Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55761 |
|---|---|
| ensemblid | ENSG00000052841.16 |
| hgncid | 25596 |
| symbol | TTC17 |
| name | tetratricopeptide repeat domain 17 |
| refseq_nuc | NM_018259.6 |
| refseq_prot | NP_060729.2 |
| ensembl_nuc | ENST00000039989.9 |
| ensembl_prot | ENSP00000039989.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 43358920 |
| end | 43494931 |
| strand | + |
| ver | v1.2 |
| region | chr11:43358920-43494931 |
| region5000 | chr11:43353920-43499931 |
| regionname0 | TTC17_chr11_43358920_43494931 |
| regionname5000 | TTC17_chr11_43353920_43499931 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1141 | 271 | 54 | 64 | 101 | 14 | 36 | 77 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0002 | 0/0 | 1141 | 21 | 19 | 2 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0003 | 0/0 | 1141 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0004 | 0/0 | 1141 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0005 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0006 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0007 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3426 | 246 | 53 | 50 | 94 | 14 | 34 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| c0002 | 0/1 | 3426 | 23 | 0 | 13 | 7 | 0 | 2 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| c0003 | 0/0 | 3426 | 21 | 19 | 2 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| c0004 | 0/0 | 3426 | 2 | 2 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| c0005 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| c0006 | 0/0 | 3426 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| c0007 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| c0008 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| c0009 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| c0010 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| 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 | 1/1 | 1063 | 256 | 57 | 60 | 94 | 11 | 32 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| t0002 | 0/0 | 1063 | 20 | 18 | 2 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| t0003 | 0/0 | 1063 | 13 | 0 | 2 | 7 | 3 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| t0004 | 0/0 | 1063 | 3 | 0 | 2 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| t0005 | 0/0 | 1063 | 3 | 0 | 0 | 3 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| t0006 | 0/0 | 1063 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| t0007 | 0/0 | 1063 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| t0008 | 0/0 | 1063 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| 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 | 2 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3426 | 246 | 53 | 50 | 94 | 14 | 34 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0002 | 0/1 | 3426 | 23 | 0 | 13 | 7 | 0 | 2 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0006 | 0/0 | 3426 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0008 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0002c0003 | 0/0 | 3426 | 21 | 19 | 2 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0003c0004 | 0/0 | 3426 | 2 | 2 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0004c0007 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0005c0010 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0006c0009 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0007c0005 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4488 | 225 | 53 | 46 | 84 | 11 | 30 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0001t0003 | 0/0 | 4488 | 13 | 0 | 2 | 7 | 3 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0001t0004 | 0/0 | 4488 | 3 | 0 | 2 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0001t0005 | 0/0 | 4488 | 3 | 0 | 0 | 3 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0001t0007 | 0/0 | 4488 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0001t0008 | 0/0 | 4488 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0002t0001 | 0/1 | 4488 | 23 | 0 | 13 | 7 | 0 | 2 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0006t0001 | 0/0 | 4488 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0001c0008t0006 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0002c0003t0001 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0002c0003t0002 | 0/0 | 4488 | 20 | 18 | 2 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0003c0004t0001 | 0/0 | 4488 | 2 | 2 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0004c0007t0001 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0005c0010t0001 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0006c0009t0001 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| a0007c0005t0001 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | copy fasta | chr11 | 43353920 | 43499931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0006t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0001c0008t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0002c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0003c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0003c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0004c0007t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0005c0010t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0006c0009t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| a0007c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | GBR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0162 | EUR | GBR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | FIN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | CHS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00738 | hp1 | a0001 | c0006 | t0001 | g0203 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0211 | AMR | PUR | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01496 | hp2 | a0002 | c0003 | t0002 | g0210 | AMR | CLM | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0033 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0032 | EUR | IBS | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0221 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01891 | hp2 | a0003 | c0004 | t0001 | g0247 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0189 | AMR | PEL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02622 | hp1 | a0002 | c0003 | t0002 | g0224 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02717 | hp1 | a0002 | c0003 | t0002 | g0217 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0195 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02809 | hp1 | a0002 | c0003 | t0002 | g0216 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02818 | hp1 | a0002 | c0003 | t0002 | g0223 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02897 | hp2 | a0002 | c0003 | t0002 | g0051 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02922 | hp1 | a0002 | c0003 | t0002 | g0222 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02965 | hp1 | a0002 | c0003 | t0002 | g0213 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02970 | hp2 | a0002 | c0003 | t0002 | g0214 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03041 | hp2 | a0002 | c0003 | t0002 | g0207 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03139 | hp2 | a0002 | c0003 | t0002 | g0220 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03195 | hp1 | a0001 | c0008 | t0006 | g0064 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03195 | hp2 | a0002 | c0003 | t0002 | g0215 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03516 | hp1 | a0002 | c0003 | t0002 | g0212 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0226 | AFR | GWD | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0179 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0204 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04199 | hp2 | a0001 | c0001 | t0008 | g0091 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | CHB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0230 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18943 | hp2 | a0006 | c0009 | t0001 | g0193 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18979 | hp2 | a0005 | c0010 | t0001 | g0113 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19084 | hp1 | a0007 | c0005 | t0001 | g0277 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA19240 | hp2 | a0002 | c0003 | t0002 | g0219 | AFR | YRI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | TSI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | TSI | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | GIH | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02109 | hp2 | a0002 | c0003 | t0002 | g0218 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG02559 | hp2 | a0002 | c0003 | t0002 | g0209 | AFR | ACB | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| HG03471 | hp2 | a0002 | c0003 | t0002 | g0003 | AFR | MSL | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | USA | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA20300 | hp2 | a0002 | c0003 | t0002 | g0225 | AFR | USA | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| NA21309 | hp2 | a0004 | c0007 | t0001 | g0045 | AFR | LWK | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0250 | REF | REF | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0148 | REF | REF | TTC17_chr11_43353920_43499931 | TTC17 | chr11 | 43353920 | 43499931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43359060
|
G | A | 1 | a0007 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.106G>A | p.Ala36Thr | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/24 | 141/4488 | 106/3426 | 36/1141 | chr11 | 43359060 | ||
| chr11:43391478
|
A | C | 1 | a0002 | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
missense_variant | MODERATE | c.433A>C | p.Ile145Leu | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 4/24 | 468/4488 | 433/3426 | 145/1141 | chr11 | 43391478 | ||
| chr11:43405577
|
G | A | 1 | a0004 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1543G>A | p.Val515Ile | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 12/24 | 1578/4488 | 1543/3426 | 515/1141 | chr11 | 43405577 | ||
| chr11:43443511
|
G | T | 1 | a0003 | 2 | HG01891.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.2438G>T | p.Gly813Val | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 17/24 | 2473/4488 | 2438/3426 | 813/1141 | chr11 | 43443511 | ||
| chr11:43448010
|
C | T | 1 | a0005 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.2674C>T | p.Arg892Cys | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/24 | 2709/4488 | 2674/3426 | 892/1141 | chr11 | 43448010 | ||
| chr11:43490341
|
G | T | 1 | a0006 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.3133G>T | p.Ala1045Ser | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/24 | 3168/4488 | 3133/3426 | 1045/1141 | chr11 | 43490341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43359083
|
C | A | 1 | a0001c0006 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.129C>A | p.Val43Val | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/24 | 164/4488 | 129/3426 | 43/1141 | chr11 | 43359083 | ||
| chr11:43444109
|
T | C | 1 | a0001c0008 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2565T>C | p.Thr855Thr | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/24 | 2600/4488 | 2565/3426 | 855/1141 | chr11 | 43444109 | ||
| chr11:43451196
|
C | T | 3 | a0001c0002a0001c0006a0006c0009 | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
synonymous_variant | LOW | c.2961C>T | p.Leu987Leu | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/24 | 2996/4488 | 2961/3426 | 987/1141 | chr11 | 43451196 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43493945
|
A | T | 1 | a0001c0001t0005 | 3 | HG00609.hp2 HG02040.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*41A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 41 | chr11 | 43493945 | |||||
| chr11:43494313
|
A | G | 1 | a0001c0001t0008 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 409 | chr11 | 43494313 | |||||
| chr11:43494358
|
G | A | 1 | a0001c0008t0006 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 454 | chr11 | 43494358 | |||||
| chr11:43494375
|
T | G | 2 | a0001c0001t0003a0001c0001t0008 | 14 | HG00099.hp2 HG01168.hp2 HG01433.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*471T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 471 | chr11 | 43494375 | |||||
