | 3 | a0001c0001t0001g0182a0001c0001t0005g0183a0001c0001t0005g0184 | 3 | HG00408.hp1 HG02071.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2490+12374G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202509196 | ||||||
| chr1:202509207
|
C | CCT | 158 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.2490+12385_2490+12 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202509207 | ||||||
| chr1:202509385
|
C | G | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2490+12563C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202509385 | ||||||
| chr1:202509824
|
G | T | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2490+13002G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202509824 | ||||||
| chr1:202509995
|
A | G | 1 | a0001c0001t0105g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2490+13173A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202509995 | ||||||
| chr1:202510064
|
T | G | 52 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(49): Show | 52 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2490+13242T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202510064 | ||||||
| chr1:202510154
|
A | T | 1 | a0001c0001t0096g0052 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2490+13332A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202510154 | ||||||
| chr1:202510381
|
A | G | 1 | a0001c0001t0012g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2490+13559A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202510381 | ||||||
| chr1:202510515
|
A | G | 1 | a0001c0001t0092g0024 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2490+13693A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202510515 | ||||||
| chr1:202510551
|
G | A | 1 | a0001c0001t0099g0138 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2490+13729G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202510551 | ||||||
| chr1:202510957
|
G | T | 132 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.2490+14135G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202510957 | ||||||
| chr1:202511222
|
GT | G | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2490+14412delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202511222 | |||||
| chr1:202511261
|
G | C | 1 | a0001c0001t0083g0081 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2490+14439G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202511261 | ||||||
| chr1:202511337
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2490+14515C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202511337 | ||||||
| chr1:202511378
|
G | A | 1 | a0001c0001t0039g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2490+14556G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202511378 | ||||||
| chr1:202511771
|
A | AT | 9 | a0001c0001t0003g0053a0001c0001t0004g0089a0001c0001t0004g0127others(6): Show | 9 | HG02027.hp2 HG02148.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.2490+14971dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202511771 | |||||
| chr1:202511771
|
AT | A | 48 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0001g0203others(45): Show | 48 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.2490+14971delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202511771 | |||||
| chr1:202511771
|
ATT | A | 70 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(67): Show | 70 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.2490+14970_2490+14 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202511771 | |||||
| chr1:202511771
|
ATTT | A | 5 | a0001c0001t0001g0191a0001c0001t0005g0222a0001c0001t0020g0217others(2): Show | 5 | HG02004.hp1 HG03471.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2490+14969_2490+14 others(9): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202511771 | |||||
| chr1:202511813
|
G | C | 1 | a0001c0001t0071g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2490+14991G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202511813 | ||||||
| chr1:202511972
|
G | T | 13 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0001g0203others(10): Show | 13 | HG00323.hp2 HG00408.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2490+15150G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202511972 | ||||||
| chr1:202512188
|
T | C | 1 | a0001c0001t0004g0092 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2490+15366T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202512188 | ||||||
| chr1:202512825
|
A | G | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2490+16003A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202512825 | ||||||
| chr1:202512877
|
C | G | 4 | a0001c0001t0002g0235a0001c0001t0006g0207a0001c0001t0006g0236others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.2490+16055C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202512877 | ||||||
| chr1:202513204
|
C | T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2490+16382C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202513204 | ||||||
| chr1:202513390
|
T | C | 1 | a0001c0001t0017g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2490+16568T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202513390 | ||||||
| chr1:202513825
|
T | A | 51 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0029others(48): Show | 51 | HG00099.hp2 HG00735.hp1 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.2490+17003T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202513825 | ||||||
| chr1:202514152
|
T | C | 1 | a0001c0001t0005g0184 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2490+17330T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202514152 | ||||||
| chr1:202514335
|
T | C | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2490+17513T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202514335 | ||||||
| chr1:202514550
|
A | G | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2490+17728A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202514550 | ||||||
| chr1:202514560
|
G | T | 1 | a0001c0001t0042g0226 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2490+17738G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202514560 | ||||||
| chr1:202515255
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2490+18433T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202515255 | ||||||
| chr1:202515264
|
C | A | 1 | a0001c0001t0016g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2490+18442C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202515264 | ||||||
| chr1:202515296
|
GTGTT | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2490+18484_2490+18 others(10): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202515296 | |||||
| chr1:202515632
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2490+18810C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202515632 | ||||||
| chr1:202515796
|
C | T | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2490+18974C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202515796 | ||||||
| chr1:202515946
|
G | A | 42 | a0001c0001t0001g0160a0001c0001t0001g0182a0001c0001t0001g0195others(39): Show | 42 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.2490+19124G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202515946 | ||||||
| chr1:202515990
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2490+19168A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202515990 | ||||||
| chr1:202516345
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2490+19523A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202516345 | ||||||
| chr1:202516383
|
T | C | 1 | a0001c0001t0006g0193 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2490+19561T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202516383 | ||||||
| chr1:202516637
|
A | T | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2490+19815A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202516637 | ||||||
| chr1:202516881
|
A | G | 1 | a0001c0001t0007g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2490+20059A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202516881 | ||||||
| chr1:202516894
|
T | G | 253 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.2490+20072T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202516894 | ||||||
| chr1:202516908
|
ATTAG | A | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2490+20092_2490+20 others(10): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202516908 | |||||
| chr1:202517460
|
A | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2490+20638A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202517460 | ||||||
| chr1:202517630
|
CT | C | 97 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2490+20821delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202517630 | |||||
| chr1:202517892
|
C | T | 1 | a0001c0001t0021g0249 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2490+21070C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202517892 | ||||||
| chr1:202518393
|
A | T | 2 | a0001c0001t0014g0238a0001c0001t0014g0243 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2490+21571A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202518393 | ||||||
| chr1:202518400
|
A | G | 1 | a0005c0007t0009g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2490+21578A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202518400 | ||||||
| chr1:202518884
|
C | T | 1 | a0001c0001t0055g0113 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2490+22062C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202518884 | ||||||
| chr1:202518901
|
T | C | 6 | a0001c0001t0015g0205a0001c0001t0015g0206a0001c0001t0015g0208others(3): Show | 6 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.2490+22079T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202518901 | ||||||
| chr1:202519260
|
A | T | 1 | a0001c0001t0004g0089 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2490+22438A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202519260 | ||||||
| chr1:202519261
|
T | A | 158 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.2490+22439T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202519261 | ||||||
| chr1:202519597
|
C | T | 1 | a0001c0001t0039g0011 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2490+22775C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202519597 | ||||||
| chr1:202519606
|
C | G | 1 | a0001c0001t0002g0179 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2490+22784C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202519606 | ||||||
| chr1:202519885
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2490+23063G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202519885 | ||||||
| chr1:202519974
|
G | A | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2490+23152G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202519974 | ||||||
| chr1:202520090
|
T | A | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2490+23268T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202520090 | ||||||
| chr1:202520291
|
A | G | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2490+23469A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202520291 | ||||||
| chr1:202520405
|
T | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2490+23583T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202520405 | ||||||
| chr1:202520436
|
C | G | 1 | a0001c0001t0002g0179 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2490+23614C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202520436 | ||||||
| chr1:202520479
|
C | T | 1 | a0001c0001t0006g0193 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2490+23657C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202520479 | ||||||
| chr1:202520525
|
T | C | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2490+23703T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202520525 | ||||||
| chr1:202520752
|
G | T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2490+23930G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202520752 | ||||||
| chr1:202520765
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0005g0183a0001c0001t0005g0184 | 3 | HG00408.hp1 HG02071.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2490+23943T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202520765 | ||||||
| chr1:202520974
|
G | A | 1 | a0001c0001t0012g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2490+24152G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202520974 | ||||||
| chr1:202521023
|
C | G | 2 | a0001c0001t0001g0223a0001c0001t0002g0224 | 2 | NA18950.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.2490+24201C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202521023 | ||||||
| chr1:202521048
|
G | T | 1 | a0001c0001t0014g0251 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2490+24226G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202521048 | ||||||
| chr1:202521070
|
C | T | 1 | a0001c0001t0004g0084 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2490+24248C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202521070 | ||||||
| chr1:202521152
|
T | A | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2490+24330T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202521152 | ||||||
| chr1:202521408
|
A | T | 1 | a0001c0001t0033g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2490+24586A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202521408 | ||||||
| chr1:202521595
|
C | A | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2490+24773C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202521595 | ||||||
| chr1:202521914
|
G | A | 1 | a0001c0001t0010g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2490+25092G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202521914 | ||||||
| chr1:202522392
|
A | G | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2490+25570A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202522392 | ||||||
| chr1:202522411
|
A | G | 2 | a0001c0001t0004g0079a0001c0001t0004g0084 | 2 | HG00609.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.2490+25589A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202522411 | ||||||
| chr1:202522554
|
T | A | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2490+25732T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202522554 | ||||||
| chr1:202522797
|
T | A | 158 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.2490+25975T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202522797 | ||||||
| chr1:202523023
|
A | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2490+26201A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202523023 | ||||||
| chr1:202523290
|
G | A | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2490+26468G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202523290 | ||||||
| chr1:202523745
|
T | A | 1 | a0001c0001t0009g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2490+26923T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202523745 | ||||||
| chr1:202524105
|
C | T | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2490+27283C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202524105 | ||||||
| chr1:202524517
|
C | G | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2490+27695C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202524517 | ||||||
| chr1:202524561
|
G | T | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2490+27739G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202524561 | ||||||
| chr1:202524933
|
G | A | 1 | a0001c0001t0054g0111 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2490+28111G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202524933 | ||||||
| chr1:202524938
|
C | T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2490+28116C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202524938 | ||||||
| chr1:202524939
|
G | A | 2 | a0001c0001t0006g0163a0001c0001t0051g0232 | 2 | HG02258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2490+28117G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202524939 | ||||||
| chr1:202524958
|
A | G | 1 | a0001c0001t0080g0086 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2490+28136A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202524958 | ||||||
| chr1:202525062
|
G | A | 132 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.2490+28240G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202525062 | ||||||
| chr1:202525213
|
C | G | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2490+28391C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202525213 | ||||||
| chr1:202525224
|
C | T | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2490+28402C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202525224 | ||||||
| chr1:202525417
|
G | C | 1 | a0001c0001t0012g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2490+28595G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202525417 | ||||||
| chr1:202525486
|
T | C | 4 | a0001c0001t0004g0070a0001c0001t0009g0062a0001c0001t0010g0071others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2490+28664T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202525486 | ||||||
| chr1:202525631
|
G | T | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2490+28809G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202525631 | ||||||
| chr1:202525847
|
G | A | 1 | a0001c0001t0002g0178 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2490+29025G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202525847 | ||||||
| chr1:202525908
|
A | C | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2490+29086A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202525908 | ||||||
| chr1:202525992
|
T | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2490+29170T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202525992 | ||||||
| chr1:202526751
|
T | C | 1 | a0001c0001t0041g0227 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2490+29929T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202526751 | ||||||
| chr1:202526887
|
G | C | 1 | a0001c0001t0002g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2490+30065G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202526887 | ||||||
| chr1:202527085
|
C | CAGAAATT others(6050): Show |
1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2490+30279_2490+30 others(6063): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202527085 | |||||
| chr1:202527085
|
C | CAGAAATT others(6052): Show |
1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2490+30279_2490+30 others(6065): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202527085 | |||||
| chr1:202527349
|
T | C | 2 | a0001c0001t0003g0048a0001c0001t0096g0052 | 2 | NA18975.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2490+30527T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202527349 | ||||||
| chr1:202527654
|
C | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2490+30832C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202527654 | ||||||
| chr1:202527855
|
T | C | 1 | a0001c0001t0056g0209 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2491-31022T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202527855 | ||||||
| chr1:202528085
|
G | T | 253 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.2491-30792G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202528085 | ||||||
| chr1:202528193
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2491-30684G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202528193 | ||||||
| chr1:202528665
|
C | T | 42 | a0001c0001t0001g0160a0001c0001t0001g0182a0001c0001t0001g0195others(39): Show | 42 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.2491-30212C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202528665 | ||||||
| chr1:202528735
|
G | A | 2 | a0001c0001t0011g0114a0001c0001t0013g0116 | 2 | HG00642.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2491-30142G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202528735 | ||||||
| chr1:202528747
|
G | GT | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2491-30121dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202528747 | |||||
| chr1:202528983
|
A | G | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2491-29894A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202528983 | ||||||
| chr1:202529072
|
A | G | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG00099.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.2491-29805A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202529072 | ||||||
| chr1:202529210
|
G | A | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2491-29667G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202529210 | ||||||
| chr1:202529305
|
GA | G | 12 | a0001c0001t0006g0171a0001c0001t0008g0154a0001c0001t0026g0008others(9): Show | 12 | HG01346.hp1 HG02074.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2491-29557delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202529305 | |||||
| chr1:202529467
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2491-29410G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202529467 | ||||||
| chr1:202529714
|
A | G | 1 | a0005c0007t0009g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2491-29163A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202529714 | ||||||
| chr1:202529795
|
A | T | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2491-29082A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202529795 | ||||||
| chr1:202529947
|
A | G | 1 | a0001c0001t0006g0229 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2491-28930A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202529947 | ||||||
| chr1:202529980
|
T | G | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2491-28897T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202529980 | ||||||
| chr1:202530111
|
T | C | 2 | a0001c0001t0014g0238a0001c0001t0014g0243 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2491-28766T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202530111 | ||||||
| chr1:202530134
|
A | G | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2491-28743A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202530134 | ||||||
| chr1:202530193
|
T | C | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2491-28684T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202530193 | ||||||
| chr1:202530402
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2491-28475T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202530402 | ||||||
