Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79867 |
|---|---|
| ensemblid | ENSG00000168778.13 |
| hgncid | 25774 |
| symbol | TCTN2 |
| name | tectonic family member 2 |
| refseq_nuc | NM_024809.5 |
| refseq_prot | NP_079085.2 |
| ensembl_nuc | ENST00000303372.7 |
| ensembl_prot | ENSP00000304941.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 123671113 |
| end | 123708399 |
| strand | + |
| ver | v1.2 |
| region | chr12:123671113-123708399 |
| region5000 | chr12:123666113-123713399 |
| regionname0 | TCTN2_chr12_123671113_123708399 |
| regionname5000 | TCTN2_chr12_123666113_123713399 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 697 | 232 | 89 | 45 | 46 | 18 | 32 | 22 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0002 | 0/0 | 697 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0003 | 0/0 | 697 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0004 | 0/0 | 697 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2094 | 116 | 61 | 17 | 15 | 6 | 17 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| c0002 | 1/1 | 2094 | 87 | 12 | 20 | 30 | 10 | 13 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| c0003 | 0/0 | 2094 | 17 | 16 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| c0004 | 0/0 | 2094 | 4 | 0 | 2 | 0 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| c0005 | 0/0 | 2094 | 3 | 0 | 3 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| c0006 | 0/0 | 2094 | 2 | 0 | 0 | 0 | 2 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| c0007 | 0/0 | 2094 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| c0008 | 0/0 | 2094 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| c0009 | 0/0 | 2094 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| c0010 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| c0011 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 815 | 95 | 24 | 19 | 29 | 10 | 11 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0002 | 0/0 | 819 | 35 | 5 | 12 | 6 | 6 | 6 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0003 | 0/0 | 819 | 26 | 9 | 2 | 7 | 1 | 7 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0004 | 0/0 | 819 | 14 | 13 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0005 | 0/0 | 819 | 9 | 4 | 3 | 0 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0006 | 0/0 | 818 | 8 | 7 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0007 | 0/0 | 819 | 6 | 6 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0008 | 0/0 | 818 | 6 | 6 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0009 | 0/0 | 820 | 5 | 2 | 3 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0010 | 0/0 | 820 | 5 | 1 | 1 | 1 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0011 | 0/0 | 816 | 5 | 1 | 1 | 2 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0012 | 0/0 | 820 | 5 | 5 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0013 | 0/0 | 820 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0014 | 0/0 | 820 | 2 | 0 | 0 | 0 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0015 | 0/0 | 819 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0016 | 0/0 | 820 | 2 | 0 | 1 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0017 | 0/0 | 819 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0018 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0019 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0020 | 0/0 | 814 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0021 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0022 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0023 | 0/0 | 815 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0024 | 0/0 | 820 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| t0025 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 23 | 10 | 1 | 5 | 4 | 3 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0002 | 0/0 | 10 | 2 | 3 | 1 | 0 | 4 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0004 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0005 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0006 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0007 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2094 | 116 | 61 | 17 | 15 | 6 | 17 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0002 | 1/1 | 2094 | 87 | 12 | 20 | 30 | 10 | 13 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0003 | 0/0 | 2094 | 17 | 16 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0004 | 0/0 | 2094 | 4 | 0 | 2 | 0 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0005 | 0/0 | 2094 | 3 | 0 | 3 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0006 | 0/0 | 2094 | 2 | 0 | 0 | 0 | 2 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0008 | 0/0 | 2094 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0010 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0002c0007 | 0/0 | 2094 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0003c0011 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0004c0009 | 0/0 | 2094 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2908 | 12 | 12 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0002 | 0/0 | 2912 | 33 | 5 | 12 | 6 | 4 | 6 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0003 | 0/0 | 2912 | 24 | 8 | 1 | 7 | 1 | 7 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0004 | 0/0 | 2912 | 14 | 13 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0006 | 0/0 | 2911 | 8 | 7 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0007 | 0/0 | 2912 | 6 | 6 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0008 | 0/0 | 2911 | 6 | 6 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0010 | 0/0 | 2913 | 5 | 1 | 1 | 1 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0011 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0014 | 0/0 | 2913 | 2 | 0 | 0 | 0 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0016 | 0/0 | 2913 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0017 | 0/0 | 2912 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0019 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0022 | 0/0 | 2912 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0001t0024 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0002t0001 | 1/1 | 2908 | 81 | 12 | 18 | 28 | 10 | 11 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0002t0011 | 0/0 | 2909 | 4 | 0 | 1 | 2 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0002t0020 | 0/0 | 2907 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0002t0023 | 0/0 | 2908 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0003t0005 | 0/0 | 2912 | 5 | 4 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0003t0009 | 0/0 | 2913 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0003t0012 | 0/0 | 2913 | 5 | 5 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0003t0013 | 0/0 | 2913 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0003t0015 | 0/0 | 2912 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0003t0025 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0004t0005 | 0/0 | 2912 | 4 | 0 | 2 | 0 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0005t0009 | 0/0 | 2913 | 3 | 0 | 3 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0006t0002 | 0/0 | 2912 | 2 | 0 | 0 | 0 | 2 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0008t0003 | 0/0 | 2912 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0008t0016 | 0/0 | 2913 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0001c0010t0001 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0002c0007t0018 | 0/0 | 2912 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0002c0007t0021 | 0/0 | 2912 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0003c0011t0003 | 0/0 | 2912 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| a0004c0009t0001 | 0/0 | 2908 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | copy fasta | chr12 | 123666113 | 123713399 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0002 | 0/0 | 9 | 2 | 3 | 1 | 0 | 3 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0008g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0010g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0010g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0010g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0011g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0014g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0016g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0017g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0019g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0022g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0001t0024g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0001 | 0/0 | 20 | 10 | 1 | 3 | 4 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0004 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0011g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0011g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0020g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0002t0023g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0005g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0009g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0013g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0013g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0003t0025g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0004t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0004t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0004t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0004t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0005t0009g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0005t0009g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0005t0009g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0006t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0006t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0008t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0008t0016g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0001c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0002c0007t0018g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0002c0007t0021g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0003c0011t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| a0004c0009t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0089 | EUR | GBR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0156 | EUR | GBR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0140 | EUR | GBR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | FIN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0107 | EUR | FIN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0131 | EUR | FIN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00408 | hp1 | a0001 | c0001 | t0016 | g0012 | EAS | CHS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CHS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | CHS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | CHS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01074 | hp2 | a0001 | c0001 | t0022 | g0082 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01099 | hp1 | a0001 | c0008 | t0016 | g0045 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01099 | hp2 | a0001 | c0003 | t0005 | g0022 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01109 | hp2 | a0001 | c0004 | t0005 | g0165 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01175 | hp1 | a0001 | c0008 | t0003 | g0046 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0136 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0127 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0120 | AMR | PUR | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01255 | hp1 | a0004 | c0009 | t0001 | g0063 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01256 | hp1 | a0001 | c0004 | t0005 | g0164 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01257 | hp1 | a0001 | c0002 | t0023 | g0096 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01346 | hp2 | a0001 | c0005 | t0009 | g0172 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0036 | EUR | IBS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01515 | hp2 | a0001 | c0006 | t0002 | g0149 | EUR | IBS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01516 | hp1 | a0001 | c0001 | t0017 | g0143 | EUR | IBS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0057 | EUR | IBS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01517 | hp1 | a0001 | c0006 | t0002 | g0150 | EUR | IBS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0124 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01975 | hp1 | a0001 | c0005 | t0009 | g0176 | AMR | PEL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01978 | hp1 | a0001 | c0002 | t0011 | g0074 | AMR | PEL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01978 | hp2 | a0001 | c0005 | t0009 | g0171 | AMR | PEL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PEL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02027 | hp1 | a0001 | c0002 | t0011 | g0073 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02145 | hp2 | a0001 | c0003 | t0005 | g0167 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | CDX | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | CDX | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0132 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | KHV | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02572 | hp1 | a0001 | c0003 | t0012 | g0174 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0122 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0125 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02630 | hp2 | a0001 | c0003 | t0009 | g0008 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02647 | hp1 | a0001 | c0003 | t0012 | g0161 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02647 | hp2 | a0001 | c0003 | t0015 | g0173 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02698 | hp1 | a0001 | c0001 | t0010 | g0007 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0086 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02735 | hp1 | a0001 | c0002 | t0020 | g0001 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02809 | hp2 | a0001 | c0003 | t0012 | g0170 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02818 | hp1 | a0001 | c0003 | t0012 | g0169 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02886 | hp1 | a0001 | c0003 | t0009 | g0008 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02895 | hp2 | a0001 | c0003 | t0025 | g0166 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02896 | hp1 | a0003 | c0011 | t0003 | g0094 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0135 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02970 | hp1 | a0001 | c0003 | t0013 | g0178 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0133 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03098 | hp2 | a0001 | c0003 | t0015 | g0008 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0134 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0126 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03453 | hp1 | a0001 | c0003 | t0013 | g0177 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03486 | hp2 | a0001 | c0001 | t0019 | g0159 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0090 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03540 | hp1 | a0001 | c0001 | t0024 | g0121 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03688 | hp1 | a0001 | c0001 | t0010 | g0007 | SAS | STU | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | STU | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03831 | hp1 | a0001 | c0001 | t0014 | g0006 | SAS | BEB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0067 | SAS | BEB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03927 | hp2 | a0001 | c0002 | t0011 | g0047 | SAS | BEB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03942 | hp1 | a0001 | c0001 | t0014 | g0002 | SAS | BEB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03942 | hp2 | a0001 | c0004 | t0005 | g0163 | SAS | BEB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | BEB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0050 | SAS | BEB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG04199 | hp1 | a0001 | c0004 | t0005 | g0162 | SAS | STU | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | STU | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | STU | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | STU | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | STU | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | YRI | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0116 | AFR | YRI | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CHB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | CHB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | CHB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | CHB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | YRI | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18906 | hp2 | a0001 | c0003 | t0005 | g0022 | AFR | YRI | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18953 | hp1 | a0001 | c0010 | t0001 | g0001 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18977 | hp2 | a0001 | c0002 | t0011 | g0001 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0100 | AFR | LWK | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0118 | AFR | LWK | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19043 | hp2 | a0001 | c0003 | t0005 | g0175 | AFR | LWK | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19086 | hp1 | a0001 | c0001 | t0010 | g0154 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19240 | hp1 | a0001 | c0003 | t0005 | g0160 | AFR | YRI | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA19240 | hp2 | a0001 | c0003 | t0012 | g0168 | AFR | YRI | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ASW | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ASW | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0060 | EUR | TSI | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0147 | EUR | TSI | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0083 | EUR | TSI | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | GIH | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | GIH | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02559 | hp1 | a0002 | c0007 | t0021 | g0026 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | MSL | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| HG06807 | hp2 | a0002 | c0007 | t0018 | g0027 | AFR | USA | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | USA | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | USA | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | LWK | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | LWK | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0084 | REF | REF | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0066 | REF | REF | TCTN2_chr12_123666113_123713399 | TCTN2 | chr12 | 123666113 | 123713399 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123672131
|
C | A | 1 | a0004 | 1 | HG01255.hp1 | missense_variant&splice_region_variant | MODERATE | c.266C>A | p.Ala89Glu | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/18 | 394/2908 | 266/2094 | 89/697 | chr12 | 123672131 | ||
| chr12:123690620
|
T | C | 1 | a0003 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.979T>C | p.Tyr327His | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/18 | 1107/2908 | 979/2094 | 327/697 | chr12 | 123690620 | ||
| chr12:123699783
|
C | G | 1 | a0002 | 2 | HG02559.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.1585C>G | p.Leu529Val | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/18 | 1713/2908 | 1585/2094 | 529/697 | chr12 | 123699783 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123672090
|
C | T | 3 | a0001c0003a0001c0004a0001c0005 | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
synonymous_variant | LOW | c.225C>T | p.Asn75Asn | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/18 | 353/2908 | 225/2094 | 75/697 | chr12 | 123672090 | ||
| chr12:123686925
|
C | T | 1 | a0001c0005 | 3 | HG01346.hp2 HG01975.hp1 HG01978.hp2 |
synonymous_variant | LOW | c.654C>T | p.Leu218Leu | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/18 | 782/2908 | 654/2094 | 218/697 | chr12 | 123686925 | ||
| chr12:123688096
|
C | T | 1 | a0001c0008 | 2 | HG01099.hp1 HG01175.hp1 |
synonymous_variant | LOW | c.810C>T | p.Asp270Asp | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/18 | 938/2908 | 810/2094 | 270/697 | chr12 | 123688096 | ||
| chr12:123688159
|
A | G | 3 | a0001c0003a0001c0004a0001c0005 | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
synonymous_variant | LOW | c.873A>G | p.Ala291Ala | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/18 | 1001/2908 | 873/2094 | 291/697 | chr12 | 123688159 | ||
| chr12:123688174
|
G | A | 1 | a0001c0010 | 1 | NA18953.hp1 | synonymous_variant | LOW | c.888G>A | p.Pro296Pro | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/18 | 1016/2908 | 888/2094 | 296/697 | chr12 | 123688174 | ||
| chr12:123690539
|
C | T | 1 | a0001c0004 | 4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
synonymous_variant | LOW | c.898C>T | p.Leu300Leu | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/18 | 1026/2908 | 898/2094 | 300/697 | chr12 | 123690539 | ||
| chr12:123694870
|
T | C | 8 | a0001c0001a0001c0003a0001c0004others(5): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
synonymous_variant | LOW | c.1128T>C | p.Pro376Pro | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 10/18 | 1256/2908 | 1128/2094 | 376/697 | chr12 | 123694870 | ||
| chr12:123706783
|
C | T | 1 | a0001c0006 | 2 | HG01515.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.1827C>T | p.Asp609Asp | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 16/18 | 1955/2908 | 1827/2094 | 609/697 | chr12 | 123706783 | ||
| chr12:123707660
|
T | C | 1 | a0001c0004 | 4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
synonymous_variant | LOW | c.2041T>C | p.Leu681Leu | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 2169/2908 | 2041/2094 | 681/697 | chr12 | 123707660 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123671146
|
G | A | 1 | a0001c0001t0007 | 6 | HG02257.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-95G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 1/18 | 95 | chr12 | 123671146 | |||||
| chr12:123671161
|
G | A | 1 | a0001c0003t0013 | 2 | HG02970.hp1 HG03453.hp1 |
5_prime_UTR_variant | MODIFIER | c.-80G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 1/18 | 80 | chr12 | 123671161 | |||||
| chr12:123671186
|
C | A | 2 | a0001c0001t0014a0001c0001t0017 | 3 | HG01516.hp1 HG03831.hp1 HG03942.hp1 |
5_prime_UTR_variant | MODIFIER | c.-55C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 1/18 | 55 | chr12 | 123671186 | |||||
| chr12:123671239
|
G | A | 1 | a0002c0007t0018 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 1/18 | 2 | chr12 | 123671239 | |||||
| chr12:123707758
|
G | A | 3 | a0001c0003t0009a0001c0003t0015a0001c0005t0009 | 7 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*45G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 45 | chr12 | 123707758 | |||||
| chr12:123707780
|
C | T | 1 | a0001c0003t0013 | 2 | HG02970.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*67C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 67 | chr12 | 123707780 | |||||
| chr12:123707800
|
C | T | 8 | a0001c0003t0005a0001c0003t0009a0001c0003t0012others(5): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*87C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 87 | chr12 | 123707800 | |||||
| chr12:123707868
|
G | A | 7 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(4): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*155G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 155 | chr12 | 123707868 | |||||
| chr12:123708007
|
C | CT | 11 | a0001c0001t0010a0001c0001t0011a0001c0001t0014others(8): Show | 27 | HG00408.hp1 HG01099.hp1 HG01175.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*317dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 318 | INFO_REALIGN_3_PRIME | chr12 | 123708007 | ||||
| chr12:123708007
|
CT | C | 5 | a0001c0001t0006a0001c0001t0008a0001c0001t0019others(2): Show | 17 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*317delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 317 | INFO_REALIGN_3_PRIME | chr12 | 123708007 | ||||
| chr12:123708040
|
T | TCTCA | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(24): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*330_*331insACTC | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 331 | INFO_REALIGN_3_PRIME | chr12 | 123708040 | ||||
| chr12:123708115
|
C | T | 1 | a0001c0001t0022 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 402 | chr12 | 123708115 | |||||
| chr12:123708125
|
T | C | 8 | a0001c0003t0005a0001c0003t0009a0001c0003t0012others(5): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*412T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 412 | chr12 | 123708125 | |||||
| chr12:123708155
|
A | G | 2 | a0002c0007t0018a0002c0007t0021 | 2 | HG02559.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*442A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 442 | chr12 | 123708155 | |||||
| chr12:123708181
|
C | T | 10 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(7): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*468C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 468 | chr12 | 123708181 | |||||
| chr12:123708258
|
G | T | 1 | a0001c0002t0023 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*545G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 545 | chr12 | 123708258 | |||||
| chr12:123708288
|
C | T | 1 | a0001c0001t0019 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 18/18 | 575 | chr12 | 123708288 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123671503
|
C | T | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.83-4C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 1/17 | chr12 | 123671503 | ||||||
| chr12:123671631
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190+17T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 2/17 | chr12 | 123671631 | ||||||
| chr12:123671705
|
CT | C | 3 | a0001c0002t0001g0009a0001c0002t0001g0024a0001c0002t0001g0025 | 4 | HG01256.hp2 HG02015.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+92delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 2/17 | chr12 | 123671705 | ||||||
| chr12:123671940
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.191-116C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 2/17 | chr12 | 123671940 | ||||||
| chr12:123672215
|
G | A | 23 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0004g0110others(20): Show | 23 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.267+83G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672215 | ||||||
| chr12:123672262
|
T | A | 1 | a0001c0001t0002g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.267+130T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672262 | ||||||
| chr12:123672291
|
G | A | 20 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(17): Show | 22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.267+159G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672291 | ||||||
| chr12:123672350
|
A | G | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.267+218A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672350 | ||||||
| chr12:123672367
|
G | A | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.267+235G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672367 | ||||||
| chr12:123672458
|
A | G | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.267+326A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672458 | ||||||
| chr12:123672505
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.267+373G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672505 | ||||||
| chr12:123672506
|
C | T | 3 | a0001c0001t0004g0128a0001c0001t0004g0129a0001c0001t0004g0130 | 3 | HG02451.hp2 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.267+374C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672506 | ||||||
| chr12:123672544
|
T | C | 9 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(6): Show | 10 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.267+412T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672544 | ||||||
| chr12:123672641
|
T | G | 91 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(88): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.267+509T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672641 | ||||||
| chr12:123672700
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.267+568G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672700 | ||||||
| chr12:123672751
|
A | G | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+619A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672751 | ||||||
| chr12:123672788
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.267+656C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672788 | ||||||
| chr12:123672789
|
G | T | 1 | a0001c0002t0001g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.267+657G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672789 | ||||||
| chr12:123672826
|
G | A | 17 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0004g0110others(14): Show | 17 | HG01243.hp2 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.267+694G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123672826 | ||||||
| chr12:123673127
|
A | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.268-488A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123673127 | ||||||
| chr12:123673198
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.268-417A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123673198 | ||||||
| chr12:123673241
|
A | G | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.268-374A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123673241 | ||||||
| chr12:123673348
|
A | C | 1 | a0001c0001t0003g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.268-267A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123673348 | ||||||
| chr12:123673394
|
C | T | 1 | a0001c0005t0009g0176 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.268-221C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123673394 | ||||||
| chr12:123673495
|
A | G | 2 | a0001c0003t0005g0167a0001c0003t0025g0166 | 2 | HG02145.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.268-120A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123673495 | ||||||
| chr12:123673529
|
G | A | 21 | a0001c0001t0004g0108a0001c0003t0005g0022a0001c0003t0005g0160others(18): Show | 23 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.268-86G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123673529 | ||||||
| chr12:123673533
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.268-82A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 3/17 | chr12 | 123673533 | ||||||
