Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5527 |
|---|---|
| ensemblid | ENSG00000078304.20 |
| hgncid | 9311 |
| symbol | PPP2R5C |
| name | protein phosphatase 2 regulatory subunit B'gamma |
| refseq_nuc | NM_001352913.2 |
| refseq_prot | NP_001339842.1 |
| ensembl_nuc | ENST00000694906.1 |
| ensembl_prot | ENSP00000511581.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 101761709 |
| end | 101927977 |
| strand | + |
| ver | v1.2 |
| region | chr14:101761709-101927977 |
| region5000 | chr14:101756709-101932977 |
| regionname0 | PPP2R5C_chr14_101761709_101927977 |
| regionname5000 | PPP2R5C_chr14_101756709_101932977 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 579 | 99 | 39 | 19 | 24 | 4 | 11 | 13 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0002 | 0/0 | 579 | 37 | 15 | 6 | 15 | 0 | 1 | 9 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0003 | 0/0 | 579 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0004 | 0/0 | 579 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1740 | 90 | 32 | 19 | 24 | 3 | 10 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| c0002 | 0/0 | 1740 | 37 | 15 | 6 | 15 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| c0003 | 0/0 | 1740 | 9 | 7 | 0 | 0 | 1 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| c0004 | 0/0 | 1740 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| c0005 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2891 | 75 | 17 | 18 | 31 | 2 | 5 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0002 | 0/0 | 2891 | 19 | 14 | 1 | 0 | 1 | 3 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0003 | 0/0 | 2891 | 12 | 1 | 1 | 7 | 1 | 2 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0004 | 0/0 | 2891 | 7 | 4 | 3 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0005 | 0/0 | 2889 | 4 | 4 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0006 | 0/0 | 2891 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0007 | 0/0 | 2889 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0008 | 0/0 | 2891 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0009 | 0/0 | 2888 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0010 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0011 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0012 | 0/0 | 2878 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0013 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0014 | 0/0 | 2891 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0015 | 0/0 | 2891 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0016 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0017 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0018 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0019 | 0/0 | 2891 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| t0020 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1740 | 90 | 32 | 19 | 24 | 3 | 10 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0003 | 0/0 | 1740 | 9 | 7 | 0 | 0 | 1 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0002c0002 | 0/0 | 1740 | 37 | 15 | 6 | 15 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0003c0004 | 0/0 | 1740 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0004c0005 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4630 | 51 | 9 | 15 | 18 | 2 | 5 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0002 | 0/0 | 4630 | 15 | 12 | 1 | 0 | 0 | 2 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0003 | 0/0 | 4630 | 8 | 1 | 0 | 5 | 1 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0005 | 0/0 | 4628 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0006 | 0/0 | 4630 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0007 | 0/0 | 4628 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0009 | 0/0 | 4627 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0010 | 0/0 | 4627 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0011 | 0/0 | 4627 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0012 | 0/0 | 4617 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0014 | 0/0 | 4630 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0015 | 0/0 | 4630 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0017 | 0/0 | 4630 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0001t0019 | 0/0 | 4630 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0003t0002 | 0/0 | 4630 | 4 | 2 | 0 | 0 | 1 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0003t0005 | 0/0 | 4628 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0003t0013 | 0/0 | 4630 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0003t0018 | 0/0 | 4630 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0001c0003t0020 | 0/0 | 4630 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0002c0002t0001 | 0/0 | 4630 | 23 | 8 | 3 | 12 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0002c0002t0003 | 0/0 | 4630 | 4 | 0 | 1 | 2 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0002c0002t0004 | 0/0 | 4630 | 6 | 4 | 2 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0002c0002t0008 | 0/0 | 4630 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0002c0002t0016 | 0/0 | 4630 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0003c0004t0004 | 0/0 | 4630 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| a0004c0005t0001 | 0/0 | 4630 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | copy fasta | chr14 | 101756709 | 101932977 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0009g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0010g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0012g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0014g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0015g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0017g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0001t0019g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0003t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0003t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0003t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0003t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0003t0013g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0003t0018g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0001c0003t0020g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0002c0002t0016g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0003c0004t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| a0004c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0132 | EAS | CHS | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00408 | hp2 | a0004 | c0005 | t0001 | g0101 | EAS | CHS | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | CHS | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0134 | EAS | CHS | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00642 | hp2 | a0001 | c0001 | t0015 | g0042 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG00733 | hp2 | a0003 | c0004 | t0004 | g0120 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01070 | hp1 | a0002 | c0002 | t0003 | g0129 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01255 | hp2 | a0001 | c0001 | t0012 | g0064 | AMR | CLM | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01256 | hp1 | a0002 | c0002 | t0004 | g0024 | AMR | CLM | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01258 | hp2 | a0002 | c0002 | t0004 | g0023 | AMR | CLM | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0122 | AMR | CLM | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02055 | hp2 | a0002 | c0002 | t0008 | g0011 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | KHV | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | KHV | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CDX | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02451 | hp2 | a0002 | c0002 | t0008 | g0010 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02572 | hp2 | a0001 | c0003 | t0005 | g0020 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0128 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02735 | hp1 | a0001 | c0003 | t0002 | g0079 | SAS | PJL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0126 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02886 | hp2 | a0001 | c0003 | t0020 | g0008 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | ESN | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0105 | AFR | ESN | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | MSL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03209 | hp2 | a0002 | c0002 | t0004 | g0017 | AFR | MSL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | MSL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | MSL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03486 | hp2 | a0002 | c0002 | t0004 | g0119 | AFR | MSL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0127 | AFR | ESN | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03516 | hp2 | a0001 | c0003 | t0005 | g0018 | AFR | ESN | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0075 | AFR | MSL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0137 | SAS | STU | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG04115 | hp1 | a0001 | c0001 | t0014 | g0110 | SAS | STU | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG04115 | hp2 | a0001 | c0001 | t0019 | g0116 | SAS | STU | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | CHB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18906 | hp1 | a0002 | c0002 | t0008 | g0009 | AFR | YRI | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0083 | AFR | YRI | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18969 | hp1 | a0001 | c0001 | t0010 | g0133 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19079 | hp1 | a0002 | c0002 | t0016 | g0103 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0097 | AFR | YRI | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0076 | AFR | YRI | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA20129 | hp1 | a0001 | c0003 | t0018 | g0089 | AFR | ASW | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0087 | AFR | ASW | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0112 | EUR | TSI | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | TSI | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02109 | hp1 | a0002 | c0002 | t0004 | g0073 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG02559 | hp2 | a0001 | c0001 | t0017 | g0085 | AFR | ACB | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0121 | AFR | MSL | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG06807 | hp1 | a0001 | c0003 | t0013 | g0019 | AFR | USA | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | USA | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| NA21309 | hp2 | a0002 | c0002 | t0004 | g0108 | AFR | LWK | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0031 | REF | REF | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0104 | REF | REF | PPP2R5C_chr14_101756709_101932977 | PPP2R5C | chr14 | 101756709 | 101932977 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:101761907
|
A | C | 1 | a0004 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.14A>C | p.Asn5Thr | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 1/16 | 199/4630 | 14/1740 | 5/579 | chr14 | 101761907 | ||
| chr14:101786027
|
G | A | 1 | a0003 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.103G>A | p.Val35Ile | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/16 | 288/4630 | 103/1740 | 35/579 | chr14 | 101786027 | ||
| chr14:101925240
|
G | C | 2 | a0002a0003 | 38 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(35): Show |
missense_variant | MODERATE | c.1708G>C | p.Ala570Pro | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 1893/4630 | 1708/1740 | 570/579 | chr14 | 101925240 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:101856756
|
T | C | 1 | a0001c0003 | 9 | HG02572.hp2 HG02717.hp1 HG02735.hp1 others(6): Show |
synonymous_variant | LOW | c.330T>C | p.Phe110Phe | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/16 | 515/4630 | 330/1740 | 110/579 | chr14 | 101856756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:101761781
|
G | GGGC | 4 | a0001c0001t0003a0001c0003t0020a0002c0002t0003others(1): Show | 16 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-94_-92dupGGC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 1/16 | 91 | INFO_REALIGN_3_PRIME | chr14 | 101761781 | ||||
| chr14:101761861
|
GGGC | G | 7 | a0001c0001t0003a0001c0001t0009a0001c0001t0010others(4): Show | 19 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-12delGGC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 1/16 | 12 | INFO_REALIGN_3_PRIME | chr14 | 101761861 | ||||
| chr14:101925723
|
G | A | 3 | a0002c0002t0004a0002c0002t0008a0003c0004t0004 | 10 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*451G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 451 | chr14 | 101925723 | |||||
| chr14:101925784
|
CGAGTTCT others(6): Show |
C | 1 | a0001c0001t0012 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*513_*525delGAGTTC others(7): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 513 | chr14 | 101925784 | |||||
| chr14:101925785
|
G | A | 3 | a0001c0001t0002a0001c0003t0002a0001c0003t0020 | 20 | HG01258.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*513G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 513 | chr14 | 101925785 | |||||
| chr14:101925799
|
C | A | 1 | a0001c0001t0012 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 527 | chr14 | 101925799 | |||||
| chr14:101925997
|
A | T | 1 | a0001c0001t0019 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*725A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 725 | chr14 | 101925997 | |||||
| chr14:101926094
|
T | C | 3 | a0001c0001t0006a0001c0001t0009a0001c0003t0013 | 5 | HG01433.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*822T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 822 | chr14 | 101926094 | |||||
| chr14:101926179
|
T | C | 1 | a0001c0001t0014 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 907 | chr14 | 101926179 | |||||
| chr14:101926680
|
CAA | C | 1 | a0001c0001t0007 | 3 | HG02622.hp1 HG02886.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1411_*1412delAA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 1411 | INFO_REALIGN_3_PRIME | chr14 | 101926680 | ||||
| chr14:101926747
|
G | A | 4 | a0001c0001t0002a0001c0001t0012a0001c0003t0002others(1): Show | 21 | HG01255.hp2 HG01258.hp1 HG01884.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1475G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 1475 | chr14 | 101926747 | |||||
| chr14:101926750
|
G | A | 1 | a0001c0001t0019 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1478G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 1478 | chr14 | 101926750 | |||||
| chr14:101926783
|
C | G | 9 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(6): Show | 28 | HG01255.hp2 HG01258.hp1 HG01884.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1511C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 1511 | chr14 | 101926783 | |||||
| chr14:101926877
|
G | C | 1 | a0001c0003t0013 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1605G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 1605 | chr14 | 101926877 | |||||
| chr14:101926971
|
A | G | 1 | a0002c0002t0016 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1699A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 1699 | chr14 | 101926971 | |||||
| chr14:101927005
|
A | T | 1 | a0001c0001t0015 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1733A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 1733 | chr14 | 101927005 | |||||
| chr14:101927480
|
G | A | 3 | a0001c0001t0005a0001c0001t0017a0001c0003t0005 | 5 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2208G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 2208 | chr14 | 101927480 | |||||
| chr14:101927965
|
CAT | C | 2 | a0001c0001t0005a0001c0003t0005 | 4 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2694_*2695delAT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 16/16 | 2694 | chr14 | 101927965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:101762124
|
G | T | 10 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0135others(7): Show | 10 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.27+204G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 1/15 | chr14 | 101762124 | ||||||
| chr14:101762125
|
C | A | 10 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0135others(7): Show | 10 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.27+205C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 1/15 | chr14 | 101762125 | ||||||
| chr14:101762133
|
C | T | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+213C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 1/15 | chr14 | 101762133 | ||||||
| chr14:101762348
|
G | T | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+428G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 1/15 | chr14 | 101762348 | ||||||
| chr14:101762511
|
G | C | 1 | a0002c0002t0001g0001 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.28-394G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 1/15 | chr14 | 101762511 | ||||||
| chr14:101762592
|
G | A | 1 | a0002c0002t0001g0002 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.28-313G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 1/15 | chr14 | 101762592 | ||||||
| chr14:101762868
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.28-37G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 1/15 | chr14 | 101762868 | ||||||
| chr14:101763103
|
T | C | 18 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(15): Show | 18 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.93+133T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763103 | ||||||
| chr14:101763190
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.93+220G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763190 | ||||||
| chr14:101763198
|
T | C | 18 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(15): Show | 18 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.93+228T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763198 | ||||||
| chr14:101763255
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.93+285T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763255 | ||||||
| chr14:101763383
|
A | G | 18 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(15): Show | 18 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.93+413A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763383 | ||||||
| chr14:101763384
|
C | A | 4 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+414C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763384 | ||||||
| chr14:101763384
|
C | CA | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+417dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101763384 | |||||
| chr14:101763387
|
A | AT | 9 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0003g0138others(6): Show | 9 | HG00733.hp2 HG01433.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.93+432dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101763387 | |||||
| chr14:101763403
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+433A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763403 | ||||||
| chr14:101763422
|
A | G | 24 | a0001c0001t0001g0123a0001c0001t0003g0005a0001c0001t0003g0006others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.93+452A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763422 | ||||||
| chr14:101763532
|
G | C | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.93+562G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763532 | ||||||
| chr14:101763543
|
C | T | 1 | a0002c0002t0004g0119 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.93+573C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763543 | ||||||
| chr14:101763552
|
T | C | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.93+582T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763552 | ||||||
| chr14:101763712
|
A | C | 1 | a0001c0001t0001g0118 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.93+742A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763712 | ||||||
| chr14:101763743
|
T | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.93+773T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763743 | ||||||
| chr14:101763796
|
T | C | 18 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(15): Show | 18 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.93+826T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763796 | ||||||
| chr14:101763856
|
C | T | 16 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(13): Show | 16 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.93+886C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101763856 | ||||||
| chr14:101764003
|
T | TTG | 15 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(12): Show | 15 | HG01071.hp2 HG01258.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.93+1058_93+1059dup others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764003 | |||||
| chr14:101764025
|
G | A | 4 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+1055G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764025 | ||||||
| chr14:101764028
|
T | TGTGTGTG others(9): Show |
1 | a0002c0002t0003g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.93+1059_93+1060ins others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764028 | |||||
| chr14:101764028
|
T | TGTGTGTG others(17): Show |
3 | a0001c0001t0003g0138a0001c0001t0010g0133a0002c0002t0003g0134 | 3 | HG00558.hp1 NA18969.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.93+1059_93+1060ins others(24): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764028 | |||||
| chr14:101764028
|
T | TGTGTGTG others(19): Show |
2 | a0001c0001t0003g0131a0002c0002t0003g0132 | 2 | HG00408.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.93+1059_93+1060ins others(26): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764028 | |||||
| chr14:101764028
|
T | TGTGTGTG others(20): Show |
1 | a0001c0001t0003g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.93+1059_93+1060ins others(27): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764028 | |||||
| chr14:101764028
|
T | TGTGTGTG others(19): Show |
2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | NA19012.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.93+1059_93+1060ins others(26): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764028 | |||||
| chr14:101764028
|
T | TGTGTGTG others(21): Show |
2 | a0002c0002t0003g0137a0002c0002t0008g0011 | 2 | HG02055.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.93+1059_93+1060ins others(28): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764028 | |||||
| chr14:101764028
|
T | TGTGTGTG others(23): Show |
2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.93+1059_93+1060ins others(30): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764028 | |||||
| chr14:101764028
|
T | TGTGTGTG others(23): Show |
1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.93+1059_93+1060ins others(30): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764028 | |||||
| chr14:101764030
|
G | C | 29 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0003g0005others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.93+1060G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764030 | ||||||
| chr14:101764030
|
G | T | 3 | a0001c0001t0001g0123a0001c0003t0005g0020a0002c0002t0004g0017 | 3 | HG02572.hp2 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.93+1060G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764030 | ||||||
| chr14:101764036
|
C | G | 13 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0135others(10): Show | 13 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.93+1066C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764036 | ||||||
| chr14:101764038
|
C | CGCGCGCG others(7): Show |
2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.93+1068_93+1069ins others(14): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764038 | ||||||
| chr14:101764038
|
C | CGCGCGCG others(5): Show |
2 | a0001c0001t0003g0007a0001c0003t0020g0008 | 2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.93+1068_93+1069ins others(12): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764038 | ||||||
| chr14:101764038
|
C | T | 13 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0135others(10): Show | 13 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.93+1068C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764038 | ||||||
| chr14:101764077
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(46): Show | 49 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.93+1107G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764077 | ||||||
| chr14:101764147
|
T | C | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.93+1177T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764147 | ||||||
| chr14:101764445
|
T | G | 1 | a0002c0002t0001g0002 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.93+1475T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764445 | ||||||
| chr14:101764575
|
G | A | 18 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(15): Show | 18 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.93+1605G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764575 | ||||||
| chr14:101764755
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+1785G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764755 | ||||||
| chr14:101764786
|
G | C | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.93+1816G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764786 | ||||||
| chr14:101764793
|
C | T | 18 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(15): Show | 18 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.93+1823C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101764793 | ||||||
| chr14:101764801
|
C | CT | 6 | a0001c0001t0009g0122a0001c0001t0012g0064a0001c0003t0005g0020others(3): Show | 6 | HG01255.hp2 HG01433.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+1849dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764801 | |||||
| chr14:101764801
|
C | CTTT | 6 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(3): Show | 6 | HG00733.hp2 HG01884.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+1847_93+1849dup others(3): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764801 | |||||
| chr14:101764801
|
CT | C | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(3): Show | 6 | HG02109.hp2 HG02165.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+1849delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764801 | |||||
| chr14:101764801
|
CTTT | C | 16 | a0001c0001t0001g0123a0001c0001t0003g0005a0001c0001t0003g0007others(13): Show | 16 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.93+1847_93+1849del others(3): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101764801 | |||||
| chr14:101765108
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+2138A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765108 | ||||||
| chr14:101765522
|
C | A | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.93+2552C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765522 | ||||||
| chr14:101765546
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+2576C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765546 | ||||||
| chr14:101765548
|
T | G | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+2578T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765548 | ||||||
| chr14:101765563
|
C | A | 1 | a0001c0001t0002g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.93+2593C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765563 | ||||||
| chr14:101765568
|
C | CT | 12 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061others(9): Show | 12 | HG02056.hp1 HG02056.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.93+2615dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101765568 | |||||
| chr14:101765568
|
CT | C | 9 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0016others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.93+2615delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101765568 | |||||
| chr14:101765611
|
T | A | 30 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+2641T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765611 | ||||||
| chr14:101765624
|
A | G | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+2654A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765624 | ||||||
| chr14:101765629
|
A | G | 30 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+2659A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765629 | ||||||
| chr14:101765631
|
A | G | 30 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+2661A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765631 | ||||||
| chr14:101765734
|
A | AT | 8 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0106others(5): Show | 8 | HG00438.hp2 HG01255.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.93+2788dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101765734 | |||||
| chr14:101765734
|
AT | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0081a0001c0001t0001g0082others(13): Show | 16 | HG01071.hp2 HG01258.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.93+2788delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101765734 | |||||
| chr14:101765734
|
ATT | A | 11 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(8): Show | 11 | HG00733.hp2 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.93+2787_93+2788del others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101765734 | |||||
| chr14:101765734
|
ATTTTTT | A | 25 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(22): Show | 25 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.93+2783_93+2788del others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101765734 | |||||
| chr14:101765813
|
G | C | 30 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+2843G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765813 | ||||||
| chr14:101765954
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+2984C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101765954 | ||||||
| chr14:101766081
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+3111T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101766081 | ||||||
| chr14:101766188
|
C | T | 10 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0135others(7): Show | 10 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.93+3218C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101766188 | ||||||
| chr14:101766358
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+3388T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101766358 | ||||||
| chr14:101766362
|
C | T | 7 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(4): Show | 7 | HG00558.hp2 HG01074.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+3392C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101766362 | ||||||
| chr14:101766370
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.93+3400T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101766370 | ||||||
| chr14:101766625
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+3655G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101766625 | ||||||
| chr14:101766636
|
C | G | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+3666C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101766636 | ||||||
| chr14:101766801
|
A | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.93+3831A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101766801 | ||||||
| chr14:101767264
|
A | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.93+4294A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101767264 | ||||||
| chr14:101767423
|
T | C | 43 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(40): Show | 43 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.93+4453T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101767423 | ||||||
| chr14:101767530
|
T | C | 9 | a0001c0001t0001g0123a0001c0001t0002g0124a0001c0001t0002g0125others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.93+4560T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101767530 | ||||||
| chr14:101767540
|
CT | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.93+4571delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101767540 | ||||||
| chr14:101767734
|
C | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.93+4764C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101767734 | ||||||
| chr14:101767778
|
C | T | 1 | a0001c0001t0003g0136 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.93+4808C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101767778 | ||||||
| chr14:101767870
|
T | A | 39 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.93+4900T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101767870 | ||||||
| chr14:101768020
|
T | G | 7 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(4): Show | 7 | HG00558.hp2 HG01074.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+5050T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768020 | ||||||
| chr14:101768126
|
C | G | 1 | a0002c0002t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.93+5156C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768126 | ||||||
| chr14:101768131
|
A | G | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.93+5161A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768131 | ||||||
| chr14:101768289
|
C | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.93+5319C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768289 | ||||||
| chr14:101768313
|
G | C | 1 | a0002c0002t0008g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.93+5343G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768313 | ||||||
| chr14:101768440
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.93+5470G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768440 | ||||||
| chr14:101768535
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.93+5565G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768535 | ||||||
| chr14:101768652
|
C | T | 1 | a0001c0003t0002g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.93+5682C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768652 | ||||||
| chr14:101768725
|
C | T | 7 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(4): Show | 7 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+5755C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768725 | ||||||
| chr14:101768825
|
CT | C | 39 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0002g0124others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.93+5872delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101768825 | |||||
| chr14:101768950
|
G | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.93+5980G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768950 | ||||||
| chr14:101768986
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+6016G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101768986 | ||||||
| chr14:101769015
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93+6045A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101769015 | ||||||
| chr14:101769045
|
C | T | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.93+6075C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101769045 | ||||||
| chr14:101769067
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0009g0122a0002c0002t0001g0121 | 3 | HG01433.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.93+6097A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101769067 | ||||||
| chr14:101769076
|
G | A | 25 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(22): Show | 25 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.93+6106G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101769076 | ||||||
| chr14:101769174
|
C | T | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.93+6204C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101769174 | ||||||
| chr14:101769231
|
CA | C | 5 | a0001c0001t0001g0078a0001c0001t0019g0116a0001c0003t0002g0079others(2): Show | 5 | HG02735.hp1 HG04115.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+6263delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101769231 | |||||
| chr14:101769813
|
A | G | 43 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(40): Show | 43 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.93+6843A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101769813 | ||||||
| chr14:101769911
|
A | G | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.93+6941A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101769911 | ||||||
| chr14:101770094
|
C | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.93+7124C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101770094 | ||||||
| chr14:101770237
|
C | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.93+7267C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101770237 | ||||||
| chr14:101770602
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0017g0085 | 2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.93+7632G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101770602 | ||||||
| chr14:101770708
|
A | G | 3 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007 | 3 | HG02486.hp1 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.93+7738A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101770708 | ||||||
| chr14:101770923
|
C | T | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.93+7953C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101770923 | ||||||
| chr14:101771125
|
T | C | 20 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(17): Show | 20 | HG02109.hp1 HG02486.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.93+8155T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101771125 | ||||||
| chr14:101771171
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.93+8201C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101771171 | ||||||
| chr14:101771202
|
A | G | 3 | a0002c0002t0001g0002a0002c0002t0001g0084a0002c0002t0001g0115 | 3 | HG01993.hp2 HG02155.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.93+8232A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101771202 | ||||||
| chr14:101771222
|
C | CGT | 23 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0061others(20): Show | 23 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.93+8293_93+8294dup others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101771222 | |||||
| chr14:101771222
|
C | CGTGT | 29 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(26): Show | 29 | HG00280.hp1 HG01070.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.93+8291_93+8294dup others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101771222 | |||||
| chr14:101771222
|
C | CGTGTGT | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(34): Show | 37 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.93+8289_93+8294dup others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101771222 | |||||
| chr14:101771222
|
C | CGTGTGTG others(1): Show |
13 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(10): Show | 13 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.93+8287_93+8294dup others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101771222 | |||||
| chr14:101771222
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0123a0001c0001t0009g0122 | 2 | HG01433.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.93+8285_93+8294dup others(10): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101771222 | |||||
| chr14:101771222
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0007g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.93+8283_93+8294dup others(12): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101771222 | |||||
| chr14:101771222
|
C | CGTGTGTG others(7): Show |
1 | a0001c0001t0003g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.93+8281_93+8294dup others(14): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101771222 | |||||
| chr14:101771222
|
CGT | C | 5 | a0001c0001t0011g0012a0002c0002t0003g0132a0002c0002t0008g0009others(2): Show | 5 | HG00408.hp1 HG00733.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+8293_93+8294del others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101771222 | |||||
| chr14:101771222
|
CGTGTGTG others(9): Show |
C | 5 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0003g0131others(2): Show | 5 | HG01106.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+8279_93+8294del others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101771222 | |||||
| chr14:101772113
|
T | C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.93+9143T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101772113 | ||||||
| chr14:101772293
|
A | G | 43 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(40): Show | 43 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.93+9323A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101772293 | ||||||
| chr14:101772347
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.93+9377C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101772347 | ||||||
| chr14:101772593
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.93+9623G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101772593 | ||||||
| chr14:101772659
|
G | A | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+9689G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101772659 | ||||||
| chr14:101772956
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.93+9986G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101772956 | ||||||
| chr14:101772976
|
C | G | 3 | a0001c0001t0001g0123a0001c0001t0011g0012a0002c0002t0008g0011 | 3 | HG02055.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.93+10006C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101772976 | ||||||
| chr14:101773521
|
A | T | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.93+10551A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101773521 | ||||||
| chr14:101773613
|
G | A | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.93+10643G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101773613 | ||||||
| chr14:101773635
|
G | T | 9 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0135others(6): Show | 9 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.93+10665G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101773635 | ||||||
| chr14:101773941
|
T | C | 1 | a0001c0001t0007g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.93+10971T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101773941 | ||||||
| chr14:101773995
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.93+11025G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101773995 | ||||||
| chr14:101774018
|
G | A | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.93+11048G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101774018 | ||||||
| chr14:101774307
|
C | A | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.93+11337C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101774307 | ||||||
| chr14:101774573
|
C | T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-11445C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101774573 | ||||||
| chr14:101774576
|
G | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-11442G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101774576 | ||||||
| chr14:101774864
|
T | C | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-11154T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101774864 | ||||||
| chr14:101775198
|
A | G | 16 | a0001c0001t0001g0123a0001c0001t0002g0124a0001c0001t0002g0125others(13): Show | 16 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.94-10820A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775198 | ||||||
| chr14:101775288
|
T | C | 16 | a0001c0001t0001g0123a0001c0001t0002g0124a0001c0001t0002g0125others(13): Show | 16 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.94-10730T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775288 | ||||||
| chr14:101775421
|
G | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-10597G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775421 | ||||||
| chr14:101775454
|
G | A | 16 | a0001c0001t0001g0123a0001c0001t0002g0124a0001c0001t0002g0125others(13): Show | 16 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.94-10564G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775454 | ||||||
| chr14:101775474
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94-10544G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775474 | ||||||
| chr14:101775475
|
G | A | 3 | a0001c0001t0007g0016a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.94-10543G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775475 | ||||||
| chr14:101775530
|
G | T | 1 | a0001c0001t0012g0064 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.94-10488G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775530 | ||||||
| chr14:101775715
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94-10303G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775715 | ||||||
| chr14:101775735
|
A | G | 42 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.94-10283A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775735 | ||||||
| chr14:101775740
|
C | A | 1 | a0001c0003t0002g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94-10278C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775740 | ||||||
| chr14:101775841
|
C | T | 1 | a0001c0001t0010g0133 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.94-10177C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775841 | ||||||
| chr14:101775853
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.94-10165G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775853 | ||||||
| chr14:101775970
|
G | A | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-10048G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101775970 | ||||||
| chr14:101776022
|
G | GC | 10 | a0001c0001t0001g0049a0001c0001t0001g0078a0001c0001t0001g0090others(7): Show | 10 | HG01433.hp2 HG01934.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.94-9986dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101776022 | |||||
| chr14:101776044
|
G | A | 1 | a0002c0002t0008g0011 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.94-9974G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776044 | ||||||
| chr14:101776176
|
A | G | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.94-9842A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776176 | ||||||
| chr14:101776213
|
AAAATAAT others(72): Show |
A | 1 | a0001c0001t0001g0048 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.94-9804_94-9726del others(79): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776213 | ||||||
| chr14:101776230
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.94-9788T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776230 | ||||||
| chr14:101776367
|
A | G | 39 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.94-9651A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776367 | ||||||
| chr14:101776399
|
C | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.94-9619C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776399 | ||||||
| chr14:101776565
|
C | T | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.94-9453C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776565 | ||||||
| chr14:101776624
|
G | A | 1 | a0001c0001t0014g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.94-9394G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776624 | ||||||
| chr14:101776793
|
A | G | 1 | a0002c0002t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94-9225A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776793 | ||||||
| chr14:101776872
|
C | T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-9146C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776872 | ||||||