| chr11:43494489
|
A | G | 1 | a0002c0003t0002 | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*585A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 585 | chr11 | 43494489 | |||||
| chr11:43494547
|
A | C | 1 | a0001c0001t0004 | 3 | HG00639.hp2 HG01106.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*643A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 643 | chr11 | 43494547 | |||||
| chr11:43494765
|
T | C | 1 | a0001c0001t0007 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*861T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 24/24 | 861 | chr11 | 43494765 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43359272
|
C | A | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.159+159C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359272 | ||||||
| chr11:43359440
|
G | A | 1 | a0002c0003t0002g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.159+327G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359440 | ||||||
| chr11:43359446
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.159+333C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359446 | ||||||
| chr11:43359484
|
C | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.159+371C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359484 | ||||||
| chr11:43359748
|
C | G | 1 | a0001c0002t0001g0294 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.159+635C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359748 | ||||||
| chr11:43359750
|
G | A | 1 | a0001c0002t0001g0294 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.159+637G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359750 | ||||||
| chr11:43359775
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.159+662G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359775 | ||||||
| chr11:43359867
|
C | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01346.hp1 HG01496.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+754C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43359867 | ||||||
| chr11:43360108
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.159+995G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360108 | ||||||
| chr11:43360122
|
GTGTAATG others(2): Show |
G | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+1011_159+1019d others(11): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43360122 | |||||
| chr11:43360165
|
A | T | 1 | a0001c0001t0001g0293 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.159+1052A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360165 | ||||||
| chr11:43360185
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.159+1072C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360185 | ||||||
| chr11:43360203
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.159+1090A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360203 | ||||||
| chr11:43360377
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.159+1264A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360377 | ||||||
| chr11:43360418
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.159+1305T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360418 | ||||||
| chr11:43360663
|
A | G | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.159+1550A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360663 | ||||||
| chr11:43360709
|
A | AT | 7 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG01884.hp2 HG02080.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+1612dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43360709 | |||||
| chr11:43360709
|
AT | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(34): Show | 37 | HG01069.hp1 HG01069.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.159+1612delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43360709 | |||||
| chr11:43360742
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.159+1629T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360742 | ||||||
| chr11:43360777
|
G | T | 23 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(20): Show | 23 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.159+1664G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360777 | ||||||
| chr11:43360793
|
A | G | 7 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(4): Show | 7 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+1680A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360793 | ||||||
| chr11:43360809
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.159+1696C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360809 | ||||||
| chr11:43360838
|
T | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.159+1725T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360838 | ||||||
| chr11:43360877
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.159+1764G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360877 | ||||||
| chr11:43360895
|
C | G | 1 | a0001c0001t0001g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.159+1782C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43360895 | ||||||
| chr11:43361178
|
C | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(60): Show | 63 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.159+2065C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361178 | ||||||
| chr11:43361332
|
C | T | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.159+2219C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361332 | ||||||
| chr11:43361397
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.159+2284G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361397 | ||||||
| chr11:43361481
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.159+2368A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361481 | ||||||
| chr11:43361733
|
A | T | 5 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 5 | NA18940.hp1 NA18967.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+2620A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361733 | ||||||
| chr11:43361777
|
G | T | 1 | a0001c0001t0001g0185 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.159+2664G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361777 | ||||||
| chr11:43361848
|
T | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.159+2735T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361848 | ||||||
| chr11:43361868
|
C | A | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.159+2755C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43361868 | ||||||
| chr11:43361978
|
C | CT | 23 | a0001c0001t0001g0030a0001c0001t0001g0290a0001c0002t0001g0294others(20): Show | 23 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.159+2884dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43361978 | |||||
| chr11:43361978
|
CT | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0059a0001c0001t0001g0068others(7): Show | 10 | HG02145.hp2 HG02486.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.159+2884delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43361978 | |||||
| chr11:43362061
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.159+2948A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362061 | ||||||
| chr11:43362149
|
T | G | 1 | a0001c0001t0001g0248 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.159+3036T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362149 | ||||||
| chr11:43362149
|
T | TTG | 17 | a0001c0001t0001g0059a0001c0001t0001g0161a0001c0001t0001g0163others(14): Show | 17 | HG00099.hp2 HG01255.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.159+3080_159+3081d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
T | TTGTG | 16 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0066others(13): Show | 16 | HG00609.hp1 HG00741.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.159+3078_159+3081d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
T | TTGTGTG | 5 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | HG02486.hp1 NA18979.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+3076_159+3081d others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.159+3072_159+3081d others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
TTG | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(33): Show | 36 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.159+3080_159+3081d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
TTGTG | T | 88 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(85): Show | 88 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.159+3078_159+3081d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
TTGTGTG | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 34 | HG00438.hp2 HG00639.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.159+3076_159+3081d others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
TTGTGTGT others(1): Show |
T | 6 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG00408.hp2 HG00438.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+3074_159+3081d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.159+3072_159+3081d others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.159+3070_159+3081d others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
TTGTGTGT others(7): Show |
T | 17 | a0001c0002t0001g0050a0001c0002t0001g0194a0001c0002t0001g0195others(14): Show | 17 | HG00558.hp2 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.159+3068_159+3081d others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
TTGTGTGT others(9): Show |
T | 8 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0188others(5): Show | 8 | HG00735.hp1 HG01070.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+3066_159+3081d others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362149
|
TTGTGTGT others(11): Show |
T | 1 | a0002c0003t0002g0209 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.159+3064_159+3081d others(20): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43362149 | |||||
| chr11:43362177
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0184 | 2 | HG00438.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.159+3064G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362177 | ||||||
| chr11:43362179
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0184 | 2 | HG00438.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.159+3066G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362179 | ||||||
| chr11:43362261
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.159+3148C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362261 | ||||||
| chr11:43362355
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+3242A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362355 | ||||||
| chr11:43362454
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159+3341G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362454 | ||||||
| chr11:43362898
|
A | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 157 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.159+3785A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43362898 | ||||||
| chr11:43363000
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.159+3887A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363000 | ||||||
| chr11:43363036
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.159+3923G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363036 | ||||||
| chr11:43363383
|
A | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(163): Show | 167 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.159+4270A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363383 | ||||||
| chr11:43363404
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.159+4291G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363404 | ||||||
| chr11:43363544
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.159+4431A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363544 | ||||||
| chr11:43363621
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+4508C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363621 | ||||||
| chr11:43363800
|
T | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG03688.hp2 HG03834.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.159+4687T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363800 | ||||||
| chr11:43363979
|