| chr12:123673903
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.463+93T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123673903 | ||||||
| chr12:123673908
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.463+98T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123673908 | ||||||
| chr12:123673955
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.463+145G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123673955 | ||||||
| chr12:123674260
|
A | T | 1 | a0001c0001t0003g0105 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.463+450A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674260 | ||||||
| chr12:123674280
|
T | TC | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.463+470_463+471ins others(1): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674280 | ||||||
| chr12:123674378
|
C | G | 1 | a0001c0001t0002g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.463+568C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674378 | ||||||
| chr12:123674395
|
C | G | 1 | a0001c0001t0006g0127 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.463+585C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674395 | ||||||
| chr12:123674424
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.463+614C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674424 | ||||||
| chr12:123674500
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.463+690C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674500 | ||||||
| chr12:123674603
|
A | C | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.463+793A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674603 | ||||||
| chr12:123674607
|
A | C | 1 | a0001c0002t0001g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.463+797A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674607 | ||||||
| chr12:123674638
|
A | C | 91 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(88): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.463+828A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674638 | ||||||
| chr12:123674665
|
G | A | 2 | a0001c0003t0005g0022a0001c0003t0005g0160 | 3 | HG01099.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.463+855G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674665 | ||||||
| chr12:123674753
|
T | C | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG00733.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.463+943T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674753 | ||||||
| chr12:123674864
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.463+1054A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674864 | ||||||
| chr12:123674937
|
G | T | 20 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(17): Show | 22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.463+1127G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674937 | ||||||
| chr12:123674999
|
T | C | 1 | a0001c0002t0001g0034 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.463+1189T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123674999 | ||||||
| chr12:123675219
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.463+1409G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123675219 | ||||||
| chr12:123675320
|
C | T | 1 | a0001c0001t0006g0127 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.463+1510C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123675320 | ||||||
| chr12:123675335
|
T | C | 1 | a0001c0002t0001g0035 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.463+1525T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123675335 | ||||||
| chr12:123675338
|
A | T | 91 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(88): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.463+1528A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123675338 | ||||||
| chr12:123675372
|
G | A | 5 | a0001c0001t0007g0020a0001c0001t0007g0132a0001c0001t0007g0133others(2): Show | 6 | HG02257.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+1562G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123675372 | ||||||
| chr12:123675378
|
G | A | 1 | a0001c0002t0001g0036 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.463+1568G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123675378 | ||||||
| chr12:123675408
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.463+1598C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123675408 | ||||||
| chr12:123675474
|
C | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.463+1664C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123675474 | ||||||
| chr12:123675598
|
A | T | 1 | a0001c0001t0019g0159 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.463+1788A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123675598 | ||||||
| chr12:123675693
|
T | C | 1 | a0001c0002t0001g0037 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.463+1883T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123675693 | ||||||
| chr12:123676217
|
C | T | 91 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(88): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.463+2407C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676217 | ||||||
| chr12:123676251
|
C | T | 5 | a0001c0001t0007g0020a0001c0001t0007g0132a0001c0001t0007g0133others(2): Show | 6 | HG02257.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+2441C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676251 | ||||||
| chr12:123676287
|
G | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.463+2477G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676287 | ||||||
| chr12:123676374
|
C | G | 2 | a0001c0002t0001g0101a0001c0002t0001g0102 | 2 | HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.463+2564C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676374 | ||||||
| chr12:123676384
|
C | T | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | HG01169.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.463+2574C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676384 | ||||||
| chr12:123676395
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.463+2585C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676395 | ||||||
| chr12:123676429
|
A | G | 1 | a0001c0002t0023g0096 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.463+2619A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676429 | ||||||
| chr12:123676436
|
C | T | 1 | a0001c0003t0005g0160 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.463+2626C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676436 | ||||||
| chr12:123676485
|
G | A | 1 | a0001c0001t0003g0011 | 2 | HG00280.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.463+2675G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676485 | ||||||
| chr12:123676509
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.464-2680A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676509 | ||||||
| chr12:123676550
|
A | T | 4 | a0001c0001t0003g0093a0001c0001t0003g0095a0001c0001t0003g0105others(1): Show | 4 | HG01891.hp1 HG02896.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-2639A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676550 | ||||||
| chr12:123676563
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.464-2626A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676563 | ||||||
| chr12:123676566
|
T | TA | 40 | a0001c0001t0001g0097a0001c0001t0002g0002a0001c0001t0002g0007others(37): Show | 54 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.464-2598dupA | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 123676566 | |||||
| chr12:123676566
|
T | TAA | 29 | a0001c0001t0002g0006a0001c0001t0002g0137a0001c0001t0002g0138others(26): Show | 29 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.464-2599_464-2598d others(4): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 123676566 | |||||
| chr12:123676566
|
T | TAAA | 17 | a0001c0001t0004g0128a0001c0001t0004g0129a0001c0001t0004g0130others(14): Show | 18 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.464-2600_464-2598d others(5): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 123676566 | |||||
| chr12:123676566
|
TAAAAAAA others(1): Show |
T | 7 | a0001c0001t0004g0108a0001c0001t0004g0117a0001c0001t0004g0119others(4): Show | 7 | HG01243.hp2 HG02818.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-2605_464-2598d others(10): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 123676566 | |||||
| chr12:123676742
|
A | T | 3 | a0001c0001t0004g0128a0001c0001t0004g0129a0001c0001t0004g0130 | 3 | HG02451.hp2 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.464-2447A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676742 | ||||||
| chr12:123676897
|
G | T | 2 | a0001c0003t0005g0167a0001c0003t0025g0166 | 2 | HG02145.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.464-2292G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676897 | ||||||
| chr12:123676947
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.464-2242A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123676947 | ||||||
| chr12:123677031
|
A | G | 2 | a0001c0002t0001g0037a0001c0002t0001g0092 | 2 | NA18612.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.464-2158A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677031 | ||||||
| chr12:123677033
|
C | G | 1 | a0001c0001t0002g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.464-2156C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677033 | ||||||
| chr12:123677039
|
A | G | 1 | a0001c0003t0005g0160 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.464-2150A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677039 | ||||||
| chr12:123677051
|
A | G | 1 | a0001c0001t0003g0091 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.464-2138A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677051 | ||||||
| chr12:123677105
|
G | A | 2 | a0001c0001t0004g0109a0001c0001t0004g0115 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.464-2084G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677105 | ||||||
| chr12:123677198
|
G | A | 1 | a0001c0001t0019g0159 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.464-1991G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677198 | ||||||
| chr12:123677500
|
G | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.464-1689G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677500 | ||||||
| chr12:123677635
|
A | G | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.464-1554A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677635 | ||||||
| chr12:123677797
|
T | C | 37 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(34): Show | 48 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.464-1392T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677797 | ||||||
| chr12:123677930
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.464-1259A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677930 | ||||||
| chr12:123677945
|
T | TA | 4 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0006g0116others(1): Show | 4 | HG02818.hp2 NA18522.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-1243dupA | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 123677945 | |||||
| chr12:123677980
|
T | C | 4 | a0001c0003t0012g0168a0001c0003t0012g0169a0001c0003t0012g0170others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-1209T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123677980 | ||||||
| chr12:123678081
|
C | T | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.464-1108C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678081 | ||||||
| chr12:123678142
|
T | C | 2 | a0001c0008t0003g0046a0001c0008t0016g0045 | 2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.464-1047T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678142 | ||||||
| chr12:123678158
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.464-1031C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678158 | ||||||
| chr12:123678172
|
G | A | 6 | a0001c0001t0003g0012a0001c0001t0003g0048a0001c0001t0003g0049others(3): Show | 6 | HG00408.hp1 HG02523.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.464-1017G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678172 | ||||||
| chr12:123678183
|
A | G | 2 | a0002c0007t0018g0027a0002c0007t0021g0026 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.464-1006A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678183 | ||||||
| chr12:123678203
|
G | A | 86 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(83): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.464-986G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678203 | ||||||
| chr12:123678222
|
A | G | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.464-967A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678222 | ||||||
| chr12:123678230
|
C | A | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.464-959C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678230 | ||||||
| chr12:123678362
|
T | A | 2 | a0001c0002t0001g0013a0001c0002t0001g0051 | 3 | HG02083.hp2 HG02132.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.464-827T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678362 | ||||||
| chr12:123678380
|
T | C | 2 | a0002c0007t0018g0027a0002c0007t0021g0026 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.464-809T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678380 | ||||||
| chr12:123678413
|
T | C | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.464-776T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678413 | ||||||
| chr12:123678480
|
G | A | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.464-709G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678480 | ||||||
| chr12:123678582
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.464-607C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678582 | ||||||
| chr12:123678642
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.464-547C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678642 | ||||||
| chr12:123678653
|
A | G | 4 | a0001c0004t0005g0162a0001c0004t0005g0163a0001c0004t0005g0164others(1): Show | 4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-536A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678653 | ||||||
| chr12:123678859
|
A | C | 1 | a0001c0002t0001g0090 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.464-330A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678859 | ||||||
| chr12:123678872
|
A | C | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.464-317A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678872 | ||||||
| chr12:123678890
|
C | T | 1 | a0002c0007t0018g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.464-299C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678890 | ||||||
| chr12:123678965
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.464-224C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123678965 | ||||||
| chr12:123679076
|
C | T | 1 | a0001c0002t0001g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.464-113C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123679076 | ||||||
| chr12:123679077
|
G | A | 1 | a0001c0003t0013g0177 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.464-112G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 4/17 | chr12 | 123679077 | ||||||
| chr12:123679435
|
C | T | 2 | a0001c0001t0007g0132a0001c0001t0007g0135 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.564+146C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123679435 | ||||||
| chr12:123679456
|