| chr1:202530478
|
A | G | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2491-28399A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202530478 | ||||||
| chr1:202530670
|
T | C | 1 | a0001c0001t0009g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2491-28207T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202530670 | ||||||
| chr1:202530818
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2491-28059G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202530818 | ||||||
| chr1:202531060
|
C | A | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2491-27817C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202531060 | ||||||
| chr1:202531221
|
C | T | 1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2491-27656C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202531221 | ||||||
| chr1:202531270
|
A | G | 2 | a0001c0001t0011g0114a0001c0001t0013g0116 | 2 | HG00642.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2491-27607A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202531270 | ||||||
| chr1:202531459
|
T | G | 1 | a0001c0001t0006g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2491-27418T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202531459 | ||||||
| chr1:202531550
|
A | T | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2491-27327A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202531550 | ||||||
| chr1:202531986
|
C | T | 4 | a0001c0001t0002g0235a0001c0001t0006g0207a0001c0001t0006g0236others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491-26891C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202531986 | ||||||
| chr1:202532563
|
G | A | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2491-26314G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202532563 | ||||||
| chr1:202532633
|
G | A | 106 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.2491-26244G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202532633 | ||||||
| chr1:202532660
|
A | G | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2491-26217A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202532660 | ||||||
| chr1:202532726
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2491-26151G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202532726 | ||||||
| chr1:202532860
|
C | CT | 33 | a0001c0001t0001g0174a0001c0001t0001g0195a0001c0001t0001g0230others(30): Show | 33 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.2491-25991dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202532860 | |||||
| chr1:202532860
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0160 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2491-26001_2491-25 others(17): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202532860 | |||||
| chr1:202532860
|
CT | C | 19 | a0001c0001t0002g0158a0001c0001t0003g0035a0001c0001t0003g0069others(16): Show | 19 | HG01070.hp2 HG01123.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.2491-25991delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202532860 | |||||
| chr1:202532954
|
C | G | 1 | a0007c0005t0010g0061 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2491-25923C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202532954 | ||||||
| chr1:202532977
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2491-25900C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202532977 | ||||||
| chr1:202533289
|
A | ATTTTG | 15 | a0001c0001t0004g0072a0001c0001t0004g0089a0001c0001t0004g0095others(12): Show | 15 | HG00673.hp2 HG01934.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.2491-25555_2491-25 others(11): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202533289 | |||||
| chr1:202533289
|
ATTTTG | A | 112 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.2491-25555_2491-25 others(11): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202533289 | |||||
| chr1:202533289
|
ATTTTGTT others(3): Show |
A | 1 | a0001c0001t0002g0094 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2491-25560_2491-25 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202533289 | |||||
| chr1:202533370
|
A | G | 1 | a0001c0001t0008g0153 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2491-25507A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202533370 | ||||||
| chr1:202533441
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2491-25436C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202533441 | ||||||
| chr1:202533463
|
G | T | 1 | a0001c0001t0016g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2491-25414G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202533463 | ||||||
| chr1:202533587
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2491-25290G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202533587 | ||||||
| chr1:202533611
|
G | A | 46 | a0001c0001t0001g0165a0001c0001t0001g0169a0001c0001t0001g0174others(43): Show | 46 | HG00280.hp2 HG00738.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.2491-25266G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202533611 | ||||||
| chr1:202533933
|
C | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2491-24944C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202533933 | ||||||
| chr1:202533949
|
C | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2491-24928C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202533949 | ||||||
| chr1:202534121
|
G | A | 1 | a0001c0001t0103g0026 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2491-24756G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202534121 | ||||||
| chr1:202534421
|
C | A | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2491-24456C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202534421 | ||||||
| chr1:202534563
|
CT | C | 120 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(117): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2491-24297delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202534563 | |||||
| chr1:202534563
|
CTT | C | 18 | a0001c0001t0005g0216a0001c0001t0006g0173a0001c0001t0008g0150others(15): Show | 18 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2491-24298_2491-24 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202534563 | |||||
| chr1:202534670
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2491-24207A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202534670 | ||||||
| chr1:202534725
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2491-24152C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202534725 | ||||||
| chr1:202534758
|
A | G | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2491-24119A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202534758 | ||||||
| chr1:202535043
|
G | GTGTGTGT others(5): Show |
2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2491-23822_2491-23 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202535043 | |||||
| chr1:202535055
|
A | ATG | 35 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0191others(32): Show | 35 | HG00280.hp2 HG01106.hp1 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.2491-23796_2491-23 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202535055 | |||||
| chr1:202535055
|
A | G | 9 | a0001c0001t0002g0158a0001c0001t0022g0105a0001c0001t0022g0112others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.2491-23822A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202535055 | ||||||
| chr1:202535409
|
TC | T | 3 | a0001c0001t0005g0198a0001c0001t0005g0202a0001c0001t0048g0197 | 3 | HG00323.hp2 HG01515.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2491-23466delC | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202535409 | |||||
| chr1:202535632
|
T | C | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2491-23245T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202535632 | ||||||
| chr1:202535638
|
C | T | 2 | a0001c0001t0011g0114a0001c0001t0013g0116 | 2 | HG00642.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2491-23239C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202535638 | ||||||
| chr1:202535814
|
C | T | 1 | a0001c0001t0079g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2491-23063C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202535814 | ||||||
| chr1:202536130
|
T | G | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2491-22747T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202536130 | ||||||
| chr1:202536155
|
T | C | 133 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(130): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.2491-22722T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202536155 | ||||||
| chr1:202536258
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2491-22619A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202536258 | ||||||
| chr1:202536319
|
C | A | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2491-22558C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202536319 | ||||||
| chr1:202536320
|
C | A | 12 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2491-22557C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202536320 | ||||||
| chr1:202536460
|
G | A | 1 | a0001c0001t0009g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2491-22417G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202536460 | ||||||
| chr1:202537124
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0211a0001c0001t0009g0062 | 3 | HG01243.hp1 NA18945.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2491-21753C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202537124 | ||||||
| chr1:202537211
|
C | G | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2491-21666C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202537211 | ||||||
| chr1:202537212
|
G | A | 25 | a0001c0001t0002g0158a0001c0001t0011g0107a0001c0001t0011g0114others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.2491-21665G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202537212 | ||||||
| chr1:202537219
|
TGGCA | T | 6 | a0001c0001t0007g0040a0001c0001t0018g0039a0001c0001t0018g0041others(3): Show | 6 | NA18943.hp1 NA18970.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.2491-21654_2491-21 others(10): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202537219 | |||||
| chr1:202537287
|
G | C | 1 | a0001c0001t0083g0081 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2491-21590G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202537287 | ||||||
| chr1:202537311
|
G | A | 1 | a0001c0001t0005g0198 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2491-21566G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202537311 | ||||||
| chr1:202537731
|
G | C | 6 | a0001c0001t0015g0205a0001c0001t0015g0206a0001c0001t0015g0208others(3): Show | 6 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.2491-21146G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202537731 | ||||||
| chr1:202538010
|
CAG | C | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2491-20864_2491-20 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202538010 | |||||
| chr1:202538147
|
C | A | 1 | a0001c0001t0023g0106 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2491-20730C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202538147 | ||||||