| chr14:101776881
|
C | CT | 6 | a0001c0001t0002g0125a0001c0001t0007g0126a0001c0003t0002g0127others(3): Show | 6 | HG02055.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-9120dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101776881 | |||||
| chr14:101776881
|
CT | C | 7 | a0001c0001t0003g0135a0001c0001t0003g0138a0002c0002t0001g0001others(4): Show | 7 | HG00733.hp2 HG01993.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-9120delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101776881 | |||||
| chr14:101776926
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-9092G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101776926 | ||||||
| chr14:101777072
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.94-8946G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101777072 | ||||||
| chr14:101777310
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.94-8708A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101777310 | ||||||
| chr14:101777381
|
G | A | 7 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(4): Show | 7 | HG01433.hp2 HG01884.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-8637G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101777381 | ||||||
| chr14:101777432
|
C | T | 1 | a0002c0002t0001g0084 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.94-8586C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101777432 | ||||||
| chr14:101777740
|
A | G | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.94-8278A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101777740 | ||||||
| chr14:101777885
|
G | A | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-8133G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101777885 | ||||||
| chr14:101777887
|
C | T | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-8131C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101777887 | ||||||
| chr14:101777997
|
C | T | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-8021C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101777997 | ||||||
| chr14:101778029
|
C | G | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.94-7989C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101778029 | ||||||
| chr14:101778139
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0049others(1): Show | 4 | HG00642.hp2 HG01074.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-7879G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101778139 | ||||||
| chr14:101778314
|
C | G | 1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94-7704C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101778314 | ||||||
| chr14:101778450
|
C | T | 42 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.94-7568C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101778450 | ||||||
| chr14:101778725
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94-7293T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101778725 | ||||||
| chr14:101778751
|
G | A | 41 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0123others(38): Show | 41 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.94-7267G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101778751 | ||||||
| chr14:101778762
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.94-7256A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101778762 | ||||||
| chr14:101779413
|
A | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-6605A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101779413 | ||||||
| chr14:101779653
|
G | T | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | NA18995.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.94-6365G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101779653 | ||||||
| chr14:101779655
|
C | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-6363C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101779655 | ||||||
| chr14:101779867
|
T | TTCTGATT others(17): Show |
1 | a0001c0001t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.94-6149_94-6126dup others(24): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101779867 | |||||
| chr14:101780069
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.94-5949A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101780069 | ||||||
| chr14:101780100
|
C | T | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-5918C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101780100 | ||||||
| chr14:101780182
|
A | G | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.94-5836A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101780182 | ||||||
| chr14:101781060
|
T | C | 14 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(11): Show | 14 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.94-4958T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101781060 | ||||||
| chr14:101781186
|
A | C | 1 | a0001c0001t0003g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.94-4832A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101781186 | ||||||
| chr14:101781338
|
G | A | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.94-4680G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101781338 | ||||||
| chr14:101781505
|
C | T | 4 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-4513C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101781505 | ||||||
| chr14:101781611
|
T | C | 1 | a0001c0001t0017g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.94-4407T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101781611 | ||||||
| chr14:101781722
|
A | G | 49 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0113others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.94-4296A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101781722 | ||||||
| chr14:101781767
|
G | T | 11 | a0001c0001t0001g0013a0001c0001t0003g0130a0001c0001t0003g0131others(8): Show | 11 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.94-4251G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101781767 | ||||||
| chr14:101781802
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.94-4216C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101781802 | ||||||
| chr14:101781823
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.94-4195T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101781823 | ||||||
| chr14:101781903
|
T | C | 9 | a0001c0001t0001g0123a0001c0001t0002g0065a0001c0001t0002g0124others(6): Show | 9 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-4115T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101781903 | ||||||
| chr14:101781913
|
T | TC | 3 | a0001c0001t0001g0033a0001c0001t0003g0131a0002c0002t0008g0011 | 3 | HG02055.hp2 NA19005.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.94-4102dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101781913 | |||||
| chr14:101782102
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.94-3916T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782102 | ||||||
| chr14:101782106
|
C | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-3912C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782106 | ||||||
| chr14:101782115
|
T | C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.94-3903T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782115 | ||||||
| chr14:101782137
|
CCCCATCC others(607): Show |
C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.94-3877_94-3264del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782137 | |||||
| chr14:101782141
|
A | C | 15 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(12): Show | 15 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.94-3877A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782141 | ||||||
| chr14:101782141
|
ATCCCTCT others(607): Show |
A | 1 | a0002c0002t0016g0103 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.94-3852_94-3239del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782141 | |||||
| chr14:101782155
|
CCT | C | 11 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(8): Show | 11 | HG01071.hp2 HG01258.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.94-3856_94-3855del others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782155 | |||||
| chr14:101782155
|
CCTCT | C | 4 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(1): Show | 4 | HG02572.hp2 HG02622.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3858_94-3855del others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782155 | |||||
| chr14:101782166
|
T | C | 15 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(12): Show | 15 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.94-3852T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782166 | ||||||
| chr14:101782172
|
C | T | 15 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(12): Show | 15 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.94-3846C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782172 | ||||||
| chr14:101782173
|
T | C | 1 | a0001c0001t0003g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.94-3845T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782173 | ||||||
| chr14:101782202
|
TCCCCCTC others(312): Show |
T | 1 | a0002c0002t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94-3811_94-3493del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782202 | |||||
| chr14:101782209
|
CCCCCTCC others(535): Show |
C | 13 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0006others(10): Show | 13 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.94-3794_94-3253del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782209 | |||||
| chr14:101782213
|
CTCCCTCT others(468): Show |
C | 1 | a0001c0001t0001g0047 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.94-3794_94-3320del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782213 | |||||
| chr14:101782224
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.94-3794C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782224 | ||||||
| chr14:101782225
|
T | C | 1 | a0001c0001t0003g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.94-3793T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782225 | ||||||
| chr14:101782250
|
CCTCTCTC others(310): Show |
C | 22 | a0001c0001t0001g0081a0001c0001t0001g0096a0001c0001t0001g0106others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.94-3627_94-3311del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782250 | |||||
| chr14:101782256
|
TC | T | 5 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0003g0138others(2): Show | 5 | HG01070.hp1 NA18969.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3755delC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782256 | |||||
| chr14:101782260
|
C | CCCCTCTC others(13): Show |
1 | a0001c0001t0001g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94-3754_94-3753ins others(20): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782260 | |||||
| chr14:101782260
|
C | CCCCTCTC others(31): Show |
1 | a0002c0002t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.94-3754_94-3753ins others(38): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782260 | |||||
| chr14:101782264
|
T | TCTCTCCC others(11): Show |
2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3754_94-3753ins others(18): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782264 | ||||||
| chr14:101782265
|
T | C | 7 | a0001c0001t0001g0066a0001c0001t0002g0094a0001c0001t0002g0114others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-3753T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782265 | ||||||
| chr14:101782265
|
T | TTCTCCCC others(13): Show |
1 | a0001c0001t0001g0052 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.94-3745_94-3726dup others(20): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782265 | |||||
| chr14:101782273
|
A | ATTCCCCT others(33): Show |
3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94-3722_94-3721ins others(40): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782273 | |||||
| chr14:101782273
|
A | C | 6 | a0001c0001t0002g0094a0001c0001t0002g0114a0002c0002t0001g0087others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-3745A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782273 | ||||||
| chr14:101782282
|
C | T | 5 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0003g0138others(2): Show | 5 | HG01070.hp1 NA18969.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3736C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782282 | ||||||
| chr14:101782283
|
CTCTCTCC others(292): Show |
C | 1 | a0001c0001t0002g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.94-3730_94-3432del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782283 | |||||
| chr14:101782293
|
CTTCCCCT others(290): Show |
C | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94-3690_94-3394del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782293 | |||||
| chr14:101782297
|
C | T | 17 | a0001c0001t0001g0066a0001c0001t0001g0113a0001c0001t0001g0117others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.94-3721C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782297 | ||||||
| chr14:101782310
|
C | CCCCTTCC others(274): Show |
1 | a0001c0001t0002g0111 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.94-3691_94-3690ins others(281): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782310 | |||||
| chr14:101782313
|
CTTCCCCT others(112): Show |
C | 1 | a0002c0002t0001g0001 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.94-3690_94-3572del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782313 | |||||
| chr14:101782313
|
CTTCCCCT others(270): Show |
C | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.94-3690_94-3414del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782313 | |||||
| chr14:101782317
|
C | T | 6 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(3): Show | 6 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-3701C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782317 | ||||||
| chr14:101782319
|
C | T | 7 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0002g0124others(4): Show | 7 | HG01884.hp2 HG02165.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-3699C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782319 | ||||||
| chr14:101782322
|
C | CCT | 17 | a0001c0001t0001g0066a0001c0001t0001g0113a0001c0001t0001g0118others(14): Show | 17 | HG01071.hp2 HG01433.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.94-3692_94-3691dup others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782322 | |||||
| chr14:101782322
|
C | CCTCTCTC others(15): Show |
4 | a0001c0001t0003g0138a0002c0002t0003g0129a0002c0002t0008g0009others(1): Show | 4 | HG01070.hp1 HG02451.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3691_94-3690ins others(22): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782322 | |||||
| chr14:101782322
|
CCTCTCCC others(292): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.94-3672_94-3374del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782322 | |||||
| chr14:101782324
|
TCTCCCCC others(308): Show |
T | 2 | a0001c0001t0001g0070a0001c0001t0001g0082 | 2 | HG02055.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.94-3690_94-3376del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782324 | |||||
| chr14:101782325
|
CTCCCCCT others(92): Show |
C | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3690_94-3592del others(99): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782325 | |||||
| chr14:101782327
|
C | CTCCCCCT others(215): Show |
1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94-3691_94-3690ins others(222): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782327 | ||||||
| chr14:101782335
|
C | T | 1 | a0001c0003t0002g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.94-3683C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782335 | ||||||
| chr14:101782337
|
C | T | 5 | a0001c0001t0001g0123a0001c0001t0003g0131a0001c0001t0003g0135others(2): Show | 5 | HG02055.hp2 HG03453.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3681C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782337 | ||||||
| chr14:101782343
|
CTCTCCCC others(74): Show |
C | 4 | a0001c0001t0001g0066a0001c0001t0001g0113a0001c0001t0009g0122others(1): Show | 4 | HG01433.hp2 HG02895.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3667_94-3587del others(81): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782343 | |||||
| chr14:101782345
|
C | CCCCCCTC others(12): Show |
1 | a0002c0002t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94-3673_94-3672ins others(19): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782345 | ||||||
| chr14:101782346
|
T | C | 1 | a0002c0002t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94-3672T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782346 | ||||||
| chr14:101782351
|
T | C | 11 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0002g0029others(8): Show | 11 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.94-3667T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782351 | ||||||
| chr14:101782352
|
T | TCCCC | 5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3665_94-3664ins others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782352 | |||||
| chr14:101782352
|
T | TTCCC | 2 | a0001c0001t0001g0123a0002c0002t0008g0011 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.94-3666_94-3665ins others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782352 | ||||||
| chr14:101782353
|
C | T | 2 | a0001c0001t0003g0135a0001c0001t0010g0133 | 2 | NA18969.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.94-3665C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782353 | ||||||
| chr14:101782353
|
CT | C | 3 | a0001c0001t0003g0131a0001c0001t0006g0099a0001c0001t0006g0105 | 3 | HG02976.hp1 HG02976.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.94-3664delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782353 | ||||||
| chr14:101782353
|
CTCTCTCT others(55): Show |
C | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3664_94-3603del others(62): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782353 | ||||||
| chr14:101782354
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0003g0135a0001c0001t0010g0133others(1): Show | 4 | HG03710.hp1 NA18969.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3664T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782354 | ||||||
| chr14:101782354
|
TCTCTCTC others(184): Show |
T | 2 | a0001c0001t0001g0067a0002c0002t0001g0102 | 2 | HG02132.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.94-3631_94-3441del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782354 | |||||
| chr14:101782356
|
T | C | 12 | a0001c0001t0001g0123a0001c0001t0002g0029a0001c0001t0002g0037others(9): Show | 12 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.94-3662T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782356 | ||||||
| chr14:101782360
|
T | C | 5 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0006g0099others(2): Show | 5 | HG02976.hp1 HG02976.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3658T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782360 | ||||||
| chr14:101782360
|
TCTTTCTC others(54): Show |
T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-3647_94-3587del others(61): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782360 | |||||
| chr14:101782362
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0003t0002g0112others(1): Show | 4 | HG02055.hp2 HG03453.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3656T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782362 | ||||||
| chr14:101782363
|
T | C | 9 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0003g0131others(6): Show | 9 | HG02055.hp2 HG02976.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-3655T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782363 | ||||||
| chr14:101782363
|
TTCTCCCC others(74): Show |
T | 1 | a0002c0002t0003g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.94-3647_94-3567del others(81): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782363 | |||||
| chr14:101782364
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0003t0002g0112others(1): Show | 4 | HG02055.hp2 HG03453.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3654T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782364 | ||||||
| chr14:101782364
|
T | TCCTCTTT others(10): Show |
5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3653_94-3652ins others(17): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782364 | |||||
| chr14:101782367
|
C | T | 4 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0003t0002g0112others(1): Show | 4 | HG02055.hp2 HG03453.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3651C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782367 | ||||||
| chr14:101782371
|
T | C | 10 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0002g0029others(7): Show | 10 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.94-3647T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782371 | ||||||
| chr14:101782374
|
C | CCCTCCCT others(36): Show |
3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94-3643_94-3642ins others(43): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782374 | |||||
| chr14:101782374
|
C | T | 5 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0006g0099others(2): Show | 5 | HG02976.hp1 HG02976.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3644C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782374 | ||||||
| chr14:101782376
|
T | C | 3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94-3642T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782376 | ||||||
| chr14:101782380
|
TCTCCCCT others(212): Show |
T | 2 | a0001c0001t0006g0099a0001c0001t0006g0105 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.94-3634_94-3416del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782380 | |||||
| chr14:101782382
|
T | C | 8 | a0001c0001t0001g0123a0001c0001t0002g0029a0001c0001t0002g0037others(5): Show | 8 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-3636T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782382 | ||||||
| chr14:101782382
|
TCCC | T | 3 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0010g0133 | 3 | NA18969.hp1 NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.94-3634_94-3632del others(3): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782382 | |||||
| chr14:101782383
|
C | T | 5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3635C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782383 | ||||||
| chr14:101782384
|
C | CT | 2 | a0001c0001t0001g0123a0002c0002t0008g0011 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.94-3634_94-3633ins others(1): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782384 | ||||||
| chr14:101782385
|
C | CCTT | 3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94-3631_94-3630ins others(3): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782385 | |||||
| chr14:101782385
|
C | T | 2 | a0001c0001t0001g0123a0002c0002t0008g0011 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.94-3633C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782385 | ||||||
| chr14:101782386
|
C | T | 3 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0010g0133 | 3 | NA18969.hp1 NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.94-3632C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782386 | ||||||
| chr14:101782387
|
T | C | 1 | a0001c0003t0002g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.94-3631T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782387 | ||||||
| chr14:101782389
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3629T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782389 | ||||||
| chr14:101782389
|
TGG | T | 5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3628_94-3627del others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782389 | ||||||
| chr14:101782390
|
G | C | 10 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0003g0131others(7): Show | 10 | HG02055.hp2 HG02572.hp2 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.94-3628G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782390 | ||||||
| chr14:101782390
|
GGCTCTTT others(151): Show |
G | 26 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 26 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.94-3627_94-3470del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782390 | ||||||
| chr14:101782391
|
G | C | 5 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0003g0138others(2): Show | 5 | NA18969.hp1 NA19009.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3627G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782391 | ||||||
| chr14:101782391
|
G | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(35): Show | 38 | HG00558.hp2 HG00733.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.94-3627G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782391 | ||||||
| chr14:101782393
|
T | C | 3 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0010g0133 | 3 | NA18969.hp1 NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.94-3625T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782393 | ||||||
| chr14:101782395
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3623T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782395 | ||||||
| chr14:101782396
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0003g0138a0001c0003t0002g0112 | 3 | HG03710.hp1 NA19081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94-3622T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782396 | ||||||
| chr14:101782396
|
TTCTC | T | 3 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0010g0133 | 3 | NA18969.hp1 NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.94-3621_94-3618del others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782396 | ||||||
| chr14:101782397
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3621T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782397 | ||||||
| chr14:101782399
|
T | C | 1 | a0001c0003t0002g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.94-3619T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782399 | ||||||
| chr14:101782399
|
T | TC | 8 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(5): Show | 8 | HG02572.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-3615dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782399 | |||||
| chr14:101782400
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3618C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782400 | ||||||
| chr14:101782402
|
CCTTCCCT others(234): Show |
C | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94-3614_94-3374del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782402 | |||||
| chr14:101782403
|
C | CCCCTTTC others(4): Show |
1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94-3615_94-3614ins others(11): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782403 | ||||||
| chr14:101782403
|
C | CCCCTTTC others(23): Show |
1 | a0002c0002t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.94-3615_94-3614ins others(30): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782403 | ||||||
| chr14:101782403
|
C | T | 1 | a0001c0003t0002g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.94-3615C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782403 | ||||||
| chr14:101782403
|
CTT | C | 3 | a0001c0001t0002g0094a0002c0002t0001g0087a0002c0002t0001g0097 | 3 | HG01884.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.94-3614_94-3613del others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782403 | ||||||
| chr14:101782404
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0003g0131a0001c0001t0003g0135others(1): Show | 4 | HG03710.hp1 NA18969.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3614T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782404 | ||||||
| chr14:101782405
|
T | C | 2 | a0001c0003t0002g0112a0002c0002t0001g0098 | 2 | HG02717.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.94-3613T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782405 | ||||||
| chr14:101782407
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94-3611C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782407 | ||||||
| chr14:101782409
|
T | C | 8 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(5): Show | 8 | HG02572.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-3609T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782409 | ||||||
| chr14:101782410
|
C | T | 3 | a0001c0001t0002g0094a0002c0002t0001g0087a0002c0002t0001g0097 | 3 | HG01884.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.94-3608C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782410 | ||||||
| chr14:101782411
|
T | C | 2 | a0001c0003t0002g0112a0002c0002t0001g0098 | 2 | HG02717.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.94-3607T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782411 | ||||||
| chr14:101782411
|
T | TC | 3 | a0001c0001t0002g0094a0002c0002t0001g0087a0002c0002t0001g0097 | 3 | HG01884.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.94-3606dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782411 | |||||
| chr14:101782412
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94-3606C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782412 | ||||||
| chr14:101782413
|
T | A | 3 | a0001c0001t0002g0094a0002c0002t0001g0087a0002c0002t0001g0097 | 3 | HG01884.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.94-3605T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782413 | ||||||
| chr14:101782415
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0003g0135a0001c0001t0010g0133 | 3 | HG03710.hp1 NA18969.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.94-3603T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782415 | ||||||
| chr14:101782415
|
T | TCCCCCCC others(311): Show |
1 | a0002c0002t0001g0043 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.94-3546_94-3545ins others(318): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782415 | |||||
| chr14:101782416
|
C | T | 3 | a0001c0001t0002g0094a0002c0002t0001g0087a0002c0002t0001g0097 | 3 | HG01884.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.94-3602C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782416 | ||||||
| chr14:101782416
|
CCCCCCCT others(150): Show |
C | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94-3595_94-3439del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782416 | |||||
| chr14:101782417
|
C | T | 5 | a0001c0001t0002g0094a0001c0003t0002g0112a0002c0002t0001g0087others(2): Show | 5 | HG01884.hp1 HG02717.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3601C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782417 | ||||||
| chr14:101782418
|
C | CTT | 2 | a0001c0001t0003g0135a0001c0001t0010g0133 | 2 | NA18969.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.94-3600_94-3599ins others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782418 | ||||||
| chr14:101782419
|
C | T | 5 | a0001c0001t0001g0117a0001c0001t0002g0094a0002c0002t0001g0087others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3599C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782419 | ||||||
| chr14:101782420
|
C | T | 1 | a0001c0001t0003g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.94-3598C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782420 | ||||||
| chr14:101782421
|
C | T | 3 | a0001c0001t0002g0094a0002c0002t0001g0087a0002c0002t0001g0097 | 3 | HG01884.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.94-3597C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782421 | ||||||
| chr14:101782423
|
T | C | 1 | a0001c0001t0003g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.94-3595T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782423 | ||||||
| chr14:101782423
|
T | TCC | 2 | a0001c0001t0003g0135a0001c0001t0010g0133 | 2 | NA18969.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.94-3595_94-3594ins others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782423 | ||||||
| chr14:101782424
|
T | C | 5 | a0001c0001t0002g0086a0001c0001t0003g0131a0001c0001t0003g0135others(2): Show | 5 | HG02451.hp1 HG03486.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3594T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782424 | ||||||
| chr14:101782427
|
T | TC | 3 | a0001c0001t0002g0094a0002c0002t0001g0087a0002c0002t0001g0097 | 3 | HG01884.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.94-3587dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782427 | |||||
| chr14:101782432
|
A | C | 18 | a0001c0001t0001g0066a0001c0001t0001g0113a0001c0001t0001g0117others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.94-3586A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782432 | ||||||
| chr14:101782432
|
ATTCCCCT others(171): Show |
A | 1 | a0001c0001t0001g0118 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94-3551_94-3374del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782432 | |||||
| chr14:101782438
|
C | T | 3 | a0001c0001t0002g0086a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.94-3580C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782438 | ||||||
| chr14:101782441
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.94-3577C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782441 | ||||||
| chr14:101782443
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.94-3575T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782443 | ||||||
| chr14:101782452
|
C | A | 5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3566C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782452 | ||||||
| chr14:101782456
|
C | T | 5 | a0001c0001t0001g0123a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-3562C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782456 | ||||||
| chr14:101782458
|
C | T | 2 | a0001c0001t0002g0086a0001c0003t0002g0112 | 2 | HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94-3560C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782458 | ||||||
| chr14:101782461
|
C | CCCTCCCT others(52): Show |
1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94-3556_94-3555ins others(59): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782461 | |||||
| chr14:101782461
|
C | T | 1 | a0002c0002t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94-3557C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782461 | ||||||
| chr14:101782461
|
CCT | C | 3 | a0001c0001t0002g0094a0002c0002t0001g0092a0002c0002t0001g0097 | 3 | HG01884.hp1 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3551_94-3550del others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782461 | |||||
| chr14:101782464
|
C | T | 1 | a0002c0002t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94-3554C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782464 | ||||||
| chr14:101782468
|
CCCCCTTC others(150): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.94-3545_94-3389del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782468 | |||||
| chr14:101782470
|
CCCTTCCG others(63): Show |
C | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-3544_94-3475del others(70): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782470 | |||||
| chr14:101782472
|
C | A | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3546C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782472 | ||||||
| chr14:101782472
|
CTTCCGCT others(111): Show |
C | 1 | a0001c0001t0001g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94-3541_94-3424del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782472 | |||||
| chr14:101782474
|
T | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3544T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782474 | ||||||
| chr14:101782475
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3543C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782475 | ||||||
| chr14:101782476
|
C | T | 4 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(1): Show | 4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3542C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782476 | ||||||
| chr14:101782476
|
CGCTCCCT others(49): Show |
C | 1 | a0002c0002t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94-3541_94-3486del others(56): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782476 | ||||||
| chr14:101782477
|
G | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(50): Show | 53 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.94-3541G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782477 | ||||||
| chr14:101782477
|
G | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3541G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782477 | ||||||
| chr14:101782478
|
C | T | 5 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0003g0138others(2): Show | 5 | HG02717.hp2 NA18969.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3540C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782478 | ||||||
| chr14:101782481
|
C | CCT | 17 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0002g0029others(14): Show | 17 | HG01884.hp1 HG02572.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.94-3533_94-3532dup others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782481 | |||||
| chr14:101782481
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3537C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782481 | ||||||
| chr14:101782481
|
CCTCTCCC others(113): Show |
C | 1 | a0001c0001t0001g0054 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.94-3512_94-3393del | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782481 | |||||
| chr14:101782482
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3536C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782482 | ||||||
| chr14:101782482
|
CTCTCCCC others(93): Show |
C | 1 | a0002c0002t0003g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.94-3528_94-3429del others(100): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782482 | |||||
| chr14:101782484
|
C | CTCTCCCC others(181): Show |
1 | a0002c0002t0008g0011 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.94-3532_94-3531ins others(188): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782484 | |||||
| chr14:101782484
|
CTCCCCCT others(91): Show |
C | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.94-3531_94-3434del others(98): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782484 | |||||
| chr14:101782487
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3531C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782487 | ||||||
| chr14:101782490
|
CTTCCCCT others(93): Show |
C | 2 | a0001c0001t0001g0113a0001c0001t0014g0110 | 2 | HG02895.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.94-3512_94-3413del others(100): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782490 | |||||
| chr14:101782491
|
T | C | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3527T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782491 | ||||||
| chr14:101782492
|
T | C | 2 | a0001c0001t0002g0086a0002c0002t0008g0011 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.94-3526T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782492 | ||||||
| chr14:101782493
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3525C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782493 | ||||||
| chr14:101782495
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3523C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782495 | ||||||
| chr14:101782496
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0009g0122 | 2 | HG01433.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.94-3522C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782496 | ||||||
| chr14:101782497
|
T | C | 1 | a0001c0001t0003g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.94-3521T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782497 | ||||||
| chr14:101782499
|
C | T | 2 | a0001c0001t0003g0131a0002c0002t0001g0092 | 2 | HG02451.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.94-3519C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782499 | ||||||
| chr14:101782500
|
CTCTCTTT others(5): Show |
C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3516_94-3505del others(12): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782500 | |||||
| chr14:101782501
|
T | C | 1 | a0001c0001t0003g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.94-3517T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782501 | ||||||
| chr14:101782502
|
CTCTTTCC others(73): Show |
C | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3512_94-3433del others(80): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782502 | |||||
| chr14:101782504
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3514C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782504 | ||||||
| chr14:101782505
|
T | TCCCCC | 5 | a0001c0001t0001g0123a0001c0001t0002g0091a0001c0001t0002g0094others(2): Show | 5 | HG01258.hp1 HG01884.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3513_94-3512ins others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782505 | ||||||
| chr14:101782505
|
T | TCCCCCTT others(75): Show |
3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94-3513_94-3512ins others(82): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782505 | ||||||
| chr14:101782505
|
T | TCCCCCTT others(18): Show |
3 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.94-3513_94-3512ins others(25): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782505 | ||||||
| chr14:101782505
|
T | TCCCCTTC others(157): Show |
1 | a0002c0002t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.94-3513_94-3512ins others(164): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782505 | ||||||
| chr14:101782506
|
T | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(22): Show | 25 | HG00558.hp2 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.94-3512T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782506 | ||||||
| chr14:101782507
|
T | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(20): Show | 23 | HG00558.hp2 HG00733.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.94-3511T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782507 | ||||||
| chr14:101782510
|
T | C | 15 | a0001c0001t0001g0117a0001c0001t0002g0029a0001c0001t0002g0037others(12): Show | 15 | HG01258.hp1 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.94-3508T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782510 | ||||||
| chr14:101782510
|
TC | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(19): Show | 22 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.94-3507delC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782510 | ||||||
| chr14:101782510
|
TCTTTCTC others(25): Show |
T | 1 | a0001c0001t0001g0055 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.94-3507_94-3476del others(32): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782510 | ||||||
| chr14:101782511
|
C | T | 3 | a0001c0001t0002g0094a0002c0002t0001g0097a0002c0002t0001g0098 | 3 | HG01884.hp1 HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3507C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782511 | ||||||
| chr14:101782512
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3506T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782512 | ||||||
| chr14:101782513
|
T | C | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(32): Show | 35 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.94-3505T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782513 | ||||||
| chr14:101782514
|
T | C | 11 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(8): Show | 11 | HG01884.hp1 HG02572.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.94-3504T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782514 | ||||||
| chr14:101782516
|
T | C | 3 | a0001c0001t0001g0123a0001c0001t0002g0111a0001c0001t0009g0122 | 3 | HG01258.hp1 HG01433.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.94-3502T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782516 | ||||||
| chr14:101782517
|
C | T | 1 | a0001c0001t0010g0133 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.94-3501C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782517 | ||||||
| chr14:101782518
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3500T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782518 | ||||||
| chr14:101782522
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.94-3496C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782522 | ||||||
| chr14:101782523
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(20): Show | 23 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.94-3495C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782523 | ||||||
| chr14:101782524
|
C | T | 24 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(21): Show | 24 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.94-3494C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782524 | ||||||
| chr14:101782527
|
C | T | 16 | a0001c0001t0001g0123a0001c0001t0002g0029a0001c0001t0002g0037others(13): Show | 16 | HG01258.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.94-3491C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782527 | ||||||
| chr14:101782528
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3490C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782528 | ||||||
| chr14:101782530
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3488C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782530 | ||||||
| chr14:101782531
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(18): Show | 21 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.94-3487C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782531 | ||||||
| chr14:101782532
|
T | C | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3486T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782532 | ||||||
| chr14:101782532
|
TCCCTC | T | 4 | a0001c0001t0001g0117a0001c0001t0003g0131a0001c0001t0003g0135others(1): Show | 4 | HG03710.hp1 NA19009.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3485_94-3481del others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782532 | ||||||
| chr14:101782536
|
T | C | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3482T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782536 | ||||||
| chr14:101782537
|
CTCTCCTC others(38): Show |
C | 1 | a0001c0003t0002g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.94-3475_94-3431del others(45): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782537 | |||||
| chr14:101782539
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3479C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782539 | ||||||
| chr14:101782540
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0003g0131a0001c0001t0003g0135others(1): Show | 4 | HG03710.hp1 NA19009.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3478T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782540 | ||||||
| chr14:101782542
|
C | CCCT | 12 | a0001c0001t0001g0123a0001c0001t0002g0029a0001c0001t0002g0037others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.94-3476_94-3475ins others(3): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782542 | ||||||
| chr14:101782542
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(18): Show | 21 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.94-3476C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782542 | ||||||
| chr14:101782543
|
T | A | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94-3475T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782543 | ||||||
| chr14:101782543
|
T | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(19): Show | 22 | HG00733.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.94-3475T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782543 | ||||||
| chr14:101782545
|
C | CTTCCCCT others(348): Show |
1 | a0001c0001t0002g0111 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.94-3473_94-3472ins others(355): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782545 | ||||||