A | T | 8 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(5): Show | 8 | HG01070.hp2 HG01081.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+4866A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43363979 | ||||||
| chr11:43364047
|
C | CT | 53 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0035others(50): Show | 53 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.159+4960dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43364047 | |||||
| chr11:43364047
|
CT | C | 33 | a0001c0001t0001g0018a0001c0001t0001g0046a0001c0001t0001g0052others(30): Show | 33 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.159+4960delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43364047 | |||||
| chr11:43364225
|
T | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+5112T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43364225 | ||||||
| chr11:43364295
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.159+5182G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43364295 | ||||||
| chr11:43364407
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+5294T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43364407 | ||||||
| chr11:43364512
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.159+5399G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43364512 | ||||||
| chr11:43364951
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.159+5838A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43364951 | ||||||
| chr11:43365146
|
G | T | 1 | a0001c0002t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.159+6033G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365146 | ||||||
| chr11:43365250
|
A | G | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.159+6137A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365250 | ||||||
| chr11:43365303
|
A | G | 1 | a0001c0006t0001g0203 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.159+6190A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365303 | ||||||
| chr11:43365305
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.159+6192G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365305 | ||||||
| chr11:43365332
|
G | A | 1 | a0001c0001t0003g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.159+6219G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365332 | ||||||
| chr11:43365399
|
G | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(11): Show | 15 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.159+6286G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365399 | ||||||
| chr11:43365445
|
T | G | 1 | a0006c0009t0001g0193 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.159+6332T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365445 | ||||||
| chr11:43365466
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.159+6353G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365466 | ||||||
| chr11:43365494
|
C | G | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.159+6381C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365494 | ||||||
| chr11:43365555
|
G | A | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.159+6442G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365555 | ||||||
| chr11:43365933
|
T | C | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.159+6820T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43365933 | ||||||
| chr11:43366063
|
C | T | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.159+6950C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366063 | ||||||
| chr11:43366105
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.159+6992C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366105 | ||||||
| chr11:43366126
|
C | T | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.159+7013C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366126 | ||||||
| chr11:43366127
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+7014G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366127 | ||||||
| chr11:43366308
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.159+7195C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366308 | ||||||
| chr11:43366433
|
G | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(33): Show | 36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.159+7320G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366433 | ||||||
| chr11:43366483
|
G | A | 7 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(4): Show | 7 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+7370G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366483 | ||||||
| chr11:43366505
|
C | CA | 35 | a0001c0001t0001g0090a0001c0001t0001g0251a0001c0001t0001g0252others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.159+7408dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43366505 | |||||
| chr11:43366505
|
CA | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(61): Show | 64 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.159+7408delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43366505 | |||||
| chr11:43366611
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.159+7498C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366611 | ||||||
| chr11:43366702
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+7589T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366702 | ||||||
| chr11:43366801
|
C | T | 24 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(21): Show | 24 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.159+7688C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366801 | ||||||
| chr11:43366813
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.159+7700A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366813 | ||||||
| chr11:43366904
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG01074.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.159+7791C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366904 | ||||||
| chr11:43366933
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.159+7820C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43366933 | ||||||
| chr11:43367260
|
G | A | 4 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(1): Show | 4 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+8147G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367260 | ||||||
| chr11:43367344
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.159+8231A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367344 | ||||||
| chr11:43367367
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(33): Show | 36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.159+8254G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367367 | ||||||
| chr11:43367520
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.159+8407C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367520 | ||||||
| chr11:43367527
|
G | C | 1 | a0001c0001t0001g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.159+8414G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367527 | ||||||
| chr11:43367617
|
C | G | 23 | a0001c0001t0001g0252a0001c0001t0001g0261a0001c0001t0001g0264others(20): Show | 23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.159+8504C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367617 | ||||||
| chr11:43367623
|
T | C | 1 | a0001c0001t0008g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.159+8510T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367623 | ||||||
| chr11:43367714
|
C | CTG | 35 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(32): Show | 35 | HG00558.hp2 HG00741.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.159+8633_159+8634d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43367714 | |||||
| chr11:43367714
|
CTG | C | 182 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.159+8633_159+8634d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43367714 | |||||
| chr11:43367714
|
CTGTG | C | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0226 | 3 | HG02145.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.159+8631_159+8634d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43367714 | |||||
| chr11:43367781
|
C | T | 158 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 159 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.159+8668C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367781 | ||||||
| chr11:43367822
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.159+8709C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43367822 | ||||||
| chr11:43368054
|
C | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.159+8941C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368054 | ||||||
| chr11:43368087
|
G | A | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.159+8974G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368087 | ||||||
| chr11:43368321
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.159+9208A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368321 | ||||||
| chr11:43368582
|
C | A | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.159+9469C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368582 | ||||||
| chr11:43368607
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.159+9494G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368607 | ||||||
| chr11:43368766
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.159+9653A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368766 | ||||||
| chr11:43368975
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159+9862C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43368975 | ||||||
| chr11:43369096
|
A | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+9983A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369096 | ||||||
| chr11:43369252
|
C | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-9981C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369252 | ||||||
| chr11:43369294
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-9939C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369294 | ||||||
| chr11:43369475
|
A | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-9758A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369475 | ||||||
| chr11:43369556
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.160-9677T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369556 | ||||||
| chr11:43369732
|
T | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.160-9501T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369732 | ||||||
| chr11:43369742
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.160-9491G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369742 | ||||||
| chr11:43369862
|
C | T | 1 | a0001c0001t0008g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.160-9371C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43369862 | ||||||
| chr11:43370098
|
C | T | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-9135C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370098 | ||||||
| chr11:43370111
|
A | G | 1 | a0001c0002t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.160-9122A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370111 | ||||||
| chr11:43370142
|
C | A | 1 | a0001c0001t0001g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160-9091C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370142 | ||||||
| chr11:43370160
|
T | A | 1 | a0001c0001t0001g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160-9073T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370160 | ||||||
| chr11:43370179
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.160-9054A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370179 | ||||||
| chr11:43370329
|
A | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.160-8904A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370329 | ||||||
| chr11:43370396
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.160-8837A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370396 | ||||||
| chr11:43370719
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0128 | 3 | NA18953.hp1 NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.160-8514G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370719 | ||||||
| chr11:43370736
|
A | C | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.160-8497A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370736 | ||||||
| chr11:43370776
|
