Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7273 |
|---|---|
| ensemblid | ENSG00000155657.29 |
| hgncid | 12403 |
| symbol | TTN |
| name | titin |
| refseq_nuc | NM_001267550.2 |
| refseq_prot | NP_001254479.2 |
| ensembl_nuc | ENST00000589042.5 |
| ensembl_prot | ENSP00000467141.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 178525989 |
| end | 178807423 |
| strand | - |
| ver | v1.2 |
| region | chr2:178525989-178807423 |
| region5000 | chr2:178520989-178812423 |
| regionname0 | TTN_chr2_178525989_178807423 |
| regionname5000 | TTN_chr2_178520989_178812423 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 35991 | 10 | 0 | 0 | 8 | 0 | 2 | 3 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0002 | 0/0 | 35991 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0003 | 0/0 | 35991 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0004 | 0/0 | 35991 | 5 | 0 | 3 | 0 | 0 | 2 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0005 | 0/0 | 35991 | 4 | 0 | 0 | 1 | 0 | 3 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0006 | 0/0 | 35991 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0007 | 0/0 | 35991 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0008 | 0/0 | 35991 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0009 | 0/0 | 35991 | 3 | 1 | 0 | 0 | 0 | 2 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0010 | 0/0 | 35991 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0011 | 0/0 | 35991 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0012 | 0/0 | 35991 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0013 | 0/0 | 35991 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0014 | 0/0 | 35991 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0015 | 0/0 | 12823 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0016 | 0/0 | 35991 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0017 | 0/0 | 35991 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0018 | 0/0 | 35991 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0019 | 0/0 | 35991 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0020 | 0/0 | 35991 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0021 | 0/0 | 35991 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0022 | 0/0 | 35991 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0023 | 0/0 | 35991 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0024 | 0/0 | 35991 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0025 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0026 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0027 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0028 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0029 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0030 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0031 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0032 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0033 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0034 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0035 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0036 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0037 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0038 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0039 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0040 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0041 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0042 | 0/0 | 12600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0043 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0044 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0045 | 0/0 | 12823 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0046 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0047 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0048 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0049 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0050 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0051 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0052 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0053 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0054 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0055 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0056 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0057 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0058 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0059 | 0/0 | 35985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0060 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0061 | 0/0 | 35985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0062 | 0/0 | 35985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0063 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0064 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0065 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0066 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0067 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0068 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0069 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0070 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0071 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0072 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0073 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0074 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0075 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0076 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0077 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0078 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0079 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0080 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0081 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0082 | 0/0 | 35489 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0083 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0084 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0085 | 0/0 | 35740 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0086 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0087 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0088 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0089 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0090 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0091 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0092 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0093 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0094 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0095 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0096 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0097 | 0/1 | 35991 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0098 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0099 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0100 | 0/0 | 35740 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0101 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0102 | 0/0 | 35740 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0103 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0104 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0105 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0106 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0107 | 0/0 | 35740 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0108 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0109 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0110 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0111 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0112 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0113 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0114 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0115 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0116 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0117 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0118 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0119 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0120 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0121 | 0/0 | 35740 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0122 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0123 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0124 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0125 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0126 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0127 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0128 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0129 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0130 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0131 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0132 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0133 | 0/0 | 35740 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0134 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0135 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0136 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0137 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0138 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0139 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0140 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0141 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0142 | 0/0 | 36003 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0143 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0144 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0145 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0146 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0147 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0148 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0149 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0150 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0151 | 0/0 | 35985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0152 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0153 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0154 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0155 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0156 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0157 | 0/0 | 35740 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0158 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0159 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0160 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0161 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0162 | 0/0 | 35740 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0163 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0164 | 0/0 | 35991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0165 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0166 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0167 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0168 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0169 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0170 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0171 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0172 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0173 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0174 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0175 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0176 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0177 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0178 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0179 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0180 | 1/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0181 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0182 | 0/0 | 35651 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0183 | 0/0 | 35991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0184 | 0/0 | 35985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0185 | 0/0 | 35991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0186 | 0/0 | 35991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0187 | 0/0 | 35985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0188 | 0/0 | 35985 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0189 | 0/0 | 35985 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0190 | 0/0 | 35985 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0191 | 0/0 | 35985 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0192 | 0/0 | 35985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0193 | 0/0 | 35985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 107976 | 4 | 0 | 0 | 2 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0002 | 0/0 | 107976 | 4 | 0 | 0 | 4 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0003 | 0/0 | 107976 | 3 | 0 | 3 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0004 | 0/0 | 107976 | 3 | 0 | 3 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0005 | 0/0 | 107976 | 3 | 0 | 0 | 1 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0006 | 0/0 | 107976 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0007 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0008 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0009 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0010 | 0/0 | 107976 | 2 | 0 | 0 | 1 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0011 | 0/0 | 107976 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0012 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0013 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0014 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0015 | 0/0 | 107976 | 2 | 0 | 0 | 0 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0016 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0017 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0018 | 0/0 | 107976 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0019 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0020 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0021 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0022 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0023 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0024 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0025 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0026 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0027 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0028 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0029 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0030 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0031 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0032 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0033 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0034 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0035 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0036 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0037 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0038 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0039 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0040 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0041 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0042 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0043 | 0/0 | 107223 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0044 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0045 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0046 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0047 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0048 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0049 | 0/0 | 107223 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0050 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0051 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0052 | 0/0 | 106470 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0053 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0054 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0055 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0056 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0057 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0058 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0059 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0060 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0061 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0062 | 0/0 | 107223 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0063 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0064 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0065 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0066 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0067 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0068 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0069 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0070 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0071 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0072 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0073 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0074 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0075 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0076 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0077 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0078 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0079 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0080 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0081 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0082 | 1/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0083 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0084 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0085 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0086 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0087 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0088 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0089 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0090 | 0/0 | 107223 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0091 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0092 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0093 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0094 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0095 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0096 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0097 | 0/0 | 108012 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0098 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0099 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0100 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0101 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0102 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0103 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0104 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0105 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0106 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0107 | 0/0 | 107223 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0108 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0109 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0110 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0111 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0112 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0113 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0114 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0115 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0116 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0117 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0118 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0119 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0120 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0121 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0122 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0123 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0124 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0125 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0126 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0127 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0128 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0129 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0130 | 0/0 | 107223 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0131 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0132 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0133 | 0/0 | 107223 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0134 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0135 | 0/0 | 107223 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0136 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0137 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0138 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0139 | 0/1 | 107976 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0140 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0141 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0142 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0143 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0144 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0145 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0146 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0147 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0148 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0149 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0150 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0151 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0152 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0153 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0154 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0155 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0156 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0157 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0158 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0159 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0160 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0161 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0162 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0163 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0164 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0165 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0166 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0167 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0168 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0169 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0170 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0171 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0172 | 0/0 | 112237 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0173 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0174 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0175 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0176 | 0/0 | 112237 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0177 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0178 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0179 | 0/0 | 112237 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0180 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0181 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0182 | 0/0 | 112237 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0183 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0184 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0185 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0186 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0187 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0188 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0189 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0190 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0191 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0192 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0193 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0194 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0195 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0196 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0197 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0198 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0199 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0200 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0201 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0202 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0203 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0204 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0205 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0206 | 0/0 | 107958 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0207 | 0/0 | 107958 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0208 | 0/0 | 107958 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0209 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0210 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| c0211 | 0/0 | 107958 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1250 | 139 | 43 | 26 | 49 | 0 | 21 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| t0002 | 1/1 | 1249 | 83 | 22 | 17 | 28 | 0 | 14 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| t0003 | 0/0 | 1250 | 11 | 0 | 0 | 11 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| t0004 | 0/0 | 1250 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| t0005 | 0/0 | 1250 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| t0006 | 0/0 | 1249 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| t0007 | 0/0 | 1250 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| t0008 | 0/0 | 1250 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| t0009 | 0/0 | 1249 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| t0010 | 0/0 | 1250 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 107976 | 4 | 0 | 0 | 2 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0001c0021 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0001c0171 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0001c0186 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0001c0195 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0001c0197 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0002c0002 | 0/0 | 107976 | 4 | 0 | 0 | 4 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0002c0022 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0003c0006 | 0/0 | 107976 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0003c0146 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0003c0147 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0004c0004 | 0/0 | 107976 | 3 | 0 | 3 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0004c0015 | 0/0 | 107976 | 2 | 0 | 0 | 0 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0005c0005 | 0/0 | 107976 | 3 | 0 | 0 | 1 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0005c0117 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0006c0018 | 0/0 | 107976 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0006c0141 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0007c0003 | 0/0 | 107976 | 3 | 0 | 3 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0008c0012 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0008c0064 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0009c0093 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0009c0095 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0009c0105 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0010c0013 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0010c0072 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0011c0007 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0012c0020 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0013c0023 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0014c0178 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0014c0180 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0015c0176 | 0/0 | 112237 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0015c0182 | 0/0 | 112237 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0016c0170 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0016c0196 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0017c0008 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0018c0009 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0019c0019 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0020c0010 | 0/0 | 107976 | 2 | 0 | 0 | 1 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0021c0011 | 0/0 | 107976 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0022c0014 | 0/0 | 107976 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0023c0016 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0024c0017 | 0/0 | 107976 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0025c0028 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0026c0027 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0027c0029 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0028c0026 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0029c0025 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0030c0165 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0031c0162 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0032c0161 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0033c0160 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0034c0159 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0035c0163 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0036c0164 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0037c0158 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0038c0166 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0039c0167 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0040c0169 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0041c0168 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0042c0172 | 0/0 | 112237 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0043c0194 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0044c0193 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0045c0179 | 0/0 | 112237 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0046c0177 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0047c0173 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0048c0185 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0049c0188 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0050c0201 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0051c0184 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0052c0183 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0053c0191 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0054c0187 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0055c0189 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0056c0190 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0057c0181 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0058c0192 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0059c0175 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0060c0174 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0061c0198 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0062c0199 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0063c0200 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0064c0202 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0065c0031 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0066c0032 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0067c0030 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0068c0156 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0069c0155 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0070c0152 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0071c0151 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0072c0154 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0073c0149 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0074c0148 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0075c0145 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0076c0150 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0077c0153 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0078c0055 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0079c0053 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0080c0054 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0081c0067 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0082c0052 | 0/0 | 106470 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0083c0142 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0084c0050 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0085c0049 | 0/0 | 107223 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0086c0118 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0087c0119 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0088c0128 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0089c0066 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0090c0127 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0091c0124 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0092c0126 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0093c0125 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0094c0123 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0095c0122 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0096c0121 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0097c0139 | 0/1 | 107976 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0098c0038 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0099c0132 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0100c0133 | 0/0 | 107223 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0101c0131 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0102c0130 | 0/0 | 107223 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0103c0157 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0104c0042 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0105c0041 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0106c0129 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0107c0043 | 0/0 | 107223 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0108c0040 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0109c0044 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0110c0045 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0111c0047 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0112c0046 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0113c0039 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0114c0048 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0115c0140 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0116c0036 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0117c0037 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0118c0035 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0119c0136 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0120c0134 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0121c0135 | 0/0 | 107223 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0122c0034 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0123c0137 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0124c0120 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0125c0138 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0126c0051 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0127c0143 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0128c0144 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0129c0115 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0130c0056 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0131c0057 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0132c0065 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0133c0062 | 0/0 | 107223 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0134c0058 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0135c0061 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0136c0060 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0137c0059 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0138c0063 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0139c0096 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0140c0094 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0141c0092 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0142c0097 | 0/0 | 108012 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0143c0103 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0144c0102 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0145c0099 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0146c0101 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0147c0098 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0148c0100 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0149c0104 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0150c0110 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0151c0112 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0152c0113 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0153c0114 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0154c0111 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0155c0108 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0156c0106 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0157c0107 | 0/0 | 107223 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0158c0109 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0159c0091 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0160c0088 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0161c0089 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0162c0090 | 0/0 | 107223 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0163c0080 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0164c0079 | 0/0 | 107976 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0165c0077 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0166c0076 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0167c0070 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0168c0075 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0169c0074 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0170c0071 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0171c0073 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0172c0078 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0173c0069 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0174c0081 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0175c0087 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0176c0086 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0177c0084 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0178c0085 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0179c0083 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0180c0082 | 1/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0181c0116 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0182c0068 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0183c0204 | 0/0 | 107976 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0184c0033 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0185c0203 | 0/0 | 107976 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0186c0024 | 0/0 | 107976 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0187c0205 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0188c0207 | 0/0 | 107958 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0189c0206 | 0/0 | 107958 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0190c0208 | 0/0 | 107958 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0191c0211 | 0/0 | 107958 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0192c0210 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0193c0209 | 0/0 | 107958 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 109225 | 4 | 0 | 0 | 2 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0001c0021t0001 | 0/0 | 109225 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0001c0171t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0001c0186t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0001c0195t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0001c0197t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0002c0002t0001 | 0/0 | 109225 | 4 | 0 | 0 | 4 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0002c0022t0001 | 0/0 | 109225 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0003c0006t0002 | 0/0 | 109224 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0003c0146t0002 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0003c0147t0002 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0004c0004t0001 | 0/0 | 109225 | 3 | 0 | 3 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0004c0015t0001 | 0/0 | 109225 | 2 | 0 | 0 | 0 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0005c0005t0001 | 0/0 | 109225 | 3 | 0 | 0 | 1 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0005c0117t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0006c0018t0002 | 0/0 | 109224 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0006c0141t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0007c0003t0002 | 0/0 | 109224 | 3 | 0 | 3 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0008c0012t0003 | 0/0 | 109225 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0008c0064t0003 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0009c0093t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0009c0095t0007 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0009c0105t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0010c0013t0002 | 0/0 | 109224 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0010c0072t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0011c0007t0002 | 0/0 | 109224 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0012c0020t0001 | 0/0 | 109225 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0013c0023t0001 | 0/0 | 109225 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0014c0178t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0014c0180t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0015c0176t0001 | 0/0 | 113486 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0015c0182t0001 | 0/0 | 113486 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0016c0170t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0016c0196t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0017c0008t0001 | 0/0 | 109225 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0018c0009t0001 | 0/0 | 109225 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0019c0019t0001 | 0/0 | 109225 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0020c0010t0002 | 0/0 | 109224 | 2 | 0 | 0 | 1 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0021c0011t0001 | 0/0 | 109225 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0022c0014t0001 | 0/0 | 109225 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0023c0016t0001 | 0/0 | 109225 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0024c0017t0001 | 0/0 | 109225 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0025c0028t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0026c0027t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0027c0029t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0028c0026t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0029c0025t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0030c0165t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0031c0162t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0032c0161t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0033c0160t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0034c0159t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0035c0163t0003 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0036c0164t0003 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0037c0158t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0038c0166t0003 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0039c0167t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0040c0169t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0041c0168t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0042c0172t0002 | 0/0 | 113485 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0043c0194t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0044c0193t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0045c0179t0001 | 0/0 | 113486 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0046c0177t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0047c0173t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0048c0185t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0049c0188t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0050c0201t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0051c0184t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0052c0183t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0053c0191t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0054c0187t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0055c0189t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0056c0190t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0057c0181t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0058c0192t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0059c0175t0004 | 0/0 | 109207 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0060c0174t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0061c0198t0001 | 0/0 | 109207 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0062c0199t0001 | 0/0 | 109207 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0063c0200t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0064c0202t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0065c0031t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0066c0032t0008 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0067c0030t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0068c0156t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0069c0155t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0070c0152t0002 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0071c0151t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0072c0154t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0073c0149t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0074c0148t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0075c0145t0002 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0076c0150t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0077c0153t0002 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0078c0055t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0079c0053t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0080c0054t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0081c0067t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0082c0052t0002 | 0/0 | 107718 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0083c0142t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0084c0050t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0085c0049t0001 | 0/0 | 108472 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0086c0118t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0087c0119t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0088c0128t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0089c0066t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0090c0127t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0091c0124t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0092c0126t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0093c0125t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0094c0123t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0095c0122t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0096c0121t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0097c0139t0002 | 0/1 | 109224 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0098c0038t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0099c0132t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0100c0133t0002 | 0/0 | 108471 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0101c0131t0009 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0102c0130t0002 | 0/0 | 108471 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0103c0157t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0104c0042t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0105c0041t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0106c0129t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0107c0043t0001 | 0/0 | 108472 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0108c0040t0002 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0109c0044t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0110c0045t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0111c0047t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0112c0046t0002 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0113c0039t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0114c0048t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0115c0140t0002 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0116c0036t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0117c0037t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0118c0035t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0119c0136t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0120c0134t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0121c0135t0001 | 0/0 | 108472 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0122c0034t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0123c0137t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0124c0120t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0125c0138t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0126c0051t0002 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0127c0143t0002 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0128c0144t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0129c0115t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0130c0056t0003 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0131c0057t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0132c0065t0003 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0133c0062t0002 | 0/0 | 108471 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0134c0058t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0135c0061t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0136c0060t0003 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0137c0059t0003 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0138c0063t0002 | 0/0 | 109224 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0139c0096t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0140c0094t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0141c0092t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0142c0097t0001 | 0/0 | 109261 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0143c0103t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0144c0102t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0145c0099t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0146c0101t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0147c0098t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0148c0100t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0149c0104t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0150c0110t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0151c0112t0001 | 0/0 | 109207 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0152c0113t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0153c0114t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0154c0111t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0155c0108t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0156c0106t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0157c0107t0001 | 0/0 | 108472 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0158c0109t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0159c0091t0010 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0160c0088t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0161c0089t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0162c0090t0002 | 0/0 | 108471 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0163c0080t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0164c0079t0001 | 0/0 | 109225 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0165c0077t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0166c0076t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0167c0070t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0168c0075t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0169c0074t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0170c0071t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0171c0073t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0172c0078t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0173c0069t0002 | 0/0 | 109224 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0174c0081t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0175c0087t0006 | 0/0 | 109224 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0176c0086t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0177c0084t0004 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0178c0085t0004 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0179c0083t0005 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0180c0082t0002 | 1/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0181c0116t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0182c0068t0002 | 0/0 | 109224 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0183c0204t0001 | 0/0 | 109225 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0184c0033t0001 | 0/0 | 109207 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0185c0203t0001 | 0/0 | 109225 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0186c0024t0001 | 0/0 | 109225 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0187c0205t0001 | 0/0 | 109207 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0188c0207t0001 | 0/0 | 109207 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0189c0206t0001 | 0/0 | 109207 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0190c0208t0003 | 0/0 | 109207 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0191c0211t0001 | 0/0 | 109207 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0192c0210t0001 | 0/0 | 109207 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| a0193c0209t0001 | 0/0 | 109207 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | copy fasta | chr2 | 178520989 | 178812423 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0001c0021t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0001c0021t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0001c0171t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0001c0186t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0001c0195t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0001c0197t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0002c0022t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0002c0022t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0003c0006t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0003c0006t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0003c0006t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0003c0146t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0003c0147t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0004c0004t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0004c0004t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0004c0004t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0004c0015t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0004c0015t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0005c0005t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0005c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0005c0117t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0006c0018t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0006c0018t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0006c0141t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0007c0003t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0007c0003t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0007c0003t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0008c0012t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0008c0012t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0008c0064t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0009c0093t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0009c0095t0007g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0009c0105t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0010c0013t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0010c0013t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0010c0072t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0011c0007t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0011c0007t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0012c0020t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0012c0020t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0013c0023t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0013c0023t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0014c0178t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0014c0180t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0015c0176t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0015c0182t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0016c0170t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0016c0196t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0017c0008t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0017c0008t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0018c0009t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0018c0009t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0019c0019t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0019c0019t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0020c0010t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0020c0010t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0021c0011t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0021c0011t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0022c0014t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0022c0014t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0023c0016t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0023c0016t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0024c0017t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0024c0017t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0025c0028t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0026c0027t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0027c0029t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0028c0026t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0029c0025t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0030c0165t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0031c0162t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0032c0161t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0033c0160t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0034c0159t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0035c0163t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0036c0164t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0037c0158t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0038c0166t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0039c0167t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0040c0169t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0041c0168t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0042c0172t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0043c0194t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0044c0193t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0045c0179t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0046c0177t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0047c0173t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0048c0185t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0049c0188t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0050c0201t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0051c0184t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0052c0183t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0053c0191t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0054c0187t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0055c0189t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0056c0190t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0057c0181t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0058c0192t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0059c0175t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0060c0174t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0061c0198t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0062c0199t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0063c0200t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0064c0202t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0065c0031t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0066c0032t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0067c0030t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0068c0156t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0069c0155t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0070c0152t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0071c0151t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0072c0154t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0073c0149t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0074c0148t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0075c0145t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0076c0150t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0077c0153t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0078c0055t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0079c0053t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0080c0054t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0081c0067t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0082c0052t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0083c0142t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0084c0050t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0085c0049t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0086c0118t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0087c0119t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0088c0128t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0089c0066t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0090c0127t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0091c0124t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0092c0126t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0093c0125t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0094c0123t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0095c0122t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0096c0121t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0097c0139t0002g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0098c0038t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0099c0132t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0100c0133t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0101c0131t0009g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0102c0130t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0103c0157t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0104c0042t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0105c0041t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0106c0129t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0107c0043t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0108c0040t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0109c0044t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0110c0045t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0111c0047t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0112c0046t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0113c0039t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0114c0048t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0115c0140t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0116c0036t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0117c0037t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0118c0035t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0119c0136t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0120c0134t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0121c0135t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0122c0034t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0123c0137t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0124c0120t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0125c0138t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0126c0051t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0127c0143t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0128c0144t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0129c0115t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0130c0056t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0131c0057t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0132c0065t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0133c0062t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0134c0058t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0135c0061t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0136c0060t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0137c0059t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0138c0063t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0139c0096t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0140c0094t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0141c0092t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0142c0097t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0143c0103t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0144c0102t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0145c0099t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0146c0101t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0147c0098t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0148c0100t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0149c0104t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0150c0110t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0151c0112t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0152c0113t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0153c0114t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0154c0111t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0155c0108t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0156c0106t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0157c0107t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0158c0109t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0159c0091t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0160c0088t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0161c0089t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0162c0090t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0163c0080t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0164c0079t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0165c0077t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0166c0076t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0167c0070t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0168c0075t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0169c0074t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0170c0071t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0171c0073t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0172c0078t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0173c0069t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0174c0081t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0175c0087t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0176c0086t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0177c0084t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0178c0085t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0179c0083t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0180c0082t0002g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0181c0116t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0182c0068t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0183c0204t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0184c0033t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0185c0203t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0186c0024t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0187c0205t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0188c0207t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0189c0206t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0190c0208t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0191c0211t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0192c0210t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| a0193c0209t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0093 | c0125 | t0002 | g0224 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00408 | hp2 | a0051 | c0184 | t0001 | g0048 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00423 | hp1 | a0113 | c0039 | t0002 | g0132 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00423 | hp2 | a0001 | c0021 | t0001 | g0075 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00438 | hp1 | a0163 | c0080 | t0002 | g0212 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00438 | hp2 | a0135 | c0061 | t0001 | g0178 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00544 | hp1 | a0050 | c0201 | t0001 | g0046 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00544 | hp2 | a0022 | c0014 | t0001 | g0193 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00558 | hp1 | a0161 | c0089 | t0002 | g0211 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00558 | hp2 | a0037 | c0158 | t0002 | g0108 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00597 | hp1 | a0136 | c0060 | t0003 | g0138 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00597 | hp2 | a0054 | c0187 | t0001 | g0037 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00609 | hp1 | a0015 | c0176 | t0001 | g0045 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00609 | hp2 | a0008 | c0012 | t0003 | g0177 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00639 | hp1 | a0117 | c0037 | t0001 | g0127 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00639 | hp2 | a0006 | c0018 | t0002 | g0102 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00642 | hp1 | a0101 | c0131 | t0009 | g0216 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00642 | hp2 | a0004 | c0004 | t0001 | g0168 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00673 | hp1 | a0032 | c0161 | t0002 | g0065 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00673 | hp2 | a0001 | c0186 | t0001 | g0017 | EAS | CHS | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00735 | hp1 | a0191 | c0211 | t0001 | g0074 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00735 | hp2 | a0112 | c0046 | t0002 | g0121 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00741 | hp1 | a0189 | c0206 | t0001 | g0069 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG00741 | hp2 | a0077 | c0153 | t0002 | g0086 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01071 | hp1 | a0075 | c0145 | t0002 | g0089 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01071 | hp2 | a0126 | c0051 | t0002 | g0123 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01099 | hp1 | a0133 | c0062 | t0002 | g0155 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01099 | hp2 | a0188 | c0207 | t0001 | g0070 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01175 | hp1 | a0122 | c0034 | t0001 | g0128 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01175 | hp2 | a0003 | c0146 | t0002 | g0079 | AMR | PUR | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01255 | hp1 | a0164 | c0079 | t0001 | g0197 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01255 | hp2 | a0070 | c0152 | t0002 | g0088 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01257 | hp1 | a0014 | c0178 | t0001 | g0062 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01257 | hp2 | a0145 | c0099 | t0001 | g0170 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01346 | hp1 | a0148 | c0100 | t0001 | g0169 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01346 | hp2 | a0015 | c0182 | t0001 | g0036 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01358 | hp1 | a0108 | c0040 | t0002 | g0124 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01358 | hp2 | a0131 | c0057 | t0001 | g0147 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01361 | hp1 | a0150 | c0110 | t0001 | g0182 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01361 | hp2 | a0006 | c0018 | t0002 | g0105 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01433 | hp1 | a0021 | c0011 | t0001 | g0149 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01433 | hp2 | a0003 | c0147 | t0002 | g0090 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01496 | hp1 | a0004 | c0004 | t0001 | g0172 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01496 | hp2 | a0115 | c0140 | t0002 | g0098 | AMR | CLM | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01884 | hp1 | a0013 | c0023 | t0001 | g0057 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01884 | hp2 | a0074 | c0148 | t0002 | g0087 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01952 | hp1 | a0021 | c0011 | t0001 | g0179 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01952 | hp2 | a0143 | c0103 | t0001 | g0171 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01975 | hp1 | a0058 | c0192 | t0001 | g0063 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01975 | hp2 | a0138 | c0063 | t0002 | g0156 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01978 | hp1 | a0045 | c0179 | t0001 | g0051 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01978 | hp2 | a0102 | c0130 | t0002 | g0103 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01981 | hp1 | a0007 | c0003 | t0002 | g0157 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG01981 | hp2 | a0118 | c0035 | t0001 | g0136 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02004 | hp1 | a0146 | c0101 | t0001 | g0176 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02004 | hp2 | a0007 | c0003 | t0002 | g0158 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02015 | hp1 | a0043 | c0194 | t0002 | g0026 | EAS | KHV | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02015 | hp2 | a0141 | c0092 | t0001 | g0194 | EAS | KHV | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02027 | hp1 | a0086 | c0118 | t0001 | g0218 | EAS | KHV | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02027 | hp2 | a0001 | c0195 | t0001 | g0042 | EAS | KHV | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02040 | hp1 | a0114 | c0048 | t0001 | g0133 | EAS | KHV | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02040 | hp2 | a0022 | c0014 | t0001 | g0195 | EAS | KHV | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02055 | hp1 | a0064 | c0202 | t0001 | g0059 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02055 | hp2 | a0003 | c0006 | t0002 | g0101 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02145 | hp1 | a0017 | c0008 | t0001 | g0107 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02145 | hp2 | a0019 | c0019 | t0001 | g0094 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02155 | hp2 | a0140 | c0094 | t0001 | g0196 | EAS | CDX | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02165 | hp1 | a0001 | c0021 | t0001 | g0076 | EAS | CDX | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02165 | hp2 | a0173 | c0069 | t0002 | g0007 | EAS | CDX | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02257 | hp1 | a0080 | c0054 | t0002 | g0011 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02257 | hp2 | a0159 | c0091 | t0010 | g0175 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02273 | hp1 | a0004 | c0004 | t0001 | g0173 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02273 | hp2 | a0044 | c0193 | t0001 | g0050 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02280 | hp1 | a0082 | c0052 | t0002 | g0113 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02280 | hp2 | a0061 | c0198 | t0001 | g0061 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02293 | hp1 | a0014 | c0180 | t0001 | g0068 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02293 | hp2 | a0144 | c0102 | t0001 | g0185 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02300 | hp1 | a0007 | c0003 | t0002 | g0154 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02300 | hp2 | a0085 | c0049 | t0001 | g0131 | AMR | PEL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02451 | hp1 | a0156 | c0106 | t0001 | g0146 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02451 | hp2 | a0028 | c0026 | t0002 | g0114 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02523 | hp1 | a0137 | c0059 | t0003 | g0148 | EAS | KHV | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02523 | hp2 | a0053 | c0191 | t0001 | g0032 | EAS | KHV | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02602 | hp2 | a0020 | c0010 | t0002 | g0134 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02615 | hp1 | a0193 | c0209 | t0001 | g0071 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02615 | hp2 | a0079 | c0053 | t0002 | g0008 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02630 | hp1 | a0151 | c0112 | t0001 | g0183 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02630 | hp2 | a0003 | c0006 | t0002 | g0083 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02647 | hp1 | a0098 | c0038 | t0001 | g0112 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02647 | hp2 | a0059 | c0175 | t0004 | g0002 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02683 | hp1 | a0182 | c0068 | t0002 | g0109 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02683 | hp2 | a0116 | c0036 | t0001 | g0126 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02698 | hp1 | a0039 | c0167 | t0001 | g0031 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02698 | hp2 | a0106 | c0129 | t0002 | g0231 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02723 | hp1 | a0187 | c0205 | t0001 | g0072 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02723 | hp2 | a0185 | c0203 | t0001 | g0240 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02735 | hp1 | a0105 | c0041 | t0002 | g0130 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02735 | hp2 | a0071 | c0151 | t0002 | g0084 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02738 | hp1 | a0081 | c0067 | t0002 | g0215 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02738 | hp2 | a0183 | c0204 | t0001 | g0139 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02809 | hp1 | a0128 | c0144 | t0001 | g0095 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02809 | hp2 | a0154 | c0111 | t0001 | g0190 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02818 | hp1 | a0026 | c0027 | t0002 | g0119 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02818 | hp2 | a0057 | c0181 | t0001 | g0043 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02895 | hp1 | a0066 | c0032 | t0008 | g0238 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02895 | hp2 | a0023 | c0016 | t0001 | g0192 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02896 | hp1 | a0018 | c0009 | t0001 | g0236 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02896 | hp2 | a0083 | c0142 | t0002 | g0080 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02897 | hp1 | a0018 | c0009 | t0001 | g0237 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02897 | hp2 | a0023 | c0016 | t0001 | g0191 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02922 | hp1 | a0006 | c0141 | t0002 | g0099 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02922 | hp2 | a0157 | c0107 | t0001 | g0145 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02965 | hp1 | a0127 | c0143 | t0002 | g0010 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02965 | hp2 | a0068 | c0156 | t0001 | g0163 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02970 | hp1 | a0181 | c0116 | t0001 | g0142 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02970 | hp2 | a0184 | c0033 | t0001 | g0159 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02976 | hp1 | a0019 | c0019 | t0001 | g0093 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02976 | hp2 | a0013 | c0023 | t0001 | g0056 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03017 | hp1 | a0073 | c0149 | t0002 | g0085 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03017 | hp2 | a0046 | c0177 | t0001 | g0054 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03041 | hp1 | a0009 | c0105 | t0001 | g0167 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03041 | hp2 | a0011 | c0007 | t0002 | g0117 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03098 | hp1 | a0069 | c0155 | t0001 | g0162 | AFR | MSL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03098 | hp2 | a0192 | c0210 | t0001 | g0073 | AFR | MSL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03130 | hp1 | a0179 | c0083 | t0005 | g0003 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03130 | hp2 | a0025 | c0028 | t0002 | g0120 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03139 | hp1 | a0063 | c0200 | t0001 | g0044 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03139 | hp2 | a0178 | c0085 | t0004 | g0004 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03195 | hp1 | a0027 | c0029 | t0001 | g0118 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03195 | hp2 | a0024 | c0017 | t0001 | g0140 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03209 | hp1 | a0109 | c0044 | t0002 | g0110 | AFR | MSL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03209 | hp2 | a0065 | c0031 | t0001 | g0235 | AFR | MSL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03453 | hp1 | a0124 | c0120 | t0001 | g0097 | AFR | MSL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03453 | hp2 | a0072 | c0154 | t0002 | g0092 | AFR | MSL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03490 | hp1 | a0005 | c0005 | t0001 | g0001 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03490 | hp2 | a0004 | c0015 | t0001 | g0186 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03492 | hp1 | a0005 | c0005 | t0001 | g0001 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03492 | hp2 | a0104 | c0042 | t0002 | g0122 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03516 | hp1 | a0158 | c0109 | t0001 | g0143 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03516 | hp2 | a0123 | c0137 | t0001 | g0096 | AFR | ESN | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03540 | hp1 | a0152 | c0113 | t0001 | g0189 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03540 | hp2 | a0129 | c0115 | t0001 | g0241 | AFR | GWD | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03669 | hp1 | a0047 | c0173 | t0001 | g0064 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03669 | hp2 | a0147 | c0098 | t0001 | g0187 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03710 | hp1 | a0099 | c0132 | t0002 | g0214 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03710 | hp2 | a0139 | c0096 | t0001 | g0181 | SAS | PJL | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03831 | hp1 | a0040 | c0169 | t0002 | g0053 | SAS | BEB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03831 | hp2 | a0005 | c0117 | t0001 | g0221 | SAS | BEB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03927 | hp1 | a0049 | c0188 | t0001 | g0078 | SAS | BEB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03927 | hp2 | a0149 | c0104 | t0001 | g0174 | SAS | BEB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03942 | hp1 | a0009 | c0093 | t0001 | g0184 | SAS | BEB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG03942 | hp2 | a0041 | c0168 | t0002 | g0052 | SAS | BEB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG04184 | hp1 | a0142 | c0097 | t0001 | g0164 | SAS | BEB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG04184 | hp2 | a0119 | c0136 | t0002 | g0234 | SAS | BEB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG04199 | hp1 | a0056 | c0190 | t0001 | g0027 | SAS | STU | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG04199 | hp2 | a0004 | c0015 | t0001 | g0165 | SAS | STU | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG04204 | hp2 | a0100 | c0133 | t0002 | g0233 | SAS | STU | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG04228 | hp1 | a0009 | c0095 | t0007 | g0166 | SAS | STU | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG04228 | hp2 | a0170 | c0071 | t0002 | g0200 | SAS | STU | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18612 | hp1 | a0190 | c0208 | t0003 | g0009 | EAS | CHB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18612 | hp2 | a0033 | c0160 | t0002 | g0024 | EAS | CHB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18906 | hp1 | a0175 | c0087 | t0006 | g0006 | AFR | YRI | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18906 | hp2 | a0024 | c0017 | t0001 | g0141 | AFR | YRI | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18943 | hp1 | a0008 | c0064 | t0003 | g0151 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18943 | hp2 | a0010 | c0072 | t0002 | g0204 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18945 | hp1 | a0005 | c0005 | t0001 | g0228 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18948 | hp1 | a0089 | c0066 | t0002 | g0220 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18948 | hp2 | a0172 | c0078 | t0001 | g0208 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18954 | hp1 | a0035 | c0163 | t0003 | g0025 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18954 | hp2 | a0134 | c0058 | t0002 | g0153 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18960 | hp2 | a0095 | c0122 | t0001 | g0226 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18964 | hp1 | a0171 | c0073 | t0002 | g0210 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18964 | hp2 | a0001 | c0197 | t0001 | g0015 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18965 | hp1 | a0002 | c0022 | t0001 | g0066 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18965 | hp2 | a0167 | c0070 | t0001 | g0199 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18966 | hp1 | a0186 | c0024 | t0001 | g0014 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18966 | hp2 | a0034 | c0159 | t0002 | g0018 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18968 | hp1 | a0165 | c0077 | t0001 | g0203 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18968 | hp2 | a0096 | c0121 | t0002 | g0227 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18970 | hp1 | a0121 | c0135 | t0001 | g0232 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18974 | hp1 | a0087 | c0119 | t0001 | g0217 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18974 | hp2 | a0132 | c0065 | t0003 | g0152 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18975 | hp1 | a0016 | c0196 | t0002 | g0047 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18975 | hp2 | a0160 | c0088 | t0001 | g0213 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18980 | hp1 | a0010 | c0013 | t0002 | g0207 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18980 | hp2 | a0012 | c0020 | t0001 | g0021 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18987 | hp1 | a0107 | c0043 | t0001 | g0161 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18987 | hp2 | a0048 | c0185 | t0002 | g0034 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18992 | hp1 | a0120 | c0134 | t0001 | g0230 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19002 | hp1 | a0038 | c0166 | t0003 | g0049 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19002 | hp2 | a0020 | c0010 | t0002 | g0160 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19004 | hp1 | a0094 | c0123 | t0001 | g0219 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19004 | hp2 | a0036 | c0164 | t0003 | g0020 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19005 | hp1 | a0091 | c0124 | t0001 | g0222 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19005 | hp2 | a0002 | c0022 | t0001 | g0067 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19007 | hp1 | a0130 | c0056 | t0003 | g0150 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19010 | hp1 | a0103 | c0157 | t0001 | g0125 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19010 | hp2 | a0052 | c0183 | t0002 | g0016 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19030 | hp1 | a0017 | c0008 | t0001 | g0106 | AFR | LWK | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19030 | hp2 | a0011 | c0007 | t0002 | g0116 | AFR | LWK | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19043 | hp1 | a0153 | c0114 | t0001 | g0188 | AFR | LWK | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19043 | hp2 | a0003 | c0006 | t0002 | g0091 | AFR | LWK | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19054 | hp1 | a0162 | c0090 | t0002 | g0198 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19054 | hp2 | a0008 | c0012 | t0003 | g0180 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19058 | hp1 | a0084 | c0050 | t0002 | g0129 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19058 | hp2 | a0174 | c0081 | t0001 | g0201 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19063 | hp1 | a0010 | c0013 | t0002 | g0206 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19063 | hp2 | a0001 | c0171 | t0001 | g0029 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19065 | hp1 | a0168 | c0075 | t0001 | g0205 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19065 | hp2 | a0016 | c0170 | t0002 | g0028 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19070 | hp1 | a0030 | c0165 | t0002 | g0022 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19070 | hp2 | a0088 | c0128 | t0001 | g0229 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19082 | hp1 | a0012 | c0020 | t0001 | g0019 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19082 | hp2 | a0092 | c0126 | t0001 | g0225 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19084 | hp1 | a0031 | c0162 | t0002 | g0023 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19084 | hp2 | a0090 | c0127 | t0001 | g0223 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19085 | hp1 | a0060 | c0174 | t0001 | g0058 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA19085 | hp2 | a0169 | c0074 | t0002 | g0209 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA20129 | hp1 | a0062 | c0199 | t0001 | g0060 | AFR | ASW | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA20129 | hp2 | a0110 | c0045 | t0002 | g0111 | AFR | ASW | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA20905 | hp1 | a0111 | c0047 | t0001 | g0135 | SAS | GIH | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA20905 | hp2 | a0125 | c0138 | t0001 | g0104 | SAS | GIH | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02486 | hp1 | a0042 | c0172 | t0002 | g0055 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02486 | hp2 | a0078 | c0055 | t0002 | g0012 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02559 | hp1 | a0177 | c0084 | t0004 | g0005 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| HG02559 | hp2 | a0029 | c0025 | t0002 | g0115 | AFR | ACB | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18955 | hp1 | a0055 | c0189 | t0001 | g0033 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA18955 | hp2 | a0166 | c0076 | t0002 | g0202 | EAS | JPT | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA20300 | hp1 | a0176 | c0086 | t0001 | g0082 | AFR | USA | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA20300 | hp2 | a0067 | c0030 | t0001 | g0239 | AFR | USA | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA21309 | hp1 | a0076 | c0150 | t0002 | g0137 | AFR | LWK | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| NA21309 | hp2 | a0155 | c0108 | t0001 | g0144 | AFR | LWK | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| homoSapiens_chm13v2 | hp1 | a0097 | c0139 | t0002 | g0100 | REF | REF | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| homoSapiens_grch38 | hp1 | a0180 | c0082 | t0002 | g0081 | REF | REF | TTN_chr2_178520989_178812423 | TTN | chr2 | 178520989 | 178812423 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:178527550
|
A | G | 2 | a0040a0041 | 2 | HG03831.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.107576T>C | p.Met35859Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 362/363 | 107801/109224 | 107576/107976 | 35859/35991 | chr2 | 178527550 | ||
| chr2:178528384
|
A | G | 20 | a0002a0012a0015others(17): Show | 27 | HG00609.hp1 HG00735.hp1 HG01346.hp2 others(24): Show |
missense_variant | MODERATE | c.107267T>C | p.Val35756Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 361/363 | 107492/109224 | 107267/107976 | 35756/35991 | chr2 | 178528384 | ||
| chr2:178528631
|
T | A | 1 | a0191 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.107120A>T | p.Gln35707Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 360/363 | 107345/109224 | 107120/107976 | 35707/35991 | chr2 | 178528631 | ||
| chr2:178528797
|
G | A | 1 | a0182 | 1 | HG02683.hp1 | stop_gained | HIGH | c.106954C>T | p.Arg35652* | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 360/363 | 107179/109224 | 106954/107976 | 35652/35991 | chr2 | 178528797 | ||
| chr2:178528893
|
C | T | 1 | a0023 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.106858G>A | p.Glu35620Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 360/363 | 107083/109224 | 106858/107976 | 35620/35991 | chr2 | 178528893 | ||
| chr2:178529132
|
A | G | 1 | a0077 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.106619T>C | p.Ile35540Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 360/363 | 106844/109224 | 106619/107976 | 35540/35991 | chr2 | 178529132 | ||
| chr2:178529171
|
T | A | 1 | a0128 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.106580A>T | p.Glu35527Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 360/363 | 106805/109224 | 106580/107976 | 35527/35991 | chr2 | 178529171 | ||
| chr2:178530273
|
G | A | 1 | a0086 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.106342C>T | p.Arg35448Trp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 106567/109224 | 106342/107976 | 35448/35991 | chr2 | 178530273 | ||
| chr2:178530573
|
T | G | 1 | a0055 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.106042A>C | p.Asn35348His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 106267/109224 | 106042/107976 | 35348/35991 | chr2 | 178530573 | ||
| chr2:178530833
|
G | A | 16 | a0002a0012a0015others(13): Show | 23 | HG00609.hp1 HG00735.hp1 HG01346.hp2 others(20): Show |
missense_variant | MODERATE | c.105782C>T | p.Pro35261Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 106007/109224 | 105782/107976 | 35261/35991 | chr2 | 178530833 | ||
| chr2:178531086
|
C | T | 3 | a0018a0019a0067 | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.105529G>A | p.Val35177Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 105754/109224 | 105529/107976 | 35177/35991 | chr2 | 178531086 | ||
| chr2:178531148
|
G | C | 1 | a0140 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.105467C>G | p.Pro35156Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 105692/109224 | 105467/107976 | 35156/35991 | chr2 | 178531148 | ||
| chr2:178531403
|
G | C | 1 | a0090 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.105212C>G | p.Ser35071Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 105437/109224 | 105212/107976 | 35071/35991 | chr2 | 178531403 | ||
| chr2:178531435
|
C | G | 7 | a0014a0021a0044others(4): Show | 9 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(6): Show |
missense_variant | MODERATE | c.105180G>C | p.Glu35060Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 105405/109224 | 105180/107976 | 35060/35991 | chr2 | 178531435 | ||
| chr2:178531488
|
G | A | 1 | a0028 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.105127C>T | p.Arg35043Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 105352/109224 | 105127/107976 | 35043/35991 | chr2 | 178531488 | ||
| chr2:178531602
|
G | A | 1 | a0171 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.105013C>T | p.His35005Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 105238/109224 | 105013/107976 | 35005/35991 | chr2 | 178531602 | ||
| chr2:178532238
|
T | G | 2 | a0177a0178 | 2 | HG02559.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.104377A>C | p.Met34793Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 104602/109224 | 104377/107976 | 34793/35991 | chr2 | 178532238 | ||
| chr2:178532706
|
G | A | 1 | a0117 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.103909C>T | p.Arg34637Trp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 104134/109224 | 103909/107976 | 34637/35991 | chr2 | 178532706 | ||
| chr2:178532834
|
C | T | 46 | a0001a0005a0013others(43): Show | 61 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
missense_variant | MODERATE | c.103781G>A | p.Arg34594His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 104006/109224 | 103781/107976 | 34594/35991 | chr2 | 178532834 | ||
| chr2:178533203
|
C | T | 2 | a0051a0092 | 2 | HG00408.hp2 NA19082.hp2 |
missense_variant | MODERATE | c.103412G>A | p.Arg34471Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 103637/109224 | 103412/107976 | 34471/35991 | chr2 | 178533203 | ||
| chr2:178533252
|
G | A | 2 | a0061a0062 | 2 | HG02280.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.103363C>T | p.Arg34455Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 103588/109224 | 103363/107976 | 34455/35991 | chr2 | 178533252 | ||
| chr2:178533297
|
T | C | 1 | a0071 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.103318A>G | p.Asn34440Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 103543/109224 | 103318/107976 | 34440/35991 | chr2 | 178533297 | ||
| chr2:178533468
|
C | G | 1 | a0149 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.103147G>C | p.Glu34383Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 103372/109224 | 103147/107976 | 34383/35991 | chr2 | 178533468 | ||
| chr2:178533782
|
C | A | 16 | a0002a0012a0015others(13): Show | 23 | HG00609.hp1 HG00735.hp1 HG01346.hp2 others(20): Show |
missense_variant | MODERATE | c.102833G>T | p.Gly34278Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 103058/109224 | 102833/107976 | 34278/35991 | chr2 | 178533782 | ||
| chr2:178534020
|
T | C | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.102595A>G | p.Ile34199Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 102820/109224 | 102595/107976 | 34199/35991 | chr2 | 178534020 | ||
| chr2:178534512
|
C | T | 1 | a0098 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.102103G>A | p.Asp34035Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 102328/109224 | 102103/107976 | 34035/35991 | chr2 | 178534512 | ||
| chr2:178534724
|
C | T | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.101891G>A | p.Arg33964His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 102116/109224 | 101891/107976 | 33964/35991 | chr2 | 178534724 | ||
| chr2:178534812
|
T | C | 4 | a0159a0177a0178others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
missense_variant | MODERATE | c.101803A>G | p.Ile33935Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 102028/109224 | 101803/107976 | 33935/35991 | chr2 | 178534812 | ||
| chr2:178535220
|
T | C | 1 | a0032 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.101395A>G | p.Thr33799Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 101620/109224 | 101395/107976 | 33799/35991 | chr2 | 178535220 | ||
| chr2:178535370
|
C | T | 2 | a0028a0029 | 2 | HG02451.hp2 HG02559.hp2 |
missense_variant | MODERATE | c.101245G>A | p.Val33749Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 101470/109224 | 101245/107976 | 33749/35991 | chr2 | 178535370 | ||
| chr2:178535403
|
G | A | 1 | a0112 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.101212C>T | p.Arg33738Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 101437/109224 | 101212/107976 | 33738/35991 | chr2 | 178535403 | ||
| chr2:178536168
|
C | T | 14 | a0002a0012a0015others(11): Show | 21 | HG00609.hp1 HG00735.hp1 HG01346.hp2 others(18): Show |
missense_variant | MODERATE | c.100579G>A | p.Val33527Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 357/363 | 100804/109224 | 100579/107976 | 33527/35991 | chr2 | 178536168 | ||
| chr2:178536288
|
G | A | 5 | a0059a0151a0187others(2): Show | 5 | HG02615.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
missense_variant | MODERATE | c.100459C>T | p.Pro33487Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 357/363 | 100684/109224 | 100459/107976 | 33487/35991 | chr2 | 178536288 | ||
| chr2:178536347
|
A | C | 1 | a0122 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.100400T>G | p.Val33467Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 357/363 | 100625/109224 | 100400/107976 | 33467/35991 | chr2 | 178536347 | ||
| chr2:178537013
|
C | T | 9 | a0008a0035a0036others(6): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
missense_variant | MODERATE | c.100096G>A | p.Val33366Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 356/363 | 100321/109224 | 100096/107976 | 33366/35991 | chr2 | 178537013 | ||
| chr2:178537015
|
C | T | 1 | a0131 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.100094G>A | p.Arg33365Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 356/363 | 100319/109224 | 100094/107976 | 33365/35991 | chr2 | 178537015 | ||
| chr2:178537118
|
A | G | 1 | a0076 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.99991T>C | p.Cys33331Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 356/363 | 100216/109224 | 99991/107976 | 33331/35991 | chr2 | 178537118 | ||
| chr2:178537647
|
T | G | 1 | a0126 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.99560A>C | p.Lys33187Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 355/363 | 99785/109224 | 99560/107976 | 33187/35991 | chr2 | 178537647 | ||
| chr2:178538753
|
C | G | 1 | a0173 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.99076G>C | p.Gly33026Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 354/363 | 99301/109224 | 99076/107976 | 33026/35991 | chr2 | 178538753 | ||
| chr2:178539023
|
C | T | 16 | a0004a0009a0022others(13): Show | 23 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(20): Show |
missense_variant | MODERATE | c.98912G>A | p.Arg32971His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 353/363 | 99137/109224 | 98912/107976 | 32971/35991 | chr2 | 178539023 | ||
| chr2:178539109
|
G | C | 1 | a0080 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.98826C>G | p.Asp32942Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 353/363 | 99051/109224 | 98826/107976 | 32942/35991 | chr2 | 178539109 | ||
| chr2:178539450
|
G | C | 1 | a0052 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.98615C>G | p.Ala32872Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 352/363 | 98840/109224 | 98615/107976 | 32872/35991 | chr2 | 178539450 | ||
| chr2:178539680
|
A | C | 1 | a0067 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.98385T>G | p.Ser32795Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 352/363 | 98610/109224 | 98385/107976 | 32795/35991 | chr2 | 178539680 | ||
| chr2:178539771
|
G | C | 1 | a0070 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.98294C>G | p.Ala32765Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 352/363 | 98519/109224 | 98294/107976 | 32765/35991 | chr2 | 178539771 | ||
| chr2:178539901
|
T | A | 5 | a0002a0012a0015others(2): Show | 12 | HG00609.hp1 HG01346.hp2 HG01981.hp2 others(9): Show |
missense_variant | MODERATE | c.98164A>T | p.Ile32722Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 352/363 | 98389/109224 | 98164/107976 | 32722/35991 | chr2 | 178539901 | ||
| chr2:178539904
|
C | T | 1 | a0134 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.98161G>A | p.Val32721Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 352/363 | 98386/109224 | 98161/107976 | 32721/35991 | chr2 | 178539904 | ||
| chr2:178541317
|
C | G | 1 | a0176 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.97760G>C | p.Arg32587Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 350/363 | 97985/109224 | 97760/107976 | 32587/35991 | chr2 | 178541317 | ||
| chr2:178541464
|
C | T | 46 | a0001a0005a0013others(43): Show | 61 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
missense_variant | MODERATE | c.97613G>A | p.Arg32538His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 350/363 | 97838/109224 | 97613/107976 | 32538/35991 | chr2 | 178541464 | ||
| chr2:178542266
|
A | G | 3 | a0042a0079a0080 | 3 | HG02257.hp1 HG02486.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.97490T>C | p.Ile32497Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 349/363 | 97715/109224 | 97490/107976 | 32497/35991 | chr2 | 178542266 | ||
| chr2:178542910
|
G | A | 7 | a0023a0027a0150others(4): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.96944C>T | p.Thr32315Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 348/363 | 97169/109224 | 96944/107976 | 32315/35991 | chr2 | 178542910 | ||
| chr2:178543986
|
A | G | 28 | a0004a0009a0017others(25): Show | 38 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(35): Show |
missense_variant | MODERATE | c.96158T>C | p.Ile32053Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 346/363 | 96383/109224 | 96158/107976 | 32053/35991 | chr2 | 178543986 | ||
| chr2:178544213
|
C | T | 1 | a0146 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.96016G>A | p.Val32006Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 345/363 | 96241/109224 | 96016/107976 | 32006/35991 | chr2 | 178544213 | ||
| chr2:178545528
|
T | C | 1 | a0082 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.95582A>G | p.Tyr31861Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 344/363 | 95807/109224 | 95582/107976 | 31861/35991 | chr2 | 178545528 | ||
| chr2:178545939
|
G | A | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.95297C>T | p.Ser31766Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 343/363 | 95522/109224 | 95297/107976 | 31766/35991 | chr2 | 178545939 | ||
| chr2:178545994
|
G | A | 1 | a0128 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.95242C>T | p.Arg31748Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 343/363 | 95467/109224 | 95242/107976 | 31748/35991 | chr2 | 178545994 | ||
| chr2:178546253
|
G | T | 2 | a0050a0135 | 2 | HG00438.hp2 HG00544.hp1 |
missense_variant | MODERATE | c.95078C>A | p.Ala31693Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 342/363 | 95303/109224 | 95078/107976 | 31693/35991 | chr2 | 178546253 | ||
| chr2:178546284
|
T | C | 9 | a0008a0035a0036others(6): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
missense_variant | MODERATE | c.95047A>G | p.Ser31683Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 342/363 | 95272/109224 | 95047/107976 | 31683/35991 | chr2 | 178546284 | ||
| chr2:178546296
|
C | T | 2 | a0068a0069 | 2 | HG02965.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.95035G>A | p.Asp31679Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 342/363 | 95260/109224 | 95035/107976 | 31679/35991 | chr2 | 178546296 | ||
| chr2:178547243
|
G | A | 1 | a0171 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.94282C>T | p.Arg31428Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 340/363 | 94507/109224 | 94282/107976 | 31428/35991 | chr2 | 178547243 | ||
| chr2:178547725
|
C | T | 8 | a0057a0063a0068others(5): Show | 8 | HG02818.hp2 HG02922.hp2 HG02965.hp2 others(5): Show |
missense_variant | MODERATE | c.93901G>A | p.Val31301Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 339/363 | 94126/109224 | 93901/107976 | 31301/35991 | chr2 | 178547725 | ||
| chr2:178549435
|
T | C | 11 | a0007a0010a0016others(8): Show | 16 | HG00558.hp2 HG01099.hp1 HG01975.hp2 others(13): Show |
missense_variant | MODERATE | c.92191A>G | p.Ile30731Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 339/363 | 92416/109224 | 92191/107976 | 30731/35991 | chr2 | 178549435 | ||
| chr2:178549591
|
C | T | 36 | a0004a0009a0017others(33): Show | 46 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(43): Show |
missense_variant | MODERATE | c.92131G>A | p.Val30711Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 338/363 | 92356/109224 | 92131/107976 | 30711/35991 | chr2 | 178549591 | ||
| chr2:178549838
|
T | A | 2 | a0068a0069 | 2 | HG02965.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.91884A>T | p.Arg30628Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 338/363 | 92109/109224 | 91884/107976 | 30628/35991 | chr2 | 178549838 | ||
| chr2:178550073
|
C | T | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.91765G>A | p.Ala30589Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 337/363 | 91990/109224 | 91765/107976 | 30589/35991 | chr2 | 178550073 | ||
| chr2:178550195
|
G | A | 1 | a0071 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.91643C>T | p.Ala30548Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 337/363 | 91868/109224 | 91643/107976 | 30548/35991 | chr2 | 178550195 | ||
| chr2:178550237
|
T | A | 1 | a0081 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.91601A>T | p.Asp30534Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 337/363 | 91826/109224 | 91601/107976 | 30534/35991 | chr2 | 178550237 | ||
| chr2:178551932
|
C | T | 8 | a0057a0063a0068others(5): Show | 8 | HG02818.hp2 HG02922.hp2 HG02965.hp2 others(5): Show |
missense_variant | MODERATE | c.90968G>A | p.Arg30323Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 335/363 | 91193/109224 | 90968/107976 | 30323/35991 | chr2 | 178551932 | ||
| chr2:178552074
|
A | C | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.90826T>G | p.Cys30276Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 335/363 | 91051/109224 | 90826/107976 | 30276/35991 | chr2 | 178552074 | ||
| chr2:178552262
|
A | G | 2 | a0066a0179 | 2 | HG02895.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.90638T>C | p.Ile30213Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 335/363 | 90863/109224 | 90638/107976 | 30213/35991 | chr2 | 178552262 | ||
| chr2:178552364
|
C | T | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.90536G>A | p.Arg30179His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 335/363 | 90761/109224 | 90536/107976 | 30179/35991 | chr2 | 178552364 | ||
| chr2:178553688
|
T | A | 3 | a0018a0019a0067 | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.89317A>T | p.Ile29773Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 334/363 | 89542/109224 | 89317/107976 | 29773/35991 | chr2 | 178553688 | ||
| chr2:178554600
|
T | C | 1 | a0187 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.88747A>G | p.Met29583Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 332/363 | 88972/109224 | 88747/107976 | 29583/35991 | chr2 | 178554600 | ||
| chr2:178554627
|
G | A | 1 | a0031 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.88720C>T | p.Arg29574Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 332/363 | 88945/109224 | 88720/107976 | 29574/35991 | chr2 | 178554627 | ||
| chr2:178554639
|
T | C | 3 | a0042a0079a0080 | 3 | HG02257.hp1 HG02486.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.88708A>G | p.Ile29570Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 332/363 | 88933/109224 | 88708/107976 | 29570/35991 | chr2 | 178554639 | ||
| chr2:178556857
|
C | T | 1 | a0123 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.88297G>A | p.Asp29433Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/363 | 88522/109224 | 88297/107976 | 29433/35991 | chr2 | 178556857 | ||
| chr2:178556967
|
A | G | 121 | a0001a0002a0004others(118): Show | 157 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(154): Show |
missense_variant | MODERATE | c.88187T>C | p.Ile29396Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/363 | 88412/109224 | 88187/107976 | 29396/35991 | chr2 | 178556967 | ||
| chr2:178557385
|
G | A | 1 | a0113 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.87877C>T | p.Arg29293Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 329/363 | 88102/109224 | 87877/107976 | 29293/35991 | chr2 | 178557385 | ||
| chr2:178557454
|
C | T | 1 | a0073 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.87808G>A | p.Val29270Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 329/363 | 88033/109224 | 87808/107976 | 29270/35991 | chr2 | 178557454 | ||
| chr2:178559409
|
T | C | 1 | a0026 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.86723A>G | p.Asn28908Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 86948/109224 | 86723/107976 | 28908/35991 | chr2 | 178559409 | ||
| chr2:178560441
|
T | A | 1 | a0156 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.85691A>T | p.Lys28564Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 85916/109224 | 85691/107976 | 28564/35991 | chr2 | 178560441 | ||
| chr2:178560481
|
G | T | 1 | a0120 | 1 | NA18992.hp1 | missense_variant | MODERATE | c.85651C>A | p.Pro28551Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 85876/109224 | 85651/107976 | 28551/35991 | chr2 | 178560481 | ||
| chr2:178560726
|
G | C | 1 | a0190 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.85406C>G | p.Ser28469Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 85631/109224 | 85406/107976 | 28469/35991 | chr2 | 178560726 | ||
| chr2:178561780
|
G | A | 7 | a0023a0027a0150others(4): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.84352C>T | p.Arg28118Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 84577/109224 | 84352/107976 | 28118/35991 | chr2 | 178561780 | ||
| chr2:178562230
|
G | A | 1 | a0121 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.83902C>T | p.Pro27968Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 84127/109224 | 83902/107976 | 27968/35991 | chr2 | 178562230 | ||
| chr2:178562392
|
T | C | 3 | a0042a0079a0080 | 3 | HG02257.hp1 HG02486.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.83740A>G | p.Thr27914Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 83965/109224 | 83740/107976 | 27914/35991 | chr2 | 178562392 | ||
| chr2:178562809
|
T | C | 121 | a0001a0002a0004others(118): Show | 157 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(154): Show |
missense_variant | MODERATE | c.83323A>G | p.Ile27775Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 83548/109224 | 83323/107976 | 27775/35991 | chr2 | 178562809 | ||
| chr2:178563069
|
C | G | 1 | a0152 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.83063G>C | p.Arg27688Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 83288/109224 | 83063/107976 | 27688/35991 | chr2 | 178563069 | ||
| chr2:178563076
|
C | T | 7 | a0023a0027a0150others(4): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.83056G>A | p.Val27686Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 83281/109224 | 83056/107976 | 27686/35991 | chr2 | 178563076 | ||
| chr2:178563334
|
C | T | 8 | a0057a0063a0068others(5): Show | 8 | HG02818.hp2 HG02922.hp2 HG02965.hp2 others(5): Show |
missense_variant | MODERATE | c.82798G>A | p.Ala27600Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 83023/109224 | 82798/107976 | 27600/35991 | chr2 | 178563334 | ||
| chr2:178563572
|
G | T | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.82560C>A | p.Asn27520Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 82785/109224 | 82560/107976 | 27520/35991 | chr2 | 178563572 | ||
| chr2:178563747
|
G | T | 5 | a0018a0019a0067others(2): Show | 7 | HG02145.hp2 HG02451.hp1 HG02809.hp1 others(4): Show |
missense_variant | MODERATE | c.82385C>A | p.Thr27462Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 82610/109224 | 82385/107976 | 27462/35991 | chr2 | 178563747 | ||
| chr2:178564174
|
C | T | 7 | a0023a0027a0150others(4): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.81958G>A | p.Ala27320Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 82183/109224 | 81958/107976 | 27320/35991 | chr2 | 178564174 | ||
| chr2:178565026
|
T | C | 1 | a0137 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.81106A>G | p.Lys27036Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 81331/109224 | 81106/107976 | 27036/35991 | chr2 | 178565026 | ||
| chr2:178565274
|
G | A | 1 | a0170 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.80858C>T | p.Thr26953Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 81083/109224 | 80858/107976 | 26953/35991 | chr2 | 178565274 | ||
| chr2:178565497
|
G | T | 3 | a0068a0069a0157 | 3 | HG02922.hp2 HG02965.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.80635C>A | p.Gln26879Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 80860/109224 | 80635/107976 | 26879/35991 | chr2 | 178565497 | ||
| chr2:178565706
|
C | T | 1 | a0130 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.80426G>A | p.Gly26809Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 80651/109224 | 80426/107976 | 26809/35991 | chr2 | 178565706 | ||
| chr2:178566031
|
A | G | 1 | a0147 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.80101T>C | p.Phe26701Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 80326/109224 | 80101/107976 | 26701/35991 | chr2 | 178566031 | ||
| chr2:178566270
|
G | A | 82 | a0001a0002a0005others(79): Show | 107 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
missense_variant | MODERATE | c.79862C>T | p.Thr26621Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 80087/109224 | 79862/107976 | 26621/35991 | chr2 | 178566270 | ||
| chr2:178566349
|
C | G | 3 | a0081a0099a0100 | 3 | HG02738.hp1 HG03710.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.79783G>C | p.Asp26595His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 80008/109224 | 79783/107976 | 26595/35991 | chr2 | 178566349 | ||
| chr2:178566432
|
T | C | 3 | a0022a0140a0141 | 4 | HG00544.hp2 HG02015.hp2 HG02040.hp2 others(1): Show |
missense_variant | MODERATE | c.79700A>G | p.Asn26567Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 79925/109224 | 79700/107976 | 26567/35991 | chr2 | 178566432 | ||
| chr2:178566612
|
G | T | 1 | a0189 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.79520C>A | p.Ala26507Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 79745/109224 | 79520/107976 | 26507/35991 | chr2 | 178566612 | ||
| chr2:178566613
|
C | T | 1 | a0189 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.79519G>A | p.Ala26507Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 79744/109224 | 79519/107976 | 26507/35991 | chr2 | 178566613 | ||
| chr2:178566813
|
C | T | 2 | a0024a0181 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.79319G>A | p.Arg26440His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 79544/109224 | 79319/107976 | 26440/35991 | chr2 | 178566813 | ||
| chr2:178566814
|
G | A | 2 | a0150a0155 | 2 | HG01361.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.79318C>T | p.Arg26440Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 79543/109224 | 79318/107976 | 26440/35991 | chr2 | 178566814 | ||
| chr2:178566867
|
A | G | 9 | a0008a0035a0036others(6): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
missense_variant | MODERATE | c.79265T>C | p.Ile26422Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 79490/109224 | 79265/107976 | 26422/35991 | chr2 | 178566867 | ||
| chr2:178566952
|
C | G | 1 | a0036 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.79180G>C | p.Glu26394Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 79405/109224 | 79180/107976 | 26394/35991 | chr2 | 178566952 | ||
| chr2:178567458
|
A | G | 11 | a0020a0040a0041others(8): Show | 12 | HG00423.hp1 HG01071.hp1 HG01358.hp1 others(9): Show |
missense_variant | MODERATE | c.78674T>C | p.Ile26225Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 78899/109224 | 78674/107976 | 26225/35991 | chr2 | 178567458 | ||
| chr2:178567494
|
A | G | 1 | a0163 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.78638T>C | p.Leu26213Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 78863/109224 | 78638/107976 | 26213/35991 | chr2 | 178567494 | ||
| chr2:178568494
|
T | C | 9 | a0008a0035a0036others(6): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
missense_variant | MODERATE | c.77638A>G | p.Thr25880Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 77863/109224 | 77638/107976 | 25880/35991 | chr2 | 178568494 | ||
| chr2:178568853
|
T | C | 9 | a0008a0035a0036others(6): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
missense_variant | MODERATE | c.77279A>G | p.Asn25760Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 77504/109224 | 77279/107976 | 25760/35991 | chr2 | 178568853 | ||
| chr2:178569412
|
A | G | 9 | a0008a0035a0036others(6): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
missense_variant | MODERATE | c.76720T>C | p.Tyr25574His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 76945/109224 | 76720/107976 | 25574/35991 | chr2 | 178569412 | ||
| chr2:178569487
|
C | T | 1 | a0148 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.76645G>A | p.Gly25549Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 76870/109224 | 76645/107976 | 25549/35991 | chr2 | 178569487 | ||
| chr2:178569789
|
C | T | 17 | a0002a0012a0015others(14): Show | 24 | HG00609.hp1 HG00735.hp1 HG01346.hp2 others(21): Show |
missense_variant | MODERATE | c.76343G>A | p.Ser25448Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 76568/109224 | 76343/107976 | 25448/35991 | chr2 | 178569789 | ||
| chr2:178570254
|
G | C | 1 | a0092 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.75878C>G | p.Ser25293Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 76103/109224 | 75878/107976 | 25293/35991 | chr2 | 178570254 | ||
| chr2:178570771
|
T | C | 1 | a0177 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.75361A>G | p.Ile25121Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 75586/109224 | 75361/107976 | 25121/35991 | chr2 | 178570771 | ||
| chr2:178571160
|
A | G | 3 | a0068a0069a0157 | 3 | HG02922.hp2 HG02965.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.74972T>C | p.Ile24991Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 75197/109224 | 74972/107976 | 24991/35991 | chr2 | 178571160 | ||
| chr2:178571241
|
G | A | 1 | a0062 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.74891C>T | p.Pro24964Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 75116/109224 | 74891/107976 | 24964/35991 | chr2 | 178571241 | ||
| chr2:178571293
|
G | A | 45 | a0001a0005a0013others(42): Show | 60 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(57): Show |
missense_variant | MODERATE | c.74839C>T | p.Arg24947Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 75064/109224 | 74839/107976 | 24947/35991 | chr2 | 178571293 | ||
| chr2:178571988
|
G | A | 1 | a0053 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.74144C>T | p.Pro24715Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 74369/109224 | 74144/107976 | 24715/35991 | chr2 | 178571988 | ||
| chr2:178572138
|
G | A | 1 | a0169 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.73994C>T | p.Thr24665Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 74219/109224 | 73994/107976 | 24665/35991 | chr2 | 178572138 | ||
| chr2:178572964
|
T | C | 1 | a0176 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.73168A>G | p.Thr24390Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 73393/109224 | 73168/107976 | 24390/35991 | chr2 | 178572964 | ||
| chr2:178573329
|
C | T | 1 | a0036 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.72803G>A | p.Arg24268His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 73028/109224 | 72803/107976 | 24268/35991 | chr2 | 178573329 | ||
| chr2:178574139
|
C | T | 21 | a0004a0009a0017others(18): Show | 30 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(27): Show |
missense_variant | MODERATE | c.71993G>A | p.Arg23998His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 72218/109224 | 71993/107976 | 23998/35991 | chr2 | 178574139 | ||
| chr2:178574763
|
C | T | 3 | a0050a0135a0160 | 3 | HG00438.hp2 HG00544.hp1 NA18975.hp2 |
missense_variant | MODERATE | c.71369G>A | p.Arg23790His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 71594/109224 | 71369/107976 | 23790/35991 | chr2 | 178574763 | ||
| chr2:178575180
|
A | C | 2 | a0123a0124 | 2 | HG03453.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.70952T>G | p.Ile23651Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 71177/109224 | 70952/107976 | 23651/35991 | chr2 | 178575180 | ||
| chr2:178575225
|
C | T | 4 | a0090a0091a0094others(1): Show | 4 | NA18948.hp2 NA19004.hp1 NA19005.hp1 others(1): Show |
missense_variant | MODERATE | c.70907G>A | p.Arg23636His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 71132/109224 | 70907/107976 | 23636/35991 | chr2 | 178575225 | ||
| chr2:178575300
|
G | A | 1 | a0178 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.70832C>T | p.Ala23611Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 71057/109224 | 70832/107976 | 23611/35991 | chr2 | 178575300 | ||
| chr2:178575882
|
A | G | 1 | a0069 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.70250T>C | p.Ile23417Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 70475/109224 | 70250/107976 | 23417/35991 | chr2 | 178575882 | ||
| chr2:178576392
|
G | A | 2 | a0064a0158 | 2 | HG02055.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.69740C>T | p.Pro23247Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 69965/109224 | 69740/107976 | 23247/35991 | chr2 | 178576392 | ||
| chr2:178577106
|
G | A | 1 | a0074 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.69229C>T | p.Leu23077Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 324/363 | 69454/109224 | 69229/107976 | 23077/35991 | chr2 | 178577106 | ||
| chr2:178577190
|
T | C | 8 | a0057a0063a0068others(5): Show | 8 | HG02818.hp2 HG02922.hp2 HG02965.hp2 others(5): Show |
missense_variant | MODERATE | c.69145A>G | p.Ile23049Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 324/363 | 69370/109224 | 69145/107976 | 23049/35991 | chr2 | 178577190 | ||
| chr2:178577354
|
G | A | 1 | a0103 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.68981C>T | p.Thr22994Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 324/363 | 69206/109224 | 68981/107976 | 22994/35991 | chr2 | 178577354 | ||
| chr2:178579070
|
C | G | 1 | a0034 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.67960G>C | p.Asp22654His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 320/363 | 68185/109224 | 67960/107976 | 22654/35991 | chr2 | 178579070 | ||
| chr2:178579324
|
C | T | 1 | a0145 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.67706G>A | p.Arg22569Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 320/363 | 67931/109224 | 67706/107976 | 22569/35991 | chr2 | 178579324 | ||
| chr2:178580041
|
C | G | 191 | a0001a0002a0003others(188): Show | 239 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(236): Show |
missense_variant | MODERATE | c.67246G>C | p.Ala22416Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 318/363 | 67471/109224 | 67246/107976 | 22416/35991 | chr2 | 178580041 | ||
| chr2:178580212
|
C | T | 87 | a0001a0002a0005others(84): Show | 112 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
missense_variant | MODERATE | c.67075G>A | p.Val22359Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 318/363 | 67300/109224 | 67075/107976 | 22359/35991 | chr2 | 178580212 | ||
| chr2:178581983
|
C | T | 1 | a0157 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.66386G>A | p.Arg22129His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 315/363 | 66611/109224 | 66386/107976 | 22129/35991 | chr2 | 178581983 | ||
| chr2:178582049
|
C | T | 1 | a0158 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.66320G>A | p.Arg22107Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 315/363 | 66545/109224 | 66320/107976 | 22107/35991 | chr2 | 178582049 | ||
| chr2:178583060
|
G | T | 3 | a0068a0069a0157 | 3 | HG02922.hp2 HG02965.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.65743C>A | p.Gln21915Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 313/363 | 65968/109224 | 65743/107976 | 21915/35991 | chr2 | 178583060 | ||
| chr2:178583666
|
G | A | 2 | a0110a0175 | 2 | NA18906.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.65516C>T | p.Ala21839Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 312/363 | 65741/109224 | 65516/107976 | 21839/35991 | chr2 | 178583666 | ||
| chr2:178583723
|
G | A | 1 | a0128 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.65459C>T | p.Thr21820Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 312/363 | 65684/109224 | 65459/107976 | 21820/35991 | chr2 | 178583723 | ||
| chr2:178584404
|
G | A | 1 | a0104 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.65147C>T | p.Ser21716Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 311/363 | 65372/109224 | 65147/107976 | 21716/35991 | chr2 | 178584404 | ||
| chr2:178584459
|
G | A | 2 | a0087a0142 | 2 | HG04184.hp1 NA18974.hp1 |
missense_variant | MODERATE | c.65092C>T | p.Arg21698Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 311/363 | 65317/109224 | 65092/107976 | 21698/35991 | chr2 | 178584459 | ||
| chr2:178584830
|
C | T | 1 | a0133 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.64811G>A | p.Arg21604Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 310/363 | 65036/109224 | 64811/107976 | 21604/35991 | chr2 | 178584830 | ||
| chr2:178584852
|
C | T | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.64789G>A | p.Val21597Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 310/363 | 65014/109224 | 64789/107976 | 21597/35991 | chr2 | 178584852 | ||
| chr2:178584879
|
C | T | 3 | a0042a0079a0080 | 3 | HG02257.hp1 HG02486.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.64762G>A | p.Gly21588Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 310/363 | 64987/109224 | 64762/107976 | 21588/35991 | chr2 | 178584879 | ||
| chr2:178586693
|
G | A | 123 | a0001a0002a0004others(120): Show | 159 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(156): Show |
missense_variant | MODERATE | c.64208C>T | p.Thr21403Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 308/363 | 64433/109224 | 64208/107976 | 21403/35991 | chr2 | 178586693 | ||
| chr2:178587701
|
G | T | 1 | a0018 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.63608C>A | p.Ala21203Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 306/363 | 63833/109224 | 63608/107976 | 21203/35991 | chr2 | 178587701 | ||
| chr2:178588699
|
C | T | 2 | a0159a0185 | 2 | HG02257.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.63026G>A | p.Arg21009Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 63251/109224 | 63026/107976 | 21009/35991 | chr2 | 178588699 | ||
| chr2:178589803
|
C | T | 1 | a0070 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.61922G>A | p.Arg20641Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 62147/109224 | 61922/107976 | 20641/35991 | chr2 | 178589803 | ||
| chr2:178590449
|
G | A | 1 | a0114 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.61276C>T | p.Leu20426Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 61501/109224 | 61276/107976 | 20426/35991 | chr2 | 178590449 | ||
| chr2:178590677
|
G | A | 1 | a0166 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.61048C>T | p.Leu20350Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 61273/109224 | 61048/107976 | 20350/35991 | chr2 | 178590677 | ||
| chr2:178590907
|
G | A | 1 | a0049 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.60818C>T | p.Ser20273Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 61043/109224 | 60818/107976 | 20273/35991 | chr2 | 178590907 | ||
| chr2:178591493
|
C | T | 2 | a0159a0185 | 2 | HG02257.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.60232G>A | p.Val20078Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 60457/109224 | 60232/107976 | 20078/35991 | chr2 | 178591493 | ||
| chr2:178591764
|
C | T | 2 | a0028a0029 | 2 | HG02451.hp2 HG02559.hp2 |
missense_variant | MODERATE | c.60055G>A | p.Glu20019Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 303/363 | 60280/109224 | 60055/107976 | 20019/35991 | chr2 | 178591764 | ||
| chr2:178592420
|
G | A | 49 | a0001a0005a0013others(46): Show | 64 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
missense_variant | MODERATE | c.59585C>T | p.Pro19862Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 301/363 | 59810/109224 | 59585/107976 | 19862/35991 | chr2 | 178592420 | ||
| chr2:178592837
|
T | C | 1 | a0036 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.59282A>G | p.Asn19761Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 300/363 | 59507/109224 | 59282/107976 | 19761/35991 | chr2 | 178592837 | ||
| chr2:178592954
|
A | G | 3 | a0123a0124a0129 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.59165T>C | p.Val19722Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 300/363 | 59390/109224 | 59165/107976 | 19722/35991 | chr2 | 178592954 | ||
| chr2:178593642
|
C | T | 1 | a0159 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.58658G>A | p.Arg19553Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 298/363 | 58883/109224 | 58658/107976 | 19553/35991 | chr2 | 178593642 | ||
| chr2:178593664
|
C | G | 1 | a0177 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.58636G>C | p.Glu19546Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 298/363 | 58861/109224 | 58636/107976 | 19546/35991 | chr2 | 178593664 | ||
| chr2:178593688
|
T | C | 1 | a0123 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.58612A>G | p.Thr19538Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 298/363 | 58837/109224 | 58612/107976 | 19538/35991 | chr2 | 178593688 | ||
| chr2:178593864
|
C | T | 49 | a0001a0005a0013others(46): Show | 64 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
missense_variant | MODERATE | c.58436G>A | p.Arg19479His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 298/363 | 58661/109224 | 58436/107976 | 19479/35991 | chr2 | 178593864 | ||
| chr2:178593967
|
C | T | 1 | a0047 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.58426G>A | p.Val19476Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 297/363 | 58651/109224 | 58426/107976 | 19476/35991 | chr2 | 178593967 | ||
| chr2:178594472
|
C | T | 1 | a0142 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.58022G>A | p.Ser19341Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 296/363 | 58247/109224 | 58022/107976 | 19341/35991 | chr2 | 178594472 | ||
| chr2:178595671
|
C | T | 1 | a0156 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.57683G>A | p.Arg19228His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/363 | 57908/109224 | 57683/107976 | 19228/35991 | chr2 | 178595671 | ||
| chr2:178597618
|
C | T | 2 | a0177a0178 | 2 | HG02559.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.57464G>A | p.Arg19155Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/363 | 57689/109224 | 57464/107976 | 19155/35991 | chr2 | 178597618 | ||
| chr2:178598550
|
A | T | 1 | a0139 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.57067T>A | p.Tyr19023Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 292/363 | 57292/109224 | 57067/107976 | 19023/35991 | chr2 | 178598550 | ||
| chr2:178598838
|
C | T | 1 | a0102 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.56872G>A | p.Asp18958Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 291/363 | 57097/109224 | 56872/107976 | 18958/35991 | chr2 | 178598838 | ||
| chr2:178599638
|
G | T | 1 | a0136 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.56263C>A | p.Arg18755Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 289/363 | 56488/109224 | 56263/107976 | 18755/35991 | chr2 | 178599638 | ||
| chr2:178599800
|
T | C | 124 | a0001a0002a0004others(121): Show | 160 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
missense_variant | MODERATE | c.56101A>G | p.Asn18701Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 289/363 | 56326/109224 | 56101/107976 | 18701/35991 | chr2 | 178599800 | ||
| chr2:178601283
|
T | C | 1 | a0042 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.55714A>G | p.Thr18572Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 287/363 | 55939/109224 | 55714/107976 | 18572/35991 | chr2 | 178601283 | ||
| chr2:178601444
|
T | C | 1 | a0128 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.55553A>G | p.Lys18518Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 287/363 | 55778/109224 | 55553/107976 | 18518/35991 | chr2 | 178601444 | ||
| chr2:178601450
|
A | G | 1 | a0191 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.55547T>C | p.Ile18516Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 287/363 | 55772/109224 | 55547/107976 | 18516/35991 | chr2 | 178601450 | ||
| chr2:178604193
|
C | T | 1 | a0142 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.54494G>A | p.Arg18165His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 282/363 | 54719/109224 | 54494/107976 | 18165/35991 | chr2 | 178604193 | ||
| chr2:178607565
|
T | A | 10 | a0008a0012a0035others(7): Show | 13 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(10): Show |
missense_variant | MODERATE | c.53123A>T | p.Lys17708Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 277/363 | 53348/109224 | 53123/107976 | 17708/35991 | chr2 | 178607565 | ||
| chr2:178609941
|
G | A | 26 | a0005a0059a0061others(23): Show | 29 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(26): Show |
missense_variant | MODERATE | c.51482C>T | p.Ala17161Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 272/363 | 51707/109224 | 51482/107976 | 17161/35991 | chr2 | 178609941 | ||
| chr2:178612802
|
C | G | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.49919G>C | p.Ser16640Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 265/363 | 50144/109224 | 49919/107976 | 16640/35991 | chr2 | 178612802 | ||
| chr2:178615707
|
G | A | 1 | a0048 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.48394C>T | p.Arg16132Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 258/363 | 48619/109224 | 48394/107976 | 16132/35991 | chr2 | 178615707 | ||
| chr2:178617348
|
G | A | 1 | a0191 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.47737C>T | p.Leu15913Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 254/363 | 47962/109224 | 47737/107976 | 15913/35991 | chr2 | 178617348 | ||
| chr2:178617806
|
G | T | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.47545C>A | p.Pro15849Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 253/363 | 47770/109224 | 47545/107976 | 15849/35991 | chr2 | 178617806 | ||
| chr2:178617949
|
G | A | 1 | a0076 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.47402C>T | p.Thr15801Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 253/363 | 47627/109224 | 47402/107976 | 15801/35991 | chr2 | 178617949 | ||
| chr2:178618036
|
C | T | 1 | a0101 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.47315G>A | p.Arg15772Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 253/363 | 47540/109224 | 47315/107976 | 15772/35991 | chr2 | 178618036 | ||
| chr2:178618703
|
G | A | 1 | a0073 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.46847C>T | p.Thr15616Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 251/363 | 47072/109224 | 46847/107976 | 15616/35991 | chr2 | 178618703 | ||
| chr2:178619737
|
A | T | 1 | a0090 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.46580T>A | p.Met15527Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 250/363 | 46805/109224 | 46580/107976 | 15527/35991 | chr2 | 178619737 | ||
| chr2:178621612
|
A | G | 1 | a0053 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.45212T>C | p.Ile15071Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/363 | 45437/109224 | 45212/107976 | 15071/35991 | chr2 | 178621612 | ||
| chr2:178621618
|
T | A | 5 | a0018a0019a0067others(2): Show | 7 | HG02145.hp2 HG02451.hp1 HG02809.hp1 others(4): Show |
missense_variant | MODERATE | c.45206A>T | p.Glu15069Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/363 | 45431/109224 | 45206/107976 | 15069/35991 | chr2 | 178621618 | ||
| chr2:178621649
|
C | T | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.45175G>A | p.Ala15059Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/363 | 45400/109224 | 45175/107976 | 15059/35991 | chr2 | 178621649 | ||
| chr2:178621704
|
A | C | 2 | a0084a0174 | 2 | NA19058.hp1 NA19058.hp2 |
missense_variant | MODERATE | c.45120T>G | p.Ile15040Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/363 | 45345/109224 | 45120/107976 | 15040/35991 | chr2 | 178621704 | ||
| chr2:178621869
|
G | A | 2 | a0014a0044 | 3 | HG01257.hp1 HG02273.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.45053C>T | p.Ala15018Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 244/363 | 45278/109224 | 45053/107976 | 15018/35991 | chr2 | 178621869 | ||