| chr14:101782545
|
C | T | 16 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0002g0029others(13): Show | 16 | HG00558.hp2 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.94-3473C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782545 | ||||||
| chr14:101782546
|
C | T | 2 | a0001c0001t0010g0133a0002c0002t0001g0092 | 2 | HG02451.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.94-3472C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782546 | ||||||
| chr14:101782548
|
C | CTG | 12 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0021others(9): Show | 12 | HG01106.hp2 HG02083.hp2 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.94-3469_94-3468ins others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782548 | |||||
| chr14:101782548
|
C | CTGTCTCT others(490): Show |
2 | a0001c0001t0001g0045a0001c0001t0001g0048 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.94-3469_94-3468ins others(497): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782548 | |||||
| chr14:101782548
|
C | CTGTCTCT others(154): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0003g0005others(1): Show | 4 | HG00733.hp1 HG03927.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3469_94-3468ins others(161): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782548 | |||||
| chr14:101782548
|
C | CTGTCTCT others(313): Show |
2 | a0001c0001t0002g0062a0002c0002t0004g0119 | 2 | HG03486.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.94-3469_94-3468ins others(320): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782548 | |||||
| chr14:101782548
|
C | G | 1 | a0001c0001t0002g0111 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.94-3470C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782548 | ||||||
| chr14:101782549
|
T | C | 1 | a0001c0001t0010g0133 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.94-3469T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782549 | ||||||
| chr14:101782552
|
CTTTCT | C | 4 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0003g0138others(1): Show | 4 | NA19009.hp1 NA19068.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3465_94-3461del others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782552 | ||||||
| chr14:101782553
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0010g0133 | 2 | HG03710.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.94-3465T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782553 | ||||||
| chr14:101782554
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0010g0133 | 2 | HG03710.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.94-3464T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782554 | ||||||
| chr14:101782555
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3463T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782555 | ||||||
| chr14:101782557
|
T | TC | 6 | a0001c0001t0002g0086a0001c0001t0009g0122a0001c0003t0005g0018others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-3457dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782557 | |||||
| chr14:101782558
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3460C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782558 | ||||||
| chr14:101782563
|
T | C | 2 | a0001c0001t0010g0133a0002c0002t0001g0092 | 2 | HG02451.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.94-3455T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782563 | ||||||
| chr14:101782566
|
CTCTCT | C | 4 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0003g0138others(1): Show | 4 | NA19009.hp1 NA19068.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-3451_94-3447del others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782566 | ||||||
| chr14:101782567
|
T | C | 9 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0002g0086others(6): Show | 9 | HG00558.hp2 HG02055.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-3451T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782567 | ||||||
| chr14:101782567
|
TCTCTCTC others(25): Show |
T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-3439_94-3408del others(32): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782567 | |||||
| chr14:101782568
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3450C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782568 | ||||||
| chr14:101782569
|
T | C | 3 | a0001c0001t0009g0122a0001c0001t0010g0133a0002c0002t0001g0092 | 3 | HG01433.hp2 HG02451.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.94-3449T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782569 | ||||||
| chr14:101782571
|
T | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3447T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782571 | ||||||
| chr14:101782575
|
C | T | 2 | a0001c0001t0010g0133a0002c0002t0001g0092 | 2 | HG02451.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.94-3443C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782575 | ||||||
| chr14:101782576
|
CCCCCTT | C | 5 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0003g0138others(2): Show | 5 | HG01433.hp2 NA19009.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3441_94-3436del others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782576 | ||||||
| chr14:101782577
|
C | CTCTGTCT others(25): Show |
1 | a0001c0001t0002g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.94-3441_94-3440ins others(32): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782577 | ||||||
| chr14:101782577
|
C | CTCTGTCT others(46): Show |
3 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.94-3441_94-3440ins others(53): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782577 | ||||||
| chr14:101782577
|
C | CTCTGTCT others(162): Show |
1 | a0002c0002t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.94-3441_94-3440ins others(169): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782577 | ||||||
| chr14:101782577
|
C | CTGTGT | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3441_94-3440ins others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782577 | ||||||
| chr14:101782579
|
C | T | 3 | a0001c0001t0002g0091a0001c0001t0002g0094a0002c0002t0001g0097 | 3 | HG01884.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3439C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782579 | ||||||
| chr14:101782582
|
T | C | 5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-3436T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782582 | ||||||
| chr14:101782588
|
CCATTCCC others(10): Show |
C | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3428_94-3412del others(17): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782588 | |||||
| chr14:101782590
|
A | ATTCCCCT others(13): Show |
1 | a0001c0001t0002g0028 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.94-3393_94-3374dup others(20): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782590 | |||||
| chr14:101782590
|
A | ATTCCCCT others(331): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0021 | 2 | HG02132.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.94-3298_94-3297ins others(338): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782590 | |||||
| chr14:101782590
|
A | C | 10 | a0001c0001t0001g0117a0001c0001t0002g0029a0001c0001t0002g0037others(7): Show | 10 | HG01433.hp2 HG02559.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.94-3428A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782590 | ||||||
| chr14:101782594
|
C | CCCTCCCT others(33): Show |
1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94-3409_94-3408ins others(40): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782594 | |||||
| chr14:101782594
|
C | T | 2 | a0001c0001t0017g0085a0002c0002t0004g0017 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.94-3424C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782594 | ||||||
| chr14:101782596
|
C | T | 3 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.94-3422C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782596 | ||||||
| chr14:101782601
|
T | TCTCTCCC others(190): Show |
1 | a0002c0002t0001g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.94-3298_94-3297ins others(197): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782601 | |||||
| chr14:101782601
|
TCTCTCCC others(31): Show |
T | 1 | a0002c0002t0003g0137 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.94-3388_94-3351del others(38): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782601 | |||||
| chr14:101782602
|
C | T | 2 | a0001c0001t0006g0099a0001c0001t0006g0105 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.94-3416C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782602 | ||||||
| chr14:101782610
|
C | A | 1 | a0002c0002t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.94-3408C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782610 | ||||||
| chr14:101782610
|
C | T | 3 | a0001c0001t0002g0094a0001c0001t0009g0122a0002c0002t0001g0097 | 3 | HG01433.hp2 HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3408C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782610 | ||||||
| chr14:101782612
|
T | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3406T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782612 | ||||||
| chr14:101782613
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3405C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782613 | ||||||
| chr14:101782614
|
C | T | 5 | a0001c0001t0001g0123a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-3404C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782614 | ||||||
| chr14:101782615
|
C | A | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3403C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782615 | ||||||
| chr14:101782615
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3403C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782615 | ||||||
| chr14:101782616
|
C | T | 11 | a0001c0001t0001g0113a0001c0001t0002g0029a0001c0001t0002g0037others(8): Show | 11 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.94-3402C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782616 | ||||||
| chr14:101782618
|
C | T | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3400C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782618 | ||||||
| chr14:101782619
|
C | CCCTCCCT others(52): Show |
3 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.94-3398_94-3397ins others(59): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782619 | |||||
| chr14:101782619
|
C | T | 3 | a0001c0001t0002g0094a0001c0001t0009g0122a0002c0002t0001g0097 | 3 | HG01433.hp2 HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3399C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782619 | ||||||
| chr14:101782621
|
TCTCTCCC others(11): Show |
T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-3373_94-3356del others(18): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782621 | |||||
| chr14:101782622
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-3396C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782622 | ||||||
| chr14:101782627
|
C | CCCCTTCC others(197): Show |
1 | a0002c0002t0008g0011 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.94-3374_94-3373ins others(204): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782627 | |||||
| chr14:101782627
|
C | CCCCTTCC others(39): Show |
1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.94-3374_94-3373ins others(46): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782627 | |||||
| chr14:101782630
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3388C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782630 | ||||||
| chr14:101782634
|
C | T | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3384C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782634 | ||||||
| chr14:101782636
|
C | T | 7 | a0001c0001t0006g0099a0001c0001t0006g0105a0002c0002t0001g0087others(4): Show | 7 | HG01070.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-3382C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782636 | ||||||
| chr14:101782639
|
C | CCT | 16 | a0001c0001t0001g0066a0001c0001t0002g0029a0001c0001t0002g0037others(13): Show | 16 | HG01070.hp1 HG02451.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.94-3375_94-3374dup others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782639 | |||||
| chr14:101782639
|
C | CCTCTCCC others(53): Show |
1 | a0001c0001t0001g0036 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.94-3371_94-3370ins others(60): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782639 | |||||
| chr14:101782639
|
C | CCTCTCCC others(432): Show |
1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.94-3298_94-3297ins others(439): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782639 | |||||
| chr14:101782639
|
C | CCTCTCTC others(112): Show |
3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94-3374_94-3373ins others(119): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782639 | |||||
| chr14:101782639
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0009g0122 | 2 | HG01433.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.94-3379C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782639 | ||||||
| chr14:101782644
|
C | CT | 2 | a0001c0001t0002g0124a0001c0001t0007g0126 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.94-3374_94-3373ins others(1): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782644 | ||||||
| chr14:101782645
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3373C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782645 | ||||||
| chr14:101782646
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3372C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782646 | ||||||
| chr14:101782647
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3371C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782647 | ||||||
| chr14:101782647
|
CCTTCCCC others(27): Show |
C | 1 | a0001c0003t0002g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.94-3368_94-3335del others(34): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782647 | |||||
| chr14:101782648
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94-3370C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782648 | ||||||
| chr14:101782650
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3368T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782650 | ||||||
| chr14:101782651
|
C | CT | 2 | a0001c0001t0002g0124a0001c0001t0007g0126 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.94-3367_94-3366ins others(1): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782651 | ||||||
| chr14:101782653
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94-3365C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782653 | ||||||
| chr14:101782653
|
C | T | 2 | a0001c0001t0002g0124a0001c0001t0007g0126 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.94-3365C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782653 | ||||||
| chr14:101782654
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3364C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782654 | ||||||
| chr14:101782656
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94-3362C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782656 | ||||||
| chr14:101782657
|
C | CCTCTCTC others(62): Show |
1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.94-3312_94-3311ins others(69): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782657 | |||||
| chr14:101782657
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0002g0124a0001c0001t0007g0126 | 3 | HG01884.hp2 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.94-3361C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782657 | ||||||
| chr14:101782660
|
C | T | 2 | a0001c0001t0002g0124a0001c0001t0007g0126 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.94-3358C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782660 | ||||||
| chr14:101782665
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3353C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782665 | ||||||
| chr14:101782669
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0002g0094a0002c0002t0001g0097 | 3 | HG01884.hp1 HG03710.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3349T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782669 | ||||||
| chr14:101782671
|
T | C | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3347T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782671 | ||||||
| chr14:101782673
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94-3345T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782673 | ||||||
| chr14:101782674
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94-3344C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782674 | ||||||
| chr14:101782675
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94-3343T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782675 | ||||||
| chr14:101782683
|
T | C | 2 | a0001c0001t0001g0107a0002c0002t0001g0001 | 2 | NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.94-3335T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782683 | ||||||
| chr14:101782684
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94-3334C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782684 | ||||||
| chr14:101782688
|
T | C | 2 | a0001c0001t0001g0032a0001c0003t0002g0112 | 2 | HG02559.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94-3330T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782688 | ||||||
| chr14:101782693
|
T | C | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3325T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782693 | ||||||
| chr14:101782705
|
C | G | 7 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0003g0138others(4): Show | 7 | HG02451.hp1 HG02717.hp2 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-3313C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782705 | ||||||
| chr14:101782706
|
TGTCTCTT others(9): Show |
T | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3311_94-3296del others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782706 | ||||||
| chr14:101782724
|
T | C | 1 | a0001c0001t0003g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.94-3294T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782724 | ||||||
| chr14:101782727
|
C | T | 1 | a0001c0001t0003g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.94-3291C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782727 | ||||||
| chr14:101782729
|
A | T | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3289A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782729 | ||||||
| chr14:101782739
|
TTTCTC | T | 2 | a0001c0001t0002g0094a0002c0002t0001g0097 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-3278_94-3274del others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782739 | ||||||
| chr14:101782751
|
T | C | 8 | a0001c0001t0001g0047a0001c0001t0002g0094a0001c0001t0002g0124others(5): Show | 8 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-3267T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782751 | ||||||
| chr14:101782751
|
T | TCCCCTCC others(65): Show |
3 | a0002c0002t0001g0087a0002c0002t0001g0092a0002c0002t0001g0098 | 3 | HG02451.hp1 HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.94-3225_94-3224ins others(72): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782751 | |||||
| chr14:101782822
|
T | TC | 4 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0019g0116others(1): Show | 4 | HG00438.hp1 HG02055.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3191dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782822 | |||||
| chr14:101782919
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.94-3099C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782919 | ||||||
| chr14:101782953
|
GC | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(6): Show | 9 | HG01993.hp2 HG02056.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-3059delC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101782953 | |||||
| chr14:101782959
|
CT | C | 2 | a0001c0003t0018g0089a0002c0002t0004g0017 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.94-3058delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782959 | ||||||
| chr14:101782980
|
C | T | 2 | a0001c0003t0018g0089a0002c0002t0004g0017 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.94-3038C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101782980 | ||||||
| chr14:101783040
|
T | C | 3 | a0001c0001t0002g0124a0001c0001t0007g0126a0001c0003t0002g0127 | 3 | HG01884.hp2 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.94-2978T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101783040 | ||||||
| chr14:101783049
|
T | TC | 4 | a0001c0001t0001g0049a0001c0001t0001g0078a0001c0001t0001g0082others(1): Show | 4 | HG01934.hp1 HG02055.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-2964dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101783049 | |||||
| chr14:101783188
|
CCTCCCCC others(20): Show |
C | 2 | a0001c0001t0001g0081a0001c0001t0001g0096 | 2 | HG01243.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.94-2817_94-2791del others(27): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101783188 | |||||
| chr14:101783229
|
T | C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.94-2789T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101783229 | ||||||
| chr14:101783376
|
C | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.94-2642C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101783376 | ||||||
| chr14:101783449
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.94-2569G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101783449 | ||||||
| chr14:101783495
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.94-2523A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101783495 | ||||||
| chr14:101783565
|
G | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.94-2453G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101783565 | ||||||
| chr14:101783571
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.94-2447C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101783571 | ||||||
| chr14:101783583
|
G | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.94-2435G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101783583 | ||||||
| chr14:101784023
|
G | C | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | NA18995.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.94-1995G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101784023 | ||||||
| chr14:101784044
|
C | T | 1 | a0002c0002t0001g0001 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.94-1974C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101784044 | ||||||
| chr14:101784513
|
G | T | 14 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(11): Show | 14 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.94-1505G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101784513 | ||||||
| chr14:101784928
|
G | GGGCCC | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-1089_94-1085dup others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 101784928 | |||||
| chr14:101784936
|
T | A | 1 | a0001c0001t0003g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.94-1082T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101784936 | ||||||
| chr14:101784952
|
G | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.94-1066G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101784952 | ||||||
| chr14:101785058
|
A | G | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.94-960A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101785058 | ||||||
| chr14:101785346
|
A | G | 2 | a0001c0001t0001g0067a0002c0002t0001g0102 | 2 | HG02132.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.94-672A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101785346 | ||||||
| chr14:101785400
|
G | C | 40 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.94-618G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101785400 | ||||||
| chr14:101785418
|
A | G | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.94-600A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101785418 | ||||||
| chr14:101785439
|
C | G | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.94-579C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101785439 | ||||||
| chr14:101785806
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.94-212G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101785806 | ||||||
| chr14:101785993
|
T | C | 14 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(11): Show | 14 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.94-25T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 2/15 | chr14 | 101785993 | ||||||
| chr14:101786313
|
GT | G | 14 | a0001c0001t0001g0057a0001c0001t0001g0078a0001c0001t0001g0113others(11): Show | 14 | HG01071.hp2 HG01074.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+143delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101786313 | |||||
| chr14:101786653
|
C | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+470C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101786653 | ||||||
| chr14:101786716
|
CA | C | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+536delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101786716 | |||||
| chr14:101786910
|
A | G | 1 | a0002c0002t0003g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.259+727A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101786910 | ||||||
| chr14:101786965
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.259+782T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101786965 | ||||||
| chr14:101786989
|
C | T | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+806C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101786989 | ||||||
| chr14:101787204
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.259+1021C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787204 | ||||||
| chr14:101787253
|
G | A | 1 | a0002c0002t0008g0011 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.259+1070G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787253 | ||||||
| chr14:101787403
|
TATGGGTG others(5): Show |
T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.259+1235_259+1246d others(14): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101787403 | |||||
| chr14:101787546
|
G | A | 1 | a0002c0002t0001g0001 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259+1363G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787546 | ||||||
| chr14:101787560
|
A | G | 2 | a0001c0001t0001g0117a0002c0002t0001g0001 | 2 | HG03710.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.259+1377A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787560 | ||||||
| chr14:101787579
|
T | C | 3 | a0001c0003t0018g0089a0002c0002t0004g0119a0002c0002t0008g0011 | 3 | HG02055.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259+1396T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787579 | ||||||
| chr14:101787580
|
G | A | 2 | a0001c0003t0018g0089a0002c0002t0004g0119 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259+1397G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787580 | ||||||
| chr14:101787581
|
G | A | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.259+1398G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787581 | ||||||
| chr14:101787586
|
AC | A | 45 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(42): Show | 45 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.259+1407delC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101787586 | |||||
| chr14:101787590
|
C | T | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.259+1407C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787590 | ||||||
| chr14:101787591
|
G | A | 1 | a0001c0001t0017g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.259+1408G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787591 | ||||||
| chr14:101787594
|
T | C | 52 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(49): Show | 52 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.259+1411T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787594 | ||||||
| chr14:101787600
|
A | G | 8 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(5): Show | 8 | HG01071.hp2 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+1417A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787600 | ||||||
| chr14:101787653
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.259+1470G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787653 | ||||||
| chr14:101787766
|
C | CA | 18 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0058others(15): Show | 18 | HG01106.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.259+1604dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101787766 | |||||
| chr14:101787766
|
CA | C | 13 | a0001c0001t0001g0067a0001c0001t0002g0124a0001c0001t0002g0125others(10): Show | 13 | HG01884.hp2 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.259+1604delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101787766 | |||||
| chr14:101787847
|
G | A | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+1664G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101787847 | ||||||
| chr14:101788672
|
T | C | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+2489T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101788672 | ||||||
| chr14:101789130
|
G | A | 5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+2947G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101789130 | ||||||
| chr14:101789491
|
C | T | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+3308C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101789491 | ||||||
| chr14:101789505
|
G | A | 14 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(11): Show | 14 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+3322G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101789505 | ||||||
| chr14:101789564
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+3381G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101789564 | ||||||
| chr14:101789684
|
T | C | 6 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(3): Show | 6 | HG00733.hp2 HG01884.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+3501T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101789684 | ||||||
| chr14:101789707
|
G | C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+3524G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101789707 | ||||||
| chr14:101789725
|
G | C | 47 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0049others(44): Show | 47 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.259+3542G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101789725 | ||||||
| chr14:101789728
|
C | T | 14 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(11): Show | 14 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+3545C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101789728 | ||||||
| chr14:101789840
|
T | G | 38 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.259+3657T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101789840 | ||||||
| chr14:101789908
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259+3725G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101789908 | ||||||
| chr14:101790088
|
T | A | 14 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(11): Show | 14 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+3905T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101790088 | ||||||
| chr14:101790856
|
G | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+4673G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101790856 | ||||||
| chr14:101790878
|
A | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0048 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.259+4695A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101790878 | ||||||
| chr14:101790951
|
T | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+4768T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101790951 | ||||||
| chr14:101790953
|
G | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+4770G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101790953 | ||||||
| chr14:101790962
|
C | T | 14 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(11): Show | 14 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+4779C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101790962 | ||||||
| chr14:101791007
|
G | A | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+4824G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101791007 | ||||||
| chr14:101791205
|
C | T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+5022C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101791205 | ||||||
| chr14:101791447
|
A | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0048a0002c0002t0001g0046 | 3 | HG00733.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.259+5264A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101791447 | ||||||
| chr14:101791543
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.259+5360T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101791543 | ||||||
| chr14:101791553
|
C | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+5370C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101791553 | ||||||
| chr14:101791654
|
G | GT | 6 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(3): Show | 6 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+5481dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101791654 | |||||
| chr14:101791680
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.259+5497T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101791680 | ||||||
| chr14:101791697
|
A | G | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+5514A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101791697 | ||||||
| chr14:101791802
|
G | A | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.259+5619G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101791802 | ||||||
| chr14:101792188
|
T | C | 3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.259+6005T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101792188 | ||||||
| chr14:101792325
|
G | A | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+6142G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101792325 | ||||||
| chr14:101792417
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.259+6234G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101792417 | ||||||
| chr14:101792828
|
T | C | 1 | a0002c0002t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259+6645T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101792828 | ||||||
| chr14:101792872
|
ATTTTTC | A | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+6694_259+6699d others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101792872 | |||||
| chr14:101792883
|
C | CT | 5 | a0001c0001t0001g0048a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG01071.hp1 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+6714dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101792883 | |||||
| chr14:101793130
|
G | A | 14 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(11): Show | 14 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+6947G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101793130 | ||||||
| chr14:101793423
|
C | G | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+7240C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101793423 | ||||||
| chr14:101793424
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.259+7241T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101793424 | ||||||
| chr14:101793659
|
A | T | 1 | a0001c0001t0007g0016 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259+7476A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101793659 | ||||||
| chr14:101793692
|
A | G | 3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.259+7509A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101793692 | ||||||
| chr14:101793914
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.259+7731C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101793914 | ||||||
| chr14:101794076
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0011g0012a0002c0002t0008g0011 | 3 | HG01074.hp1 HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.259+7893A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101794076 | ||||||
| chr14:101794324
|
A | T | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.259+8141A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101794324 | ||||||
| chr14:101794325
|
AT | A | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.259+8143delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101794325 | ||||||
| chr14:101794422
|
A | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+8239A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101794422 | ||||||
| chr14:101794763
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.259+8580C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101794763 | ||||||
| chr14:101794986
|
G | A | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+8803G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101794986 | ||||||
| chr14:101795223
|
A | G | 14 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(11): Show | 14 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+9040A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101795223 | ||||||
| chr14:101795481
|
A | T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+9298A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101795481 | ||||||
| chr14:101795701
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+9518G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101795701 | ||||||
| chr14:101795735
|
T | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.259+9552T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101795735 | ||||||
| chr14:101795763
|
A | T | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.259+9580A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101795763 | ||||||
| chr14:101795878
|
A | G | 1 | a0001c0003t0002g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.259+9695A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101795878 | ||||||
| chr14:101796285
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.259+10102T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101796285 | ||||||
| chr14:101796305
|
G | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+10122G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101796305 | ||||||
| chr14:101796566
|
T | G | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+10383T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101796566 | ||||||
| chr14:101796618
|
A | G | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.259+10435A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101796618 | ||||||
| chr14:101796819
|
G | A | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+10636G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101796819 | ||||||
| chr14:101796915
|
A | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+10732A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101796915 | ||||||
| chr14:101796927
|
G | A | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+10744G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101796927 | ||||||
| chr14:101796976
|
T | C | 4 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+10793T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101796976 | ||||||
| chr14:101796986
|
G | A | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+10803G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101796986 | ||||||
| chr14:101797127
|
A | C | 6 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG01071.hp2 HG01258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+10944A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101797127 | ||||||
| chr14:101797636
|
C | T | 43 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(40): Show | 43 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.259+11453C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101797636 | ||||||
| chr14:101797870
|
C | G | 1 | a0002c0002t0008g0011 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.259+11687C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101797870 | ||||||
| chr14:101797935
|
C | T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+11752C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101797935 | ||||||
| chr14:101798167
|
A | G | 1 | a0002c0002t0001g0102 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.259+11984A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101798167 | ||||||
| chr14:101798288
|
T | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+12105T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101798288 | ||||||
| chr14:101798297
|
A | G | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+12114A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101798297 | ||||||
| chr14:101798382
|
C | T | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.259+12199C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101798382 | ||||||
| chr14:101798422
|
G | T | 14 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(11): Show | 14 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+12239G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101798422 | ||||||
| chr14:101798531
|
C | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+12348C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101798531 | ||||||
| chr14:101798538
|
C | G | 45 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(42): Show | 45 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.259+12355C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101798538 | ||||||
| chr14:101798692
|
T | G | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+12509T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101798692 | ||||||
| chr14:101798883
|
A | G | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+12700A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101798883 | ||||||
| chr14:101798898
|
A | G | 45 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(42): Show | 45 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.259+12715A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101798898 | ||||||
| chr14:101799061
|
T | C | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+12878T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101799061 | ||||||
| chr14:101799224
|
C | T | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.259+13041C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101799224 | ||||||
| chr14:101799274
|
A | G | 1 | a0001c0001t0007g0016 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.259+13091A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101799274 | ||||||
| chr14:101799719
|
G | A | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.259+13536G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101799719 | ||||||
| chr14:101799977
|
T | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+13794T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101799977 | ||||||
| chr14:101800157
|
G | A | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+13974G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101800157 | ||||||
| chr14:101800241
|
T | C | 1 | a0002c0002t0004g0119 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.259+14058T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101800241 | ||||||
| chr14:101800270
|
C | T | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.259+14087C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101800270 | ||||||
| chr14:101800383
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.259+14200G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101800383 | ||||||
| chr14:101800406
|
T | A | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+14223T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101800406 | ||||||
| chr14:101800651
|
C | CA | 8 | a0001c0001t0001g0123a0001c0001t0007g0016a0001c0001t0011g0012others(5): Show | 8 | HG02055.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+14482dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101800651 | |||||
| chr14:101800651
|
CA | C | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+14482delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101800651 | |||||
| chr14:101800775
|
T | G | 14 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(11): Show | 14 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+14592T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101800775 | ||||||
| chr14:101800790
|
C | T | 14 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(11): Show | 14 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+14607C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101800790 | ||||||
| chr14:101800865
|
T | C | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+14682T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101800865 | ||||||
| chr14:101800889
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.259+14706A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101800889 | ||||||
| chr14:101801330
|
A | C | 40 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.259+15147A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101801330 | ||||||
| chr14:101802055
|
A | C | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.259+15872A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101802055 | ||||||
| chr14:101802141
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.259+15958G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101802141 | ||||||
| chr14:101802316
|
G | A | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+16133G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101802316 | ||||||
| chr14:101802349
|
T | C | 1 | a0002c0002t0001g0084 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.259+16166T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101802349 | ||||||
| chr14:101802484
|
G | A | 1 | a0002c0002t0001g0102 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.259+16301G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101802484 | ||||||
| chr14:101802505
|
G | A | 1 | a0002c0002t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.259+16322G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101802505 | ||||||
| chr14:101802743
|
T | C | 1 | a0002c0002t0001g0115 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.259+16560T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101802743 | ||||||
| chr14:101802951
|
T | A | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.259+16768T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101802951 | ||||||
| chr14:101802951
|
T | TA | 7 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0005g0069others(4): Show | 7 | HG00558.hp1 HG01070.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+16791dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101802951 | |||||
| chr14:101802951
|
T | TAA | 26 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0057others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.259+16790_259+1679 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101802951 | |||||
| chr14:101802980
|
A | G | 46 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(43): Show | 46 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.259+16797A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101802980 | ||||||
| chr14:101803079
|
T | C | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+16896T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101803079 | ||||||
| chr14:101803440
|
C | G | 1 | a0001c0003t0020g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.259+17257C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101803440 | ||||||
| chr14:101803450
|
C | T | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+17267C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101803450 | ||||||