| chr1:202539002
|
G | A | 2 | a0001c0001t0011g0114a0001c0001t0013g0116 | 2 | HG00642.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2491-19875G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202539002 | ||||||
| chr1:202539475
|
C | T | 1 | a0001c0001t0047g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2491-19402C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202539475 | ||||||
| chr1:202540020
|
T | C | 1 | a0008c0006t0001g0190 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2491-18857T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202540020 | ||||||
| chr1:202540421
|
C | T | 2 | a0001c0001t0032g0057a0001c0001t0032g0058 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2491-18456C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202540421 | ||||||
| chr1:202540878
|
A | C | 1 | a0001c0001t0079g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2491-17999A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202540878 | ||||||
| chr1:202541124
|
T | G | 1 | a0001c0001t0071g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2491-17753T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202541124 | ||||||
| chr1:202541229
|
G | GT | 145 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(142): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2491-17639dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202541229 | |||||
| chr1:202541239
|
C | T | 1 | a0001c0001t0094g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2491-17638C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202541239 | ||||||
| chr1:202541347
|
GAATACCA others(7): Show |
G | 1 | a0001c0001t0006g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2491-17528_2491-17 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202541347 | |||||
| chr1:202541666
|
A | G | 1 | a0001c0001t0017g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2491-17211A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202541666 | ||||||
| chr1:202541753
|
C | T | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2491-17124C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202541753 | ||||||
| chr1:202542066
|
G | A | 1 | a0001c0001t0004g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2491-16811G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202542066 | ||||||
| chr1:202542095
|
T | C | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2491-16782T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202542095 | ||||||
| chr1:202542167
|
C | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2491-16710C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202542167 | ||||||
| chr1:202542725
|
C | T | 1 | a0001c0001t0078g0050 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2491-16152C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202542725 | ||||||
| chr1:202542769
|
A | C | 46 | a0001c0001t0001g0165a0001c0001t0001g0169a0001c0001t0001g0174others(43): Show | 46 | HG00280.hp2 HG00738.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.2491-16108A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202542769 | ||||||
| chr1:202542948
|
A | G | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2491-15929A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202542948 | ||||||
| chr1:202543090
|
A | G | 1 | a0001c0001t0069g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2491-15787A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202543090 | ||||||
| chr1:202543118
|
T | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2491-15759T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202543118 | ||||||
| chr1:202543399
|
T | C | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2491-15478T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202543399 | ||||||
| chr1:202543523
|
C | T | 3 | a0001c0001t0027g0129a0001c0001t0027g0130a0001c0001t0046g0170 | 3 | HG02818.hp2 HG03710.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2491-15354C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202543523 | ||||||
| chr1:202543558
|
T | C | 2 | a0001c0001t0026g0008a0001c0001t0026g0009 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2491-15319T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202543558 | ||||||
| chr1:202543569
|
A | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2491-15308A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202543569 | ||||||
| chr1:202543667
|
G | C | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2491-15210G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202543667 | ||||||
| chr1:202544234
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2491-14643C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202544234 | ||||||
| chr1:202544336
|
A | G | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2491-14541A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202544336 | ||||||
| chr1:202544693
|
A | G | 2 | a0001c0001t0015g0205a0001c0001t0015g0208 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2491-14184A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202544693 | ||||||
| chr1:202544964
|
C | T | 158 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.2491-13913C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202544964 | ||||||
| chr1:202545110
|
G | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2491-13767G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202545110 | ||||||
| chr1:202545247
|
T | G | 2 | a0001c0001t0014g0251a0001c0001t0058g0250 | 2 | HG02080.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2491-13630T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202545247 | ||||||
| chr1:202545277
|
A | G | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2491-13600A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202545277 | ||||||
| chr1:202545304
|
G | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0002g0168others(4): Show | 7 | HG01261.hp2 HG01346.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.2491-13573G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202545304 | ||||||
| chr1:202545401
|
T | C | 2 | a0001c0001t0014g0238a0001c0001t0014g0243 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2491-13476T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202545401 | ||||||
| chr1:202545432
|
G | A | 1 | a0001c0001t0046g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2491-13445G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202545432 | ||||||
| chr1:202545484
|
T | G | 2 | a0001c0001t0100g0142a0001c0001t0101g0144 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2491-13393T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202545484 | ||||||
| chr1:202545818
|
G | A | 96 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2491-13059G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202545818 | ||||||
| chr1:202545822
|
A | G | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2491-13055A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202545822 | ||||||
| chr1:202546350
|
A | G | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2491-12527A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202546350 | ||||||
| chr1:202546532
|
A | G | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2491-12345A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202546532 | ||||||
| chr1:202546807
|
A | G | 1 | a0001c0001t0098g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2491-12070A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202546807 | ||||||
| chr1:202546914
|
A | G | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2491-11963A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202546914 | ||||||
| chr1:202546992
|
A | G | 253 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.2491-11885A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202546992 | ||||||
| chr1:202547038
|
CAA | C | 96 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2491-11837_2491-11 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202547038 | |||||
| chr1:202547068
|
A | G | 1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2491-11809A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202547068 | ||||||
| chr1:202547538
|
T | C | 2 | a0001c0001t0009g0065a0001c0001t0009g0066 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2491-11339T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202547538 | ||||||
| chr1:202547747
|
A | C | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2491-11130A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202547747 | ||||||
| chr1:202547995
|
A | C | 5 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2491-10882A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202547995 | ||||||
| chr1:202548022
|
A | G | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2491-10855A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548022 | ||||||
| chr1:202548068
|
G | A | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2491-10809G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548068 | ||||||
| chr1:202548236
|
C | A | 96 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2491-10641C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548236 | ||||||
| chr1:202548348
|
ATGTTTTG others(3): Show |
A | 1 | a0001c0001t0044g0252 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2491-10512_2491-10 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548348 | |||||
| chr1:202548570
|
C | T | 1 | a0001c0001t0079g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2491-10307C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548570 | ||||||
| chr1:202548614
|
T | A | 1 | a0001c0001t0104g0101 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2491-10263T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548614 | ||||||
| chr1:202548769
|
GCTCGCTG others(3): Show |
G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2491-10104_2491-10 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548769 | |||||
| chr1:202548773
|
GCTGTCTC others(1): Show |
G | 12 | a0001c0001t0001g0165a0001c0001t0001g0219a0001c0001t0001g0221others(9): Show | 12 | HG00642.hp2 HG01099.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2491-10101_2491-10 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548773 | |||||
| chr1:202548773
|
GCTGTCTC others(3): Show |
G | 16 | a0001c0001t0001g0169a0001c0001t0001g0186a0001c0001t0001g0211others(13): Show | 16 | HG02027.hp1 HG02155.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2491-10101_2491-10 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548773 | |||||
| chr1:202548773
|
GCTGTCTC others(5): Show |
G | 2 | a0001c0001t0005g0220a0001c0001t0025g0233 | 2 | HG01934.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2491-10101_2491-10 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548773 | |||||
| chr1:202548773
|
GCTGTCTC others(7): Show |
G | 2 | a0001c0001t0006g0193a0001c0001t0045g0189 | 2 | HG01106.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2491-10101_2491-10 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548773 | |||||
| chr1:202548776
|
G | C | 68 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0182others(65): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2491-10101G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548776 | ||||||