| chr2:178624681
|
C | T | 1 | a0094 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.44599G>A | p.Gly14867Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/363 | 44824/109224 | 44599/107976 | 14867/35991 | chr2 | 178624681 | ||
| chr2:178632291
|
G | A | 3 | a0007a0133a0138 | 5 | HG01099.hp1 HG01975.hp2 HG01981.hp1 others(2): Show |
missense_variant | MODERATE | c.43603C>T | p.Arg14535Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 236/363 | 43828/109224 | 43603/107976 | 14535/35991 | chr2 | 178632291 | ||
| chr2:178633315
|
T | C | 3 | a0097a0115a0182 | 3 | HG01496.hp2 HG02683.hp1 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.42958A>G | p.Lys14320Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 233/363 | 43183/109224 | 42958/107976 | 14320/35991 | chr2 | 178633315 | ||
| chr2:178634803
|
T | C | 11 | a0008a0012a0035others(8): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
missense_variant | MODERATE | c.42071A>G | p.His14024Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 229/363 | 42296/109224 | 42071/107976 | 14024/35991 | chr2 | 178634803 | ||
| chr2:178636002
|
C | T | 1 | a0095 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.41569G>A | p.Ala13857Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 226/363 | 41794/109224 | 41569/107976 | 13857/35991 | chr2 | 178636002 | ||
| chr2:178636491
|
T | C | 1 | a0099 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.41236A>G | p.Ile13746Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 225/363 | 41461/109224 | 41236/107976 | 13746/35991 | chr2 | 178636491 | ||
| chr2:178649608
|
C | A | 1 | a0139 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.39919G>T | p.Val13307Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 212/363 | 40144/109224 | 39919/107976 | 13307/35991 | chr2 | 178649608 | ||
| chr2:178650214
|
TTTTCCTC others(11): Show |
T | 12 | a0059a0061a0062others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(9): Show |
disruptive_inframe_deletion | MODERATE | c.39749_39766delTTGC others(14): Show |
p.Ile13250_Glu13255d others(2): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 210/363 | 39991/109224 | 39749/107976 | 13250/35991 | chr2 | 178650214 | ||
| chr2:178650756
|
G | C | 14 | a0005a0087a0088others(11): Show | 17 | HG00408.hp1 HG03490.hp1 HG03492.hp1 others(14): Show |
missense_variant | MODERATE | c.39704C>G | p.Pro13235Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 209/363 | 39929/109224 | 39704/107976 | 13235/35991 | chr2 | 178650756 | ||
| chr2:178651252
|
G | A | 1 | a0087 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.39616C>T | p.Pro13206Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 208/363 | 39841/109224 | 39616/107976 | 13206/35991 | chr2 | 178651252 | ||
| chr2:178652500
|
G | T | 1 | a0106 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.39085C>A | p.Pro13029Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 202/363 | 39310/109224 | 39085/107976 | 13029/35991 | chr2 | 178652500 | ||
| chr2:178652503
|
C | T | 2 | a0057a0063 | 2 | HG02818.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.39082G>A | p.Val13028Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 202/363 | 39307/109224 | 39082/107976 | 13028/35991 | chr2 | 178652503 | ||
| chr2:178653276
|
A | G | 26 | a0004a0008a0009others(23): Show | 37 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(34): Show |
missense_variant | MODERATE | c.38753T>C | p.Leu12918Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 198/363 | 38978/109224 | 38753/107976 | 12918/35991 | chr2 | 178653276 | ||
| chr2:178653866
|
T | G | 1 | a0054 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.38496A>C | p.Lys12832Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 195/363 | 38721/109224 | 38496/107976 | 12832/35991 | chr2 | 178653866 | ||
| chr2:178654210
|
T | C | 1 | a0055 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.38378A>G | p.Lys12793Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 193/363 | 38603/109224 | 38378/107976 | 12793/35991 | chr2 | 178654210 | ||
| chr2:178654252
|
A | ACTTTCTT others(4254): Show |
2 | a0015a0045 | 3 | HG00609.hp1 HG01346.hp2 HG01978.hp1 |
frameshift_variant&stop_gained | HIGH | c.38335_38336insCATC others(4257): Show |
p.Val12779fs | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 193/363 | 38560/109224 | 38335/107976 | 12779/35991 | chr2 | 178654252 | ||
| chr2:178654252
|
A | G | 14 | a0004a0009a0017others(11): Show | 22 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(19): Show |
missense_variant | MODERATE | c.38336T>C | p.Val12779Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 193/363 | 38561/109224 | 38336/107976 | 12779/35991 | chr2 | 178654252 | ||
| chr2:178654265
|
G | A | 2 | a0068a0069 | 2 | HG02965.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.38323C>T | p.Leu12775Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 193/363 | 38548/109224 | 38323/107976 | 12775/35991 | chr2 | 178654265 | ||
| chr2:178654766
|
G | A | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.38185C>T | p.Pro12729Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 191/363 | 38410/109224 | 38185/107976 | 12729/35991 | chr2 | 178654766 | ||
| chr2:178654790
|
CCTTCTTT others(8514): Show |
C | 1 | a0082 | 1 | HG02280.hp1 | exon_loss_variant | HIGH | c.36655_38160del | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 190/363 | 38385/109224 | chr2 | 178654790 | |||||
| chr2:178654801
|
G | A | 1 | a0047 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.38150C>T | p.Pro12717Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 191/363 | 38375/109224 | 38150/107976 | 12717/35991 | chr2 | 178654801 | ||
| chr2:178654965
|
T | TCTTCAGG others(29): Show |
1 | a0142 | 1 | HG04184.hp1 | conservative_inframe_insertion | MODERATE | c.38068_38069insTGCC others(32): Show |
p.Pro12689_Glu12690i others(38): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 190/363 | 38293/109224 | 38068/107976 | 12690/35991 | chr2 | 178654965 | ||
| chr2:178655278
|
ATATCTCA others(4253): Show |
A | 7 | a0085a0100a0102others(4): Show | 7 | HG01099.hp1 HG01978.hp2 HG02300.hp2 others(4): Show |
exon_loss_variant | HIGH | c.37286-283_38039-28 others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/363 | chr2 | 178655278 | ||||||
| chr2:178656457
|
TACTACCA others(4254): Show |
T | 1 | a0157 | 1 | HG02922.hp2 | exon_loss_variant | HIGH | c.37285+1041_38038+1 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/363 | chr2 | 178656457 | ||||||
| chr2:178657534
|
T | C | 31 | a0004a0008a0009others(28): Show | 42 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
missense_variant | MODERATE | c.38002A>G | p.Thr12668Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/363 | 38227/109224 | 38002/107976 | 12668/35991 | chr2 | 178657534 | ||
| chr2:178657916
|
G | A | 2 | a0037a0161 | 2 | HG00558.hp1 HG00558.hp2 |
missense_variant | MODERATE | c.37838C>T | p.Ala12613Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 187/363 | 38063/109224 | 37838/107976 | 12613/35991 | chr2 | 178657916 | ||
| chr2:178657949
|
T | G | 1 | a0181 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.37805A>C | p.Gln12602Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 187/363 | 38030/109224 | 37805/107976 | 12602/35991 | chr2 | 178657949 | ||
| chr2:178658134
|
C | CGGCTTCT others(4254): Show |
1 | a0042 | 1 | HG02486.hp1 | frameshift_variant&stop_gained | HIGH | c.36982_37734dupACAG others(4257): Show |
p.Ala12579fs | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 186/363 | 37959/109224 | 37734/107976 | 12578/35991 | chr2 | 178658134 | ||
| chr2:178658134
|
C | T | 1 | a0137 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.37735G>A | p.Ala12579Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 186/363 | 37960/109224 | 37735/107976 | 12579/35991 | chr2 | 178658134 | ||
| chr2:178658278
|
C | T | 12 | a0024a0057a0064others(9): Show | 13 | HG02055.hp1 HG02818.hp2 HG02895.hp1 others(10): Show |
missense_variant | MODERATE | c.37705G>A | p.Val12569Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 185/363 | 37930/109224 | 37705/107976 | 12569/35991 | chr2 | 178658278 | ||
| chr2:178658281
|
C | T | 1 | a0159 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.37702G>A | p.Ala12568Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 185/363 | 37927/109224 | 37702/107976 | 12568/35991 | chr2 | 178658281 | ||
| chr2:178658787
|
T | A | 12 | a0008a0012a0035others(9): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
missense_variant | MODERATE | c.37461A>T | p.Glu12487Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 183/363 | 37686/109224 | 37461/107976 | 12487/35991 | chr2 | 178658787 | ||
| chr2:178659026
|
G | A | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.37432C>T | p.Pro12478Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 182/363 | 37657/109224 | 37432/107976 | 12478/35991 | chr2 | 178659026 | ||
| chr2:178661795
|
C | T | 12 | a0023a0027a0066others(9): Show | 13 | HG00438.hp1 HG01361.hp1 HG02809.hp2 others(10): Show |
missense_variant | MODERATE | c.37249G>A | p.Ala12417Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/363 | 37474/109224 | 37249/107976 | 12417/35991 | chr2 | 178661795 | ||
| chr2:178662395
|
T | C | 82 | a0001a0002a0004others(79): Show | 111 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
missense_variant | MODERATE | c.36982A>G | p.Thr12328Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 177/363 | 37207/109224 | 36982/107976 | 12328/35991 | chr2 | 178662395 | ||
| chr2:178662539
|
C | T | 9 | a0023a0027a0066others(6): Show | 10 | HG01361.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
missense_variant | MODERATE | c.36952G>A | p.Val12318Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 176/363 | 37177/109224 | 36952/107976 | 12318/35991 | chr2 | 178662539 | ||
| chr2:178662773
|
G | A | 1 | a0056 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.36830C>T | p.Ala12277Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 175/363 | 37055/109224 | 36830/107976 | 12277/35991 | chr2 | 178662773 | ||
| chr2:178663311
|
A | C | 89 | a0001a0002a0004others(86): Show | 121 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(118): Show |
missense_variant | MODERATE | c.36655T>G | p.Leu12219Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 173/363 | 36880/109224 | 36655/107976 | 12219/35991 | chr2 | 178663311 | ||
| chr2:178663341
|
C | A | 15 | a0005a0087a0088others(12): Show | 18 | HG00408.hp1 HG03490.hp1 HG03492.hp1 others(15): Show |
missense_variant | MODERATE | c.36625G>T | p.Val12209Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 173/363 | 36850/109224 | 36625/107976 | 12209/35991 | chr2 | 178663341 | ||
| chr2:178663651
|
C | T | 69 | a0004a0008a0009others(66): Show | 84 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(81): Show |
missense_variant | MODERATE | c.36508G>A | p.Glu12170Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 171/363 | 36733/109224 | 36508/107976 | 12170/35991 | chr2 | 178663651 | ||
| chr2:178664080
|
T | A | 5 | a0028a0029a0082others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
missense_variant | MODERATE | c.36299A>T | p.Glu12100Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 169/363 | 36524/109224 | 36299/107976 | 12100/35991 | chr2 | 178664080 | ||
| chr2:178664730
|
T | G | 2 | a0066a0179 | 2 | HG02895.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.36126A>C | p.Glu12042Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 167/363 | 36351/109224 | 36126/107976 | 12042/35991 | chr2 | 178664730 | ||
| chr2:178671131
|
G | A | 1 | a0135 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.35267C>T | p.Pro11756Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 156/363 | 35492/109224 | 35267/107976 | 11756/35991 | chr2 | 178671131 | ||
| chr2:178671134
|
T | G | 1 | a0176 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.35264A>C | p.Lys11755Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 156/363 | 35489/109224 | 35264/107976 | 11755/35991 | chr2 | 178671134 | ||
| chr2:178672228
|
C | T | 2 | a0066a0179 | 2 | HG02895.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.34970G>A | p.Arg11657His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 155/363 | 35195/109224 | 34970/107976 | 11657/35991 | chr2 | 178672228 | ||
| chr2:178672635
|
C | T | 1 | a0063 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.34855G>A | p.Val11619Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 153/363 | 35080/109224 | 34855/107976 | 11619/35991 | chr2 | 178672635 | ||
| chr2:178673650
|
T | C | 1 | a0156 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.34769A>G | p.Glu11590Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 152/363 | 34994/109224 | 34769/107976 | 11590/35991 | chr2 | 178673650 | ||
| chr2:178675085
|
T | G | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.34566A>C | p.Glu11522Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 150/363 | 34791/109224 | 34566/107976 | 11522/35991 | chr2 | 178675085 | ||
| chr2:178675703
|
C | A | 1 | a0156 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.34505G>T | p.Gly11502Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 149/363 | 34730/109224 | 34505/107976 | 11502/35991 | chr2 | 178675703 | ||
| chr2:178675977
|
T | G | 1 | a0172 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.34397A>C | p.Lys11466Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 148/363 | 34622/109224 | 34397/107976 | 11466/35991 | chr2 | 178675977 | ||
| chr2:178677272
|
T | C | 1 | a0176 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.34307A>G | p.Lys11436Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 147/363 | 34532/109224 | 34307/107976 | 11436/35991 | chr2 | 178677272 | ||
| chr2:178680256
|
C | G | 1 | a0108 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.33416G>C | p.Arg11139Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 139/363 | 33641/109224 | 33416/107976 | 11139/35991 | chr2 | 178680256 | ||
| chr2:178681132
|
C | T | 9 | a0020a0103a0104others(6): Show | 10 | HG00423.hp1 HG01071.hp2 HG01358.hp1 others(7): Show |
missense_variant | MODERATE | c.33287G>A | p.Arg11096His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 138/363 | 33512/109224 | 33287/107976 | 11096/35991 | chr2 | 178681132 | ||
| chr2:178681669
|
G | A | 1 | a0089 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.33164C>T | p.Pro11055Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 136/363 | 33389/109224 | 33164/107976 | 11055/35991 | chr2 | 178681669 | ||
| chr2:178684702
|
T | C | 1 | a0143 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.32602A>G | p.Lys10868Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 131/363 | 32827/109224 | 32602/107976 | 10868/35991 | chr2 | 178684702 | ||
| chr2:178685560
|
G | C | 1 | a0128 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.32350C>G | p.Leu10784Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 128/363 | 32575/109224 | 32350/107976 | 10784/35991 | chr2 | 178685560 | ||
| chr2:178688168
|
C | T | 5 | a0059a0151a0187others(2): Show | 5 | HG02615.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
missense_variant | MODERATE | c.32254G>A | p.Val10752Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/363 | 32479/109224 | 32254/107976 | 10752/35991 | chr2 | 178688168 | ||
| chr2:178689578
|
C | T | 85 | a0004a0008a0009others(82): Show | 101 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(98): Show |
missense_variant | MODERATE | c.31864G>A | p.Gly10622Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 123/363 | 32089/109224 | 31864/107976 | 10622/35991 | chr2 | 178689578 | ||
| chr2:178693639
|
T | C | 106 | a0001a0002a0004others(103): Show | 140 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(137): Show |
missense_variant | MODERATE | c.31564A>G | p.Ile10522Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 119/363 | 31789/109224 | 31564/107976 | 10522/35991 | chr2 | 178693639 | ||
| chr2:178696120
|
C | T | 9 | a0057a0063a0068others(6): Show | 9 | HG02451.hp1 HG02818.hp2 HG02922.hp2 others(6): Show |
missense_variant | MODERATE | c.30952G>A | p.Glu10318Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 114/363 | 31177/109224 | 30952/107976 | 10318/35991 | chr2 | 178696120 | ||
| chr2:178704534
|
C | T | 1 | a0113 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.29938G>A | p.Ala9980Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 105/363 | 30163/109224 | 29938/107976 | 9980/35991 | chr2 | 178704534 | ||
| chr2:178704660
|
T | A | 5 | a0081a0099a0100others(2): Show | 5 | HG00642.hp1 HG01255.hp1 HG02738.hp1 others(2): Show |
missense_variant | MODERATE | c.29812A>T | p.Thr9938Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 105/363 | 30037/109224 | 29812/107976 | 9938/35991 | chr2 | 178704660 | ||
| chr2:178706560
|
C | T | 1 | a0072 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.29314G>A | p.Val9772Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 102/363 | 29539/109224 | 29314/107976 | 9772/35991 | chr2 | 178706560 | ||
| chr2:178706721
|
A | G | 30 | a0004a0009a0022others(27): Show | 37 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(34): Show |
missense_variant | MODERATE | c.29153T>C | p.Ile9718Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 102/363 | 29378/109224 | 29153/107976 | 9718/35991 | chr2 | 178706721 | ||
| chr2:178707711
|
A | G | 1 | a0141 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.28856T>C | p.Ile9619Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 100/363 | 29081/109224 | 28856/107976 | 9619/35991 | chr2 | 178707711 | ||
| chr2:178707784
|
G | A | 1 | a0058 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.28783C>T | p.His9595Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 100/363 | 29008/109224 | 28783/107976 | 9595/35991 | chr2 | 178707784 | ||
| chr2:178709772
|
C | T | 1 | a0174 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.28547G>A | p.Arg9516His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/363 | 28772/109224 | 28547/107976 | 9516/35991 | chr2 | 178709772 | ||
| chr2:178710784
|
C | T | 8 | a0014a0021a0040others(5): Show | 10 | HG01257.hp1 HG01358.hp2 HG01433.hp1 others(7): Show |
missense_variant | MODERATE | c.28313G>A | p.Arg9438Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 98/363 | 28538/109224 | 28313/107976 | 9438/35991 | chr2 | 178710784 | ||
| chr2:178711166
|
G | A | 1 | a0191 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.28070C>T | p.Thr9357Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 97/363 | 28295/109224 | 28070/107976 | 9357/35991 | chr2 | 178711166 | ||
| chr2:178713271
|
T | C | 1 | a0149 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.26863A>G | p.Ile8955Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 93/363 | 27088/109224 | 26863/107976 | 8955/35991 | chr2 | 178713271 | ||
| chr2:178713977
|
G | A | 26 | a0004a0009a0022others(23): Show | 33 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(30): Show |
missense_variant | MODERATE | c.26681C>T | p.Pro8894Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/363 | 26906/109224 | 26681/107976 | 8894/35991 | chr2 | 178713977 | ||
| chr2:178713986
|
T | C | 1 | a0076 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.26672A>G | p.Asn8891Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/363 | 26897/109224 | 26672/107976 | 8891/35991 | chr2 | 178713986 | ||
| chr2:178714366
|
T | C | 46 | a0001a0002a0013others(43): Show | 66 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(63): Show |
missense_variant | MODERATE | c.26408A>G | p.Asn8803Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 91/363 | 26633/109224 | 26408/107976 | 8803/35991 | chr2 | 178714366 | ||
| chr2:178714529
|
C | T | 2 | a0013a0098 | 3 | HG01884.hp1 HG02647.hp1 HG02976.hp2 |
missense_variant | MODERATE | c.26245G>A | p.Val8749Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 91/363 | 26470/109224 | 26245/107976 | 8749/35991 | chr2 | 178714529 | ||
| chr2:178715208
|
C | T | 1 | a0063 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.25978G>A | p.Val8660Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 90/363 | 26203/109224 | 25978/107976 | 8660/35991 | chr2 | 178715208 | ||
| chr2:178715250
|
G | A | 4 | a0081a0099a0100others(1): Show | 4 | HG00642.hp1 HG02738.hp1 HG03710.hp1 others(1): Show |
missense_variant | MODERATE | c.25936C>T | p.Arg8646Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 90/363 | 26161/109224 | 25936/107976 | 8646/35991 | chr2 | 178715250 | ||
| chr2:178715585
|
T | C | 1 | a0114 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.25829A>G | p.His8610Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 89/363 | 26054/109224 | 25829/107976 | 8610/35991 | chr2 | 178715585 | ||
| chr2:178717108
|
C | A | 18 | a0008a0012a0030others(15): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
missense_variant | MODERATE | c.25626G>T | p.Gln8542His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 88/363 | 25851/109224 | 25626/107976 | 8542/35991 | chr2 | 178717108 | ||
| chr2:178717244
|
C | T | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.25490G>A | p.Arg8497His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 88/363 | 25715/109224 | 25490/107976 | 8497/35991 | chr2 | 178717244 | ||
| chr2:178717336
|
A | T | 9 | a0018a0024a0063others(6): Show | 11 | HG02738.hp2 HG02895.hp1 HG02896.hp1 others(8): Show |
missense_variant | MODERATE | c.25398T>A | p.Asp8466Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 88/363 | 25623/109224 | 25398/107976 | 8466/35991 | chr2 | 178717336 | ||
| chr2:178717600
|
C | T | 45 | a0001a0002a0013others(42): Show | 65 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(62): Show |
missense_variant | MODERATE | c.25274G>A | p.Ser8425Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 87/363 | 25499/109224 | 25274/107976 | 8425/35991 | chr2 | 178717600 | ||
| chr2:178717810
|
G | T | 101 | a0001a0002a0004others(98): Show | 133 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(130): Show |
missense_variant&splice_region_variant | MODERATE | c.25064C>A | p.Ala8355Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 87/363 | 25289/109224 | 25064/107976 | 8355/35991 | chr2 | 178717810 | ||
| chr2:178718126
|
T | C | 1 | a0071 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.24880A>G | p.Arg8294Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 86/363 | 25105/109224 | 24880/107976 | 8294/35991 | chr2 | 178718126 | ||
| chr2:178718769
|
T | G | 41 | a0001a0002a0013others(38): Show | 61 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
missense_variant | MODERATE | c.24431A>C | p.Glu8144Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 84/363 | 24656/109224 | 24431/107976 | 8144/35991 | chr2 | 178718769 | ||
| chr2:178719230
|
T | A | 2 | a0159a0185 | 2 | HG02257.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.24160A>T | p.Ile8054Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 83/363 | 24385/109224 | 24160/107976 | 8054/35991 | chr2 | 178719230 | ||
| chr2:178719817
|
A | G | 1 | a0193 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.23675T>C | p.Ile7892Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 82/363 | 23900/109224 | 23675/107976 | 7892/35991 | chr2 | 178719817 | ||
| chr2:178720064
|
C | T | 1 | a0060 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.23578G>A | p.Ala7860Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 81/363 | 23803/109224 | 23578/107976 | 7860/35991 | chr2 | 178720064 | ||
| chr2:178720104
|
G | C | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.23538C>G | p.Phe7846Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 81/363 | 23763/109224 | 23538/107976 | 7846/35991 | chr2 | 178720104 | ||
| chr2:178720530
|
G | C | 1 | a0119 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.23232C>G | p.Asn7744Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 80/363 | 23457/109224 | 23232/107976 | 7744/35991 | chr2 | 178720530 | ||
| chr2:178721053
|
T | C | 1 | a0088 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.22966A>G | p.Asn7656Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 79/363 | 23191/109224 | 22966/107976 | 7656/35991 | chr2 | 178721053 | ||
| chr2:178721877
|
C | G | 2 | a0097a0115 | 2 | HG01496.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.22786G>C | p.Asp7596His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 78/363 | 23011/109224 | 22786/107976 | 7596/35991 | chr2 | 178721877 | ||
| chr2:178721912
|
T | A | 1 | a0044 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.22751A>T | p.Gln7584Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 78/363 | 22976/109224 | 22751/107976 | 7584/35991 | chr2 | 178721912 | ||
| chr2:178722403
|
C | G | 45 | a0001a0002a0013others(42): Show | 65 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(62): Show |
missense_variant | MODERATE | c.22384G>C | p.Asp7462His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 77/363 | 22609/109224 | 22384/107976 | 7462/35991 | chr2 | 178722403 | ||
| chr2:178724086
|
C | T | 1 | a0128 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.21173G>A | p.Gly7058Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 73/363 | 21398/109224 | 21173/107976 | 7058/35991 | chr2 | 178724086 | ||
| chr2:178724096
|
C | A | 1 | a0042 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.21163G>T | p.Gly7055Trp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 73/363 | 21388/109224 | 21163/107976 | 7055/35991 | chr2 | 178724096 | ||
| chr2:178724269
|
C | T | 6 | a0018a0063a0065others(3): Show | 7 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
missense_variant | MODERATE | c.21106G>A | p.Asp7036Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 72/363 | 21331/109224 | 21106/107976 | 7036/35991 | chr2 | 178724269 | ||
| chr2:178724331
|
G | A | 14 | a0005a0087a0088others(11): Show | 17 | HG00408.hp1 HG03490.hp1 HG03492.hp1 others(14): Show |
missense_variant | MODERATE | c.21044C>T | p.Ala7015Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 72/363 | 21269/109224 | 21044/107976 | 7015/35991 | chr2 | 178724331 | ||
| chr2:178724356
|
T | A | 2 | a0068a0069 | 2 | HG02965.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.21019A>T | p.Ile7007Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 72/363 | 21244/109224 | 21019/107976 | 7007/35991 | chr2 | 178724356 | ||
| chr2:178724514
|
G | A | 10 | a0004a0125a0142others(7): Show | 14 | HG00642.hp2 HG01257.hp2 HG01346.hp1 others(11): Show |
missense_variant | MODERATE | c.20861C>T | p.Ala6954Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 72/363 | 21086/109224 | 20861/107976 | 6954/35991 | chr2 | 178724514 | ||
| chr2:178725968
|
G | A | 1 | a0070 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.20354C>T | p.Ser6785Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 70/363 | 20579/109224 | 20354/107976 | 6785/35991 | chr2 | 178725968 | ||
| chr2:178726005
|
G | A | 1 | a0030 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.20317C>T | p.Leu6773Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 70/363 | 20542/109224 | 20317/107976 | 6773/35991 | chr2 | 178726005 | ||
| chr2:178727190
|
T | C | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.20175A>G | p.Ile6725Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/363 | 20400/109224 | 20175/107976 | 6725/35991 | chr2 | 178727190 | ||
| chr2:178727602
|
G | A | 2 | a0013a0098 | 3 | HG01884.hp1 HG02647.hp1 HG02976.hp2 |
missense_variant | MODERATE | c.19976C>T | p.Thr6659Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 68/363 | 20201/109224 | 19976/107976 | 6659/35991 | chr2 | 178727602 | ||
| chr2:178727840
|
G | A | 1 | a0017 | 2 | HG02145.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.19738C>T | p.Pro6580Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 68/363 | 19963/109224 | 19738/107976 | 6580/35991 | chr2 | 178727840 | ||
| chr2:178727854
|
C | T | 1 | a0042 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.19724G>A | p.Ser6575Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 68/363 | 19949/109224 | 19724/107976 | 6575/35991 | chr2 | 178727854 | ||
| chr2:178728625
|
C | T | 22 | a0004a0009a0022others(19): Show | 29 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(26): Show |
missense_variant | MODERATE | c.19301G>A | p.Ser6434Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 66/363 | 19526/109224 | 19301/107976 | 6434/35991 | chr2 | 178728625 | ||
| chr2:178728722
|
T | C | 6 | a0018a0063a0065others(3): Show | 7 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
missense_variant | MODERATE | c.19204A>G | p.Met6402Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 66/363 | 19429/109224 | 19204/107976 | 6402/35991 | chr2 | 178728722 | ||
| chr2:178728776
|
G | T | 1 | a0173 | 1 | HG02165.hp2 | missense_variant&splice_region_variant | MODERATE | c.19150C>A | p.Pro6384Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 66/363 | 19375/109224 | 19150/107976 | 6384/35991 | chr2 | 178728776 | ||
| chr2:178729034
|
T | C | 4 | a0018a0065a0066others(1): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.19004A>G | p.Asp6335Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 65/363 | 19229/109224 | 19004/107976 | 6335/35991 | chr2 | 178729034 | ||
| chr2:178729077
|
T | C | 1 | a0017 | 2 | HG02145.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.18961A>G | p.Ile6321Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 65/363 | 19186/109224 | 18961/107976 | 6321/35991 | chr2 | 178729077 | ||
| chr2:178729300
|
C | T | 1 | a0017 | 2 | HG02145.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.18856G>A | p.Val6286Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 64/363 | 19081/109224 | 18856/107976 | 6286/35991 | chr2 | 178729300 | ||
| chr2:178729332
|
T | C | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.18824A>G | p.Asn6275Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 64/363 | 19049/109224 | 18824/107976 | 6275/35991 | chr2 | 178729332 | ||
| chr2:178729497
|
C | G | 1 | a0179 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.18659G>C | p.Cys6220Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 64/363 | 18884/109224 | 18659/107976 | 6220/35991 | chr2 | 178729497 | ||
| chr2:178729928
|
T | C | 1 | a0082 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.18325A>G | p.Lys6109Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 63/363 | 18550/109224 | 18325/107976 | 6109/35991 | chr2 | 178729928 | ||
| chr2:178730544
|
C | T | 1 | a0154 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.17989G>A | p.Ala5997Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 61/363 | 18214/109224 | 17989/107976 | 5997/35991 | chr2 | 178730544 | ||
| chr2:178730656
|
T | C | 1 | a0138 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.17877A>G | p.Ile5959Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 61/363 | 18102/109224 | 17877/107976 | 5959/35991 | chr2 | 178730656 | ||
| chr2:178731113
|
T | C | 1 | a0077 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.17552A>G | p.Glu5851Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 60/363 | 17777/109224 | 17552/107976 | 5851/35991 | chr2 | 178731113 | ||
| chr2:178731756
|
A | G | 1 | a0182 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.17119T>C | p.Tyr5707His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 58/363 | 17344/109224 | 17119/107976 | 5707/35991 | chr2 | 178731756 | ||
| chr2:178732532
|
T | C | 2 | a0163a0174 | 2 | HG00438.hp1 NA19058.hp2 |
missense_variant | MODERATE | c.16529A>G | p.Tyr5510Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 56/363 | 16754/109224 | 16529/107976 | 5510/35991 | chr2 | 178732532 | ||
| chr2:178733386
|
C | T | 1 | a0041 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.15907G>A | p.Ala5303Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 54/363 | 16132/109224 | 15907/107976 | 5303/35991 | chr2 | 178733386 | ||
| chr2:178733443
|
C | T | 1 | a0155 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.15850G>A | p.Val5284Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 54/363 | 16075/109224 | 15850/107976 | 5284/35991 | chr2 | 178733443 | ||
| chr2:178733730
|
T | C | 1 | a0174 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.15659A>G | p.Asn5220Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 53/363 | 15884/109224 | 15659/107976 | 5220/35991 | chr2 | 178733730 | ||
| chr2:178733805
|
T | C | 1 | a0185 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.15584A>G | p.Glu5195Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 53/363 | 15809/109224 | 15584/107976 | 5195/35991 | chr2 | 178733805 | ||
| chr2:178734746
|
C | G | 2 | a0040a0041 | 2 | HG03831.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.15178G>C | p.Val5060Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 51/363 | 15403/109224 | 15178/107976 | 5060/35991 | chr2 | 178734746 | ||
| chr2:178734884
|
T | A | 1 | a0132 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.15040A>T | p.Thr5014Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 51/363 | 15265/109224 | 15040/107976 | 5014/35991 | chr2 | 178734884 | ||
| chr2:178735921
|
C | T | 45 | a0007a0008a0012others(42): Show | 54 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
missense_variant | MODERATE | c.14525G>A | p.Arg4842Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 50/363 | 14750/109224 | 14525/107976 | 4842/35991 | chr2 | 178735921 | ||
| chr2:178739374
|
C | T | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.13859G>A | p.Gly4620Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 14084/109224 | 13859/107976 | 4620/35991 | chr2 | 178739374 | ||
| chr2:178739433
|
T | G | 23 | a0007a0008a0012others(20): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
missense_variant | MODERATE | c.13800A>C | p.Leu4600Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 14025/109224 | 13800/107976 | 4600/35991 | chr2 | 178739433 | ||
| chr2:178739639
|
T | G | 23 | a0007a0008a0012others(20): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
missense_variant | MODERATE | c.13594A>C | p.Thr4532Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 13819/109224 | 13594/107976 | 4532/35991 | chr2 | 178739639 | ||
| chr2:178740031
|
C | T | 2 | a0061a0097 | 2 | HG02280.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.13202G>A | p.Arg4401Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 13427/109224 | 13202/107976 | 4401/35991 | chr2 | 178740031 | ||
| chr2:178741000
|
G | A | 2 | a0024a0181 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.12233C>T | p.Thr4078Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 12458/109224 | 12233/107976 | 4078/35991 | chr2 | 178741000 | ||
| chr2:178741445
|
C | T | 1 | a0122 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.11788G>A | p.Glu3930Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 12013/109224 | 11788/107976 | 3930/35991 | chr2 | 178741445 | ||
| chr2:178741514
|
G | C | 5 | a0017a0018a0065others(2): Show | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
missense_variant | MODERATE | c.11719C>G | p.Leu3907Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 11944/109224 | 11719/107976 | 3907/35991 | chr2 | 178741514 | ||
| chr2:178741811
|
G | A | 77 | a0004a0007a0008others(74): Show | 94 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(91): Show |
missense_variant | MODERATE | c.11422C>T | p.Pro3808Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 11647/109224 | 11422/107976 | 3808/35991 | chr2 | 178741811 | ||
| chr2:178756224
|
C | T | 144 | a0001a0002a0003others(141): Show | 180 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
missense_variant&splice_region_variant | MODERATE | c.11252G>A | p.Gly3751Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/363 | 11477/109224 | 11252/107976 | 3751/35991 | chr2 | 178756224 | ||
| chr2:178756545
|
C | T | 10 | a0005a0088a0089others(7): Show | 13 | HG00408.hp1 HG03490.hp1 HG03492.hp1 others(10): Show |
missense_variant | MODERATE | c.10931G>A | p.Ser3644Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/363 | 11156/109224 | 10931/107976 | 3644/35991 | chr2 | 178756545 | ||
| chr2:178756622
|
T | G | 1 | a0155 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.10854A>C | p.Gln3618His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/363 | 11079/109224 | 10854/107976 | 3618/35991 | chr2 | 178756622 | ||
| chr2:178756626
|
G | A | 4 | a0175a0177a0178others(1): Show | 4 | HG02559.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
missense_variant | MODERATE | c.10850C>T | p.Ser3617Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/363 | 11075/109224 | 10850/107976 | 3617/35991 | chr2 | 178756626 | ||
| chr2:178756750
|
T | C | 1 | a0176 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.10726A>G | p.Thr3576Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/363 | 10951/109224 | 10726/107976 | 3576/35991 | chr2 | 178756750 | ||
| chr2:178757842
|
G | C | 1 | a0175 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.10378C>G | p.Pro3460Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/363 | 10603/109224 | 10378/107976 | 3460/35991 | chr2 | 178757842 | ||
| chr2:178759031
|
C | T | 144 | a0001a0002a0003others(141): Show | 180 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
missense_variant | MODERATE | c.10256G>A | p.Ser3419Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/363 | 10481/109224 | 10256/107976 | 3419/35991 | chr2 | 178759031 | ||
| chr2:178759124
|
C | T | 1 | a0186 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.10163G>A | p.Arg3388Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/363 | 10388/109224 | 10163/107976 | 3388/35991 | chr2 | 178759124 | ||
| chr2:178764191
|
C | T | 2 | a0087a0131 | 2 | HG01358.hp2 NA18974.hp1 |
missense_variant | MODERATE | c.10100G>A | p.Arg3367Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/363 | 10325/109224 | 10100/107976 | 3367/35991 | chr2 | 178764191 | ||
| chr2:178764203
|
C | T | 1 | a0158 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.10088G>A | p.Arg3363His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/363 | 10313/109224 | 10088/107976 | 3363/35991 | chr2 | 178764203 | ||
| chr2:178764734
|
C | T | 144 | a0001a0002a0003others(141): Show | 180 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
missense_variant | MODERATE | c.9781G>A | p.Val3261Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 42/363 | 10006/109224 | 9781/107976 | 3261/35991 | chr2 | 178764734 | ||
| chr2:178767769
|
T | C | 18 | a0004a0009a0022others(15): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
missense_variant | MODERATE | c.9461A>G | p.Lys3154Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/363 | 9686/109224 | 9461/107976 | 3154/35991 | chr2 | 178767769 | ||
| chr2:178767871
|
C | T | 1 | a0039 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.9359G>A | p.Arg3120Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/363 | 9584/109224 | 9359/107976 | 3120/35991 | chr2 | 178767871 | ||
| chr2:178767892
|
C | T | 2 | a0086a0130 | 2 | HG02027.hp1 NA19007.hp1 |
missense_variant | MODERATE | c.9338G>A | p.Arg3113His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/363 | 9563/109224 | 9338/107976 | 3113/35991 | chr2 | 178767892 | ||
| chr2:178768110
|
A | G | 1 | a0037 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.9209T>C | p.Leu3070Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 39/363 | 9434/109224 | 9209/107976 | 3070/35991 | chr2 | 178768110 | ||
| chr2:178768898
|
C | T | 1 | a0184 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.8938G>A | p.Ala2980Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 38/363 | 9163/109224 | 8938/107976 | 2980/35991 | chr2 | 178768898 | ||
| chr2:178770209
|
C | T | 23 | a0007a0008a0012others(20): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
missense_variant | MODERATE | c.8492G>A | p.Ser2831Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 36/363 | 8717/109224 | 8492/107976 | 2831/35991 | chr2 | 178770209 | ||
| chr2:178770234
|
C | A | 1 | a0085 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.8467G>T | p.Val2823Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 36/363 | 8692/109224 | 8467/107976 | 2823/35991 | chr2 | 178770234 | ||
| chr2:178771258
|
G | A | 1 | a0084 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.8069C>T | p.Thr2690Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 34/363 | 8294/109224 | 8069/107976 | 2690/35991 | chr2 | 178771258 | ||
| chr2:178773134
|
C | G | 21 | a0007a0008a0012others(18): Show | 27 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(24): Show |
missense_variant | MODERATE | c.7830G>C | p.Met2610Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/363 | 8055/109224 | 7830/107976 | 2610/35991 | chr2 | 178773134 | ||
| chr2:178773224
|
A | C | 1 | a0159 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.7740T>G | p.Ile2580Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/363 | 7965/109224 | 7740/107976 | 2580/35991 | chr2 | 178773224 | ||
| chr2:178773714
|
T | C | 1 | a0126 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.7342A>G | p.Ile2448Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 32/363 | 7567/109224 | 7342/107976 | 2448/35991 | chr2 | 178773714 | ||
| chr2:178773994
|
C | T | 18 | a0004a0009a0022others(15): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
missense_variant | MODERATE | c.7174G>A | p.Gly2392Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 31/363 | 7399/109224 | 7174/107976 | 2392/35991 | chr2 | 178773994 | ||
| chr2:178774107
|
C | T | 1 | a0150 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.7061G>A | p.Arg2354His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 31/363 | 7286/109224 | 7061/107976 | 2354/35991 | chr2 | 178774107 | ||
| chr2:178774984
|
C | A | 2 | a0064a0158 | 2 | HG02055.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.6727G>T | p.Asp2243Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 29/363 | 6952/109224 | 6727/107976 | 2243/35991 | chr2 | 178774984 | ||
| chr2:178775511
|
A | G | 2 | a0024a0181 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.6353T>C | p.Ile2118Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 28/363 | 6578/109224 | 6353/107976 | 2118/35991 | chr2 | 178775511 | ||
| chr2:178775871
|
C | T | 1 | a0183 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.5993G>A | p.Arg1998His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 28/363 | 6218/109224 | 5993/107976 | 1998/35991 | chr2 | 178775871 | ||
| chr2:178776196
|
G | A | 1 | a0083 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.5668C>T | p.Arg1890Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 28/363 | 5893/109224 | 5668/107976 | 1890/35991 | chr2 | 178776196 | ||
| chr2:178776633
|
G | A | 3 | a0160a0161a0162 | 3 | HG00558.hp1 NA18975.hp2 NA19054.hp1 |
missense_variant | MODERATE | c.5231C>T | p.Pro1744Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 28/363 | 5456/109224 | 5231/107976 | 1744/35991 | chr2 | 178776633 | ||
| chr2:178777224
|
G | A | 1 | a0082 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.4739C>T | p.Thr1580Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 27/363 | 4964/109224 | 4739/107976 | 1580/35991 | chr2 | 178777224 | ||
| chr2:178777248
|
C | T | 21 | a0007a0008a0012others(18): Show | 27 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(24): Show |
missense_variant | MODERATE | c.4715G>A | p.Arg1572Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 27/363 | 4940/109224 | 4715/107976 | 1572/35991 | chr2 | 178777248 | ||
| chr2:178777435
|
T | C | 2 | a0127a0128 | 2 | HG02809.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.4630A>G | p.Ile1544Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 26/363 | 4855/109224 | 4630/107976 | 1544/35991 | chr2 | 178777435 | ||
| chr2:178777862
|
C | G | 3 | a0188a0189a0190 | 3 | HG00741.hp1 HG01099.hp2 NA18612.hp1 |
missense_variant | MODERATE | c.4322G>C | p.Arg1441Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 25/363 | 4547/109224 | 4322/107976 | 1441/35991 | chr2 | 178777862 | ||
| chr2:178777938
|
G | A | 6 | a0023a0150a0151others(3): Show | 7 | HG01361.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
missense_variant | MODERATE | c.4246C>T | p.Arg1416Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 25/363 | 4471/109224 | 4246/107976 | 1416/35991 | chr2 | 178777938 | ||
| chr2:178778883
|
C | G | 2 | a0028a0029 | 2 | HG02451.hp2 HG02559.hp2 |
missense_variant | MODERATE | c.4199G>C | p.Ser1400Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/363 | 4424/109224 | 4199/107976 | 1400/35991 | chr2 | 178778883 | ||
| chr2:178778905
|
T | C | 11 | a0023a0064a0150others(8): Show | 12 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
missense_variant | MODERATE | c.4177A>G | p.Ile1393Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/363 | 4402/109224 | 4177/107976 | 1393/35991 | chr2 | 178778905 | ||
| chr2:178778913
|
G | A | 1 | a0129 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.4169C>T | p.Pro1390Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/363 | 4394/109224 | 4169/107976 | 1390/35991 | chr2 | 178778913 | ||
| chr2:178778922
|
A | G | 1 | a0159 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.4160T>C | p.Leu1387Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/363 | 4385/109224 | 4160/107976 | 1387/35991 | chr2 | 178778922 | ||
| chr2:178779237
|
A | T | 1 | a0187 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.3955T>A | p.Leu1319Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 23/363 | 4180/109224 | 3955/107976 | 1319/35991 | chr2 | 178779237 | ||
| chr2:178779308
|
G | A | 164 | a0001a0002a0003others(161): Show | 209 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
missense_variant | MODERATE | c.3884C>T | p.Ser1295Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 23/363 | 4109/109224 | 3884/107976 | 1295/35991 | chr2 | 178779308 | ||
| chr2:178780061
|
G | A | 2 | a0024a0181 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.3668C>T | p.Ala1223Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 22/363 | 3893/109224 | 3668/107976 | 1223/35991 | chr2 | 178780061 | ||
| chr2:178780128
|
T | C | 71 | a0003a0005a0006others(68): Show | 83 | HG00408.hp1 HG00423.hp1 HG00639.hp1 others(80): Show |
missense_variant | MODERATE | c.3601A>G | p.Lys1201Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 22/363 | 3826/109224 | 3601/107976 | 1201/35991 | chr2 | 178780128 | ||
| chr2:178781121
|
C | T | 1 | a0182 | 1 | HG02683.hp1 | missense_variant&splice_region_variant | MODERATE | c.3523G>A | p.Ala1175Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 21/363 | 3748/109224 | 3523/107976 | 1175/35991 | chr2 | 178781121 | ||
| chr2:178782806
|
C | T | 1 | a0081 | 1 | HG02738.hp1 | missense_variant&splice_region_variant | MODERATE | c.3100G>A | p.Val1034Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 18/363 | 3325/109224 | 3100/107976 | 1034/35991 | chr2 | 178782806 | ||
| chr2:178784080
|
C | T | 3 | a0078a0079a0080 | 3 | HG02257.hp1 HG02486.hp2 HG02615.hp2 |
missense_variant | MODERATE | c.2765G>A | p.Arg922His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 16/363 | 2990/109224 | 2765/107976 | 922/35991 | chr2 | 178784080 | ||
| chr2:178785681
|
G | A | 10 | a0003a0019a0070others(7): Show | 15 | HG00741.hp2 HG01071.hp1 HG01175.hp2 others(12): Show |
missense_variant | MODERATE | c.2432C>T | p.Thr811Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/363 | 2657/109224 | 2432/107976 | 811/35991 | chr2 | 178785681 | ||
| chr2:178785948
|
G | A | 2 | a0068a0069 | 2 | HG02965.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.2270C>T | p.Pro757Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 14/363 | 2495/109224 | 2270/107976 | 757/35991 | chr2 | 178785948 | ||
| chr2:178795088
|
C | G | 2 | a0183a0184 | 2 | HG02738.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.1079G>C | p.Arg360Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 7/363 | 1304/109224 | 1079/107976 | 360/35991 | chr2 | 178795088 | ||
| chr2:178795164
|
C | T | 5 | a0017a0018a0065others(2): Show | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
missense_variant | MODERATE | c.1003G>A | p.Val335Met | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 7/363 | 1228/109224 | 1003/107976 | 335/35991 | chr2 | 178795164 | ||
| chr2:178795185
|
G | A | 50 | a0001a0002a0012others(47): Show | 69 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(66): Show |
missense_variant | MODERATE | c.982C>T | p.Arg328Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 7/363 | 1207/109224 | 982/107976 | 328/35991 | chr2 | 178795185 | ||
| chr2:178795197
|
G | A | 1 | a0185 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.970C>T | p.Pro324Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 7/363 | 1195/109224 | 970/107976 | 324/35991 | chr2 | 178795197 | ||
| chr2:178800436
|
C | T | 6 | a0011a0025a0026others(3): Show | 7 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(4): Show |
missense_variant | MODERATE | c.542G>A | p.Ser181Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 4/363 | 767/109224 | 542/107976 | 181/35991 | chr2 | 178800436 | ||
| chr2:178800631
|
C | G | 1 | a0186 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.347G>C | p.Arg116Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 4/363 | 572/109224 | 347/107976 | 116/35991 | chr2 | 178800631 | ||
| chr2:178802255
|
C | A | 7 | a0187a0188a0189others(4): Show | 7 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(4): Show |
missense_variant | MODERATE | c.178G>T | p.Asp60Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/363 | 403/109224 | 178/107976 | 60/35991 | chr2 | 178802255 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:178527288
|
T | C | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.107700A>G | p.Glu35900Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 363/363 | 107925/109224 | 107700/107976 | 35900/35991 | chr2 | 178527288 | ||
| chr2:178528894
|
G | A | 1 | a0156c0106 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.106857C>T | p.Asn35619Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 360/363 | 107082/109224 | 106857/107976 | 35619/35991 | chr2 | 178528894 | ||
| chr2:178529113
|
C | T | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.106638G>A | p.Arg35546Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 360/363 | 106863/109224 | 106638/107976 | 35546/35991 | chr2 | 178529113 | ||
| chr2:178529173
|
A | T | 1 | a0128c0144 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.106578T>A | p.Ser35526Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 360/363 | 106803/109224 | 106578/107976 | 35526/35991 | chr2 | 178529173 | ||
| chr2:178530015
|
A | G | 4 | a0159c0091a0177c0084a0178c0085others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.106476T>C | p.Cys35492Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 359/363 | 106701/109224 | 106476/107976 | 35492/35991 | chr2 | 178530015 | ||
| chr2:178530340
|
C | G | 5 | a0006c0018a0078c0055a0102c0130others(2): Show | 6 | HG00639.hp2 HG01361.hp2 HG01978.hp2 others(3): Show |
synonymous_variant | LOW | c.106275G>C | p.Gly35425Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 106500/109224 | 106275/107976 | 35425/35991 | chr2 | 178530340 | ||
| chr2:178531033
|
G | A | 22 | a0002c0002a0002c0022a0012c0020others(19): Show | 27 | HG00609.hp1 HG00735.hp1 HG01346.hp2 others(24): Show |
synonymous_variant | LOW | c.105582C>T | p.Ser35194Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 105807/109224 | 105582/107976 | 35194/35991 | chr2 | 178531033 | ||
| chr2:178531231
|
T | C | 134 | a0001c0001a0001c0021a0001c0171others(131): Show | 157 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(154): Show |
synonymous_variant | LOW | c.105384A>G | p.Ala35128Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 105609/109224 | 105384/107976 | 35128/35991 | chr2 | 178531231 | ||
| chr2:178531387
|
C | T | 1 | a0076c0150 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.105228G>A | p.Ser35076Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 105453/109224 | 105228/107976 | 35076/35991 | chr2 | 178531387 | ||
| chr2:178531627
|
G | A | 60 | a0001c0001a0001c0021a0001c0171others(57): Show | 70 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
synonymous_variant | LOW | c.104988C>T | p.Val34996Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 105213/109224 | 104988/107976 | 34996/35991 | chr2 | 178531627 | ||
| chr2:178532023
|
C | T | 1 | a0009c0105 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.104592G>A | p.Pro34864Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 104817/109224 | 104592/107976 | 34864/35991 | chr2 | 178532023 | ||
| chr2:178532641
|
G | A | 1 | a0045c0179 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.103974C>T | p.Ile34658Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 104199/109224 | 103974/107976 | 34658/35991 | chr2 | 178532641 | ||
| chr2:178533562
|
G | A | 1 | a0036c0164 | 1 | NA19004.hp2 | synonymous_variant | LOW | c.103053C>T | p.Thr34351Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 103278/109224 | 103053/107976 | 34351/35991 | chr2 | 178533562 | ||
| chr2:178534096
|
G | A | 60 | a0001c0001a0001c0021a0001c0171others(57): Show | 70 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
synonymous_variant | LOW | c.102519C>T | p.Gly34173Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 102744/109224 | 102519/107976 | 34173/35991 | chr2 | 178534096 | ||
| chr2:178534918
|
G | A | 2 | a0028c0026a0029c0025 | 2 | HG02451.hp2 HG02559.hp2 |
synonymous_variant | LOW | c.101697C>T | p.Asp33899Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 101922/109224 | 101697/107976 | 33899/35991 | chr2 | 178534918 | ||
| chr2:178535209
|
G | C | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.101406C>G | p.Val33802Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 101631/109224 | 101406/107976 | 33802/35991 | chr2 | 178535209 | ||
| chr2:178535551
|
A | G | 1 | a0156c0106 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.101064T>C | p.Asp33688Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 358/363 | 101289/109224 | 101064/107976 | 33688/35991 | chr2 | 178535551 | ||
| chr2:178537050
|
A | T | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.100059T>A | p.Ile33353Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 356/363 | 100284/109224 | 100059/107976 | 33353/35991 | chr2 | 178537050 | ||
| chr2:178537862
|
A | C | 1 | a0001c0197 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.99345T>G | p.Gly33115Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 355/363 | 99570/109224 | 99345/107976 | 33115/35991 | chr2 | 178537862 | ||
| chr2:178538718
|
A | G | 2 | a0064c0202a0158c0109 | 2 | HG02055.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.99111T>C | p.Tyr33037Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 354/363 | 99336/109224 | 99111/107976 | 33037/35991 | chr2 | 178538718 | ||
| chr2:178539566
|
G | A | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.98499C>T | p.Leu32833Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 352/363 | 98724/109224 | 98499/107976 | 32833/35991 | chr2 | 178539566 | ||
| chr2:178539626
|
C | T | 1 | a0156c0106 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.98439G>A | p.Val32813Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 352/363 | 98664/109224 | 98439/107976 | 32813/35991 | chr2 | 178539626 | ||
| chr2:178541556
|
C | T | 1 | a0044c0193 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.97521G>A | p.Gln32507Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 350/363 | 97746/109224 | 97521/107976 | 32507/35991 | chr2 | 178541556 | ||
| chr2:178543472
|
A | G | 3 | a0042c0172a0079c0053a0080c0054 | 3 | HG02257.hp1 HG02486.hp1 HG02615.hp2 |
synonymous_variant | LOW | c.96501T>C | p.Ser32167Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 347/363 | 96726/109224 | 96501/107976 | 32167/35991 | chr2 | 178543472 | ||
| chr2:178544036
|
C | T | 1 | a0156c0106 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.96108G>A | p.Val32036Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 346/363 | 96333/109224 | 96108/107976 | 32036/35991 | chr2 | 178544036 | ||
| chr2:178544214
|
G | A | 1 | a0080c0054 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.96015C>T | p.Pro32005Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 345/363 | 96240/109224 | 96015/107976 | 32005/35991 | chr2 | 178544214 | ||
| chr2:178545557
|
G | A | 7 | a0023c0016a0027c0029a0150c0110others(4): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
synonymous_variant | LOW | c.95553C>T | p.Ser31851Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 344/363 | 95778/109224 | 95553/107976 | 31851/35991 | chr2 | 178545557 | ||
| chr2:178546088
|
G | A | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.95148C>T | p.Thr31716Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 343/363 | 95373/109224 | 95148/107976 | 31716/35991 | chr2 | 178546088 | ||
| chr2:178548239
|
G | A | 2 | a0085c0049a0122c0034 | 2 | HG01175.hp1 HG02300.hp2 |
synonymous_variant | LOW | c.93387C>T | p.Ser31129Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 339/363 | 93612/109224 | 93387/107976 | 31129/35991 | chr2 | 178548239 | ||
| chr2:178548383
|
G | A | 60 | a0001c0001a0001c0021a0001c0171others(57): Show | 70 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
synonymous_variant | LOW | c.93243C>T | p.Ala31081Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 339/363 | 93468/109224 | 93243/107976 | 31081/35991 | chr2 | 178548383 | ||
| chr2:178548725
|
G | A | 1 | a0003c0147 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.92901C>T | p.Ser30967Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 339/363 | 93126/109224 | 92901/107976 | 30967/35991 | chr2 | 178548725 | ||
| chr2:178548911
|
G | A | 1 | a0161c0089 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.92715C>T | p.Gly30905Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 339/363 | 92940/109224 | 92715/107976 | 30905/35991 | chr2 | 178548911 | ||
| chr2:178551829
|
A | C | 39 | a0004c0004a0004c0015a0009c0093others(36): Show | 46 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(43): Show |
synonymous_variant | LOW | c.91071T>G | p.Thr30357Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 335/363 | 91296/109224 | 91071/107976 | 30357/35991 | chr2 | 178551829 | ||
| chr2:178552906
|
C | T | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.89994G>A | p.Ser29998Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 335/363 | 90219/109224 | 89994/107976 | 29998/35991 | chr2 | 178552906 | ||
| chr2:178554145
|
T | G | 1 | a0130c0056 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.88966A>C | p.Arg29656Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 333/363 | 89191/109224 | 88966/107976 | 29656/35991 | chr2 | 178554145 | ||
| chr2:178554489
|
G | A | 2 | a0066c0032a0179c0083 | 2 | HG02895.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.88858C>T | p.Leu29620Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 332/363 | 89083/109224 | 88858/107976 | 29620/35991 | chr2 | 178554489 | ||
| chr2:178554736
|
A | C | 1 | a0037c0158 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.88611T>G | p.Pro29537Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 332/363 | 88836/109224 | 88611/107976 | 29537/35991 | chr2 | 178554736 | ||
| chr2:178556882
|
C | T | 20 | a0004c0004a0004c0015a0009c0093others(17): Show | 25 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(22): Show |
synonymous_variant | LOW | c.88272G>A | p.Glu29424Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/363 | 88497/109224 | 88272/107976 | 29424/35991 | chr2 | 178556882 | ||
| chr2:178557685
|
A | G | 7 | a0023c0016a0027c0029a0150c0110others(4): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
synonymous_variant | LOW | c.87669T>C | p.His29223His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 328/363 | 87894/109224 | 87669/107976 | 29223/35991 | chr2 | 178557685 | ||
| chr2:178558372
|
A | G | 10 | a0008c0012a0008c0064a0035c0163others(7): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
synonymous_variant | LOW | c.87087T>C | p.Leu29029Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 327/363 | 87312/109224 | 87087/107976 | 29029/35991 | chr2 | 178558372 | ||
| chr2:178559321
|
T | C | 2 | a0097c0139a0115c0140 | 2 | HG01496.hp2 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.86811A>G | p.Val28937Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 87036/109224 | 86811/107976 | 28937/35991 | chr2 | 178559321 | ||
| chr2:178560080
|
A | G | 1 | a0174c0081 | 1 | NA19058.hp2 | synonymous_variant | LOW | c.86052T>C | p.Thr28684Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 86277/109224 | 86052/107976 | 28684/35991 | chr2 | 178560080 | ||
| chr2:178561679
|
T | C | 2 | a0057c0181a0063c0200 | 2 | HG02818.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.84453A>G | p.Pro28151Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 84678/109224 | 84453/107976 | 28151/35991 | chr2 | 178561679 | ||
| chr2:178562459
|
A | G | 134 | a0001c0001a0001c0021a0001c0171others(131): Show | 157 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(154): Show |
synonymous_variant | LOW | c.83673T>C | p.Gly27891Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 83898/109224 | 83673/107976 | 27891/35991 | chr2 | 178562459 | ||
| chr2:178563392
|
C | T | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.82740G>A | p.Thr27580Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 82965/109224 | 82740/107976 | 27580/35991 | chr2 | 178563392 | ||
| chr2:178563440
|
C | T | 1 | a0056c0190 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.82692G>A | p.Ala27564Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 82917/109224 | 82692/107976 | 27564/35991 | chr2 | 178563440 | ||
| chr2:178563557
|
C | T | 3 | a0123c0137a0124c0120a0129c0115 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.82575G>A | p.Thr27525Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 82800/109224 | 82575/107976 | 27525/35991 | chr2 | 178563557 | ||
| chr2:178564277
|
G | A | 9 | a0008c0012a0008c0064a0035c0163others(6): Show | 10 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(7): Show |
synonymous_variant | LOW | c.81855C>T | p.Ile27285Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 82080/109224 | 81855/107976 | 27285/35991 | chr2 | 178564277 | ||
| chr2:178565075
|
A | G | 2 | a0064c0202a0158c0109 | 2 | HG02055.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.81057T>C | p.Thr27019Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 81282/109224 | 81057/107976 | 27019/35991 | chr2 | 178565075 | ||
| chr2:178565228
|
G | A | 1 | a0003c0147 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.80904C>T | p.Ile26968Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 81129/109224 | 80904/107976 | 26968/35991 | chr2 | 178565228 | ||
| chr2:178565333
|
G | T | 9 | a0008c0012a0008c0064a0035c0163others(6): Show | 10 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(7): Show |
synonymous_variant | LOW | c.80799C>A | p.Thr26933Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 81024/109224 | 80799/107976 | 26933/35991 | chr2 | 178565333 | ||
| chr2:178565810
|
G | A | 2 | a0015c0182a0055c0189 | 2 | HG01346.hp2 NA18955.hp1 |
synonymous_variant | LOW | c.80322C>T | p.Ala26774Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 80547/109224 | 80322/107976 | 26774/35991 | chr2 | 178565810 | ||
| chr2:178565861
|
G | A | 1 | a0106c0129 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.80271C>T | p.Val26757Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 80496/109224 | 80271/107976 | 26757/35991 | chr2 | 178565861 | ||
| chr2:178566443
|
G | T | 2 | a0006c0141a0083c0142 | 2 | HG02896.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.79689C>A | p.Val26563Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 79914/109224 | 79689/107976 | 26563/35991 | chr2 | 178566443 | ||
| chr2:178567070
|
A | T | 23 | a0002c0002a0002c0022a0012c0020others(20): Show | 28 | HG00609.hp1 HG00735.hp1 HG01346.hp2 others(25): Show |
synonymous_variant | LOW | c.79062T>A | p.Gly26354Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 79287/109224 | 79062/107976 | 26354/35991 | chr2 | 178567070 | ||
| chr2:178570019
|
T | C | 1 | a0191c0211 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.76113A>G | p.Glu25371Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 76338/109224 | 76113/107976 | 25371/35991 | chr2 | 178570019 | ||
| chr2:178570610
|
T | G | 34 | a0004c0004a0004c0015a0009c0093others(31): Show | 40 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(37): Show |
synonymous_variant | LOW | c.75522A>C | p.Ala25174Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 75747/109224 | 75522/107976 | 25174/35991 | chr2 | 178570610 | ||
| chr2:178570940
|
A | G | 1 | a0057c0181 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.75192T>C | p.Thr25064Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 75417/109224 | 75192/107976 | 25064/35991 | chr2 | 178570940 | ||
| chr2:178571129
|
A | G | 1 | a0139c0096 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.75003T>C | p.Tyr25001Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 75228/109224 | 75003/107976 | 25001/35991 | chr2 | 178571129 | ||
| chr2:178573508
|
T | C | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.72624A>G | p.Pro24208Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 72849/109224 | 72624/107976 | 24208/35991 | chr2 | 178573508 | ||
| chr2:178574027
|
A | G | 2 | a0009c0093a0139c0096 | 2 | HG03710.hp2 HG03942.hp1 |
synonymous_variant | LOW | c.72105T>C | p.Phe24035Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 72330/109224 | 72105/107976 | 24035/35991 | chr2 | 178574027 | ||
| chr2:178574099
|
T | C | 2 | a0150c0110a0155c0108 | 2 | HG01361.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.72033A>G | p.Pro24011Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 72258/109224 | 72033/107976 | 24011/35991 | chr2 | 178574099 | ||
| chr2:178574192
|
C | T | 2 | a0150c0110a0155c0108 | 2 | HG01361.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.71940G>A | p.Leu23980Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 72165/109224 | 71940/107976 | 23980/35991 | chr2 | 178574192 | ||
| chr2:178574792
|
G | A | 1 | a0009c0095 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.71340C>T | p.Thr23780Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 71565/109224 | 71340/107976 | 23780/35991 | chr2 | 178574792 | ||
| chr2:178575302
|
G | A | 13 | a0020c0010a0028c0026a0029c0025others(10): Show | 14 | HG00423.hp1 HG01071.hp1 HG01358.hp1 others(11): Show |
synonymous_variant | LOW | c.70830C>T | p.Ser23610Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/363 | 71055/109224 | 70830/107976 | 23610/35991 | chr2 | 178575302 | ||
| chr2:178577104
|
A | G | 1 | a0038c0166 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.69231T>C | p.Leu23077Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 324/363 | 69456/109224 | 69231/107976 | 23077/35991 | chr2 | 178577104 | ||
| chr2:178578813
|
A | G | 32 | a0004c0004a0004c0015a0009c0093others(29): Show | 38 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(35): Show |
synonymous_variant | LOW | c.68217T>C | p.His22739His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 320/363 | 68442/109224 | 68217/107976 | 22739/35991 | chr2 | 178578813 | ||
| chr2:178578948
|
G | A | 1 | a0002c0022 | 2 | NA18965.hp1 NA19005.hp2 |
synonymous_variant | LOW | c.68082C>T | p.Cys22694Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 320/363 | 68307/109224 | 68082/107976 | 22694/35991 | chr2 | 178578948 | ||
| chr2:178578951
|
C | T | 2 | a0068c0156a0069c0155 | 2 | HG02965.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.68079G>A | p.Thr22693Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 320/363 | 68304/109224 | 68079/107976 | 22693/35991 | chr2 | 178578951 | ||
| chr2:178579562
|
A | G | 11 | a0008c0012a0008c0064a0035c0163others(8): Show | 12 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(9): Show |
synonymous_variant | LOW | c.67635T>C | p.Val22545Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 319/363 | 67860/109224 | 67635/107976 | 22545/35991 | chr2 | 178579562 | ||
| chr2:178583121
|
T | C | 137 | a0001c0001a0001c0021a0001c0171others(134): Show | 160 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
synonymous_variant | LOW | c.65682A>G | p.Thr21894Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 313/363 | 65907/109224 | 65682/107976 | 21894/35991 | chr2 | 178583121 | ||
| chr2:178587179
|
G | A | 3 | a0043c0194a0173c0069a0183c0204 | 3 | HG02015.hp1 HG02165.hp2 HG02738.hp2 |
synonymous_variant | LOW | c.64032C>T | p.Asn21344Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 307/363 | 64257/109224 | 64032/107976 | 21344/35991 | chr2 | 178587179 | ||
| chr2:178588560
|
C | T | 1 | a0085c0049 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.63165G>A | p.Pro21055Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 63390/109224 | 63165/107976 | 21055/35991 | chr2 | 178588560 | ||
| chr2:178589547
|
A | G | 4 | a0159c0091a0177c0084a0178c0085others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.62178T>C | p.Thr20726Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 62403/109224 | 62178/107976 | 20726/35991 | chr2 | 178589547 | ||
| chr2:178589667
|
A | G | 137 | a0001c0001a0001c0021a0001c0171others(134): Show | 160 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
synonymous_variant | LOW | c.62058T>C | p.Tyr20686Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 62283/109224 | 62058/107976 | 20686/35991 | chr2 | 178589667 | ||
| chr2:178590480
|
T | C | 137 | a0001c0001a0001c0021a0001c0171others(134): Show | 160 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
synonymous_variant | LOW | c.61245A>G | p.Thr20415Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 61470/109224 | 61245/107976 | 20415/35991 | chr2 | 178590480 | ||
| chr2:178591344
|
A | T | 1 | a0026c0027 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.60381T>A | p.Val20127Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 304/363 | 60606/109224 | 60381/107976 | 20127/35991 | chr2 | 178591344 | ||
| chr2:178591876
|