| chr14:101803462
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.259+17279C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101803462 | ||||||
| chr14:101803507
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.259+17324G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101803507 | ||||||
| chr14:101803585
|
G | C | 1 | a0001c0003t0005g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.259+17402G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101803585 | ||||||
| chr14:101803633
|
A | G | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.259+17450A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101803633 | ||||||
| chr14:101803729
|
C | CA | 5 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+17561dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101803729 | |||||
| chr14:101803875
|
G | A | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.259+17692G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101803875 | ||||||
| chr14:101804268
|
G | C | 1 | a0004c0005t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.259+18085G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101804268 | ||||||
| chr14:101804500
|
AAT | A | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.259+18329_259+1833 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101804500 | |||||
| chr14:101805206
|
C | T | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+19023C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101805206 | ||||||
| chr14:101805674
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.259+19491G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101805674 | ||||||
| chr14:101806097
|
T | A | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+19914T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101806097 | ||||||
| chr14:101806099
|
G | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+19916G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101806099 | ||||||
| chr14:101806705
|
A | G | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259+20522A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101806705 | ||||||
| chr14:101807172
|
T | TAA | 45 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(42): Show | 45 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.259+20990_259+2099 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101807172 | |||||
| chr14:101807559
|
T | C | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG01074.hp2 HG01256.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+21376T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101807559 | ||||||
| chr14:101807950
|
G | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+21767G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101807950 | ||||||
| chr14:101807968
|
T | C | 2 | a0001c0001t0001g0107a0002c0002t0001g0038 | 2 | NA18995.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.259+21785T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101807968 | ||||||
| chr14:101808118
|
G | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+21935G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101808118 | ||||||
| chr14:101808234
|
A | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0030a0002c0002t0001g0041 | 3 | HG00280.hp1 HG00642.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.259+22051A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101808234 | ||||||
| chr14:101808405
|
G | A | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+22222G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101808405 | ||||||
| chr14:101808561
|
T | C | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+22378T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101808561 | ||||||
| chr14:101808796
|
T | A | 1 | a0002c0002t0001g0074 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.259+22613T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101808796 | ||||||
| chr14:101808816
|
G | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+22633G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101808816 | ||||||
| chr14:101808838
|
G | A | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259+22655G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101808838 | ||||||
| chr14:101809219
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+23036G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101809219 | ||||||
| chr14:101809272
|
G | C | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+23089G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101809272 | ||||||
| chr14:101809392
|
T | TA | 7 | a0001c0001t0007g0016a0001c0001t0011g0012a0001c0003t0005g0018others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+23221dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101809392 | |||||
| chr14:101809404
|
A | C | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+23221A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101809404 | ||||||
| chr14:101809405
|
C | A | 30 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.259+23222C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101809405 | ||||||
| chr14:101809552
|
C | CT | 29 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0093others(26): Show | 29 | HG00642.hp1 HG01255.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.259+23395dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101809552 | |||||
| chr14:101809577
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.259+23394T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101809577 | ||||||
| chr14:101810095
|
A | C | 1 | a0002c0002t0001g0115 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.259+23912A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101810095 | ||||||
| chr14:101810380
|
T | C | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+24197T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101810380 | ||||||
| chr14:101810391
|
G | T | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+24208G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101810391 | ||||||
| chr14:101810822
|
T | C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+24639T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101810822 | ||||||
| chr14:101811157
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.259+24974A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101811157 | ||||||
| chr14:101811535
|
G | A | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+25352G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101811535 | ||||||
| chr14:101811787
|
T | C | 1 | a0002c0002t0001g0102 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.259+25604T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101811787 | ||||||
| chr14:101811858
|
T | A | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0007g0126others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+25675T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101811858 | ||||||
| chr14:101811872
|
A | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0047a0001c0001t0011g0012others(4): Show | 7 | HG01106.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+25689A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101811872 | ||||||
| chr14:101811962
|
C | T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+25779C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101811962 | ||||||
| chr14:101812301
|
A | G | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+26118A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101812301 | ||||||
| chr14:101812321
|
G | C | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.259+26138G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101812321 | ||||||
| chr14:101812375
|
G | T | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+26192G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101812375 | ||||||
| chr14:101812416
|
C | A | 1 | a0001c0001t0001g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.259+26233C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101812416 | ||||||
| chr14:101812864
|
G | A | 3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.259+26681G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101812864 | ||||||
| chr14:101813008
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.259+26825C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101813008 | ||||||
| chr14:101813078
|
T | C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+26895T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101813078 | ||||||
| chr14:101813091
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.259+26908G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101813091 | ||||||
| chr14:101813506
|
C | T | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+27323C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101813506 | ||||||
| chr14:101813578
|
C | T | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+27395C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101813578 | ||||||
| chr14:101813682
|
G | T | 1 | a0001c0001t0001g0022 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.259+27499G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101813682 | ||||||
| chr14:101813960
|
A | T | 2 | a0001c0001t0011g0012a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.259+27777A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101813960 | ||||||
| chr14:101814026
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.259+27843A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814026 | ||||||
| chr14:101814112
|
A | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+27929A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814112 | ||||||
| chr14:101814185
|
C | T | 1 | a0002c0002t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259+28002C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814185 | ||||||
| chr14:101814315
|
C | A | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259+28132C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814315 | ||||||
| chr14:101814392
|
G | A | 1 | a0002c0002t0003g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.259+28209G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814392 | ||||||
| chr14:101814437
|
G | C | 1 | a0001c0001t0017g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.259+28254G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814437 | ||||||
| chr14:101814656
|
A | G | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.259+28473A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814656 | ||||||
| chr14:101814778
|
T | A | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259+28595T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814778 | ||||||
| chr14:101814788
|
T | C | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+28605T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814788 | ||||||
| chr14:101814790
|
T | A | 5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+28607T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814790 | ||||||
| chr14:101814804
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.259+28621G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101814804 | ||||||
| chr14:101815079
|
A | G | 1 | a0002c0002t0004g0119 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.259+28896A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815079 | ||||||
| chr14:101815126
|
C | T | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+28943C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815126 | ||||||
| chr14:101815133
|
C | A | 3 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.259+28950C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815133 | ||||||
| chr14:101815149
|
C | T | 14 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0005others(11): Show | 14 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+28966C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815149 | ||||||
| chr14:101815425
|
G | A | 1 | a0002c0002t0001g0102 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.259+29242G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815425 | ||||||
| chr14:101815461
|
T | C | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259+29278T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815461 | ||||||
| chr14:101815505
|
C | T | 32 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.259+29322C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815505 | ||||||
| chr14:101815731
|
G | A | 2 | a0001c0001t0009g0122a0002c0002t0001g0121 | 2 | HG01433.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.259+29548G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815731 | ||||||
| chr14:101815741
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0096 | 2 | HG01243.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.259+29558C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815741 | ||||||
| chr14:101815845
|
T | G | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+29662T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815845 | ||||||
| chr14:101815935
|
A | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+29752A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815935 | ||||||
| chr14:101815966
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.259+29783G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101815966 | ||||||
| chr14:101816148
|
T | C | 1 | a0001c0001t0006g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.259+29965T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101816148 | ||||||
| chr14:101816299
|
G | A | 4 | a0001c0001t0001g0078a0001c0001t0006g0075a0001c0003t0002g0079others(1): Show | 4 | HG02735.hp1 HG03579.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+30116G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101816299 | ||||||
| chr14:101816479
|
C | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+30296C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101816479 | ||||||
| chr14:101816508
|
C | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+30325C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101816508 | ||||||
| chr14:101816856
|
A | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0049 | 2 | HG01934.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.259+30673A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101816856 | ||||||
| chr14:101816881
|
TTA | T | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0003t0002g0127others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+30708_259+3070 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101816881 | |||||
| chr14:101816884
|
TA | T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+30702delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101816884 | ||||||
| chr14:101816907
|
T | TA | 47 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(44): Show | 47 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.259+30725dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101816907 | |||||
| chr14:101816917
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.259+30734A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101816917 | ||||||
| chr14:101816927
|
A | AAT | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+30752_259+3075 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101816927 | |||||
| chr14:101816966
|
T | A | 55 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0047others(52): Show | 55 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.259+30783T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101816966 | ||||||
| chr14:101816967
|
T | A | 1 | a0002c0002t0004g0073 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.259+30784T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101816967 | ||||||
| chr14:101816968
|
T | A | 16 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(13): Show | 16 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.259+30785T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101816968 | ||||||
| chr14:101817208
|
G | A | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0003t0002g0127others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+31025G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101817208 | ||||||
| chr14:101817289
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.259+31106G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101817289 | ||||||
| chr14:101817340
|
G | T | 26 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(23): Show | 26 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.259+31157G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101817340 | ||||||
| chr14:101817521
|
C | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(2): Show | 5 | HG02486.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+31338C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101817521 | ||||||
| chr14:101818115
|
C | T | 3 | a0001c0001t0009g0122a0001c0003t0018g0089a0002c0002t0001g0121 | 3 | HG01433.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259+31932C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101818115 | ||||||
| chr14:101818156
|
C | T | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0003t0002g0127others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+31973C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101818156 | ||||||
| chr14:101818257
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG00558.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.259+32074G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101818257 | ||||||
| chr14:101818633
|
C | CA | 20 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(17): Show | 20 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.259+32466dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101818633 | |||||
| chr14:101818742
|
T | C | 16 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0002g0124others(13): Show | 16 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.259+32559T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101818742 | ||||||
| chr14:101818887
|
T | A | 1 | a0001c0003t0002g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.259+32704T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101818887 | ||||||
| chr14:101818942
|
A | C | 16 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(13): Show | 16 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.259+32759A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101818942 | ||||||
| chr14:101819209
|
TC | T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+33027delC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819209 | ||||||
| chr14:101819370
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.259+33187T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819370 | ||||||
| chr14:101819375
|
C | T | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0003t0002g0127others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+33192C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819375 | ||||||
| chr14:101819401
|
G | T | 1 | a0001c0001t0003g0131 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.259+33218G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819401 | ||||||
| chr14:101819456
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.259+33273G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819456 | ||||||
| chr14:101819458
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.259+33275T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819458 | ||||||
| chr14:101819470
|
A | G | 3 | a0001c0003t0018g0089a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.259+33287A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819470 | ||||||
| chr14:101819640
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.259+33457T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819640 | ||||||
| chr14:101819677
|
G | T | 1 | a0002c0002t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.259+33494G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819677 | ||||||
| chr14:101819945
|
G | A | 5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+33762G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819945 | ||||||
| chr14:101819963
|
G | A | 41 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(38): Show | 41 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.259+33780G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101819963 | ||||||
| chr14:101820227
|
A | C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+34044A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101820227 | ||||||
| chr14:101820364
|
T | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.259+34181T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101820364 | ||||||
| chr14:101820368
|
C | T | 5 | a0001c0001t0007g0016a0001c0003t0005g0018a0001c0003t0005g0020others(2): Show | 5 | HG02572.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+34185C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101820368 | ||||||
| chr14:101820679
|
A | G | 12 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0006g0075others(9): Show | 12 | HG00733.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+34496A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101820679 | ||||||
| chr14:101820695
|
T | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(2): Show | 5 | HG02486.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+34512T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101820695 | ||||||
| chr14:101820713
|
C | T | 2 | a0001c0001t0001g0033a0002c0002t0001g0035 | 2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.259+34530C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101820713 | ||||||
| chr14:101820725
|
C | G | 12 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0006g0075others(9): Show | 12 | HG00733.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+34542C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101820725 | ||||||
| chr14:101821011
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.259+34828T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821011 | ||||||
| chr14:101821053
|
A | C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.259+34870A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821053 | ||||||
| chr14:101821089
|
A | AT | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259+34906_259+3490 others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821089 | ||||||
| chr14:101821094
|
TAAAATA | T | 16 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0002g0124others(13): Show | 16 | HG00733.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.259+34928_259+3493 others(10): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101821094 | |||||
| chr14:101821117
|
A | T | 1 | a0002c0002t0001g0002 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.259+34934A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821117 | ||||||
| chr14:101821135
|
G | A | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.259+34952G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821135 | ||||||
| chr14:101821231
|
T | G | 47 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(44): Show | 47 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.259+35048T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821231 | ||||||
| chr14:101821369
|
C | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(2): Show | 5 | HG02486.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+35186C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821369 | ||||||
| chr14:101821410
|
G | A | 15 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(12): Show | 15 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(12): Show |
intron_variant | MODIFIER | c.259+35227G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821410 | ||||||
| chr14:101821440
|
G | T | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-35246G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821440 | ||||||
| chr14:101821444
|
G | GGTGT | 3 | a0001c0001t0002g0124a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG01884.hp2 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.260-35239_260-3523 others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101821444 | |||||
| chr14:101821444
|
G | GGTGTGT | 3 | a0001c0001t0002g0125a0001c0003t0002g0127a0001c0003t0002g0128 | 3 | HG02717.hp1 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.260-35239_260-3523 others(10): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101821444 | |||||
| chr14:101821444
|
G | T | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-35242G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821444 | ||||||
| chr14:101821444
|
GGTGGGTG others(3): Show |
G | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.260-35238_260-3522 others(14): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101821444 | |||||
| chr14:101821444
|
GGTGGGTG others(5): Show |
G | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.260-35238_260-3522 others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101821444 | |||||
| chr14:101821446
|
TGG | T | 20 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(17): Show | 20 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.260-35238_260-3523 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101821446 | |||||
| chr14:101821448
|
G | T | 18 | a0001c0001t0001g0072a0001c0001t0002g0124a0001c0001t0002g0125others(15): Show | 18 | HG01433.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.260-35238G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821448 | ||||||
| chr14:101821452
|
G | GGT | 25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(22): Show | 25 | HG00408.hp2 HG00642.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.260-35203_260-3520 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101821452 | |||||
| chr14:101821452
|
G | GGTGT | 48 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.260-35205_260-3520 others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101821452 | |||||
| chr14:101821452
|
G | GGTGTGT | 6 | a0001c0001t0001g0060a0001c0001t0002g0094a0001c0001t0002g0111others(3): Show | 6 | HG01258.hp1 HG01884.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.260-35207_260-3520 others(10): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101821452 | |||||
| chr14:101821452
|
G | GTGT | 2 | a0001c0001t0001g0047a0001c0001t0001g0109 | 2 | HG01106.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.260-35234_260-3523 others(7): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821452 | ||||||
| chr14:101821452
|
G | T | 43 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0031others(40): Show | 43 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.260-35234G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821452 | ||||||
| chr14:101821452
|
GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.260-35213_260-3520 others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101821452 | |||||
| chr14:101821526
|
A | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.260-35160A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821526 | ||||||
| chr14:101821567
|
A | C | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.260-35119A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821567 | ||||||
| chr14:101821603
|
T | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007others(2): Show | 5 | HG02486.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-35083T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821603 | ||||||
| chr14:101821717
|
G | T | 1 | a0001c0001t0002g0111 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.260-34969G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821717 | ||||||
| chr14:101821806
|
G | A | 18 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(15): Show | 18 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.260-34880G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821806 | ||||||
| chr14:101821860
|
C | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.260-34826C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821860 | ||||||
| chr14:101821876
|
C | T | 1 | a0001c0003t0002g0112 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.260-34810C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101821876 | ||||||
| chr14:101822000
|
A | G | 18 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(15): Show | 18 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.260-34686A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101822000 | ||||||
| chr14:101822058
|
A | AC | 3 | a0001c0001t0001g0078a0001c0001t0001g0123a0002c0002t0001g0071 | 3 | HG02630.hp2 HG03453.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.260-34624dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101822058 | |||||
| chr14:101822063
|
A | C | 17 | a0001c0001t0001g0022a0001c0001t0001g0072a0001c0001t0001g0078others(14): Show | 17 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.260-34623A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101822063 | ||||||
| chr14:101822079
|
G | GC | 12 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0049others(9): Show | 12 | HG00280.hp1 HG01255.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.260-34597dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101822079 | |||||
| chr14:101822079
|
GC | G | 10 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 10 | HG00280.hp2 HG01074.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.260-34597delC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101822079 | |||||
| chr14:101822088
|
C | A | 1 | a0001c0001t0003g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.260-34598C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101822088 | ||||||
| chr14:101822088
|
CCA | C | 12 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(9): Show | 12 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.260-34587_260-3458 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101822088 | |||||
| chr14:101822089
|
CA | C | 3 | a0001c0001t0002g0124a0001c0001t0007g0076a0002c0002t0004g0017 | 3 | HG01884.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.260-34596delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101822089 | ||||||
| chr14:101822090
|
A | C | 6 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0066others(3): Show | 6 | HG01884.hp1 HG01934.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.260-34596A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101822090 | ||||||
| chr14:101822326
|
A | G | 38 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(35): Show | 38 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.260-34360A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101822326 | ||||||
| chr14:101822766
|
C | CTTATGCG others(1): Show |
2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.260-33919_260-3391 others(12): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101822766 | |||||
| chr14:101822997
|
C | T | 39 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(36): Show | 39 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.260-33689C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101822997 | ||||||
| chr14:101823333
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.260-33353G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101823333 | ||||||
| chr14:101823376
|
T | C | 2 | a0001c0001t0001g0123a0003c0004t0004g0120 | 2 | HG00733.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.260-33310T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101823376 | ||||||
| chr14:101824005
|
T | C | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0003t0002g0127others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-32681T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101824005 | ||||||
| chr14:101824283
|
G | T | 1 | a0002c0002t0003g0132 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.260-32403G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101824283 | ||||||
| chr14:101824693
|
C | T | 4 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019others(1): Show | 4 | HG02572.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-31993C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101824693 | ||||||
| chr14:101824748
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.260-31938T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101824748 | ||||||
| chr14:101824988
|
G | C | 2 | a0001c0001t0001g0123a0003c0004t0004g0120 | 2 | HG00733.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.260-31698G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101824988 | ||||||
| chr14:101824996
|
G | A | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-31690G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101824996 | ||||||
| chr14:101825158
|
A | G | 1 | a0001c0001t0006g0105 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.260-31528A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101825158 | ||||||
| chr14:101825211
|
C | CATGTGTG others(5): Show |
1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.260-31475_260-3147 others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101825211 | ||||||
| chr14:101825211
|
C | CGT | 10 | a0001c0001t0001g0117a0001c0001t0002g0111a0001c0001t0002g0114others(7): Show | 10 | HG01258.hp1 HG01884.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-31438_260-3143 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101825211 | |||||
| chr14:101825211
|
C | CGTGT | 14 | a0001c0001t0001g0072a0001c0001t0006g0075a0001c0001t0006g0105others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.260-31440_260-3143 others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101825211 | |||||
| chr14:101825211
|
C | CGTGTGT | 10 | a0001c0001t0001g0022a0001c0001t0001g0078a0001c0001t0001g0081others(7): Show | 10 | HG00280.hp2 HG01243.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.260-31442_260-3143 others(10): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101825211 | |||||
| chr14:101825211
|
C | CGTGTGTG others(1): Show |
7 | a0001c0001t0001g0057a0001c0001t0003g0007a0001c0001t0003g0138others(4): Show | 7 | HG00558.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-31444_260-3143 others(12): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101825211 | |||||
| chr14:101825211
|
C | CGTGTGTG others(3): Show |
12 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0002g0125others(9): Show | 12 | HG00408.hp1 HG00438.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.260-31446_260-3143 others(14): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101825211 | |||||
| chr14:101825211
|
C | CGTGTGTG others(5): Show |
5 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0002g0094others(2): Show | 5 | HG01884.hp1 HG01934.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-31448_260-3143 others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101825211 | |||||
| chr14:101825211
|
CGT | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0021others(55): Show | 58 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.260-31438_260-3143 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101825211 | |||||
| chr14:101825211
|
CGTGT | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0107a0002c0002t0001g0038 | 3 | NA18612.hp1 NA18995.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.260-31440_260-3143 others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101825211 | |||||
| chr14:101825211
|
CGTGTGT | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0002g0065 | 3 | HG02056.hp1 HG02165.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.260-31442_260-3143 others(10): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101825211 | |||||
| chr14:101825258
|
T | G | 52 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(49): Show | 52 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.260-31428T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101825258 | ||||||
| chr14:101825268
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.260-31418T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101825268 | ||||||
| chr14:101825509
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.260-31177G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101825509 | ||||||
| chr14:101825785
|
G | A | 24 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(21): Show | 24 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.260-30901G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101825785 | ||||||
| chr14:101825991
|
A | G | 52 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(49): Show | 52 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.260-30695A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101825991 | ||||||
| chr14:101826080
|
T | C | 1 | a0001c0001t0012g0064 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.260-30606T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101826080 | ||||||
| chr14:101826183
|
GTC | G | 24 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(21): Show | 24 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.260-30500_260-3049 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101826183 | |||||
| chr14:101826531
|
T | C | 52 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(49): Show | 52 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.260-30155T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101826531 | ||||||
| chr14:101826924
|
G | A | 8 | a0001c0001t0001g0072a0001c0001t0006g0105a0001c0001t0007g0076others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-29762G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101826924 | ||||||
| chr14:101826969
|
C | CT | 7 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0049others(4): Show | 7 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-29693dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101826969 | |||||
| chr14:101826969
|
CT | C | 32 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(29): Show | 32 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.260-29693delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101826969 | |||||
| chr14:101827031
|
A | C | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0003t0002g0127others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-29655A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101827031 | ||||||
| chr14:101827924
|
C | CT | 4 | a0001c0001t0009g0122a0002c0002t0004g0017a0002c0002t0008g0009others(1): Show | 4 | HG01433.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-28757dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101827924 | |||||
| chr14:101828000
|
A | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-28686A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828000 | ||||||
| chr14:101828137
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.260-28549A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828137 | ||||||
| chr14:101828160
|
T | G | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-28526T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828160 | ||||||
| chr14:101828247
|
G | T | 5 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-28439G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828247 | ||||||
| chr14:101828268
|
C | T | 28 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.260-28418C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828268 | ||||||
| chr14:101828457
|
T | G | 4 | a0001c0001t0001g0066a0001c0001t0002g0094a0002c0002t0001g0121others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-28229T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828457 | ||||||
| chr14:101828676
|
C | CT | 11 | a0001c0001t0001g0015a0001c0001t0001g0047a0001c0001t0001g0048others(8): Show | 11 | HG01071.hp1 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-27990dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101828676 | |||||
| chr14:101828676
|
CT | C | 29 | a0001c0001t0001g0022a0001c0001t0001g0051a0001c0001t0001g0052others(26): Show | 29 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.260-27990delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101828676 | |||||
| chr14:101828696
|
T | A | 1 | a0002c0002t0001g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.260-27990T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828696 | ||||||
| chr14:101828747
|
G | A | 5 | a0001c0001t0001g0066a0001c0001t0002g0094a0002c0002t0001g0121others(2): Show | 5 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-27939G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828747 | ||||||
| chr14:101828756
|
C | T | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-27930C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828756 | ||||||
| chr14:101828809
|
C | G | 43 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(40): Show | 43 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.260-27877C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828809 | ||||||
| chr14:101828877
|
T | C | 51 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(48): Show | 51 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.260-27809T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101828877 | ||||||
| chr14:101829006
|
A | G | 47 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(44): Show | 47 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.260-27680A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101829006 | ||||||
| chr14:101829258
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0002g0094a0002c0002t0001g0121others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-27428A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101829258 | ||||||
| chr14:101829554
|
A | G | 2 | a0001c0001t0001g0067a0002c0002t0001g0102 | 2 | HG02132.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.260-27132A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101829554 | ||||||
| chr14:101829609
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0002g0094a0002c0002t0001g0121others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-27077G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101829609 | ||||||
| chr14:101829681
|
G | A | 51 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(48): Show | 51 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.260-27005G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101829681 | ||||||
| chr14:101829687
|
T | G | 4 | a0001c0001t0001g0066a0001c0001t0002g0094a0002c0002t0001g0121others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-26999T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101829687 | ||||||
| chr14:101829701
|
T | C | 16 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(13): Show | 16 | HG00733.hp2 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.260-26985T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101829701 | ||||||
| chr14:101829721
|
C | T | 2 | a0002c0002t0004g0023a0002c0002t0004g0024 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.260-26965C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101829721 | ||||||
| chr14:101829746
|
G | C | 51 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(48): Show | 51 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.260-26940G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101829746 | ||||||
| chr14:101829942
|
CA | C | 50 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(47): Show | 50 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.260-26733delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101829942 | |||||
| chr14:101829993
|
C | T | 3 | a0001c0001t0002g0124a0001c0003t0002g0127a0001c0003t0002g0128 | 3 | HG01884.hp2 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.260-26693C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101829993 | ||||||
| chr14:101830046
|
C | T | 5 | a0001c0001t0001g0066a0001c0001t0002g0094a0001c0001t0007g0016others(2): Show | 5 | HG00733.hp2 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-26640C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101830046 | ||||||
| chr14:101830082
|
A | G | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-26604A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101830082 | ||||||
| chr14:101830147
|
A | G | 32 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(29): Show | 32 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.260-26539A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101830147 | ||||||
| chr14:101830195
|
G | T | 3 | a0001c0001t0001g0066a0001c0001t0002g0094a0002c0002t0001g0121 | 3 | HG01884.hp1 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.260-26491G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101830195 | ||||||
| chr14:101830241
|
C | T | 28 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.260-26445C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101830241 | ||||||
| chr14:101830403
|
G | A | 34 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(31): Show | 34 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.260-26283G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101830403 | ||||||
| chr14:101830878
|
C | G | 43 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(40): Show | 43 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.260-25808C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101830878 | ||||||
| chr14:101831052
|
T | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.260-25634T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101831052 | ||||||
| chr14:101831321
|
G | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-25365G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101831321 | ||||||
| chr14:101831384
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.260-25302A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101831384 | ||||||
| chr14:101831421
|
T | C | 49 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(46): Show | 49 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.260-25265T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101831421 | ||||||
| chr14:101831491
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0051others(1): Show | 4 | HG02056.hp1 HG02056.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-25195T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101831491 | ||||||
| chr14:101831549
|
C | G | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0003t0002g0127others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-25137C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101831549 | ||||||
| chr14:101831674
|
A | T | 1 | a0002c0002t0001g0115 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.260-25012A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101831674 | ||||||
| chr14:101831865
|
T | C | 5 | a0001c0001t0002g0114a0002c0002t0001g0087a0002c0002t0001g0092others(2): Show | 5 | HG02451.hp1 HG02717.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-24821T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101831865 | ||||||
| chr14:101832410
|
T | C | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.260-24276T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101832410 | ||||||
| chr14:101832550
|
G | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(12): Show | 15 | HG00733.hp2 HG01243.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-24136G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101832550 | ||||||
| chr14:101832577
|
T | C | 1 | a0001c0001t0003g0135 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.260-24109T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101832577 | ||||||
| chr14:101832704
|
G | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-23982G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101832704 | ||||||
| chr14:101832708
|
G | T | 48 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.260-23978G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101832708 | ||||||
| chr14:101832745
|
G | A | 3 | a0001c0001t0001g0066a0001c0001t0002g0094a0002c0002t0001g0121 | 3 | HG01884.hp1 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.260-23941G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101832745 | ||||||