| chr1:202548776
|
G | GTC | 23 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0067others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.2491-10069_2491-10 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548776 | |||||
| chr1:202548776
|
G | GTCTC | 18 | a0001c0001t0003g0043a0001c0001t0003g0053a0001c0001t0009g0065others(15): Show | 18 | HG01123.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2491-10071_2491-10 others(10): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548776 | |||||
| chr1:202548776
|
G | GTCTCTCT others(1): Show |
4 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(1): Show | 4 | HG01192.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491-10075_2491-10 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548776 | |||||
| chr1:202548776
|
G | GTCTCTCT others(5): Show |
1 | a0001c0001t0004g0092 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2491-10079_2491-10 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548776 | |||||
| chr1:202548776
|
GTCTCTCT others(3): Show |
G | 1 | a0001c0001t0004g0127 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2491-10077_2491-10 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548776 | |||||
| chr1:202548798
|
CTCTCTCT others(7): Show |
C | 5 | a0001c0001t0001g0191a0001c0001t0002g0200a0001c0001t0002g0204others(2): Show | 5 | HG01515.hp2 HG01517.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.2491-10077_2491-10 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548798 | |||||
| chr1:202548800
|
CTCTCTCT others(5): Show |
C | 5 | a0001c0001t0005g0248a0001c0001t0015g0206a0001c0001t0026g0008others(2): Show | 5 | HG00639.hp1 HG02523.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2491-10075_2491-10 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548800 | |||||
| chr1:202548800
|
CTCTCTCT others(7): Show |
C | 5 | a0001c0001t0005g0194a0001c0001t0005g0198a0001c0001t0005g0202others(2): Show | 5 | HG00323.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2491-10075_2491-10 others(20): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548800 | |||||
| chr1:202548802
|
CTCTCTCT others(3): Show |
C | 16 | a0001c0001t0001g0242a0001c0001t0001g0246a0001c0001t0002g0172others(13): Show | 16 | HG00597.hp2 HG01069.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.2491-10073_2491-10 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548802 | |||||
| chr1:202548802
|
CTCTCTCT others(5): Show |
C | 1 | a0001c0001t0021g0249 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2491-10073_2491-10 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548802 | |||||
| chr1:202548804
|
C | A | 3 | a0001c0001t0034g0044a0001c0001t0034g0045a0001c0001t0088g0085 | 3 | HG00673.hp2 HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2491-10073C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548804 | ||||||
| chr1:202548804
|
CTCTCTAT others(1): Show |
C | 7 | a0001c0001t0001g0201a0001c0001t0001g0230a0001c0001t0002g0196others(4): Show | 7 | HG00735.hp2 HG01993.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2491-10071_2491-10 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548804 | |||||
| chr1:202548804
|
CTCTCTAT others(3): Show |
C | 16 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0192others(13): Show | 16 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(13): Show |
intron_variant | MODIFIER | c.2491-10071_2491-10 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548804 | |||||
| chr1:202548804
|
CTCTCTAT others(5): Show |
C | 1 | a0001c0001t0021g0254 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2491-10071_2491-10 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548804 | |||||
| chr1:202548806
|
C | A | 8 | a0001c0001t0003g0021a0001c0001t0003g0031a0001c0001t0004g0127others(5): Show | 8 | HG00673.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2491-10071C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548806 | ||||||
| chr1:202548806
|
CTCTATA | C | 5 | a0001c0001t0002g0239a0001c0001t0024g0164a0001c0001t0027g0129others(2): Show | 5 | HG02818.hp2 HG04199.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.2491-10069_2491-10 others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548806 | |||||
| chr1:202548806
|
CTCTATAT others(1): Show |
C | 5 | a0001c0001t0001g0160a0001c0001t0001g0195a0001c0001t0001g0244others(2): Show | 5 | HG00609.hp2 HG02559.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.2491-10069_2491-10 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548806 | |||||
| chr1:202548806
|
CTCTATAT others(3): Show |
C | 2 | a0001c0001t0037g0006a0001c0001t0049g0245 | 2 | HG03041.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.2491-10069_2491-10 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548806 | |||||
| chr1:202548808
|
C | A | 28 | a0001c0001t0001g0165a0001c0001t0001g0225a0001c0001t0002g0094others(25): Show | 28 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.2491-10069C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548808 | ||||||
| chr1:202548808
|
C | CTA | 3 | a0001c0001t0004g0087a0001c0001t0031g0001a0001c0001t0099g0138 | 3 | HG02055.hp1 HG02559.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2491-10042_2491-10 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548808 | |||||
| chr1:202548808
|
C | CTATA | 6 | a0001c0001t0003g0013a0001c0001t0003g0034a0001c0001t0003g0035others(3): Show | 6 | HG01515.hp1 HG01517.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2491-10044_2491-10 others(10): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548808 | |||||
| chr1:202548808
|
C | CTCTA | 5 | a0001c0001t0003g0048a0001c0001t0016g0022a0001c0001t0016g0023others(2): Show | 5 | HG02523.hp2 NA18522.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.2491-10068_2491-10 others(10): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548808 | |||||
| chr1:202548808
|
C | CTCTCTA | 3 | a0001c0001t0003g0030a0001c0001t0096g0052a0007c0005t0010g0061 | 3 | HG01993.hp1 NA18975.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2491-10068_2491-10 others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548808 | |||||
| chr1:202548808
|
C | CTCTCTAT others(17): Show |
1 | a0001c0001t0097g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2491-10068_2491-10 others(30): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548808 | |||||
| chr1:202548808
|
C | CTCTCTCT others(3): Show |
1 | a0001c0001t0007g0049 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2491-10068_2491-10 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548808 | |||||
| chr1:202548808
|
CTA | C | 10 | a0001c0001t0008g0156a0001c0001t0023g0106a0001c0001t0023g0110others(7): Show | 10 | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2491-10042_2491-10 others(8): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548808 | |||||
| chr1:202548808
|
CTATATA | C | 3 | a0001c0001t0006g0173a0001c0001t0006g0237a0001c0001t0072g0012 | 3 | HG01433.hp1 HG02622.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.2491-10046_2491-10 others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548808 | |||||
| chr1:202548808
|
CTATATAT others(3): Show |
C | 1 | a0001c0001t0050g0175 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2491-10050_2491-10 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202548808 | |||||
| chr1:202548810
|
A | C | 80 | a0001c0001t0001g0169a0001c0001t0001g0186a0001c0001t0001g0211others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2491-10067A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548810 | ||||||
| chr1:202548812
|
A | C | 43 | a0001c0001t0002g0158a0001c0001t0003g0032a0001c0001t0004g0070others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.2491-10065A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548812 | ||||||
| chr1:202548814
|
A | C | 24 | a0001c0001t0004g0070a0001c0001t0004g0075a0001c0001t0004g0092others(21): Show | 24 | HG00639.hp2 HG00733.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.2491-10063A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548814 | ||||||
| chr1:202548816
|
A | C | 7 | a0001c0001t0006g0173a0001c0001t0012g0148a0001c0001t0013g0126others(4): Show | 7 | HG01192.hp2 HG02071.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2491-10061A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548816 | ||||||
| chr1:202548818
|
A | C | 1 | a0001c0001t0066g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2491-10059A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548818 | ||||||
| chr1:202548889
|
A | G | 28 | a0001c0001t0004g0145a0001c0001t0008g0150a0001c0001t0008g0152others(25): Show | 28 | HG01123.hp1 HG01192.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.2491-9988A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548889 | ||||||
| chr1:202548973
|
C | G | 1 | a0001c0001t0015g0206 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2491-9904C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202548973 | ||||||
| chr1:202549163
|
C | G | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2491-9714C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202549163 | ||||||
| chr1:202549180
|
C | T | 1 | a0001c0001t0008g0154 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2491-9697C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202549180 | ||||||
| chr1:202549291
|
G | A | 1 | a0001c0001t0011g0107 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2491-9586G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202549291 | ||||||
| chr1:202549420
|
C | CT | 8 | a0001c0001t0003g0030a0001c0001t0015g0206a0001c0001t0021g0254others(5): Show | 8 | HG00639.hp1 HG00738.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.2491-9440dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202549420 | |||||
| chr1:202549443
|
G | A | 2 | a0001c0001t0027g0129a0001c0001t0027g0130 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2491-9434G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202549443 | ||||||
| chr1:202549481
|
G | A | 1 | a0001c0001t0006g0173 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2491-9396G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202549481 | ||||||
| chr1:202549534
|
C | T | 2 | a0001c0001t0072g0012a0001c0001t0073g0010 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2491-9343C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202549534 | ||||||
| chr1:202549643
|
C | T | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2491-9234C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202549643 | ||||||
| chr1:202549708
|
G | A | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2491-9169G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202549708 | ||||||
| chr1:202549786
|
G | A | 1 | a0001c0001t0007g0049 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2491-9091G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202549786 | ||||||
| chr1:202549822
|
A | G | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2491-9055A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202549822 | ||||||
| chr1:202550167
|