T | A | 11 | a0002c0003t0002g0051a0002c0003t0002g0207a0002c0003t0002g0210others(8): Show | 11 | HG01496.hp2 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.160-8457T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43370776 | ||||||
| chr11:43370782
|
AAG | A | 10 | a0002c0003t0002g0051a0002c0003t0002g0207a0002c0003t0002g0210others(7): Show | 10 | HG01496.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.160-8446_160-8445d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43370782 | |||||
| chr11:43370795
|
G | GGTTT | 80 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0001t0001g0251others(77): Show | 80 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.160-8409_160-8406d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43370795 | |||||
| chr11:43370795
|
G | GGTTTGTT others(1): Show |
5 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0003g0031others(2): Show | 5 | HG01070.hp2 HG01081.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-8413_160-8406d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43370795 | |||||
| chr11:43370795
|
GGTTTGTT others(1): Show |
G | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.160-8413_160-8406d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43370795 | |||||
| chr11:43371023
|
T | TG | 26 | a0001c0001t0001g0034a0001c0001t0001g0074a0001c0001t0001g0084others(23): Show | 26 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.160-8199dupG | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43371023 | |||||
| chr11:43371023
|
TG | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 82 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.160-8199delG | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43371023 | |||||
| chr11:43371023
|
TGG | T | 61 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(58): Show | 61 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.160-8200_160-8199d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43371023 | |||||
| chr11:43371025
|
G | C | 1 | a0002c0003t0002g0219 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.160-8208G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371025 | ||||||
| chr11:43371025
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.160-8208G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371025 | ||||||
| chr11:43371143
|
A | G | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-8090A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371143 | ||||||
| chr11:43371346
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.160-7887A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371346 | ||||||
| chr11:43371402
|
T | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.160-7831T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371402 | ||||||
| chr11:43371404
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.160-7829C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371404 | ||||||
| chr11:43371440
|
T | C | 1 | a0002c0003t0002g0051 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.160-7793T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371440 | ||||||
| chr11:43371534
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(19): Show | 23 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.160-7699A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371534 | ||||||
| chr11:43371560
|
G | A | 2 | a0001c0001t0003g0105a0001c0001t0005g0104 | 2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.160-7673G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43371560 | ||||||
| chr11:43372051
|
G | A | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.160-7182G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372051 | ||||||
| chr11:43372149
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.160-7084A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372149 | ||||||
| chr11:43372202
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.160-7031A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372202 | ||||||
| chr11:43372231
|
G | GTA | 34 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(31): Show | 34 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.160-6999_160-6998d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372231 | |||||
| chr11:43372305
|
C | T | 25 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(22): Show | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.160-6928C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372305 | ||||||
| chr11:43372306
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(60): Show | 63 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.160-6927A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372306 | ||||||
| chr11:43372372
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.160-6861C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372372 | ||||||
| chr11:43372428
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.160-6805G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372428 | ||||||
| chr11:43372482
|
T | TTTTA | 58 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(55): Show | 58 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.160-6719_160-6716d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372482 | |||||
| chr11:43372482
|
T | TTTTATTT others(1): Show |
6 | a0002c0003t0001g0226a0002c0003t0002g0211a0002c0003t0002g0219others(3): Show | 6 | HG01243.hp2 HG01891.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-6723_160-6716d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372482 | |||||
| chr11:43372482
|
T | TTTTATTT others(5): Show |
14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(11): Show | 15 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.160-6727_160-6716d others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372482 | |||||
| chr11:43372482
|
T | TTTTATTT others(9): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.160-6731_160-6716d others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372482 | |||||
| chr11:43372482
|
T | TTTTATTT others(13): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG01261.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.160-6735_160-6716d others(22): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43372482 | |||||
| chr11:43372571
|
A | T | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.160-6662A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372571 | ||||||
| chr11:43372971
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-6262A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43372971 | ||||||
| chr11:43373082
|
T | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-6151T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373082 | ||||||
| chr11:43373324
|
C | CT | 11 | a0001c0001t0001g0023a0001c0001t0001g0102a0001c0001t0001g0130others(8): Show | 11 | HG01168.hp2 HG01361.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.160-5892dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43373324 | |||||
| chr11:43373351
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.160-5882T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373351 | ||||||
| chr11:43373361
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0128 | 3 | NA18953.hp1 NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.160-5872T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373361 | ||||||
| chr11:43373384
|
C | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0172others(1): Show | 4 | NA18962.hp1 NA18970.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-5849C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373384 | ||||||
| chr11:43373427
|
C | T | 44 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(41): Show | 44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.160-5806C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373427 | ||||||
| chr11:43373504
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(12): Show | 15 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.160-5729T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373504 | ||||||
| chr11:43373566
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.160-5667A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373566 | ||||||
| chr11:43373972
|
A | G | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-5261A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373972 | ||||||
| chr11:43373979
|
G | C | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.160-5254G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43373979 | ||||||
| chr11:43374018
|
T | C | 10 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-5215T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43374018 | ||||||
| chr11:43374390
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160-4843A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43374390 | ||||||
| chr11:43374636
|
C | A | 1 | a0001c0001t0001g0262 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.160-4597C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43374636 | ||||||
| chr11:43374663
|
A | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.160-4570A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43374663 | ||||||
| chr11:43374749
|
C | CA | 20 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0027others(17): Show | 20 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-4468dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43374749 | |||||
| chr11:43374749
|
CA | C | 44 | a0001c0001t0001g0040a0001c0001t0001g0251a0001c0001t0001g0252others(41): Show | 44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.160-4468delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43374749 | |||||
| chr11:43374752
|
A | G | 5 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(2): Show | 5 | NA18943.hp1 NA18953.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-4481A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43374752 | ||||||
| chr11:43375284
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.160-3949G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375284 | ||||||
| chr11:43375330
|
G | C | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.160-3903G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375330 | ||||||
| chr11:43375340
|
T | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(19): Show | 23 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.160-3893T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375340 | ||||||
| chr11:43375641
|
C | T | 1 | a0001c0002t0001g0190 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.160-3592C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375641 | ||||||
| chr11:43375682
|
AG | A | 33 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(30): Show | 33 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.160-3550delG | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375682 | ||||||
| chr11:43375684
|
A | C | 33 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(30): Show | 33 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.160-3549A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375684 | ||||||
| chr11:43375687
|
A | G | 33 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(30): Show | 33 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.160-3546A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375687 | ||||||
| chr11:43375827
|
A | C | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.160-3406A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43375827 | ||||||
| chr11:43376115
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.160-3118C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43376115 | ||||||
| chr11:43376591
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.160-2642C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43376591 | ||||||
| chr11:43376613
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0231 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.160-2620G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43376613 | ||||||
| chr11:43377020
|
C | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(33): Show | 36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.160-2213C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377020 | ||||||
| chr11:43377065
|
G | A | 26 | a0001c0001t0001g0052a0001c0002t0001g0050a0001c0002t0001g0186others(23): Show | 26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.160-2168G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377065 | ||||||