G | A | 3 | a0001c0005t0009g0171a0001c0005t0009g0172a0001c0005t0009g0176 | 3 | HG01346.hp2 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.564+167G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123679456 | ||||||
| chr12:123679736
|
G | GT | 42 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(39): Show | 53 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.564+468dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123679736 | |||||
| chr12:123679778
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.564+489C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123679778 | ||||||
| chr12:123679808
|
T | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(36): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.564+519T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123679808 | ||||||
| chr12:123679833
|
G | A | 10 | a0001c0003t0009g0008a0001c0003t0012g0168a0001c0003t0012g0169others(7): Show | 11 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.564+544G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123679833 | ||||||
| chr12:123679840
|
T | C | 1 | a0001c0002t0001g0052 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.564+551T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123679840 | ||||||
| chr12:123679960
|
T | C | 6 | a0001c0001t0004g0108a0001c0001t0004g0117a0001c0001t0004g0119others(3): Show | 6 | HG01243.hp2 HG02818.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+671T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123679960 | ||||||
| chr12:123679975
|
G | A | 6 | a0001c0001t0004g0108a0001c0001t0004g0117a0001c0001t0004g0119others(3): Show | 6 | HG01243.hp2 HG02818.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+686G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123679975 | ||||||
| chr12:123680010
|
A | C | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.564+721A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680010 | ||||||
| chr12:123680028
|
C | T | 20 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(17): Show | 22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.564+739C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680028 | ||||||
| chr12:123680029
|
G | A | 6 | a0001c0001t0004g0108a0001c0001t0004g0117a0001c0001t0004g0119others(3): Show | 6 | HG01243.hp2 HG02818.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+740G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680029 | ||||||
| chr12:123680030
|
C | T | 1 | a0001c0001t0004g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.564+741C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680030 | ||||||
| chr12:123680114
|
T | A | 3 | a0001c0002t0001g0014a0001c0002t0001g0053a0001c0002t0001g0107 | 4 | HG00323.hp1 HG00738.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.564+825T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680114 | ||||||
| chr12:123680144
|
G | A | 1 | a0001c0001t0003g0011 | 2 | HG00280.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.564+855G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680144 | ||||||
| chr12:123680203
|
T | C | 2 | a0001c0001t0007g0133a0001c0001t0007g0134 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.564+914T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680203 | ||||||
| chr12:123680348
|
G | A | 23 | a0001c0002t0001g0037a0001c0003t0005g0022a0001c0003t0005g0160others(20): Show | 25 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.564+1059G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680348 | ||||||
| chr12:123680352
|
C | CA | 29 | a0001c0001t0001g0098a0001c0001t0004g0108a0001c0001t0004g0109others(26): Show | 30 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.564+1079dupA | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123680352 | |||||
| chr12:123680352
|
C | CAA | 38 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(35): Show | 49 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.564+1078_564+1079d others(4): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123680352 | |||||
| chr12:123680388
|
AT | A | 6 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+1111delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123680388 | |||||
| chr12:123680406
|
G | A | 3 | a0001c0001t0004g0128a0001c0001t0004g0129a0001c0001t0004g0130 | 3 | HG02451.hp2 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.564+1117G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680406 | ||||||
| chr12:123680481
|
A | AG | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.564+1192_564+1193i others(3): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680481 | ||||||
| chr12:123680509
|
C | G | 1 | a0001c0001t0003g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.564+1220C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680509 | ||||||
| chr12:123680509
|
C | T | 86 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(83): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.564+1220C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680509 | ||||||
| chr12:123680512
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.564+1223T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680512 | ||||||
| chr12:123680520
|
CT | C | 20 | a0001c0001t0017g0143a0001c0003t0005g0022a0001c0003t0005g0160others(17): Show | 22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.564+1245delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123680520 | |||||
| chr12:123680532
|
T | C | 19 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(16): Show | 21 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.564+1243T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680532 | ||||||
| chr12:123680564
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.564+1275T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680564 | ||||||
| chr12:123680666
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.564+1377G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680666 | ||||||
| chr12:123680705
|
C | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 5 | HG01884.hp2 HG02145.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+1416C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680705 | ||||||
| chr12:123680989
|
C | A | 2 | a0001c0001t0003g0054a0001c0001t0003g0086 | 2 | HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.564+1700C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680989 | ||||||
| chr12:123680994
|
C | T | 6 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+1705C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123680994 | ||||||
| chr12:123681037
|
T | C | 1 | a0001c0001t0001g0015 | 2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.564+1748T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681037 | ||||||
| chr12:123681130
|
C | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.564+1841C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681130 | ||||||
| chr12:123681256
|
C | CAAAAAAA others(1): Show |
5 | a0001c0001t0002g0155a0001c0004t0005g0162a0001c0004t0005g0163others(2): Show | 5 | HG01109.hp2 HG01256.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+1969_564+1976d others(10): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123681256 | |||||
| chr12:123681256
|
C | CAAAAAAA others(2): Show |
72 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(69): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.564+1968_564+1976d others(11): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123681256 | |||||
| chr12:123681256
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.564+1976_564+1977i others(12): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123681256 | |||||
| chr12:123681282
|
T | A | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.564+1993T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681282 | ||||||
| chr12:123681405
|
C | T | 1 | a0001c0001t0010g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.564+2116C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681405 | ||||||
| chr12:123681494
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.564+2205T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681494 | ||||||
| chr12:123681729
|
A | T | 1 | a0001c0002t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.564+2440A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681729 | ||||||
| chr12:123681730
|
T | C | 1 | a0001c0002t0001g0034 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.564+2441T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681730 | ||||||
| chr12:123681851
|
C | G | 1 | a0001c0001t0024g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.564+2562C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681851 | ||||||
| chr12:123681864
|
G | T | 86 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(83): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.564+2575G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681864 | ||||||
| chr12:123681872
|
T | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 5 | HG01884.hp2 HG02145.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+2583T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681872 | ||||||
| chr12:123681953
|
T | C | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.564+2664T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123681953 | ||||||
| chr12:123682107
|
A | C | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.564+2818A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682107 | ||||||
| chr12:123682197
|
C | T | 1 | a0001c0002t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.564+2908C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682197 | ||||||
| chr12:123682211
|
A | G | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.564+2922A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682211 | ||||||
| chr12:123682390
|
G | A | 90 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 104 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.564+3101G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682390 | ||||||
| chr12:123682407
|
G | A | 6 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+3118G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682407 | ||||||
| chr12:123682431
|
G | T | 39 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(36): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.564+3142G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682431 | ||||||
| chr12:123682459
|
C | CT | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.564+3178dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123682459 | |||||
| chr12:123682474
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.564+3185T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682474 | ||||||
| chr12:123682512
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.564+3223G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682512 | ||||||
| chr12:123682538
|
A | T | 1 | a0001c0002t0001g0025 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.564+3249A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682538 | ||||||
| chr12:123682628
|
C | T | 37 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(34): Show | 48 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.564+3339C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682628 | ||||||
| chr12:123682638
|
C | A | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.564+3349C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682638 | ||||||
| chr12:123682724
|
C | T | 7 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.564+3435C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682724 | ||||||
| chr12:123682823
|
A | G | 1 | a0001c0001t0002g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.564+3534A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682823 | ||||||
| chr12:123682889
|
ATATT | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.564+3602_564+3605d others(6): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123682889 | |||||
| chr12:123682902
|
C | T | 3 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0012g0161 | 4 | HG01099.hp2 HG02647.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+3613C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682902 | ||||||
| chr12:123682989
|
C | T | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.564+3700C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123682989 | ||||||
| chr12:123683061
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.564+3772T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123683061 | ||||||
| chr12:123683117
|
G | A | 17 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0004g0110others(14): Show | 17 | HG01243.hp2 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.565-3719G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123683117 | ||||||
| chr12:123683304
|
A | G | 2 | a0001c0001t0007g0133a0001c0001t0007g0134 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.565-3532A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123683304 | ||||||
| chr12:123683409
|
C | T | 86 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(83): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.565-3427C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123683409 | ||||||
| chr12:123683523
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.565-3313T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123683523 | ||||||
| chr12:123683783
|
C | T | 2 | a0001c0002t0001g0037a0001c0002t0001g0092 | 2 | NA18612.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.565-3053C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123683783 | ||||||
| chr12:123683875
|
G | A | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.565-2961G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123683875 | ||||||
| chr12:123683895
|
T | C | 1 | a0001c0001t0001g0015 | 2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565-2941T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123683895 | ||||||
| chr12:123683996
|
A | C | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.565-2840A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123683996 | ||||||
| chr12:123684151
|
A | G | 2 | a0002c0007t0018g0027a0002c0007t0021g0026 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.565-2685A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123684151 | ||||||
| chr12:123684260
|
G | GTTGTT | 2 | a0001c0002t0001g0037a0001c0002t0001g0092 | 2 | NA18612.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.565-2564_565-2560d others(7): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123684260 | |||||
| chr12:123684309
|
T | C | 4 | a0001c0001t0003g0093a0001c0001t0003g0095a0001c0001t0003g0105others(1): Show | 4 | HG01891.hp1 HG02896.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-2527T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123684309 | ||||||
| chr12:123684399
|
C | CT | 12 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0004g0108others(9): Show | 12 | HG01243.hp2 HG02145.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.565-2418dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123684399 | |||||
| chr12:123684399
|
CT | C | 12 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0146others(9): Show | 12 | HG01169.hp1 HG01256.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.565-2418delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123684399 | |||||
| chr12:123684463
|
C | T | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.565-2373C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123684463 | ||||||
| chr12:123684545
|