G | T | 1 | a0106c0129 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.59943C>A | p.Pro19981Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 303/363 | 60168/109224 | 59943/107976 | 19981/35991 | chr2 | 178591876 | ||
| chr2:178592069
|
G | A | 1 | a0062c0199 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.59835C>T | p.Asn19945Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 302/363 | 60060/109224 | 59835/107976 | 19945/35991 | chr2 | 178592069 | ||
| chr2:178593275
|
G | A | 13 | a0007c0003a0010c0013a0010c0072others(10): Show | 16 | HG00558.hp2 HG01099.hp1 HG01975.hp2 others(13): Show |
synonymous_variant | LOW | c.58933C>T | p.Leu19645Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 299/363 | 59158/109224 | 58933/107976 | 19645/35991 | chr2 | 178593275 | ||
| chr2:178593339
|
T | C | 1 | a0184c0033 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.58869A>G | p.Lys19623Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 299/363 | 59094/109224 | 58869/107976 | 19623/35991 | chr2 | 178593339 | ||
| chr2:178595706
|
G | A | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.57648C>T | p.Ile19216Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/363 | 57873/109224 | 57648/107976 | 19216/35991 | chr2 | 178595706 | ||
| chr2:178597620
|
C | T | 2 | a0177c0084a0178c0085 | 2 | HG02559.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.57462G>A | p.Gln19154Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/363 | 57687/109224 | 57462/107976 | 19154/35991 | chr2 | 178597620 | ||
| chr2:178597767
|
A | G | 9 | a0020c0010a0048c0185a0052c0183others(6): Show | 10 | HG00423.hp1 HG01071.hp1 HG01358.hp1 others(7): Show |
synonymous_variant | LOW | c.57315T>C | p.His19105His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/363 | 57540/109224 | 57315/107976 | 19105/35991 | chr2 | 178597767 | ||
| chr2:178599723
|
A | T | 1 | a0055c0189 | 1 | NA18955.hp1 | synonymous_variant | LOW | c.56178T>A | p.Pro18726Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 289/363 | 56403/109224 | 56178/107976 | 18726/35991 | chr2 | 178599723 | ||
| chr2:178601548
|
G | A | 1 | a0015c0182 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.55449C>T | p.Pro18483Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 287/363 | 55674/109224 | 55449/107976 | 18483/35991 | chr2 | 178601548 | ||
| chr2:178604988
|
A | G | 2 | a0010c0013a0089c0066 | 3 | NA18948.hp1 NA18980.hp1 NA19063.hp1 |
splice_region_variant&synonymous_variant | LOW | c.54189T>C | p.Tyr18063Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 280/363 | 54414/109224 | 54189/107976 | 18063/35991 | chr2 | 178604988 | ||
| chr2:178607870
|
A | G | 5 | a0057c0181a0063c0200a0123c0137others(2): Show | 5 | HG02818.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
synonymous_variant | LOW | c.52917T>C | p.Asp17639Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 276/363 | 53142/109224 | 52917/107976 | 17639/35991 | chr2 | 178607870 | ||
| chr2:178607966
|
A | G | 11 | a0008c0012a0008c0064a0012c0020others(8): Show | 13 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(10): Show |
synonymous_variant | LOW | c.52821T>C | p.Asp17607Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 276/363 | 53046/109224 | 52821/107976 | 17607/35991 | chr2 | 178607966 | ||
| chr2:178608227
|
A | G | 1 | a0185c0203 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.52656T>C | p.Pro17552Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 275/363 | 52881/109224 | 52656/107976 | 17552/35991 | chr2 | 178608227 | ||
| chr2:178609739
|
C | T | 10 | a0008c0012a0008c0064a0012c0020others(7): Show | 12 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(9): Show |
synonymous_variant | LOW | c.51684G>A | p.Ala17228Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 272/363 | 51909/109224 | 51684/107976 | 17228/35991 | chr2 | 178609739 | ||
| chr2:178612990
|
A | G | 27 | a0005c0005a0005c0117a0059c0175others(24): Show | 29 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(26): Show |
synonymous_variant | LOW | c.49731T>C | p.His16577His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 265/363 | 49956/109224 | 49731/107976 | 16577/35991 | chr2 | 178612990 | ||
| chr2:178613840
|
T | G | 2 | a0064c0202a0158c0109 | 2 | HG02055.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.49443A>C | p.Pro16481Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 263/363 | 49668/109224 | 49443/107976 | 16481/35991 | chr2 | 178613840 | ||
| chr2:178613912
|
T | A | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.49371A>T | p.Leu16457Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 263/363 | 49596/109224 | 49371/107976 | 16457/35991 | chr2 | 178613912 | ||
| chr2:178614518
|
C | T | 27 | a0005c0005a0005c0117a0059c0175others(24): Show | 29 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(26): Show |
synonymous_variant | LOW | c.48996G>A | p.Glu16332Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 261/363 | 49221/109224 | 48996/107976 | 16332/35991 | chr2 | 178614518 | ||
| chr2:178615459
|
A | G | 1 | a0071c0151 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.48486T>C | p.Val16162Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 259/363 | 48711/109224 | 48486/107976 | 16162/35991 | chr2 | 178615459 | ||
| chr2:178617951
|
C | T | 3 | a0018c0009a0019c0019a0067c0030 | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.47400G>A | p.Lys15800Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 253/363 | 47625/109224 | 47400/107976 | 15800/35991 | chr2 | 178617951 | ||
| chr2:178618080
|
A | G | 2 | a0068c0156a0069c0155 | 2 | HG02965.hp2 HG03098.hp1 |
splice_region_variant&synonymous_variant | LOW | c.47271T>C | p.Asp15757Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 253/363 | 47496/109224 | 47271/107976 | 15757/35991 | chr2 | 178618080 | ||
| chr2:178618750
|
T | C | 1 | a0120c0134 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.46800A>G | p.Glu15600Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 251/363 | 47025/109224 | 46800/107976 | 15600/35991 | chr2 | 178618750 | ||
| chr2:178620872
|
A | G | 13 | a0008c0012a0008c0064a0012c0020others(10): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
synonymous_variant | LOW | c.45738T>C | p.Ala15246Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 247/363 | 45963/109224 | 45738/107976 | 15246/35991 | chr2 | 178620872 | ||
| chr2:178621192
|
G | A | 5 | a0028c0026a0029c0025a0082c0052others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
synonymous_variant | LOW | c.45526C>T | p.Leu15176Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 246/363 | 45751/109224 | 45526/107976 | 15176/35991 | chr2 | 178621192 | ||
| chr2:178621626
|
C | T | 1 | a0119c0136 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.45198G>A | p.Gly15066Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/363 | 45423/109224 | 45198/107976 | 15066/35991 | chr2 | 178621626 | ||
| chr2:178625292
|
G | A | 2 | a0001c0186a0001c0197 | 2 | HG00673.hp2 NA18964.hp2 |
synonymous_variant | LOW | c.44529C>T | p.His14843His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 241/363 | 44754/109224 | 44529/107976 | 14843/35991 | chr2 | 178625292 | ||
| chr2:178632298
|
A | G | 15 | a0005c0005a0005c0117a0087c0119others(12): Show | 17 | HG00408.hp1 HG03490.hp1 HG03492.hp1 others(14): Show |
synonymous_variant | LOW | c.43596T>C | p.Asn14532Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 236/363 | 43821/109224 | 43596/107976 | 14532/35991 | chr2 | 178632298 | ||
| chr2:178633576
|
T | C | 25 | a0004c0004a0004c0015a0009c0093others(22): Show | 31 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(28): Show |
synonymous_variant | LOW | c.42783A>G | p.Lys14261Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 232/363 | 43008/109224 | 42783/107976 | 14261/35991 | chr2 | 178633576 | ||
| chr2:178634562
|
G | A | 2 | a0064c0202a0158c0109 | 2 | HG02055.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.42219C>T | p.Phe14073Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 230/363 | 42444/109224 | 42219/107976 | 14073/35991 | chr2 | 178634562 | ||
| chr2:178634625
|
G | A | 2 | a0150c0110a0155c0108 | 2 | HG01361.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.42156C>T | p.Ile14052Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 230/363 | 42381/109224 | 42156/107976 | 14052/35991 | chr2 | 178634625 | ||
| chr2:178636063
|
A | G | 13 | a0008c0012a0008c0064a0012c0020others(10): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
synonymous_variant | LOW | c.41508T>C | p.Ala13836Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 226/363 | 41733/109224 | 41508/107976 | 13836/35991 | chr2 | 178636063 | ||
| chr2:178636624
|
G | A | 1 | a0122c0034 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.41103C>T | p.Gly13701Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 225/363 | 41328/109224 | 41103/107976 | 13701/35991 | chr2 | 178636624 | ||
| chr2:178636729
|
C | T | 1 | a0023c0016 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.40998G>A | p.Glu13666Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 225/363 | 41223/109224 | 40998/107976 | 13666/35991 | chr2 | 178636729 | ||
| chr2:178652852
|
A | C | 1 | a0105c0041 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.38955T>G | p.Val12985Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 200/363 | 39180/109224 | 38955/107976 | 12985/35991 | chr2 | 178652852 | ||
| chr2:178652927
|
T | C | 13 | a0008c0012a0008c0064a0012c0020others(10): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
synonymous_variant | LOW | c.38880A>G | p.Pro12960Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 200/363 | 39105/109224 | 38880/107976 | 12960/35991 | chr2 | 178652927 | ||
| chr2:178653827
|
T | C | 8 | a0028c0026a0029c0025a0036c0164others(5): Show | 8 | HG01978.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
synonymous_variant | LOW | c.38535A>G | p.Pro12845Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 195/363 | 38760/109224 | 38535/107976 | 12845/35991 | chr2 | 178653827 | ||
| chr2:178654025
|
G | A | 1 | a0049c0188 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.38451C>T | p.Ala12817Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 194/363 | 38676/109224 | 38451/107976 | 12817/35991 | chr2 | 178654025 | ||
| chr2:178654485
|
C | T | 1 | a0017c0008 | 2 | HG02145.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.38256G>A | p.Pro12752Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 192/363 | 38481/109224 | 38256/107976 | 12752/35991 | chr2 | 178654485 | ||
| chr2:178654967
|
A | T | 1 | a0142c0097 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.38067T>A | p.Pro12689Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 190/363 | 38292/109224 | 38067/107976 | 12689/35991 | chr2 | 178654967 | ||
| chr2:178658087
|
C | T | 38 | a0004c0004a0004c0015a0009c0093others(35): Show | 43 | HG00544.hp2 HG00642.hp2 HG00735.hp1 others(40): Show |
synonymous_variant | LOW | c.37782G>A | p.Pro12594Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 186/363 | 38007/109224 | 37782/107976 | 12594/35991 | chr2 | 178658087 | ||
| chr2:178658147
|
A | G | 2 | a0064c0202a0158c0109 | 2 | HG02055.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.37722T>C | p.Val12574Val | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 186/363 | 37947/109224 | 37722/107976 | 12574/35991 | chr2 | 178658147 | ||
| chr2:178662348
|
T | C | 5 | a0090c0127a0163c0080a0166c0076others(2): Show | 5 | HG00438.hp1 HG02738.hp2 NA18955.hp2 others(2): Show |
synonymous_variant | LOW | c.37029A>G | p.Pro12343Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 177/363 | 37254/109224 | 37029/107976 | 12343/35991 | chr2 | 178662348 | ||
| chr2:178662748
|
C | T | 12 | a0059c0175a0061c0198a0062c0199others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(9): Show |
synonymous_variant | LOW | c.36855G>A | p.Pro12285Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 175/363 | 37080/109224 | 36855/107976 | 12285/35991 | chr2 | 178662748 | ||
| chr2:178663670
|
C | T | 3 | a0013c0023a0065c0031a0098c0038 | 4 | HG01884.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.36489G>A | p.Ala12163Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 171/363 | 36714/109224 | 36489/107976 | 12163/35991 | chr2 | 178663670 | ||
| chr2:178664061
|
T | C | 6 | a0018c0009a0019c0019a0067c0030others(3): Show | 8 | HG02145.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
synonymous_variant | LOW | c.36318A>G | p.Lys12106Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 169/363 | 36543/109224 | 36318/107976 | 12106/35991 | chr2 | 178664061 | ||
| chr2:178677238
|
G | A | 1 | a0053c0191 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.34341C>T | p.Pro11447Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 147/363 | 34566/109224 | 34341/107976 | 11447/35991 | chr2 | 178677238 | ||
| chr2:178678490
|
C | T | 52 | a0001c0001a0001c0021a0001c0171others(49): Show | 64 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(61): Show |
synonymous_variant | LOW | c.33834G>A | p.Glu11278Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 144/363 | 34059/109224 | 33834/107976 | 11278/35991 | chr2 | 178678490 | ||
| chr2:178702461
|
G | A | 1 | a0066c0032 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.30426C>T | p.Asp10142Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 107/363 | 30651/109224 | 30426/107976 | 10142/35991 | chr2 | 178702461 | ||
| chr2:178702503
|
A | G | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.30384T>C | p.Asp10128Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 107/363 | 30609/109224 | 30384/107976 | 10128/35991 | chr2 | 178702503 | ||
| chr2:178704673
|
C | T | 28 | a0008c0012a0008c0064a0012c0020others(25): Show | 31 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(28): Show |
synonymous_variant | LOW | c.29799G>A | p.Ser9933Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 105/363 | 30024/109224 | 29799/107976 | 9933/35991 | chr2 | 178704673 | ||
| chr2:178704709
|
A | G | 32 | a0008c0012a0008c0064a0012c0020others(29): Show | 36 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(33): Show |
synonymous_variant | LOW | c.29763T>C | p.Ile9921Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 105/363 | 29988/109224 | 29763/107976 | 9921/35991 | chr2 | 178704709 | ||
| chr2:178706696
|
G | T | 3 | a0043c0194a0167c0070a0173c0069 | 3 | HG02015.hp1 HG02165.hp2 NA18965.hp2 |
synonymous_variant | LOW | c.29178C>A | p.Ile9726Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 102/363 | 29403/109224 | 29178/107976 | 9726/35991 | chr2 | 178706696 | ||
| chr2:178709657
|
C | T | 26 | a0008c0012a0008c0064a0012c0020others(23): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
synonymous_variant | LOW | c.28662G>A | p.Arg9554Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/363 | 28887/109224 | 28662/107976 | 9554/35991 | chr2 | 178709657 | ||
| chr2:178710738
|
G | A | 1 | a0185c0203 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.28359C>T | p.His9453His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 98/363 | 28584/109224 | 28359/107976 | 9453/35991 | chr2 | 178710738 | ||
| chr2:178712128
|
A | G | 1 | a0118c0035 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.27702T>C | p.Ile9234Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 96/363 | 27927/109224 | 27702/107976 | 9234/35991 | chr2 | 178712128 | ||
| chr2:178713143
|
T | C | 5 | a0128c0144a0175c0087a0177c0084others(2): Show | 5 | HG02559.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.26991A>G | p.Thr8997Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 93/363 | 27216/109224 | 26991/107976 | 8997/35991 | chr2 | 178713143 | ||
| chr2:178714003
|
G | A | 113 | a0001c0001a0001c0021a0001c0171others(110): Show | 132 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(129): Show |
synonymous_variant | LOW | c.26655C>T | p.Ser8885Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/363 | 26880/109224 | 26655/107976 | 8885/35991 | chr2 | 178714003 | ||
| chr2:178714308
|
G | C | 1 | a0191c0211 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.26466C>G | p.Ala8822Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 91/363 | 26691/109224 | 26466/107976 | 8822/35991 | chr2 | 178714308 | ||
| chr2:178714335
|
G | A | 1 | a0077c0153 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.26439C>T | p.Asn8813Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 91/363 | 26664/109224 | 26439/107976 | 8813/35991 | chr2 | 178714335 | ||
| chr2:178714485
|
T | C | 124 | a0001c0001a0001c0021a0001c0171others(121): Show | 144 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
synonymous_variant | LOW | c.26289A>G | p.Glu8763Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 91/363 | 26514/109224 | 26289/107976 | 8763/35991 | chr2 | 178714485 | ||
| chr2:178715095
|
T | A | 113 | a0001c0001a0001c0021a0001c0171others(110): Show | 132 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(129): Show |
synonymous_variant | LOW | c.26091A>T | p.Leu8697Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 90/363 | 26316/109224 | 26091/107976 | 8697/35991 | chr2 | 178715095 | ||
| chr2:178715707
|
A | G | 19 | a0008c0012a0008c0064a0012c0020others(16): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
synonymous_variant | LOW | c.25707T>C | p.Tyr8569Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 89/363 | 25932/109224 | 25707/107976 | 8569/35991 | chr2 | 178715707 | ||
| chr2:178717740
|
T | C | 1 | a0176c0086 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.25134A>G | p.Ala8378Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 87/363 | 25359/109224 | 25134/107976 | 8378/35991 | chr2 | 178717740 | ||
| chr2:178717998
|
G | A | 1 | a0019c0019 | 2 | HG02145.hp2 HG02976.hp1 |
synonymous_variant | LOW | c.25008C>T | p.Cys8336Cys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 86/363 | 25233/109224 | 25008/107976 | 8336/35991 | chr2 | 178717998 | ||
| chr2:178718097
|
C | T | 9 | a0017c0008a0059c0175a0187c0205others(6): Show | 10 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(7): Show |
synonymous_variant | LOW | c.24909G>A | p.Lys8303Lys | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 86/363 | 25134/109224 | 24909/107976 | 8303/35991 | chr2 | 178718097 | ||
| chr2:178718527
|
T | C | 2 | a0159c0091a0185c0203 | 2 | HG02257.hp2 HG02723.hp2 |
synonymous_variant | LOW | c.24579A>G | p.Thr8193Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 85/363 | 24804/109224 | 24579/107976 | 8193/35991 | chr2 | 178718527 | ||
| chr2:178718590
|
G | A | 6 | a0006c0141a0083c0142a0084c0050others(3): Show | 6 | HG01496.hp2 HG02683.hp1 HG02896.hp2 others(3): Show |
synonymous_variant | LOW | c.24516C>T | p.Thr8172Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 85/363 | 24741/109224 | 24516/107976 | 8172/35991 | chr2 | 178718590 | ||
| chr2:178718729
|
G | A | 2 | a0024c0017a0181c0116 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.24471C>T | p.Gly8157Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 84/363 | 24696/109224 | 24471/107976 | 8157/35991 | chr2 | 178718729 | ||
| chr2:178718855
|
G | A | 2 | a0159c0091a0185c0203 | 2 | HG02257.hp2 HG02723.hp2 |
synonymous_variant | LOW | c.24345C>T | p.Ser8115Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 84/363 | 24570/109224 | 24345/107976 | 8115/35991 | chr2 | 178718855 | ||
| chr2:178719240
|
G | A | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.24150C>T | p.Ser8050Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 83/363 | 24375/109224 | 24150/107976 | 8050/35991 | chr2 | 178719240 | ||
| chr2:178719639
|
G | T | 1 | a0142c0097 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.23853C>A | p.Ala7951Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 82/363 | 24078/109224 | 23853/107976 | 7951/35991 | chr2 | 178719639 | ||
| chr2:178720539
|
C | T | 204 | a0001c0001a0001c0021a0001c0171others(201): Show | 234 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(231): Show |
synonymous_variant | LOW | c.23223G>A | p.Gln7741Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 80/363 | 23448/109224 | 23223/107976 | 7741/35991 | chr2 | 178720539 | ||
| chr2:178721018
|
C | T | 2 | a0013c0023a0098c0038 | 3 | HG01884.hp1 HG02647.hp1 HG02976.hp2 |
synonymous_variant | LOW | c.23001G>A | p.Thr7667Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 79/363 | 23226/109224 | 23001/107976 | 7667/35991 | chr2 | 178721018 | ||
| chr2:178722052
|
A | G | 4 | a0175c0087a0177c0084a0178c0085others(1): Show | 4 | HG02559.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.22611T>C | p.His7537His | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 78/363 | 22836/109224 | 22611/107976 | 7537/35991 | chr2 | 178722052 | ||
| chr2:178722819
|
A | G | 26 | a0004c0004a0004c0015a0009c0093others(23): Show | 30 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(27): Show |
synonymous_variant | LOW | c.22080T>C | p.Asp7360Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 76/363 | 22305/109224 | 22080/107976 | 7360/35991 | chr2 | 178722819 | ||
| chr2:178723485
|
C | T | 1 | a0047c0173 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.21615G>A | p.Gly7205Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 74/363 | 21840/109224 | 21615/107976 | 7205/35991 | chr2 | 178723485 | ||
| chr2:178723611
|
G | C | 1 | a0001c0195 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.21489C>G | p.Thr7163Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 74/363 | 21714/109224 | 21489/107976 | 7163/35991 | chr2 | 178723611 | ||
| chr2:178728537
|
G | A | 1 | a0124c0120 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.19389C>T | p.Phe6463Phe | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 66/363 | 19614/109224 | 19389/107976 | 6463/35991 | chr2 | 178728537 | ||
| chr2:178728735
|
C | T | 1 | a0001c0021 | 2 | HG00423.hp2 HG02165.hp1 |
synonymous_variant | LOW | c.19191G>A | p.Thr6397Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 66/363 | 19416/109224 | 19191/107976 | 6397/35991 | chr2 | 178728735 | ||
| chr2:178729135
|
G | A | 7 | a0004c0004a0143c0103a0144c0102others(4): Show | 9 | HG00642.hp2 HG01257.hp2 HG01346.hp1 others(6): Show |
synonymous_variant | LOW | c.18903C>T | p.Thr6301Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 65/363 | 19128/109224 | 18903/107976 | 6301/35991 | chr2 | 178729135 | ||
| chr2:178729863
|
T | A | 3 | a0155c0108a0156c0106a0157c0107 | 3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.18390A>T | p.Thr6130Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 63/363 | 18615/109224 | 18390/107976 | 6130/35991 | chr2 | 178729863 | ||
| chr2:178731420
|
G | A | 1 | a0081c0067 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.17346C>T | p.Asn5782Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 59/363 | 17571/109224 | 17346/107976 | 5782/35991 | chr2 | 178731420 | ||
| chr2:178733063
|
A | G | 2 | a0001c0171a0016c0170 | 2 | NA19063.hp2 NA19065.hp2 |
synonymous_variant | LOW | c.16113T>C | p.Asn5371Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 55/363 | 16338/109224 | 16113/107976 | 5371/35991 | chr2 | 178733063 | ||
| chr2:178733081
|
G | A | 2 | a0063c0200a0128c0144 | 2 | HG02809.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.16095C>T | p.Asn5365Asn | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 55/363 | 16320/109224 | 16095/107976 | 5365/35991 | chr2 | 178733081 | ||
| chr2:178733501
|
A | G | 5 | a0085c0049a0116c0036a0117c0037others(2): Show | 5 | HG00639.hp1 HG01175.hp1 HG01981.hp2 others(2): Show |
synonymous_variant | LOW | c.15792T>C | p.Ile5264Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 54/363 | 16017/109224 | 15792/107976 | 5264/35991 | chr2 | 178733501 | ||
| chr2:178733672
|
C | T | 8 | a0078c0055a0079c0053a0080c0054others(5): Show | 8 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
synonymous_variant | LOW | c.15717G>A | p.Thr5239Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 53/363 | 15942/109224 | 15717/107976 | 5239/35991 | chr2 | 178733672 | ||
| chr2:178733837
|
G | A | 1 | a0016c0196 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.15552C>T | p.Thr5184Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 53/363 | 15777/109224 | 15552/107976 | 5184/35991 | chr2 | 178733837 | ||
| chr2:178734747
|
G | A | 1 | a0008c0064 | 1 | NA18943.hp1 | synonymous_variant | LOW | c.15177C>T | p.Asp5059Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 51/363 | 15402/109224 | 15177/107976 | 5059/35991 | chr2 | 178734747 | ||
| chr2:178734774
|
C | A | 1 | a0063c0200 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.15150G>T | p.Gly5050Gly | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 51/363 | 15375/109224 | 15150/107976 | 5050/35991 | chr2 | 178734774 | ||
| chr2:178734942
|
G | A | 1 | a0009c0105 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.14982C>T | p.Leu4994Leu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 51/363 | 15207/109224 | 14982/107976 | 4994/35991 | chr2 | 178734942 | ||
| chr2:178735836
|
G | A | 204 | a0001c0001a0001c0021a0001c0171others(201): Show | 234 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(231): Show |
synonymous_variant | LOW | c.14610C>T | p.Ser4870Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 50/363 | 14835/109224 | 14610/107976 | 4870/35991 | chr2 | 178735836 | ||
| chr2:178739229
|
G | A | 1 | a0176c0086 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.14004C>T | p.Thr4668Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 14229/109224 | 14004/107976 | 4668/35991 | chr2 | 178739229 | ||
| chr2:178740015
|
G | A | 24 | a0007c0003a0008c0012a0008c0064others(21): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
synonymous_variant | LOW | c.13218C>T | p.Ala4406Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 13443/109224 | 13218/107976 | 4406/35991 | chr2 | 178740015 | ||
| chr2:178740453
|
C | A | 24 | a0007c0003a0008c0012a0008c0064others(21): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
synonymous_variant | LOW | c.12780G>T | p.Ala4260Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 13005/109224 | 12780/107976 | 4260/35991 | chr2 | 178740453 | ||
| chr2:178740453
|
C | T | 53 | a0001c0001a0001c0021a0001c0171others(50): Show | 62 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
synonymous_variant | LOW | c.12780G>A | p.Ala4260Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 13005/109224 | 12780/107976 | 4260/35991 | chr2 | 178740453 | ||
| chr2:178740978
|
A | G | 24 | a0007c0003a0008c0012a0008c0064others(21): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
synonymous_variant | LOW | c.12255T>C | p.Ile4085Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 12480/109224 | 12255/107976 | 4085/35991 | chr2 | 178740978 | ||
| chr2:178741116
|
G | A | 8 | a0078c0055a0079c0053a0080c0054others(5): Show | 8 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
synonymous_variant | LOW | c.12117C>T | p.Pro4039Pro | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 12342/109224 | 12117/107976 | 4039/35991 | chr2 | 178741116 | ||
| chr2:178741119
|
G | C | 1 | a0001c0197 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.12114C>G | p.Thr4038Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 12339/109224 | 12114/107976 | 4038/35991 | chr2 | 178741119 | ||
| chr2:178741521
|
A | G | 1 | a0072c0154 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.11712T>C | p.Ser3904Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/363 | 11937/109224 | 11712/107976 | 3904/35991 | chr2 | 178741521 | ||
| chr2:178756499
|
C | T | 1 | a0126c0051 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.10977G>A | p.Ala3659Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/363 | 11202/109224 | 10977/107976 | 3659/35991 | chr2 | 178756499 | ||
| chr2:178757612
|
C | T | 1 | a0124c0120 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.10608G>A | p.Gln3536Gln | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/363 | 10833/109224 | 10608/107976 | 3536/35991 | chr2 | 178757612 | ||
| chr2:178759123
|
C | A | 1 | a0050c0201 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.10164G>T | p.Arg3388Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/363 | 10389/109224 | 10164/107976 | 3388/35991 | chr2 | 178759123 | ||
| chr2:178764636
|
T | C | 204 | a0001c0001a0001c0021a0001c0171others(201): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
synonymous_variant | LOW | c.9879A>G | p.Glu3293Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 42/363 | 10104/109224 | 9879/107976 | 3293/35991 | chr2 | 178764636 | ||
| chr2:178766487
|
T | C | 46 | a0004c0004a0004c0015a0007c0003others(43): Show | 55 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(52): Show |
synonymous_variant | LOW | c.9597A>G | p.Glu3199Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/363 | 9822/109224 | 9597/107976 | 3199/35991 | chr2 | 178766487 | ||
| chr2:178768686
|
T | C | 1 | a0185c0203 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.9150A>G | p.Thr3050Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 38/363 | 9375/109224 | 9150/107976 | 3050/35991 | chr2 | 178768686 | ||
| chr2:178768917
|
G | C | 21 | a0004c0004a0004c0015a0009c0093others(18): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
synonymous_variant | LOW | c.8919C>G | p.Ser2973Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 38/363 | 9144/109224 | 8919/107976 | 2973/35991 | chr2 | 178768917 | ||
| chr2:178773511
|
G | A | 6 | a0006c0141a0083c0142a0084c0050others(3): Show | 6 | HG01496.hp2 HG02683.hp1 HG02896.hp2 others(3): Show |
synonymous_variant | LOW | c.7545C>T | p.Tyr2515Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 32/363 | 7770/109224 | 7545/107976 | 2515/35991 | chr2 | 178773511 | ||
| chr2:178776476
|
A | G | 1 | a0185c0203 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.5388T>C | p.Asp1796Asp | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 28/363 | 5613/109224 | 5388/107976 | 1796/35991 | chr2 | 178776476 | ||
| chr2:178776863
|
A | G | 1 | a0005c0117 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.5001T>C | p.Tyr1667Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 28/363 | 5226/109224 | 5001/107976 | 1667/35991 | chr2 | 178776863 | ||
| chr2:178777837
|
T | C | 5 | a0017c0008a0018c0009a0065c0031others(2): Show | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
synonymous_variant | LOW | c.4347A>G | p.Ser1449Ser | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 25/363 | 4572/109224 | 4347/107976 | 1449/35991 | chr2 | 178777837 | ||
| chr2:178779089
|
G | A | 6 | a0017c0008a0018c0009a0065c0031others(3): Show | 8 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
synonymous_variant | LOW | c.3993C>T | p.Ile1331Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/363 | 4218/109224 | 3993/107976 | 1331/35991 | chr2 | 178779089 | ||
| chr2:178779433
|
T | C | 22 | a0007c0003a0008c0012a0008c0064others(19): Show | 27 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(24): Show |
synonymous_variant | LOW | c.3759A>G | p.Arg1253Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 23/363 | 3984/109224 | 3759/107976 | 1253/35991 | chr2 | 178779433 | ||
| chr2:178782819
|
A | G | 23 | a0007c0003a0008c0012a0008c0064others(20): Show | 28 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(25): Show |
synonymous_variant | LOW | c.3087T>C | p.Tyr1029Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 18/363 | 3312/109224 | 3087/107976 | 1029/35991 | chr2 | 178782819 | ||
| chr2:178782957
|
G | A | 2 | a0003c0006a0072c0154 | 4 | HG02055.hp2 HG02630.hp2 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.2949C>T | p.Ile983Ile | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 18/363 | 3174/109224 | 2949/107976 | 983/35991 | chr2 | 178782957 | ||
| chr2:178783780
|
T | G | 6 | a0017c0008a0018c0009a0065c0031others(3): Show | 8 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
synonymous_variant | LOW | c.2781A>C | p.Thr927Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 17/363 | 3006/109224 | 2781/107976 | 927/35991 | chr2 | 178783780 | ||
| chr2:178785974
|
C | T | 27 | a0011c0007a0020c0010a0025c0028others(24): Show | 29 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(26): Show |
synonymous_variant | LOW | c.2244G>A | p.Glu748Glu | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 14/363 | 2469/109224 | 2244/107976 | 748/35991 | chr2 | 178785974 | ||
| chr2:178795030
|
T | C | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1137A>G | p.Arg379Arg | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 7/363 | 1362/109224 | 1137/107976 | 379/35991 | chr2 | 178795030 | ||
| chr2:178795165
|
G | A | 1 | a0103c0157 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.1002C>T | p.Thr334Thr | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 7/363 | 1227/109224 | 1002/107976 | 334/35991 | chr2 | 178795165 | ||
| chr2:178800552
|
G | A | 1 | a0183c0204 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.426C>T | p.Ala142Ala | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 4/363 | 651/109224 | 426/107976 | 142/35991 | chr2 | 178800552 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:178525997
|
T | C | 1 | a0101c0131t0009 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1015A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 363/363 | 1015 | chr2 | 178525997 | |||||
| chr2:178526348
|
C | A | 10 | a0008c0012t0003a0008c0064t0003a0035c0163t0003others(7): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*664G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 363/363 | 664 | chr2 | 178526348 | |||||
| chr2:178526425
|
A | T | 2 | a0066c0032t0008a0179c0083t0005 | 2 | HG02895.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*587T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 363/363 | 587 | chr2 | 178526425 | |||||
| chr2:178526835
|
A | G | 1 | a0009c0095t0007 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*177T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 363/363 | 177 | chr2 | 178526835 | |||||
| chr2:178526912
|
C | CT | 134 | a0001c0001t0001a0001c0021t0001a0001c0171t0001others(131): Show | 157 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*99dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 363/363 | 99 | chr2 | 178526912 | |||||
| chr2:178526969
|
G | A | 1 | a0159c0091t0010 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*43C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 363/363 | 43 | chr2 | 178526969 | |||||
| chr2:178807306
|
C | T | 5 | a0059c0175t0004a0175c0087t0006a0177c0084t0004others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-108G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/363 | 2664 | chr2 | 178807306 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:178527336
|
C | A | 1 | a0071c0151t0002g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.107681-29G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 362/362 | chr2 | 178527336 | ||||||
| chr2:178527353
|
A | T | 60 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(57): Show | 61 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.107681-46T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 362/362 | chr2 | 178527353 | ||||||
| chr2:178528024
|
G | A | 1 | a0002c0002t0001g0040 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.107377+250C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 361/362 | chr2 | 178528024 | ||||||
| chr2:178528058
|
G | A | 23 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040others(20): Show | 23 | HG00609.hp1 HG00735.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.107377+216C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 361/362 | chr2 | 178528058 | ||||||
| chr2:178528243
|
A | G | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.107377+31T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 361/362 | chr2 | 178528243 | ||||||
| chr2:178529485
|
G | A | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.106532-266C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 359/362 | chr2 | 178529485 | ||||||
| chr2:178529525
|
C | T | 1 | a0004c0015t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.106532-306G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 359/362 | chr2 | 178529525 | ||||||
| chr2:178529635
|
C | T | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.106531+325G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 359/362 | chr2 | 178529635 | ||||||
| chr2:178535859
|
A | G | 12 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.100766-10T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 357/362 | chr2 | 178535859 | ||||||
| chr2:178535941
|
C | T | 2 | a0177c0084t0004g0005a0178c0085t0004g0004 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.100765+41G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 357/362 | chr2 | 178535941 | ||||||
| chr2:178536793
|
A | T | 45 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(42): Show | 45 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.100171+145T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 356/362 | chr2 | 178536793 | ||||||
| chr2:178538451
|
C | G | 3 | a0068c0156t0001g0163a0069c0155t0001g0162a0157c0107t0001g0145 | 3 | HG02922.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.99289+89G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 354/362 | chr2 | 178538451 | ||||||
| chr2:178538470
|
G | C | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.99289+70C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 354/362 | chr2 | 178538470 | ||||||
| chr2:178538866
|
G | A | 56 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(53): Show | 57 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.98990-27C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 353/362 | chr2 | 178538866 | ||||||
| chr2:178540059
|
A | T | 69 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(66): Show | 70 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.98098+9T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 351/362 | chr2 | 178540059 | ||||||
| chr2:178540681
|
A | C | 1 | a0170c0071t0002g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.97796-311T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 350/362 | chr2 | 178540681 | ||||||
| chr2:178540746
|
A | G | 1 | a0003c0006t0002g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.97796-376T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 350/362 | chr2 | 178540746 | ||||||
| chr2:178541080
|
A | G | 156 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(153): Show | 157 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.97795+202T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 350/362 | chr2 | 178541080 | ||||||
| chr2:178541090
|
G | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.97795+192C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 350/362 | chr2 | 178541090 | ||||||
| chr2:178541129
|
C | T | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.97795+153G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 350/362 | chr2 | 178541129 | ||||||
| chr2:178541158
|
T | C | 60 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(57): Show | 61 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.97795+124A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 350/362 | chr2 | 178541158 | ||||||
| chr2:178541276
|
C | A | 155 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(152): Show | 156 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(153): Show |
splice_region_variant&intron_variant | LOW | c.97795+6G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 350/362 | chr2 | 178541276 | ||||||
| chr2:178541785
|
A | T | 1 | a0009c0105t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.97493-201T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 349/362 | chr2 | 178541785 | ||||||
| chr2:178541862
|
T | C | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.97493-278A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 349/362 | chr2 | 178541862 | ||||||
| chr2:178542001
|
A | G | 13 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(10): Show | 13 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.97492+263T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 349/362 | chr2 | 178542001 | ||||||
| chr2:178544645
|
C | T | 1 | a0078c0055t0002g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.95723-139G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 344/362 | chr2 | 178544645 | ||||||
| chr2:178544648
|
A | G | 8 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(5): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.95723-142T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 344/362 | chr2 | 178544648 | ||||||
| chr2:178544939
|
G | T | 3 | a0123c0137t0001g0096a0124c0120t0001g0097a0129c0115t0001g0241 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.95723-433C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 344/362 | chr2 | 178544939 | ||||||
| chr2:178545350
|
G | GTCCTCAA others(21): Show |
1 | a0121c0135t0001g0232 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.95722+37_95722+38i others(30): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 344/362 | chr2 | 178545350 | ||||||
| chr2:178545355
|
G | A | 1 | a0121c0135t0001g0232 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.95722+33C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 344/362 | chr2 | 178545355 | ||||||
| chr2:178545741
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.95417-48T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 343/362 | chr2 | 178545741 | ||||||
| chr2:178546938
|
A | G | 98 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(95): Show | 99 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.94523-33T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 340/362 | chr2 | 178546938 | ||||||
| chr2:178549906
|
C | A | 97 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(94): Show | 98 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.91853-37G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 337/362 | chr2 | 178549906 | ||||||
| chr2:178549978
|
A | T | 11 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(8): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.91852+8T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 337/362 | chr2 | 178549978 | ||||||
| chr2:178550286
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91565-13C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 336/362 | chr2 | 178550286 | ||||||
| chr2:178550440
|
T | C | 16 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(13): Show | 16 | HG00558.hp2 HG01099.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.91565-167A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 336/362 | chr2 | 178550440 | ||||||
| chr2:178550495
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91565-222T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 336/362 | chr2 | 178550495 | ||||||
| chr2:178550611
|
G | T | 1 | a0125c0138t0001g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.91565-338C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 336/362 | chr2 | 178550611 | ||||||
| chr2:178550717
|
T | C | 3 | a0123c0137t0001g0096a0124c0120t0001g0097a0129c0115t0001g0241 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.91564+250A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 336/362 | chr2 | 178550717 | ||||||
| chr2:178551294
|
A | G | 5 | a0001c0171t0001g0029a0050c0201t0001g0046a0135c0061t0001g0178others(2): Show | 5 | HG00438.hp2 HG00544.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.91271-34T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 335/362 | chr2 | 178551294 | ||||||
| chr2:178551327
|
G | A | 2 | a0021c0011t0001g0149a0021c0011t0001g0179 | 2 | HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.91271-67C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 335/362 | chr2 | 178551327 | ||||||
| chr2:178554234
|
G | A | 2 | a0001c0001t0001g0077a0049c0188t0001g0078 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.88895-18C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 332/362 | chr2 | 178554234 | ||||||
| chr2:178554424
|
T | G | 1 | a0004c0015t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.88894+29A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 332/362 | chr2 | 178554424 | ||||||
| chr2:178555236
|
T | TTAAAGTA others(3): Show |
1 | a0156c0106t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.88307-85_88307-84i others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178555236 | ||||||
| chr2:178555346
|
CTG | C | 8 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(5): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.88307-196_88307-19 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178555346 | ||||||
| chr2:178555443
|
A | G | 4 | a0159c0091t0010g0175a0177c0084t0004g0005a0178c0085t0004g0004others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.88307-291T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178555443 | ||||||
| chr2:178555492
|
C | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.88307-340G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178555492 | ||||||
| chr2:178555671
|
G | A | 1 | a0175c0087t0006g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.88307-519C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178555671 | ||||||
| chr2:178556161
|
G | A | 1 | a0182c0068t0002g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.88306+687C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556161 | ||||||
| chr2:178556172
|
G | A | 8 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(5): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.88306+676C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556172 | ||||||
| chr2:178556259
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.88306+589C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556259 | ||||||
| chr2:178556431
|
A | AAAAC | 21 | a0010c0013t0002g0207a0018c0009t0001g0236a0018c0009t0001g0237others(18): Show | 21 | HG01361.hp1 HG01981.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.88306+413_88306+41 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556431 | ||||||
| chr2:178556431
|
A | AAAACAAA others(1): Show |
18 | a0002c0002t0001g0039a0002c0002t0001g0040a0002c0002t0001g0041others(15): Show | 18 | HG00609.hp1 HG00735.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.88306+409_88306+41 others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556431 | ||||||
| chr2:178556455
|
C | A | 2 | a0096c0121t0002g0227a0188c0207t0001g0070 | 2 | HG01099.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.88306+393G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556455 | ||||||
| chr2:178556455
|
CAAAA | C | 8 | a0002c0002t0001g0038a0048c0185t0002g0034a0057c0181t0001g0043others(5): Show | 8 | HG02818.hp2 HG02922.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.88306+389_88306+39 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556455 | ||||||
| chr2:178556459
|
A | C | 120 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(117): Show | 121 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.88306+389T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556459 | ||||||
| chr2:178556463
|
A | C | 2 | a0157c0107t0001g0145a0193c0209t0001g0071 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.88306+385T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556463 | ||||||
| chr2:178556567
|
C | T | 109 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(106): Show | 110 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.88306+281G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556567 | ||||||
| chr2:178556672
|
G | A | 1 | a0128c0144t0001g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88306+176C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556672 | ||||||
| chr2:178556743
|
T | G | 70 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(67): Show | 71 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.88306+105A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556743 | ||||||
| chr2:178556795
|
C | T | 1 | a0043c0194t0002g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.88306+53G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 330/362 | chr2 | 178556795 | ||||||
| chr2:178557231
|
C | A | 8 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(5): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.88009+22G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 329/362 | chr2 | 178557231 | ||||||
| chr2:178557248
|
C | T | 1 | a0094c0123t0001g0219 | 1 | NA19004.hp1 | splice_region_variant&intron_variant | LOW | c.88009+5G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 329/362 | chr2 | 178557248 | ||||||
| chr2:178558758
|
G | A | 8 | a0057c0181t0001g0043a0063c0200t0001g0044a0068c0156t0001g0163others(5): Show | 8 | HG02818.hp2 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.86822-121C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/362 | chr2 | 178558758 | ||||||
| chr2:178558952
|
A | G | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.86822-315T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/362 | chr2 | 178558952 | ||||||
| chr2:178559023
|
G | GTA | 44 | a0001c0171t0001g0029a0004c0004t0001g0168a0004c0004t0001g0172others(41): Show | 44 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.86821+286_86821+28 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/362 | chr2 | 178559023 | ||||||
| chr2:178559023
|
G | GTATA | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.86821+284_86821+28 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/362 | chr2 | 178559023 | ||||||
| chr2:178559155
|
A | G | 46 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(43): Show | 46 | HG00544.hp2 HG00642.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.86821+156T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 326/362 | chr2 | 178559155 | ||||||
| chr2:178577565
|
TA | T | 5 | a0006c0141t0002g0099a0083c0142t0002g0080a0097c0139t0002g0100others(2): Show | 5 | HG01496.hp2 HG02683.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.68824+36delT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 323/362 | chr2 | 178577565 | ||||||
| chr2:178578490
|
T | G | 160 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(157): Show | 161 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.68329+121A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 321/362 | chr2 | 178578490 | ||||||
| chr2:178578531
|
G | A | 1 | a0055c0189t0001g0033 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.68329+80C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 321/362 | chr2 | 178578531 | ||||||
| chr2:178579410
|
A | G | 109 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(106): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.67637-17T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 319/362 | chr2 | 178579410 | ||||||
| chr2:178579899
|
A | C | 11 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(8): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.67348+40T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 318/362 | chr2 | 178579899 | ||||||
| chr2:178580258
|
G | C | 1 | a0190c0208t0003g0009 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.67058-29C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 317/362 | chr2 | 178580258 | ||||||
| chr2:178580783
|
T | A | 1 | a0156c0106t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.66770-174A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 316/362 | chr2 | 178580783 | ||||||
| chr2:178580829
|
C | G | 1 | a0186c0024t0001g0014 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.66770-220G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 316/362 | chr2 | 178580829 | ||||||
| chr2:178581015
|
T | C | 12 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.66770-406A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 316/362 | chr2 | 178581015 | ||||||
| chr2:178581028
|
A | T | 12 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.66770-419T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 316/362 | chr2 | 178581028 | ||||||
| chr2:178581080
|
T | C | 2 | a0066c0032t0008g0238a0179c0083t0005g0003 | 2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.66769+419A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 316/362 | chr2 | 178581080 | ||||||
| chr2:178582280
|
C | T | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66160+16G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 314/362 | chr2 | 178582280 | ||||||
| chr2:178582672
|
T | G | 1 | a0153c0114t0001g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65864-80A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 313/362 | chr2 | 178582672 | ||||||
| chr2:178582900
|
CA | C | 17 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(14): Show | 17 | HG00558.hp1 HG00558.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.65863+39delT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 313/362 | chr2 | 178582900 | ||||||
| chr2:178583588
|
A | C | 17 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.65575+19T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 312/362 | chr2 | 178583588 | ||||||
| chr2:178583939
|
C | G | 1 | a0077c0153t0002g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.65276-33G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 311/362 | chr2 | 178583939 | ||||||
| chr2:178583952
|
G | A | 1 | a0165c0077t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.65276-46C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 311/362 | chr2 | 178583952 | ||||||
| chr2:178584184
|
G | A | 113 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(110): Show | 114 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.65275+92C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 311/362 | chr2 | 178584184 | ||||||
| chr2:178584240
|
A | AAAC | 28 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(25): Show | 28 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.65275+33_65275+35d others(5): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 311/362 | chr2 | 178584240 | ||||||
| chr2:178584998
|
G | T | 1 | a0189c0206t0001g0069 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.64673-30C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 309/362 | chr2 | 178584998 | ||||||
| chr2:178585048
|
C | T | 1 | a0139c0096t0001g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.64672+24G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 309/362 | chr2 | 178585048 | ||||||
| chr2:178585377
|
T | G | 2 | a0057c0181t0001g0043a0063c0200t0001g0044 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.64397-30A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 308/362 | chr2 | 178585377 | ||||||
| chr2:178585454
|
T | A | 1 | a0101c0131t0009g0216 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.64397-107A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 308/362 | chr2 | 178585454 | ||||||
| chr2:178585688
|
T | G | 1 | a0142c0097t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64397-341A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 308/362 | chr2 | 178585688 | ||||||
| chr2:178586933
|
A | G | 76 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(73): Show | 77 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.64094-126T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 307/362 | chr2 | 178586933 | ||||||
| chr2:178587454
|
T | C | 2 | a0043c0194t0002g0026a0173c0069t0002g0007 | 2 | HG02015.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.63794-37A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 306/362 | chr2 | 178587454 | ||||||
| chr2:178592303
|
A | G | 1 | a0119c0136t0002g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.59627-26T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 301/362 | chr2 | 178592303 | ||||||
| chr2:178592719
|
A | G | 30 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040others(27): Show | 30 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.59344+56T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 300/362 | chr2 | 178592719 | ||||||
| chr2:178593889
|
G | A | 4 | a0005c0005t0001g0228a0005c0117t0001g0221a0088c0128t0001g0229others(1): Show | 4 | HG03831.hp2 NA18945.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.58433-22C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 297/362 | chr2 | 178593889 | ||||||
| chr2:178594932
|
C | T | 4 | a0003c0146t0002g0079a0003c0147t0002g0090a0073c0149t0002g0085others(1): Show | 4 | HG01071.hp2 HG01175.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.57848-286G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/362 | chr2 | 178594932 | ||||||
| chr2:178594971
|
T | G | 1 | a0147c0098t0001g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.57848-325A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/362 | chr2 | 178594971 | ||||||
| chr2:178595029
|
C | T | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.57848-383G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/362 | chr2 | 178595029 | ||||||
| chr2:178595096
|
C | A | 1 | a0004c0004t0001g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.57847+411G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/362 | chr2 | 178595096 | ||||||
| chr2:178595200
|
G | C | 2 | a0110c0045t0002g0111a0175c0087t0006g0006 | 2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.57847+307C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/362 | chr2 | 178595200 | ||||||
| chr2:178595285
|
G | GA | 29 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040others(26): Show | 29 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.57847+221dupT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/362 | chr2 | 178595285 | ||||||
| chr2:178595285
|
GA | G | 70 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(67): Show | 71 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.57847+221delT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/362 | chr2 | 178595285 | ||||||
| chr2:178595348
|
A | G | 1 | a0004c0015t0001g0186 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.57847+159T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/362 | chr2 | 178595348 | ||||||
| chr2:178595363
|
C | A | 1 | a0014c0180t0001g0068 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.57847+144G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/362 | chr2 | 178595363 | ||||||
| chr2:178595487
|
AT | A | 9 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(6): Show | 9 | HG00642.hp2 HG01257.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.57847+19delA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 295/362 | chr2 | 178595487 | ||||||
| chr2:178595830
|
A | T | 12 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.57545-21T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178595830 | ||||||
| chr2:178595984
|
C | CT | 31 | a0002c0022t0001g0067a0003c0006t0002g0101a0003c0146t0002g0079others(28): Show | 31 | HG00597.hp1 HG00609.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.57545-176dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178595984 | ||||||
| chr2:178596004
|
T | C | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.57545-195A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178596004 | ||||||
| chr2:178596494
|
C | A | 183 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(180): Show | 184 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.57545-685G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178596494 | ||||||
| chr2:178596749
|
G | T | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.57544+789C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178596749 | ||||||
| chr2:178596840
|
G | A | 2 | a0177c0084t0004g0005a0178c0085t0004g0004 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.57544+698C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178596840 | ||||||
| chr2:178597046
|
A | C | 21 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(18): Show | 21 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.57544+492T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178597046 | ||||||
| chr2:178597137
|
A | G | 5 | a0001c0171t0001g0029a0050c0201t0001g0046a0135c0061t0001g0178others(2): Show | 5 | HG00438.hp2 HG00544.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.57544+401T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178597137 | ||||||
| chr2:178597227
|
A | G | 1 | a0106c0129t0002g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.57544+311T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178597227 | ||||||
| chr2:178597232
|
C | T | 41 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(38): Show | 41 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.57544+306G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178597232 | ||||||
| chr2:178597406
|
A | G | 2 | a0068c0156t0001g0163a0069c0155t0001g0162 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.57544+132T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178597406 | ||||||
| chr2:178597415
|
A | G | 159 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(156): Show | 160 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.57544+123T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 294/362 | chr2 | 178597415 | ||||||
| chr2:178598135
|
C | T | 5 | a0057c0181t0001g0043a0063c0200t0001g0044a0123c0137t0001g0096others(2): Show | 5 | HG02818.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.57112-77G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 292/362 | chr2 | 178598135 | ||||||
| chr2:178598310
|
A | G | 1 | a0049c0188t0001g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.57111+196T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 292/362 | chr2 | 178598310 | ||||||
| chr2:178598672
|
A | G | 1 | a0123c0137t0001g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56963-18T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 291/362 | chr2 | 178598672 | ||||||
| chr2:178598673
|
C | A | 1 | a0123c0137t0001g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56963-19G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 291/362 | chr2 | 178598673 | ||||||
| chr2:178598679
|
T | G | 5 | a0001c0171t0001g0029a0050c0201t0001g0046a0135c0061t0001g0178others(2): Show | 5 | HG00438.hp2 HG00544.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.56963-25A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 291/362 | chr2 | 178598679 | ||||||
| chr2:178598719
|
T | TA | 11 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(8): Show | 11 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.56962+28dupT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 291/362 | chr2 | 178598719 | ||||||
| chr2:178599096
|
T | A | 2 | a0188c0207t0001g0070a0189c0206t0001g0069 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.56648-34A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 290/362 | chr2 | 178599096 | ||||||
| chr2:178599518
|
A | G | 12 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.56347+36T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 289/362 | chr2 | 178599518 | ||||||
| chr2:178599910
|
A | T | 1 | a0149c0104t0001g0174 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.56051-60T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178599910 | ||||||
| chr2:178599972
|
T | C | 1 | a0039c0167t0001g0031 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.56051-122A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178599972 | ||||||
| chr2:178600227
|
G | T | 70 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(67): Show | 71 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.56051-377C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600227 | ||||||
| chr2:178600348
|
G | A | 1 | a0036c0164t0003g0020 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.56051-498C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600348 | ||||||
| chr2:178600410
|
C | CAT | 7 | a0006c0141t0002g0099a0043c0194t0002g0026a0080c0054t0002g0011others(4): Show | 7 | HG01358.hp1 HG02015.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.56050+442_56050+44 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
C | CATAT | 3 | a0006c0018t0002g0102a0020c0010t0002g0160a0052c0183t0002g0016 | 3 | HG00639.hp2 NA19002.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.56050+440_56050+44 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
C | CATATATA others(3): Show |
1 | a0008c0064t0003g0151 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.56050+434_56050+44 others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
C | CATATATA others(5): Show |
5 | a0008c0012t0003g0180a0130c0056t0003g0150a0132c0065t0003g0152others(2): Show | 5 | HG00597.hp1 HG02523.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.56050+432_56050+44 others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
C | CATATATA others(7): Show |
1 | a0038c0166t0003g0049 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.56050+430_56050+44 others(18): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
C | CATATATA others(9): Show |
1 | a0036c0164t0003g0020 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.56050+428_56050+44 others(20): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
CAT | C | 50 | a0003c0006t0002g0091a0003c0006t0002g0101a0003c0146t0002g0079others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.56050+442_56050+44 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
CATAT | C | 4 | a0087c0119t0001g0217a0099c0132t0002g0214a0104c0042t0002g0122others(1): Show | 4 | HG02738.hp2 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.56050+440_56050+44 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
CATATAT | C | 23 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040others(20): Show | 23 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.56050+438_56050+44 others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
CATATATA others(1): Show |
C | 4 | a0012c0020t0001g0019a0012c0020t0001g0021a0177c0084t0004g0005others(1): Show | 4 | HG02559.hp1 HG03139.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.56050+436_56050+44 others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
CATATATA others(5): Show |
C | 1 | a0015c0182t0001g0036 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.56050+432_56050+44 others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
CATATATA others(15): Show |
C | 116 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(113): Show | 117 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.56050+422_56050+44 others(26): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600410
|
CATATATA others(17): Show |
C | 1 | a0009c0105t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.56050+420_56050+44 others(28): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600410 | ||||||
| chr2:178600745
|
T | TC | 3 | a0084c0050t0002g0129a0163c0080t0002g0212a0166c0076t0002g0202 | 3 | HG00438.hp1 NA18955.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.56050+108_56050+10 others(5): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600745 | ||||||
| chr2:178600746
|
A | T | 3 | a0084c0050t0002g0129a0163c0080t0002g0212a0166c0076t0002g0202 | 3 | HG00438.hp1 NA18955.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.56050+108T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600746 | ||||||
| chr2:178600750
|
G | C | 3 | a0084c0050t0002g0129a0163c0080t0002g0212a0166c0076t0002g0202 | 3 | HG00438.hp1 NA18955.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.56050+104C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600750 | ||||||
| chr2:178600805
|
G | C | 1 | a0036c0164t0003g0020 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.56050+49C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600805 | ||||||
| chr2:178600821
|
G | A | 1 | a0112c0046t0002g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.56050+33C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 288/362 | chr2 | 178600821 | ||||||
| chr2:178601603
|
A | C | 1 | a0091c0124t0001g0222 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.55433-39T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 286/362 | chr2 | 178601603 | ||||||
| chr2:178602657
|
C | T | 3 | a0123c0137t0001g0096a0124c0120t0001g0097a0129c0115t0001g0241 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.54812-67G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 282/362 | chr2 | 178602657 | ||||||
| chr2:178603055
|
C | G | 1 | a0104c0042t0002g0122 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.54812-465G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 282/362 | chr2 | 178603055 | ||||||
| chr2:178603279
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.54811+597A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 282/362 | chr2 | 178603279 | ||||||
| chr2:178603419
|
A | G | 12 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.54811+457T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 282/362 | chr2 | 178603419 | ||||||
| chr2:178603485
|
T | C | 32 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(29): Show | 33 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.54811+391A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 282/362 | chr2 | 178603485 | ||||||
| chr2:178603508
|
A | G | 2 | a0061c0198t0001g0061a0062c0199t0001g0060 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54811+368T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 282/362 | chr2 | 178603508 | ||||||
| chr2:178603578
|
A | C | 3 | a0068c0156t0001g0163a0069c0155t0001g0162a0157c0107t0001g0145 | 3 | HG02922.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.54811+298T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 282/362 | chr2 | 178603578 | ||||||
| chr2:178603654
|
T | A | 5 | a0057c0181t0001g0043a0063c0200t0001g0044a0123c0137t0001g0096others(2): Show | 5 | HG02818.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.54811+222A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 282/362 | chr2 | 178603654 | ||||||
| chr2:178604457
|
CT | C | 32 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(29): Show | 33 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.54382-153delA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 281/362 | chr2 | 178604457 | ||||||
| chr2:178604659
|
A | G | 45 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(42): Show | 46 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.54381+49T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 281/362 | chr2 | 178604659 | ||||||
| chr2:178604954
|
T | A | 1 | a0117c0037t0001g0127 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.54190+33A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 280/362 | chr2 | 178604954 | ||||||
| chr2:178605320
|