| chr14:101832776
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.260-23910C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101832776 | ||||||
| chr14:101832825
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-23861C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101832825 | ||||||
| chr14:101832845
|
T | C | 48 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.260-23841T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101832845 | ||||||
| chr14:101832996
|
A | G | 48 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.260-23690A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101832996 | ||||||
| chr14:101833083
|
T | C | 19 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(16): Show | 19 | HG01243.hp1 HG01884.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.260-23603T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101833083 | ||||||
| chr14:101833276
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.260-23410C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101833276 | ||||||
| chr14:101833495
|
C | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.260-23191C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101833495 | ||||||
| chr14:101833515
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.260-23171A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101833515 | ||||||
| chr14:101833897
|
G | T | 3 | a0001c0001t0001g0066a0001c0001t0002g0094a0002c0002t0001g0121 | 3 | HG01884.hp1 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.260-22789G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101833897 | ||||||
| chr14:101833970
|
G | A | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-22716G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101833970 | ||||||
| chr14:101834021
|
T | C | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-22665T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101834021 | ||||||
| chr14:101834104
|
C | T | 15 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(12): Show | 15 | HG00733.hp2 HG01243.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-22582C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101834104 | ||||||
| chr14:101834189
|
C | T | 10 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(7): Show | 10 | HG01243.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-22497C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101834189 | ||||||
| chr14:101834386
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.260-22300T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101834386 | ||||||
| chr14:101834583
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.260-22103G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101834583 | ||||||
| chr14:101834740
|
G | A | 3 | a0001c0001t0002g0124a0001c0003t0002g0127a0001c0003t0002g0128 | 3 | HG01884.hp2 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.260-21946G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101834740 | ||||||
| chr14:101834774
|
A | ACT | 49 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(46): Show | 49 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.260-21909_260-2190 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101834774 | |||||
| chr14:101834931
|
G | T | 1 | a0001c0001t0006g0075 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.260-21755G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101834931 | ||||||
| chr14:101835061
|
A | G | 1 | a0001c0001t0007g0016 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.260-21625A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835061 | ||||||
| chr14:101835092
|
C | T | 8 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(5): Show | 8 | HG01243.hp1 HG02486.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-21594C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835092 | ||||||
| chr14:101835326
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-21360C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835326 | ||||||
| chr14:101835426
|
A | G | 11 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(8): Show | 11 | HG01243.hp1 HG02486.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-21260A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835426 | ||||||
| chr14:101835499
|
C | T | 25 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(22): Show | 25 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.260-21187C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835499 | ||||||
| chr14:101835562
|
A | G | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.260-21124A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835562 | ||||||
| chr14:101835567
|
C | A | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-21119C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835567 | ||||||
| chr14:101835657
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.260-21029G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835657 | ||||||
| chr14:101835706
|
C | G | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-20980C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835706 | ||||||
| chr14:101835755
|
G | A | 4 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019others(1): Show | 4 | HG02572.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-20931G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835755 | ||||||
| chr14:101835965
|
C | T | 24 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(21): Show | 24 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.260-20721C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101835965 | ||||||
| chr14:101836035
|
A | G | 25 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(22): Show | 25 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.260-20651A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101836035 | ||||||
| chr14:101836373
|
C | T | 1 | a0001c0001t0006g0075 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.260-20313C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101836373 | ||||||
| chr14:101836570
|
T | C | 48 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.260-20116T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101836570 | ||||||
| chr14:101836582
|
G | C | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-20104G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101836582 | ||||||
| chr14:101836813
|
C | T | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-19873C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101836813 | ||||||
| chr14:101836822
|
T | C | 1 | a0004c0005t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.260-19864T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101836822 | ||||||
| chr14:101836955
|
G | A | 8 | a0001c0001t0001g0003a0002c0002t0001g0002a0002c0002t0001g0025others(5): Show | 8 | HG01993.hp2 HG02155.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-19731G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101836955 | ||||||
| chr14:101837091
|
T | C | 49 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(46): Show | 49 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.260-19595T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837091 | ||||||
| chr14:101837300
|
C | T | 33 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(30): Show | 33 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.260-19386C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837300 | ||||||
| chr14:101837317
|
AT | A | 51 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(48): Show | 51 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.260-19360delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101837317 | |||||
| chr14:101837335
|
T | C | 48 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.260-19351T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837335 | ||||||
| chr14:101837367
|
C | G | 48 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.260-19319C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837367 | ||||||
| chr14:101837427
|
G | A | 3 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007 | 3 | HG02486.hp1 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.260-19259G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837427 | ||||||
| chr14:101837443
|
G | A | 24 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(21): Show | 24 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.260-19243G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837443 | ||||||
| chr14:101837497
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-19189C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837497 | ||||||
| chr14:101837513
|
A | T | 4 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019others(1): Show | 4 | HG02572.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-19173A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837513 | ||||||
| chr14:101837516
|
T | C | 3 | a0001c0001t0001g0066a0001c0001t0002g0094a0002c0002t0001g0121 | 3 | HG01884.hp1 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.260-19170T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837516 | ||||||
| chr14:101837654
|
C | T | 10 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(7): Show | 10 | HG01243.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-19032C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837654 | ||||||
| chr14:101837769
|
T | C | 8 | a0001c0001t0001g0072a0001c0001t0006g0105a0001c0001t0007g0076others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-18917T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837769 | ||||||
| chr14:101837831
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.260-18855G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837831 | ||||||
| chr14:101837843
|
G | A | 13 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(10): Show | 13 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.260-18843G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837843 | ||||||
| chr14:101837933
|
A | G | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.260-18753A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837933 | ||||||
| chr14:101837964
|
T | C | 5 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0003t0002g0127others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-18722T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101837964 | ||||||
| chr14:101838043
|
A | C | 1 | a0001c0001t0002g0028 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.260-18643A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838043 | ||||||
| chr14:101838055
|
T | C | 48 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(45): Show | 48 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.260-18631T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838055 | ||||||
| chr14:101838212
|
C | T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.260-18474C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838212 | ||||||
| chr14:101838272
|
G | T | 15 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(12): Show | 15 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-18414G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838272 | ||||||
| chr14:101838294
|
A | C | 20 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(17): Show | 20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.260-18392A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838294 | ||||||
| chr14:101838521
|
C | T | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.260-18165C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838521 | ||||||
| chr14:101838543
|
G | A | 9 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(6): Show | 9 | HG01243.hp1 HG02486.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-18143G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838543 | ||||||
| chr14:101838586
|
T | C | 49 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(46): Show | 49 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.260-18100T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838586 | ||||||
| chr14:101838737
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.260-17949T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838737 | ||||||
| chr14:101838819
|
G | A | 1 | a0001c0001t0007g0016 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.260-17867G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838819 | ||||||
| chr14:101838916
|
C | T | 1 | a0001c0001t0006g0075 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.260-17770C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838916 | ||||||
| chr14:101838923
|
T | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.260-17763T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101838923 | ||||||
| chr14:101839055
|
GA | G | 45 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(42): Show | 45 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.260-17616delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101839055 | |||||
| chr14:101839105
|
A | C | 1 | a0002c0002t0001g0102 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.260-17581A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101839105 | ||||||
| chr14:101839176
|
T | C | 5 | a0001c0001t0001g0066a0001c0001t0002g0094a0002c0002t0001g0121others(2): Show | 5 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-17510T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101839176 | ||||||
| chr14:101839179
|
C | A | 2 | a0002c0002t0008g0009a0002c0002t0008g0010 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.260-17507C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101839179 | ||||||
| chr14:101839350
|
CA | C | 26 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(23): Show | 26 | HG00733.hp2 HG01243.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.260-17324delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101839350 | |||||
| chr14:101839505
|
C | G | 4 | a0001c0001t0002g0124a0001c0001t0009g0122a0001c0003t0002g0127others(1): Show | 4 | HG01433.hp2 HG01884.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-17181C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101839505 | ||||||
| chr14:101839725
|
C | G | 52 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(49): Show | 52 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.260-16961C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101839725 | ||||||
| chr14:101839879
|
C | T | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.260-16807C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101839879 | ||||||
| chr14:101839948
|
AT | A | 26 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(23): Show | 26 | HG00733.hp2 HG01243.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.260-16727delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101839948 | |||||
| chr14:101840095
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.260-16591C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101840095 | ||||||
| chr14:101840144
|
C | T | 10 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0009g0122others(7): Show | 10 | HG01433.hp2 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.260-16542C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101840144 | ||||||
| chr14:101840384
|
GCAGC | G | 17 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(14): Show | 17 | HG00733.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.260-16297_260-1629 others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101840384 | |||||
| chr14:101840476
|
C | G | 9 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0096others(6): Show | 9 | HG01243.hp1 HG02486.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-16210C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101840476 | ||||||
| chr14:101840482
|
C | CA | 12 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0056others(9): Show | 12 | HG01934.hp1 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.260-16177dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101840482 | |||||
| chr14:101840482
|
CA | C | 24 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0113others(21): Show | 24 | HG01070.hp1 HG01433.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.260-16177delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101840482 | |||||
| chr14:101840482
|
CAA | C | 12 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0002g0094others(9): Show | 12 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.260-16178_260-1617 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101840482 | |||||
| chr14:101840482
|
CAAAAAAA others(6): Show |
C | 8 | a0001c0001t0001g0047a0001c0001t0001g0081a0001c0001t0001g0096others(5): Show | 8 | HG00642.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-16189_260-1617 others(17): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101840482 | |||||
| chr14:101840523
|
G | A | 17 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(14): Show | 17 | HG00733.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.260-16163G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101840523 | ||||||
| chr14:101840634
|
C | T | 3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.260-16052C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101840634 | ||||||
| chr14:101840731
|
A | G | 21 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(18): Show | 21 | HG00733.hp2 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.260-15955A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101840731 | ||||||
| chr14:101840759
|
T | G | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-15927T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101840759 | ||||||
| chr14:101840884
|
A | G | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.260-15802A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101840884 | ||||||
| chr14:101841007
|
C | G | 18 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(15): Show | 18 | HG00733.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.260-15679C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841007 | ||||||
| chr14:101841043
|
T | C | 6 | a0001c0001t0001g0047a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG00642.hp1 HG01071.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-15643T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841043 | ||||||
| chr14:101841059
|
C | G | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-15627C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841059 | ||||||
| chr14:101841121
|
G | A | 2 | a0001c0001t0007g0016a0003c0004t0004g0120 | 2 | HG00733.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.260-15565G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841121 | ||||||
| chr14:101841194
|
C | T | 29 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(26): Show | 29 | HG00733.hp2 HG01243.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.260-15492C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841194 | ||||||
| chr14:101841412
|
C | T | 2 | a0001c0001t0007g0016a0003c0004t0004g0120 | 2 | HG00733.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.260-15274C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841412 | ||||||
| chr14:101841431
|
G | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-15255G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841431 | ||||||
| chr14:101841506
|
G | A | 1 | a0001c0001t0001g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.260-15180G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841506 | ||||||
| chr14:101841511
|
C | T | 4 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019others(1): Show | 4 | HG02572.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-15175C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841511 | ||||||
| chr14:101841516
|
C | G | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-15170C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841516 | ||||||
| chr14:101841672
|
G | T | 2 | a0001c0001t0007g0016a0003c0004t0004g0120 | 2 | HG00733.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.260-15014G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841672 | ||||||
| chr14:101841810
|
C | A | 15 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-14876C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841810 | ||||||
| chr14:101841838
|
G | A | 15 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-14848G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841838 | ||||||
| chr14:101841910
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0002g0094others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-14776A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101841910 | ||||||
| chr14:101842011
|
G | A | 1 | a0001c0001t0006g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.260-14675G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101842011 | ||||||
| chr14:101842035
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.260-14651C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101842035 | ||||||
| chr14:101842063
|
G | A | 28 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0081others(25): Show | 28 | HG00733.hp2 HG01243.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.260-14623G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101842063 | ||||||
| chr14:101842372
|
G | A | 1 | a0001c0001t0007g0016 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.260-14314G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101842372 | ||||||
| chr14:101842375
|
C | T | 4 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019others(1): Show | 4 | HG02572.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-14311C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101842375 | ||||||
| chr14:101842376
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0048 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.260-14310G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101842376 | ||||||
| chr14:101842632
|
G | A | 1 | a0001c0001t0007g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.260-14054G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101842632 | ||||||
| chr14:101842757
|
C | CT | 98 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(95): Show | 98 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.260-13913dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101842757 | |||||
| chr14:101842863
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0002g0094others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-13823A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101842863 | ||||||
| chr14:101843155
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.260-13531G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101843155 | ||||||
| chr14:101843313
|
C | T | 3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.260-13373C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101843313 | ||||||
| chr14:101843356
|
C | T | 19 | a0001c0001t0002g0068a0001c0001t0002g0124a0001c0001t0002g0125others(16): Show | 19 | HG00733.hp2 HG01433.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.260-13330C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101843356 | ||||||
| chr14:101843411
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.260-13275T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101843411 | ||||||
| chr14:101843679
|
G | A | 5 | a0001c0001t0002g0068a0001c0001t0007g0016a0002c0002t0008g0009others(2): Show | 5 | HG00733.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-13007G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101843679 | ||||||
| chr14:101843832
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.260-12854C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101843832 | ||||||
| chr14:101843995
|
G | T | 23 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0002g0068others(20): Show | 23 | HG00733.hp2 HG01433.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.260-12691G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101843995 | ||||||
| chr14:101844062
|
C | T | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.260-12624C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844062 | ||||||
| chr14:101844087
|
C | T | 1 | a0002c0002t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.260-12599C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844087 | ||||||
| chr14:101844099
|
A | G | 7 | a0001c0001t0006g0105a0001c0001t0007g0076a0001c0001t0007g0126others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-12587A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844099 | ||||||
| chr14:101844142
|
G | GTT | 7 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0003t0002g0127others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-12529_260-1252 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101844142 | |||||
| chr14:101844150
|
T | TG | 14 | a0001c0001t0002g0068a0001c0001t0003g0005a0001c0001t0003g0006others(11): Show | 14 | HG00733.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.260-12536_260-1253 others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844150 | ||||||
| chr14:101844192
|
G | A | 2 | a0001c0001t0001g0033a0002c0002t0001g0035 | 2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.260-12494G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844192 | ||||||
| chr14:101844288
|
G | T | 3 | a0001c0001t0002g0068a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.260-12398G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844288 | ||||||
| chr14:101844352
|
A | G | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-12334A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844352 | ||||||
| chr14:101844367
|
T | C | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-12319T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844367 | ||||||
| chr14:101844387
|
C | T | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.260-12299C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844387 | ||||||
| chr14:101844493
|
C | T | 1 | a0002c0002t0001g0001 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.260-12193C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844493 | ||||||
| chr14:101844659
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0002g0094others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-12027G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844659 | ||||||
| chr14:101844666
|
G | A | 26 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0002g0068others(23): Show | 26 | HG00733.hp2 HG01433.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.260-12020G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844666 | ||||||
| chr14:101844757
|
A | G | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.260-11929A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844757 | ||||||
| chr14:101844864
|
A | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-11822A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101844864 | ||||||
| chr14:101845043
|
G | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 35 | HG00280.hp1 HG00558.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.260-11643G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101845043 | ||||||
| chr14:101845138
|
T | TA | 47 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0001g0052others(44): Show | 47 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.260-11533dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101845138 | |||||
| chr14:101845138
|
TA | T | 8 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0088others(5): Show | 8 | HG00642.hp1 HG01070.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-11533delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101845138 | |||||
| chr14:101845179
|
C | T | 3 | a0001c0003t0002g0127a0001c0003t0002g0128a0001c0003t0020g0008 | 3 | HG02717.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.260-11507C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101845179 | ||||||
| chr14:101845419
|
T | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-11267T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101845419 | ||||||
| chr14:101845463
|
T | TCCACC | 16 | a0001c0001t0001g0123a0001c0001t0002g0124a0001c0001t0002g0125others(13): Show | 16 | HG01884.hp2 HG02486.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.260-11216_260-1121 others(9): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101845463 | |||||
| chr14:101845537
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.260-11149G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101845537 | ||||||
| chr14:101846094
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0002g0125 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.260-10592C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101846094 | ||||||
| chr14:101846261
|
G | A | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-10425G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101846261 | ||||||
| chr14:101846756
|
G | T | 1 | a0001c0001t0006g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.260-9930G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101846756 | ||||||
| chr14:101846924
|
C | A | 1 | a0001c0001t0001g0003 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.260-9762C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101846924 | ||||||
| chr14:101846995
|
A | C | 1 | a0001c0001t0002g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.260-9691A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101846995 | ||||||
| chr14:101847217
|
G | GA | 3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.260-9465dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101847217 | |||||
| chr14:101847663
|
C | CT | 10 | a0001c0001t0001g0118a0001c0001t0002g0094a0001c0001t0003g0138others(7): Show | 10 | HG01071.hp2 HG01884.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.260-9004dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101847663 | |||||
| chr14:101847663
|
C | CTTT | 15 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0123others(12): Show | 15 | HG01255.hp1 HG01993.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.260-9006_260-9004d others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101847663 | |||||
| chr14:101847703
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0002g0095others(17): Show | 20 | HG01255.hp1 HG01993.hp2 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.260-8983G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101847703 | ||||||
| chr14:101847732
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0048others(36): Show | 39 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.260-8954A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101847732 | ||||||
| chr14:101847918
|
T | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0048others(30): Show | 33 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.260-8768T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101847918 | ||||||
| chr14:101847963
|
G | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0002g0095others(8): Show | 11 | HG01255.hp1 HG01993.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-8723G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101847963 | ||||||
| chr14:101848011
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(28): Show | 31 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.260-8675A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848011 | ||||||
| chr14:101848023
|
C | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0002g0095others(8): Show | 11 | HG01255.hp1 HG01993.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-8663C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848023 | ||||||
| chr14:101848046
|
T | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0047others(34): Show | 37 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.260-8640T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848046 | ||||||
| chr14:101848446
|
G | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0002g0095others(8): Show | 11 | HG01255.hp1 HG01993.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-8240G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848446 | ||||||
| chr14:101848478
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.260-8208C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848478 | ||||||
| chr14:101848579
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.260-8107G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848579 | ||||||
| chr14:101848586
|
C | T | 14 | a0001c0001t0002g0068a0001c0001t0009g0122a0001c0003t0002g0079others(11): Show | 14 | HG00733.hp2 HG01433.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.260-8100C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848586 | ||||||
| chr14:101848644
|
C | T | 1 | a0002c0002t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.260-8042C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848644 | ||||||
| chr14:101848689
|
A | G | 36 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0047others(33): Show | 36 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.260-7997A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848689 | ||||||
| chr14:101848720
|
G | A | 2 | a0001c0003t0002g0079a0001c0003t0002g0112 | 2 | HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.260-7966G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848720 | ||||||
| chr14:101848834
|
A | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0113others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-7852A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101848834 | ||||||
| chr14:101849122
|
C | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(27): Show | 30 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.260-7564C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101849122 | ||||||
| chr14:101849235
|
C | T | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.260-7451C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101849235 | ||||||
| chr14:101849454
|
G | A | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-7232G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101849454 | ||||||
| chr14:101849507
|
ATTC | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(27): Show | 30 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.260-7174_260-7172d others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101849507 | |||||
| chr14:101849579
|
A | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(27): Show | 30 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.260-7107A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101849579 | ||||||
| chr14:101849584
|
T | G | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-7102T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101849584 | ||||||
| chr14:101849611
|
G | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-7075G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101849611 | ||||||
| chr14:101849672
|
G | GATCAACC others(152): Show |
1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.260-7012_260-7011i others(161): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101849672 | |||||
| chr14:101849672
|
G | GATCAACC others(152): Show |
29 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(26): Show | 29 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.260-7012_260-7011i others(161): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101849672 | |||||
| chr14:101849675
|
A | G | 4 | a0001c0001t0001g0047a0001c0001t0001g0117a0001c0001t0002g0111others(1): Show | 4 | HG00642.hp1 HG01106.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-7011A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101849675 | ||||||
| chr14:101849716
|
C | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(27): Show | 30 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.260-6970C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101849716 | ||||||
| chr14:101849860
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(28): Show | 31 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.260-6826A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101849860 | ||||||
| chr14:101850000
|
T | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(12): Show | 15 | HG00642.hp1 HG01106.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-6686T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101850000 | ||||||
| chr14:101850006
|
C | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(27): Show | 30 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.260-6680C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101850006 | ||||||
| chr14:101850057
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(27): Show | 30 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.260-6629G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101850057 | ||||||
| chr14:101850136
|
GC | G | 15 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(12): Show | 15 | HG00642.hp1 HG01106.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.260-6549delC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101850136 | ||||||
| chr14:101850915
|
G | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0002g0095others(8): Show | 11 | HG01255.hp1 HG01993.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-5771G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101850915 | ||||||
| chr14:101850948
|
C | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0002g0095others(8): Show | 11 | HG01255.hp1 HG01993.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-5738C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101850948 | ||||||
| chr14:101851012
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(27): Show | 30 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.260-5674G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101851012 | ||||||
| chr14:101851075
|
CTT | C | 3 | a0001c0003t0002g0127a0001c0003t0002g0128a0001c0003t0020g0008 | 3 | HG02717.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.260-5610_260-5609d others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101851075 | ||||||
| chr14:101851146
|
T | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(27): Show | 30 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.260-5540T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101851146 | ||||||
| chr14:101851212
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(28): Show | 31 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.260-5474A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101851212 | ||||||
| chr14:101851487
|
C | T | 6 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0113others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-5199C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101851487 | ||||||
| chr14:101851514
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(27): Show | 30 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.260-5172G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101851514 | ||||||
| chr14:101851820
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.260-4866T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101851820 | ||||||
| chr14:101851884
|
C | T | 6 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0113others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-4802C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101851884 | ||||||
| chr14:101851994
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0093a0002c0002t0001g0002others(6): Show | 9 | HG01255.hp1 HG01993.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.260-4692T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101851994 | ||||||
| chr14:101852006
|
C | T | 15 | a0001c0001t0002g0068a0001c0001t0009g0122a0001c0003t0002g0079others(12): Show | 15 | HG00733.hp2 HG01433.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.260-4680C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101852006 | ||||||
| chr14:101852091
|
A | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0002g0095others(8): Show | 11 | HG01255.hp1 HG01993.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-4595A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101852091 | ||||||
| chr14:101852373
|
C | G | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-4313C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101852373 | ||||||
| chr14:101852469
|
C | CT | 17 | a0001c0001t0001g0015a0001c0001t0001g0052a0001c0001t0001g0053others(14): Show | 17 | HG01074.hp2 HG01106.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.260-4200dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101852469 | |||||
| chr14:101852645
|
AT | A | 19 | a0001c0001t0001g0047a0001c0001t0001g0117a0001c0001t0002g0068others(16): Show | 19 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.260-4035delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101852645 | |||||
| chr14:101852720
|
T | C | 36 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0047others(33): Show | 36 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.260-3966T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101852720 | ||||||
| chr14:101853157
|
A | G | 8 | a0001c0003t0002g0079a0001c0003t0002g0112a0001c0003t0002g0127others(5): Show | 8 | HG02572.hp2 HG02717.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-3529A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101853157 | ||||||
| chr14:101853339
|
G | A | 9 | a0001c0003t0002g0079a0001c0003t0002g0112a0001c0003t0002g0127others(6): Show | 9 | HG02572.hp2 HG02717.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-3347G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101853339 | ||||||
| chr14:101853521
|
A | C | 4 | a0001c0001t0002g0068a0002c0002t0008g0009a0002c0002t0008g0010others(1): Show | 4 | HG00733.hp2 HG02451.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-3165A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101853521 | ||||||
| chr14:101853549
|
T | A | 4 | a0001c0001t0001g0047a0001c0001t0001g0117a0001c0001t0002g0111others(1): Show | 4 | HG00642.hp1 HG01106.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-3137T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101853549 | ||||||
| chr14:101853566
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0117a0001c0001t0002g0111others(2): Show | 5 | HG00642.hp1 HG01106.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-3120G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101853566 | ||||||
| chr14:101854059
|
G | A | 6 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0113others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-2627G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101854059 | ||||||
| chr14:101854218
|
C | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0070 | 2 | HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.260-2468C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101854218 | ||||||
| chr14:101854548
|
G | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-2138G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101854548 | ||||||
| chr14:101854680
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.260-2006G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101854680 | ||||||
| chr14:101854873
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.260-1813T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101854873 | ||||||
| chr14:101854886
|
T | C | 1 | a0002c0002t0001g0074 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.260-1800T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101854886 | ||||||
| chr14:101854896
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.260-1790G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101854896 | ||||||
| chr14:101855102
|
A | G | 36 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0047others(33): Show | 36 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.260-1584A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101855102 | ||||||
| chr14:101855320
|
A | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.260-1366A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101855320 | ||||||
| chr14:101855320
|
A | G | 25 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(22): Show | 25 | HG00642.hp1 HG01106.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.260-1366A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101855320 | ||||||
| chr14:101855486
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(123): Show | 126 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.260-1200T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101855486 | ||||||
| chr14:101855861
|
T | C | 9 | a0001c0003t0002g0079a0001c0003t0002g0112a0001c0003t0002g0127others(6): Show | 9 | HG02572.hp2 HG02717.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-825T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101855861 | ||||||
| chr14:101856507
|
C | CGACTAGC others(1): Show |
9 | a0001c0003t0002g0079a0001c0003t0002g0112a0001c0003t0002g0127others(6): Show | 9 | HG02572.hp2 HG02717.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-177_260-170dup others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101856507 | |||||
| chr14:101856563
|
A | AC | 33 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0113others(30): Show | 33 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.260-120dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 101856563 | |||||
| chr14:101856659
|
C | G | 36 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0045others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.260-27C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 3/15 | chr14 | 101856659 | ||||||
| chr14:101856931
|
A | G | 10 | a0001c0001t0001g0113a0001c0001t0002g0068a0001c0001t0002g0094others(7): Show | 10 | HG00733.hp2 HG01433.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+46A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101856931 | ||||||
| chr14:101857138
|
C | T | 3 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0007 | 3 | HG02486.hp1 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.459+253C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101857138 | ||||||
| chr14:101857339
|
T | A | 36 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0045others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.459+454T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101857339 | ||||||
| chr14:101857509
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.459+624A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101857509 | ||||||
| chr14:101857552
|
CAGTT | C | 5 | a0001c0003t0002g0079a0001c0003t0002g0112a0001c0003t0005g0018others(2): Show | 5 | HG02572.hp2 HG02735.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+672_459+675del others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101857552 | |||||
| chr14:101857928
|
T | C | 8 | a0001c0001t0002g0068a0001c0001t0002g0094a0001c0001t0009g0122others(5): Show | 8 | HG01433.hp2 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+1043T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101857928 | ||||||
| chr14:101858159
|
A | G | 17 | a0001c0001t0001g0047a0001c0001t0001g0088a0001c0001t0001g0090others(14): Show | 17 | HG01106.hp1 HG01258.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.459+1274A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101858159 | ||||||
| chr14:101858515
|
G | GT | 23 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0067others(20): Show | 23 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.459+1639dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101858515 | |||||
| chr14:101858838
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+1953G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101858838 | ||||||
| chr14:101858850
|
A | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+1965A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101858850 | ||||||
| chr14:101859051
|
C | T | 1 | a0001c0001t0003g0136 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.459+2166C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101859051 | ||||||