| chr11:43377110
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.160-2123G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377110 | ||||||
| chr11:43377111
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.160-2122G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377111 | ||||||
| chr11:43377208
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-2025G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377208 | ||||||
| chr11:43377276
|
G | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.160-1957G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377276 | ||||||
| chr11:43377301
|
A | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-1932A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377301 | ||||||
| chr11:43377545
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.160-1688G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377545 | ||||||
| chr11:43377627
|
TCTG | T | 4 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0158others(1): Show | 4 | HG01928.hp1 HG01952.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-1603_160-1601d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | 43377627 | |||||
| chr11:43377652
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.160-1581C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377652 | ||||||
| chr11:43377751
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.160-1482A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377751 | ||||||
| chr11:43377810
|
C | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.160-1423C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377810 | ||||||
| chr11:43377851
|
A | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(4): Show | 7 | HG01255.hp1 HG01515.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-1382A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377851 | ||||||
| chr11:43377934
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.160-1299C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377934 | ||||||
| chr11:43377990
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(60): Show | 63 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.160-1243A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43377990 | ||||||
| chr11:43378108
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(33): Show | 36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.160-1125G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378108 | ||||||
| chr11:43378154
|
C | T | 1 | a0001c0002t0001g0202 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.160-1079C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378154 | ||||||
| chr11:43378205
|
G | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(12): Show | 15 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.160-1028G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378205 | ||||||
| chr11:43378243
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.160-990G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378243 | ||||||
| chr11:43378387
|
T | C | 1 | a0002c0003t0002g0212 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160-846T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378387 | ||||||
| chr11:43378575
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.160-658T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378575 | ||||||
| chr11:43378734
|
C | T | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-499C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378734 | ||||||
| chr11:43378913
|
A | G | 27 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.160-320A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43378913 | ||||||
| chr11:43379202
|
C | A | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-31C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 1/23 | chr11 | 43379202 | ||||||
| chr11:43379458
|
A | ATG | 22 | a0001c0001t0001g0079a0001c0001t0001g0134a0001c0001t0001g0135others(19): Show | 22 | HG01243.hp1 HG01243.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.249+158_249+159dup others(2): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43379458 | |||||
| chr11:43379480
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.249+158G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43379480 | ||||||
| chr11:43379482
|
T | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(33): Show | 36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.249+160T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43379482 | ||||||
| chr11:43379776
|
T | C | 48 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 49 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.249+454T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43379776 | ||||||
| chr11:43379792
|
C | A | 1 | a0002c0003t0002g0211 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.249+470C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43379792 | ||||||
| chr11:43379818
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.249+496A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43379818 | ||||||
| chr11:43380083
|
T | A | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.249+761T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380083 | ||||||
| chr11:43380235
|
G | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+913G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380235 | ||||||
| chr11:43380302
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.249+980C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380302 | ||||||
| chr11:43380444
|
C | T | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+1122C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380444 | ||||||
| chr11:43380500
|
C | A | 1 | a0001c0001t0007g0179 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.249+1178C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380500 | ||||||
| chr11:43380530
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+1208C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380530 | ||||||
| chr11:43380545
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.249+1223G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380545 | ||||||
| chr11:43380546
|
T | C | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.249+1224T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380546 | ||||||
| chr11:43380637
|
G | A | 25 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(22): Show | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.249+1315G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380637 | ||||||
| chr11:43380678
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.249+1356T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380678 | ||||||
| chr11:43380941
|
G | A | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+1619G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380941 | ||||||
| chr11:43380974
|
A | T | 23 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(20): Show | 23 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.249+1652A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43380974 | ||||||
| chr11:43381239
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.249+1917T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43381239 | ||||||
| chr11:43381308
|
C | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02922.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.249+1986C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43381308 | ||||||
| chr11:43381311
|
TA | T | 4 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0048others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+1992delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43381311 | |||||
| chr11:43381368
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.249+2046T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43381368 | ||||||
| chr11:43381616
|
A | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0231 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.249+2294A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43381616 | ||||||
| chr11:43381966
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.249+2644T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43381966 | ||||||
| chr11:43382152
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(33): Show | 36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.249+2830A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382152 | ||||||
| chr11:43382199
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.249+2877T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382199 | ||||||
| chr11:43382224
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.249+2902G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382224 | ||||||
| chr11:43382241
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.249+2919C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382241 | ||||||
| chr11:43382369
|
C | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0077others(1): Show | 4 | HG00408.hp2 HG00438.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+3047C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382369 | ||||||
| chr11:43382475
|
G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.249+3153G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382475 | ||||||
| chr11:43382590
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+3268A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382590 | ||||||
| chr11:43382625
|
A | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0231 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.249+3303A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382625 | ||||||
| chr11:43382646
|
T | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.249+3324T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382646 | ||||||
| chr11:43382721
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.249+3399T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382721 | ||||||
| chr11:43382791
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.249+3469C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382791 | ||||||
| chr11:43382849
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.249+3527C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43382849 | ||||||
| chr11:43382889
|
ATTTTCTT others(8): Show |
A | 5 | a0002c0003t0002g0210a0002c0003t0002g0213a0002c0003t0002g0214others(2): Show | 5 | HG01496.hp2 HG02109.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+3581_249+3595d others(17): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43382889 | |||||
| chr11:43383004
|
A | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.249+3682A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383004 | ||||||
| chr11:43383232
|
G | A | 23 | a0001c0001t0001g0252a0001c0001t0001g0261a0001c0001t0001g0264others(20): Show | 23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.249+3910G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383232 | ||||||
| chr11:43383554
|
G | A | 1 | a0001c0001t0003g0146 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.249+4232G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383554 | ||||||
| chr11:43383608
|
G | A | 60 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(57): Show | 60 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.249+4286G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383608 | ||||||
| chr11:43383619
|
C | T | 6 | a0001c0001t0003g0095a0001c0001t0003g0096a0001c0001t0003g0097others(3): Show | 6 | HG02080.hp2 NA18944.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+4297C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383619 | ||||||
| chr11:43383658
|
C | T | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.249+4336C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383658 | ||||||
| chr11:43383796
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.249+4474C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383796 | ||||||
| chr11:43383832
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+4510G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383832 | ||||||
| chr11:43383880
|
A | G | 26 | a0001c0001t0001g0052a0001c0002t0001g0050a0001c0002t0001g0186others(23): Show | 26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.249+4558A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383880 | ||||||