C | G | 7 | a0001c0001t0004g0095a0001c0001t0004g0127a0001c0001t0010g0083others(4): Show | 7 | HG00673.hp2 NA18952.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.2491-8710C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202550167 | ||||||
| chr1:202550290
|
C | T | 2 | a0001c0001t0027g0129a0001c0001t0027g0130 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2491-8587C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202550290 | ||||||
| chr1:202550501
|
A | C | 1 | a0001c0001t0082g0097 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2491-8376A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202550501 | ||||||
| chr1:202550772
|
G | C | 96 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.2491-8105G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202550772 | ||||||
| chr1:202551030
|
A | T | 3 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007 | 3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2491-7847A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202551030 | ||||||
| chr1:202551461
|
C | T | 28 | a0001c0001t0001g0165a0001c0001t0001g0186a0001c0001t0001g0191others(25): Show | 28 | HG00280.hp2 HG01106.hp1 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.2491-7416C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202551461 | ||||||
| chr1:202551527
|
A | AT | 101 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2491-7340dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202551527 | |||||
| chr1:202551585
|
A | AG | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2491-7291dupG | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202551585 | |||||
| chr1:202551797
|
A | T | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2491-7080A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202551797 | ||||||
| chr1:202551837
|
G | A | 15 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0001g0203others(12): Show | 15 | HG00323.hp2 HG00408.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.2491-7040G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202551837 | ||||||
| chr1:202552044
|
T | C | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2491-6833T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202552044 | ||||||
| chr1:202552157
|
A | C | 5 | a0001c0001t0004g0004a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2491-6720A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202552157 | ||||||
| chr1:202552505
|
G | A | 11 | a0001c0001t0008g0150a0001c0001t0008g0152a0001c0001t0008g0153others(8): Show | 11 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2491-6372G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202552505 | ||||||
| chr1:202552529
|
C | G | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2491-6348C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202552529 | ||||||
| chr1:202552619
|
C | A | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2491-6258C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202552619 | ||||||
| chr1:202552774
|
T | C | 1 | a0001c0001t0066g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2491-6103T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202552774 | ||||||
| chr1:202552806
|
A | G | 5 | a0001c0001t0013g0093a0001c0001t0013g0126a0001c0001t0029g0123others(2): Show | 5 | HG02071.hp1 NA18954.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2491-6071A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202552806 | ||||||
| chr1:202552911
|
C | T | 2 | a0001c0001t0041g0227a0001c0001t0042g0226 | 2 | NA18944.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.2491-5966C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202552911 | ||||||
| chr1:202553226
|
G | A | 8 | a0001c0001t0004g0004a0001c0001t0004g0070a0001c0001t0004g0075others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2491-5651G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202553226 | ||||||
| chr1:202553321
|
T | G | 1 | a0001c0001t0005g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2491-5556T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202553321 | ||||||
| chr1:202553374
|
G | T | 1 | a0001c0001t0005g0194 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2491-5503G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202553374 | ||||||
| chr1:202553411
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2491-5466A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202553411 | ||||||
| chr1:202553506
|
A | G | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2491-5371A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202553506 | ||||||
| chr1:202553543
|
G | T | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2491-5334G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202553543 | ||||||
| chr1:202553633
|
G | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0037 | 2 | NA18960.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2491-5244G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202553633 | ||||||
| chr1:202554766
|
C | A | 2 | a0001c0001t0014g0238a0001c0001t0014g0243 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2491-4111C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202554766 | ||||||
| chr1:202554836
|
G | A | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2491-4041G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202554836 | ||||||
| chr1:202554890
|
T | C | 1 | a0001c0001t0070g0136 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2491-3987T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202554890 | ||||||
| chr1:202555028
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2491-3849C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202555028 | ||||||
| chr1:202555325
|
G | GA | 7 | a0001c0001t0004g0087a0001c0001t0008g0153a0001c0001t0013g0093others(4): Show | 7 | HG02572.hp1 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2491-3524dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
G | GAA | 7 | a0001c0001t0017g0137a0001c0001t0017g0141a0001c0001t0017g0143others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2491-3525_2491-352 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
G | GAAAAAAA others(1): Show |
7 | a0001c0001t0001g0160a0001c0001t0002g0172a0001c0001t0002g0204others(4): Show | 7 | HG00408.hp1 HG00609.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.2491-3531_2491-352 others(12): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
G | GAAAAAAA others(2): Show |
30 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0001g0182others(27): Show | 30 | HG00280.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2491-3532_2491-352 others(13): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
G | GAAAAAAA others(3): Show |
34 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0203others(31): Show | 34 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.2491-3533_2491-352 others(14): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
G | GAAAAAAA others(4): Show |
12 | a0001c0001t0001g0219a0001c0001t0001g0223a0001c0001t0001g0242others(9): Show | 12 | HG01106.hp1 HG01258.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.2491-3534_2491-352 others(15): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
G | GAAAAAAA others(5): Show |
7 | a0001c0001t0001g0244a0001c0001t0002g0253a0001c0001t0005g0222others(4): Show | 7 | HG00597.hp2 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2491-3535_2491-352 others(16): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
G | GAAAAAAA others(6): Show |
4 | a0001c0001t0001g0165a0001c0001t0001g0221a0001c0001t0020g0215others(1): Show | 4 | HG02056.hp2 NA18963.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491-3536_2491-352 others(17): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
G | GAAAAAAA others(7): Show |
1 | a0001c0001t0005g0220 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2491-3537_2491-352 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
G | GAAAAAAA others(10): Show |
1 | a0001c0001t0006g0229 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2491-3540_2491-352 others(21): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
GA | G | 54 | a0001c0001t0002g0158a0001c0001t0003g0021a0001c0001t0003g0048others(51): Show | 54 | HG00639.hp2 HG00673.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.2491-3524delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
GAA | G | 36 | a0001c0001t0003g0013a0001c0001t0003g0029a0001c0001t0003g0030others(33): Show | 36 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2491-3525_2491-352 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555325
|
GAAAAAAA others(7): Show |
G | 1 | a0001c0001t0067g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2491-3537_2491-352 others(18): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555325 | |||||
| chr1:202555349
|
A | G | 1 | a0001c0001t0098g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2491-3528A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202555349 | ||||||
| chr1:202555418
|
T | A | 1 | a0001c0001t0102g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2491-3459T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202555418 | ||||||
| chr1:202555463
|
T | TA | 9 | a0001c0001t0002g0094a0001c0001t0013g0093a0001c0001t0031g0001others(6): Show | 9 | HG01175.hp1 HG02055.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.2491-3394dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555463 | |||||
| chr1:202555463
|
TA | T | 10 | a0001c0001t0002g0235a0001c0001t0003g0035a0001c0001t0004g0015others(7): Show | 10 | HG00099.hp1 HG00323.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.2491-3394delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr1 | 202555463 | |||||
| chr1:202555637
|
A | G | 2 | a0001c0001t0031g0001a0001c0001t0031g0002 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2491-3240A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202555637 | ||||||
| chr1:202555714
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2491-3163G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202555714 | ||||||
| chr1:202555793
|
G | A | 4 | a0001c0001t0002g0235a0001c0001t0006g0207a0001c0001t0006g0236others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491-3084G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202555793 | ||||||
| chr1:202555861
|
A | G | 2 | a0001c0001t0061g0132a0004c0008t0064g0134 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2491-3016A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202555861 | ||||||
| chr1:202556155
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2491-2722C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202556155 | ||||||
| chr1:202556182
|
G | A | 10 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(7): Show | 10 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2491-2695G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202556182 | ||||||
| chr1:202556601
|
A | G | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2491-2276A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202556601 | ||||||
| chr1:202556732
|
G | C | 4 | a0001c0001t0004g0070a0001c0001t0009g0062a0001c0001t0010g0071others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491-2145G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202556732 | ||||||
| chr1:202557514