| chr14:101859159
|
G | A | 1 | a0001c0001t0006g0105 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459+2274G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101859159 | ||||||
| chr14:101859295
|
A | T | 1 | a0001c0001t0014g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.459+2410A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101859295 | ||||||
| chr14:101859400
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(86): Show | 89 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.459+2515T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101859400 | ||||||
| chr14:101859541
|
G | A | 1 | a0002c0002t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.459+2656G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101859541 | ||||||
| chr14:101859599
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.459+2714A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101859599 | ||||||
| chr14:101859682
|
A | G | 22 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0096others(19): Show | 22 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+2797A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101859682 | ||||||
| chr14:101859755
|
C | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+2870C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101859755 | ||||||
| chr14:101859869
|
G | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0045others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.459+2984G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101859869 | ||||||
| chr14:101859914
|
C | CT | 25 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0050others(22): Show | 25 | HG01071.hp2 HG01106.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.459+3042dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101859914 | |||||
| chr14:101860317
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.459+3432C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101860317 | ||||||
| chr14:101860365
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0003g0006 | 2 | HG01243.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.459+3480G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101860365 | ||||||
| chr14:101860404
|
T | C | 1 | a0002c0002t0001g0115 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.459+3519T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101860404 | ||||||
| chr14:101860454
|
A | G | 26 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0053others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.459+3569A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101860454 | ||||||
| chr14:101860610
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0048 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.459+3725G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101860610 | ||||||
| chr14:101860846
|
C | T | 1 | a0001c0001t0006g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459+3961C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101860846 | ||||||
| chr14:101860892
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.459+4007C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101860892 | ||||||
| chr14:101861074
|
CCTT | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082 | 3 | HG02055.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.459+4195_459+4197d others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101861074 | |||||
| chr14:101861237
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0003t0002g0079others(1): Show | 4 | HG02735.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+4352A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101861237 | ||||||
| chr14:101861419
|
T | C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.459+4534T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101861419 | ||||||
| chr14:101861481
|
T | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(80): Show | 83 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.459+4596T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101861481 | ||||||
| chr14:101861682
|
G | A | 5 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0073others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+4797G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101861682 | ||||||
| chr14:101861704
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.459+4819G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101861704 | ||||||
| chr14:101861737
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0118 | 3 | HG00280.hp2 HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+4852G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101861737 | ||||||
| chr14:101861751
|
A | T | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.459+4866A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101861751 | ||||||
| chr14:101861939
|
C | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(80): Show | 83 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.459+5054C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101861939 | ||||||
| chr14:101862118
|
A | G | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.459+5233A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101862118 | ||||||
| chr14:101862381
|
G | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+5496G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101862381 | ||||||
| chr14:101862608
|
A | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(87): Show | 90 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.459+5723A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101862608 | ||||||
| chr14:101862761
|
T | C | 22 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0053others(19): Show | 22 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+5876T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101862761 | ||||||
| chr14:101862769
|
A | AATATAGT others(1): Show |
5 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0073others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+5887_459+5894d others(10): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101862769 | |||||
| chr14:101862816
|
A | AT | 21 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0082others(18): Show | 21 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.459+5953dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101862816 | |||||
| chr14:101862816
|
AT | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0118a0001c0001t0002g0114others(5): Show | 8 | HG00733.hp2 HG01071.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+5953delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101862816 | |||||
| chr14:101862891
|
C | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0047others(37): Show | 40 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.459+6006C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101862891 | ||||||
| chr14:101862980
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.459+6095T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101862980 | ||||||
| chr14:101862982
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0045others(39): Show | 42 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.459+6097C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101862982 | ||||||
| chr14:101863037
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.459+6152G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101863037 | ||||||
| chr14:101863307
|
C | CA | 41 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0047others(38): Show | 41 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.459+6432dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101863307 | |||||
| chr14:101863418
|
C | A | 27 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0053others(24): Show | 27 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.459+6533C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101863418 | ||||||
| chr14:101863420
|
G | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(80): Show | 83 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.459+6535G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101863420 | ||||||
| chr14:101863498
|
T | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0047others(38): Show | 41 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.459+6613T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101863498 | ||||||
| chr14:101863543
|
C | T | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.459+6658C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101863543 | ||||||
| chr14:101863650
|
A | C | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.459+6765A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101863650 | ||||||
| chr14:101863671
|
C | T | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.459+6786C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101863671 | ||||||
| chr14:101863735
|
A | G | 5 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0073others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+6850A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101863735 | ||||||
| chr14:101863916
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+7031A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101863916 | ||||||
| chr14:101864423
|
A | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(87): Show | 90 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.459+7538A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101864423 | ||||||
| chr14:101864546
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.459+7661G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101864546 | ||||||
| chr14:101864574
|
C | G | 8 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG01074.hp2 HG01256.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+7689C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101864574 | ||||||
| chr14:101864616
|
C | T | 1 | a0001c0001t0014g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.459+7731C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101864616 | ||||||
| chr14:101864701
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.459+7816C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101864701 | ||||||
| chr14:101864735
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+7850C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101864735 | ||||||
| chr14:101865031
|
C | T | 2 | a0002c0002t0001g0121a0003c0004t0004g0120 | 2 | HG00733.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.459+8146C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101865031 | ||||||
| chr14:101865270
|
A | G | 22 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0096others(19): Show | 22 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+8385A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101865270 | ||||||
| chr14:101865319
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.459+8434G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101865319 | ||||||
| chr14:101865433
|
T | G | 5 | a0001c0001t0017g0085a0002c0002t0001g0071a0002c0002t0001g0074others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+8548T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101865433 | ||||||
| chr14:101865466
|
A | T | 5 | a0001c0001t0017g0085a0002c0002t0001g0071a0002c0002t0001g0074others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+8581A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101865466 | ||||||
| chr14:101865525
|
A | G | 23 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0053others(20): Show | 23 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.459+8640A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101865525 | ||||||
| chr14:101865739
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+8854C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101865739 | ||||||
| chr14:101865940
|
C | T | 1 | a0001c0001t0006g0105 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459+9055C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101865940 | ||||||
| chr14:101865961
|
C | T | 1 | a0001c0001t0007g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.459+9076C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101865961 | ||||||
| chr14:101865962
|
G | A | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.459+9077G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101865962 | ||||||
| chr14:101866168
|
A | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.459+9283A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101866168 | ||||||
| chr14:101866272
|
G | A | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.459+9387G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101866272 | ||||||
| chr14:101866524
|
G | T | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.459+9639G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101866524 | ||||||
| chr14:101866673
|
A | T | 4 | a0001c0001t0001g0027a0001c0001t0003g0005a0001c0001t0003g0006others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+9788A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101866673 | ||||||
| chr14:101866834
|
A | C | 2 | a0002c0002t0001g0121a0003c0004t0004g0120 | 2 | HG00733.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.459+9949A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101866834 | ||||||
| chr14:101866897
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+10012C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101866897 | ||||||
| chr14:101867086
|
G | GCAT | 2 | a0001c0001t0001g0015a0001c0001t0012g0064 | 2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.459+10202_459+1020 others(7): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101867086 | |||||
| chr14:101867138
|
A | G | 3 | a0001c0001t0007g0016a0001c0001t0007g0076a0001c0001t0007g0126 | 3 | HG02622.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.459+10253A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101867138 | ||||||
| chr14:101867356
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0048 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.459+10471G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101867356 | ||||||
| chr14:101867517
|
C | T | 11 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.459+10632C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101867517 | ||||||
| chr14:101867754
|
A | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(80): Show | 83 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.459+10869A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101867754 | ||||||
| chr14:101867796
|
T | TA | 22 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0096others(19): Show | 22 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+10916dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101867796 | |||||
| chr14:101868457
|
C | T | 24 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0048others(21): Show | 24 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.459+11572C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101868457 | ||||||
| chr14:101868842
|
T | A | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.459+11957T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101868842 | ||||||
| chr14:101868856
|
A | G | 2 | a0002c0002t0001g0121a0003c0004t0004g0120 | 2 | HG00733.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.459+11971A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101868856 | ||||||
| chr14:101868906
|
TTTTG | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0003t0002g0079others(4): Show | 7 | HG02572.hp2 HG02735.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+12045_459+1204 others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101868906 | |||||
| chr14:101868941
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.459+12056G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101868941 | ||||||
| chr14:101869203
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.459+12318C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101869203 | ||||||
| chr14:101869244
|
C | T | 1 | a0002c0002t0003g0134 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.459+12359C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101869244 | ||||||
| chr14:101869398
|
C | A | 2 | a0002c0002t0004g0023a0002c0002t0004g0024 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.459+12513C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101869398 | ||||||
| chr14:101869450
|
T | C | 3 | a0001c0003t0018g0089a0002c0002t0001g0121a0003c0004t0004g0120 | 3 | HG00733.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.459+12565T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101869450 | ||||||
| chr14:101869653
|
G | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.460-12508G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101869653 | ||||||
| chr14:101869872
|
G | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0045others(71): Show | 74 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.460-12289G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101869872 | ||||||
| chr14:101870040
|
CT | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0081others(9): Show | 12 | HG01258.hp1 HG01934.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.460-12095delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101870040 | |||||
| chr14:101870040
|
CTT | C | 48 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0050others(45): Show | 48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.460-12096_460-1209 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101870040 | |||||
| chr14:101870040
|
CTTTT | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0048others(17): Show | 20 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.460-12098_460-1209 others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101870040 | |||||
| chr14:101870040
|
CTTTTT | C | 5 | a0001c0001t0001g0045a0002c0002t0001g0001a0002c0002t0001g0025others(2): Show | 5 | HG01070.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-12099_460-1209 others(9): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101870040 | |||||
| chr14:101870060
|
T | G | 17 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0096others(14): Show | 17 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.460-12101T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870060 | ||||||
| chr14:101870061
|
T | A | 17 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0096others(14): Show | 17 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.460-12100T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870061 | ||||||
| chr14:101870062
|
T | G | 17 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0096others(14): Show | 17 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.460-12099T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870062 | ||||||
| chr14:101870294
|
A | G | 50 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0050others(47): Show | 50 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.460-11867A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870294 | ||||||
| chr14:101870336
|
A | G | 4 | a0001c0001t0002g0068a0001c0001t0011g0012a0002c0002t0008g0009others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-11825A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870336 | ||||||
| chr14:101870350
|
T | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0048others(21): Show | 24 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.460-11811T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870350 | ||||||
| chr14:101870500
|
C | T | 33 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0053others(30): Show | 33 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.460-11661C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870500 | ||||||
| chr14:101870764
|
T | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(79): Show | 82 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.460-11397T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870764 | ||||||
| chr14:101870854
|
T | A | 1 | a0001c0003t0020g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.460-11307T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870854 | ||||||
| chr14:101870922
|
C | G | 26 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0053others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-11239C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870922 | ||||||
| chr14:101870936
|
A | G | 2 | a0002c0002t0001g0121a0003c0004t0004g0120 | 2 | HG00733.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.460-11225A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101870936 | ||||||
| chr14:101871141
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.460-11020A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871141 | ||||||
| chr14:101871220
|
T | TTTTGG | 71 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0045others(68): Show | 71 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.460-10937_460-1093 others(9): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101871220 | |||||
| chr14:101871228
|
T | TGGTTTTT others(4): Show |
6 | a0002c0002t0004g0017a0002c0002t0004g0023a0002c0002t0004g0024others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-10933_460-1093 others(15): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871228 | ||||||
| chr14:101871228
|
T | TGGTTTTT others(7): Show |
1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.460-10933_460-1093 others(18): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871228 | ||||||
| chr14:101871228
|
T | TGGTTTTT others(13): Show |
1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.460-10933_460-1093 others(24): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871228 | ||||||
| chr14:101871230
|
T | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.460-10931T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871230 | ||||||
| chr14:101871234
|
G | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.460-10927G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871234 | ||||||
| chr14:101871236
|
TG | T | 71 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0045others(68): Show | 71 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.460-10924delG | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871236 | ||||||
| chr14:101871298
|
G | A | 73 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(70): Show | 73 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.460-10863G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871298 | ||||||
| chr14:101871330
|
C | T | 17 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0096others(14): Show | 17 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.460-10831C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871330 | ||||||
| chr14:101871393
|
A | G | 51 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0050others(48): Show | 51 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.460-10768A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871393 | ||||||
| chr14:101871619
|
G | C | 1 | a0001c0001t0002g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.460-10542G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871619 | ||||||
| chr14:101871623
|
G | A | 3 | a0001c0001t0002g0068a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.460-10538G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871623 | ||||||
| chr14:101871687
|
C | CTCTT | 35 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0045others(32): Show | 35 | HG00733.hp2 HG01070.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.460-10473_460-1047 others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101871687 | |||||
| chr14:101871775
|
A | G | 17 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0096others(14): Show | 17 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.460-10386A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871775 | ||||||
| chr14:101871941
|
C | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0118 | 2 | HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.460-10220C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101871941 | ||||||
| chr14:101872018
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.460-10143C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101872018 | ||||||
| chr14:101872219
|
C | CT | 10 | a0001c0001t0001g0056a0001c0001t0001g0117a0001c0003t0018g0089others(7): Show | 10 | HG00408.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-9920dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101872219 | |||||
| chr14:101872219
|
C | CTT | 26 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0050others(23): Show | 26 | HG01070.hp1 HG01106.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-9921_460-9920d others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101872219 | |||||
| chr14:101872219
|
C | CTTT | 50 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0045others(47): Show | 50 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.460-9922_460-9920d others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101872219 | |||||
| chr14:101872641
|
A | G | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.460-9520A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101872641 | ||||||
| chr14:101872913
|
A | G | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.460-9248A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101872913 | ||||||
| chr14:101872926
|
C | CT | 26 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0053others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-9223dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101872926 | |||||
| chr14:101873204
|
C | T | 89 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(86): Show | 89 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.460-8957C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101873204 | ||||||
| chr14:101873224
|
T | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0040others(86): Show | 89 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.460-8937T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101873224 | ||||||
| chr14:101873263
|
T | C | 9 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0096others(6): Show | 9 | HG01106.hp1 HG01243.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-8898T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101873263 | ||||||
| chr14:101873549
|
G | A | 1 | a0001c0001t0006g0105 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.460-8612G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101873549 | ||||||
| chr14:101873612
|
G | T | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.460-8549G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101873612 | ||||||
| chr14:101873788
|
G | A | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.460-8373G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101873788 | ||||||
| chr14:101873843
|
G | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0048others(21): Show | 24 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.460-8318G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101873843 | ||||||
| chr14:101874262
|
G | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0048others(28): Show | 31 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.460-7899G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101874262 | ||||||
| chr14:101874312
|
A | G | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.460-7849A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101874312 | ||||||
| chr14:101874371
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.460-7790G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101874371 | ||||||
| chr14:101874476
|
A | G | 1 | a0002c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.460-7685A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101874476 | ||||||
| chr14:101874589
|
T | C | 3 | a0001c0001t0002g0068a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.460-7572T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101874589 | ||||||
| chr14:101874612
|
A | G | 10 | a0001c0001t0001g0066a0001c0003t0018g0089a0002c0002t0001g0121others(7): Show | 10 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-7549A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101874612 | ||||||
| chr14:101874778
|
C | T | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.460-7383C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101874778 | ||||||
| chr14:101874946
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0048others(26): Show | 29 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-7215G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101874946 | ||||||
| chr14:101875313
|
T | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0045others(81): Show | 84 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.460-6848T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101875313 | ||||||
| chr14:101875481
|
A | T | 12 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0096others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-6680A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101875481 | ||||||
| chr14:101875720
|
A | G | 3 | a0001c0001t0002g0068a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.460-6441A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101875720 | ||||||
| chr14:101875854
|
C | T | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.460-6307C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101875854 | ||||||
| chr14:101875979
|
G | A | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.460-6182G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101875979 | ||||||
| chr14:101876129
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.460-6032A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876129 | ||||||
| chr14:101876409
|
G | A | 68 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0045others(65): Show | 68 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.460-5752G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876409 | ||||||
| chr14:101876414
|
C | T | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.460-5747C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876414 | ||||||
| chr14:101876603
|
A | G | 27 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(24): Show | 27 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.460-5558A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876603 | ||||||
| chr14:101876611
|
A | T | 1 | a0002c0002t0001g0025 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.460-5550A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876611 | ||||||
| chr14:101876766
|
C | G | 15 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(12): Show | 15 | HG00280.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-5395C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876766 | ||||||
| chr14:101876774
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-5387C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876774 | ||||||
| chr14:101876813
|
C | T | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.460-5348C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876813 | ||||||
| chr14:101876836
|
C | T | 15 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(12): Show | 15 | HG00280.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-5325C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876836 | ||||||
| chr14:101876885
|
T | C | 77 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0045others(74): Show | 77 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.460-5276T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876885 | ||||||
| chr14:101876886
|
G | A | 1 | a0002c0002t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.460-5275G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876886 | ||||||
| chr14:101876940
|
C | CT | 26 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0056others(23): Show | 26 | HG01243.hp2 HG01433.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.460-5195dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101876940 | |||||
| chr14:101876940
|
CT | C | 16 | a0001c0001t0001g0026a0001c0001t0001g0066a0001c0001t0001g0082others(13): Show | 16 | HG01074.hp1 HG01433.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.460-5195delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101876940 | |||||
| chr14:101876940
|
CTT | C | 5 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0114others(2): Show | 5 | HG01884.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-5196_460-5195d others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101876940 | |||||
| chr14:101876985
|
A | G | 20 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(17): Show | 20 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.460-5176A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101876985 | ||||||
| chr14:101877047
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.460-5114C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877047 | ||||||
| chr14:101877198
|
C | G | 2 | a0001c0001t0001g0022a0001c0001t0012g0064 | 2 | HG00280.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.460-4963C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877198 | ||||||
| chr14:101877280
|
G | A | 20 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(17): Show | 20 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.460-4881G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877280 | ||||||
| chr14:101877386
|
C | T | 1 | a0002c0002t0001g0001 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.460-4775C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877386 | ||||||
| chr14:101877387
|
G | T | 1 | a0001c0001t0001g0004 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.460-4774G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877387 | ||||||
| chr14:101877394
|
C | T | 3 | a0001c0001t0002g0068a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.460-4767C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877394 | ||||||
| chr14:101877395
|
C | A | 4 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0003t0002g0128others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-4766C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877395 | ||||||
| chr14:101877622
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-4539C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877622 | ||||||
| chr14:101877883
|
C | T | 1 | a0002c0002t0001g0001 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.460-4278C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877883 | ||||||
| chr14:101877901
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.460-4260G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877901 | ||||||
| chr14:101877917
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0118a0001c0003t0018g0089 | 3 | HG01071.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.460-4244C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877917 | ||||||
| chr14:101877943
|
G | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082 | 3 | HG02055.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.460-4218G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101877943 | ||||||
| chr14:101878037
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0012g0064a0002c0002t0004g0017 | 3 | HG00280.hp2 HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.460-4124G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101878037 | ||||||
| chr14:101878248
|
A | G | 26 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-3913A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101878248 | ||||||
| chr14:101878348
|
A | C | 26 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-3813A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101878348 | ||||||
| chr14:101878448
|
G | A | 5 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0073others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-3713G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101878448 | ||||||
| chr14:101878649
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.460-3512G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101878649 | ||||||
| chr14:101879108
|
A | G | 4 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0003t0002g0128others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-3053A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101879108 | ||||||
| chr14:101879179
|
G | GGGGCTTT | 15 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(12): Show | 15 | HG00280.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-2980_460-2974d others(9): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 101879179 | |||||
| chr14:101879356
|
G | A | 78 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0040others(75): Show | 78 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.460-2805G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101879356 | ||||||
| chr14:101879415
|
G | A | 11 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(8): Show | 11 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-2746G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101879415 | ||||||
| chr14:101879689
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.460-2472C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101879689 | ||||||
| chr14:101879843
|
G | A | 84 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0045others(81): Show | 84 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.460-2318G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101879843 | ||||||
| chr14:101880026
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.460-2135G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880026 | ||||||
| chr14:101880201
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.460-1960G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880201 | ||||||
| chr14:101880221
|
T | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0118a0001c0001t0017g0085others(8): Show | 11 | HG00733.hp2 HG01071.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-1940T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880221 | ||||||
| chr14:101880305
|
C | G | 15 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(12): Show | 15 | HG00280.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-1856C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880305 | ||||||
| chr14:101880321
|
G | A | 1 | a0002c0002t0008g0011 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.460-1840G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880321 | ||||||
| chr14:101880336
|
G | A | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.460-1825G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880336 | ||||||
| chr14:101880393
|
C | T | 26 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-1768C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880393 | ||||||
| chr14:101880411
|
A | G | 84 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0045others(81): Show | 84 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.460-1750A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880411 | ||||||
| chr14:101880496
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.460-1665G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880496 | ||||||
| chr14:101880531
|
C | T | 15 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(12): Show | 15 | HG00280.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-1630C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880531 | ||||||
| chr14:101880659
|
T | C | 41 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(38): Show | 41 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.460-1502T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880659 | ||||||
| chr14:101880712
|
G | A | 5 | a0001c0001t0002g0068a0001c0001t0011g0012a0001c0003t0002g0127others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-1449G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880712 | ||||||
| chr14:101880718
|
A | G | 5 | a0001c0001t0002g0068a0001c0001t0011g0012a0001c0003t0002g0127others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-1443A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880718 | ||||||
| chr14:101880878
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.460-1283C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880878 | ||||||
| chr14:101880901
|
C | G | 1 | a0002c0002t0001g0035 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.460-1260C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101880901 | ||||||
| chr14:101881127
|
G | A | 15 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(12): Show | 15 | HG00280.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-1034G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101881127 | ||||||
| chr14:101881216
|
G | A | 15 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(12): Show | 15 | HG00280.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-945G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101881216 | ||||||
| chr14:101881315
|
A | G | 84 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0045others(81): Show | 84 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.460-846A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101881315 | ||||||
| chr14:101881389
|
G | A | 3 | a0001c0001t0017g0085a0002c0002t0001g0121a0003c0004t0004g0120 | 3 | HG00733.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.460-772G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101881389 | ||||||
| chr14:101881455
|
G | A | 26 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-706G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101881455 | ||||||
| chr14:101881696
|
T | C | 75 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(72): Show | 75 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.460-465T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101881696 | ||||||
| chr14:101881777
|
G | A | 5 | a0001c0001t0002g0068a0001c0001t0011g0012a0001c0003t0002g0127others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-384G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101881777 | ||||||
| chr14:101881931
|
G | A | 82 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.460-230G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101881931 | ||||||
| chr14:101881937
|
T | C | 50 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(47): Show | 50 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.460-224T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101881937 | ||||||
| chr14:101881962
|
T | C | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.460-199T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101881962 | ||||||
| chr14:101882021
|
A | G | 45 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(42): Show | 45 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.460-140A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 4/15 | chr14 | 101882021 | ||||||
| chr14:101882276
|
C | T | 5 | a0001c0001t0002g0068a0001c0001t0011g0012a0001c0003t0002g0127others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.570+5C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 5/15 | chr14 | 101882276 | ||||||
| chr14:101882513
|
G | T | 16 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(13): Show | 16 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.570+242G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 5/15 | chr14 | 101882513 | ||||||
| chr14:101882709
|
G | A | 68 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(65): Show | 68 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.570+438G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 5/15 | chr14 | 101882709 | ||||||
| chr14:101882720
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.570+449C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 5/15 | chr14 | 101882720 | ||||||
| chr14:101882887
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.571-370C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 5/15 | chr14 | 101882887 | ||||||
| chr14:101883181
|
T | A | 4 | a0001c0001t0002g0068a0001c0001t0011g0012a0002c0002t0008g0009others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-76T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 5/15 | chr14 | 101883181 | ||||||
| chr14:101883203
|
C | T | 82 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.571-54C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 5/15 | chr14 | 101883203 | ||||||
| chr14:101883205
|
G | T | 82 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.571-52G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 5/15 | chr14 | 101883205 | ||||||
| chr14:101883371
|
AC | A | 5 | a0001c0001t0002g0068a0001c0001t0011g0012a0001c0003t0002g0127others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.663+23delC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 6/15 | chr14 | 101883371 | ||||||
| chr14:101883570
|
A | G | 82 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
splice_region_variant&intron_variant | LOW | c.794+8A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101883570 | ||||||
| chr14:101883663
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0012g0064a0002c0002t0004g0017 | 3 | HG00280.hp2 HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.794+101G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101883663 | ||||||
| chr14:101883980
|
C | G | 4 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0003t0002g0128others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+418C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101883980 | ||||||
| chr14:101884059
|
A | G | 75 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(72): Show | 75 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.794+497A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884059 | ||||||
| chr14:101884064
|
T | C | 1 | a0001c0003t0002g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.794+502T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884064 | ||||||
| chr14:101884076
|
G | A | 8 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0068others(5): Show | 8 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.794+514G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884076 | ||||||
| chr14:101884200
|
A | T | 7 | a0001c0001t0017g0085a0002c0002t0001g0121a0002c0002t0004g0023others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+638A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884200 | ||||||
| chr14:101884215
|
C | G | 26 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.794+653C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884215 | ||||||
| chr14:101884225
|
T | G | 26 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.794+663T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884225 | ||||||
| chr14:101884230
|
C | A | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.794+668C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884230 | ||||||
| chr14:101884254
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.794+692C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884254 | ||||||
| chr14:101884259
|
G | A | 1 | a0002c0002t0001g0002 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.794+697G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884259 | ||||||
| chr14:101884525
|
A | T | 1 | a0001c0001t0001g0078 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.794+963A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884525 | ||||||
| chr14:101884587
|
G | A | 3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.794+1025G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101884587 | ||||||
| chr14:101885085
|
G | A | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.794+1523G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885085 | ||||||
| chr14:101885204
|
G | A | 1 | a0002c0002t0001g0001 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.794+1642G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885204 | ||||||
| chr14:101885291
|