C | A | 32 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(29): Show | 33 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.53882-25G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 279/362 | chr2 | 178605320 | ||||||
| chr2:178605356
|
T | C | 1 | a0108c0040t0002g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.53881+58A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 279/362 | chr2 | 178605356 | ||||||
| chr2:178605778
|
C | T | 2 | a0066c0032t0008g0238a0179c0083t0005g0003 | 2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.53582-65G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 278/362 | chr2 | 178605778 | ||||||
| chr2:178606022
|
T | G | 1 | a0032c0161t0002g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.53582-309A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 278/362 | chr2 | 178606022 | ||||||
| chr2:178606073
|
G | T | 1 | a0001c0195t0001g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.53582-360C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 278/362 | chr2 | 178606073 | ||||||
| chr2:178606110
|
A | G | 1 | a0100c0133t0002g0233 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.53582-397T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 278/362 | chr2 | 178606110 | ||||||
| chr2:178606280
|
A | G | 4 | a0159c0091t0010g0175a0177c0084t0004g0005a0178c0085t0004g0004others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.53582-567T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 278/362 | chr2 | 178606280 | ||||||
| chr2:178606315
|
G | T | 1 | a0127c0143t0002g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.53582-602C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 278/362 | chr2 | 178606315 | ||||||
| chr2:178606334
|
G | A | 9 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040others(6): Show | 9 | HG00609.hp1 HG01346.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.53582-621C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 278/362 | chr2 | 178606334 | ||||||
| chr2:178606365
|
T | C | 46 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(43): Show | 47 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.53582-652A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 278/362 | chr2 | 178606365 | ||||||
| chr2:178606449
|
T | C | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.53581+572A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 278/362 | chr2 | 178606449 | ||||||
| chr2:178607332
|
C | A | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.53288-18G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 277/362 | chr2 | 178607332 | ||||||
| chr2:178608098
|
T | C | 2 | a0116c0036t0001g0126a0118c0035t0001g0136 | 2 | HG01981.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.52706-17A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 275/362 | chr2 | 178608098 | ||||||
| chr2:178608151
|
C | G | 4 | a0159c0091t0010g0175a0177c0084t0004g0005a0178c0085t0004g0004others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.52705+27G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 275/362 | chr2 | 178608151 | ||||||
| chr2:178608997
|
G | C | 1 | a0170c0071t0002g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.52103-89C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 273/362 | chr2 | 178608997 | ||||||
| chr2:178609081
|
G | A | 1 | a0137c0059t0003g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.52102+127C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 273/362 | chr2 | 178609081 | ||||||
| chr2:178610060
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.51436+30A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 271/362 | chr2 | 178610060 | ||||||
| chr2:178610537
|
C | T | 1 | a0159c0091t0010g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.51137-148G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 270/362 | chr2 | 178610537 | ||||||
| chr2:178611734
|
T | G | 1 | a0013c0023t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.50551+24A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 268/362 | chr2 | 178611734 | ||||||
| chr2:178611738
|
G | A | 4 | a0003c0006t0002g0083a0042c0172t0002g0055a0079c0053t0002g0008others(1): Show | 4 | HG02257.hp1 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.50551+20C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 268/362 | chr2 | 178611738 | ||||||
| chr2:178612235
|
C | T | 2 | a0013c0023t0001g0056a0013c0023t0001g0057 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.50248+42G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 266/362 | chr2 | 178612235 | ||||||
| chr2:178612605
|
AT | A | 162 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0077others(159): Show | 163 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.49949-30delA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 265/362 | chr2 | 178612605 | ||||||
| chr2:178612749
|
T | G | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.49948+24A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 265/362 | chr2 | 178612749 | ||||||
| chr2:178613126
|
C | G | 1 | a0107c0043t0001g0161 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.49648+35G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 264/362 | chr2 | 178613126 | ||||||
| chr2:178613145
|
A | G | 8 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(5): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.49648+16T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 264/362 | chr2 | 178613145 | ||||||
| chr2:178613948
|
G | A | 1 | a0015c0182t0001g0036 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.49346-11C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 262/362 | chr2 | 178613948 | ||||||
| chr2:178614382
|
T | A | 1 | a0004c0015t0001g0186 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.49049-34A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 261/362 | chr2 | 178614382 | ||||||
| chr2:178614391
|
A | AT | 17 | a0002c0022t0001g0066a0008c0012t0003g0177a0008c0012t0003g0180others(14): Show | 17 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.49049-44dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 261/362 | chr2 | 178614391 | ||||||
| chr2:178615014
|
G | A | 28 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(25): Show | 28 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.48639-46C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 259/362 | chr2 | 178615014 | ||||||
| chr2:178615128
|
A | G | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.48639-160T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 259/362 | chr2 | 178615128 | ||||||
| chr2:178615195
|
C | T | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.48638+112G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 259/362 | chr2 | 178615195 | ||||||
| chr2:178615215
|
T | A | 5 | a0057c0181t0001g0043a0063c0200t0001g0044a0123c0137t0001g0096others(2): Show | 5 | HG02818.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.48638+92A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 259/362 | chr2 | 178615215 | ||||||
| chr2:178615553
|
C | T | 2 | a0018c0009t0001g0236a0018c0009t0001g0237 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.48461-69G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 258/362 | chr2 | 178615553 | ||||||
| chr2:178615633
|
G | A | 6 | a0031c0162t0002g0023a0032c0161t0002g0065a0033c0160t0002g0024others(3): Show | 6 | HG00558.hp1 HG00673.hp1 NA18612.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.48460+8C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 258/362 | chr2 | 178615633 | ||||||
| chr2:178616168
|
A | G | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.48312+311T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 257/362 | chr2 | 178616168 | ||||||
| chr2:178616181
|
A | C | 1 | a0001c0195t0001g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.48312+298T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 257/362 | chr2 | 178616181 | ||||||
| chr2:178616306
|
T | C | 3 | a0068c0156t0001g0163a0069c0155t0001g0162a0157c0107t0001g0145 | 3 | HG02922.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.48312+173A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 257/362 | chr2 | 178616306 | ||||||
| chr2:178616316
|
C | T | 1 | a0139c0096t0001g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.48312+163G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 257/362 | chr2 | 178616316 | ||||||
| chr2:178616336
|
G | T | 1 | a0128c0144t0001g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.48312+143C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 257/362 | chr2 | 178616336 | ||||||
| chr2:178617112
|
C | A | 1 | a0171c0073t0002g0210 | 1 | NA18964.hp1 | splice_region_variant&intron_variant | LOW | c.47875+8G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 255/362 | chr2 | 178617112 | ||||||
| chr2:178617574
|
G | A | 3 | a0048c0185t0002g0034a0128c0144t0001g0095a0156c0106t0001g0146 | 3 | HG02451.hp1 HG02809.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.47573-62C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 253/362 | chr2 | 178617574 | ||||||
| chr2:178617582
|
CAATT | C | 31 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(28): Show | 32 | HG00408.hp1 HG00741.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.47573-74_47573-71d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 253/362 | chr2 | 178617582 | ||||||
| chr2:178617620
|
CTAAG | C | 10 | a0001c0197t0001g0015a0006c0018t0002g0102a0006c0018t0002g0105others(7): Show | 10 | HG00639.hp2 HG01361.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.47573-112_47573-10 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 253/362 | chr2 | 178617620 | ||||||
| chr2:178617698
|
A | G | 2 | a0028c0026t0002g0114a0029c0025t0002g0115 | 2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.47572+81T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 253/362 | chr2 | 178617698 | ||||||
| chr2:178619017
|
TTTG | T | 27 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(24): Show | 28 | HG00408.hp1 HG00741.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.46697-167_46697-16 others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 250/362 | chr2 | 178619017 | ||||||
| chr2:178619121
|
A | G | 2 | a0066c0032t0008g0238a0179c0083t0005g0003 | 2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.46697-268T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 250/362 | chr2 | 178619121 | ||||||
| chr2:178619327
|
C | T | 23 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(20): Show | 23 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.46696+294G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 250/362 | chr2 | 178619327 | ||||||
| chr2:178619522
|
A | G | 5 | a0059c0175t0004g0002a0151c0112t0001g0183a0187c0205t0001g0072others(2): Show | 5 | HG02615.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.46696+99T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 250/362 | chr2 | 178619522 | ||||||
| chr2:178620165
|
T | A | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.46304+52A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 248/362 | chr2 | 178620165 | ||||||
| chr2:178621381
|
A | G | 2 | a0066c0032t0008g0238a0179c0083t0005g0003 | 2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.45350-13T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/362 | chr2 | 178621381 | ||||||
| chr2:178621385
|
A | T | 1 | a0031c0162t0002g0023 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.45350-17T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/362 | chr2 | 178621385 | ||||||
| chr2:178621411
|
G | T | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.45350-43C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/362 | chr2 | 178621411 | ||||||
| chr2:178621439
|
TTAGAAAT others(2): Show |
T | 28 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(25): Show | 28 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.45349+27_45349+35d others(11): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/362 | chr2 | 178621439 | ||||||
| chr2:178621450
|
A | G | 28 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(25): Show | 28 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.45349+25T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/362 | chr2 | 178621450 | ||||||
| chr2:178621451
|
G | T | 28 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(25): Show | 28 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.45349+24C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/362 | chr2 | 178621451 | ||||||
| chr2:178621452
|
A | T | 28 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(25): Show | 28 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.45349+23T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 245/362 | chr2 | 178621452 | ||||||
| chr2:178622123
|
T | A | 2 | a0002c0022t0001g0066a0002c0022t0001g0067 | 2 | NA18965.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.44914-115A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 243/362 | chr2 | 178622123 | ||||||
| chr2:178622283
|
C | T | 1 | a0015c0176t0001g0045 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.44914-275G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 243/362 | chr2 | 178622283 | ||||||
| chr2:178622411
|
A | T | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.44913+259T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 243/362 | chr2 | 178622411 | ||||||
| chr2:178622587
|
C | CT | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.44913+82dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 243/362 | chr2 | 178622587 | ||||||
| chr2:178622956
|
T | G | 23 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(20): Show | 23 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.44816-189A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178622956 | ||||||
| chr2:178623353
|
T | TACTAATT others(27): Show |
4 | a0008c0012t0003g0177a0008c0012t0003g0180a0038c0166t0003g0049others(1): Show | 4 | HG00438.hp2 HG00609.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.44816-587_44816-58 others(38): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178623353 | ||||||
| chr2:178623356
|
G | T | 4 | a0008c0012t0003g0177a0008c0012t0003g0180a0038c0166t0003g0049others(1): Show | 4 | HG00438.hp2 HG00609.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.44816-589C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178623356 | ||||||
| chr2:178623467
|
C | T | 158 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(155): Show | 159 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.44816-700G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178623467 | ||||||
| chr2:178623469
|
G | C | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.44816-702C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178623469 | ||||||
| chr2:178623628
|
T | G | 1 | a0075c0145t0002g0089 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.44815+837A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178623628 | ||||||
| chr2:178624009
|
C | T | 1 | a0075c0145t0002g0089 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.44815+456G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178624009 | ||||||
| chr2:178624265
|
C | G | 2 | a0016c0196t0002g0047a0050c0201t0001g0046 | 2 | HG00544.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.44815+200G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178624265 | ||||||
| chr2:178624279
|
A | T | 3 | a0042c0172t0002g0055a0079c0053t0002g0008a0080c0054t0002g0011 | 3 | HG02257.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.44815+186T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178624279 | ||||||
| chr2:178624289
|
T | G | 1 | a0190c0208t0003g0009 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.44815+176A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178624289 | ||||||
| chr2:178624290
|
T | A | 1 | a0190c0208t0003g0009 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.44815+175A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 242/362 | chr2 | 178624290 | ||||||
| chr2:178624999
|
A | G | 68 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(65): Show | 68 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.44549-268T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 241/362 | chr2 | 178624999 | ||||||
| chr2:178625044
|
T | TAAAAACA others(6058): Show |
1 | a0062c0199t0001g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.44548+228_44548+22 others(6069): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 241/362 | chr2 | 178625044 | ||||||
| chr2:178625721
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.44425-325C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178625721 | ||||||
| chr2:178625751
|
T | C | 115 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(112): Show | 116 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.44425-355A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178625751 | ||||||
| chr2:178625883
|
G | A | 2 | a0177c0084t0004g0005a0178c0085t0004g0004 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.44425-487C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178625883 | ||||||
| chr2:178626058
|
C | T | 158 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(155): Show | 159 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.44425-662G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626058 | ||||||
| chr2:178626084
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.44425-688C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626084 | ||||||
| chr2:178626136
|
C | A | 5 | a0057c0181t0001g0043a0063c0200t0001g0044a0123c0137t0001g0096others(2): Show | 5 | HG02818.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.44425-740G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626136 | ||||||
| chr2:178626227
|
C | T | 100 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(97): Show | 101 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.44425-831G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626227 | ||||||
| chr2:178626490
|
G | A | 24 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(21): Show | 25 | HG00408.hp1 HG00741.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.44425-1094C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626490 | ||||||
| chr2:178626508
|
T | G | 158 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(155): Show | 159 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.44425-1112A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626508 | ||||||
| chr2:178626530
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.44425-1134C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626530 | ||||||
| chr2:178626543
|
A | G | 8 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.44425-1147T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626543 | ||||||
| chr2:178626551
|
G | T | 10 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(7): Show | 10 | HG01361.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.44425-1155C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626551 | ||||||
| chr2:178626603
|
C | T | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.44425-1207G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626603 | ||||||
| chr2:178626604
|
A | G | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.44425-1208T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626604 | ||||||
| chr2:178626678
|
G | C | 1 | a0072c0154t0002g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.44425-1282C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626678 | ||||||
| chr2:178626725
|
T | C | 1 | a0021c0011t0001g0179 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.44425-1329A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178626725 | ||||||
| chr2:178627062
|
T | A | 3 | a0068c0156t0001g0163a0069c0155t0001g0162a0157c0107t0001g0145 | 3 | HG02922.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.44425-1666A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178627062 | ||||||
| chr2:178627158
|
T | C | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.44425-1762A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178627158 | ||||||
| chr2:178627308
|
T | C | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.44425-1912A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178627308 | ||||||
| chr2:178627549
|
C | T | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.44424+1752G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178627549 | ||||||
| chr2:178627591
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.44424+1710C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178627591 | ||||||
| chr2:178628267
|
A | G | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.44424+1034T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178628267 | ||||||
| chr2:178628307
|
T | C | 6 | a0008c0064t0003g0151a0035c0163t0003g0025a0086c0118t0001g0218others(3): Show | 6 | HG00597.hp1 HG02027.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.44424+994A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178628307 | ||||||
| chr2:178628477
|
A | G | 1 | a0154c0111t0001g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.44424+824T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178628477 | ||||||
| chr2:178628484
|
A | G | 1 | a0163c0080t0002g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.44424+817T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178628484 | ||||||
| chr2:178628688
|
G | A | 1 | a0058c0192t0001g0063 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.44424+613C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178628688 | ||||||
| chr2:178629069
|
G | T | 1 | a0096c0121t0002g0227 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.44424+232C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178629069 | ||||||
| chr2:178629109
|
A | G | 1 | a0138c0063t0002g0156 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.44424+192T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 240/362 | chr2 | 178629109 | ||||||
| chr2:178629476
|
C | T | 1 | a0001c0021t0001g0075 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.44282-33G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 239/362 | chr2 | 178629476 | ||||||
| chr2:178629593
|
C | T | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.44282-150G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 239/362 | chr2 | 178629593 | ||||||
| chr2:178629731
|
G | A | 1 | a0128c0144t0001g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.44282-288C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 239/362 | chr2 | 178629731 | ||||||
| chr2:178629731
|
GTA | G | 7 | a0009c0093t0001g0184a0009c0095t0007g0166a0022c0014t0001g0193others(4): Show | 7 | HG00544.hp2 HG02015.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.44282-290_44282-28 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 239/362 | chr2 | 178629731 | ||||||
| chr2:178629757
|
C | T | 1 | a0098c0038t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.44282-314G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 239/362 | chr2 | 178629757 | ||||||
| chr2:178629812
|
A | G | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.44282-369T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 239/362 | chr2 | 178629812 | ||||||
| chr2:178630071
|
C | T | 8 | a0001c0186t0001g0017a0001c0197t0001g0015a0066c0032t0008g0238others(5): Show | 8 | HG00673.hp2 HG02040.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.44281+170G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 239/362 | chr2 | 178630071 | ||||||
| chr2:178630616
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.44154+188C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 238/362 | chr2 | 178630616 | ||||||
| chr2:178630672
|
C | T | 1 | a0156c0106t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.44154+132G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 238/362 | chr2 | 178630672 | ||||||
| chr2:178631015
|
C | G | 1 | a0001c0197t0001g0015 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.44014+19G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 237/362 | chr2 | 178631015 | ||||||
| chr2:178631533
|
T | A | 1 | a0111c0047t0001g0135 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.43748-233A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 236/362 | chr2 | 178631533 | ||||||
| chr2:178631554
|
A | G | 2 | a0002c0022t0001g0066a0002c0022t0001g0067 | 2 | NA18965.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.43748-254T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 236/362 | chr2 | 178631554 | ||||||
| chr2:178631807
|
A | C | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.43747+340T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 236/362 | chr2 | 178631807 | ||||||
| chr2:178633144
|
C | T | 2 | a0061c0198t0001g0061a0062c0199t0001g0060 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.43086+43G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 233/362 | chr2 | 178633144 | ||||||
| chr2:178633384
|
G | T | 1 | a0137c0059t0003g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.42946+29C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 232/362 | chr2 | 178633384 | ||||||
| chr2:178634199
|
T | C | 1 | a0125c0138t0001g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.42416-116A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 230/362 | chr2 | 178634199 | ||||||
| chr2:178634311
|
A | G | 31 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(28): Show | 31 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.42415+55T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 230/362 | chr2 | 178634311 | ||||||
| chr2:178635159
|
A | G | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.42024+6T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 228/362 | chr2 | 178635159 | ||||||
| chr2:178635398
|
T | A | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.41884+42A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 227/362 | chr2 | 178635398 | ||||||
| chr2:178635436
|
A | G | 1 | a0042c0172t0002g0055 | 1 | HG02486.hp1 | splice_region_variant&intron_variant | LOW | c.41884+4T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 227/362 | chr2 | 178635436 | ||||||
| chr2:178635742
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.41609-27A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 226/362 | chr2 | 178635742 | ||||||
| chr2:178635819
|
C | A | 3 | a0042c0172t0002g0055a0079c0053t0002g0008a0080c0054t0002g0011 | 3 | HG02257.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.41609-104G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 226/362 | chr2 | 178635819 | ||||||
| chr2:178635896
|
G | A | 1 | a0080c0054t0002g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41608+67C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 226/362 | chr2 | 178635896 | ||||||
| chr2:178637146
|
G | GAT | 23 | a0001c0171t0001g0029a0001c0186t0001g0017a0003c0006t0002g0091others(20): Show | 23 | HG00558.hp1 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.40927+221_40927+22 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
G | GATAGATA others(15): Show |
1 | a0132c0065t0003g0152 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.40927+222_40927+22 others(26): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
G | GATAT | 14 | a0003c0146t0002g0079a0006c0141t0002g0099a0014c0178t0001g0062others(11): Show | 14 | HG00544.hp1 HG01071.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.40927+219_40927+22 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
G | GATATAT | 25 | a0001c0001t0001g0035a0002c0022t0001g0066a0006c0018t0002g0102others(22): Show | 25 | HG00639.hp2 HG01358.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.40927+217_40927+22 others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
G | GATATATA others(1): Show |
36 | a0001c0001t0001g0077a0001c0021t0001g0075a0001c0021t0001g0076others(33): Show | 36 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.40927+215_40927+22 others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
G | GATATATA others(3): Show |
10 | a0001c0001t0001g0030a0003c0006t0002g0101a0008c0012t0003g0180others(7): Show | 10 | HG02055.hp2 HG02155.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.40927+213_40927+22 others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
G | GATATATA others(5): Show |
6 | a0001c0195t0001g0042a0068c0156t0001g0163a0069c0155t0001g0162others(3): Show | 6 | HG01071.hp2 HG02027.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.40927+211_40927+22 others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
G | GATATATA others(7): Show |
2 | a0002c0022t0001g0067a0171c0073t0002g0210 | 2 | NA18964.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.40927+209_40927+22 others(18): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
G | GATATATA others(11): Show |
2 | a0012c0020t0001g0021a0136c0060t0003g0138 | 2 | HG00597.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.40927+205_40927+22 others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
GAT | G | 23 | a0010c0072t0002g0204a0025c0028t0002g0120a0031c0162t0002g0023others(20): Show | 23 | HG00408.hp2 HG00673.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.40927+221_40927+22 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
GATAT | G | 9 | a0007c0003t0002g0157a0009c0093t0001g0184a0011c0007t0002g0117others(6): Show | 9 | HG00544.hp2 HG00642.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.40927+219_40927+22 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
GATATAT | G | 9 | a0001c0001t0001g0013a0003c0147t0002g0090a0042c0172t0002g0055others(6): Show | 9 | HG01433.hp2 HG02486.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.40927+217_40927+22 others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
GATATATA others(3): Show |
G | 1 | a0108c0040t0002g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.40927+213_40927+22 others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
GATATATA others(5): Show |
G | 3 | a0015c0176t0001g0045a0087c0119t0001g0217a0088c0128t0001g0229 | 3 | HG00609.hp1 NA18974.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.40927+211_40927+22 others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
GATATATA others(7): Show |
G | 1 | a0142c0097t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.40927+209_40927+22 others(18): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
GATATATA others(9): Show |
G | 23 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(20): Show | 24 | HG00408.hp1 HG00741.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.40927+207_40927+22 others(20): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
GATATATA others(13): Show |
G | 2 | a0057c0181t0001g0043a0063c0200t0001g0044 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.40927+203_40927+22 others(24): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
GATATATA others(15): Show |
G | 3 | a0123c0137t0001g0096a0124c0120t0001g0097a0129c0115t0001g0241 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.40927+201_40927+22 others(26): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637146
|
GATATATA others(25): Show |
G | 7 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.40927+191_40927+22 others(36): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637146 | ||||||
| chr2:178637187
|
A | ATATATAT others(7): Show |
1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40927+181_40927+18 others(18): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637187 | ||||||
| chr2:178637187
|
A | ATATATAT others(3): Show |
1 | a0083c0142t0002g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.40927+181_40927+18 others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637187 | ||||||
| chr2:178637187
|
A | ATATATCT others(11): Show |
1 | a0159c0091t0010g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.40927+181_40927+18 others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637187 | ||||||
| chr2:178637187
|
A | C | 1 | a0177c0084t0004g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.40927+182T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637187 | ||||||
| chr2:178637191
|
C | A | 1 | a0147c0098t0001g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.40927+178G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637191 | ||||||
| chr2:178637226
|
T | C | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.40927+143A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637226 | ||||||
| chr2:178637262
|
A | G | 5 | a0059c0175t0004g0002a0151c0112t0001g0183a0187c0205t0001g0072others(2): Show | 5 | HG02615.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.40927+107T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 224/362 | chr2 | 178637262 | ||||||
| chr2:178637448
|
A | G | 1 | a0066c0032t0008g0238 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.40877-29T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178637448 | ||||||
| chr2:178637662
|
A | G | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.40877-243T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178637662 | ||||||
| chr2:178637782
|
G | A | 1 | a0002c0022t0001g0066 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.40877-363C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178637782 | ||||||
| chr2:178637938
|
C | G | 1 | a0127c0143t0002g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.40877-519G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178637938 | ||||||
| chr2:178638123
|
A | C | 1 | a0083c0142t0002g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.40877-704T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178638123 | ||||||
| chr2:178638484
|
T | A | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.40877-1065A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178638484 | ||||||
| chr2:178638513
|
G | C | 2 | a0177c0084t0004g0005a0178c0085t0004g0004 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.40877-1094C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178638513 | ||||||
| chr2:178638531
|
A | G | 1 | a0137c0059t0003g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.40877-1112T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178638531 | ||||||
| chr2:178638555
|
T | C | 1 | a0177c0084t0004g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.40877-1136A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178638555 | ||||||
| chr2:178638838
|
A | G | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.40876+861T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178638838 | ||||||
| chr2:178639151
|
T | C | 1 | a0139c0096t0001g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.40876+548A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178639151 | ||||||
| chr2:178639561
|
A | G | 2 | a0177c0084t0004g0005a0178c0085t0004g0004 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.40876+138T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 223/362 | chr2 | 178639561 | ||||||
| chr2:178640639
|
T | C | 1 | a0057c0181t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.40634-9A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 220/362 | chr2 | 178640639 | ||||||
| chr2:178640789
|
C | G | 4 | a0159c0091t0010g0175a0177c0084t0004g0005a0178c0085t0004g0004others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.40634-159G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 220/362 | chr2 | 178640789 | ||||||
| chr2:178641169
|
A | G | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.40633+72T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 220/362 | chr2 | 178641169 | ||||||
| chr2:178641687
|
A | C | 11 | a0014c0178t0001g0062a0014c0180t0001g0068a0021c0011t0001g0149others(8): Show | 11 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.40559-372T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 219/362 | chr2 | 178641687 | ||||||
| chr2:178642062
|
T | A | 1 | a0082c0052t0002g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.40558+175A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 219/362 | chr2 | 178642062 | ||||||
| chr2:178642063
|
A | T | 9 | a0006c0018t0002g0102a0006c0018t0002g0105a0078c0055t0002g0012others(6): Show | 9 | HG00639.hp2 HG01361.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.40558+174T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 219/362 | chr2 | 178642063 | ||||||
| chr2:178642133
|
C | T | 2 | a0028c0026t0002g0114a0029c0025t0002g0115 | 2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.40558+104G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 219/362 | chr2 | 178642133 | ||||||
| chr2:178642134
|
G | A | 1 | a0064c0202t0001g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.40558+103C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 219/362 | chr2 | 178642134 | ||||||
| chr2:178642522
|
C | T | 1 | a0039c0167t0001g0031 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.40478-205G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178642522 | ||||||
| chr2:178642614
|
A | G | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.40478-297T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178642614 | ||||||
| chr2:178642615
|
G | C | 4 | a0022c0014t0001g0193a0022c0014t0001g0195a0140c0094t0001g0196others(1): Show | 4 | HG00544.hp2 HG02015.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.40478-298C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178642615 | ||||||
| chr2:178643215
|
T | G | 3 | a0025c0028t0002g0120a0177c0084t0004g0005a0178c0085t0004g0004 | 3 | HG02559.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.40478-898A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178643215 | ||||||
| chr2:178643348
|
G | A | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.40478-1031C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178643348 | ||||||
| chr2:178643645
|
C | T | 1 | a0156c0106t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.40477+903G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178643645 | ||||||
| chr2:178643646
|
C | G | 8 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.40477+902G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178643646 | ||||||
| chr2:178643719
|
CA | C | 4 | a0013c0023t0001g0056a0013c0023t0001g0057a0065c0031t0001g0235others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.40477+828delT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178643719 | ||||||
| chr2:178643792
|
C | G | 5 | a0059c0175t0004g0002a0151c0112t0001g0183a0187c0205t0001g0072others(2): Show | 5 | HG02615.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.40477+756G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178643792 | ||||||
| chr2:178644032
|
C | T | 1 | a0041c0168t0002g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.40477+516G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178644032 | ||||||
| chr2:178644458
|
G | A | 1 | a0006c0018t0002g0105 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.40477+90C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 218/362 | chr2 | 178644458 | ||||||
| chr2:178644773
|
G | A | 24 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(21): Show | 24 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.40409-157C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 217/362 | chr2 | 178644773 | ||||||
| chr2:178644815
|
GTTAA | G | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.40409-203_40409-20 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 217/362 | chr2 | 178644815 | ||||||
| chr2:178645098
|
T | C | 7 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.40409-482A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 217/362 | chr2 | 178645098 | ||||||
| chr2:178645422
|
A | T | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.40408+498T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 217/362 | chr2 | 178645422 | ||||||
| chr2:178645598
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.40408+322A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 217/362 | chr2 | 178645598 | ||||||
| chr2:178645777
|
G | C | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.40408+143C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 217/362 | chr2 | 178645777 | ||||||
| chr2:178646103
|
A | ATT | 3 | a0009c0095t0007g0166a0017c0008t0001g0106a0017c0008t0001g0107 | 3 | HG02145.hp1 HG04228.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.40298-75_40298-74d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646103 | ||||||
| chr2:178646104
|
T | TATATATA others(8): Show |
1 | a0107c0043t0001g0161 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.40298-75_40298-74i others(17): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTA | 30 | a0001c0001t0001g0013a0001c0195t0001g0042a0003c0146t0002g0079others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.40298-76_40298-75d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTATA | 34 | a0001c0001t0001g0077a0001c0197t0001g0015a0002c0022t0001g0066others(31): Show | 34 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.40298-78_40298-75d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTATATA | 16 | a0001c0001t0001g0035a0003c0147t0002g0090a0012c0020t0001g0019others(13): Show | 16 | HG00423.hp1 HG00735.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.40298-80_40298-75d others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTATATAT others(1): Show |
16 | a0002c0002t0001g0038a0002c0002t0001g0040a0007c0003t0002g0154others(13): Show | 16 | HG00438.hp1 HG00597.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.40298-82_40298-75d others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTATATAT others(3): Show |
11 | a0001c0001t0001g0030a0007c0003t0002g0157a0007c0003t0002g0158others(8): Show | 11 | HG01255.hp1 HG01257.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.40298-84_40298-75d others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTATATAT others(5): Show |
15 | a0001c0021t0001g0076a0002c0002t0001g0039a0010c0013t0002g0206others(12): Show | 15 | HG00597.hp1 HG00673.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.40298-86_40298-75d others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTATATAT others(7): Show |
14 | a0016c0170t0002g0028a0020c0010t0002g0134a0021c0011t0001g0179others(11): Show | 14 | HG00408.hp2 HG01952.hp1 HG02273.hp2 others(11): Show |
intron_variant | MODIFIER | c.40298-88_40298-75d others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTATATAT others(9): Show |
6 | a0002c0002t0001g0041a0006c0141t0002g0099a0008c0064t0003g0151others(3): Show | 6 | HG02027.hp1 HG02293.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.40298-90_40298-75d others(18): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTATATAT others(13): Show |
3 | a0142c0097t0001g0164a0168c0075t0001g0205a0183c0204t0001g0139 | 3 | HG02738.hp2 HG04184.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.40298-94_40298-75d others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTATATAT others(15): Show |
4 | a0001c0021t0001g0075a0096c0121t0002g0227a0117c0037t0001g0127others(1): Show | 4 | HG00423.hp2 HG00639.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.40298-96_40298-75d others(24): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTATATAT others(17): Show |
1 | a0167c0070t0001g0199 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.40298-98_40298-75d others(26): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTTATATA others(4): Show |
1 | a0004c0004t0001g0173 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.40298-75_40298-74i others(13): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTTTATA | 4 | a0004c0015t0001g0186a0022c0014t0001g0193a0022c0014t0001g0195others(1): Show | 4 | HG00544.hp2 HG02004.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.40298-75_40298-74i others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTTTATAT others(1): Show |
6 | a0024c0017t0001g0140a0024c0017t0001g0141a0125c0138t0001g0104others(3): Show | 6 | HG03195.hp2 HG03540.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.40298-75_40298-74i others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTTTATAT others(3): Show |
7 | a0004c0004t0001g0168a0009c0093t0001g0184a0023c0016t0001g0191others(4): Show | 7 | HG00642.hp2 HG02015.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.40298-75_40298-74i others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTTTATAT others(5): Show |
4 | a0004c0015t0001g0165a0009c0105t0001g0167a0143c0103t0001g0171others(1): Show | 4 | HG01952.hp2 HG02293.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.40298-75_40298-74i others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTTTATAT others(7): Show |
1 | a0181c0116t0001g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.40298-75_40298-74i others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTTTATAT others(9): Show |
2 | a0140c0094t0001g0196a0148c0100t0001g0169 | 2 | HG01346.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.40298-75_40298-74i others(18): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
T | TTTTATAT others(13): Show |
1 | a0149c0104t0001g0174 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.40298-75_40298-74i others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTA | T | 3 | a0018c0009t0001g0236a0018c0009t0001g0237a0166c0076t0002g0202 | 3 | HG02896.hp1 HG02897.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.40298-76_40298-75d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTATA | T | 2 | a0006c0018t0002g0102a0072c0154t0002g0092 | 2 | HG00639.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.40298-78_40298-75d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTATATA | T | 5 | a0006c0018t0002g0105a0019c0019t0001g0093a0019c0019t0001g0094others(2): Show | 5 | HG01361.hp2 HG01978.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.40298-80_40298-75d others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTATATAT others(3): Show |
T | 3 | a0067c0030t0001g0239a0080c0054t0002g0011a0174c0081t0001g0201 | 3 | HG02257.hp1 NA19058.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.40298-84_40298-75d others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTATATAT others(5): Show |
T | 2 | a0060c0174t0001g0058a0127c0143t0002g0010 | 2 | HG02965.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.40298-86_40298-75d others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTATATAT others(7): Show |
T | 3 | a0027c0029t0001g0118a0084c0050t0002g0129a0154c0111t0001g0190 | 3 | HG02809.hp2 HG03195.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.40298-88_40298-75d others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTATATAT others(9): Show |
T | 2 | a0188c0207t0001g0070a0189c0206t0001g0069 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.40298-90_40298-75d others(18): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTATATAT others(11): Show |
T | 2 | a0177c0084t0004g0005a0178c0085t0004g0004 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.40298-92_40298-75d others(20): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTATATAT others(13): Show |
T | 15 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(12): Show | 16 | HG00408.hp1 HG03490.hp1 HG03492.hp1 others(13): Show |
intron_variant | MODIFIER | c.40298-94_40298-75d others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTATATAT others(15): Show |
T | 1 | a0004c0004t0001g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.40298-96_40298-75d others(24): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646104
|
TTATATAT others(17): Show |
T | 2 | a0003c0006t0002g0083a0159c0091t0010g0175 | 2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.40298-98_40298-75d others(26): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646104 | ||||||
| chr2:178646106
|
A | T | 1 | a0155c0108t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.40298-76T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646106 | ||||||
| chr2:178646111
|
T | C | 1 | a0175c0087t0006g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40298-81A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646111 | ||||||
| chr2:178646120
|
A | T | 2 | a0027c0029t0001g0118a0154c0111t0001g0190 | 2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.40298-90T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646120 | ||||||
| chr2:178646123
|
T | TATATATA others(6): Show |
1 | a0133c0062t0002g0155 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.40298-106_40298-94 others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646123 | ||||||
| chr2:178646128
|
A | T | 1 | a0004c0004t0001g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.40298-98T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646128 | ||||||
| chr2:178646170
|
A | G | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.40298-140T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 216/362 | chr2 | 178646170 | ||||||
| chr2:178646702
|
C | T | 4 | a0008c0012t0003g0177a0008c0012t0003g0180a0038c0166t0003g0049others(1): Show | 4 | HG00438.hp2 HG00609.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.40223-143G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 215/362 | chr2 | 178646702 | ||||||
| chr2:178646767
|
C | A | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.40223-208G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 215/362 | chr2 | 178646767 | ||||||
| chr2:178646974
|
A | G | 1 | a0004c0004t0001g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.40222+90T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 215/362 | chr2 | 178646974 | ||||||
| chr2:178647040
|
G | GTA | 10 | a0001c0171t0001g0029a0016c0170t0002g0028a0021c0011t0001g0149others(7): Show | 10 | HG00423.hp1 HG00639.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.40222+22_40222+23d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 215/362 | chr2 | 178647040 | ||||||
| chr2:178647040
|
G | GTATA | 6 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0094others(3): Show | 6 | HG02015.hp1 HG02145.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.40222+20_40222+23d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 215/362 | chr2 | 178647040 | ||||||
| chr2:178647040
|
G | GTATATAT others(1): Show |
11 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.40222+16_40222+23d others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 215/362 | chr2 | 178647040 | ||||||
| chr2:178647040
|
G | GTATATAT others(3): Show |
1 | a0038c0166t0003g0049 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.40222+14_40222+23d others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 215/362 | chr2 | 178647040 | ||||||
| chr2:178647040
|
G | GTATATAT others(5): Show |
2 | a0130c0056t0003g0150a0137c0059t0003g0148 | 2 | HG02523.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.40222+12_40222+23d others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 215/362 | chr2 | 178647040 | ||||||
| chr2:178647040
|
G | GTATATAT others(17): Show |
1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.40222+23_40222+24i others(26): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 215/362 | chr2 | 178647040 | ||||||
| chr2:178647040
|
GTA | G | 61 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(58): Show | 61 | HG00544.hp2 HG00642.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.40222+22_40222+23d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 215/362 | chr2 | 178647040 | ||||||
| chr2:178647165
|
T | G | 5 | a0037c0158t0002g0108a0160c0088t0001g0213a0161c0089t0002g0211others(2): Show | 5 | HG00558.hp1 HG00558.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.40142-21A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 214/362 | chr2 | 178647165 | ||||||
| chr2:178647374
|
C | T | 3 | a0068c0156t0001g0163a0069c0155t0001g0162a0157c0107t0001g0145 | 3 | HG02922.hp2 HG02965.hp2 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.40141+7G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 214/362 | chr2 | 178647374 | ||||||
| chr2:178647656
|
A | G | 1 | a0167c0070t0001g0199 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.40058-192T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 213/362 | chr2 | 178647656 | ||||||
| chr2:178648295
|
A | G | 1 | a0113c0039t0002g0132 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.40058-831T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 213/362 | chr2 | 178648295 | ||||||
| chr2:178648371
|
A | G | 1 | a0147c0098t0001g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.40057+877T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 213/362 | chr2 | 178648371 | ||||||
| chr2:178648411
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.40057+837A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 213/362 | chr2 | 178648411 | ||||||
| chr2:178648540
|
G | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.40057+708C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 213/362 | chr2 | 178648540 | ||||||
| chr2:178648690
|
G | A | 1 | a0175c0087t0006g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40057+558C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 213/362 | chr2 | 178648690 | ||||||
| chr2:178648826
|
C | G | 8 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(5): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.40057+422G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 213/362 | chr2 | 178648826 | ||||||
| chr2:178649019
|
G | C | 1 | a0050c0201t0001g0046 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.40057+229C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 213/362 | chr2 | 178649019 | ||||||
| chr2:178649074
|
C | T | 232 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(229): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.40057+174G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 213/362 | chr2 | 178649074 | ||||||
| chr2:178649196
|
A | T | 27 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(24): Show | 27 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.40057+52T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 213/362 | chr2 | 178649196 | ||||||
| chr2:178649481
|
G | A | 12 | a0059c0175t0004g0002a0061c0198t0001g0061a0062c0199t0001g0060others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.39973+73C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 212/362 | chr2 | 178649481 | ||||||
| chr2:178649693
|
G | A | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.39896-62C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 211/362 | chr2 | 178649693 | ||||||
| chr2:178649706
|
T | C | 97 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(94): Show | 97 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.39896-75A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 211/362 | chr2 | 178649706 | ||||||
| chr2:178649781
|
A | C | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.39895+36T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 211/362 | chr2 | 178649781 | ||||||
| chr2:178650707
|
T | G | 1 | a0055c0189t0001g0033 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.39709+44A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 209/362 | chr2 | 178650707 | ||||||
| chr2:178650710
|
T | G | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.39709+41A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 209/362 | chr2 | 178650710 | ||||||
| chr2:178650712
|
G | A | 1 | a0162c0090t0002g0198 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.39709+39C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 209/362 | chr2 | 178650712 | ||||||
| chr2:178650838
|
T | C | 1 | a0122c0034t0001g0128 | 1 | HG01175.hp1 | splice_region_variant&intron_variant | LOW | c.39626-4A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 208/362 | chr2 | 178650838 | ||||||
| chr2:178650960
|
T | C | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.39626-126A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 208/362 | chr2 | 178650960 | ||||||
| chr2:178651047
|
A | G | 66 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(63): Show | 66 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.39625+196T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 208/362 | chr2 | 178651047 | ||||||
| chr2:178651163
|
G | A | 7 | a0030c0165t0002g0022a0031c0162t0002g0023a0032c0161t0002g0065others(4): Show | 7 | HG00673.hp1 NA18612.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.39625+80C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 208/362 | chr2 | 178651163 | ||||||
| chr2:178651853
|
G | C | 1 | a0111c0047t0001g0135 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.39379+31C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 205/362 | chr2 | 178651853 | ||||||
| chr2:178652550
|
A | T | 1 | a0112c0046t0002g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.39044-9T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 201/362 | chr2 | 178652550 | ||||||
| chr2:178652649
|
A | G | 1 | a0003c0146t0002g0079 | 1 | HG01175.hp2 | splice_region_variant&intron_variant | LOW | c.39043+4T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 201/362 | chr2 | 178652649 | ||||||
| chr2:178653175
|
A | G | 1 | a0105c0041t0002g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.38792-51T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 198/362 | chr2 | 178653175 | ||||||
| chr2:178653348
|
G | A | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.38708-27C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 197/362 | chr2 | 178653348 | ||||||
| chr2:178653350
|
A | G | 22 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(19): Show | 22 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.38708-29T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 197/362 | chr2 | 178653350 | ||||||
| chr2:178653546
|
G | A | 1 | a0039c0167t0001g0031 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.38627-39C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 196/362 | chr2 | 178653546 | ||||||
| chr2:178653784
|
C | G | 1 | a0128c0144t0001g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.38545+33G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 195/362 | chr2 | 178653784 | ||||||
| chr2:178654127
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.38381-32C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 193/362 | chr2 | 178654127 | ||||||
| chr2:178654133
|
C | T | 13 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(10): Show | 13 | HG02145.hp2 HG02818.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.38381-38G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 193/362 | chr2 | 178654133 | ||||||
| chr2:178654171
|
A | G | 22 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(19): Show | 22 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.38380+37T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 193/362 | chr2 | 178654171 | ||||||
| chr2:178654172
|
G | A | 22 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(19): Show | 22 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.38380+36C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 193/362 | chr2 | 178654172 | ||||||
| chr2:178654179
|
A | T | 23 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(20): Show | 23 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.38380+29T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 193/362 | chr2 | 178654179 | ||||||
| chr2:178654184
|
TAGC | T | 9 | a0006c0018t0002g0102a0006c0018t0002g0105a0006c0141t0002g0099others(6): Show | 9 | HG00639.hp2 HG01361.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.38380+21_38380+23d others(5): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 193/362 | chr2 | 178654184 | ||||||
| chr2:178654359
|
A | T | 16 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(13): Show | 17 | HG00408.hp1 HG03490.hp1 HG03492.hp1 others(14): Show |
intron_variant | MODIFIER | c.38297-68T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 192/362 | chr2 | 178654359 | ||||||
| chr2:178654396
|
A | G | 22 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(19): Show | 22 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.38296+49T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 192/362 | chr2 | 178654396 | ||||||
| chr2:178654576
|
T | C | 107 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(104): Show | 107 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.38207-42A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 191/362 | chr2 | 178654576 | ||||||
| chr2:178654603
|
C | A | 92 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0077others(89): Show | 92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.38207-69G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 191/362 | chr2 | 178654603 | ||||||
| chr2:178654624
|
T | C | 115 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0077others(112): Show | 115 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.38207-90A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 191/362 | chr2 | 178654624 | ||||||
| chr2:178654662
|
A | T | 92 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(89): Show | 92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.38206+83T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 191/362 | chr2 | 178654662 | ||||||
| chr2:178655186
|
G | A | 86 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(83): Show | 86 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.38039-191C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178655186 | ||||||
| chr2:178655278
|
A | G | 69 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(66): Show | 69 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.38039-283T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178655278 | ||||||
| chr2:178655920
|
GA | G | 22 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(19): Show | 22 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.38039-926delT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178655920 | ||||||
| chr2:178656012
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.38039-1017C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656012 | ||||||
| chr2:178656036
|
A | T | 2 | a0012c0020t0001g0019a0012c0020t0001g0021 | 2 | NA18980.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.38039-1041T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656036 | ||||||
| chr2:178656144
|
C | A | 2 | a0177c0084t0004g0005a0178c0085t0004g0004 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.38039-1149G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656144 | ||||||
| chr2:178656221
|
A | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.38039-1226T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656221 | ||||||
| chr2:178656261
|
A | C | 2 | a0066c0032t0008g0238a0179c0083t0005g0003 | 2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.38038+1237T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656261 | ||||||
| chr2:178656320
|
A | G | 1 | a0021c0011t0001g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.38038+1178T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656320 | ||||||
| chr2:178656417
|
T | C | 7 | a0057c0181t0001g0043a0063c0200t0001g0044a0068c0156t0001g0163others(4): Show | 7 | HG02818.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.38038+1081A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656417 | ||||||
| chr2:178656456
|
G | A | 2 | a0157c0107t0001g0145a0192c0210t0001g0073 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.38038+1042C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656456 | ||||||
| chr2:178656456
|
G | GA | 225 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(222): Show | 226 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.38038+1041_38038+1 others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656456 | ||||||
| chr2:178656456
|
G | GAAACTAC others(4255): Show |
2 | a0023c0016t0001g0191a0023c0016t0001g0192 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.38038+1041_38038+1 others(4268): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656456 | ||||||
| chr2:178656456
|
G | GAAACTAC others(4255): Show |
1 | a0009c0095t0007g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.38038+1041_38038+1 others(4268): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656456 | ||||||
| chr2:178656456
|
G | GAAACTAC others(4255): Show |
1 | a0039c0167t0001g0031 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.38038+1041_38038+1 others(4268): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656456 | ||||||
| chr2:178656456
|
G | GAAACTAC others(4255): Show |
1 | a0020c0010t0002g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.38038+1041_38038+1 others(4268): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656456 | ||||||
| chr2:178656457
|
T | A | 231 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(228): Show | 232 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.38038+1041A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656457 | ||||||
| chr2:178656564
|
C | T | 2 | a0006c0018t0002g0102a0006c0018t0002g0105 | 2 | HG00639.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.38038+934G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656564 | ||||||
| chr2:178656904
|
C | T | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.38038+594G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178656904 | ||||||
| chr2:178657200
|
T | C | 10 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(7): Show | 10 | HG01361.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.38038+298A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178657200 | ||||||
| chr2:178657230
|
C | T | 1 | a0137c0059t0003g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.38038+268G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178657230 | ||||||
| chr2:178657320
|
G | A | 1 | a0004c0015t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.38038+178C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178657320 | ||||||
| chr2:178657418
|
T | A | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.38038+80A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178657418 | ||||||
| chr2:178657432
|
A | T | 13 | a0017c0008t0001g0106a0059c0175t0004g0002a0061c0198t0001g0061others(10): Show | 13 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.38038+66T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/362 | chr2 | 178657432 | ||||||
| chr2:178657585
|
A | G | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.37955-4T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 188/362 | chr2 | 178657585 | ||||||
| chr2:178657610
|
G | A | 57 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(54): Show | 57 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.37955-29C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 188/362 | chr2 | 178657610 | ||||||
| chr2:178658431
|
G | A | 2 | a0061c0198t0001g0061a0062c0199t0001g0060 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.37627+37C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 184/362 | chr2 | 178658431 | ||||||
| chr2:178658432
|
A | G | 2 | a0061c0198t0001g0061a0062c0199t0001g0060 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.37627+36T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 184/362 | chr2 | 178658432 | ||||||
| chr2:178658439
|
T | A | 2 | a0061c0198t0001g0061a0062c0199t0001g0060 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.37627+29A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 184/362 | chr2 | 178658439 | ||||||
| chr2:178658641
|
G | A | 8 | a0003c0146t0002g0079a0003c0147t0002g0090a0073c0149t0002g0085others(5): Show | 8 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.37543+64C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 183/362 | chr2 | 178658641 | ||||||
| chr2:178658656
|
A | G | 26 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(23): Show | 26 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.37543+49T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 183/362 | chr2 | 178658656 | ||||||
| chr2:178658661
|
C | G | 1 | a0167c0070t0001g0199 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.37543+44G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 183/362 | chr2 | 178658661 | ||||||
| chr2:178658836
|
C | T | 5 | a0004c0015t0001g0165a0159c0091t0010g0175a0177c0084t0004g0005others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.37454-42G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 182/362 | chr2 | 178658836 | ||||||
| chr2:178658863
|
C | A | 2 | a0122c0034t0001g0128a0156c0106t0001g0146 | 2 | HG01175.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.37454-69G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 182/362 | chr2 | 178658863 | ||||||
| chr2:178658884
|
T | C | 44 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(41): Show | 44 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.37454-90A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 182/362 | chr2 | 178658884 | ||||||
| chr2:178658884
|
T | TGATTGAC others(4254): Show |
1 | a0070c0152t0002g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.37454-91_37454-90i others(4263): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 182/362 | chr2 | 178658884 | ||||||
| chr2:178658922
|
A | T | 2 | a0122c0034t0001g0128a0156c0106t0001g0146 | 2 | HG01175.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.37453+83T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 182/362 | chr2 | 178658922 | ||||||
| chr2:178659411
|
T | C | 1 | a0150c0110t0001g0182 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.37286-156A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178659411 | ||||||
| chr2:178659446
|
A | G | 25 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(22): Show | 26 | HG00408.hp1 HG00639.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.37286-191T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178659446 | ||||||
| chr2:178659459
|
T | C | 1 | a0087c0119t0001g0217 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.37286-204A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178659459 | ||||||
| chr2:178659538
|
G | A | 3 | a0122c0034t0001g0128a0123c0137t0001g0096a0124c0120t0001g0097 | 3 | HG01175.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.37286-283C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178659538 | ||||||
| chr2:178660033
|
C | T | 2 | a0006c0018t0002g0105a0102c0130t0002g0103 | 2 | HG01361.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.37286-778G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660033 | ||||||
| chr2:178660237
|
A | T | 2 | a0016c0196t0002g0047a0050c0201t0001g0046 | 2 | HG00544.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.37286-982T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660237 | ||||||
| chr2:178660296
|
A | T | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.37286-1041T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660296 | ||||||
| chr2:178660481
|
A | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.37286-1226T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660481 | ||||||
| chr2:178660622
|
G | C | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.37285+1137C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660622 | ||||||
| chr2:178660677
|
T | C | 3 | a0057c0181t0001g0043a0063c0200t0001g0044a0129c0115t0001g0241 | 3 | HG02818.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.37285+1082A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660677 | ||||||
| chr2:178660715
|
G | A | 73 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(70): Show | 73 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.37285+1044C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660715 | ||||||
| chr2:178660715
|
G | GGAAACTA others(4254): Show |
1 | a0129c0115t0001g0241 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.37285+1043_37285+1 others(4267): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660715 | ||||||
| chr2:178660715
|
G | GGAAACTA others(4254): Show |
2 | a0057c0181t0001g0043a0063c0200t0001g0044 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.37285+1043_37285+1 others(4267): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660715 | ||||||
| chr2:178660825
|
C | T | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.37285+934G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660825 | ||||||
| chr2:178660990
|
A | T | 1 | a0118c0035t0001g0136 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.37285+769T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178660990 | ||||||
| chr2:178661224
|
A | T | 1 | a0061c0198t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.37285+535T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178661224 | ||||||
| chr2:178661288
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.37285+471T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178661288 | ||||||
| chr2:178661461
|
T | C | 2 | a0066c0032t0008g0238a0179c0083t0005g0003 | 2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.37285+298A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178661461 | ||||||
| chr2:178661598
|
A | T | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.37285+161T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178661598 | ||||||
| chr2:178661679
|
T | A | 1 | a0145c0099t0001g0170 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.37285+80A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 180/362 | chr2 | 178661679 | ||||||
| chr2:178661846
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | splice_region_variant&intron_variant | LOW | c.37202-4T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 179/362 | chr2 | 178661846 | ||||||
| chr2:178661871
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.37202-29C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 179/362 | chr2 | 178661871 | ||||||
| chr2:178662235
|
T | C | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.37040-13A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 177/362 | chr2 | 178662235 | ||||||
| chr2:178662305
|
C | G | 8 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.37039+33G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 177/362 | chr2 | 178662305 | ||||||
| chr2:178662654
|
T | C | 1 | a0022c0014t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.36875-38A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 175/362 | chr2 | 178662654 | ||||||
| chr2:178662863
|
G | A | 3 | a0021c0011t0001g0149a0021c0011t0001g0179a0131c0057t0001g0147 | 3 | HG01358.hp2 HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.36791-51C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 174/362 | chr2 | 178662863 | ||||||
| chr2:178662901
|
C | T | 1 | a0159c0091t0010g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.36790+65G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 174/362 | chr2 | 178662901 | ||||||
| chr2:178662904
|
C | T | 1 | a0171c0073t0002g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.36790+62G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 174/362 | chr2 | 178662904 | ||||||
| chr2:178663097
|
T | C | 1 | a0004c0004t0001g0173 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.36701-42A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 173/362 | chr2 | 178663097 | ||||||
| chr2:178663145
|
C | T | 2 | a0114c0048t0001g0133a0184c0033t0001g0159 | 2 | HG02040.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.36701-90G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 173/362 | chr2 | 178663145 | ||||||
| chr2:178663608
|
T | C | 20 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(17): Show | 20 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.36532+19A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 171/362 | chr2 | 178663608 | ||||||
| chr2:178663792
|
C | G | 1 | a0030c0165t0002g0022 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.36448+27G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 170/362 | chr2 | 178663792 | ||||||
| chr2:178664262
|
C | T | 84 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(81): Show | 84 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.36281-164G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 168/362 | chr2 | 178664262 | ||||||
| chr2:178664284
|
A | T | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.36280+176T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 168/362 | chr2 | 178664284 | ||||||
| chr2:178664363
|
C | A | 1 | a0060c0174t0001g0058 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.36280+97G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 168/362 | chr2 | 178664363 | ||||||
| chr2:178664546
|
A | G | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.36203-9T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 167/362 | chr2 | 178664546 | ||||||
| chr2:178664770
|
T | G | 16 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(13): Show | 16 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.36119-33A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 166/362 | chr2 | 178664770 | ||||||
| chr2:178664825
|
T | G | 1 | a0068c0156t0001g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.36118+27A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 166/362 | chr2 | 178664825 | ||||||
| chr2:178665372
|
C | T | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | splice_region_variant&intron_variant | LOW | c.36043+5G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 165/362 | chr2 | 178665372 | ||||||
| chr2:178665592
|
T | C | 2 | a0057c0181t0001g0043a0063c0200t0001g0044 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.35959+116A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 164/362 | chr2 | 178665592 | ||||||
| chr2:178665668
|
C | T | 1 | a0073c0149t0002g0085 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.35959+40G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 164/362 | chr2 | 178665668 | ||||||
| chr2:178665836
|
G | A | 1 | a0003c0006t0002g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.35876-45C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 163/362 | chr2 | 178665836 | ||||||
| chr2:178666228
|
T | C | 1 | a0193c0209t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.35876-437A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 163/362 | chr2 | 178666228 | ||||||
| chr2:178666351
|
A | AATGT | 120 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(117): Show | 120 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.35875+472_35875+47 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 163/362 | chr2 | 178666351 | ||||||
| chr2:178666395
|
G | T | 1 | a0063c0200t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.35875+429C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 163/362 | chr2 | 178666395 | ||||||
| chr2:178666402
|
G | A | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.35875+422C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 163/362 | chr2 | 178666402 | ||||||
| chr2:178666966
|
A | G | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.35798-65T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 162/362 | chr2 | 178666966 | ||||||
| chr2:178667129
|
G | A | 45 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(42): Show | 45 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.35797+107C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 162/362 | chr2 | 178667129 | ||||||
| chr2:178667795
|
T | C | 1 | a0114c0048t0001g0133 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.35546-74A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178667795 | ||||||
| chr2:178667878
|
C | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.35546-157G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178667878 | ||||||
| chr2:178667923
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.35546-202T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178667923 | ||||||
| chr2:178667930
|
T | C | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.35546-209A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178667930 | ||||||
| chr2:178668134
|
T | C | 1 | a0008c0012t0003g0180 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.35546-413A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178668134 | ||||||
| chr2:178668335
|
A | C | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.35546-614T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178668335 | ||||||
| chr2:178668399
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.35546-678C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178668399 | ||||||
| chr2:178668445
|
A | T | 15 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(12): Show | 15 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.35546-724T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178668445 | ||||||
| chr2:178668882
|
A | C | 56 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(53): Show | 56 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.35545+491T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178668882 | ||||||
| chr2:178668986
|
T | TA | 13 | a0059c0175t0004g0002a0061c0198t0001g0061a0062c0199t0001g0060others(10): Show | 13 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.35545+386dupT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178668986 | ||||||
| chr2:178669179
|
C | T | 2 | a0015c0182t0001g0036a0055c0189t0001g0033 | 2 | HG01346.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.35545+194G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 159/362 | chr2 | 178669179 | ||||||
| chr2:178669497
|
C | T | 1 | a0010c0072t0002g0204 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.35471-50G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 158/362 | chr2 | 178669497 | ||||||
| chr2:178669498
|
G | A | 1 | a0111c0047t0001g0135 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.35471-51C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 158/362 | chr2 | 178669498 | ||||||
| chr2:178669716
|
T | C | 1 | a0007c0003t0002g0154 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.35387-41A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 157/362 | chr2 | 178669716 | ||||||
| chr2:178670552
|
T | C | 10 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(7): Show | 10 | HG01361.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.35309-257A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 156/362 | chr2 | 178670552 | ||||||
| chr2:178670688
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.35309-393A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 156/362 | chr2 | 178670688 | ||||||
| chr2:178671631
|
C | G | 1 | a0021c0011t0001g0179 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.35227+340G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 155/362 | chr2 | 178671631 | ||||||
| chr2:178671770
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.35227+201A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 155/362 | chr2 | 178671770 | ||||||
| chr2:178672548
|
A | C | 2 | a0028c0026t0002g0114a0029c0025t0002g0115 | 2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.34856-67T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 153/362 | chr2 | 178672548 | ||||||
| chr2:178673123
|
A | C | 1 | a0003c0006t0002g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.34787-420T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 152/362 | chr2 | 178673123 | ||||||
| chr2:178673314
|
C | T | 5 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.34786+319G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 152/362 | chr2 | 178673314 | ||||||
| chr2:178673321
|
C | T | 12 | a0059c0175t0004g0002a0061c0198t0001g0061a0062c0199t0001g0060others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.34786+312G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 152/362 | chr2 | 178673321 | ||||||
| chr2:178673562
|
A | G | 2 | a0177c0084t0004g0005a0178c0085t0004g0004 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.34786+71T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 152/362 | chr2 | 178673562 | ||||||
| chr2:178673595
|
G | A | 2 | a0015c0182t0001g0036a0055c0189t0001g0033 | 2 | HG01346.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.34786+38C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 152/362 | chr2 | 178673595 | ||||||
| chr2:178674037
|
A | G | 2 | a0150c0110t0001g0182a0155c0108t0001g0144 | 2 | HG01361.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.34708+277T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 151/362 | chr2 | 178674037 | ||||||
| chr2:178675176
|
C | A | 140 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(137): Show | 140 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.34538-63G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 149/362 | chr2 | 178675176 | ||||||
| chr2:178675223
|
A | G | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.34538-110T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 149/362 | chr2 | 178675223 | ||||||
| chr2:178675236
|
T | C | 28 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(25): Show | 28 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.34538-123A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 149/362 | chr2 | 178675236 | ||||||
| chr2:178675294
|
T | C | 1 | a0159c0091t0010g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.34538-181A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 149/362 | chr2 | 178675294 | ||||||
| chr2:178675359
|
C | CT | 47 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(44): Show | 47 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(44): Show |
intron_variant | MODIFIER | c.34538-247dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 149/362 | chr2 | 178675359 | ||||||
| chr2:178675374
|
AGGAAGAA others(3): Show |
A | 1 | a0106c0129t0002g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.34538-271_34538-26 others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 149/362 | chr2 | 178675374 | ||||||
| chr2:178675389
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.34538-276A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 149/362 | chr2 | 178675389 | ||||||
| chr2:178675845
|
C | T | 1 | a0038c0166t0003g0049 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.34453+76G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 148/362 | chr2 | 178675845 | ||||||
| chr2:178675907
|
C | T | 1 | a0004c0015t0001g0186 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.34453+14G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 148/362 | chr2 | 178675907 | ||||||
| chr2:178675909
|
G | T | 6 | a0008c0064t0003g0151a0035c0163t0003g0025a0086c0118t0001g0218others(3): Show | 6 | HG00597.hp1 HG02027.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.34453+12C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 148/362 | chr2 | 178675909 | ||||||
| chr2:178676023
|
A | G | 1 | a0123c0137t0001g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.34379-28T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 147/362 | chr2 | 178676023 | ||||||
| chr2:178676675
|
A | AG | 103 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(100): Show | 103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.34378+525dupC | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 147/362 | chr2 | 178676675 | ||||||
| chr2:178676764
|
A | T | 1 | a0186c0024t0001g0014 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.34378+437T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 147/362 | chr2 | 178676764 | ||||||
| chr2:178676885
|
C | T | 56 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(53): Show | 56 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.34378+316G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 147/362 | chr2 | 178676885 | ||||||
| chr2:178677172
|
C | G | 182 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(179): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.34378+29G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 147/362 | chr2 | 178677172 | ||||||
| chr2:178677335
|
C | CAT | 21 | a0006c0141t0002g0099a0014c0180t0001g0068a0015c0176t0001g0045others(18): Show | 21 | HG00423.hp1 HG00609.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.34292-50_34292-49d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATAT | 17 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(14): Show | 17 | HG00438.hp2 HG00609.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.34292-52_34292-49d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATACA others(3): Show |
1 | a0148c0100t0001g0169 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.34292-49_34292-48i others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATACA others(11): Show |
1 | a0125c0138t0001g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.34292-49_34292-48i others(20): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATACA others(13): Show |
5 | a0004c0004t0001g0172a0004c0015t0001g0186a0009c0093t0001g0184others(2): Show | 5 | HG01496.hp1 HG03490.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.34292-49_34292-48i others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATACA others(15): Show |
8 | a0004c0004t0001g0168a0004c0004t0001g0173a0004c0015t0001g0165others(5): Show | 8 | HG00642.hp2 HG02004.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.34292-49_34292-48i others(24): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATACA others(17): Show |
3 | a0022c0014t0001g0193a0140c0094t0001g0196a0145c0099t0001g0170 | 3 | HG00544.hp2 HG01257.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.34292-49_34292-48i others(26): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATACA others(19): Show |
1 | a0009c0095t0007g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.34292-49_34292-48i others(28): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATACA others(29): Show |
1 | a0009c0105t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.34292-49_34292-48i others(38): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATACA others(33): Show |
1 | a0143c0103t0001g0171 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.34292-49_34292-48i others(42): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(1): Show |
5 | a0038c0166t0003g0049a0082c0052t0002g0113a0085c0049t0001g0131others(2): Show | 5 | HG02280.hp1 HG02300.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.34292-56_34292-49d others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(3): Show |
3 | a0014c0178t0001g0062a0062c0199t0001g0060a0117c0037t0001g0127 | 3 | HG00639.hp1 HG01257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.34292-58_34292-49d others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(5): Show |
5 | a0021c0011t0001g0149a0021c0011t0001g0179a0122c0034t0001g0128others(2): Show | 5 | HG01175.hp1 HG01358.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.34292-60_34292-49d others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(7): Show |
6 | a0024c0017t0001g0140a0024c0017t0001g0141a0055c0189t0001g0033others(3): Show | 6 | HG02280.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.34292-62_34292-49d others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(9): Show |
12 | a0001c0001t0001g0035a0001c0186t0001g0017a0002c0002t0001g0038others(9): Show | 12 | HG00673.hp2 HG01975.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.34292-64_34292-49d others(18): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(11): Show |
10 | a0001c0171t0001g0029a0001c0197t0001g0015a0017c0008t0001g0106others(7): Show | 10 | HG00544.hp1 HG02145.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.34292-66_34292-49d others(20): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(13): Show |
15 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0021t0001g0075others(12): Show | 15 | HG00423.hp2 HG01346.hp2 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.34292-68_34292-49d others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(15): Show |
10 | a0001c0001t0001g0077a0016c0196t0002g0047a0046c0177t0001g0054others(7): Show | 10 | HG00597.hp2 HG02040.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.34292-70_34292-49d others(24): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(17): Show |
6 | a0023c0016t0001g0191a0051c0184t0001g0048a0053c0191t0001g0032others(3): Show | 6 | HG00408.hp2 HG02523.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.34292-72_34292-49d others(26): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(19): Show |
7 | a0002c0022t0001g0067a0023c0016t0001g0192a0066c0032t0008g0238others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.34292-74_34292-49d others(28): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(21): Show |
5 | a0002c0022t0001g0066a0184c0033t0001g0159a0187c0205t0001g0072others(2): Show | 5 | HG01099.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.34292-49_34292-48i others(30): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(23): Show |
6 | a0013c0023t0001g0057a0065c0031t0001g0235a0068c0156t0001g0163others(3): Show | 6 | HG00741.hp1 HG01361.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.34292-49_34292-48i others(32): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(25): Show |
4 | a0039c0167t0001g0031a0048c0185t0002g0034a0155c0108t0001g0144others(1): Show | 4 | HG02698.hp1 NA18612.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.34292-49_34292-48i others(34): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(27): Show |
4 | a0013c0023t0001g0056a0052c0183t0002g0016a0063c0200t0001g0044others(1): Show | 4 | HG00735.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.34292-49_34292-48i others(36): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(29): Show |
1 | a0098c0038t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.34292-49_34292-48i others(38): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
C | CATATATA others(35): Show |
1 | a0177c0084t0004g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.34292-49_34292-48i others(44): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677335
|
CAT | C | 6 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(3): Show | 6 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.34292-50_34292-49d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677335 | ||||||
| chr2:178677431
|
A | G | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.34292-144T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677431 | ||||||
| chr2:178677506
|
G | A | 85 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(82): Show | 85 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.34291+115C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677506 | ||||||
| chr2:178677550
|
T | C | 3 | a0123c0137t0001g0096a0124c0120t0001g0097a0129c0115t0001g0241 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.34291+71A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 146/362 | chr2 | 178677550 | ||||||
| chr2:178677947
|
C | T | 1 | a0085c0049t0001g0131 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.33995-30G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 145/362 | chr2 | 178677947 | ||||||
| chr2:178678332
|
A | G | 7 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.33910+82T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 144/362 | chr2 | 178678332 | ||||||
| chr2:178678672
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.33826+75G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 143/362 | chr2 | 178678672 | ||||||
| chr2:178678713
|
A | C | 3 | a0014c0178t0001g0062a0014c0180t0001g0068a0044c0193t0001g0050 | 3 | HG01257.hp1 HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.33826+34T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 143/362 | chr2 | 178678713 | ||||||
| chr2:178678978
|
G | A | 3 | a0082c0052t0002g0113a0109c0044t0002g0110a0110c0045t0002g0111 | 3 | HG02280.hp1 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.33743-148C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 142/362 | chr2 | 178678978 | ||||||
| chr2:178679000
|
A | T | 5 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.33743-170T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 142/362 | chr2 | 178679000 | ||||||
| chr2:178679093
|
G | T | 2 | a0166c0076t0002g0202a0174c0081t0001g0201 | 2 | NA18955.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.33742+246C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 142/362 | chr2 | 178679093 | ||||||
| chr2:178679328
|
T | C | 1 | a0128c0144t0001g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.33742+11A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 142/362 | chr2 | 178679328 | ||||||
| chr2:178679455
|
G | A | 1 | a0156c0106t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.33665-39C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 141/362 | chr2 | 178679455 | ||||||
| chr2:178679518
|
A | G | 1 | a0031c0162t0002g0023 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.33664+81T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 141/362 | chr2 | 178679518 | ||||||
| chr2:178679700
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.33581-18T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 140/362 | chr2 | 178679700 | ||||||
| chr2:178679842
|
C | A | 9 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(6): Show | 9 | HG01361.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.33580+52G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 140/362 | chr2 | 178679842 | ||||||
| chr2:178680577
|
G | A | 1 | a0097c0139t0002g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.33341-246C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 138/362 | chr2 | 178680577 | ||||||
| chr2:178680709
|
T | C | 1 | a0169c0074t0002g0209 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.33340+370A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 138/362 | chr2 | 178680709 | ||||||
| chr2:178680973
|
A | G | 3 | a0123c0137t0001g0096a0124c0120t0001g0097a0129c0115t0001g0241 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.33340+106T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 138/362 | chr2 | 178680973 | ||||||
| chr2:178681069
|
A | G | 2 | a0006c0141t0002g0099a0083c0142t0002g0080 | 2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.33340+10T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 138/362 | chr2 | 178681069 | ||||||
| chr2:178682302
|
A | G | 2 | a0015c0182t0001g0036a0055c0189t0001g0033 | 2 | HG01346.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.33094+395T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 135/362 | chr2 | 178682302 | ||||||
| chr2:178682374
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.33094+323G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 135/362 | chr2 | 178682374 | ||||||
| chr2:178682428
|
T | A | 1 | a0004c0004t0001g0173 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.33094+269A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 135/362 | chr2 | 178682428 | ||||||
| chr2:178682475
|
C | T | 5 | a0059c0175t0004g0002a0151c0112t0001g0183a0187c0205t0001g0072others(2): Show | 5 | HG02615.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.33094+222G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 135/362 | chr2 | 178682475 | ||||||
| chr2:178682566
|
G | A | 28 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(25): Show | 28 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.33094+131C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 135/362 | chr2 | 178682566 | ||||||
| chr2:178682623
|
T | G | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.33094+74A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 135/362 | chr2 | 178682623 | ||||||
| chr2:178683133
|
A | G | 80 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(77): Show | 80 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.32887+78T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 134/362 | chr2 | 178683133 | ||||||
| chr2:178683301
|
A | T | 2 | a0048c0185t0002g0034a0114c0048t0001g0133 | 2 | HG02040.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.32807-10T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 133/362 | chr2 | 178683301 | ||||||
| chr2:178683475
|
C | A | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.32807-184G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 133/362 | chr2 | 178683475 | ||||||
| chr2:178683551
|
A | G | 1 | a0106c0129t0002g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.32807-260T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 133/362 | chr2 | 178683551 | ||||||
| chr2:178683812
|
T | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.32806+187A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 133/362 | chr2 | 178683812 | ||||||
| chr2:178683968
|
A | AT | 5 | a0001c0021t0001g0076a0159c0091t0010g0175a0179c0083t0005g0003others(2): Show | 5 | HG02165.hp1 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.32806+30dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 133/362 | chr2 | 178683968 | ||||||
| chr2:178683977
|
T | C | 1 | a0116c0036t0001g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.32806+22A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 133/362 | chr2 | 178683977 | ||||||
| chr2:178684227
|
T | TCAA | 60 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.32722+100_32722+10 others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 132/362 | chr2 | 178684227 | ||||||
| chr2:178684773
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.32555-24T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 130/362 | chr2 | 178684773 | ||||||
| chr2:178685095
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.32471-106G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 129/362 | chr2 | 178685095 | ||||||
| chr2:178685342
|
T | C | 12 | a0059c0175t0004g0002a0061c0198t0001g0061a0062c0199t0001g0060others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.32393-12A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 128/362 | chr2 | 178685342 | ||||||
| chr2:178685400
|
T | A | 2 | a0068c0156t0001g0163a0069c0155t0001g0162 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32393-70A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 128/362 | chr2 | 178685400 | ||||||
| chr2:178685489
|
G | C | 1 | a0122c0034t0001g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.32392+29C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 128/362 | chr2 | 178685489 | ||||||
| chr2:178685666
|
T | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.32312-68A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178685666 | ||||||
| chr2:178685712
|
A | G | 2 | a0188c0207t0001g0070a0189c0206t0001g0069 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.32312-114T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178685712 | ||||||
| chr2:178686113
|
A | AT | 23 | a0003c0006t0002g0101a0006c0018t0002g0105a0006c0141t0002g0099others(20): Show | 23 | HG00438.hp1 HG01099.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.32312-516dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATT | 16 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040others(13): Show | 16 | HG00423.hp1 HG01071.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.32312-517_32312-51 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTT | 18 | a0002c0022t0001g0066a0008c0012t0003g0177a0008c0012t0003g0180others(15): Show | 18 | HG00609.hp1 HG00609.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.32312-518_32312-51 others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTT | 37 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0077others(34): Show | 37 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.32312-519_32312-51 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTT | 10 | a0001c0001t0001g0035a0001c0021t0001g0075a0001c0186t0001g0017others(7): Show | 10 | HG00423.hp2 HG00597.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.32312-520_32312-51 others(9): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(1): Show |
8 | a0059c0175t0004g0002a0061c0198t0001g0061a0147c0098t0001g0187others(5): Show | 8 | HG02280.hp2 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.32312-523_32312-51 others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(2): Show |
5 | a0062c0199t0001g0060a0157c0107t0001g0145a0184c0033t0001g0159others(2): Show | 5 | HG01099.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.32312-524_32312-51 others(13): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(3): Show |
2 | a0189c0206t0001g0069a0191c0211t0001g0074 | 2 | HG00735.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.32312-525_32312-51 others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(5): Show |
1 | a0156c0106t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.32312-527_32312-51 others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(7): Show |
4 | a0024c0017t0001g0140a0024c0017t0001g0141a0128c0144t0001g0095others(1): Show | 4 | HG02809.hp1 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.32312-529_32312-51 others(18): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(8): Show |
5 | a0019c0019t0001g0093a0123c0137t0001g0096a0129c0115t0001g0241others(2): Show | 5 | HG02976.hp1 HG03516.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.32312-530_32312-51 others(19): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(9): Show |
5 | a0009c0095t0007g0166a0017c0008t0001g0106a0017c0008t0001g0107others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.32312-531_32312-51 others(20): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(10): Show |
1 | a0064c0202t0001g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.32312-532_32312-51 others(21): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(11): Show |
1 | a0141c0092t0001g0194 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.32312-533_32312-51 others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(12): Show |
6 | a0004c0004t0001g0172a0004c0004t0001g0173a0018c0009t0001g0236others(3): Show | 6 | HG01496.hp1 HG02004.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.32312-534_32312-51 others(23): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(13): Show |
9 | a0009c0093t0001g0184a0018c0009t0001g0237a0022c0014t0001g0193others(6): Show | 9 | HG00544.hp2 HG01257.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.32312-535_32312-51 others(24): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(14): Show |
4 | a0068c0156t0001g0163a0139c0096t0001g0181a0149c0104t0001g0174others(1): Show | 4 | HG02965.hp2 HG03130.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.32312-536_32312-51 others(25): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(15): Show |
3 | a0023c0016t0001g0191a0023c0016t0001g0192a0066c0032t0008g0238 | 3 | HG02895.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.32312-537_32312-51 others(26): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(16): Show |
5 | a0027c0029t0001g0118a0063c0200t0001g0044a0067c0030t0001g0239others(2): Show | 5 | HG02809.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32312-538_32312-51 others(27): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(17): Show |
5 | a0004c0004t0001g0168a0004c0015t0001g0165a0004c0015t0001g0186others(2): Show | 5 | HG00642.hp2 HG03041.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.32312-539_32312-51 others(28): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
A | ATTTTTTT others(18): Show |
3 | a0144c0102t0001g0185a0150c0110t0001g0182a0155c0108t0001g0144 | 3 | HG01361.hp1 HG02293.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.32312-540_32312-51 others(29): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686113
|
ATTTTTTT others(5): Show |
A | 1 | a0118c0035t0001g0136 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.32312-527_32312-51 others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686113 | ||||||
| chr2:178686177
|
G | A | 3 | a0123c0137t0001g0096a0124c0120t0001g0097a0129c0115t0001g0241 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.32312-579C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686177 | ||||||
| chr2:178686183
|
G | C | 3 | a0123c0137t0001g0096a0124c0120t0001g0097a0129c0115t0001g0241 | 3 | HG03453.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.32312-585C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686183 | ||||||
| chr2:178686227
|
TCTC | T | 8 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.32312-632_32312-63 others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686227 | ||||||
| chr2:178686281
|
C | T | 1 | a0113c0039t0002g0132 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.32312-683G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686281 | ||||||
| chr2:178686356
|
G | A | 55 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(52): Show | 55 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.32312-758C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686356 | ||||||
| chr2:178686363
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.32312-765T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686363 | ||||||
| chr2:178686385
|
G | C | 14 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.32312-787C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686385 | ||||||
| chr2:178686427
|
A | AT | 222 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(219): Show | 223 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.32312-830dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686427 | ||||||
| chr2:178686615
|
A | G | 1 | a0128c0144t0001g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.32312-1017T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686615 | ||||||
| chr2:178686735
|
A | G | 1 | a0120c0134t0001g0230 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.32312-1137T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686735 | ||||||
| chr2:178686865
|
C | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.32311+1246G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686865 | ||||||
| chr2:178686937
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.32311+1174C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178686937 | ||||||
| chr2:178687079
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.32311+1032G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178687079 | ||||||
| chr2:178687394
|
T | TAAGAAAC others(318): Show |
9 | a0059c0175t0004g0002a0061c0198t0001g0061a0062c0199t0001g0060others(6): Show | 9 | HG00741.hp1 HG01099.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.32311+716_32311+71 others(329): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178687394 | ||||||
| chr2:178687394
|
T | TAAGAAAC others(319): Show |
3 | a0184c0033t0001g0159a0191c0211t0001g0074a0193c0209t0001g0071 | 3 | HG00735.hp1 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.32311+716_32311+71 others(330): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178687394 | ||||||
| chr2:178687394
|
T | TAAGAAAC others(328): Show |
1 | a0177c0084t0004g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.32311+716_32311+71 others(339): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178687394 | ||||||
| chr2:178687394
|
T | TAAGAAAC others(329): Show |
1 | a0178c0085t0004g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.32311+716_32311+71 others(340): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178687394 | ||||||
| chr2:178687394
|
T | TAAGAAAC others(342): Show |
1 | a0159c0091t0010g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.32311+716_32311+71 others(353): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178687394 | ||||||
| chr2:178687394
|
T | TAAGAAAC others(349): Show |
1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.32311+716_32311+71 others(360): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178687394 | ||||||
| chr2:178687828
|
T | C | 3 | a0068c0156t0001g0163a0069c0155t0001g0162a0157c0107t0001g0145 | 3 | HG02922.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32311+283A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178687828 | ||||||
| chr2:178687858
|
A | C | 9 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(6): Show | 9 | HG01099.hp1 HG01975.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.32311+253T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178687858 | ||||||
| chr2:178687900
|
G | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.32311+211C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 127/362 | chr2 | 178687900 | ||||||
| chr2:178688536
|
A | G | 1 | a0177c0084t0004g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.32197+141T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 126/362 | chr2 | 178688536 | ||||||
| chr2:178688584
|
C | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.32197+93G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 126/362 | chr2 | 178688584 | ||||||
| chr2:178688839
|
A | G | 2 | a0188c0207t0001g0070a0189c0206t0001g0069 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.32096-61T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 125/362 | chr2 | 178688839 | ||||||
| chr2:178689003
|
A | AT | 6 | a0010c0013t0002g0207a0081c0067t0002g0215a0099c0132t0002g0214others(3): Show | 6 | HG00438.hp2 HG02738.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.32095+49dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 125/362 | chr2 | 178689003 | ||||||
| chr2:178689003
|
AT | A | 141 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(138): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.32095+49delA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 125/362 | chr2 | 178689003 | ||||||
| chr2:178689003
|
ATTTTTTT others(1): Show |
A | 8 | a0018c0009t0001g0236a0018c0009t0001g0237a0019c0019t0001g0093others(5): Show | 8 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.32095+42_32095+49d others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 125/362 | chr2 | 178689003 | ||||||
| chr2:178689190
|
G | A | 83 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(80): Show | 83 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.32012-54C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 124/362 | chr2 | 178689190 | ||||||
| chr2:178689795
|
C | T | 1 | a0164c0079t0001g0197 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.31846+18G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 122/362 | chr2 | 178689795 | ||||||
| chr2:178690214
|
T | C | 2 | a0166c0076t0002g0202a0174c0081t0001g0201 | 2 | NA18955.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.31763-318A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 121/362 | chr2 | 178690214 | ||||||
| chr2:178690235
|
A | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.31763-339T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 121/362 | chr2 | 178690235 | ||||||
| chr2:178690419
|
A | C | 2 | a0017c0008t0001g0106a0017c0008t0001g0107 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.31763-523T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 121/362 | chr2 | 178690419 | ||||||
| chr2:178690679
|
G | A | 1 | a0017c0008t0001g0107 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.31763-783C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 121/362 | chr2 | 178690679 | ||||||
| chr2:178690909
|
CACAA | C | 6 | a0030c0165t0002g0022a0031c0162t0002g0023a0032c0161t0002g0065others(3): Show | 6 | HG00673.hp1 NA18612.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.31763-1017_31763-1 others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 121/362 | chr2 | 178690909 | ||||||
| chr2:178690948
|
G | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.31763-1052C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 121/362 | chr2 | 178690948 | ||||||
| chr2:178691248
|
T | G | 2 | a0109c0044t0002g0110a0110c0045t0002g0111 | 2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.31762+768A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 121/362 | chr2 | 178691248 | ||||||
| chr2:178691320
|
G | A | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.31762+696C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 121/362 | chr2 | 178691320 | ||||||
| chr2:178692011
|
C | T | 4 | a0005c0005t0001g0228a0070c0152t0002g0088a0088c0128t0001g0229others(1): Show | 4 | HG01255.hp2 NA18945.hp1 NA18968.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.31762+5G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 121/362 | chr2 | 178692011 | ||||||
| chr2:178692198
|
G | T | 1 | a0145c0099t0001g0170 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.31679-99C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 120/362 | chr2 | 178692198 | ||||||
| chr2:178692350
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.31678+147G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 120/362 | chr2 | 178692350 | ||||||
| chr2:178692457
|
T | C | 8 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(5): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.31678+40A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 120/362 | chr2 | 178692457 | ||||||
| chr2:178692984
|
G | T | 1 | a0173c0069t0002g0007 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.31595-404C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 119/362 | chr2 | 178692984 | ||||||
| chr2:178693120
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.31594+489G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 119/362 | chr2 | 178693120 | ||||||
| chr2:178693355
|
G | T | 1 | a0114c0048t0001g0133 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.31594+254C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 119/362 | chr2 | 178693355 | ||||||
| chr2:178693433
|
C | T | 1 | a0003c0146t0002g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.31594+176G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 119/362 | chr2 | 178693433 | ||||||
| chr2:178693462
|
G | A | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.31594+147C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 119/362 | chr2 | 178693462 | ||||||
| chr2:178693555
|
T | A | 93 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(90): Show | 93 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.31594+54A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 119/362 | chr2 | 178693555 | ||||||
| chr2:178693862
|
G | T | 1 | a0061c0198t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.31513+60C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 118/362 | chr2 | 178693862 | ||||||
| chr2:178693883
|
C | T | 1 | a0031c0162t0002g0023 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.31513+39G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 118/362 | chr2 | 178693883 | ||||||
| chr2:178694124
|
G | A | 1 | a0056c0190t0001g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.31427-116C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 117/362 | chr2 | 178694124 | ||||||
| chr2:178694128
|
G | C | 1 | a0075c0145t0002g0089 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.31427-120C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 117/362 | chr2 | 178694128 | ||||||
| chr2:178694325
|
A | T | 2 | a0028c0026t0002g0114a0029c0025t0002g0115 | 2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.31426+274T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 117/362 | chr2 | 178694325 | ||||||
| chr2:178694731
|
A | G | 1 | a0008c0012t0003g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.31349-55T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 116/362 | chr2 | 178694731 | ||||||
| chr2:178695216
|
A | C | 1 | a0008c0012t0003g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.31270+132T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 115/362 | chr2 | 178695216 | ||||||
| chr2:178695441
|
T | C | 9 | a0057c0181t0001g0043a0063c0200t0001g0044a0068c0156t0001g0163others(6): Show | 9 | HG02451.hp1 HG02818.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.31208-31A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 114/362 | chr2 | 178695441 | ||||||
| chr2:178695462
|
T | C | 1 | a0140c0094t0001g0196 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.31208-52A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 114/362 | chr2 | 178695462 | ||||||
| chr2:178695855
|
T | G | 1 | a0186c0024t0001g0014 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.31207+10A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 114/362 | chr2 | 178695855 | ||||||
| chr2:178696535
|
TTCCATGA others(4): Show |
T | 1 | a0020c0010t0002g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.30803-277_30803-26 others(15): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 113/362 | chr2 | 178696535 | ||||||
| chr2:178696552
|
T | C | 1 | a0077c0153t0002g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.30803-283A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 113/362 | chr2 | 178696552 | ||||||
| chr2:178696619
|
T | G | 18 | a0059c0175t0004g0002a0061c0198t0001g0061a0062c0199t0001g0060others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.30803-350A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 113/362 | chr2 | 178696619 | ||||||
| chr2:178696801
|
T | C | 20 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(17): Show | 20 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.30802+320A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 113/362 | chr2 | 178696801 | ||||||
| chr2:178696869
|
C | T | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.30802+252G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 113/362 | chr2 | 178696869 | ||||||
| chr2:178697413
|
T | C | 56 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(53): Show | 56 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.30755-245A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 112/362 | chr2 | 178697413 | ||||||
| chr2:178697494
|
A | G | 1 | a0135c0061t0001g0178 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.30755-326T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 112/362 | chr2 | 178697494 | ||||||
| chr2:178697627
|
T | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.30755-459A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 112/362 | chr2 | 178697627 | ||||||
| chr2:178697740
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.30755-572A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 112/362 | chr2 | 178697740 | ||||||
| chr2:178697904
|
T | C | 2 | a0072c0154t0002g0092a0074c0148t0002g0087 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.30755-736A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 112/362 | chr2 | 178697904 | ||||||
| chr2:178698154
|
C | T | 1 | a0155c0108t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.30754+689G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 112/362 | chr2 | 178698154 | ||||||
| chr2:178698272
|
C | CTTAG | 141 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(138): Show | 141 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.30754+567_30754+57 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 112/362 | chr2 | 178698272 | ||||||
| chr2:178698363
|
TAA | T | 8 | a0014c0178t0001g0062a0014c0180t0001g0068a0021c0011t0001g0149others(5): Show | 8 | HG01257.hp1 HG01358.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.30754+478_30754+47 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 112/362 | chr2 | 178698363 | ||||||
| chr2:178698475
|
A | T | 9 | a0023c0016t0001g0191a0023c0016t0001g0192a0027c0029t0001g0118others(6): Show | 9 | HG01361.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.30754+368T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 112/362 | chr2 | 178698475 | ||||||
| chr2:178698553
|
T | C | 1 | a0095c0122t0001g0226 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.30754+290A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 112/362 | chr2 | 178698553 | ||||||
| chr2:178698922
|
AAAAAAAA others(3): Show |
A | 1 | a0168c0075t0001g0205 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.30683-18_30683-9de others(11): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178698922 | ||||||
| chr2:178698929
|
AAAGAAAA others(6): Show |
A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.30683-28_30683-16d others(15): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178698929 | ||||||
| chr2:178698975
|
C | T | 4 | a0081c0067t0002g0215a0099c0132t0002g0214a0100c0133t0002g0233others(1): Show | 4 | HG00642.hp1 HG02738.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.30683-61G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178698975 | ||||||
| chr2:178699215
|
A | T | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30683-301T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699215 | ||||||
| chr2:178699378
|
ACACTCTT others(325): Show |
A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.30683-796_30683-46 others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699378 | ||||||
| chr2:178699383
|
C | CTTTT | 5 | a0003c0006t0002g0091a0006c0018t0002g0102a0097c0139t0002g0100others(2): Show | 5 | HG00639.hp2 HG01358.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.30683-473_30683-47 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
C | CTTTTTTT others(4): Show |
1 | a0003c0006t0002g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.30683-480_30683-47 others(15): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
C | CTTTTTTT others(6): Show |
1 | a0083c0142t0002g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.30683-482_30683-47 others(17): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTT | C | 6 | a0003c0146t0002g0079a0010c0013t0002g0207a0011c0007t0002g0116others(3): Show | 6 | HG01175.hp2 HG02738.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.30683-473_30683-47 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTT | C | 10 | a0003c0147t0002g0090a0011c0007t0002g0117a0073c0149t0002g0085others(7): Show | 10 | HG00642.hp1 HG01071.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.30683-474_30683-47 others(9): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTT | C | 7 | a0010c0013t0002g0206a0020c0010t0002g0134a0077c0153t0002g0086others(4): Show | 7 | HG00558.hp1 HG00741.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.30683-475_30683-47 others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(3): Show |
C | 8 | a0022c0014t0001g0193a0023c0016t0001g0191a0113c0039t0002g0132others(5): Show | 8 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(5): Show |
intron_variant | MODIFIER | c.30683-479_30683-47 others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(4): Show |
C | 3 | a0029c0025t0002g0115a0042c0172t0002g0055a0191c0211t0001g0074 | 3 | HG00735.hp1 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.30683-480_30683-47 others(15): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(5): Show |
C | 11 | a0009c0093t0001g0184a0022c0014t0001g0195a0023c0016t0001g0192others(8): Show | 11 | HG02015.hp2 HG02040.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.30683-481_30683-47 others(16): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(6): Show |
C | 9 | a0004c0015t0001g0165a0009c0095t0007g0166a0059c0175t0004g0002others(6): Show | 9 | HG01257.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.30683-482_30683-47 others(17): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(7): Show |
C | 16 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(13): Show | 16 | HG00642.hp2 HG01346.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.30683-483_30683-47 others(18): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(8): Show |
C | 7 | a0017c0008t0001g0107a0019c0019t0001g0094a0078c0055t0002g0012others(4): Show | 7 | HG02145.hp1 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.30683-484_30683-47 others(19): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(9): Show |
C | 12 | a0002c0022t0001g0066a0002c0022t0001g0067a0018c0009t0001g0236others(9): Show | 12 | HG01099.hp1 HG01496.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.30683-485_30683-47 others(20): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(10): Show |
C | 14 | a0001c0195t0001g0042a0018c0009t0001g0237a0019c0019t0001g0093others(11): Show | 14 | HG01175.hp1 HG02027.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.30683-486_30683-47 others(21): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(11): Show |
C | 44 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(41): Show | 44 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.30683-487_30683-47 others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(12): Show |
C | 14 | a0005c0117t0001g0221a0006c0141t0002g0099a0007c0003t0002g0154others(11): Show | 14 | HG01975.hp2 HG01981.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.30683-488_30683-47 others(23): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(13): Show |
C | 10 | a0005c0005t0001g0001a0005c0005t0001g0228a0088c0128t0001g0229others(7): Show | 11 | HG00408.hp1 HG03490.hp1 HG03492.hp1 others(8): Show |
intron_variant | MODIFIER | c.30683-489_30683-47 others(24): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(14): Show |
C | 5 | a0008c0012t0003g0180a0094c0123t0001g0219a0107c0043t0001g0161others(2): Show | 5 | HG03209.hp1 NA18974.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.30683-490_30683-47 others(25): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(15): Show |
C | 19 | a0008c0012t0003g0177a0008c0064t0003g0151a0012c0020t0001g0019others(16): Show | 19 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.30683-491_30683-47 others(26): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(16): Show |
C | 2 | a0033c0160t0002g0024a0070c0152t0002g0088 | 2 | HG01255.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.30683-492_30683-47 others(27): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(17): Show |
C | 1 | a0175c0087t0006g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.30683-493_30683-47 others(28): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(20): Show |
C | 1 | a0144c0102t0001g0185 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.30683-496_30683-47 others(31): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699383
|
CTTTTTTT others(22): Show |
C | 6 | a0057c0181t0001g0043a0063c0200t0001g0044a0182c0068t0002g0109others(3): Show | 6 | HG00741.hp1 HG01099.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.30683-498_30683-47 others(33): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699383 | ||||||
| chr2:178699442
|
C | T | 1 | a0100c0133t0002g0233 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.30683-528G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699442 | ||||||
| chr2:178699458
|
C | T | 1 | a0152c0113t0001g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30683-544G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699458 | ||||||
| chr2:178699497
|
C | T | 43 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(40): Show | 43 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.30683-583G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699497 | ||||||
| chr2:178699560
|
C | T | 1 | a0070c0152t0002g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.30683-646G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699560 | ||||||
| chr2:178699561
|
G | A | 8 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(5): Show | 8 | HG00642.hp2 HG01257.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.30683-647C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699561 | ||||||
| chr2:178699567
|
G | A | 3 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011 | 3 | HG02257.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.30683-653C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699567 | ||||||
| chr2:178699613
|
G | A | 1 | a0105c0041t0002g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.30683-699C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699613 | ||||||
| chr2:178699723
|
A | AT | 8 | a0017c0008t0001g0106a0023c0016t0001g0191a0023c0016t0001g0192others(5): Show | 8 | HG01361.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.30683-810dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699723 | ||||||
| chr2:178699723
|
AT | A | 180 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(177): Show | 181 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.30683-810delA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699723 | ||||||
| chr2:178699790
|
G | C | 8 | a0057c0181t0001g0043a0063c0200t0001g0044a0068c0156t0001g0163others(5): Show | 8 | HG02818.hp2 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.30683-876C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699790 | ||||||
| chr2:178699872
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.30683-958A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699872 | ||||||
| chr2:178699958
|
G | A | 1 | a0067c0030t0001g0239 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.30683-1044C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699958 | ||||||
| chr2:178699967
|
G | A | 1 | a0085c0049t0001g0131 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.30683-1053C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699967 | ||||||
| chr2:178699985
|
G | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.30683-1071C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178699985 | ||||||
| chr2:178700006
|
C | T | 1 | a0148c0100t0001g0169 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.30683-1092G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178700006 | ||||||
| chr2:178700341
|
A | G | 1 | a0104c0042t0002g0122 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.30682+779T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178700341 | ||||||
| chr2:178700437
|
A | AT | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.30682+682dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178700437 | ||||||
| chr2:178700656
|
C | T | 8 | a0057c0181t0001g0043a0063c0200t0001g0044a0068c0156t0001g0163others(5): Show | 8 | HG02818.hp2 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.30682+464G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178700656 | ||||||
| chr2:178700752
|
A | G | 9 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(6): Show | 9 | HG01099.hp1 HG01975.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.30682+368T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178700752 | ||||||
| chr2:178700775
|
T | C | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.30682+345A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178700775 | ||||||
| chr2:178700828
|
ATAG | A | 5 | a0024c0017t0001g0140a0024c0017t0001g0141a0139c0096t0001g0181others(2): Show | 5 | HG02922.hp2 HG02970.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.30682+289_30682+29 others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178700828 | ||||||
| chr2:178700831
|
G | GT | 41 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(38): Show | 41 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.30682+288dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 111/362 | chr2 | 178700831 | ||||||
| chr2:178701311
|
C | T | 4 | a0006c0018t0002g0102a0006c0018t0002g0105a0042c0172t0002g0055others(1): Show | 4 | HG00639.hp2 HG01361.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.30599-108G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 110/362 | chr2 | 178701311 | ||||||
| chr2:178701324
|
C | T | 4 | a0006c0018t0002g0102a0006c0018t0002g0105a0042c0172t0002g0055others(1): Show | 4 | HG00639.hp2 HG01361.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.30599-121G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 110/362 | chr2 | 178701324 | ||||||
| chr2:178701364
|
C | CT | 21 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.30599-162dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 110/362 | chr2 | 178701364 | ||||||
| chr2:178701365
|
T | G | 5 | a0159c0091t0010g0175a0177c0084t0004g0005a0178c0085t0004g0004others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.30599-162A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 110/362 | chr2 | 178701365 | ||||||
| chr2:178701419
|
T | G | 232 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(229): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.30598+109A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 110/362 | chr2 | 178701419 | ||||||
| chr2:178701430
|
C | G | 1 | a0139c0096t0001g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30598+98G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 110/362 | chr2 | 178701430 | ||||||
| chr2:178701671
|
C | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.30539-84G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 109/362 | chr2 | 178701671 | ||||||
| chr2:178701682
|
T | G | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.30539-95A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 109/362 | chr2 | 178701682 | ||||||
| chr2:178702075
|
T | TA | 39 | a0001c0171t0001g0029a0004c0004t0001g0168a0004c0004t0001g0172others(36): Show | 39 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.30512-10dupT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 108/362 | chr2 | 178702075 | ||||||
| chr2:178702699
|
T | C | 1 | a0006c0018t0002g0102 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.30224-36A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178702699 | ||||||
| chr2:178702704
|
A | C | 2 | a0125c0138t0001g0104a0142c0097t0001g0164 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.30224-41T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178702704 | ||||||
| chr2:178702810
|
T | C | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.30224-147A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178702810 | ||||||
| chr2:178702816
|
C | G | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.30224-153G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178702816 | ||||||
| chr2:178702907
|
T | C | 46 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(43): Show | 46 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(43): Show |
intron_variant | MODIFIER | c.30224-244A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178702907 | ||||||
| chr2:178703057
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.30224-394C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703057 | ||||||
| chr2:178703065
|
G | A | 2 | a0019c0019t0001g0093a0019c0019t0001g0094 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.30224-402C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703065 | ||||||
| chr2:178703121
|
G | A | 18 | a0059c0175t0004g0002a0061c0198t0001g0061a0062c0199t0001g0060others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.30224-458C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703121 | ||||||
| chr2:178703287
|
T | C | 1 | a0003c0006t0002g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.30224-624A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703287 | ||||||
| chr2:178703297
|
A | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.30224-634T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703297 | ||||||
| chr2:178703426
|
T | C | 2 | a0012c0020t0001g0019a0012c0020t0001g0021 | 2 | NA18980.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.30223+721A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703426 | ||||||
| chr2:178703514
|
C | T | 1 | a0136c0060t0003g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.30223+633G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703514 | ||||||
| chr2:178703700
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.30223+447T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703700 | ||||||
| chr2:178703883
|
C | T | 2 | a0061c0198t0001g0061a0062c0199t0001g0060 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.30223+264G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703883 | ||||||
| chr2:178703943
|
G | A | 3 | a0013c0023t0001g0056a0013c0023t0001g0057a0065c0031t0001g0235 | 3 | HG01884.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.30223+204C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703943 | ||||||
| chr2:178703955
|
C | T | 82 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(79): Show | 82 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.30223+192G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703955 | ||||||
| chr2:178703981
|
G | A | 3 | a0003c0146t0002g0079a0003c0147t0002g0090a0073c0149t0002g0085 | 3 | HG01175.hp2 HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.30223+166C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178703981 | ||||||
| chr2:178704146
|
C | T | 1 | a0004c0004t0001g0168 | 1 | HG00642.hp2 | splice_donor_variant&intron_variant | HIGH | c.30223+1G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 106/362 | chr2 | 178704146 | ||||||
| chr2:178704427
|
C | T | 1 | a0193c0209t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.29963-20G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 105/362 | chr2 | 178704427 | ||||||
| chr2:178704856
|
T | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.29694+21A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 104/362 | chr2 | 178704856 | ||||||
| chr2:178704978
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.29605-12T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 103/362 | chr2 | 178704978 | ||||||
| chr2:178705129
|
T | C | 1 | a0019c0019t0001g0094 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.29604+45A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 103/362 | chr2 | 178705129 | ||||||
| chr2:178705387
|
A | T | 34 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(31): Show | 34 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.29421-30T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 102/362 | chr2 | 178705387 | ||||||
| chr2:178705395
|
C | A | 21 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.29421-38G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 102/362 | chr2 | 178705395 | ||||||
| chr2:178705727
|