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2491-1363G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202557514 | ||||||
| chr1:202557794
|
A | T | 5 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007others(2): Show | 5 | HG02622.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2491-1083A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202557794 | ||||||
| chr1:202558634
|
T | C | 1 | a0001c0001t0076g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2491-243T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202558634 | ||||||
| chr1:202558825
|
G | A | 2 | a0001c0001t0011g0114a0001c0001t0013g0116 | 2 | HG00642.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2491-52G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 18/23 | chr1 | 202558825 | ||||||
| chr1:202559136
|
A | G | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2507+243A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202559136 | ||||||
| chr1:202559165
|
G | A | 2 | a0001c0001t0009g0065a0001c0001t0009g0066 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2507+272G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202559165 | ||||||
| chr1:202559379
|
A | C | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2507+486A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202559379 | ||||||
| chr1:202559517
|
C | A | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2507+624C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202559517 | ||||||
| chr1:202559538
|
C | T | 1 | a0001c0001t0072g0012 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2507+645C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202559538 | ||||||
| chr1:202559619
|
C | T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2507+726C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202559619 | ||||||
| chr1:202559659
|
A | G | 1 | a0001c0001t0009g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2507+766A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202559659 | ||||||
| chr1:202559872
|
G | A | 2 | a0002c0002t0007g0055a0002c0002t0007g0056 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2507+979G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202559872 | ||||||
| chr1:202559908
|
C | T | 1 | a0001c0001t0005g0199 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2507+1015C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202559908 | ||||||
| chr1:202559934
|
A | G | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2507+1041A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202559934 | ||||||
| chr1:202560302
|
C | T | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2507+1409C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202560302 | ||||||
| chr1:202560705
|
T | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2507+1812T>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202560705 | ||||||
| chr1:202560830
|
A | T | 1 | a0001c0001t0063g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2507+1937A>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202560830 | ||||||
| chr1:202560912
|
C | T | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2508-1866C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202560912 | ||||||
| chr1:202561091
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2508-1687A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202561091 | ||||||
| chr1:202561231
|
TAAG | T | 3 | a0001c0001t0034g0044a0001c0001t0034g0045a0001c0001t0105g0014 | 3 | HG02258.hp1 HG02280.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2508-1543_2508-154 others(7): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr1 | 202561231 | |||||
| chr1:202561385
|
C | CT | 26 | a0001c0001t0002g0158a0001c0001t0004g0127a0001c0001t0011g0107others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.2508-1379dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr1 | 202561385 | |||||
| chr1:202561834
|
C | T | 3 | a0001c0001t0024g0164a0001c0001t0024g0185a0001c0001t0056g0209 | 3 | HG02698.hp2 HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2508-944C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202561834 | ||||||
| chr1:202562043
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2508-735G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202562043 | ||||||
| chr1:202562238
|
A | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2508-540A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202562238 | ||||||
| chr1:202562518
|
T | G | 158 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.2508-260T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202562518 | ||||||
| chr1:202562545
|
A | G | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2508-233A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202562545 | ||||||
| chr1:202562574
|
A | G | 1 | a0001c0001t0022g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2508-204A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202562574 | ||||||
| chr1:202562588
|
A | G | 1 | a0001c0001t0097g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2508-190A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202562588 | ||||||
| chr1:202562613
|
C | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2508-165C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 19/23 | chr1 | 202562613 | ||||||
| chr1:202563154
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2652+232T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/23 | chr1 | 202563154 | ||||||
| chr1:202563187
|
G | A | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2652+265G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/23 | chr1 | 202563187 | ||||||
| chr1:202563444
|
A | G | 3 | a0001c0001t0034g0044a0001c0001t0034g0045a0001c0001t0105g0014 | 3 | HG02258.hp1 HG02280.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2652+522A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/23 | chr1 | 202563444 | ||||||
| chr1:202563598
|
A | C | 1 | a0001c0001t0054g0111 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2652+676A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/23 | chr1 | 202563598 | ||||||
| chr1:202563626
|
T | TA | 35 | a0001c0001t0002g0158a0001c0001t0003g0034a0001c0001t0003g0035others(32): Show | 35 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.2652+722dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr1 | 202563626 | |||||
| chr1:202563626
|
TA | T | 20 | a0001c0001t0002g0178a0001c0001t0004g0092a0001c0001t0008g0150others(17): Show | 20 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.2652+722delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr1 | 202563626 | |||||
| chr1:202563626
|
TAA | T | 9 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(6): Show | 9 | HG01123.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2652+721_2652+722d others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr1 | 202563626 | |||||
| chr1:202563808
|
C | T | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2653-635C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/23 | chr1 | 202563808 | ||||||
| chr1:202564388
|
G | C | 26 | a0001c0001t0002g0158a0001c0001t0011g0107a0001c0001t0011g0114others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.2653-55G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/23 | chr1 | 202564388 | ||||||
| chr1:202564414
|
G | A | 1 | a0001c0001t0005g0248 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2653-29G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 20/23 | chr1 | 202564414 | ||||||
| chr1:202564554
|
C | T | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2757+7C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202564554 | ||||||
| chr1:202564752
|
C | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2757+205C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202564752 | ||||||
| chr1:202564980
|
G | A | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2757+433G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202564980 | ||||||
| chr1:202565261
|
T | C | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2757+714T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202565261 | ||||||
| chr1:202566141
|
G | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2757+1594G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202566141 | ||||||
| chr1:202566409
|
G | C | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2758-1369G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202566409 | ||||||
| chr1:202566669
|
G | A | 1 | a0001c0001t0087g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2758-1109G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202566669 | ||||||
| chr1:202566756
|
C | A | 1 | a0001c0001t0101g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2758-1022C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202566756 | ||||||
| chr1:202567012
|
C | T | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2758-766C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202567012 | ||||||
| chr1:202567135
|
C | A | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2758-643C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202567135 | ||||||
| chr1:202567347
|
C | T | 1 | a0001c0001t0087g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2758-431C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202567347 | ||||||
| chr1:202567380
|
C | CT | 102 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.2758-384dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr1 | 202567380 | |||||
| chr1:202567417
|
A | G | 1 | a0001c0001t0004g0095 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2758-361A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202567417 | ||||||
| chr1:202567720
|
C | T | 95 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2758-58C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 21/23 | chr1 | 202567720 | ||||||
| chr1:202567933
|
G | A | 1 | a0001c0001t0091g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2811+102G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 22/23 | chr1 | 202567933 | ||||||
| chr1:202567937
|
G | A | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2811+106G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 22/23 | chr1 | 202567937 | ||||||
| chr1:202568093
|
G | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0037 | 2 | NA18960.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2811+262G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 22/23 | chr1 | 202568093 | ||||||
| chr1:202568169
|
T | TAC | 47 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0001g0244others(44): Show | 47 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.2811+366_2811+367d others(4): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr1 | 202568169 | |||||
| chr1:202568169
|
TACAC | T | 4 | a0001c0001t0003g0031a0001c0001t0003g0034a0001c0001t0003g0035others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.2811+364_2811+367d others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr1 | 202568169 | |||||
| chr1:202568216
|
G | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2811+385G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 22/23 | chr1 | 202568216 | ||||||
| chr1:202568278
|