T | A | 22 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(19): Show | 22 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.794+1729T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885291 | ||||||
| chr14:101885314
|
C | CCTCCCAT others(251): Show |
26 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.794+1805_794+1806i others(260): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101885314 | |||||
| chr14:101885330
|
G | GGCTTGCA others(337): Show |
7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+1805_794+1806i others(346): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101885330 | |||||
| chr14:101885368
|
G | A | 2 | a0001c0001t0001g0109a0004c0005t0001g0101 | 2 | HG00408.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.794+1806G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885368 | ||||||
| chr14:101885368
|
G | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+1806G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885368 | ||||||
| chr14:101885416
|
G | A | 58 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(55): Show | 58 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.794+1854G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885416 | ||||||
| chr14:101885432
|
G | A | 15 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(12): Show | 15 | HG00280.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.794+1870G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885432 | ||||||
| chr14:101885435
|
GGGAGCAC others(79): Show |
G | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.794+1893_794+1978d others(88): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101885435 | |||||
| chr14:101885451
|
TCCCTCTG others(80): Show |
T | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.794+1904_794+1990d others(89): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101885451 | |||||
| chr14:101885454
|
C | CTCTGCAG others(79): Show |
2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.794+1911_794+1912i others(88): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101885454 | |||||
| chr14:101885474
|
A | G | 7 | a0001c0001t0017g0085a0002c0002t0001g0121a0002c0002t0004g0023others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+1912A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885474 | ||||||
| chr14:101885507
|
G | GCACAGCC others(79): Show |
5 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0073others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+1958_794+1959i others(88): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101885507 | |||||
| chr14:101885517
|
C | T | 5 | a0001c0001t0002g0068a0001c0001t0011g0012a0001c0003t0002g0127others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.794+1955C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885517 | ||||||
| chr14:101885521
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(93): Show | 96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.794+1959A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885521 | ||||||
| chr14:101885597
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.794+2035C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885597 | ||||||
| chr14:101885663
|
G | A | 7 | a0001c0001t0017g0085a0002c0002t0001g0121a0002c0002t0004g0023others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+2101G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885663 | ||||||
| chr14:101885708
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+2146C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885708 | ||||||
| chr14:101885720
|
C | T | 1 | a0001c0003t0020g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.794+2158C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885720 | ||||||
| chr14:101885771
|
G | C | 1 | a0001c0001t0017g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.794+2209G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885771 | ||||||
| chr14:101885831
|
A | G | 11 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0001t0017g0085others(8): Show | 11 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.794+2269A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101885831 | ||||||
| chr14:101886019
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.794+2457C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101886019 | ||||||
| chr14:101886088
|
T | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+2526T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101886088 | ||||||
| chr14:101886138
|
G | A | 1 | a0001c0003t0002g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.794+2576G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101886138 | ||||||
| chr14:101886154
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.794+2592A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101886154 | ||||||
| chr14:101886160
|
A | G | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794+2598A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101886160 | ||||||
| chr14:101886280
|
CA | C | 66 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(63): Show | 66 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.794+2735delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101886280 | |||||
| chr14:101886427
|
CTGTGTGC others(26): Show |
C | 4 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0003t0002g0128others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.794+2968_794+3000d others(35): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101886427 | |||||
| chr14:101886462
|
G | A | 16 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(13): Show | 16 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.794+2900G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101886462 | ||||||
| chr14:101886498
|
T | C | 1 | a0002c0002t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.794+2936T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101886498 | ||||||
| chr14:101886572
|
C | T | 1 | a0002c0002t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.794+3010C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101886572 | ||||||
| chr14:101886773
|
TGGA | T | 16 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(13): Show | 16 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.794+3213_794+3215d others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101886773 | |||||
| chr14:101887454
|
T | C | 23 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(20): Show | 23 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.795-2783T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101887454 | ||||||
| chr14:101887512
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.795-2725G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101887512 | ||||||
| chr14:101887523
|
G | A | 5 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0073others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-2714G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101887523 | ||||||
| chr14:101887785
|
A | G | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.795-2452A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101887785 | ||||||
| chr14:101887871
|
G | C | 4 | a0001c0001t0002g0068a0001c0001t0011g0012a0002c0002t0008g0009others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-2366G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101887871 | ||||||
| chr14:101887973
|
G | A | 4 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0003t0002g0128others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-2264G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101887973 | ||||||
| chr14:101888032
|
A | G | 3 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0003g0138 | 3 | NA19009.hp1 NA19068.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.795-2205A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101888032 | ||||||
| chr14:101888213
|
A | T | 1 | a0001c0003t0002g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.795-2024A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101888213 | ||||||
| chr14:101888248
|
A | G | 4 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0003t0002g0128others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-1989A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101888248 | ||||||
| chr14:101888309
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.795-1928G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101888309 | ||||||
| chr14:101888579
|
GTTGTTTT others(3): Show |
G | 3 | a0001c0001t0001g0022a0001c0001t0012g0064a0002c0002t0004g0017 | 3 | HG00280.hp2 HG01255.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.795-1640_795-1631d others(12): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101888579 | |||||
| chr14:101888753
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.795-1484G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101888753 | ||||||
| chr14:101888793
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.795-1444T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101888793 | ||||||
| chr14:101889010
|
T | TA | 7 | a0001c0001t0017g0085a0002c0002t0001g0121a0002c0002t0004g0023others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-1215dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 101889010 | |||||
| chr14:101889050
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.795-1187A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101889050 | ||||||
| chr14:101889411
|
T | C | 12 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0002g0028others(9): Show | 12 | HG01243.hp1 HG01258.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.795-826T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101889411 | ||||||
| chr14:101889458
|
G | A | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.795-779G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101889458 | ||||||
| chr14:101889615
|
G | A | 3 | a0001c0001t0007g0016a0001c0001t0007g0076a0001c0001t0007g0126 | 3 | HG02622.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.795-622G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101889615 | ||||||
| chr14:101889766
|
A | G | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.795-471A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101889766 | ||||||
| chr14:101890138
|
C | T | 26 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.795-99C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101890138 | ||||||
| chr14:101890142
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.795-95T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 7/15 | chr14 | 101890142 | ||||||
| chr14:101890327
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.854+31G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101890327 | ||||||
| chr14:101890376
|
C | T | 4 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0003t0002g0128others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.854+80C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101890376 | ||||||
| chr14:101890462
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.854+166T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101890462 | ||||||
| chr14:101890655
|
T | C | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.854+359T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101890655 | ||||||
| chr14:101890683
|
A | G | 82 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.854+387A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101890683 | ||||||
| chr14:101890700
|
T | C | 4 | a0001c0001t0002g0068a0001c0001t0011g0012a0002c0002t0008g0009others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.854+404T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101890700 | ||||||
| chr14:101890764
|
C | CT | 5 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0083others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.854+492dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr14 | 101890764 | |||||
| chr14:101890764
|
CTT | C | 38 | a0001c0001t0001g0022a0001c0001t0001g0048a0001c0001t0001g0061others(35): Show | 38 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.854+491_854+492del others(2): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr14 | 101890764 | |||||
| chr14:101890764
|
CTTT | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0117a0001c0001t0002g0095others(4): Show | 7 | HG01070.hp2 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.854+490_854+492del others(3): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr14 | 101890764 | |||||
| chr14:101890775
|
T | C | 15 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(12): Show | 15 | HG01070.hp1 HG01433.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.854+479T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101890775 | ||||||
| chr14:101890887
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.854+591C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101890887 | ||||||
| chr14:101890921
|
C | T | 5 | a0001c0003t0002g0127a0002c0002t0001g0025a0002c0002t0001g0038others(2): Show | 5 | HG03516.hp1 NA18995.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.854+625C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101890921 | ||||||
| chr14:101891211
|
C | T | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.854+915C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101891211 | ||||||
| chr14:101891297
|
C | T | 4 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0003t0002g0128others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.854+1001C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101891297 | ||||||
| chr14:101891419
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.854+1123C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101891419 | ||||||
| chr14:101891464
|
CCT | C | 58 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(55): Show | 58 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.854+1173_854+1174d others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr14 | 101891464 | |||||
| chr14:101891542
|
T | C | 59 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(56): Show | 59 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.854+1246T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101891542 | ||||||
| chr14:101891608
|
G | A | 43 | a0001c0001t0001g0022a0001c0001t0001g0066a0001c0001t0001g0072others(40): Show | 43 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.854+1312G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101891608 | ||||||
| chr14:101891622
|
G | A | 27 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(24): Show | 27 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.854+1326G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101891622 | ||||||
| chr14:101891642
|
A | G | 4 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0003t0002g0128others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.854+1346A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101891642 | ||||||
| chr14:101891724
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.855-1276C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101891724 | ||||||
| chr14:101891750
|
G | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.855-1250G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101891750 | ||||||
| chr14:101891763
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.855-1237C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101891763 | ||||||
| chr14:101892037
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0107 | 2 | NA18964.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.855-963A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892037 | ||||||
| chr14:101892038
|
A | G | 3 | a0001c0001t0002g0068a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.855-962A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892038 | ||||||
| chr14:101892042
|
T | C | 16 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(13): Show | 16 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.855-958T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892042 | ||||||
| chr14:101892111
|
G | A | 41 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(38): Show | 41 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.855-889G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892111 | ||||||
| chr14:101892121
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.855-879A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892121 | ||||||
| chr14:101892162
|
G | A | 1 | a0001c0001t0006g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.855-838G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892162 | ||||||
| chr14:101892223
|
C | G | 1 | a0001c0001t0001g0004 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.855-777C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892223 | ||||||
| chr14:101892223
|
C | T | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.855-777C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892223 | ||||||
| chr14:101892247
|
G | A | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.855-753G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892247 | ||||||
| chr14:101892276
|
C | G | 22 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(19): Show | 22 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.855-724C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892276 | ||||||
| chr14:101892350
|
G | T | 70 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0066others(67): Show | 70 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.855-650G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892350 | ||||||
| chr14:101892393
|
GT | G | 52 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0096others(49): Show | 52 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.855-606delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892393 | ||||||
| chr14:101892394
|
T | C | 19 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(16): Show | 19 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.855-606T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892394 | ||||||
| chr14:101892395
|
G | C | 52 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0096others(49): Show | 52 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.855-605G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892395 | ||||||
| chr14:101892398
|
G | A | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.855-602G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892398 | ||||||
| chr14:101892421
|
G | A | 3 | a0001c0001t0002g0068a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.855-579G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892421 | ||||||
| chr14:101892484
|
C | T | 9 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(6): Show | 9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.855-516C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892484 | ||||||
| chr14:101892577
|
C | T | 81 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0066others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.855-423C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892577 | ||||||
| chr14:101892791
|
G | A | 32 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0090others(29): Show | 32 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.855-209G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892791 | ||||||
| chr14:101892827
|
G | C | 81 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0066others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.855-173G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892827 | ||||||
| chr14:101892829
|
C | T | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.855-171C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892829 | ||||||
| chr14:101892967
|
A | G | 28 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(25): Show | 28 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.855-33A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 8/15 | chr14 | 101892967 | ||||||
| chr14:101893152
|
A | G | 58 | a0001c0001t0001g0022a0001c0001t0001g0066a0001c0001t0001g0072others(55): Show | 58 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.963+44A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893152 | ||||||
| chr14:101893180
|
C | T | 1 | a0001c0001t0006g0075 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.963+72C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893180 | ||||||
| chr14:101893217
|
G | T | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.963+109G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893217 | ||||||
| chr14:101893231
|
A | G | 28 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0117others(25): Show | 28 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.963+123A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893231 | ||||||
| chr14:101893422
|
G | A | 19 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(16): Show | 19 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.963+314G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893422 | ||||||
| chr14:101893517
|
T | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+409T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893517 | ||||||
| chr14:101893580
|
G | A | 8 | a0001c0001t0001g0061a0001c0003t0018g0089a0002c0002t0004g0023others(5): Show | 8 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+472G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893580 | ||||||
| chr14:101893611
|
A | G | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.963+503A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893611 | ||||||
| chr14:101893619
|
A | G | 8 | a0001c0001t0001g0061a0001c0003t0018g0089a0002c0002t0004g0023others(5): Show | 8 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+511A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893619 | ||||||
| chr14:101893636
|
G | C | 8 | a0001c0001t0001g0061a0001c0003t0018g0089a0002c0002t0004g0023others(5): Show | 8 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+528G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893636 | ||||||
| chr14:101893715
|
A | G | 18 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(15): Show | 18 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.963+607A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893715 | ||||||
| chr14:101893735
|
A | C | 4 | a0001c0001t0002g0086a0001c0001t0002g0091a0001c0001t0002g0124others(1): Show | 4 | HG01884.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+627A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893735 | ||||||
| chr14:101893837
|
A | G | 1 | a0001c0001t0003g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.964-670A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893837 | ||||||
| chr14:101893964
|
A | G | 65 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0088others(62): Show | 65 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.964-543A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101893964 | ||||||
| chr14:101894344
|
A | G | 3 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0119 | 3 | HG01256.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.964-163A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101894344 | ||||||
| chr14:101894408
|
T | C | 19 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(16): Show | 19 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.964-99T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 9/15 | chr14 | 101894408 | ||||||
| chr14:101894579
|
G | A | 44 | a0001c0001t0001g0022a0001c0001t0001g0066a0001c0001t0001g0072others(41): Show | 44 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.1017+19G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101894579 | ||||||
| chr14:101894727
|
A | C | 19 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(16): Show | 19 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1017+167A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101894727 | ||||||
| chr14:101894797
|
G | A | 21 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(18): Show | 21 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1017+237G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101894797 | ||||||
| chr14:101895063
|
C | T | 72 | a0001c0001t0001g0022a0001c0001t0001g0066a0001c0001t0001g0072others(69): Show | 72 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1017+503C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101895063 | ||||||
| chr14:101895128
|
T | C | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1017+568T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101895128 | ||||||
| chr14:101895220
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1017+660A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101895220 | ||||||
| chr14:101895354
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1017+794C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101895354 | ||||||
| chr14:101895377
|
G | A | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1017+817G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101895377 | ||||||
| chr14:101895400
|
G | A | 19 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(16): Show | 19 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1017+840G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101895400 | ||||||
| chr14:101895603
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0005g0069others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017+1043G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101895603 | ||||||
| chr14:101895668
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1017+1108G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101895668 | ||||||
| chr14:101895725
|
A | G | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1017+1165A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101895725 | ||||||
| chr14:101895798
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1017+1238A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101895798 | ||||||
| chr14:101896081
|
G | A | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1017+1521G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101896081 | ||||||
| chr14:101896162
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0078 | 2 | NA18963.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1017+1602G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101896162 | ||||||
| chr14:101896520
|
G | T | 16 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0002g0028others(13): Show | 16 | HG01243.hp1 HG01258.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1017+1960G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101896520 | ||||||
| chr14:101896636
|
C | CA | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(61): Show | 64 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1017+2095dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 101896636 | |||||
| chr14:101896636
|
C | CAA | 24 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0003g0130others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1017+2094_1017+209 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 101896636 | |||||
| chr14:101896652
|
A | T | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1017+2092A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101896652 | ||||||
| chr14:101896724
|
T | A | 1 | a0001c0001t0017g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1017+2164T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101896724 | ||||||
| chr14:101896729
|
A | T | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1017+2169A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101896729 | ||||||
| chr14:101896877
|
T | C | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1017+2317T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101896877 | ||||||
| chr14:101896899
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0090 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1017+2339C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101896899 | ||||||
| chr14:101896938
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1017+2378C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101896938 | ||||||
| chr14:101897402
|
A | AT | 20 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0048others(17): Show | 20 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1017+2857dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 101897402 | |||||
| chr14:101897402
|
AT | A | 28 | a0001c0001t0001g0050a0001c0001t0001g0088a0001c0001t0001g0090others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.1017+2857delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 101897402 | |||||
| chr14:101897414
|
T | C | 1 | a0001c0003t0002g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1017+2854T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101897414 | ||||||
| chr14:101897430
|
C | T | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1017+2870C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101897430 | ||||||
| chr14:101897518
|
C | T | 1 | a0002c0002t0001g0115 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1017+2958C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101897518 | ||||||
| chr14:101897520
|
G | A | 19 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(16): Show | 19 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1017+2960G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101897520 | ||||||
| chr14:101897526
|
C | T | 16 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0002g0028others(13): Show | 16 | HG01243.hp1 HG01258.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1017+2966C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101897526 | ||||||
| chr14:101897544
|
G | A | 26 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0003g0130others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.1017+2984G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101897544 | ||||||
| chr14:101897669
|
G | C | 26 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0003g0130others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.1017+3109G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101897669 | ||||||
| chr14:101897807
|
T | TA | 30 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0002g0068others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1017+3263dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 101897807 | |||||
| chr14:101897896
|
C | G | 36 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0096others(33): Show | 36 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1017+3336C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101897896 | ||||||
| chr14:101897992
|
C | CA | 37 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0096others(34): Show | 37 | HG00280.hp2 HG00733.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1017+3445dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 101897992 | |||||
| chr14:101898256
|
G | A | 4 | a0001c0001t0002g0086a0001c0001t0002g0091a0001c0001t0002g0124others(1): Show | 4 | HG01884.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-3463G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101898256 | ||||||
| chr14:101898581
|
G | A | 16 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0002g0028others(13): Show | 16 | HG01243.hp1 HG01258.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1018-3138G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101898581 | ||||||
| chr14:101898779
|
A | G | 1 | a0001c0003t0002g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1018-2940A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101898779 | ||||||
| chr14:101898977
|
G | A | 1 | a0002c0002t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1018-2742G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101898977 | ||||||
| chr14:101899327
|
G | C | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1018-2392G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101899327 | ||||||
| chr14:101899387
|
G | A | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1018-2332G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101899387 | ||||||
| chr14:101899634
|
T | G | 3 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0119 | 3 | HG01256.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1018-2085T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101899634 | ||||||
| chr14:101899684
|
T | C | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1018-2035T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101899684 | ||||||
| chr14:101899734
|
C | T | 16 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(13): Show | 16 | HG01070.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1018-1985C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101899734 | ||||||
| chr14:101899737
|
A | C | 2 | a0002c0002t0001g0035a0002c0002t0001g0102 | 2 | HG02132.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1018-1982A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101899737 | ||||||
| chr14:101899965
|
C | T | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1018-1754C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101899965 | ||||||
| chr14:101900049
|
G | A | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1018-1670G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101900049 | ||||||
| chr14:101900366
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1018-1353T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101900366 | ||||||
| chr14:101900456
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1018-1263T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101900456 | ||||||
| chr14:101900458
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1018-1261G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101900458 | ||||||
| chr14:101900496
|
G | C | 81 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0066others(78): Show | 81 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1018-1223G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101900496 | ||||||
| chr14:101900504
|
C | G | 2 | a0002c0002t0001g0035a0002c0002t0001g0102 | 2 | HG02132.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1018-1215C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101900504 | ||||||
| chr14:101900676
|
T | C | 80 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0066others(77): Show | 80 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1018-1043T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101900676 | ||||||
| chr14:101900707
|
T | C | 1 | a0002c0002t0004g0119 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1018-1012T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101900707 | ||||||
| chr14:101900805
|
C | T | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1018-914C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101900805 | ||||||
| chr14:101900890
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1018-829C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101900890 | ||||||
| chr14:101901332
|
T | G | 1 | a0001c0001t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1018-387T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101901332 | ||||||
| chr14:101901636
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1018-83C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 10/15 | chr14 | 101901636 | ||||||
| chr14:101901983
|
T | G | 1 | a0004c0005t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1188+94T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101901983 | ||||||
| chr14:101902458
|
A | C | 75 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(72): Show | 75 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1188+569A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101902458 | ||||||
| chr14:101902515
|
CATT | C | 4 | a0001c0001t0002g0086a0001c0001t0002g0091a0001c0001t0002g0124others(1): Show | 4 | HG01884.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1188+627_1188+629d others(5): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101902515 | ||||||
| chr14:101902523
|
G | A | 1 | a0002c0002t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1188+634G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101902523 | ||||||
| chr14:101902666
|
G | A | 1 | a0002c0002t0001g0084 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1188+777G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101902666 | ||||||
| chr14:101902669
|
G | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(5): Show | 8 | HG01433.hp2 HG02055.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188+780G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101902669 | ||||||
| chr14:101903015
|
G | GT | 7 | a0001c0001t0001g0014a0001c0001t0001g0058a0001c0001t0001g0106others(4): Show | 7 | HG00438.hp2 HG01433.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1188+1144dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr14 | 101903015 | |||||
| chr14:101903015
|
GT | G | 67 | a0001c0001t0001g0056a0001c0001t0001g0093a0001c0001t0001g0096others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1188+1144delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr14 | 101903015 | |||||
| chr14:101903130
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1188+1241C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903130 | ||||||
| chr14:101903192
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0011g0012 | 2 | HG02630.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1188+1303G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903192 | ||||||
| chr14:101903216
|
G | A | 78 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(75): Show | 78 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1188+1327G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903216 | ||||||
| chr14:101903288
|
T | C | 43 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(40): Show | 43 | HG00733.hp2 HG01243.hp1 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.1188+1399T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903288 | ||||||
| chr14:101903312
|
A | T | 8 | a0001c0001t0002g0068a0001c0001t0002g0095a0001c0001t0002g0114others(5): Show | 8 | HG01255.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188+1423A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903312 | ||||||
| chr14:101903379
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0049 | 3 | HG01074.hp1 HG01934.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1188+1490C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903379 | ||||||
| chr14:101903430
|
G | A | 3 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0119 | 3 | HG01256.hp1 HG01258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1188+1541G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903430 | ||||||
| chr14:101903495
|
C | T | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1188+1606C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903495 | ||||||
| chr14:101903539
|
C | G | 5 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1188+1650C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903539 | ||||||
| chr14:101903543
|
C | G | 4 | a0001c0001t0001g0027a0001c0001t0003g0005a0001c0001t0003g0006others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+1654C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903543 | ||||||
| chr14:101903658
|
G | A | 1 | a0001c0001t0006g0075 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1188+1769G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903658 | ||||||
| chr14:101903800
|
C | T | 3 | a0001c0003t0005g0018a0001c0003t0005g0020a0001c0003t0013g0019 | 3 | HG02572.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1188+1911C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903800 | ||||||
| chr14:101903917
|
G | A | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1188+2028G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101903917 | ||||||
| chr14:101904087
|
G | T | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1188+2198G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101904087 | ||||||
| chr14:101904088
|
C | T | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1188+2199C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101904088 | ||||||
| chr14:101904338
|
C | T | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1189-2064C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101904338 | ||||||
| chr14:101904545
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1189-1857C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101904545 | ||||||
| chr14:101904607
|
A | T | 8 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(5): Show | 8 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1189-1795A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101904607 | ||||||
| chr14:101904687
|
A | G | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1189-1715A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101904687 | ||||||
| chr14:101904749
|
G | A | 1 | a0001c0001t0006g0075 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1189-1653G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101904749 | ||||||
| chr14:101904947
|
C | T | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1189-1455C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101904947 | ||||||
| chr14:101905079
|
T | A | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1189-1323T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905079 | ||||||
| chr14:101905099
|
G | A | 5 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-1303G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905099 | ||||||
| chr14:101905111
|
T | C | 5 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-1291T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905111 | ||||||
| chr14:101905303
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0060 | 2 | HG02056.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1189-1099G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905303 | ||||||
| chr14:101905571
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1189-831C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905571 | ||||||
| chr14:101905709
|
G | A | 5 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-693G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905709 | ||||||
| chr14:101905764
|
C | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0048 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1189-638C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905764 | ||||||
| chr14:101905774
|
C | T | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1189-628C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905774 | ||||||
| chr14:101905781
|
A | C | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1189-621A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905781 | ||||||
| chr14:101905784
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1189-618G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905784 | ||||||
| chr14:101905878
|
G | C | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1189-524G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905878 | ||||||
| chr14:101905888
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1189-514C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101905888 | ||||||
| chr14:101906023
|
T | C | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1189-379T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101906023 | ||||||
| chr14:101906087
|
G | A | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1189-315G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101906087 | ||||||
| chr14:101906233
|
G | C | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1189-169G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101906233 | ||||||
| chr14:101906391
|
G | A | 1 | a0001c0001t0010g0133 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1189-11G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 11/15 | chr14 | 101906391 | ||||||
| chr14:101906862
|
A | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0082 | 2 | HG02055.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1316+333A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101906862 | ||||||
| chr14:101906883
|
G | A | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1316+354G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101906883 | ||||||
| chr14:101906889
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0049 | 2 | HG01934.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1316+360A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101906889 | ||||||
| chr14:101907215
|
G | A | 5 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316+686G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101907215 | ||||||
| chr14:101907233
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1316+704C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101907233 | ||||||
| chr14:101907325
|
T | C | 79 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(76): Show | 79 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1316+796T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101907325 | ||||||
| chr14:101907646
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1316+1117G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101907646 | ||||||
| chr14:101907796
|
T | C | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1316+1267T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101907796 | ||||||
| chr14:101907858
|
A | G | 42 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(39): Show | 42 | HG00733.hp2 HG01243.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.1316+1329A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101907858 | ||||||
| chr14:101907942
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082 | 3 | HG02055.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1316+1413C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101907942 | ||||||
| chr14:101907964
|
C | T | 5 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316+1435C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101907964 | ||||||
| chr14:101908084
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1317-1505T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101908084 | ||||||
| chr14:101908172
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1317-1417A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101908172 | ||||||
| chr14:101908312
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1317-1277G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101908312 | ||||||
| chr14:101908442
|
T | C | 70 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(67): Show | 70 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1317-1147T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101908442 | ||||||
| chr14:101908678
|
T | C | 9 | a0001c0003t0018g0089a0002c0002t0004g0017a0002c0002t0004g0023others(6): Show | 9 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1317-911T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101908678 | ||||||
| chr14:101908803
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1317-786C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101908803 | ||||||
| chr14:101908975
|
C | T | 9 | a0001c0003t0018g0089a0002c0002t0004g0017a0002c0002t0004g0023others(6): Show | 9 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1317-614C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101908975 | ||||||
| chr14:101909321
|
T | C | 33 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(30): Show | 33 | HG01243.hp1 HG01255.hp2 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.1317-268T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101909321 | ||||||
| chr14:101909428
|
G | C | 9 | a0001c0003t0018g0089a0002c0002t0004g0017a0002c0002t0004g0023others(6): Show | 9 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1317-161G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101909428 | ||||||
| chr14:101909515
|
C | G | 1 | a0001c0001t0012g0064 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1317-74C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101909515 | ||||||
| chr14:101909571