C | T | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.565-2291C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123684545 | ||||||
| chr12:123684546
|
A | G | 115 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(112): Show | 135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.565-2290A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123684546 | ||||||
| chr12:123684693
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.565-2143C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123684693 | ||||||
| chr12:123684695
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.565-2141T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123684695 | ||||||
| chr12:123684773
|
C | T | 1 | a0001c0001t0004g0130 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.565-2063C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123684773 | ||||||
| chr12:123684826
|
T | G | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.565-2010T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123684826 | ||||||
| chr12:123684914
|
T | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.565-1922T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123684914 | ||||||
| chr12:123685049
|
C | CA | 6 | a0001c0001t0003g0012a0001c0001t0003g0048a0001c0001t0003g0049others(3): Show | 6 | HG00408.hp1 HG02523.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.565-1771dupA | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123685049 | |||||
| chr12:123685084
|
A | C | 5 | a0001c0001t0004g0110a0001c0001t0004g0111a0001c0001t0004g0112others(2): Show | 5 | HG02486.hp1 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-1752A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123685084 | ||||||
| chr12:123685159
|
C | G | 1 | a0001c0001t0002g0153 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.565-1677C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123685159 | ||||||
| chr12:123685210
|
C | T | 1 | a0001c0002t0001g0056 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.565-1626C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123685210 | ||||||
| chr12:123685283
|
T | C | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.565-1553T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123685283 | ||||||
| chr12:123685341
|
A | C | 2 | a0002c0007t0018g0027a0002c0007t0021g0026 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.565-1495A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123685341 | ||||||
| chr12:123685460
|
C | T | 5 | a0001c0001t0004g0110a0001c0001t0004g0111a0001c0001t0004g0112others(2): Show | 5 | HG02486.hp1 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-1376C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123685460 | ||||||
| chr12:123685662
|
G | A | 1 | a0001c0002t0001g0024 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.565-1174G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123685662 | ||||||
| chr12:123685718
|
CTT | C | 64 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(61): Show | 75 | HG00323.hp2 HG00621.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.565-1096_565-1095d others(4): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123685718 | |||||
| chr12:123685718
|
CTTT | C | 45 | a0001c0001t0002g0140a0001c0001t0002g0147a0001c0001t0002g0156others(42): Show | 54 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.565-1097_565-1095d others(5): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123685718 | |||||
| chr12:123685718
|
CTTTT | C | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0008g0029others(2): Show | 5 | HG02559.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.565-1098_565-1095d others(6): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123685718 | |||||
| chr12:123685746
|
A | G | 114 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(111): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.565-1090A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123685746 | ||||||
| chr12:123685890
|
A | AT | 15 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(12): Show | 17 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.565-931dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123685890 | |||||
| chr12:123685890
|
AT | A | 9 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0003g0091others(6): Show | 9 | HG01256.hp2 HG02015.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.565-931delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123685890 | |||||
| chr12:123686029
|
T | G | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.565-807T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123686029 | ||||||
| chr12:123686036
|
A | AATTT | 2 | a0001c0001t0002g0021a0001c0001t0002g0142 | 3 | HG00738.hp1 HG01074.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.565-775_565-772dup others(4): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123686036 | |||||
| chr12:123686221
|
AT | A | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.565-610delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123686221 | |||||
| chr12:123686338
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0152 | 2 | NA18977.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.565-498C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123686338 | ||||||
| chr12:123686351
|
G | A | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.565-485G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123686351 | ||||||
| chr12:123686361
|
GATGAC | G | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.565-472_565-468del others(5): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 123686361 | |||||
| chr12:123686418
|
A | G | 10 | a0001c0003t0009g0008a0001c0003t0012g0168a0001c0003t0012g0169others(7): Show | 11 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.565-418A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123686418 | ||||||
| chr12:123686604
|
C | T | 86 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(83): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.565-232C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123686604 | ||||||
| chr12:123686629
|
A | G | 114 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(111): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.565-207A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123686629 | ||||||
| chr12:123686713
|
A | G | 4 | a0001c0001t0003g0093a0001c0001t0003g0095a0001c0001t0003g0105others(1): Show | 4 | HG01891.hp1 HG02896.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-123A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123686713 | ||||||
| chr12:123686773
|
C | T | 3 | a0001c0001t0007g0020a0001c0001t0007g0132a0001c0001t0007g0135 | 4 | HG02257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-63C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123686773 | ||||||
| chr12:123686776
|
T | C | 86 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(83): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.565-60T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123686776 | ||||||
| chr12:123686787
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.565-49G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 5/17 | chr12 | 123686787 | ||||||
| chr12:123687063
|
G | C | 6 | a0001c0003t0013g0177a0001c0003t0013g0178a0001c0004t0005g0162others(3): Show | 6 | HG01109.hp2 HG01256.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.764+28G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687063 | ||||||
| chr12:123687063
|
G | T | 16 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(13): Show | 18 | HG01099.hp2 HG01346.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.764+28G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687063 | ||||||
| chr12:123687093
|
A | G | 19 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(16): Show | 25 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.764+58A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687093 | ||||||
| chr12:123687111
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.764+76C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687111 | ||||||
| chr12:123687279
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.764+244T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687279 | ||||||
| chr12:123687356
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.764+321A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687356 | ||||||
| chr12:123687580
|
C | A | 2 | a0002c0007t0018g0027a0002c0007t0021g0026 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.765-471C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687580 | ||||||
| chr12:123687670
|
CAAAGT | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.765-376_765-372del others(5): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr12 | 123687670 | |||||
| chr12:123687760
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.765-291C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687760 | ||||||
| chr12:123687795
|
T | C | 114 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(111): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.765-256T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687795 | ||||||
| chr12:123687829
|
G | C | 1 | a0001c0002t0001g0052 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.765-222G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687829 | ||||||
| chr12:123687830
|
G | T | 1 | a0001c0002t0001g0052 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.765-221G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687830 | ||||||
| chr12:123687952
|
A | C | 4 | a0001c0004t0005g0162a0001c0004t0005g0163a0001c0004t0005g0164others(1): Show | 4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-99A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123687952 | ||||||
| chr12:123688008
|
A | T | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.765-43A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 6/17 | chr12 | 123688008 | ||||||
| chr12:123688184
|
G | A | 86 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(83): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
splice_region_variant&intron_variant | LOW | c.891+7G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123688184 | ||||||
| chr12:123688199
|
T | C | 114 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(111): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.891+22T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123688199 | ||||||
| chr12:123688213
|
C | CT | 4 | a0001c0001t0001g0097a0001c0001t0003g0003a0001c0001t0003g0050others(1): Show | 7 | HG02109.hp1 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+54dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 123688213 | |||||
| chr12:123688213
|
CT | C | 9 | a0001c0001t0002g0023a0001c0001t0002g0140a0001c0001t0008g0030others(6): Show | 9 | HG00140.hp1 HG01109.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.891+54delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 123688213 | |||||
| chr12:123688231
|
T | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.891+54T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123688231 | ||||||
| chr12:123688358
|
G | T | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.891+181G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123688358 | ||||||
| chr12:123688458
|
T | G | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.891+281T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123688458 | ||||||
| chr12:123688763
|
C | CT | 22 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(19): Show | 28 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.891+595dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 123688763 | |||||
| chr12:123688832
|
C | G | 10 | a0001c0003t0009g0008a0001c0003t0012g0168a0001c0003t0012g0169others(7): Show | 11 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+655C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123688832 | ||||||
| chr12:123688901
|
C | T | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.891+724C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123688901 | ||||||
| chr12:123688992
|
G | A | 2 | a0001c0001t0002g0023a0001c0001t0019g0159 | 2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.891+815G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123688992 | ||||||
| chr12:123689042
|
CT | C | 6 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(3): Show | 7 | HG01099.hp2 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+877delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 123689042 | |||||
| chr12:123689054
|
T | A | 16 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(13): Show | 18 | HG01099.hp2 HG01346.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.891+877T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689054 | ||||||
| chr12:123689054
|
T | TA | 5 | a0001c0003t0013g0178a0001c0004t0005g0162a0001c0004t0005g0163others(2): Show | 5 | HG01109.hp2 HG01256.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+880dupA | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 123689054 | |||||
| chr12:123689066
|
A | G | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.891+889A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689066 | ||||||
| chr12:123689206
|
C | T | 1 | a0001c0002t0001g0078 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.891+1029C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689206 | ||||||
| chr12:123689227
|
A | T | 1 | a0001c0001t0004g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.891+1050A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689227 | ||||||
| chr12:123689270
|
T | A | 1 | a0001c0001t0003g0050 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.891+1093T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689270 | ||||||
| chr12:123689388
|
A | C | 1 | a0001c0002t0001g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.892-1145A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689388 | ||||||
| chr12:123689400
|
C | T | 16 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(13): Show | 18 | HG01099.hp2 HG01346.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.892-1133C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689400 | ||||||
| chr12:123689445
|
G | A | 15 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(12): Show | 17 | HG01099.hp2 HG01346.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.892-1088G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689445 | ||||||
| chr12:123689518
|
T | A | 86 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(83): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.892-1015T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689518 | ||||||
| chr12:123689687
|
G | A | 68 | a0001c0001t0001g0098a0001c0001t0002g0002a0001c0001t0002g0006others(65): Show | 80 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.892-846G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689687 | ||||||
| chr12:123689729
|
C | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.892-804C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689729 | ||||||
| chr12:123689818
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.892-715A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689818 | ||||||
| chr12:123689986
|
G | C | 1 | a0001c0002t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.892-547G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123689986 | ||||||
| chr12:123690109
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.892-424T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123690109 | ||||||