G | A | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.29421-370C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 102/362 | chr2 | 178705727 | ||||||
| chr2:178706220
|
G | A | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.29420+234C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 102/362 | chr2 | 178706220 | ||||||
| chr2:178706423
|
T | A | 2 | a0068c0156t0001g0163a0069c0155t0001g0162 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.29420+31A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 102/362 | chr2 | 178706423 | ||||||
| chr2:178706785
|
A | G | 2 | a0011c0007t0002g0116a0011c0007t0002g0117 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.29135-46T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 101/362 | chr2 | 178706785 | ||||||
| chr2:178706829
|
G | C | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.29134+33C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 101/362 | chr2 | 178706829 | ||||||
| chr2:178706970
|
C | T | 30 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(27): Show | 30 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.29042-16G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 100/362 | chr2 | 178706970 | ||||||
| chr2:178707206
|
G | A | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.29042-252C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 100/362 | chr2 | 178707206 | ||||||
| chr2:178707215
|
C | T | 28 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(25): Show | 28 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.29042-261G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 100/362 | chr2 | 178707215 | ||||||
| chr2:178707245
|
G | C | 21 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.29041+281C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 100/362 | chr2 | 178707245 | ||||||
| chr2:178707381
|
A | G | 21 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(18): Show | 21 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.29041+145T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 100/362 | chr2 | 178707381 | ||||||
| chr2:178707949
|
G | A | 1 | a0056c0190t0001g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.28754-136C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178707949 | ||||||
| chr2:178708119
|
T | C | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.28754-306A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708119 | ||||||
| chr2:178708170
|
C | G | 4 | a0084c0050t0002g0129a0097c0139t0002g0100a0115c0140t0002g0098others(1): Show | 4 | HG01496.hp2 HG02683.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.28754-357G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708170 | ||||||
| chr2:178708374
|
G | A | 32 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(29): Show | 32 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.28754-561C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708374 | ||||||
| chr2:178708628
|
A | G | 2 | a0159c0091t0010g0175a0185c0203t0001g0240 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.28754-815T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708628 | ||||||
| chr2:178708638
|
G | T | 32 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(29): Show | 32 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.28754-825C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708638 | ||||||
| chr2:178708667
|
A | G | 32 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(29): Show | 32 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.28754-854T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708667 | ||||||
| chr2:178708680
|
T | G | 32 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(29): Show | 32 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.28754-867A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708680 | ||||||
| chr2:178708697
|
C | T | 29 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.28753+869G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708697 | ||||||
| chr2:178708727
|
C | T | 29 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.28753+839G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708727 | ||||||
| chr2:178708894
|
T | C | 11 | a0018c0009t0001g0236a0018c0009t0001g0237a0024c0017t0001g0140others(8): Show | 11 | HG02738.hp2 HG02895.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.28753+672A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708894 | ||||||
| chr2:178708906
|
T | C | 31 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(28): Show | 31 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.28753+660A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178708906 | ||||||
| chr2:178709190
|
A | C | 1 | a0104c0042t0002g0122 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.28753+376T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 99/362 | chr2 | 178709190 | ||||||
| chr2:178709976
|
C | T | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.28463-120G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 98/362 | chr2 | 178709976 | ||||||
| chr2:178709988
|
A | G | 29 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.28463-132T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 98/362 | chr2 | 178709988 | ||||||
| chr2:178710057
|
A | G | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.28463-201T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 98/362 | chr2 | 178710057 | ||||||
| chr2:178710274
|
C | T | 1 | a0156c0106t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.28462+361G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 98/362 | chr2 | 178710274 | ||||||
| chr2:178710944
|
A | G | 1 | a0190c0208t0003g0009 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.28175-22T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 97/362 | chr2 | 178710944 | ||||||
| chr2:178711427
|
C | T | 1 | a0142c0097t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.27887-78G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 96/362 | chr2 | 178711427 | ||||||
| chr2:178711428
|
G | A | 1 | a0083c0142t0002g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.27887-79C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 96/362 | chr2 | 178711428 | ||||||
| chr2:178711497
|
A | G | 1 | a0099c0132t0002g0214 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27887-148T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 96/362 | chr2 | 178711497 | ||||||
| chr2:178711589
|
G | C | 1 | a0112c0046t0002g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.27887-240C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 96/362 | chr2 | 178711589 | ||||||
| chr2:178711674
|
C | T | 62 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.27886+270G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 96/362 | chr2 | 178711674 | ||||||
| chr2:178711741
|
A | G | 1 | a0159c0091t0010g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.27886+203T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 96/362 | chr2 | 178711741 | ||||||
| chr2:178711869
|
A | T | 132 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(129): Show | 132 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.27886+75T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 96/362 | chr2 | 178711869 | ||||||
| chr2:178713009
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.27050-34C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 93/362 | chr2 | 178713009 | ||||||
| chr2:178713381
|
T | TACAAA | 98 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(95): Show | 98 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.26762-14_26762-10d others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/362 | chr2 | 178713381 | ||||||
| chr2:178713381
|
T | TACAAAAC others(3): Show |
6 | a0068c0156t0001g0163a0069c0155t0001g0162a0123c0137t0001g0096others(3): Show | 6 | HG02451.hp1 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.26762-19_26762-10d others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/362 | chr2 | 178713381 | ||||||
| chr2:178713381
|
T | TACAAAAC others(8): Show |
1 | a0036c0164t0003g0020 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.26762-24_26762-10d others(17): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/362 | chr2 | 178713381 | ||||||
| chr2:178713381
|
T | TACAAAAC others(18): Show |
17 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(14): Show | 17 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.26762-34_26762-10d others(27): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/362 | chr2 | 178713381 | ||||||
| chr2:178713381
|
T | TACAAAAC others(23): Show |
3 | a0012c0020t0001g0019a0012c0020t0001g0021a0086c0118t0001g0218 | 3 | HG02027.hp1 NA18980.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.26762-39_26762-10d others(32): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/362 | chr2 | 178713381 | ||||||
| chr2:178713429
|
A | G | 1 | a0121c0135t0001g0232 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.26762-57T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/362 | chr2 | 178713429 | ||||||
| chr2:178713432
|
A | G | 1 | a0131c0057t0001g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.26762-60T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/362 | chr2 | 178713432 | ||||||
| chr2:178713610
|
A | C | 233 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(230): Show | 234 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.26762-238T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/362 | chr2 | 178713610 | ||||||
| chr2:178713751
|
C | A | 28 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(25): Show | 28 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.26761+146G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 92/362 | chr2 | 178713751 | ||||||
| chr2:178714210
|
A | G | 32 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(29): Show | 32 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.26483-35T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 91/362 | chr2 | 178714210 | ||||||
| chr2:178714639
|
G | A | 32 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(29): Show | 32 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.26201-66C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 90/362 | chr2 | 178714639 | ||||||
| chr2:178714967
|
T | A | 29 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.26200+19A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 90/362 | chr2 | 178714967 | ||||||
| chr2:178715341
|
A | C | 29 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.25922-77T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 89/362 | chr2 | 178715341 | ||||||
| chr2:178715366
|
A | C | 70 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(67): Show | 70 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.25922-102T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 89/362 | chr2 | 178715366 | ||||||
| chr2:178715473
|
C | T | 1 | a0191c0211t0001g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.25921+20G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 89/362 | chr2 | 178715473 | ||||||
| chr2:178715483
|
G | A | 33 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(30): Show | 33 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.25921+10C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 89/362 | chr2 | 178715483 | ||||||
| chr2:178715798
|
C | T | 33 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(30): Show | 33 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.25640-24G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 88/362 | chr2 | 178715798 | ||||||
| chr2:178715856
|
T | C | 95 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(92): Show | 95 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.25640-82A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 88/362 | chr2 | 178715856 | ||||||
| chr2:178716021
|
T | G | 1 | a0190c0208t0003g0009 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.25640-247A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 88/362 | chr2 | 178716021 | ||||||
| chr2:178716882
|
G | T | 1 | a0043c0194t0002g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.25639+213C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 88/362 | chr2 | 178716882 | ||||||
| chr2:178716895
|
T | C | 1 | a0171c0073t0002g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.25639+200A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 88/362 | chr2 | 178716895 | ||||||
| chr2:178716913
|
T | A | 69 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(66): Show | 69 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.25639+182A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 88/362 | chr2 | 178716913 | ||||||
| chr2:178716914
|
T | A | 1 | a0177c0084t0004g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.25639+181A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 88/362 | chr2 | 178716914 | ||||||
| chr2:178717435
|
C | T | 65 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(62): Show | 65 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.25352-53G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 87/362 | chr2 | 178717435 | ||||||
| chr2:178717466
|
G | A | 1 | a0190c0208t0003g0009 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.25351+57C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 87/362 | chr2 | 178717466 | ||||||
| chr2:178717878
|
A | G | 78 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.25063+65T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 86/362 | chr2 | 178717878 | ||||||
| chr2:178718641
|
A | G | 1 | a0003c0006t0002g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.24506-41T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 84/362 | chr2 | 178718641 | ||||||
| chr2:178718671
|
T | C | 74 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.24505+24A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 84/362 | chr2 | 178718671 | ||||||
| chr2:178719019
|
C | T | 2 | a0023c0016t0001g0191a0023c0016t0001g0192 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.24227-46G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 83/362 | chr2 | 178719019 | ||||||
| chr2:178719475
|
C | T | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.23939-24G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 82/362 | chr2 | 178719475 | ||||||
| chr2:178719493
|
A | G | 1 | a0042c0172t0002g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.23939-42T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 82/362 | chr2 | 178719493 | ||||||
| chr2:178719916
|
A | G | 1 | a0120c0134t0001g0230 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.23659+67T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 81/362 | chr2 | 178719916 | ||||||
| chr2:178719931
|
G | C | 1 | a0056c0190t0001g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.23659+52C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 81/362 | chr2 | 178719931 | ||||||
| chr2:178719933
|
T | C | 1 | a0020c0010t0002g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.23659+50A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 81/362 | chr2 | 178719933 | ||||||
| chr2:178720666
|
A | G | 139 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(136): Show | 139 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(136): Show |
splice_region_variant&intron_variant | LOW | c.23099-3T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 79/362 | chr2 | 178720666 | ||||||
| chr2:178720690
|
G | C | 1 | a0175c0087t0006g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.23099-27C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 79/362 | chr2 | 178720690 | ||||||
| chr2:178721236
|
A | G | 21 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.22817-34T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 78/362 | chr2 | 178721236 | ||||||
| chr2:178721244
|
T | C | 1 | a0128c0144t0001g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.22817-42A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 78/362 | chr2 | 178721244 | ||||||
| chr2:178721280
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.22817-78G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 78/362 | chr2 | 178721280 | ||||||
| chr2:178721377
|
A | G | 1 | a0116c0036t0001g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.22817-175T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 78/362 | chr2 | 178721377 | ||||||
| chr2:178721379
|
A | T | 10 | a0018c0009t0001g0236a0018c0009t0001g0237a0024c0017t0001g0140others(7): Show | 10 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.22817-177T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 78/362 | chr2 | 178721379 | ||||||
| chr2:178721788
|
T | A | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.22816+59A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 78/362 | chr2 | 178721788 | ||||||
| chr2:178722185
|
A | G | 6 | a0008c0064t0003g0151a0035c0163t0003g0025a0086c0118t0001g0218others(3): Show | 6 | HG00597.hp1 HG02027.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.22529-51T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 77/362 | chr2 | 178722185 | ||||||
| chr2:178722246
|
C | T | 1 | a0003c0006t0002g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.22528+13G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 77/362 | chr2 | 178722246 | ||||||
| chr2:178722581
|
A | T | 1 | a0190c0208t0003g0009 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.22241-35T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 76/362 | chr2 | 178722581 | ||||||
| chr2:178722614
|
G | C | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.22240+45C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 76/362 | chr2 | 178722614 | ||||||
| chr2:178722960
|
T | C | 144 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(141): Show | 144 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.21962-23A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 75/362 | chr2 | 178722960 | ||||||
| chr2:178724181
|
A | C | 1 | a0149c0104t0001g0174 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.21116-38T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 72/362 | chr2 | 178724181 | ||||||
| chr2:178724644
|
G | T | 21 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.20837-106C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 71/362 | chr2 | 178724644 | ||||||
| chr2:178724689
|
A | T | 1 | a0157c0107t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.20837-151T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 71/362 | chr2 | 178724689 | ||||||
| chr2:178724753
|
TG | T | 8 | a0024c0017t0001g0140a0024c0017t0001g0141a0128c0144t0001g0095others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.20837-216delC | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 71/362 | chr2 | 178724753 | ||||||
| chr2:178724823
|
C | T | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.20837-285G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 71/362 | chr2 | 178724823 | ||||||
| chr2:178724914
|
T | C | 5 | a0018c0009t0001g0236a0018c0009t0001g0237a0065c0031t0001g0235others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.20837-376A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 71/362 | chr2 | 178724914 | ||||||
| chr2:178725042
|
A | C | 21 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.20836+326T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 71/362 | chr2 | 178725042 | ||||||
| chr2:178725143
|
T | C | 5 | a0018c0009t0001g0236a0018c0009t0001g0237a0065c0031t0001g0235others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.20836+225A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 71/362 | chr2 | 178725143 | ||||||
| chr2:178725192
|
A | C | 21 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.20836+176T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 71/362 | chr2 | 178725192 | ||||||
| chr2:178726317
|
T | A | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.20276-271A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726317 | ||||||
| chr2:178726328
|
A | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(46): Show | 49 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.20276-282T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726328 | ||||||
| chr2:178726372
|
T | A | 1 | a0174c0081t0001g0201 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.20276-326A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726372 | ||||||
| chr2:178726457
|
G | A | 2 | a0123c0137t0001g0096a0128c0144t0001g0095 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.20276-411C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726457 | ||||||
| chr2:178726527
|
T | C | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.20276-481A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726527 | ||||||
| chr2:178726533
|
C | CAA | 66 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(63): Show | 66 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.20276-489_20276-48 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726533 | ||||||
| chr2:178726737
|
T | C | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.20275+353A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726737 | ||||||
| chr2:178726835
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.20275+255G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726835 | ||||||
| chr2:178726954
|
G | A | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.20275+136C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726954 | ||||||
| chr2:178726981
|
C | T | 1 | a0071c0151t0002g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.20275+109G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726981 | ||||||
| chr2:178726983
|
A | G | 1 | a0020c0010t0002g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.20275+107T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 69/362 | chr2 | 178726983 | ||||||
| chr2:178727434
|
A | G | 21 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.19994-63T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 68/362 | chr2 | 178727434 | ||||||
| chr2:178727990
|
A | C | 1 | a0115c0140t0002g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.19714+120T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 67/362 | chr2 | 178727990 | ||||||
| chr2:178727997
|
A | G | 58 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(55): Show | 58 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.19714+113T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 67/362 | chr2 | 178727997 | ||||||
| chr2:178728008
|
C | A | 21 | a0008c0012t0003g0177a0008c0012t0003g0180a0008c0064t0003g0151others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.19714+102G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 67/362 | chr2 | 178728008 | ||||||
| chr2:178730390
|
C | G | 101 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(98): Show | 101 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.18029-19G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 61/362 | chr2 | 178730390 | ||||||
| chr2:178730801
|
T | C | 5 | a0018c0009t0001g0236a0018c0009t0001g0237a0065c0031t0001g0235others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.17741-9A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 60/362 | chr2 | 178730801 | ||||||
| chr2:178730822
|
A | C | 1 | a0054c0187t0001g0037 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.17741-30T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 60/362 | chr2 | 178730822 | ||||||
| chr2:178730850
|
G | GT | 30 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(27): Show | 30 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.17741-59dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 60/362 | chr2 | 178730850 | ||||||
| chr2:178730850
|
GT | G | 37 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(34): Show | 37 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.17741-59delA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 60/362 | chr2 | 178730850 | ||||||
| chr2:178730852
|
T | C | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.17741-60A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 60/362 | chr2 | 178730852 | ||||||
| chr2:178730861
|
TA | T | 4 | a0021c0011t0001g0149a0021c0011t0001g0179a0131c0057t0001g0147others(1): Show | 4 | HG01358.hp2 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.17740+63delT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 60/362 | chr2 | 178730861 | ||||||
| chr2:178730862
|
A | T | 2 | a0018c0009t0001g0236a0018c0009t0001g0237 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.17740+63T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 60/362 | chr2 | 178730862 | ||||||
| chr2:178731590
|
G | A | 1 | a0125c0138t0001g0104 | 1 | NA20905.hp2 | splice_region_variant&intron_variant | LOW | c.17183-7C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 58/362 | chr2 | 178731590 | ||||||
| chr2:178732433
|
T | A | 1 | a0009c0105t0001g0167 | 1 | HG03041.hp1 | splice_region_variant&intron_variant | LOW | c.16621+7A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 56/362 | chr2 | 178732433 | ||||||
| chr2:178733592
|
G | A | 3 | a0155c0108t0001g0144a0156c0106t0001g0146a0157c0107t0001g0145 | 3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.15775+22C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 53/362 | chr2 | 178733592 | ||||||
| chr2:178733921
|
A | T | 1 | a0074c0148t0002g0087 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.15497-29T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 52/362 | chr2 | 178733921 | ||||||
| chr2:178734155
|
G | A | 2 | a0188c0207t0001g0070a0189c0206t0001g0069 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.15496+173C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 52/362 | chr2 | 178734155 | ||||||
| chr2:178734155
|
G | C | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.15496+173C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 52/362 | chr2 | 178734155 | ||||||
| chr2:178734171
|
G | GAA | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.15496+155_15496+15 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 52/362 | chr2 | 178734171 | ||||||
| chr2:178734179
|
C | A | 1 | a0004c0004t0001g0173 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.15496+149G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 52/362 | chr2 | 178734179 | ||||||
| chr2:178734628
|
G | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.15218-22C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 51/362 | chr2 | 178734628 | ||||||
| chr2:178734992
|
C | A | 1 | a0164c0079t0001g0197 | 1 | HG01255.hp1 | splice_region_variant&intron_variant | LOW | c.14936-4G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 50/362 | chr2 | 178734992 | ||||||
| chr2:178735208
|
A | C | 9 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(6): Show | 9 | HG00642.hp2 HG01257.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.14936-220T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 50/362 | chr2 | 178735208 | ||||||
| chr2:178736147
|
C | T | 1 | a0128c0144t0001g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.14372-73G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178736147 | ||||||
| chr2:178736175
|
T | C | 1 | a0106c0129t0002g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.14372-101A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178736175 | ||||||
| chr2:178736277
|
C | T | 1 | a0074c0148t0002g0087 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.14372-203G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178736277 | ||||||
| chr2:178736330
|
A | G | 41 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.14372-256T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178736330 | ||||||
| chr2:178736428
|
G | A | 14 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(11): Show | 15 | HG00408.hp1 HG03490.hp1 HG03492.hp1 others(12): Show |
intron_variant | MODIFIER | c.14372-354C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178736428 | ||||||
| chr2:178736555
|
T | C | 8 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011others(5): Show | 8 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.14372-481A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178736555 | ||||||
| chr2:178736767
|
G | A | 1 | a0190c0208t0003g0009 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.14372-693C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178736767 | ||||||
| chr2:178737248
|
A | G | 54 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(51): Show | 54 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.14371+834T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178737248 | ||||||
| chr2:178737474
|
A | G | 1 | a0176c0086t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.14371+608T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178737474 | ||||||
| chr2:178737558
|
C | T | 1 | a0119c0136t0002g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.14371+524G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178737558 | ||||||
| chr2:178737615
|
T | C | 12 | a0023c0016t0001g0191a0023c0016t0001g0192a0064c0202t0001g0059others(9): Show | 12 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.14371+467A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178737615 | ||||||
| chr2:178737681
|
T | C | 4 | a0081c0067t0002g0215a0099c0132t0002g0214a0100c0133t0002g0233others(1): Show | 4 | HG00642.hp1 HG02738.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.14371+401A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178737681 | ||||||
| chr2:178737806
|
T | C | 1 | a0076c0150t0002g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.14371+276A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178737806 | ||||||
| chr2:178737905
|
T | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.14371+177A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178737905 | ||||||
| chr2:178737972
|
G | T | 1 | a0044c0193t0001g0050 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.14371+110C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178737972 | ||||||
| chr2:178737989
|
G | A | 1 | a0123c0137t0001g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.14371+93C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 49/362 | chr2 | 178737989 | ||||||
| chr2:178738389
|
T | G | 1 | a0177c0084t0004g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.14093-29A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/362 | chr2 | 178738389 | ||||||
| chr2:178738458
|
A | C | 12 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(9): Show | 12 | HG00558.hp1 NA18943.hp2 NA18948.hp2 others(9): Show |
intron_variant | MODIFIER | c.14093-98T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/362 | chr2 | 178738458 | ||||||
| chr2:178738498
|
G | A | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.14093-138C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/362 | chr2 | 178738498 | ||||||
| chr2:178738554
|
A | T | 1 | a0190c0208t0003g0009 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.14093-194T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/362 | chr2 | 178738554 | ||||||
| chr2:178738708
|
G | GTGA | 28 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(25): Show | 28 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.14093-351_14093-34 others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/362 | chr2 | 178738708 | ||||||
| chr2:178739110
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.14092+31G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 48/362 | chr2 | 178739110 | ||||||
| chr2:178742130
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.11312-209T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178742130 | ||||||
| chr2:178742184
|
C | T | 8 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011others(5): Show | 8 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.11312-263G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178742184 | ||||||
| chr2:178742665
|
A | G | 13 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(10): Show | 13 | HG02145.hp1 HG02809.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.11312-744T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178742665 | ||||||
| chr2:178742760
|
T | C | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.11312-839A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178742760 | ||||||
| chr2:178742867
|
C | T | 8 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011others(5): Show | 8 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.11312-946G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178742867 | ||||||
| chr2:178743248
|
G | T | 8 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011others(5): Show | 8 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.11312-1327C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178743248 | ||||||
| chr2:178743357
|
G | A | 1 | a0182c0068t0002g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.11312-1436C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178743357 | ||||||
| chr2:178743480
|
C | T | 38 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(35): Show | 38 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.11312-1559G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178743480 | ||||||
| chr2:178743693
|
T | C | 2 | a0163c0080t0002g0212a0174c0081t0001g0201 | 2 | HG00438.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.11312-1772A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178743693 | ||||||
| chr2:178743716
|
C | T | 1 | a0124c0120t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.11312-1795G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178743716 | ||||||
| chr2:178743765
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.11312-1844C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178743765 | ||||||
| chr2:178744078
|
T | C | 1 | a0054c0187t0001g0037 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.11312-2157A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178744078 | ||||||
| chr2:178744113
|
A | G | 7 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.11312-2192T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178744113 | ||||||
| chr2:178744278
|
G | A | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.11312-2357C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178744278 | ||||||
| chr2:178744419
|
C | T | 1 | a0009c0105t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.11312-2498G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178744419 | ||||||
| chr2:178744448
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.11312-2527G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178744448 | ||||||
| chr2:178744517
|
T | TAAAGAGT others(321): Show |
1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.11312-2597_11312-2 others(334): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178744517 | ||||||
| chr2:178744518
|
A | G | 63 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(60): Show | 63 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.11312-2597T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178744518 | ||||||
| chr2:178744580
|
G | A | 1 | a0127c0143t0002g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.11312-2659C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178744580 | ||||||
| chr2:178744979
|
C | T | 14 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.11312-3058G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178744979 | ||||||
| chr2:178745074
|
T | C | 7 | a0064c0202t0001g0059a0158c0109t0001g0143a0175c0087t0006g0006others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.11312-3153A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178745074 | ||||||
| chr2:178745234
|
T | C | 2 | a0006c0141t0002g0099a0083c0142t0002g0080 | 2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.11312-3313A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178745234 | ||||||
| chr2:178745251
|
A | C | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.11312-3330T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178745251 | ||||||
| chr2:178745282
|
T | G | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.11312-3361A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178745282 | ||||||
| chr2:178745436
|
A | T | 22 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(19): Show | 22 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.11312-3515T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178745436 | ||||||
| chr2:178745445
|
T | A | 21 | a0005c0005t0001g0001a0005c0005t0001g0228a0005c0117t0001g0221others(18): Show | 22 | HG00408.hp1 HG00642.hp1 HG02698.hp2 others(19): Show |
intron_variant | MODIFIER | c.11312-3524A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178745445 | ||||||
| chr2:178745514
|
C | T | 2 | a0184c0033t0001g0159a0185c0203t0001g0240 | 2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.11312-3593G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178745514 | ||||||
| chr2:178745529
|
A | T | 1 | a0152c0113t0001g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.11312-3608T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178745529 | ||||||
| chr2:178745750
|
A | G | 1 | a0175c0087t0006g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.11312-3829T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178745750 | ||||||
| chr2:178745968
|
C | T | 14 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.11312-4047G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178745968 | ||||||
| chr2:178746176
|
A | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.11312-4255T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178746176 | ||||||
| chr2:178746240
|
C | T | 1 | a0164c0079t0001g0197 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.11312-4319G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178746240 | ||||||
| chr2:178746953
|
G | A | 16 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(13): Show | 16 | HG02055.hp1 HG02145.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.11312-5032C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178746953 | ||||||
| chr2:178746976
|
C | T | 1 | a0192c0210t0001g0073 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.11312-5055G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178746976 | ||||||
| chr2:178746984
|
C | A | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.11312-5063G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178746984 | ||||||
| chr2:178747087
|
GCTCTAGA others(59): Show |
G | 1 | a0001c0197t0001g0015 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.11312-5232_11312-5 others(72): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178747087 | ||||||
| chr2:178747124
|
C | T | 14 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.11312-5203G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178747124 | ||||||
| chr2:178747148
|
A | G | 14 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.11312-5227T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178747148 | ||||||
| chr2:178747172
|
G | T | 2 | a0017c0008t0001g0106a0017c0008t0001g0107 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.11312-5251C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178747172 | ||||||
| chr2:178747519
|
G | A | 1 | a0035c0163t0003g0025 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.11312-5598C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178747519 | ||||||
| chr2:178747646
|
A | C | 2 | a0125c0138t0001g0104a0142c0097t0001g0164 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.11311+5478T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178747646 | ||||||
| chr2:178747908
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.11311+5216G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178747908 | ||||||
| chr2:178748073
|
A | G | 1 | a0125c0138t0001g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.11311+5051T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748073 | ||||||
| chr2:178748420
|
G | C | 14 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(11): Show | 14 | HG02145.hp1 HG02559.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.11311+4704C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748420 | ||||||
| chr2:178748531
|
A | C | 5 | a0175c0087t0006g0006a0176c0086t0001g0082a0177c0084t0004g0005others(2): Show | 5 | HG02559.hp1 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.11311+4593T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748531 | ||||||
| chr2:178748537
|
C | T | 4 | a0008c0012t0003g0177a0008c0012t0003g0180a0038c0166t0003g0049others(1): Show | 4 | HG00438.hp2 HG00609.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.11311+4587G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748537 | ||||||
| chr2:178748541
|
T | G | 4 | a0022c0014t0001g0193a0022c0014t0001g0195a0140c0094t0001g0196others(1): Show | 4 | HG00544.hp2 HG02015.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.11311+4583A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748541 | ||||||
| chr2:178748767
|
C | T | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.11311+4357G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748767 | ||||||
| chr2:178748768
|
G | A | 1 | a0002c0002t0001g0041 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.11311+4356C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748768 | ||||||
| chr2:178748786
|
T | G | 1 | a0084c0050t0002g0129 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.11311+4338A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748786 | ||||||
| chr2:178748792
|
G | A | 7 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.11311+4332C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748792 | ||||||
| chr2:178748839
|
T | C | 1 | a0008c0012t0003g0180 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.11311+4285A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748839 | ||||||
| chr2:178748922
|
T | G | 7 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.11311+4202A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178748922 | ||||||
| chr2:178749053
|
T | C | 2 | a0028c0026t0002g0114a0029c0025t0002g0115 | 2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.11311+4071A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178749053 | ||||||
| chr2:178749235
|
C | T | 4 | a0175c0087t0006g0006a0177c0084t0004g0005a0178c0085t0004g0004others(1): Show | 4 | HG02559.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.11311+3889G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178749235 | ||||||
| chr2:178749355
|
G | T | 2 | a0011c0007t0002g0116a0011c0007t0002g0117 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.11311+3769C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178749355 | ||||||
| chr2:178749837
|
G | C | 1 | a0009c0095t0007g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.11311+3287C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178749837 | ||||||
| chr2:178750225
|
A | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(231): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.11311+2899T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178750225 | ||||||
| chr2:178750759
|
C | T | 2 | a0012c0020t0001g0019a0012c0020t0001g0021 | 2 | NA18980.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.11311+2365G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178750759 | ||||||
| chr2:178751123
|
A | G | 1 | a0022c0014t0001g0193 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.11311+2001T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178751123 | ||||||
| chr2:178751160
|
T | C | 153 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(150): Show | 154 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.11311+1964A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178751160 | ||||||
| chr2:178751204
|
C | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(231): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.11311+1920G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178751204 | ||||||
| chr2:178751232
|
G | A | 1 | a0105c0041t0002g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.11311+1892C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178751232 | ||||||
| chr2:178751267
|
T | C | 234 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(231): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.11311+1857A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178751267 | ||||||
| chr2:178751394
|
T | C | 1 | a0127c0143t0002g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.11311+1730A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178751394 | ||||||
| chr2:178751483
|
G | A | 2 | a0188c0207t0001g0070a0189c0206t0001g0069 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.11311+1641C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178751483 | ||||||
| chr2:178751752
|
G | A | 1 | a0191c0211t0001g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.11311+1372C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178751752 | ||||||
| chr2:178751806
|
T | A | 1 | a0091c0124t0001g0222 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.11311+1318A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178751806 | ||||||
| chr2:178752043
|
GA | G | 193 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(190): Show | 194 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.11311+1080delT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752043 | ||||||
| chr2:178752043
|
GAA | G | 5 | a0021c0011t0001g0179a0084c0050t0002g0129a0097c0139t0002g0100others(2): Show | 5 | HG01496.hp2 HG01952.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.11311+1079_11311+1 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752043 | ||||||
| chr2:178752053
|
A | AC | 3 | a0177c0084t0004g0005a0178c0085t0004g0004a0179c0083t0005g0003 | 3 | HG02559.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.11311+1070_11311+1 others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752053 | ||||||
| chr2:178752264
|
T | C | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.11311+860A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752264 | ||||||
| chr2:178752334
|
G | T | 1 | a0170c0071t0002g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.11311+790C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752334 | ||||||
| chr2:178752643
|
T | C | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.11311+481A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752643 | ||||||
| chr2:178752698
|
A | G | 21 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(18): Show | 21 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.11311+426T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752698 | ||||||
| chr2:178752785
|
G | A | 1 | a0131c0057t0001g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.11311+339C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752785 | ||||||
| chr2:178752807
|
A | G | 4 | a0018c0009t0001g0236a0018c0009t0001g0237a0065c0031t0001g0235others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.11311+317T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752807 | ||||||
| chr2:178752840
|
C | T | 239 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(236): Show | 240 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.11311+284G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752840 | ||||||
| chr2:178752911
|
A | G | 3 | a0021c0011t0001g0149a0021c0011t0001g0179a0131c0057t0001g0147 | 3 | HG01358.hp2 HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.11311+213T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752911 | ||||||
| chr2:178752929
|
A | G | 1 | a0042c0172t0002g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.11311+195T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178752929 | ||||||
| chr2:178753015
|
A | G | 2 | a0113c0039t0002g0132a0114c0048t0001g0133 | 2 | HG00423.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.11311+109T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 47/362 | chr2 | 178753015 | ||||||
| chr2:178753292
|
T | A | 179 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(176): Show | 180 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.11255-112A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178753292 | ||||||
| chr2:178753396
|
T | G | 11 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(8): Show | 11 | HG00597.hp1 HG01099.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.11255-216A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178753396 | ||||||
| chr2:178753550
|
C | T | 7 | a0023c0016t0001g0191a0023c0016t0001g0192a0150c0110t0001g0182others(4): Show | 7 | HG01361.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.11255-370G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178753550 | ||||||
| chr2:178753564
|
C | T | 4 | a0010c0072t0002g0204a0165c0077t0001g0203a0168c0075t0001g0205others(1): Show | 4 | NA18943.hp2 NA18968.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.11255-384G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178753564 | ||||||
| chr2:178753735
|
C | T | 93 | a0003c0006t0002g0083a0003c0006t0002g0091a0003c0006t0002g0101others(90): Show | 94 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.11255-555G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178753735 | ||||||
| chr2:178753777
|
C | T | 2 | a0009c0093t0001g0184a0183c0204t0001g0139 | 2 | HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.11255-597G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178753777 | ||||||
| chr2:178754063
|
G | A | 239 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(236): Show | 240 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.11255-883C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178754063 | ||||||
| chr2:178754448
|
C | G | 2 | a0061c0198t0001g0061a0062c0199t0001g0060 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.11255-1268G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178754448 | ||||||
| chr2:178754458
|
T | C | 1 | a0084c0050t0002g0129 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.11255-1278A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178754458 | ||||||
| chr2:178754670
|
G | C | 234 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(231): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.11255-1490C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178754670 | ||||||
| chr2:178754673
|
T | C | 55 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(52): Show | 55 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.11255-1493A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178754673 | ||||||
| chr2:178755111
|
T | C | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.11254+1111A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755111 | ||||||
| chr2:178755226
|
T | TTC | 3 | a0003c0147t0002g0090a0073c0149t0002g0085a0075c0145t0002g0089 | 3 | HG01071.hp1 HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.11254+995_11254+99 others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755226 | ||||||
| chr2:178755228
|
G | T | 3 | a0003c0147t0002g0090a0073c0149t0002g0085a0075c0145t0002g0089 | 3 | HG01071.hp1 HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.11254+994C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755228 | ||||||
| chr2:178755231
|
C | A | 60 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.11254+991G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755231 | ||||||
| chr2:178755358
|
A | G | 4 | a0003c0006t0002g0083a0003c0006t0002g0091a0003c0006t0002g0101others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.11254+864T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755358 | ||||||
| chr2:178755490
|
C | T | 1 | a0120c0134t0001g0230 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.11254+732G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755490 | ||||||
| chr2:178755504
|
C | T | 1 | a0159c0091t0010g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.11254+718G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755504 | ||||||
| chr2:178755538
|
C | T | 1 | a0167c0070t0001g0199 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.11254+684G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755538 | ||||||
| chr2:178755729
|
T | C | 234 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(231): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.11254+493A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755729 | ||||||
| chr2:178755826
|
C | A | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.11254+396G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755826 | ||||||
| chr2:178755984
|
A | G | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.11254+238T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755984 | ||||||
| chr2:178755996
|
C | T | 1 | a0098c0038t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.11254+226G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178755996 | ||||||
| chr2:178756177
|
C | T | 1 | a0182c0068t0002g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.11254+45G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 46/362 | chr2 | 178756177 | ||||||
| chr2:178757137
|
G | A | 55 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(52): Show | 55 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.10679-340C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757137 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(53): Show |
2 | a0040c0169t0002g0053a0041c0168t0002g0052 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.10679-350_10679-34 others(64): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(203): Show |
1 | a0073c0149t0002g0085 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.10679-350_10679-34 others(214): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(53): Show |
5 | a0001c0195t0001g0042a0001c0197t0001g0015a0015c0176t0001g0045others(2): Show | 5 | HG00609.hp1 HG01981.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.10679-350_10679-34 others(64): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(233): Show |
4 | a0003c0147t0002g0090a0070c0152t0002g0088a0075c0145t0002g0089others(1): Show | 4 | HG00741.hp2 HG01071.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.10679-350_10679-34 others(244): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(263): Show |
1 | a0076c0150t0002g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.10679-350_10679-34 others(274): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(83): Show |
5 | a0014c0178t0001g0062a0014c0180t0001g0068a0044c0193t0001g0050others(2): Show | 5 | HG00639.hp1 HG01257.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.10679-350_10679-34 others(94): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(113): Show |
6 | a0018c0009t0001g0236a0018c0009t0001g0237a0062c0199t0001g0060others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.10679-350_10679-34 others(124): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(143): Show |
2 | a0006c0018t0002g0105a0125c0138t0001g0104 | 2 | HG01361.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.10679-350_10679-34 others(154): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(203): Show |
2 | a0010c0013t0002g0207a0172c0078t0001g0208 | 2 | NA18948.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.10679-350_10679-34 others(214): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(173): Show |
4 | a0006c0141t0002g0099a0071c0151t0002g0084a0083c0142t0002g0080others(1): Show | 4 | HG01978.hp2 HG02735.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.10679-350_10679-34 others(184): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(203): Show |
9 | a0003c0006t0002g0083a0005c0005t0001g0228a0006c0018t0002g0102others(6): Show | 9 | HG00639.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.10679-350_10679-34 others(214): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(233): Show |
44 | a0003c0006t0002g0101a0003c0146t0002g0079a0010c0013t0002g0206others(41): Show | 44 | HG00408.hp1 HG00558.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.10679-350_10679-34 others(244): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(263): Show |
21 | a0003c0006t0002g0091a0005c0005t0001g0001a0005c0117t0001g0221others(18): Show | 22 | HG00423.hp1 HG00438.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.10679-350_10679-34 others(274): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(293): Show |
2 | a0126c0051t0002g0123a0128c0144t0001g0095 | 2 | HG01071.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.10679-350_10679-34 others(304): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(323): Show |
3 | a0103c0157t0001g0125a0105c0041t0002g0130a0110c0045t0002g0111 | 3 | HG02735.hp1 NA19010.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.10679-350_10679-34 others(334): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757146
|
A | ATGCTTTA others(259): Show |
1 | a0173c0069t0002g0007 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.10679-350_10679-34 others(270): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757146 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(23): Show |
1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.10679-352_10679-35 others(34): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(23): Show |
2 | a0040c0169t0002g0053a0041c0168t0002g0052 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.10678+364_10679-35 others(34): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(53): Show |
3 | a0177c0084t0004g0005a0178c0085t0004g0004a0179c0083t0005g0003 | 3 | HG02559.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.10678+334_10679-35 others(64): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(173): Show |
1 | a0142c0097t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.10679-352_10679-35 others(184): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(83): Show |
1 | a0009c0093t0001g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.10679-352_10679-35 others(94): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(113): Show |
4 | a0139c0096t0001g0181a0140c0094t0001g0196a0141c0092t0001g0194others(1): Show | 4 | HG02015.hp2 HG02155.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.10679-352_10679-35 others(124): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(143): Show |
14 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(11): Show | 14 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.10679-352_10679-35 others(154): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(173): Show |
2 | a0009c0095t0007g0166a0068c0156t0001g0163 | 2 | HG02965.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.10679-352_10679-35 others(184): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(203): Show |
2 | a0149c0104t0001g0174a0159c0091t0010g0175 | 2 | HG02257.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.10679-352_10679-35 others(214): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(53): Show |
1 | a0116c0036t0001g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.10679-352_10679-35 others(64): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(83): Show |
44 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(41): Show | 44 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.10679-352_10679-35 others(94): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(113): Show |
9 | a0016c0196t0002g0047a0023c0016t0001g0191a0023c0016t0001g0192others(6): Show | 9 | HG00544.hp1 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.10679-352_10679-35 others(124): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(113): Show |
3 | a0055c0189t0001g0033a0061c0198t0001g0061a0191c0211t0001g0074 | 3 | HG00735.hp1 HG02280.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.10679-352_10679-35 others(124): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(143): Show |
3 | a0151c0112t0001g0183a0153c0114t0001g0188a0156c0106t0001g0146 | 3 | HG02451.hp1 HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.10679-352_10679-35 others(154): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(173): Show |
1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.10679-352_10679-35 others(184): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757148
|
G | GCTTTAAG others(143): Show |
3 | a0017c0008t0001g0106a0017c0008t0001g0107a0150c0110t0001g0182 | 3 | HG01361.hp1 HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.10679-352_10679-35 others(154): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757148 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(499): Show |
2 | a0130c0056t0003g0150a0138c0063t0002g0156 | 2 | HG01975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.10679-361_10679-36 others(510): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(439): Show |
1 | a0007c0003t0002g0158 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.10679-361_10679-36 others(450): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(499): Show |
1 | a0007c0003t0002g0157 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.10679-361_10679-36 others(510): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(499): Show |
1 | a0033c0160t0002g0024 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.10679-361_10679-36 others(510): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(469): Show |
1 | a0133c0062t0002g0155 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.10679-361_10679-36 others(480): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(495): Show |
1 | a0008c0012t0003g0180 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.10679-361_10679-36 others(506): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(405): Show |
1 | a0012c0020t0001g0019 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.10679-361_10679-36 others(416): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(469): Show |
2 | a0031c0162t0002g0023a0086c0118t0001g0218 | 2 | HG02027.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.10679-361_10679-36 others(480): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(495): Show |
1 | a0038c0166t0003g0049 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.10679-361_10679-36 others(506): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(439): Show |
2 | a0034c0159t0002g0018a0037c0158t0002g0108 | 2 | HG00558.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.10679-361_10679-36 others(450): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(465): Show |
1 | a0008c0012t0003g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.10679-361_10679-36 others(476): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(409): Show |
2 | a0012c0020t0001g0021a0030c0165t0002g0022 | 2 | NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.10679-361_10679-36 others(420): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(409): Show |
1 | a0135c0061t0001g0178 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.10679-361_10679-36 others(420): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(499): Show |
1 | a0136c0060t0003g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.10679-361_10679-36 others(510): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(469): Show |
1 | a0008c0064t0003g0151 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.10679-361_10679-36 others(480): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(499): Show |
1 | a0021c0011t0001g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.10679-361_10679-36 others(510): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(379): Show |
1 | a0036c0164t0003g0020 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.10679-361_10679-36 others(390): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(435): Show |
1 | a0131c0057t0001g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.10679-361_10679-36 others(446): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757157
|
A | ACAGTAAG others(431): Show |
1 | a0137c0059t0003g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.10679-361_10679-36 others(442): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757157 | ||||||
| chr2:178757162
|
A | AAGTAATA others(19): Show |
3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10679-366_10679-36 others(30): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757162 | ||||||
| chr2:178757171
|
T | C | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.10678+371A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757171 | ||||||
| chr2:178757174
|
A | ACTTACTT others(143): Show |
1 | a0022c0014t0001g0195 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.10678+367_10678+36 others(154): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757174 | ||||||
| chr2:178757178
|
A | G | 95 | a0003c0006t0002g0083a0003c0006t0002g0091a0003c0006t0002g0101others(92): Show | 96 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.10678+364T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757178 | ||||||
| chr2:178757187
|
A | ACAGTAAG others(469): Show |
1 | a0007c0003t0002g0154 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.10678+354_10678+35 others(480): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757187 | ||||||
| chr2:178757187
|
A | ACAGTAAG others(559): Show |
1 | a0021c0011t0001g0179 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.10678+354_10678+35 others(570): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757187 | ||||||
| chr2:178757187
|
A | ACAGTAAG others(555): Show |
1 | a0134c0058t0002g0153 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.10678+354_10678+35 others(566): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757187 | ||||||
| chr2:178757187
|
A | ACAGTAAG others(439): Show |
1 | a0035c0163t0003g0025 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.10678+354_10678+35 others(450): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757187 | ||||||
| chr2:178757187
|
A | ACAGTAAG others(469): Show |
1 | a0032c0161t0002g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.10678+354_10678+35 others(480): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757187 | ||||||
| chr2:178757192
|
A | AAGTAATA others(49): Show |
1 | a0175c0087t0006g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.10678+349_10678+35 others(60): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757192 | ||||||
| chr2:178757201
|
T | C | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.10678+341A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757201 | ||||||
| chr2:178757208
|
A | G | 77 | a0003c0006t0002g0101a0005c0005t0001g0001a0005c0005t0001g0228others(74): Show | 78 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.10678+334T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757208 | ||||||
| chr2:178757217
|
A | ACAGTAAG others(533): Show |
1 | a0132c0065t0003g0152 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.10678+324_10678+32 others(544): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757217 | ||||||
| chr2:178757217
|
A | ACAGTAAG others(323): Show |
1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10678+324_10678+32 others(334): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757217 | ||||||
| chr2:178757395
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10678+147A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757395 | ||||||
| chr2:178757407
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10678+135A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757407 | ||||||
| chr2:178757511
|
ATCAAAG | A | 7 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.10678+25_10678+30d others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 45/362 | chr2 | 178757511 | ||||||
| chr2:178758046
|
C | A | 1 | a0124c0120t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.10304-130G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758046 | ||||||
| chr2:178758078
|
A | G | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.10304-162T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758078 | ||||||
| chr2:178758099
|
G | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10304-183C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758099 | ||||||
| chr2:178758123
|
C | T | 7 | a0014c0178t0001g0062a0014c0180t0001g0068a0040c0169t0002g0053others(4): Show | 7 | HG01257.hp1 HG01978.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.10304-207G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758123 | ||||||
| chr2:178758281
|
A | G | 235 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(232): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.10304-365T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758281 | ||||||
| chr2:178758298
|
A | G | 1 | a0001c0195t0001g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.10304-382T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758298 | ||||||
| chr2:178758415
|
A | G | 56 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(53): Show | 56 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.10304-499T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758415 | ||||||
| chr2:178758444
|
A | G | 1 | a0173c0069t0002g0007 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.10304-528T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758444 | ||||||
| chr2:178758610
|
C | T | 1 | a0012c0020t0001g0019 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.10303+374G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758610 | ||||||
| chr2:178758850
|
G | T | 56 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(53): Show | 56 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.10303+134C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758850 | ||||||
| chr2:178758941
|
C | A | 1 | a0120c0134t0001g0230 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.10303+43G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 44/362 | chr2 | 178758941 | ||||||
| chr2:178759212
|
T | C | 239 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(236): Show | 240 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.10115-40A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178759212 | ||||||
| chr2:178759598
|
T | C | 25 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(22): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.10115-426A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178759598 | ||||||
| chr2:178759677
|
C | T | 3 | a0160c0088t0001g0213a0161c0089t0002g0211a0162c0090t0002g0198 | 3 | HG00558.hp1 NA18975.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.10115-505G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178759677 | ||||||
| chr2:178759715
|
A | T | 1 | a0006c0018t0002g0102 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.10115-543T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178759715 | ||||||
| chr2:178759778
|
A | C | 1 | a0009c0095t0007g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.10115-606T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178759778 | ||||||