| chr11:43383946
|
T | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0042 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.249+4624T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43383946 | ||||||
| chr11:43384037
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+4715G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384037 | ||||||
| chr11:43384144
|
CA | C | 255 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.249+4835delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43384144 | |||||
| chr11:43384144
|
CAA | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(13): Show | 16 | HG00741.hp2 HG01069.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.249+4834_249+4835d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43384144 | |||||
| chr11:43384175
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.249+4853A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384175 | ||||||
| chr11:43384387
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.249+5065G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384387 | ||||||
| chr11:43384446
|
G | A | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+5124G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384446 | ||||||
| chr11:43384618
|
C | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.250-5034C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384618 | ||||||
| chr11:43384903
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.250-4749A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384903 | ||||||
| chr11:43384928
|
C | G | 9 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(6): Show | 9 | HG01070.hp2 HG01081.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-4724C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43384928 | ||||||
| chr11:43385174
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.250-4478C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385174 | ||||||
| chr11:43385256
|
T | A | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.250-4396T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385256 | ||||||
| chr11:43385421
|
AAG | A | 7 | a0001c0001t0003g0095a0001c0001t0003g0096a0001c0001t0003g0097others(4): Show | 7 | HG02040.hp2 HG02080.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-4225_250-4224d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43385421 | |||||
| chr11:43385456
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.250-4196G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385456 | ||||||
| chr11:43385508
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(33): Show | 36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.250-4144A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385508 | ||||||
| chr11:43385536
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA18747.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.250-4116C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385536 | ||||||
| chr11:43385541
|
A | G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.250-4111A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385541 | ||||||
| chr11:43385787
|
A | C | 7 | a0001c0001t0003g0095a0001c0001t0003g0096a0001c0001t0003g0097others(4): Show | 7 | HG02040.hp2 HG02080.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-3865A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43385787 | ||||||
| chr11:43386104
|
A | G | 2 | a0003c0004t0001g0230a0003c0004t0001g0247 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.250-3548A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386104 | ||||||
| chr11:43386323
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.250-3329C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386323 | ||||||
| chr11:43386357
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.250-3295G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386357 | ||||||
| chr11:43386694
|
G | A | 5 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041others(2): Show | 5 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-2958G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386694 | ||||||
| chr11:43386768
|
C | CGTAT | 3 | a0001c0001t0001g0129a0001c0001t0003g0094a0001c0002t0001g0197 | 3 | HG02129.hp2 HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.250-2875_250-2872d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43386768 | |||||
| chr11:43386777
|
G | GTATT | 23 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(20): Show | 23 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.250-2858_250-2855d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43386777 | |||||
| chr11:43386781
|
T | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(19): Show | 23 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.250-2871T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386781 | ||||||
| chr11:43386869
|
C | T | 60 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(57): Show | 60 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.250-2783C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43386869 | ||||||
| chr11:43387025
|
C | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0033 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.250-2627C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43387025 | ||||||
| chr11:43387232
|
A | G | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.250-2420A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43387232 | ||||||
| chr11:43387269
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.250-2383G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43387269 | ||||||
| chr11:43387507
|
TTAA | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.250-2138_250-2136d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43387507 | |||||
| chr11:43387692
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.250-1960G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43387692 | ||||||
| chr11:43387800
|
A | G | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-1852A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43387800 | ||||||
| chr11:43388008
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.250-1644T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388008 | ||||||
| chr11:43388120
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.250-1532A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388120 | ||||||
| chr11:43388166
|
T | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.250-1486T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388166 | ||||||
| chr11:43388167
|
TAAAG | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-1482_250-1479d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43388167 | |||||
| chr11:43388183
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.250-1469A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388183 | ||||||
| chr11:43388258
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0229 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.250-1394G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388258 | ||||||
| chr11:43388397
|
TAGG | T | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.250-1252_250-1250d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43388397 | |||||
| chr11:43388612
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.250-1040A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388612 | ||||||
| chr11:43388782
|
T | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.250-870T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388782 | ||||||
| chr11:43388974
|
C | CA | 45 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0068others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.250-662dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43388974 | |||||
| chr11:43388990
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.250-662A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43388990 | ||||||
| chr11:43389017
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-635T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43389017 | ||||||
| chr11:43389138
|
C | CA | 32 | a0001c0001t0001g0052a0001c0001t0001g0085a0001c0001t0001g0166others(29): Show | 32 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.250-501dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | 43389138 | |||||
| chr11:43389393
|
C | T | 2 | a0001c0001t0001g0208a0001c0002t0001g0204 | 2 | HG03834.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.250-259C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43389393 | ||||||
| chr11:43389396
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.250-256G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43389396 | ||||||
| chr11:43389543
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.250-109C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 2/23 | chr11 | 43389543 | ||||||
| chr11:43389978
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.419+157A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43389978 | ||||||
| chr11:43389990
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.419+169A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43389990 | ||||||
| chr11:43390033
|
G | A | 31 | a0001c0001t0001g0035a0001c0001t0001g0071a0001c0001t0001g0085others(28): Show | 31 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.419+212G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390033 | ||||||
| chr11:43390117
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.419+296G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390117 | ||||||
| chr11:43390127
|
C | T | 42 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(39): Show | 42 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.419+306C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390127 | ||||||
| chr11:43390156
|
T | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0184 | 3 | HG00438.hp2 NA18957.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.419+335T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390156 | ||||||
| chr11:43390212
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.419+391A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390212 | ||||||
| chr11:43390336
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.419+515C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390336 | ||||||
| chr11:43390343
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(33): Show | 36 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.419+522G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390343 | ||||||
| chr11:43390561
|
AGCCAAGA others(3): Show |
A | 32 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(29): Show | 32 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.419+741_419+750del others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390561 | ||||||
| chr11:43390571
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.419+750G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390571 | ||||||
| chr11:43390574
|
C | G | 32 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(29): Show | 32 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.419+753C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390574 | ||||||
| chr11:43390575
|
CACTG | C | 32 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(29): Show | 32 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.419+755_419+758del others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390575 | ||||||
| chr11:43390582
|
C | G | 32 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(29): Show | 32 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.419+761C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390582 | ||||||
| chr11:43390583
|
T | C | 32 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(29): Show | 32 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.419+762T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390583 | ||||||
| chr11:43390610
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.419+789C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390610 | ||||||
| chr11:43390650
|
AAAAAATA others(6): Show |
A | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02976.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.420-803_420-791del others(13): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | 43390650 | |||||