| chr12:123690390
|
A | T | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.892-143A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123690390 | ||||||
| chr12:123690410
|
G | A | 15 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(12): Show | 17 | HG01099.hp2 HG01346.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.892-123G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 7/17 | chr12 | 123690410 | ||||||
| chr12:123691158
|
C | T | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1033+484C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691158 | ||||||
| chr12:123691232
|
C | T | 1 | a0001c0001t0006g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1033+558C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691232 | ||||||
| chr12:123691256
|
C | T | 5 | a0001c0002t0001g0076a0001c0004t0005g0162a0001c0004t0005g0163others(2): Show | 5 | HG00621.hp2 HG01109.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1033+582C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691256 | ||||||
| chr12:123691397
|
A | G | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1033+723A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691397 | ||||||
| chr12:123691466
|
T | C | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1033+792T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691466 | ||||||
| chr12:123691472
|
G | A | 1 | a0001c0001t0004g0115 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1033+798G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691472 | ||||||
| chr12:123691524
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0061 | 3 | HG02723.hp1 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1033+850G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691524 | ||||||
| chr12:123691545
|
C | T | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1033+871C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691545 | ||||||
| chr12:123691629
|
T | A | 1 | a0001c0002t0001g0088 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1033+955T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691629 | ||||||
| chr12:123691701
|
T | C | 3 | a0001c0001t0004g0128a0001c0001t0004g0129a0001c0001t0004g0130 | 3 | HG02451.hp2 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1034-957T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691701 | ||||||
| chr12:123691719
|
G | GT | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034-929dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 123691719 | |||||
| chr12:123691738
|
G | GT | 60 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(57): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1034-920_1034-919i others(3): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691738 | ||||||
| chr12:123691738
|
G | GTT | 2 | a0001c0001t0002g0151a0001c0001t0002g0158 | 2 | HG01934.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1034-920_1034-919i others(4): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691738 | ||||||
| chr12:123691739
|
G | T | 114 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(111): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1034-919G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691739 | ||||||
| chr12:123691793
|
G | A | 1 | a0001c0003t0012g0161 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1034-865G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691793 | ||||||
| chr12:123691800
|
C | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0145 | 2 | HG02027.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1034-858C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691800 | ||||||
| chr12:123691898
|
AT | A | 86 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(83): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1034-747delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr12 | 123691898 | |||||
| chr12:123691925
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1034-733G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691925 | ||||||
| chr12:123691963
|
C | T | 9 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(6): Show | 10 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1034-695C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691963 | ||||||
| chr12:123691969
|
A | G | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1034-689A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123691969 | ||||||
| chr12:123692052
|
G | A | 1 | a0001c0001t0004g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1034-606G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123692052 | ||||||
| chr12:123692201
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1034-457A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123692201 | ||||||
| chr12:123692204
|
C | T | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1034-454C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123692204 | ||||||
| chr12:123692301
|
T | C | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1034-357T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123692301 | ||||||
| chr12:123692356
|
A | G | 1 | a0001c0001t0022g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1034-302A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123692356 | ||||||
| chr12:123692469
|
C | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1034-189C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 8/17 | chr12 | 123692469 | ||||||
| chr12:123692742
|
T | C | 114 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(111): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1099+19T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123692742 | ||||||
| chr12:123692930
|
C | G | 1 | a0001c0001t0003g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1099+207C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123692930 | ||||||
| chr12:123692959
|
G | C | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099+236G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123692959 | ||||||
| chr12:123692991
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1099+268C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123692991 | ||||||
| chr12:123693018
|
C | CT | 14 | a0001c0001t0008g0028a0001c0001t0008g0031a0001c0002t0001g0075others(11): Show | 14 | HG01109.hp2 HG01192.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1099+320dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123693018 | |||||
| chr12:123693018
|
CT | C | 33 | a0001c0001t0002g0138a0001c0001t0002g0151a0001c0001t0003g0005others(30): Show | 37 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.1099+320delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123693018 | |||||
| chr12:123693018
|
CTT | C | 55 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(52): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1099+319_1099+320d others(4): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123693018 | |||||
| chr12:123693096
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1099+373G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693096 | ||||||
| chr12:123693112
|
C | T | 1 | a0001c0002t0001g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1099+389C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693112 | ||||||
| chr12:123693284
|
C | T | 1 | a0001c0001t0001g0015 | 2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1099+561C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693284 | ||||||
| chr12:123693316
|
G | A | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1099+593G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693316 | ||||||
| chr12:123693318
|
G | A | 23 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0004g0110others(20): Show | 23 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1099+595G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693318 | ||||||
| chr12:123693376
|
C | CT | 73 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(70): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1099+674dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123693376 | |||||
| chr12:123693376
|
CT | C | 6 | a0001c0001t0003g0054a0001c0002t0001g0032a0001c0002t0001g0092others(3): Show | 6 | HG01169.hp2 HG02735.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099+674delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123693376 | |||||
| chr12:123693437
|
T | C | 2 | a0002c0007t0018g0027a0002c0007t0021g0026 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1099+714T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693437 | ||||||
| chr12:123693452
|
A | AG | 2 | a0001c0001t0003g0003a0001c0001t0003g0081 | 5 | HG02109.hp1 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099+730dupG | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123693452 | |||||
| chr12:123693454
|
A | AT | 22 | a0001c0001t0003g0005a0001c0001t0003g0011a0001c0001t0003g0012others(19): Show | 25 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1099+747dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123693454 | |||||
| chr12:123693454
|
A | ATT | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099+746_1099+747d others(4): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123693454 | |||||
| chr12:123693454
|
A | T | 2 | a0001c0001t0003g0003a0001c0001t0003g0081 | 5 | HG02109.hp1 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099+731A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693454 | ||||||
| chr12:123693468
|
T | TC | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1099+745_1099+746i others(3): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693468 | ||||||
| chr12:123693743
|
G | C | 114 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(111): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1099+1020G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693743 | ||||||
| chr12:123693751
|
G | T | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1099+1028G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693751 | ||||||
| chr12:123693782
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1099+1059G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693782 | ||||||
| chr12:123693818
|
CT | C | 13 | a0001c0001t0002g0157a0001c0001t0010g0154a0001c0003t0009g0008others(10): Show | 14 | HG01169.hp1 HG01255.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1100-1012delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123693818 | |||||
| chr12:123693834
|
T | C | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1100-1008T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123693834 | ||||||
| chr12:123694002
|
A | AT | 6 | a0001c0001t0008g0028a0001c0002t0001g0016a0001c0002t0001g0043others(3): Show | 7 | HG02258.hp1 HG02738.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1100-827dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123694002 | |||||
| chr12:123694002
|
AT | A | 12 | a0001c0003t0009g0008a0001c0003t0012g0168a0001c0003t0012g0169others(9): Show | 13 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1100-827delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 123694002 | |||||
| chr12:123694049
|
A | G | 2 | a0001c0001t0002g0146a0001c0001t0002g0152 | 2 | NA18977.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1100-793A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123694049 | ||||||
| chr12:123694118
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1100-724C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123694118 | ||||||
| chr12:123694228
|
C | T | 23 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0004g0110others(20): Show | 23 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1100-614C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123694228 | ||||||
| chr12:123694268
|
C | G | 1 | a0001c0004t0005g0164 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1100-574C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123694268 | ||||||
| chr12:123694273
|
G | A | 4 | a0001c0004t0005g0162a0001c0004t0005g0163a0001c0004t0005g0164others(1): Show | 4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1100-569G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123694273 | ||||||
| chr12:123694352
|
C | T | 1 | a0001c0003t0005g0022 | 2 | HG01099.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1100-490C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123694352 | ||||||
| chr12:123694537
|
C | T | 5 | a0001c0001t0004g0110a0001c0001t0004g0111a0001c0001t0004g0112others(2): Show | 5 | HG02486.hp1 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1100-305C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123694537 | ||||||
| chr12:123694606
|
G | T | 1 | a0001c0003t0013g0178 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1100-236G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123694606 | ||||||
| chr12:123694815
|
T | A | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1100-27T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 9/17 | chr12 | 123694815 | ||||||
| chr12:123695017
|
G | C | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234+41G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 10/17 | chr12 | 123695017 | ||||||
| chr12:123695073
|
G | A | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1234+97G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 10/17 | chr12 | 123695073 | ||||||
| chr12:123695092
|
A | G | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1234+116A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 10/17 | chr12 | 123695092 | ||||||
| chr12:123695109
|
C | G | 1 | a0001c0001t0006g0122 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1235-111C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 10/17 | chr12 | 123695109 | ||||||
| chr12:123695109
|
C | T | 6 | a0001c0003t0009g0008a0001c0003t0015g0008a0001c0003t0015g0173others(3): Show | 7 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1235-111C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 10/17 | chr12 | 123695109 | ||||||
| chr12:123695165
|
ATTTCT | A | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1235-50_1235-46del others(5): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 123695165 | |||||
| chr12:123695168
|
T | C | 1 | a0001c0002t0001g0064 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1235-52T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 10/17 | chr12 | 123695168 | ||||||
| chr12:123695192
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1235-28A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 10/17 | chr12 | 123695192 | ||||||
| chr12:123695334
|
C | T | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1312+37C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | chr12 | 123695334 | ||||||
| chr12:123695381
|
T | A | 20 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(17): Show | 22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1312+84T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | chr12 | 123695381 | ||||||
| chr12:123695464
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1312+167T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | chr12 | 123695464 | ||||||
| chr12:123695585
|
CT | C | 94 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(91): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1312+305delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 123695585 | |||||
| chr12:123695662
|
G | A | 1 | a0001c0004t0005g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1312+365G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | chr12 | 123695662 | ||||||