| chr2:178760002
|
C | T | 12 | a0023c0016t0001g0191a0023c0016t0001g0192a0064c0202t0001g0059others(9): Show | 12 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.10115-830G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760002 | ||||||
| chr2:178760061
|
A | T | 56 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(53): Show | 56 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.10115-889T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760061 | ||||||
| chr2:178760151
|
C | A | 1 | a0001c0171t0001g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.10115-979G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760151 | ||||||
| chr2:178760273
|
T | C | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.10115-1101A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760273 | ||||||
| chr2:178760314
|
G | A | 1 | a0051c0184t0001g0048 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.10115-1142C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760314 | ||||||
| chr2:178760414
|
C | A | 1 | a0001c0197t0001g0015 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.10115-1242G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760414 | ||||||
| chr2:178760460
|
G | T | 1 | a0104c0042t0002g0122 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.10115-1288C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760460 | ||||||
| chr2:178760462
|
G | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10115-1290C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760462 | ||||||
| chr2:178760520
|
A | G | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10115-1348T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760520 | ||||||
| chr2:178760660
|
T | A | 3 | a0177c0084t0004g0005a0178c0085t0004g0004a0179c0083t0005g0003 | 3 | HG02559.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.10115-1488A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760660 | ||||||
| chr2:178760848
|
G | GGT | 68 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(65): Show | 69 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.10115-1678_10115-1 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760848 | ||||||
| chr2:178760848
|
G | GGTGT | 3 | a0016c0196t0002g0047a0050c0201t0001g0046a0184c0033t0001g0159 | 3 | HG00544.hp1 HG02970.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.10115-1680_10115-1 others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760848 | ||||||
| chr2:178760848
|
G | GGTGTGTG others(1): Show |
7 | a0023c0016t0001g0191a0023c0016t0001g0192a0150c0110t0001g0182others(4): Show | 7 | HG01361.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.10115-1684_10115-1 others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760848 | ||||||
| chr2:178760848
|
G | GGTGTGTG others(9): Show |
2 | a0156c0106t0001g0146a0157c0107t0001g0145 | 2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.10115-1692_10115-1 others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760848 | ||||||
| chr2:178760848
|
GGT | G | 76 | a0001c0195t0001g0042a0003c0006t0002g0083a0003c0006t0002g0101others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.10115-1678_10115-1 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760848 | ||||||
| chr2:178760848
|
GGTGT | G | 53 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(50): Show | 53 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.10115-1680_10115-1 others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178760848 | ||||||
| chr2:178761112
|
G | A | 12 | a0023c0016t0001g0191a0023c0016t0001g0192a0064c0202t0001g0059others(9): Show | 12 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.10115-1940C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761112 | ||||||
| chr2:178761142
|
T | C | 3 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011 | 3 | HG02257.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.10115-1970A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761142 | ||||||
| chr2:178761154
|
C | CT | 25 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(22): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.10115-1983dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761154 | ||||||
| chr2:178761265
|
C | T | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.10115-2093G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761265 | ||||||
| chr2:178761290
|
C | T | 56 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(53): Show | 56 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.10115-2118G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761290 | ||||||
| chr2:178761353
|
T | A | 23 | a0011c0007t0002g0116a0011c0007t0002g0117a0020c0010t0002g0134others(20): Show | 23 | HG00423.hp1 HG00735.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.10115-2181A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761353 | ||||||
| chr2:178761631
|
G | A | 1 | a0007c0003t0002g0158 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.10115-2459C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761631 | ||||||
| chr2:178761754
|
A | C | 1 | a0053c0191t0001g0032 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.10114+2423T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761754 | ||||||
| chr2:178761832
|
T | C | 234 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(231): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.10114+2345A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761832 | ||||||
| chr2:178761880
|
G | C | 234 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(231): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.10114+2297C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761880 | ||||||
| chr2:178761892
|
C | T | 1 | a0139c0096t0001g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.10114+2285G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178761892 | ||||||
| chr2:178762074
|
A | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(231): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.10114+2103T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178762074 | ||||||
| chr2:178762213
|
T | C | 235 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(232): Show | 236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.10114+1964A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178762213 | ||||||
| chr2:178762428
|
C | T | 7 | a0023c0016t0001g0191a0023c0016t0001g0192a0150c0110t0001g0182others(4): Show | 7 | HG01361.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.10114+1749G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178762428 | ||||||
| chr2:178762449
|
G | C | 25 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(22): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.10114+1728C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178762449 | ||||||
| chr2:178762513
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.10114+1664G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178762513 | ||||||
| chr2:178762638
|
A | G | 234 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(231): Show | 235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.10114+1539T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178762638 | ||||||
| chr2:178762847
|
A | G | 7 | a0011c0007t0002g0116a0011c0007t0002g0117a0025c0028t0002g0120others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.10114+1330T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178762847 | ||||||
| chr2:178762852
|
C | T | 1 | a0151c0112t0001g0183 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.10114+1325G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178762852 | ||||||
| chr2:178762875
|
C | T | 4 | a0175c0087t0006g0006a0177c0084t0004g0005a0178c0085t0004g0004others(1): Show | 4 | HG02559.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.10114+1302G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178762875 | ||||||
| chr2:178762995
|
T | A | 8 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.10114+1182A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178762995 | ||||||
| chr2:178763363
|
C | T | 2 | a0017c0008t0001g0106a0017c0008t0001g0107 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.10114+814G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763363 | ||||||
| chr2:178763476
|
C | T | 1 | a0178c0085t0004g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.10114+701G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763476 | ||||||
| chr2:178763504
|
T | C | 25 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(22): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.10114+673A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763504 | ||||||
| chr2:178763513
|
C | T | 9 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(6): Show | 9 | HG02145.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.10114+664G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763513 | ||||||
| chr2:178763610
|
T | C | 209 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(206): Show | 210 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.10114+567A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763610 | ||||||
| chr2:178763625
|
C | A | 25 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(22): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.10114+552G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763625 | ||||||
| chr2:178763635
|
G | A | 172 | a0003c0006t0002g0083a0003c0006t0002g0091a0003c0006t0002g0101others(169): Show | 173 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.10114+542C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763635 | ||||||
| chr2:178763642
|
G | T | 147 | a0003c0006t0002g0083a0003c0006t0002g0091a0003c0006t0002g0101others(144): Show | 148 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.10114+535C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763642 | ||||||
| chr2:178763790
|
G | A | 62 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.10114+387C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763790 | ||||||
| chr2:178763932
|
T | G | 1 | a0170c0071t0002g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.10114+245A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763932 | ||||||
| chr2:178763934
|
A | AT | 208 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(205): Show | 209 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.10114+242dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763934 | ||||||
| chr2:178763953
|
G | C | 93 | a0003c0006t0002g0083a0003c0006t0002g0091a0003c0006t0002g0101others(90): Show | 94 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.10114+224C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178763953 | ||||||
| chr2:178764013
|
T | C | 2 | a0019c0019t0001g0093a0019c0019t0001g0094 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.10114+164A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 43/362 | chr2 | 178764013 | ||||||
| chr2:178764378
|
T | C | 2 | a0002c0022t0001g0066a0002c0022t0001g0067 | 2 | NA18965.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.9989-76A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 42/362 | chr2 | 178764378 | ||||||
| chr2:178764866
|
C | T | 1 | a0056c0190t0001g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.9704-55G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178764866 | ||||||
| chr2:178765091
|
T | G | 1 | a0079c0053t0002g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.9704-280A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178765091 | ||||||
| chr2:178765095
|
G | C | 1 | a0079c0053t0002g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.9704-284C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178765095 | ||||||
| chr2:178765148
|
C | T | 1 | a0186c0024t0001g0014 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.9704-337G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178765148 | ||||||
| chr2:178765517
|
C | G | 1 | a0118c0035t0001g0136 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.9704-706G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178765517 | ||||||
| chr2:178765529
|
A | T | 25 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(22): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.9704-718T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178765529 | ||||||
| chr2:178765574
|
G | T | 1 | a0163c0080t0002g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.9704-763C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178765574 | ||||||
| chr2:178765580
|
T | C | 1 | a0030c0165t0002g0022 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.9704-769A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178765580 | ||||||
| chr2:178765601
|
C | T | 1 | a0113c0039t0002g0132 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.9703+780G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178765601 | ||||||
| chr2:178765808
|
C | T | 2 | a0019c0019t0001g0093a0019c0019t0001g0094 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.9703+573G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178765808 | ||||||
| chr2:178765980
|
A | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.9703+401T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 41/362 | chr2 | 178765980 | ||||||
| chr2:178766635
|
A | C | 48 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(45): Show | 48 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.9472-23T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/362 | chr2 | 178766635 | ||||||
| chr2:178766637
|
AC | A | 25 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(22): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.9472-26delG | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/362 | chr2 | 178766637 | ||||||
| chr2:178766656
|
C | T | 1 | a0051c0184t0001g0048 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.9472-44G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/362 | chr2 | 178766656 | ||||||
| chr2:178766829
|
C | T | 1 | a0130c0056t0003g0150 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.9472-217G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/362 | chr2 | 178766829 | ||||||
| chr2:178766961
|
C | T | 1 | a0139c0096t0001g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.9472-349G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/362 | chr2 | 178766961 | ||||||
| chr2:178767124
|
C | A | 30 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(27): Show | 30 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.9472-512G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/362 | chr2 | 178767124 | ||||||
| chr2:178767309
|
T | A | 1 | a0177c0084t0004g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.9471+450A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/362 | chr2 | 178767309 | ||||||
| chr2:178767406
|
A | G | 172 | a0003c0006t0002g0083a0003c0006t0002g0091a0003c0006t0002g0101others(169): Show | 173 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.9471+353T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/362 | chr2 | 178767406 | ||||||
| chr2:178767410
|
C | G | 1 | a0179c0083t0005g0003 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9471+349G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 40/362 | chr2 | 178767410 | ||||||
| chr2:178767955
|
G | A | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.9306-31C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 39/362 | chr2 | 178767955 | ||||||
| chr2:178767983
|
T | C | 92 | a0003c0006t0002g0083a0003c0006t0002g0091a0003c0006t0002g0101others(89): Show | 92 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.9305+31A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 39/362 | chr2 | 178767983 | ||||||
| chr2:178768244
|
T | C | 4 | a0021c0011t0001g0149a0021c0011t0001g0179a0131c0057t0001g0147others(1): Show | 4 | HG01358.hp2 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.9164-89A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 38/362 | chr2 | 178768244 | ||||||
| chr2:178768363
|
A | G | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.9164-208T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 38/362 | chr2 | 178768363 | ||||||
| chr2:178768460
|
T | C | 25 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(22): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.9163+213A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 38/362 | chr2 | 178768460 | ||||||
| chr2:178768550
|
C | T | 25 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(22): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.9163+123G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 38/362 | chr2 | 178768550 | ||||||
| chr2:178768571
|
G | T | 114 | a0003c0006t0002g0083a0003c0006t0002g0091a0003c0006t0002g0101others(111): Show | 114 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.9163+102C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 38/362 | chr2 | 178768571 | ||||||
| chr2:178768617
|
T | C | 2 | a0057c0181t0001g0043a0063c0200t0001g0044 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.9163+56A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 38/362 | chr2 | 178768617 | ||||||
| chr2:178769089
|
A | G | 1 | a0008c0064t0003g0151 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.8903-156T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 37/362 | chr2 | 178769089 | ||||||
| chr2:178769341
|
C | A | 5 | a0031c0162t0002g0023a0032c0161t0002g0065a0033c0160t0002g0024others(2): Show | 5 | HG00558.hp2 HG00673.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.8902+338G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 37/362 | chr2 | 178769341 | ||||||
| chr2:178769443
|
T | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.8902+236A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 37/362 | chr2 | 178769443 | ||||||
| chr2:178769649
|
GTA | G | 238 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(235): Show | 239 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.8902+28_8902+29del others(2): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 37/362 | chr2 | 178769649 | ||||||
| chr2:178769663
|
A | T | 4 | a0016c0170t0002g0028a0050c0201t0001g0046a0060c0174t0001g0058others(1): Show | 4 | HG00544.hp1 HG03540.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.8902+16T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 37/362 | chr2 | 178769663 | ||||||
| chr2:178769665
|
A | T | 68 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(65): Show | 69 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.8902+14T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 37/362 | chr2 | 178769665 | ||||||
| chr2:178771062
|
A | T | 224 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(221): Show | 225 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.8116+149T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 34/362 | chr2 | 178771062 | ||||||
| chr2:178771123
|
T | C | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.8116+88A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 34/362 | chr2 | 178771123 | ||||||
| chr2:178771155
|
C | T | 233 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(230): Show | 234 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.8116+56G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 34/362 | chr2 | 178771155 | ||||||
| chr2:178771192
|
C | T | 3 | a0085c0049t0001g0131a0117c0037t0001g0127a0122c0034t0001g0128 | 3 | HG00639.hp1 HG01175.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.8116+19G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 34/362 | chr2 | 178771192 | ||||||
| chr2:178771530
|
T | A | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.7856-59A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178771530 | ||||||
| chr2:178771546
|
T | C | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.7856-75A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178771546 | ||||||
| chr2:178771857
|
A | T | 3 | a0085c0049t0001g0131a0117c0037t0001g0127a0122c0034t0001g0128 | 3 | HG00639.hp1 HG01175.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.7856-386T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178771857 | ||||||
| chr2:178771881
|
C | G | 1 | a0157c0107t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7856-410G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178771881 | ||||||
| chr2:178771911
|
A | G | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7856-440T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178771911 | ||||||
| chr2:178771933
|
G | A | 2 | a0089c0066t0002g0220a0094c0123t0001g0219 | 2 | NA18948.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.7856-462C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178771933 | ||||||
| chr2:178771941
|
T | C | 29 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.7856-470A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178771941 | ||||||
| chr2:178772256
|
C | T | 26 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(23): Show | 26 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.7856-785G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178772256 | ||||||
| chr2:178772524
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7855+585G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178772524 | ||||||
| chr2:178772539
|
A | G | 212 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(209): Show | 213 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.7855+570T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178772539 | ||||||
| chr2:178772874
|
A | G | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7855+235T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178772874 | ||||||
| chr2:178773029
|
G | A | 1 | a0015c0176t0001g0045 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.7855+80C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178773029 | ||||||
| chr2:178773078
|
C | T | 1 | a0175c0087t0006g0006 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7855+31G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 33/362 | chr2 | 178773078 | ||||||
| chr2:178774181
|
A | G | 1 | a0139c0096t0001g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.7057+26T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 30/362 | chr2 | 178774181 | ||||||
| chr2:178774570
|
C | T | 202 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(199): Show | 203 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.6791-97G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 29/362 | chr2 | 178774570 | ||||||
| chr2:178774675
|
A | G | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.6791-202T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 29/362 | chr2 | 178774675 | ||||||
| chr2:178774771
|
C | G | 209 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(206): Show | 210 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.6790+150G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 29/362 | chr2 | 178774771 | ||||||
| chr2:178774797
|
T | G | 1 | a0013c0023t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6790+124A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 29/362 | chr2 | 178774797 | ||||||
| chr2:178777075
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4815-26T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 27/362 | chr2 | 178777075 | ||||||
| chr2:178777698
|
G | A | 207 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(204): Show | 208 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(205): Show |
splice_region_variant&intron_variant | LOW | c.4480+6C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 25/362 | chr2 | 178777698 | ||||||
| chr2:178778035
|
C | T | 2 | a0018c0009t0001g0236a0018c0009t0001g0237 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4209-60G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/362 | chr2 | 178778035 | ||||||
| chr2:178778098
|
G | A | 2 | a0016c0196t0002g0047a0050c0201t0001g0046 | 2 | HG00544.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.4209-123C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/362 | chr2 | 178778098 | ||||||
| chr2:178778155
|
T | C | 21 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(18): Show | 21 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.4209-180A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/362 | chr2 | 178778155 | ||||||
| chr2:178778198
|
T | C | 239 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(236): Show | 240 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.4209-223A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/362 | chr2 | 178778198 | ||||||
| chr2:178778367
|
T | C | 25 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(22): Show | 25 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.4209-392A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/362 | chr2 | 178778367 | ||||||
| chr2:178778818
|
T | C | 12 | a0023c0016t0001g0191a0023c0016t0001g0192a0064c0202t0001g0059others(9): Show | 12 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.4208+56A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/362 | chr2 | 178778818 | ||||||
| chr2:178778848
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4208+26T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 24/362 | chr2 | 178778848 | ||||||
| chr2:178779135
|
G | C | 1 | a0014c0180t0001g0068 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3964-17C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 23/362 | chr2 | 178779135 | ||||||
| chr2:178779159
|
A | G | 208 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(205): Show | 209 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.3964-41T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 23/362 | chr2 | 178779159 | ||||||
| chr2:178779207
|
A | G | 208 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(205): Show | 209 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.3963+22T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 23/362 | chr2 | 178779207 | ||||||
| chr2:178779577
|
G | A | 209 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(206): Show | 210 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.3730-115C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 22/362 | chr2 | 178779577 | ||||||
| chr2:178779700
|
C | T | 9 | a0023c0016t0001g0191a0023c0016t0001g0192a0150c0110t0001g0182others(6): Show | 9 | HG01361.hp1 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3730-238G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 22/362 | chr2 | 178779700 | ||||||
| chr2:178779728
|
A | C | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3730-266T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 22/362 | chr2 | 178779728 | ||||||
| chr2:178780241
|
C | T | 1 | a0065c0031t0001g0235 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3524-36G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 21/362 | chr2 | 178780241 | ||||||
| chr2:178780379
|
A | T | 208 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(205): Show | 209 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.3524-174T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 21/362 | chr2 | 178780379 | ||||||
| chr2:178780402
|
A | G | 1 | a0193c0209t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3524-197T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 21/362 | chr2 | 178780402 | ||||||
| chr2:178780457
|
C | T | 2 | a0001c0171t0001g0029a0016c0170t0002g0028 | 2 | NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.3524-252G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 21/362 | chr2 | 178780457 | ||||||
| chr2:178780558
|
C | G | 27 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(24): Show | 27 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.3524-353G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 21/362 | chr2 | 178780558 | ||||||
| chr2:178780562
|
G | C | 7 | a0023c0016t0001g0191a0023c0016t0001g0192a0150c0110t0001g0182others(4): Show | 7 | HG01361.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3524-357C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 21/362 | chr2 | 178780562 | ||||||
| chr2:178780850
|
C | T | 152 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(149): Show | 153 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.3523+271G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 21/362 | chr2 | 178780850 | ||||||
| chr2:178781004
|
C | A | 27 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(24): Show | 27 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.3523+117G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 21/362 | chr2 | 178781004 | ||||||
| chr2:178781383
|
C | T | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3381-120G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781383 | ||||||
| chr2:178781485
|
T | G | 1 | a0047c0173t0001g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3381-222A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781485 | ||||||
| chr2:178781538
|
A | T | 4 | a0068c0156t0001g0163a0069c0155t0001g0162a0129c0115t0001g0241others(1): Show | 4 | HG02257.hp2 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3381-275T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781538 | ||||||
| chr2:178781583
|
A | AT | 27 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(24): Show | 27 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.3381-321dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781583 | ||||||
| chr2:178781607
|
G | A | 208 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(205): Show | 209 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.3381-344C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781607 | ||||||
| chr2:178781803
|
T | G | 208 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(205): Show | 209 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.3380+409A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781803 | ||||||
| chr2:178781905
|
A | AGT | 110 | a0001c0021t0001g0075a0001c0021t0001g0076a0003c0006t0002g0083others(107): Show | 111 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.3380+305_3380+306d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781905 | ||||||
| chr2:178781905
|
A | AGTGT | 54 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0077others(51): Show | 54 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.3380+303_3380+306d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781905 | ||||||
| chr2:178781905
|
A | AGTGTGT | 3 | a0001c0001t0001g0013a0044c0193t0001g0050a0056c0190t0001g0027 | 3 | HG02273.hp2 HG02602.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3380+301_3380+306d others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781905 | ||||||
| chr2:178781905
|
AGT | A | 34 | a0011c0007t0002g0116a0011c0007t0002g0117a0020c0010t0002g0134others(31): Show | 34 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.3380+305_3380+306d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781905 | ||||||
| chr2:178781905
|
AGTGT | A | 25 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(22): Show | 25 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.3380+303_3380+306d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781905 | ||||||
| chr2:178781911
|
T | C | 1 | a0107c0043t0001g0161 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3380+301A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781911 | ||||||
| chr2:178781931
|
G | T | 1 | a0043c0194t0002g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3380+281C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 20/362 | chr2 | 178781931 | ||||||
| chr2:178783096
|
C | T | 31 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(28): Show | 31 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.2842-32G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 17/362 | chr2 | 178783096 | ||||||
| chr2:178783097
|
G | A | 7 | a0014c0178t0001g0062a0014c0180t0001g0068a0040c0169t0002g0053others(4): Show | 7 | HG01257.hp1 HG01978.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.2842-33C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 17/362 | chr2 | 178783097 | ||||||
| chr2:178783175
|
G | T | 30 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(27): Show | 30 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.2842-111C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 17/362 | chr2 | 178783175 | ||||||
| chr2:178783235
|
ATATAT | A | 56 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(53): Show | 56 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.2842-176_2842-172d others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 17/362 | chr2 | 178783235 | ||||||
| chr2:178783391
|
G | A | 1 | a0106c0129t0002g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2842-327C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 17/362 | chr2 | 178783391 | ||||||
| chr2:178783458
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2841+262G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 17/362 | chr2 | 178783458 | ||||||
| chr2:178783522
|
A | G | 18 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(15): Show | 18 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.2841+198T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 17/362 | chr2 | 178783522 | ||||||
| chr2:178783585
|
G | A | 4 | a0013c0023t0001g0056a0013c0023t0001g0057a0042c0172t0002g0055others(1): Show | 4 | HG01884.hp1 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2841+135C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 17/362 | chr2 | 178783585 | ||||||
| chr2:178784622
|
G | A | 29 | a0011c0007t0002g0116a0011c0007t0002g0117a0020c0010t0002g0134others(26): Show | 29 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2494-271C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178784622 | ||||||
| chr2:178784647
|
C | T | 8 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2494-296G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178784647 | ||||||
| chr2:178784734
|
G | A | 4 | a0006c0018t0002g0102a0006c0018t0002g0105a0102c0130t0002g0103others(1): Show | 4 | HG00639.hp2 HG01361.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2494-383C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178784734 | ||||||
| chr2:178784843
|
A | G | 3 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011 | 3 | HG02257.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2494-492T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178784843 | ||||||
| chr2:178785023
|
C | A | 104 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(101): Show | 104 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2493+597G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178785023 | ||||||
| chr2:178785144
|
G | A | 29 | a0011c0007t0002g0116a0011c0007t0002g0117a0020c0010t0002g0134others(26): Show | 29 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2493+476C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178785144 | ||||||
| chr2:178785185
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2493+435A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178785185 | ||||||
| chr2:178785198
|
GA | G | 68 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(65): Show | 68 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2493+421delT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178785198 | ||||||
| chr2:178785280
|
T | A | 7 | a0023c0016t0001g0191a0023c0016t0001g0192a0150c0110t0001g0182others(4): Show | 7 | HG01361.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2493+340A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178785280 | ||||||
| chr2:178785344
|
G | A | 1 | a0108c0040t0002g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2493+276C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178785344 | ||||||
| chr2:178785501
|
C | T | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2493+119G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178785501 | ||||||
| chr2:178785507
|
C | A | 2 | a0116c0036t0001g0126a0118c0035t0001g0136 | 2 | HG01981.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.2493+113G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 15/362 | chr2 | 178785507 | ||||||
| chr2:178786227
|
G | A | 48 | a0003c0147t0002g0090a0007c0003t0002g0154a0007c0003t0002g0157others(45): Show | 48 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2077-86C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178786227 | ||||||
| chr2:178786523
|
T | C | 7 | a0003c0146t0002g0079a0003c0147t0002g0090a0070c0152t0002g0088others(4): Show | 7 | HG00741.hp2 HG01071.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.2077-382A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178786523 | ||||||
| chr2:178786528
|
G | T | 3 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011 | 3 | HG02257.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2077-387C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178786528 | ||||||
| chr2:178786529
|
A | T | 3 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011 | 3 | HG02257.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2077-388T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178786529 | ||||||
| chr2:178786646
|
A | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2077-505T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178786646 | ||||||
| chr2:178786665
|
A | C | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2077-524T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178786665 | ||||||
| chr2:178787019
|
C | T | 4 | a0175c0087t0006g0006a0177c0084t0004g0005a0178c0085t0004g0004others(1): Show | 4 | HG02559.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2077-878G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178787019 | ||||||
| chr2:178787091
|
AAAGT | A | 24 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(21): Show | 24 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.2077-954_2077-951d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178787091 | ||||||
| chr2:178787320
|
C | T | 42 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(39): Show | 42 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.2077-1179G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178787320 | ||||||
| chr2:178787467
|
A | G | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2077-1326T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178787467 | ||||||
| chr2:178787517
|
A | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2077-1376T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178787517 | ||||||
| chr2:178787712
|
T | C | 75 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(72): Show | 75 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.2077-1571A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178787712 | ||||||
| chr2:178787734
|
A | G | 57 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(54): Show | 57 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.2077-1593T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178787734 | ||||||
| chr2:178787786
|
T | C | 57 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(54): Show | 57 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.2076+1574A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178787786 | ||||||
| chr2:178787962
|
G | A | 2 | a0019c0019t0001g0093a0019c0019t0001g0094 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2076+1398C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178787962 | ||||||
| chr2:178787964
|
G | C | 18 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(15): Show | 18 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.2076+1396C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178787964 | ||||||
| chr2:178788075
|
A | G | 185 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(182): Show | 185 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.2076+1285T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178788075 | ||||||
| chr2:178788180
|
T | C | 9 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(6): Show | 9 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2076+1180A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178788180 | ||||||
| chr2:178788238
|
G | C | 1 | a0060c0174t0001g0058 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2076+1122C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178788238 | ||||||
| chr2:178788841
|
T | C | 1 | a0129c0115t0001g0241 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2076+519A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 13/362 | chr2 | 178788841 | ||||||
| chr2:178789586
|
A | G | 21 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(18): Show | 21 | HG00544.hp2 HG00642.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1939-89T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 12/362 | chr2 | 178789586 | ||||||
| chr2:178789863
|
G | A | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1938+115C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 12/362 | chr2 | 178789863 | ||||||
| chr2:178789968
|
C | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1938+10G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 12/362 | chr2 | 178789968 | ||||||
| chr2:178790319
|
G | GA | 33 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(30): Show | 33 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1801-205dupT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 11/362 | chr2 | 178790319 | ||||||
| chr2:178790468
|
C | T | 15 | a0005c0005t0001g0228a0005c0117t0001g0221a0086c0118t0001g0218others(12): Show | 15 | HG00408.hp1 HG02027.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.1800+240G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 11/362 | chr2 | 178790468 | ||||||
| chr2:178790897
|
T | C | 10 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(7): Show | 10 | HG00597.hp1 HG01099.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1663-52A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178790897 | ||||||
| chr2:178790916
|
C | T | 6 | a0156c0106t0001g0146a0157c0107t0001g0145a0175c0087t0006g0006others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-71G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178790916 | ||||||
| chr2:178790942
|
T | C | 1 | a0103c0157t0001g0125 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1663-97A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178790942 | ||||||
| chr2:178791385
|
G | A | 1 | a0060c0174t0001g0058 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1663-540C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791385 | ||||||
| chr2:178791388
|
C | T | 1 | a0142c0097t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1663-543G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791388 | ||||||
| chr2:178791415
|
A | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1663-570T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791415 | ||||||
| chr2:178791506
|
C | T | 1 | a0077c0153t0002g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1662+566G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791506 | ||||||
| chr2:178791663
|
A | ATG | 30 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(27): Show | 30 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1662+407_1662+408d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791663 | ||||||
| chr2:178791663
|
A | ATGTG | 32 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(29): Show | 32 | HG00642.hp2 HG01257.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1662+405_1662+408d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791663 | ||||||
| chr2:178791663
|
A | ATGTGTG | 32 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(29): Show | 32 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1662+403_1662+408d others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791663 | ||||||
| chr2:178791663
|
A | ATGTGTGT others(1): Show |
19 | a0008c0064t0003g0151a0020c0010t0002g0134a0020c0010t0002g0160others(16): Show | 19 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1662+401_1662+408d others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791663 | ||||||
| chr2:178791663
|
A | ATGTGTGT others(3): Show |
5 | a0098c0038t0001g0112a0109c0044t0002g0110a0110c0045t0002g0111others(2): Show | 5 | HG00639.hp1 HG01175.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+399_1662+408d others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791663 | ||||||
| chr2:178791755
|
G | A | 99 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(96): Show | 99 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1662+317C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791755 | ||||||
| chr2:178791765
|
A | G | 1 | a0184c0033t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1662+307T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791765 | ||||||
| chr2:178791952
|
T | C | 12 | a0023c0016t0001g0191a0023c0016t0001g0192a0064c0202t0001g0059others(9): Show | 12 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1662+120A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178791952 | ||||||
| chr2:178792030
|
T | C | 2 | a0163c0080t0002g0212a0174c0081t0001g0201 | 2 | HG00438.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1662+42A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 10/362 | chr2 | 178792030 | ||||||
| chr2:178792201
|
C | T | 2 | a0001c0186t0001g0017a0001c0197t0001g0015 | 2 | HG00673.hp2 NA18964.hp2 |
splice_region_variant&intron_variant | LOW | c.1537-4G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792201 | ||||||
| chr2:178792238
|
C | A | 8 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1537-41G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792238 | ||||||
| chr2:178792250
|
A | C | 3 | a0188c0207t0001g0070a0189c0206t0001g0069a0190c0208t0003g0009 | 3 | HG00741.hp1 HG01099.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1537-53T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792250 | ||||||
| chr2:178792266
|
A | C | 1 | a0073c0149t0002g0085 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1537-69T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792266 | ||||||
| chr2:178792527
|
G | A | 4 | a0160c0088t0001g0213a0161c0089t0002g0211a0162c0090t0002g0198others(1): Show | 4 | HG00558.hp1 NA18964.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537-330C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792527 | ||||||
| chr2:178792561
|
T | C | 1 | a0163c0080t0002g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1537-364A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792561 | ||||||
| chr2:178792704
|
G | T | 2 | a0068c0156t0001g0163a0069c0155t0001g0162 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1537-507C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792704 | ||||||
| chr2:178792737
|
T | G | 33 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(30): Show | 33 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1537-540A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792737 | ||||||
| chr2:178792778
|
C | T | 2 | a0064c0202t0001g0059a0158c0109t0001g0143 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1537-581G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792778 | ||||||
| chr2:178792784
|
C | T | 7 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1537-587G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792784 | ||||||
| chr2:178792848
|
G | C | 2 | a0123c0137t0001g0096a0124c0120t0001g0097 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1536+556C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792848 | ||||||
| chr2:178792895
|
C | T | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1536+509G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792895 | ||||||
| chr2:178792938
|
G | T | 3 | a0177c0084t0004g0005a0178c0085t0004g0004a0179c0083t0005g0003 | 3 | HG02559.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1536+466C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178792938 | ||||||
| chr2:178793020
|
T | C | 6 | a0003c0006t0002g0083a0003c0006t0002g0091a0003c0006t0002g0101others(3): Show | 6 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+384A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178793020 | ||||||
| chr2:178793051
|
C | T | 2 | a0086c0118t0001g0218a0087c0119t0001g0217 | 2 | HG02027.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1536+353G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178793051 | ||||||
| chr2:178793173
|
C | T | 1 | a0116c0036t0001g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1536+231G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178793173 | ||||||
| chr2:178793200
|
T | C | 1 | a0121c0135t0001g0232 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1536+204A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178793200 | ||||||
| chr2:178793275
|
A | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1536+129T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 9/362 | chr2 | 178793275 | ||||||
| chr2:178793694
|
C | T | 1 | a0071c0151t0002g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1399-153G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 8/362 | chr2 | 178793694 | ||||||
| chr2:178794048
|
A | G | 6 | a0156c0106t0001g0146a0157c0107t0001g0145a0175c0087t0006g0006others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1398+351T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 8/362 | chr2 | 178794048 | ||||||
| chr2:178794161
|
A | ATATAGCC others(15): Show |
18 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(15): Show | 18 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.1398+216_1398+237d others(24): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 8/362 | chr2 | 178794161 | ||||||
| chr2:178794370
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1398+29G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 8/362 | chr2 | 178794370 | ||||||
| chr2:178794383
|
G | A | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1398+16C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 8/362 | chr2 | 178794383 | ||||||
| chr2:178794391
|
G | A | 7 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1398+8C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 8/362 | chr2 | 178794391 | ||||||
| chr2:178794607
|
A | C | 33 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(30): Show | 33 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1246-56T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 7/362 | chr2 | 178794607 | ||||||
| chr2:178795303
|
T | C | 34 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(31): Show | 34 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.915-51A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795303 | ||||||
| chr2:178795375
|
C | T | 34 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(31): Show | 34 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.915-123G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795375 | ||||||
| chr2:178795452
|
T | C | 18 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(15): Show | 18 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.915-200A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795452 | ||||||
| chr2:178795510
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.915-258G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795510 | ||||||
| chr2:178795515
|
T | TA | 5 | a0014c0178t0001g0062a0061c0198t0001g0061a0062c0199t0001g0060others(2): Show | 5 | HG01257.hp1 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.915-264dupT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795515 | ||||||
| chr2:178795515
|
TA | T | 43 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(40): Show |
intron_variant | MODIFIER | c.915-264delT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795515 | ||||||
| chr2:178795551
|
T | C | 3 | a0024c0017t0001g0140a0024c0017t0001g0141a0181c0116t0001g0142 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.915-299A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795551 | ||||||
| chr2:178795672
|
G | C | 1 | a0058c0192t0001g0063 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.915-420C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795672 | ||||||
| chr2:178795723
|
AT | A | 20 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(17): Show | 20 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.915-472delA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795723 | ||||||
| chr2:178795797
|
G | A | 40 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(37): Show | 40 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.915-545C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795797 | ||||||
| chr2:178795799
|
G | C | 3 | a0078c0055t0002g0012a0079c0053t0002g0008a0080c0054t0002g0011 | 3 | HG02257.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.915-547C>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178795799 | ||||||
| chr2:178796078
|
G | A | 1 | a0032c0161t0002g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.915-826C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178796078 | ||||||
| chr2:178796200
|
A | T | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.915-948T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178796200 | ||||||
| chr2:178796227
|
A | T | 17 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(14): Show | 17 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.915-975T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178796227 | ||||||
| chr2:178796618
|
T | G | 1 | a0097c0139t0002g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.915-1366A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178796618 | ||||||
| chr2:178797126
|
T | C | 33 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(30): Show | 33 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.915-1874A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797126 | ||||||
| chr2:178797242
|
A | AT | 17 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(14): Show | 17 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.915-1991dupA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797242 | ||||||
| chr2:178797245
|
T | A | 2 | a0156c0106t0001g0146a0157c0107t0001g0145 | 2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.915-1993A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797245 | ||||||
| chr2:178797376
|
TTCA | T | 6 | a0006c0141t0002g0099a0083c0142t0002g0080a0097c0139t0002g0100others(3): Show | 6 | HG01496.hp2 HG02683.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.914+2108_914+2110d others(5): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797376 | ||||||
| chr2:178797379
|
A | G | 1 | a0103c0157t0001g0125 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.914+2108T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797379 | ||||||
| chr2:178797380
|
CAT | C | 32 | a0005c0005t0001g0228a0005c0117t0001g0221a0006c0018t0002g0102others(29): Show | 32 | HG00408.hp1 HG00639.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.914+2105_914+2106d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797380 | ||||||
| chr2:178797382
|
T | C | 6 | a0006c0141t0002g0099a0083c0142t0002g0080a0097c0139t0002g0100others(3): Show | 6 | HG01496.hp2 HG02683.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.914+2105A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797382 | ||||||
| chr2:178797438
|
CT | C | 9 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(6): Show | 9 | HG00597.hp1 HG01099.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.914+2048delA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797438 | ||||||
| chr2:178797653
|
T | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.914+1834A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797653 | ||||||
| chr2:178797693
|
T | C | 1 | a0003c0006t0002g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.914+1794A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797693 | ||||||
| chr2:178797740
|
T | G | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.914+1747A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178797740 | ||||||
| chr2:178798049
|
A | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.914+1438T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178798049 | ||||||
| chr2:178798176
|
A | T | 1 | a0103c0157t0001g0125 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.914+1311T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178798176 | ||||||
| chr2:178798213
|
A | T | 1 | a0109c0044t0002g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.914+1274T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178798213 | ||||||
| chr2:178798310
|
C | T | 1 | a0003c0006t0002g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.914+1177G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178798310 | ||||||
| chr2:178798473
|
T | G | 12 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(9): Show | 12 | HG00558.hp1 NA18943.hp2 NA18948.hp2 others(9): Show |
intron_variant | MODIFIER | c.914+1014A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178798473 | ||||||
| chr2:178798497
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.914+990G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178798497 | ||||||
| chr2:178798528
|
G | A | 18 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(15): Show | 18 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.914+959C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178798528 | ||||||
| chr2:178799089
|
C | G | 2 | a0020c0010t0002g0160a0107c0043t0001g0161 | 2 | NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.914+398G>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178799089 | ||||||
| chr2:178799254
|
A | G | 7 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(4): Show | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.914+233T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178799254 | ||||||
| chr2:178799323
|
A | G | 4 | a0104c0042t0002g0122a0108c0040t0002g0124a0112c0046t0002g0121others(1): Show | 4 | HG00735.hp2 HG01071.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.914+164T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178799323 | ||||||
| chr2:178799366
|
C | A | 2 | a0025c0028t0002g0120a0026c0027t0002g0119 | 2 | HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.914+121G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178799366 | ||||||
| chr2:178799390
|
G | A | 1 | a0146c0101t0001g0176 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.914+97C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 6/362 | chr2 | 178799390 | ||||||
| chr2:178799795
|
G | T | 1 | a0001c0197t0001g0015 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.669+30C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 5/362 | chr2 | 178799795 | ||||||
| chr2:178799822
|
T | C | 1 | a0008c0012t0003g0180 | 1 | NA19054.hp2 | splice_region_variant&intron_variant | LOW | c.669+3A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 5/362 | chr2 | 178799822 | ||||||
| chr2:178800113
|
T | C | 239 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(236): Show | 240 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.584-203A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 4/362 | chr2 | 178800113 | ||||||
| chr2:178800321
|
G | A | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.583+74C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 4/362 | chr2 | 178800321 | ||||||
| chr2:178800977
|
T | G | 3 | a0156c0106t0001g0146a0157c0107t0001g0145a0175c0087t0006g0006 | 3 | HG02451.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.296-295A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178800977 | ||||||
| chr2:178801096
|
C | T | 69 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(66): Show | 69 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.296-414G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801096 | ||||||
| chr2:178801286
|
G | A | 38 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(35): Show | 38 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.296-604C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801286 | ||||||
| chr2:178801439
|
T | C | 18 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(15): Show | 18 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.295+699A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801439 | ||||||
| chr2:178801465
|
T | C | 2 | a0002c0022t0001g0066a0002c0022t0001g0067 | 2 | NA18965.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.295+673A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801465 | ||||||
| chr2:178801504
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.295+634T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801504 | ||||||
| chr2:178801517
|
C | T | 4 | a0082c0052t0002g0113a0098c0038t0001g0112a0109c0044t0002g0110others(1): Show | 4 | HG02280.hp1 HG02647.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+621G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801517 | ||||||
| chr2:178801519
|
T | A | 17 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(14): Show | 17 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.295+619A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801519 | ||||||
| chr2:178801524
|
C | T | 22 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(19): Show | 22 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.295+614G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801524 | ||||||
| chr2:178801635
|
T | C | 1 | a0014c0180t0001g0068 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.295+503A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801635 | ||||||
| chr2:178801638
|
GT | G | 24 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(21): Show | 24 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.295+499delA | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801638 | ||||||
| chr2:178801698
|
G | A | 17 | a0007c0003t0002g0154a0007c0003t0002g0157a0007c0003t0002g0158others(14): Show | 17 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.295+440C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178801698 | ||||||
| chr2:178802103
|
G | A | 4 | a0006c0018t0002g0102a0006c0018t0002g0105a0102c0130t0002g0103others(1): Show | 4 | HG00639.hp2 HG01361.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+35C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 3/362 | chr2 | 178802103 | ||||||
| chr2:178802363
|
C | T | 187 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(184): Show | 188 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.92-22G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178802363 | ||||||
| chr2:178802434
|
G | A | 7 | a0023c0016t0001g0191a0023c0016t0001g0192a0150c0110t0001g0182others(4): Show | 7 | HG01361.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-93C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178802434 | ||||||
| chr2:178802505
|
A | C | 2 | a0167c0070t0001g0199a0173c0069t0002g0007 | 2 | HG02165.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.92-164T>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178802505 | ||||||
| chr2:178802612
|
T | C | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.92-271A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178802612 | ||||||
| chr2:178802888
|
A | G | 4 | a0081c0067t0002g0215a0099c0132t0002g0214a0100c0133t0002g0233others(1): Show | 4 | HG00642.hp1 HG02738.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-547T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178802888 | ||||||
| chr2:178803079
|
C | T | 30 | a0011c0007t0002g0116a0011c0007t0002g0117a0020c0010t0002g0134others(27): Show | 30 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.92-738G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803079 | ||||||
| chr2:178803144
|
G | A | 5 | a0023c0016t0001g0191a0023c0016t0001g0192a0152c0113t0001g0189others(2): Show | 5 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-803C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803144 | ||||||
| chr2:178803213
|
G | A | 1 | a0191c0211t0001g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.92-872C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803213 | ||||||
| chr2:178803214
|
C | A | 1 | a0191c0211t0001g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.92-873G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803214 | ||||||
| chr2:178803324
|
C | T | 1 | a0083c0142t0002g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92-983G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803324 | ||||||
| chr2:178803395
|
CTGAG | C | 8 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(5): Show | 8 | HG02145.hp1 HG02723.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-1058_92-1055del others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803395 | ||||||
| chr2:178803464
|
T | C | 2 | a0001c0021t0001g0075a0001c0021t0001g0076 | 2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.91+1088A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803464 | ||||||
| chr2:178803525
|
T | C | 1 | a0147c0098t0001g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.91+1027A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803525 | ||||||
| chr2:178803612
|
A | G | 1 | a0003c0146t0002g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.91+940T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803612 | ||||||
| chr2:178803624
|
T | C | 2 | a0001c0001t0001g0077a0049c0188t0001g0078 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.91+928A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803624 | ||||||
| chr2:178803651
|
A | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91+901T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803651 | ||||||
| chr2:178803767
|
T | C | 1 | a0139c0096t0001g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.91+785A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178803767 | ||||||
| chr2:178804123
|
G | A | 38 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(35): Show | 38 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.91+429C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178804123 | ||||||
| chr2:178804445
|
C | T | 1 | a0183c0204t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91+107G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178804445 | ||||||
| chr2:178804497
|
T | C | 8 | a0017c0008t0001g0106a0017c0008t0001g0107a0018c0009t0001g0236others(5): Show | 8 | HG02145.hp1 HG02723.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.91+55A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178804497 | ||||||
| chr2:178804500
|
CTGGAG | C | 22 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(19): Show | 22 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.91+47_91+51delCTCC others(1): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 2/362 | chr2 | 178804500 | ||||||
| chr2:178805114
|
G | A | 28 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(25): Show | 28 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.-13-459C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805114 | ||||||
| chr2:178805204
|
C | T | 70 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0035others(67): Show | 71 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-13-549G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805204 | ||||||
| chr2:178805343
|
C | CA | 31 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(28): Show | 31 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.-13-689dupT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805343 | ||||||
| chr2:178805343
|
C | CAA | 11 | a0004c0015t0001g0186a0009c0093t0001g0184a0022c0014t0001g0195others(8): Show | 11 | HG02040.hp2 HG02155.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13-690_-13-689dup others(2): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805343 | ||||||
| chr2:178805343
|
C | CAAAAAA | 6 | a0018c0009t0001g0236a0018c0009t0001g0237a0065c0031t0001g0235others(3): Show | 6 | HG02723.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-694_-13-689dup others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805343 | ||||||
| chr2:178805343
|
CA | C | 36 | a0011c0007t0002g0116a0011c0007t0002g0117a0020c0010t0002g0134others(33): Show | 36 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.-13-689delT | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805343 | ||||||
| chr2:178805361
|
A | T | 1 | a0079c0053t0002g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-13-706T>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805361 | ||||||
| chr2:178805365
|
T | A | 4 | a0022c0014t0001g0193a0022c0014t0001g0195a0140c0094t0001g0196others(1): Show | 4 | HG00544.hp2 HG02015.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-710A>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805365 | ||||||
| chr2:178805533
|
C | T | 29 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(26): Show | 29 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13-878G>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805533 | ||||||
| chr2:178805549
|
G | A | 116 | a0004c0004t0001g0168a0004c0004t0001g0172a0004c0004t0001g0173others(113): Show | 116 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-13-894C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805549 | ||||||
| chr2:178805577
|
C | A | 17 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(14): Show | 17 | HG00438.hp1 HG00558.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13-922G>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805577 | ||||||
| chr2:178805633
|
G | A | 29 | a0010c0013t0002g0206a0010c0013t0002g0207a0010c0072t0002g0204others(26): Show | 29 | HG00438.hp1 HG00558.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13-978C>T | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805633 | ||||||
| chr2:178805912
|
A | G | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-13-1257T>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805912 | ||||||
| chr2:178805956
|
T | C | 21 | a0005c0005t0001g0228a0005c0117t0001g0221a0081c0067t0002g0215others(18): Show | 21 | HG00408.hp1 HG00642.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.-14+1256A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178805956 | ||||||
| chr2:178806070
|
T | C | 1 | a0185c0203t0001g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-14+1142A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178806070 | ||||||
| chr2:178806101
|
T | G | 6 | a0018c0009t0001g0236a0018c0009t0001g0237a0065c0031t0001g0235others(3): Show | 6 | HG02723.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+1111A>C | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178806101 | ||||||
| chr2:178806635
|
T | C | 1 | a0129c0115t0001g0241 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14+577A>G | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178806635 | ||||||
| chr2:178806901
|
G | T | 1 | a0173c0069t0002g0007 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-14+311C>A | TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 1/362 | chr2 | 178806901 |