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1317-18G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 12/15 | chr14 | 101909571 | ||||||
| chr14:101909875
|
G | T | 70 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(67): Show | 70 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1418+185G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101909875 | ||||||
| chr14:101910173
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0070 | 2 | HG02165.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1418+483G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101910173 | ||||||
| chr14:101910399
|
C | G | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1418+709C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101910399 | ||||||
| chr14:101910401
|
ATG | A | 69 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(66): Show | 69 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1418+729_1418+730d others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 101910401 | |||||
| chr14:101910637
|
G | C | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1418+947G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101910637 | ||||||
| chr14:101910961
|
G | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(5): Show | 8 | HG01433.hp2 HG02055.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1418+1271G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101910961 | ||||||
| chr14:101910973
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1418+1283A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101910973 | ||||||
| chr14:101910977
|
G | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(5): Show | 8 | HG01433.hp2 HG02055.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1418+1287G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101910977 | ||||||
| chr14:101910996
|
C | CA | 2 | a0001c0003t0005g0018a0001c0003t0005g0020 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1418+1307dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 101910996 | |||||
| chr14:101911097
|
C | T | 1 | a0001c0001t0017g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1419-1304C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911097 | ||||||
| chr14:101911098
|
G | A | 9 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(6): Show | 9 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1419-1303G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911098 | ||||||
| chr14:101911102
|
C | CA | 45 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0078others(42): Show | 45 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1419-1285dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 101911102 | |||||
| chr14:101911104
|
A | G | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1419-1297A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911104 | ||||||
| chr14:101911265
|
C | A | 1 | a0001c0001t0002g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1419-1136C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911265 | ||||||
| chr14:101911437
|
A | G | 79 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(76): Show | 79 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1419-964A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911437 | ||||||
| chr14:101911471
|
C | T | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1419-930C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911471 | ||||||
| chr14:101911548
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1419-853C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911548 | ||||||
| chr14:101911623
|
C | T | 3 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1419-778C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911623 | ||||||
| chr14:101911690
|
C | T | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1419-711C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911690 | ||||||
| chr14:101911810
|
G | C | 1 | a0001c0001t0017g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1419-591G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911810 | ||||||
| chr14:101911883
|
CA | C | 45 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(42): Show | 45 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1419-503delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 101911883 | |||||
| chr14:101911917
|
G | A | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1419-484G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911917 | ||||||
| chr14:101911929
|
T | C | 39 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1419-472T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911929 | ||||||
| chr14:101911969
|
G | A | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1419-432G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101911969 | ||||||
| chr14:101912157
|
G | A | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1419-244G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101912157 | ||||||
| chr14:101912204
|
A | C | 1 | a0002c0002t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1419-197A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101912204 | ||||||
| chr14:101912270
|
G | T | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1419-131G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101912270 | ||||||
| chr14:101912336
|
T | A | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1419-65T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 13/15 | chr14 | 101912336 | ||||||
| chr14:101912553
|
T | TG | 33 | a0001c0001t0001g0117a0001c0001t0002g0028a0001c0001t0002g0029others(30): Show | 33 | HG00733.hp2 HG01255.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.1491+88dupG | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 101912553 | |||||
| chr14:101912761
|
A | G | 1 | a0002c0002t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1491+288A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101912761 | ||||||
| chr14:101912800
|
C | G | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1491+327C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101912800 | ||||||
| chr14:101913024
|
C | T | 26 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0002g0028others(23): Show | 26 | HG01243.hp1 HG01255.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1491+551C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101913024 | ||||||
| chr14:101913137
|
C | T | 1 | a0002c0002t0003g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1491+664C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101913137 | ||||||
| chr14:101913291
|
G | A | 3 | a0001c0001t0002g0068a0002c0002t0008g0009a0002c0002t0008g0010 | 3 | HG02451.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1491+818G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101913291 | ||||||
| chr14:101913344
|
T | C | 11 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(8): Show | 11 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1491+871T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101913344 | ||||||
| chr14:101913484
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1491+1011T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101913484 | ||||||
| chr14:101913533
|
T | C | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1491+1060T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101913533 | ||||||
| chr14:101913639
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1491+1166C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101913639 | ||||||
| chr14:101913799
|
T | C | 1 | a0001c0001t0012g0064 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1491+1326T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101913799 | ||||||
| chr14:101913978
|
T | C | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1491+1505T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101913978 | ||||||
| chr14:101914090
|
T | C | 1 | a0001c0003t0005g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1491+1617T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101914090 | ||||||
| chr14:101914299
|
C | G | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1491+1826C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101914299 | ||||||
| chr14:101914319
|
C | A | 1 | a0001c0003t0020g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1491+1846C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101914319 | ||||||
| chr14:101914421
|
C | T | 11 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(8): Show | 11 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1491+1948C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101914421 | ||||||
| chr14:101914482
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1491+2009T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101914482 | ||||||
| chr14:101914535
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1491+2062T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101914535 | ||||||
| chr14:101914548
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1491+2075T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101914548 | ||||||
| chr14:101914557
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0081a0001c0001t0015g0042 | 3 | HG00642.hp2 HG02559.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1491+2084G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101914557 | ||||||
| chr14:101914667
|
G | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(5): Show | 8 | HG01433.hp2 HG02055.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1491+2194G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101914667 | ||||||
| chr14:101915020
|
A | G | 30 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0010g0133others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1491+2547A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101915020 | ||||||
| chr14:101915057
|
GTTTGGTT others(13): Show |
G | 2 | a0001c0001t0005g0069a0001c0001t0005g0083 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1491+2599_1491+261 others(24): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 101915057 | |||||
| chr14:101915157
|
A | G | 9 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(6): Show | 9 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1492-2674A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101915157 | ||||||
| chr14:101915188
|
G | A | 4 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(1): Show | 4 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1492-2643G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101915188 | ||||||
| chr14:101915321
|
C | A | 3 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1492-2510C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101915321 | ||||||
| chr14:101915367
|
A | G | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1492-2464A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101915367 | ||||||
| chr14:101915542
|
C | T | 4 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(1): Show | 4 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1492-2289C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101915542 | ||||||
| chr14:101915610
|
C | T | 11 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(8): Show | 11 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1492-2221C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101915610 | ||||||
| chr14:101915664
|
G | A | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1492-2167G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101915664 | ||||||
| chr14:101916010
|
C | T | 34 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0005g0069others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1492-1821C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101916010 | ||||||
| chr14:101916535
|
T | C | 80 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(77): Show | 80 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1492-1296T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101916535 | ||||||
| chr14:101916678
|
C | G | 35 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0002g0028others(32): Show | 35 | HG00733.hp2 HG01243.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1492-1153C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101916678 | ||||||
| chr14:101916838
|
G | A | 34 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0005g0069others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1492-993G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101916838 | ||||||
| chr14:101916984
|
A | C | 9 | a0001c0003t0018g0089a0002c0002t0004g0017a0002c0002t0004g0023others(6): Show | 9 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1492-847A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101916984 | ||||||
| chr14:101917156
|
A | G | 11 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(8): Show | 11 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1492-675A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101917156 | ||||||
| chr14:101917302
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1492-529C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101917302 | ||||||
| chr14:101917494
|
C | G | 2 | a0001c0001t0017g0085a0002c0002t0001g0121 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1492-337C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | chr14 | 101917494 | ||||||
| chr14:101917574
|
TGGGC | T | 34 | a0001c0001t0003g0130a0001c0001t0003g0136a0001c0001t0005g0069others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1492-252_1492-249d others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 101917574 | |||||
| chr14:101918097
|
G | A | 3 | a0002c0002t0001g0025a0002c0002t0001g0038a0002c0002t0001g0039 | 3 | NA18995.hp2 NA19005.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1608+150G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918097 | ||||||
| chr14:101918139
|
A | ATTAAGTA others(32): Show |
25 | a0001c0001t0001g0096a0001c0001t0002g0028a0001c0001t0002g0029others(22): Show | 25 | HG01243.hp1 HG01255.hp2 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1608+228_1608+229i others(41): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918139 | |||||
| chr14:101918233
|
C | T | 13 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(10): Show | 13 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1608+286C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918233 | ||||||
| chr14:101918247
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1608+300C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918247 | ||||||
| chr14:101918401
|
C | T | 2 | a0001c0003t0005g0018a0001c0003t0005g0020 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1608+454C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918401 | ||||||
| chr14:101918403
|
T | TC | 5 | a0001c0001t0001g0053a0001c0001t0001g0072a0001c0001t0014g0110others(2): Show | 5 | HG01256.hp1 HG01934.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1608+462dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918403 | |||||
| chr14:101918420
|
A | AC | 6 | a0001c0001t0001g0036a0001c0001t0001g0058a0001c0001t0001g0072others(3): Show | 6 | HG00438.hp2 HG01255.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608+479dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918420 | |||||
| chr14:101918423
|
C | T | 38 | a0001c0001t0003g0130a0001c0001t0005g0069a0001c0001t0005g0083others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1608+476C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918423 | ||||||
| chr14:101918456
|
TTCATCCC others(60): Show |
T | 14 | a0001c0001t0001g0066a0001c0001t0006g0075a0001c0001t0006g0099others(11): Show | 14 | HG00733.hp1 HG00733.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1608+529_1608+595d others(69): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918456 | |||||
| chr14:101918475
|
T | TC | 24 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0082others(21): Show | 24 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1608+528_1608+529i others(3): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918475 | ||||||
| chr14:101918475
|
T | TCGCCCCC others(62): Show |
2 | a0002c0002t0001g0098a0002c0002t0003g0129 | 2 | HG01070.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1608+528_1608+529i others(71): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918475 | ||||||
| chr14:101918476
|
G | C | 5 | a0001c0001t0001g0072a0001c0001t0003g0130a0001c0003t0013g0019others(2): Show | 5 | HG00438.hp1 HG02132.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1608+529G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918476 | ||||||
| chr14:101918477
|
G | C | 26 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0082others(23): Show | 26 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1608+530G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918477 | ||||||
| chr14:101918477
|
G | GCCCCCCA others(61): Show |
2 | a0001c0001t0001g0059a0001c0001t0001g0107 | 2 | NA18964.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1608+569_1608+636d others(70): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918477 | |||||
| chr14:101918477
|
G | GCCCCCCA others(62): Show |
1 | a0001c0001t0001g0004 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1608+536_1608+604d others(71): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918477 | |||||
| chr14:101918477
|
G | GCCCCCCA others(129): Show |
3 | a0001c0001t0001g0118a0001c0001t0002g0065a0001c0001t0003g0007 | 3 | HG01071.hp2 HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1608+636_1608+637i others(138): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918477 | |||||
| chr14:101918477
|
G | GCCCCCCA others(196): Show |
3 | a0001c0001t0002g0091a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG01884.hp2 HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1608+636_1608+637i others(205): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918477 | |||||
| chr14:101918477
|
G | GCCCCCCA others(197): Show |
4 | a0001c0001t0002g0028a0001c0001t0019g0116a0001c0003t0002g0079others(1): Show | 4 | HG02735.hp1 HG03834.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+636_1608+637i others(206): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918477 | |||||
| chr14:101918477
|
G | GCCCCCCA others(265): Show |
1 | a0001c0001t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1608+636_1608+637i others(274): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918477 | |||||
| chr14:101918477
|
G | GCCCCCCA others(333): Show |
1 | a0001c0001t0002g0111 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1608+636_1608+637i others(342): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918477 | |||||
| chr14:101918477
|
G | GCCCCCCA others(537): Show |
1 | a0001c0003t0002g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1608+636_1608+637i others(546): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918477 | |||||
| chr14:101918477
|
G | GCCCCCCA others(264): Show |
1 | a0001c0001t0002g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1608+595_1608+596i others(273): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918477 | |||||
| chr14:101918477
|
G | GCCCCCCA others(197): Show |
3 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1608+547_1608+548i others(206): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918477 | |||||
| chr14:101918478
|
CCCCCCAC others(59): Show |
C | 3 | a0001c0001t0001g0072a0001c0003t0013g0019a0002c0002t0001g0102 | 3 | HG02132.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1608+537_1608+602d others(68): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918478 | |||||
| chr14:101918490
|
C | CCCCCCAC others(195): Show |
1 | a0001c0001t0002g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1608+636_1608+637i others(204): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918490 | |||||
| chr14:101918510
|
T | TCCCCTCA others(53): Show |
6 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0073others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+569_1608+570i others(62): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918510 | |||||
| chr14:101918516
|
C | CGCCCCCC others(61): Show |
4 | a0001c0001t0002g0095a0001c0001t0002g0114a0001c0003t0002g0128others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+588_1608+655d others(70): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918516 | |||||
| chr14:101918516
|
CGCCCCCC others(61): Show |
C | 2 | a0001c0001t0001g0056a0001c0001t0001g0070 | 2 | HG02165.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1608+588_1608+655d others(70): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918516 | |||||
| chr14:101918517
|
G | A | 6 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0073others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+570G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918517 | ||||||
| chr14:101918523
|
C | CTCATCCC others(884): Show |
1 | a0001c0001t0005g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1608+604_1608+605i others(893): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918523 | |||||
| chr14:101918523
|
C | CTCATCCC others(610): Show |
1 | a0001c0001t0005g0083 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1608+604_1608+605i others(619): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918523 | |||||
| chr14:101918523
|
C | T | 6 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0073others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+576C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918523 | ||||||
| chr14:101918544
|
G | GC | 19 | a0001c0001t0001g0058a0001c0001t0003g0005a0001c0001t0003g0130others(16): Show | 19 | HG00438.hp1 HG00558.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1608+604dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918544 | |||||
| chr14:101918545
|
CCCCCCCA others(60): Show |
C | 3 | a0001c0001t0001g0061a0001c0001t0001g0082a0002c0002t0001g0121 | 3 | HG02055.hp1 HG03471.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1608+605_1608+671d others(69): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918545 | |||||
| chr14:101918584
|
T | C | 50 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0066others(47): Show | 50 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1608+637T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918584 | ||||||
| chr14:101918584
|
T | TGCCCCCC others(61): Show |
1 | a0001c0001t0017g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1608+655_1608+656i others(70): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918584 | |||||
| chr14:101918603
|
A | G | 77 | a0001c0001t0001g0030a0001c0001t0001g0066a0001c0001t0001g0072others(74): Show | 77 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1608+656A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918603 | ||||||
| chr14:101918642
|
A | AC | 6 | a0001c0001t0001g0093a0001c0001t0007g0016a0001c0001t0007g0076others(3): Show | 6 | HG00733.hp2 HG01255.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608+701dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918642 | |||||
| chr14:101918642
|
A | ACC | 29 | a0001c0001t0003g0130a0001c0001t0010g0133a0002c0002t0001g0001others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1608+700_1608+701d others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101918642 | |||||
| chr14:101918648
|
C | G | 1 | a0001c0001t0017g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1608+701C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918648 | ||||||
| chr14:101918659
|
C | T | 31 | a0001c0001t0003g0130a0001c0001t0007g0016a0001c0001t0007g0076others(28): Show | 31 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1608+712C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918659 | ||||||
| chr14:101918704
|
C | T | 2 | a0001c0001t0005g0069a0001c0001t0005g0083 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1608+757C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918704 | ||||||
| chr14:101918722
|
G | A | 1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1608+775G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918722 | ||||||
| chr14:101918885
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1608+938G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101918885 | ||||||
| chr14:101919046
|
G | A | 22 | a0001c0001t0002g0094a0001c0001t0005g0069a0001c0001t0005g0083others(19): Show | 22 | HG00733.hp1 HG00733.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1608+1099G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919046 | ||||||
| chr14:101919101
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1608+1154G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919101 | ||||||
| chr14:101919120
|
C | T | 40 | a0001c0001t0002g0094a0001c0001t0003g0130a0001c0001t0005g0069others(37): Show | 40 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1608+1173C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919120 | ||||||
| chr14:101919199
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1608+1252G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919199 | ||||||
| chr14:101919432
|
T | G | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1608+1485T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919432 | ||||||
| chr14:101919601
|
T | C | 50 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(47): Show | 50 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1608+1654T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919601 | ||||||
| chr14:101919930
|
C | T | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1608+1983C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919930 | ||||||
| chr14:101919968
|
T | TC | 14 | a0001c0001t0003g0130a0002c0002t0001g0001a0002c0002t0001g0044others(11): Show | 14 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.1608+2022dupC | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919968 | |||||
| chr14:101919968
|
T | TCAAAAAA others(4): Show |
3 | a0001c0001t0006g0075a0001c0001t0006g0099a0001c0003t0013g0019 | 3 | HG02976.hp1 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1608+2022_1608+203 others(15): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919968 | |||||
| chr14:101919969
|
C | CA | 36 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1608+2045dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919969 | |||||
| chr14:101919969
|
C | CAA | 13 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0027others(10): Show | 13 | HG01243.hp2 HG01993.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1608+2044_1608+204 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919969 | |||||
| chr14:101919969
|
C | CAAA | 9 | a0001c0001t0002g0068a0001c0001t0002g0114a0001c0001t0012g0064others(6): Show | 9 | HG01255.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1608+2043_1608+204 others(7): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919969 | |||||
| chr14:101919969
|
C | CAAAA | 11 | a0001c0001t0002g0028a0001c0001t0002g0037a0001c0001t0002g0062others(8): Show | 11 | HG01884.hp2 HG02486.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1608+2042_1608+204 others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919969 | |||||
| chr14:101919969
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0066a0001c0001t0001g0082 | 2 | HG02055.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1608+2033_1608+204 others(17): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919969 | |||||
| chr14:101919969
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1608+2029_1608+204 others(21): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919969 | |||||
| chr14:101919969
|
C | CCA | 13 | a0002c0002t0001g0002a0002c0002t0001g0025a0002c0002t0001g0034others(10): Show | 13 | HG00642.hp1 HG02083.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1608+2022_1608+202 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919969 | ||||||
| chr14:101919969
|
C | CCAA | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | NA18995.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1608+2022_1608+202 others(7): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919969 | ||||||
| chr14:101919979
|
A | AAAAAAAA others(8): Show |
1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1608+2045_1608+204 others(19): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919979 | |||||
| chr14:101919980
|
A | AAAAAAAA others(9): Show |
1 | a0002c0002t0004g0023 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1608+2045_1608+204 others(20): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919980 | |||||
| chr14:101919980
|
A | AAAAAAAA others(8): Show |
3 | a0002c0002t0004g0024a0002c0002t0004g0108a0002c0002t0004g0119 | 3 | HG01256.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1608+2045_1608+204 others(19): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919980 | |||||
| chr14:101919980
|
A | AAAAAAAA others(7): Show |
2 | a0002c0002t0004g0073a0002c0002t0008g0011 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1608+2045_1608+204 others(18): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919980 | |||||
| chr14:101919980
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0009g0122 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1608+2044_1608+204 others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919980 | |||||
| chr14:101919980
|
A | AAAAACAA others(3): Show |
1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1608+2037_1608+203 others(14): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919980 | |||||
| chr14:101919980
|
A | C | 3 | a0001c0001t0006g0075a0001c0001t0006g0099a0001c0003t0013g0019 | 3 | HG02976.hp1 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1608+2033A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919980 | ||||||
| chr14:101919981
|
A | AAAAAAAA others(4): Show |
1 | a0001c0003t0005g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1608+2044_1608+204 others(15): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919981 | |||||
| chr14:101919981
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0005g0069a0001c0001t0005g0083 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1608+2043_1608+204 others(14): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101919981 | |||||
| chr14:101919993
|
C | A | 18 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(15): Show | 18 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1608+2046C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919993 | ||||||
| chr14:101919993
|
C | CAAAAAAA others(5): Show |
1 | a0001c0003t0005g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1608+2046_1608+204 others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919993 | ||||||
| chr14:101919993
|
C | CAAAAAAA others(6): Show |
26 | a0001c0001t0003g0130a0002c0002t0001g0001a0002c0002t0001g0002others(23): Show | 26 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.1608+2046_1608+204 others(17): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919993 | ||||||
| chr14:101919993
|
C | CAAAAAAA others(7): Show |
3 | a0002c0002t0001g0046a0002c0002t0001g0087a0002c0002t0003g0137 | 3 | HG00733.hp1 HG03688.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1608+2046_1608+204 others(18): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101919993 | ||||||
| chr14:101920152
|
T | C | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1608+2205T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920152 | ||||||
| chr14:101920229
|
G | C | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1608+2282G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920229 | ||||||
| chr14:101920301
|
G | T | 1 | a0001c0001t0006g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1608+2354G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920301 | ||||||
| chr14:101920305
|
C | T | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1608+2358C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920305 | ||||||
| chr14:101920320
|
G | A | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1608+2373G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920320 | ||||||
| chr14:101920357
|
A | G | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1608+2410A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920357 | ||||||
| chr14:101920522
|
T | C | 4 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(1): Show | 4 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+2575T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920522 | ||||||
| chr14:101920591
|
C | T | 7 | a0001c0001t0002g0068a0001c0001t0002g0095a0001c0001t0002g0114others(4): Show | 7 | HG02451.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1608+2644C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920591 | ||||||
| chr14:101920694
|
G | A | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1608+2747G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920694 | ||||||
| chr14:101920923
|
G | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0060 | 2 | HG02056.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1608+2976G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920923 | ||||||
| chr14:101920941
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1608+2994T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101920941 | ||||||
| chr14:101921035
|
T | G | 1 | a0001c0001t0001g0004 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1608+3088T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101921035 | ||||||
| chr14:101921054
|
C | CT | 5 | a0001c0001t0001g0032a0001c0001t0003g0131a0001c0001t0003g0135others(2): Show | 5 | HG02559.hp1 HG02559.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1608+3138dupT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101921054 | |||||
| chr14:101921054
|
CT | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0021others(43): Show | 46 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1608+3138delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101921054 | |||||
| chr14:101921054
|
CTT | C | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0002g0029others(2): Show | 5 | HG00558.hp2 HG01433.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1608+3137_1608+313 others(6): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101921054 | |||||
| chr14:101921054
|
CTTTTTTT | C | 7 | a0001c0001t0001g0072a0001c0001t0006g0075a0001c0001t0006g0099others(4): Show | 7 | HG01433.hp2 HG02976.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.1608+3132_1608+313 others(11): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101921054 | |||||
| chr14:101921054
|
CTTTTTTT others(1): Show |
C | 35 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0003g0130others(32): Show | 35 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1608+3131_1608+313 others(12): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101921054 | |||||
| chr14:101921054
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(1): Show | 4 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+3129_1608+313 others(14): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101921054 | |||||
| chr14:101921054
|
CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0002g0068a0001c0001t0002g0095a0001c0001t0002g0114others(4): Show | 7 | HG02451.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1608+3127_1608+313 others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101921054 | |||||
| chr14:101921262
|
A | C | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1608+3315A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101921262 | ||||||
| chr14:101921356
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1608+3409G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101921356 | ||||||
| chr14:101921529
|
T | TA | 6 | a0001c0001t0002g0068a0001c0001t0002g0095a0001c0001t0002g0114others(3): Show | 6 | HG02451.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608+3593dupA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101921529 | |||||
| chr14:101921562
|
C | T | 74 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(71): Show | 74 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1609-3579C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101921562 | ||||||
| chr14:101921803
|
A | G | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-3338A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101921803 | ||||||
| chr14:101921845
|
C | T | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-3296C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101921845 | ||||||
| chr14:101922138
|
T | G | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-3003T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922138 | ||||||
| chr14:101922304
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0049 | 2 | HG01934.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1609-2837C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922304 | ||||||
| chr14:101922421
|
G | A | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-2720G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922421 | ||||||
| chr14:101922480
|
CTCTGTGT others(23): Show |
C | 48 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(45): Show | 48 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1609-2659_1609-263 others(34): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101922480 | |||||
| chr14:101922481
|
TCTGTGTC others(29): Show |
T | 1 | a0001c0001t0003g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1609-2659_1609-262 others(40): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922481 | ||||||
| chr14:101922518
|
G | T | 1 | a0001c0001t0003g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1609-2623G>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922518 | ||||||
| chr14:101922540
|
A | C | 1 | a0001c0001t0011g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1609-2601A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922540 | ||||||
| chr14:101922600
|
A | G | 74 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(71): Show | 74 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1609-2541A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922600 | ||||||
| chr14:101922656
|
GA | G | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-2471delA | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101922656 | |||||
| chr14:101922748
|
T | G | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1609-2393T>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922748 | ||||||
| chr14:101922783
|
A | G | 7 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(4): Show | 7 | HG01433.hp2 HG02055.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609-2358A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922783 | ||||||
| chr14:101922824
|
A | T | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-2317A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922824 | ||||||
| chr14:101922833
|
A | T | 20 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(17): Show | 20 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1609-2308A>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922833 | ||||||
| chr14:101922903
|
G | C | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-2238G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922903 | ||||||
| chr14:101922950
|
A | C | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-2191A>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101922950 | ||||||
| chr14:101923106
|
G | C | 74 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(71): Show | 74 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1609-2035G>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101923106 | ||||||
| chr14:101923329
|
T | A | 1 | a0001c0001t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1609-1812T>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101923329 | ||||||
| chr14:101923434
|
C | T | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-1707C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101923434 | ||||||
| chr14:101923500
|
G | A | 1 | a0002c0002t0004g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1609-1641G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101923500 | ||||||
| chr14:101923615
|
G | A | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-1526G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101923615 | ||||||
| chr14:101923757
|
G | A | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-1384G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101923757 | ||||||
| chr14:101923780
|
T | C | 1 | a0001c0001t0012g0064 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1609-1361T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101923780 | ||||||
| chr14:101923805
|
ACTTTACA others(115): Show |
A | 22 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0037others(19): Show | 22 | HG01255.hp2 HG01258.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1609-1335_1609-121 others(4): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101923805 | ||||||
| chr14:101923826
|
C | T | 1 | a0002c0002t0001g0115 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1609-1315C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101923826 | ||||||
| chr14:101923940
|
AGACT | A | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-1196_1609-119 others(8): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101923940 | |||||
| chr14:101924131
|
G | A | 74 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(71): Show | 74 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1609-1010G>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101924131 | ||||||
| chr14:101924400
|
T | C | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-741T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101924400 | ||||||
| chr14:101924445
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG01074.hp2 HG01256.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-684_1609-683i others(15): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0088 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1609-684_1609-683i others(16): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0113 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1609-684_1609-683i others(17): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0027a0001c0001t0003g0006 | 2 | HG01243.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1609-684_1609-683i others(19): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1609-684_1609-683i others(20): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0007g0076a0001c0003t0020g0008 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1609-684_1609-683i others(23): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0060 | 2 | HG02056.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1609-684_1609-683i others(25): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0096 | 3 | HG01243.hp1 HG02132.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1609-684_1609-683i others(26): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1609-684_1609-683i others(27): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0026 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1609-684_1609-683i others(28): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(20): Show |
4 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0117others(1): Show | 4 | HG01934.hp1 HG02630.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-684_1609-683i others(29): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(21): Show |
2 | a0001c0001t0001g0123a0002c0002t0008g0010 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1609-684_1609-683i others(30): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(22): Show |
7 | a0001c0001t0002g0065a0001c0001t0002g0068a0001c0001t0002g0095others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609-684_1609-683i others(31): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(23): Show |
2 | a0001c0001t0002g0111a0001c0001t0012g0064 | 2 | HG01255.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1609-684_1609-683i others(32): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(24): Show |
7 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0080others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609-684_1609-683i others(33): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0017g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1609-684_1609-683i others(36): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(29): Show |
1 | a0001c0001t0002g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1609-684_1609-683i others(38): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(30): Show |
3 | a0001c0001t0002g0086a0001c0001t0002g0124a0001c0001t0006g0105 | 3 | HG01884.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1609-684_1609-683i others(39): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(31): Show |
6 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0078others(3): Show | 6 | HG00408.hp2 HG02083.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1609-684_1609-683i others(40): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(32): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0040others(5): Show | 8 | HG01433.hp1 HG02559.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1609-684_1609-683i others(41): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(33): Show |
3 | a0001c0001t0003g0007a0001c0001t0007g0016a0001c0001t0015g0042 | 3 | HG00642.hp2 HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1609-684_1609-683i others(42): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(34): Show |
1 | a0001c0001t0001g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1609-684_1609-683i others(43): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
C | CTTTTTTT others(36): Show |
1 | a0001c0001t0001g0118 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1609-684_1609-683i others(45): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924445
|
CT | C | 49 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1609-684delT | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 101924445 | |||||
| chr14:101924465
|
A | G | 1 | a0001c0003t0018g0089 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1609-676A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101924465 | ||||||
| chr14:101924604
|
A | G | 1 | a0003c0004t0004g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1609-537A>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101924604 | ||||||
| chr14:101924770
|
T | C | 37 | a0001c0001t0003g0130a0002c0002t0001g0001a0002c0002t0001g0002others(34): Show | 37 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1609-371T>C | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101924770 | ||||||
| chr14:101924844
|
C | T | 48 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(45): Show | 48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1609-297C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101924844 | ||||||
| chr14:101924875
|
C | A | 48 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0082others(45): Show | 48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1609-266C>A | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101924875 | ||||||
| chr14:101924940
|
C | T | 4 | a0001c0001t0005g0069a0001c0001t0005g0083a0001c0003t0005g0018others(1): Show | 4 | HG02109.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-201C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101924940 | ||||||
| chr14:101924998
|
C | G | 1 | a0002c0002t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1609-143C>G | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101924998 | ||||||
| chr14:101925102
|
C | T | 2 | a0002c0002t0004g0017a0003c0004t0004g0120 | 2 | HG00733.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1609-39C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101925102 | ||||||
| chr14:101925118
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1609-23C>T | PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | chr14 | 101925118 |