| chr12:123695927
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1313-488T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | chr12 | 123695927 | ||||||
| chr12:123695960
|
C | T | 4 | a0001c0004t0005g0162a0001c0004t0005g0163a0001c0004t0005g0164others(1): Show | 4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-455C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | chr12 | 123695960 | ||||||
| chr12:123696119
|
C | T | 2 | a0002c0007t0018g0027a0002c0007t0021g0026 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1313-296C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | chr12 | 123696119 | ||||||
| chr12:123696174
|
A | AT | 8 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(5): Show | 9 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1313-229dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 123696174 | |||||
| chr12:123696174
|
A | ATT | 6 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 7 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1313-230_1313-229d others(4): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 123696174 | |||||
| chr12:123696174
|
AT | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1313-229delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 123696174 | |||||
| chr12:123696252
|
GT | G | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1313-155delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 123696252 | |||||
| chr12:123696367
|
G | T | 1 | a0001c0002t0001g0104 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1313-48G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 11/17 | chr12 | 123696367 | ||||||
| chr12:123696502
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
splice_region_variant&intron_variant | LOW | c.1393+7C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 12/17 | chr12 | 123696502 | ||||||
| chr12:123696820
|
A | G | 1 | a0001c0002t0001g0071 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1394-267A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 12/17 | chr12 | 123696820 | ||||||
| chr12:123696853
|
G | A | 3 | a0001c0003t0009g0008a0001c0003t0015g0008a0001c0003t0015g0173 | 4 | HG02630.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1394-234G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 12/17 | chr12 | 123696853 | ||||||
| chr12:123697201
|
G | C | 2 | a0002c0007t0018g0027a0002c0007t0021g0026 | 2 | HG02559.hp1 HG06807.hp2 |
splice_region_variant&intron_variant | LOW | c.1505+3G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123697201 | ||||||
| chr12:123697273
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1505+75A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123697273 | ||||||
| chr12:123697573
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1505+375C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123697573 | ||||||
| chr12:123697596
|
T | C | 33 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(30): Show | 44 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1505+398T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123697596 | ||||||
| chr12:123697688
|
G | T | 1 | a0001c0001t0002g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1505+490G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123697688 | ||||||
| chr12:123697783
|
C | T | 4 | a0001c0001t0004g0117a0001c0001t0004g0119a0001c0001t0006g0116others(1): Show | 4 | HG02818.hp2 NA18522.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1505+585C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123697783 | ||||||
| chr12:123697860
|
CTTTTT | C | 20 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(17): Show | 22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1505+676_1505+680d others(7): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 123697860 | |||||
| chr12:123697887
|
G | T | 10 | a0001c0003t0009g0008a0001c0003t0012g0168a0001c0003t0012g0169others(7): Show | 11 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1505+689G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123697887 | ||||||
| chr12:123697928
|
A | G | 1 | a0001c0003t0012g0174 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1505+730A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123697928 | ||||||
| chr12:123698020
|
C | T | 23 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0004g0110others(20): Show | 23 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1505+822C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123698020 | ||||||
| chr12:123698112
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1505+914A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123698112 | ||||||
| chr12:123698365
|
GT | G | 22 | a0001c0002t0001g0064a0001c0003t0005g0022a0001c0003t0005g0160others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1505+1178delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 123698365 | |||||
| chr12:123698404
|
G | T | 1 | a0001c0001t0019g0159 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1505+1206G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123698404 | ||||||
| chr12:123698506
|
C | T | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1506-1198C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123698506 | ||||||
| chr12:123698511
|
C | T | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1506-1193C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123698511 | ||||||
| chr12:123698702
|
G | C | 4 | a0001c0004t0005g0162a0001c0004t0005g0163a0001c0004t0005g0164others(1): Show | 4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506-1002G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123698702 | ||||||
| chr12:123698750
|
G | A | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1506-954G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123698750 | ||||||
| chr12:123698804
|
TG | T | 19 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(16): Show | 21 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1506-895delG | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 123698804 | |||||
| chr12:123699013
|
A | T | 6 | a0001c0003t0009g0008a0001c0003t0015g0008a0001c0003t0015g0173others(3): Show | 7 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1506-691A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123699013 | ||||||
| chr12:123699052
|
C | T | 3 | a0001c0002t0001g0070a0001c0003t0005g0175a0001c0004t0005g0165 | 3 | HG01109.hp2 HG01496.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1506-652C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123699052 | ||||||
| chr12:123699129
|
T | C | 1 | a0001c0002t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1506-575T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123699129 | ||||||
| chr12:123699155
|
A | AT | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1506-533dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 123699155 | |||||
| chr12:123699257
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1506-447C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123699257 | ||||||
| chr12:123699280
|
A | G | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1506-424A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123699280 | ||||||
| chr12:123699394
|
A | G | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1506-310A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123699394 | ||||||
| chr12:123699497
|
TA | T | 20 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(17): Show | 22 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1506-206delA | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123699497 | ||||||
| chr12:123699518
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1506-186G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123699518 | ||||||
| chr12:123699630
|
C | T | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1506-74C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123699630 | ||||||
| chr12:123699638
|
C | G | 1 | a0001c0002t0001g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1506-66C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 13/17 | chr12 | 123699638 | ||||||
| chr12:123699822
|
C | T | 1 | a0001c0002t0001g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1612+12C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123699822 | ||||||
| chr12:123699831
|
A | G | 1 | a0001c0003t0013g0177 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1612+21A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123699831 | ||||||
| chr12:123699842
|
A | G | 1 | a0001c0003t0015g0173 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1612+32A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123699842 | ||||||
| chr12:123699921
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1612+111C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123699921 | ||||||
| chr12:123699935
|
G | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1612+125G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123699935 | ||||||
| chr12:123699995
|
C | A | 1 | a0001c0002t0001g0064 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1612+185C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123699995 | ||||||
| chr12:123700092
|
T | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1612+282T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700092 | ||||||
| chr12:123700157
|
G | A | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1612+347G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700157 | ||||||
| chr12:123700250
|
A | G | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1612+440A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700250 | ||||||
| chr12:123700273
|
ACCCCAAC others(1): Show |
A | 114 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(111): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1612+464_1612+471d others(10): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700273 | ||||||
| chr12:123700282
|
A | G | 114 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(111): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1612+472A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700282 | ||||||
| chr12:123700330
|
T | A | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1612+520T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700330 | ||||||
| chr12:123700339
|
A | G | 1 | a0001c0003t0012g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1612+529A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700339 | ||||||
| chr12:123700347
|
G | C | 2 | a0001c0001t0006g0116a0001c0001t0006g0118 | 2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1612+537G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700347 | ||||||
| chr12:123700356
|
C | T | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1612+546C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700356 | ||||||
| chr12:123700364
|
C | T | 1 | a0001c0002t0001g0036 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1612+554C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700364 | ||||||
| chr12:123700419
|
A | G | 1 | a0001c0002t0001g0079 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1612+609A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700419 | ||||||
| chr12:123700454
|
C | T | 1 | a0001c0002t0001g0036 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1612+644C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700454 | ||||||
| chr12:123700577
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1612+767C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700577 | ||||||
| chr12:123700579
|
C | T | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1612+769C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700579 | ||||||
| chr12:123700614
|
A | G | 19 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(16): Show | 21 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1612+804A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700614 | ||||||
| chr12:123700622
|
G | A | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1612+812G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700622 | ||||||
| chr12:123700665
|
C | T | 114 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(111): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1612+855C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700665 | ||||||
| chr12:123700666
|
C | T | 10 | a0001c0003t0009g0008a0001c0003t0012g0168a0001c0003t0012g0169others(7): Show | 11 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1612+856C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700666 | ||||||
| chr12:123700720
|
C | A | 1 | a0001c0001t0022g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1612+910C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700720 | ||||||
| chr12:123700840
|
T | G | 3 | a0001c0002t0001g0013a0001c0002t0001g0051a0001c0002t0001g0065 | 4 | HG02040.hp1 HG02083.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1612+1030T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700840 | ||||||
| chr12:123700862
|
C | T | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1612+1052C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123700862 | ||||||
| chr12:123700897
|
C | CT | 3 | a0001c0005t0009g0171a0001c0005t0009g0172a0001c0005t0009g0176 | 3 | HG01346.hp2 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1612+1088dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 123700897 | |||||
| chr12:123701308
|
G | A | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1612+1498G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123701308 | ||||||
| chr12:123701387
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1612+1577G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123701387 | ||||||
| chr12:123701401
|
T | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1612+1591T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123701401 | ||||||
| chr12:123701477
|
A | G | 186 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(183): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1612+1667A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123701477 | ||||||
| chr12:123701478
|
T | C | 186 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(183): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1612+1668T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123701478 | ||||||
| chr12:123701504
|
C | T | 1 | a0001c0003t0013g0178 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1612+1694C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123701504 | ||||||
| chr12:123701581
|
TA | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(38): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1612+1783delA | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 123701581 | |||||
| chr12:123701801
|
T | C | 5 | a0001c0001t0002g0007a0001c0001t0002g0144a0001c0001t0002g0151others(2): Show | 6 | HG00733.hp1 HG01934.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1612+1991T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123701801 | ||||||
| chr12:123701882
|
A | G | 186 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(183): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1612+2072A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123701882 | ||||||
| chr12:123701971
|
C | T | 1 | a0002c0007t0021g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1612+2161C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123701971 | ||||||
| chr12:123702247
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1613-2285C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702247 | ||||||