G | A | 8 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0037g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2811+447G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 22/23 | chr1 | 202568278 | ||||||
| chr1:202568728
|
C | T | 1 | a0001c0001t0002g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2812-419C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 22/23 | chr1 | 202568728 | ||||||
| chr1:202569029
|
C | T | 1 | a0001c0001t0065g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2812-118C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 22/23 | chr1 | 202569029 | ||||||
| chr1:202569125
|
C | T | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2812-22C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 22/23 | chr1 | 202569125 | ||||||
| chr1:202569275
|
G | T | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2862+78G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202569275 | ||||||
| chr1:202569344
|
C | G | 1 | a0001c0001t0006g0173 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2862+147C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202569344 | ||||||
| chr1:202569344
|
C | T | 6 | a0001c0001t0011g0119a0001c0001t0011g0120a0001c0001t0030g0115others(3): Show | 6 | HG00673.hp1 HG02074.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.2862+147C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202569344 | ||||||
| chr1:202569533
|
G | A | 3 | a0001c0001t0033g0090a0001c0001t0033g0091a0001c0001t0069g0098 | 3 | HG02109.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2862+336G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202569533 | ||||||
| chr1:202569607
|
C | T | 1 | a0001c0001t0010g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2862+410C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202569607 | ||||||
| chr1:202569782
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2862+585C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202569782 | ||||||
| chr1:202569970
|
C | G | 104 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2862+773C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202569970 | ||||||
| chr1:202570121
|
T | C | 1 | a0001c0001t0046g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2862+924T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202570121 | ||||||
| chr1:202571445
|
G | GT | 102 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.2862+2258dupT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr1 | 202571445 | |||||
| chr1:202571623
|
T | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2862+2426T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202571623 | ||||||
| chr1:202571746
|
GCGTCTGG others(6): Show |
G | 1 | a0001c0001t0053g0109 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2862+2551_2862+256 others(17): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr1 | 202571746 | |||||
| chr1:202571780
|
A | C | 1 | a0001c0001t0009g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2862+2583A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202571780 | ||||||
| chr1:202572254
|
A | G | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2862+3057A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202572254 | ||||||
| chr1:202573074
|
T | C | 6 | a0001c0001t0001g0230a0001c0001t0002g0161a0001c0001t0002g0162others(3): Show | 6 | HG00735.hp2 HG01099.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2862+3877T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202573074 | ||||||
| chr1:202573150
|
CT | C | 11 | a0001c0001t0004g0145a0001c0001t0017g0137a0001c0001t0017g0141others(8): Show | 11 | HG01123.hp1 HG01123.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2862+3957delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr1 | 202573150 | |||||
| chr1:202573219
|
T | C | 1 | a0004c0008t0064g0134 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2862+4022T>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202573219 | ||||||
| chr1:202573478
|
C | T | 1 | a0001c0001t0106g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2862+4281C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202573478 | ||||||
| chr1:202573487
|
G | C | 1 | a0001c0001t0104g0101 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2862+4290G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202573487 | ||||||
| chr1:202573535
|
A | G | 1 | a0001c0001t0012g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2862+4338A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202573535 | ||||||
| chr1:202574167
|
C | CA | 5 | a0001c0001t0003g0013a0001c0001t0003g0033a0001c0001t0009g0065others(2): Show | 5 | HG01099.hp2 HG02451.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.2862+4987dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr1 | 202574167 | |||||
| chr1:202574167
|
CA | C | 143 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(140): Show | 143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.2862+4987delA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr1 | 202574167 | |||||
| chr1:202574167
|
CAA | C | 10 | a0001c0001t0021g0254a0001c0001t0026g0008a0001c0001t0026g0009others(7): Show | 10 | HG02148.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2862+4986_2862+498 others(6): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr1 | 202574167 | |||||
| chr1:202574169
|
A | C | 1 | a0001c0001t0069g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2862+4972A>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202574169 | ||||||
| chr1:202574215
|
T | TAAAAATA others(326): Show |
1 | a0001c0001t0025g0234 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2862+5029_2862+503 others(337): Show |
PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr1 | 202574215 | |||||
| chr1:202574491
|
G | A | 1 | a0001c0001t0025g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2862+5294G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202574491 | ||||||
| chr1:202574927
|
A | G | 1 | a0001c0001t0002g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2863-5547A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202574927 | ||||||
| chr1:202575213
|
G | A | 2 | a0001c0001t0032g0057a0001c0001t0032g0058 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2863-5261G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202575213 | ||||||
| chr1:202575237
|
G | A | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2863-5237G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202575237 | ||||||
| chr1:202575259
|
G | C | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2863-5215G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202575259 | ||||||
| chr1:202575392
|
A | G | 2 | a0001c0001t0003g0013a0001c0001t0003g0037 | 2 | NA18960.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2863-5082A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202575392 | ||||||
| chr1:202576097
|
G | C | 1 | a0001c0001t0004g0079 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2863-4377G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202576097 | ||||||
| chr1:202576511
|
C | T | 1 | a0001c0001t0038g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2863-3963C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202576511 | ||||||
| chr1:202576825
|
G | GA | 101 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.2863-3637dupA | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr1 | 202576825 | |||||
| chr1:202576993
|
G | A | 3 | a0001c0001t0034g0044a0001c0001t0034g0045a0001c0001t0105g0014 | 3 | HG02258.hp1 HG02280.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2863-3481G>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202576993 | ||||||
| chr1:202577478
|
AT | A | 4 | a0001c0001t0026g0008a0001c0001t0026g0009a0001c0001t0060g0007others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-2992delT | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr1 | 202577478 | |||||
| chr1:202577973
|
G | T | 56 | a0001c0001t0001g0160a0001c0001t0001g0169a0001c0001t0001g0182others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2863-2501G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202577973 | ||||||
| chr1:202578373
|
A | G | 1 | a0001c0001t0078g0050 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2863-2101A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202578373 | ||||||
| chr1:202578781
|
T | G | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2863-1693T>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202578781 | ||||||
| chr1:202578794
|
A | G | 221 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2863-1680A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202578794 | ||||||
| chr1:202578823
|
C | T | 3 | a0001c0001t0076g0051a0001c0001t0078g0050a0001c0001t0079g0046 | 3 | HG00735.hp1 HG01346.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2863-1651C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202578823 | ||||||
| chr1:202578846
|
G | C | 2 | a0001c0001t0062g0131a0001c0001t0063g0159 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2863-1628G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202578846 | ||||||
| chr1:202579164
|
C | T | 1 | a0001c0001t0068g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2863-1310C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202579164 | ||||||
| chr1:202579203
|
C | T | 3 | a0001c0001t0034g0044a0001c0001t0034g0045a0001c0001t0105g0014 | 3 | HG02258.hp1 HG02280.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2863-1271C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202579203 | ||||||
| chr1:202579283
|
G | T | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2863-1191G>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202579283 | ||||||
| chr1:202579442
|
C | T | 1 | a0001c0001t0010g0083 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2863-1032C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202579442 | ||||||
| chr1:202579694
|
C | T | 105 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0169others(102): Show | 105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2863-780C>T | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202579694 | ||||||
| chr1:202579705
|
C | A | 1 | a0001c0001t0077g0059 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2863-769C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202579705 | ||||||
| chr1:202580111
|
C | G | 3 | a0001c0001t0037g0006a0001c0001t0038g0005a0001c0001t0039g0011 | 3 | HG02451.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2863-363C>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202580111 | ||||||
| chr1:202580131
|
G | C | 1 | a0001c0001t0071g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2863-343G>C | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202580131 | ||||||
| chr1:202580194
|
A | G | 1 | a0001c0001t0098g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2863-280A>G | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202580194 | ||||||
| chr1:202580451
|
C | A | 7 | a0001c0001t0017g0137a0001c0001t0017g0141a0001c0001t0017g0143others(4): Show | 7 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2863-23C>A | PPP1R12B | ENSG00000077157.23 | transcript | ENST00000608999.6 | protein_coding | 23/23 | chr1 | 202580451 |