| chr12:123702378
|
A | C | 25 | a0001c0001t0003g0054a0001c0001t0003g0095a0001c0001t0003g0105others(22): Show | 27 | HG01099.hp2 HG01109.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.1613-2154A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702378 | ||||||
| chr12:123702450
|
C | T | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1613-2082C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702450 | ||||||
| chr12:123702453
|
T | TG | 58 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(55): Show | 67 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.1613-2079_1613-207 others(5): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702453 | ||||||
| chr12:123702533
|
A | AC | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1613-1998dupC | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 123702533 | |||||
| chr12:123702535
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1613-1997T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702535 | ||||||
| chr12:123702543
|
C | T | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1613-1989C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702543 | ||||||
| chr12:123702638
|
G | A | 23 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(20): Show | 29 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1613-1894G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702638 | ||||||
| chr12:123702641
|
C | T | 1 | a0001c0002t0001g0042 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1613-1891C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702641 | ||||||
| chr12:123702735
|
G | A | 1 | a0001c0003t0013g0178 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1613-1797G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702735 | ||||||
| chr12:123702779
|
G | A | 1 | a0001c0002t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1613-1753G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702779 | ||||||
| chr12:123702843
|
T | C | 1 | a0001c0001t0001g0015 | 2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1613-1689T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123702843 | ||||||
| chr12:123703010
|
T | C | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1613-1522T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703010 | ||||||
| chr12:123703059
|
C | T | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1613-1473C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703059 | ||||||
| chr12:123703079
|
T | C | 1 | a0001c0003t0013g0178 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1613-1453T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703079 | ||||||
| chr12:123703169
|
TA | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG00733.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1613-1362delA | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703169 | ||||||
| chr12:123703173
|
T | A | 6 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(3): Show | 7 | HG02257.hp2 HG02258.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1613-1359T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703173 | ||||||
| chr12:123703190
|
CATT | C | 5 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(2): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1613-1338_1613-133 others(7): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 123703190 | |||||
| chr12:123703193
|
TA | T | 32 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(29): Show | 43 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1613-1338delA | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703193 | ||||||
| chr12:123703339
|
A | G | 123 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(120): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1613-1193A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703339 | ||||||
| chr12:123703354
|
G | C | 2 | a0001c0001t0004g0109a0001c0001t0004g0115 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1613-1178G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703354 | ||||||
| chr12:123703377
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1613-1155T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703377 | ||||||
| chr12:123703457
|
C | G | 10 | a0001c0003t0009g0008a0001c0003t0012g0168a0001c0003t0012g0169others(7): Show | 11 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1613-1075C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703457 | ||||||
| chr12:123703477
|
C | T | 10 | a0001c0003t0009g0008a0001c0003t0012g0168a0001c0003t0012g0169others(7): Show | 11 | HG01346.hp2 HG01975.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1613-1055C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703477 | ||||||
| chr12:123703517
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1613-1015C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703517 | ||||||
| chr12:123703556
|
C | T | 19 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(16): Show | 21 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1613-976C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703556 | ||||||
| chr12:123703599
|
C | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0152 | 2 | NA18977.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1613-933C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703599 | ||||||
| chr12:123703700
|
G | A | 2 | a0001c0001t0003g0003a0001c0001t0003g0081 | 5 | HG02109.hp1 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613-832G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703700 | ||||||
| chr12:123703756
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1613-776C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703756 | ||||||
| chr12:123703887
|
T | G | 6 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1613-645T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123703887 | ||||||
| chr12:123704004
|
C | CT | 5 | a0001c0001t0001g0097a0001c0002t0001g0024a0001c0002t0001g0041others(2): Show | 5 | HG00621.hp2 HG01109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613-507dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 123704004 | |||||
| chr12:123704004
|
CT | C | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1613-507delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 123704004 | |||||
| chr12:123704004
|
CTT | C | 9 | a0001c0001t0004g0109a0001c0001t0004g0117a0001c0001t0004g0119others(6): Show | 9 | HG01243.hp2 HG01515.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1613-508_1613-507d others(4): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 123704004 | |||||
| chr12:123704004
|
CTTT | C | 18 | a0001c0001t0004g0115a0001c0003t0005g0160a0001c0003t0005g0167others(15): Show | 19 | HG01109.hp2 HG01256.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.1613-509_1613-507d others(5): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 123704004 | |||||
| chr12:123704034
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1613-498G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123704034 | ||||||
| chr12:123704208
|
T | C | 1 | a0001c0001t0003g0011 | 2 | HG00280.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1613-324T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123704208 | ||||||
| chr12:123704248
|
G | T | 1 | a0001c0002t0001g0040 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1613-284G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123704248 | ||||||
| chr12:123704252
|
G | A | 1 | a0001c0001t0006g0122 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1613-280G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123704252 | ||||||
| chr12:123704260
|
C | G | 19 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0011others(16): Show | 25 | HG00280.hp1 HG00408.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1613-272C>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 14/17 | chr12 | 123704260 | ||||||
| chr12:123704711
|
C | T | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1769+23C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123704711 | ||||||
| chr12:123705110
|
T | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(36): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1769+422T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705110 | ||||||
| chr12:123705115
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1769+427C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705115 | ||||||
| chr12:123705161
|
G | GT | 49 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(46): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1769+493dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 123705161 | |||||
| chr12:123705161
|
G | GTT | 15 | a0001c0001t0002g0137a0001c0001t0002g0141a0001c0001t0002g0153others(12): Show | 15 | HG00733.hp1 HG01175.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1769+492_1769+493d others(4): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 123705161 | |||||
| chr12:123705161
|
G | GTTT | 6 | a0001c0001t0004g0108a0001c0001t0004g0117a0001c0001t0004g0119others(3): Show | 6 | HG01243.hp2 HG02818.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.1769+491_1769+493d others(5): Show |
TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 123705161 | |||||
| chr12:123705161
|
GT | G | 17 | a0001c0001t0008g0010a0001c0001t0008g0028a0001c0001t0008g0029others(14): Show | 19 | HG01109.hp2 HG01256.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1769+493delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 123705161 | |||||
| chr12:123705216
|
G | A | 4 | a0001c0001t0002g0007a0001c0001t0002g0144a0001c0001t0002g0153others(1): Show | 5 | HG00733.hp1 HG02698.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1769+528G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705216 | ||||||
| chr12:123705232
|
G | A | 4 | a0001c0004t0005g0162a0001c0004t0005g0163a0001c0004t0005g0164others(1): Show | 4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1769+544G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705232 | ||||||
| chr12:123705412
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1769+724C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705412 | ||||||
| chr12:123705471
|
G | A | 1 | a0001c0001t0003g0095 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1769+783G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705471 | ||||||
| chr12:123705755
|
C | T | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1770-971C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705755 | ||||||
| chr12:123705759
|
C | CT | 19 | a0001c0003t0005g0167a0001c0003t0005g0175a0001c0003t0009g0008others(16): Show | 20 | HG01109.hp2 HG01256.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-953dupT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 123705759 | |||||
| chr12:123705759
|
CT | C | 65 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(62): Show | 76 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1770-953delT | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 123705759 | |||||
| chr12:123705843
|
A | G | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-883A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705843 | ||||||
| chr12:123705846
|
A | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1770-880A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705846 | ||||||
| chr12:123705847
|
A | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1770-879A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705847 | ||||||
| chr12:123705847
|
A | G | 4 | a0001c0004t0005g0162a0001c0004t0005g0163a0001c0004t0005g0164others(1): Show | 4 | HG01109.hp2 HG01256.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1770-879A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705847 | ||||||
| chr12:123705852
|
G | T | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1770-874G>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705852 | ||||||
| chr12:123705878
|
T | C | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-848T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705878 | ||||||
| chr12:123705879
|
C | T | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-847C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705879 | ||||||
| chr12:123705882
|
A | G | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-844A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705882 | ||||||
| chr12:123705891
|
A | G | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-835A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705891 | ||||||
| chr12:123705893
|
G | A | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-833G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705893 | ||||||
| chr12:123705899
|
A | G | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-827A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705899 | ||||||
| chr12:123705905
|
T | C | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-821T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705905 | ||||||
| chr12:123705907
|
G | C | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-819G>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705907 | ||||||
| chr12:123705912
|
T | A | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-814T>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705912 | ||||||
| chr12:123705913
|
C | A | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-813C>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705913 | ||||||
| chr12:123705917
|
T | C | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-809T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705917 | ||||||
| chr12:123705922
|
A | T | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0155others(2): Show | 5 | HG00140.hp1 HG01257.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-804A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123705922 | ||||||
| chr12:123706035
|
C | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1770-691C>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123706035 | ||||||
| chr12:123706058
|
T | G | 2 | a0001c0003t0013g0177a0001c0003t0013g0178 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1770-668T>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123706058 | ||||||
| chr12:123706101
|
G | A | 22 | a0001c0003t0005g0022a0001c0003t0005g0160a0001c0003t0005g0167others(19): Show | 24 | HG01099.hp2 HG01109.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1770-625G>A | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123706101 | ||||||
| chr12:123706289
|
T | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1770-437T>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123706289 | ||||||
| chr12:123706392
|
A | G | 1 | a0001c0001t0001g0019 | 2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1770-334A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123706392 | ||||||
| chr12:123706678
|
A | C | 1 | a0001c0001t0002g0147 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1770-48A>C | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 15/17 | chr12 | 123706678 | ||||||
| chr12:123707125
|
A | T | 1 | a0001c0001t0004g0111 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1984+52A>T | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 17/17 | chr12 | 123707125 | ||||||
| chr12:123707525
|
A | G | 1 | a0001c0003t0005g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1985-79A>G | TCTN2 | ENSG00000168778.13 | transcript | ENST00000303372.7 | protein_coding | 17/17 | chr12 | 123707525 |