| chr11:43390901
|
C | G | 1 | a0001c0002t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.420-564C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390901 | ||||||
| chr11:43390935
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0229 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.420-530A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43390935 | ||||||
| chr11:43391126
|
C | CA | 44 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(41): Show | 44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.420-338dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | 43391126 | |||||
| chr11:43391393
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.420-72T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 3/23 | chr11 | 43391393 | ||||||
| chr11:43391596
|
A | AT | 33 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(30): Show | 33 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.531+33dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | 43391596 | |||||
| chr11:43391596
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.531+20A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 4/23 | chr11 | 43391596 | ||||||
| chr11:43391608
|
TTGCG | T | 240 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.531+34_531+37delGC others(2): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | 43391608 | |||||
| chr11:43391609
|
TGCG | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0026others(15): Show | 18 | HG01069.hp1 HG01168.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.531+34_531+36delGC others(1): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 4/23 | chr11 | 43391609 | ||||||
| chr11:43392187
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.663+235C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43392187 | ||||||
| chr11:43392379
|
C | CT | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.663+430dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | 43392379 | |||||
| chr11:43392582
|
A | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.663+630A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43392582 | ||||||
| chr11:43392950
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.663+998C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43392950 | ||||||
| chr11:43393378
|
C | T | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.663+1426C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393378 | ||||||
| chr11:43393384
|
A | C | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.663+1432A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393384 | ||||||
| chr11:43393394
|
A | G | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.663+1442A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393394 | ||||||
| chr11:43393437
|
TC | T | 24 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(21): Show | 24 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.663+1487delC | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | 43393437 | |||||
| chr11:43393528
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.663+1576C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393528 | ||||||
| chr11:43393620
|
G | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.663+1668G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393620 | ||||||
| chr11:43393661
|
C | T | 2 | a0003c0004t0001g0230a0003c0004t0001g0247 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.663+1709C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43393661 | ||||||
| chr11:43394020
|
A | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(15): Show | 18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.663+2068A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43394020 | ||||||
| chr11:43394330
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.663+2378G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43394330 | ||||||
| chr11:43394788
|
G | C | 1 | a0001c0002t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.664-1921G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43394788 | ||||||
| chr11:43395099
|
C | CT | 6 | a0001c0001t0001g0048a0001c0001t0001g0121a0001c0001t0001g0144others(3): Show | 6 | HG01175.hp2 HG02083.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.664-1591dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | 43395099 | |||||
| chr11:43395136
|
T | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.664-1573T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395136 | ||||||
| chr11:43395139
|
C | T | 7 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(4): Show | 7 | HG01928.hp2 NA18943.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.664-1570C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395139 | ||||||
| chr11:43395201
|
C | T | 4 | a0001c0002t0001g0198a0001c0002t0001g0199a0001c0002t0001g0250others(1): Show | 4 | HG00738.hp1 HG01257.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.664-1508C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395201 | ||||||
| chr11:43395231
|
G | C | 5 | a0001c0001t0001g0092a0001c0001t0001g0102a0001c0001t0001g0154others(2): Show | 5 | HG01978.hp2 NA18949.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-1478G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395231 | ||||||
| chr11:43395247
|
C | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.664-1462C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395247 | ||||||
| chr11:43395422
|
C | G | 5 | a0001c0001t0001g0092a0001c0001t0001g0102a0001c0001t0001g0154others(2): Show | 5 | HG01978.hp2 NA18949.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-1287C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43395422 | ||||||
| chr11:43396069
|
A | G | 1 | a0001c0001t0008g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.664-640A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396069 | ||||||
| chr11:43396114
|
T | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-595T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396114 | ||||||
| chr11:43396118
|
T | C | 1 | a0002c0003t0002g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.664-591T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396118 | ||||||
| chr11:43396172
|
C | A | 1 | a0001c0001t0001g0038 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.664-537C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396172 | ||||||
| chr11:43396232
|
T | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.664-477T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396232 | ||||||
| chr11:43396353
|
A | G | 23 | a0001c0001t0001g0252a0001c0001t0001g0261a0001c0001t0001g0264others(20): Show | 23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.664-356A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396353 | ||||||
| chr11:43396634
|
A | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.664-75A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396634 | ||||||
| chr11:43396646
|
T | C | 1 | a0001c0001t0003g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.664-63T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 5/23 | chr11 | 43396646 | ||||||
| chr11:43396957
|
C | CA | 26 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(23): Show | 27 | HG00639.hp1 HG00639.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.773+155dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr11 | 43396957 | |||||
| chr11:43397123
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0132 | 2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.774-224C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 6/23 | chr11 | 43397123 | ||||||
| chr11:43397181
|
T | G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.774-166T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 6/23 | chr11 | 43397181 | ||||||
| chr11:43397321
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0183 | 2 | NA18985.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.774-26C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 6/23 | chr11 | 43397321 | ||||||
| chr11:43397536
|
T | C | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.918+45T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | chr11 | 43397536 | ||||||
| chr11:43397537
|
C | CT | 150 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 151 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.918+62dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397537 | |||||
| chr11:43397568
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.918+77G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | chr11 | 43397568 | ||||||
| chr11:43397684
|
A | G | 26 | a0001c0001t0001g0052a0001c0002t0001g0050a0001c0002t0001g0186others(23): Show | 26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.918+193A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | chr11 | 43397684 | ||||||
| chr11:43397789
|
C | CTGGTCAC others(12): Show |
3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0231 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919-175_919-157dup others(19): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397789 | |||||
| chr11:43397873
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.919-101A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | chr11 | 43397873 | ||||||
| chr11:43397901
|
C | CGT | 12 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0079others(9): Show | 12 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.919-24_919-23dupGT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
C | CGTGT | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0093 | 3 | HG01256.hp2 HG01258.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.919-26_919-23dupGT others(2): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0003g0105 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.919-34_919-23dupGT others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGT | C | 28 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0034others(25): Show | 28 | HG01081.hp1 HG01099.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.919-24_919-23delGT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGT | C | 45 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0044others(42): Show | 45 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.919-26_919-23delGT others(2): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGT | C | 55 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(52): Show | 55 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.919-28_919-23delGT others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(1): Show |
C | 18 | a0001c0001t0001g0052a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00099.hp1 HG00738.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.919-30_919-23delGT others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(3): Show |
C | 22 | a0001c0001t0001g0055a0001c0001t0001g0059a0001c0001t0001g0065others(19): Show | 22 | HG00408.hp1 HG00639.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.919-32_919-23delGT others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(5): Show |
C | 18 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0029others(15): Show | 18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.919-34_919-23delGT others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(7): Show |
C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0002c0003t0002g0217 | 3 | HG01884.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.919-36_919-23delGT others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(9): Show |
C | 20 | a0001c0001t0001g0040a0002c0003t0002g0003a0002c0003t0002g0051others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.919-38_919-23delGT others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0001g0151 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.919-40_919-23delGT others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(13): Show |
C | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.919-42_919-23delGT others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(15): Show |
C | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 19 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.919-44_919-23delGT others(20): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(19): Show |
C | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.919-48_919-23delGT others(24): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(21): Show |
C | 15 | a0001c0001t0001g0280a0001c0001t0003g0031a0001c0001t0003g0032others(12): Show | 15 | HG00099.hp2 HG01168.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.919-50_919-23delGT others(26): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43397901
|
CGTGTGTG others(25): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.919-54_919-23delGT others(30): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | 43397901 | |||||
| chr11:43398227
|
C | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1058+114C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398227 | ||||||
| chr11:43398305
|
T | C | 5 | a0001c0001t0001g0092a0001c0001t0001g0102a0001c0001t0001g0154others(2): Show | 5 | HG01978.hp2 NA18949.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+192T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398305 | ||||||
| chr11:43398360
|
A | G | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1058+247A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398360 | ||||||
| chr11:43398603
|
G | A | 1 | a0002c0003t0002g0209 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1058+490G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398603 | ||||||
| chr11:43398847
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1058+734A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398847 | ||||||
| chr11:43398889
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1058+776A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398889 | ||||||
| chr11:43398935
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1058+822T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43398935 | ||||||
| chr11:43398971
|
ATCTT | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG01074.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1058+860_1058+863d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr11 | 43398971 | |||||
| chr11:43399056
|
C | A | 1 | a0001c0001t0001g0163 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1059-832C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43399056 | ||||||
| chr11:43399057
|
A | G | 1 | a0001c0002t0001g0206 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1059-831A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43399057 | ||||||
| chr11:43399158
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0128 | 3 | NA18953.hp1 NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1059-730G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43399158 | ||||||
| chr11:43399835
|
A | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0128 | 2 | NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1059-53A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 8/23 | chr11 | 43399835 | ||||||
| chr11:43400090
|
T | G | 1 | a0004c0007t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1219+42T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400090 | ||||||
| chr11:43400172
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1219+124C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400172 | ||||||
| chr11:43400173
|
G | A | 23 | a0001c0001t0001g0252a0001c0001t0001g0261a0001c0001t0001g0264others(20): Show | 23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.1219+125G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400173 | ||||||
| chr11:43400277
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1219+229T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400277 | ||||||
| chr11:43400457
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0262 | 2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1219+409C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400457 | ||||||
| chr11:43400535
|
A | G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1219+487A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400535 | ||||||
| chr11:43400673
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1219+625T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43400673 | ||||||
| chr11:43401011
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1220-435T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43401011 | ||||||
| chr11:43401085
|
A | G | 23 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(20): Show | 23 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1220-361A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43401085 | ||||||
| chr11:43401318
|
C | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1220-128C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43401318 | ||||||
| chr11:43401398
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1220-48C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 9/23 | chr11 | 43401398 | ||||||
| chr11:43401607
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1332+49G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43401607 | ||||||
| chr11:43401884
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1332+326G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43401884 | ||||||
| chr11:43401963
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0229 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1332+405G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43401963 | ||||||
| chr11:43401980
|
A | AAAAT | 16 | a0001c0001t0001g0044a0001c0001t0001g0077a0001c0001t0001g0080others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.1332+470_1332+473d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | |||||
| chr11:43401980
|
AAAAT | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1332+470_1332+473d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | |||||
| chr11:43401980
|
AAAATAAA others(1): Show |
A | 43 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 43 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1332+466_1332+473d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | |||||
| chr11:43401980
|
AAAATAAA others(5): Show |
A | 8 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG02055.hp2 HG02622.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332+462_1332+473d others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | |||||
| chr11:43401980
|
AAAATAAA others(9): Show |
A | 39 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0027others(36): Show | 39 | HG00438.hp1 HG01069.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.1332+458_1332+473d others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | |||||
| chr11:43401980
|
AAAATAAA others(13): Show |
A | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1332+454_1332+473d others(22): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | |||||
| chr11:43401980
|
AAAATAAA others(21): Show |
A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1332+446_1332+473d others(30): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43401980 | |||||
| chr11:43402032
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1332+474G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402032 | ||||||
| chr11:43402062
|
T | C | 1 | a0002c0003t0002g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1332+504T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402062 | ||||||
| chr11:43402112
|
A | G | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1332+554A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402112 | ||||||
| chr11:43402190
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0228 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1332+632G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402190 | ||||||
| chr11:43402228
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1332+670G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402228 | ||||||
| chr11:43402256
|
A | T | 1 | a0001c0001t0001g0160 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1332+698A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402256 | ||||||
| chr11:43402404
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0001g0261a0001c0001t0001g0268others(2): Show | 5 | NA18942.hp1 NA18948.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332+846C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402404 | ||||||
| chr11:43402434
|
G | A | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.1332+876G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402434 | ||||||
| chr11:43402616
|
A | G | 25 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(22): Show | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1332+1058A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402616 | ||||||
| chr11:43402709
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1332+1151A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402709 | ||||||
| chr11:43402762
|
G | T | 26 | a0001c0001t0001g0052a0001c0002t0001g0050a0001c0002t0001g0186others(23): Show | 26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1332+1204G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402762 | ||||||
| chr11:43402828
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0001g0262 | 2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1333-1170G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402828 | ||||||
| chr11:43402862
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1333-1136G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402862 | ||||||
| chr11:43402920
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1333-1078C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43402920 | ||||||
| chr11:43403014
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0077others(1): Show | 4 | HG00408.hp2 HG00438.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333-984G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403014 | ||||||
| chr11:43403078
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1333-920A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403078 | ||||||
| chr11:43403079
|
TAAAG | T | 42 | a0001c0001t0001g0182a0001c0001t0001g0251a0001c0001t0001g0252others(39): Show | 42 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1333-916_1333-913d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43403079 | |||||
| chr11:43403117
|
C | CT | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0172 | 3 | NA18962.hp1 NA18970.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1333-878dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43403117 | |||||
| chr11:43403221
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1333-777C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403221 | ||||||
| chr11:43403261
|
A | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1333-737A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403261 | ||||||
| chr11:43403275
|
C | T | 14 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(11): Show | 14 | HG00099.hp2 HG01168.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1333-723C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403275 | ||||||
| chr11:43403399
|
A | T | 1 | a0001c0001t0001g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1333-599A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403399 | ||||||
| chr11:43403493
|
C | T | 1 | a0005c0010t0001g0113 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1333-505C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403493 | ||||||
| chr11:43403622
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333-376C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403622 | ||||||
| chr11:43403632
|
A | G | 1 | a0002c0003t0002g0225 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1333-366A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403632 | ||||||
| chr11:43403694
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1333-304A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403694 | ||||||
| chr11:43403743
|
G | GGGACAGG others(33): Show |
19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1333-216_1333-215i others(42): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr11 | 43403743 | |||||
| chr11:43403756
|
G | A | 27 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1333-242G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403756 | ||||||
| chr11:43403862
|
A | G | 9 | a0001c0001t0001g0142a0001c0001t0001g0157a0001c0001t0001g0169others(6): Show | 9 | HG00558.hp2 HG01256.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.1333-136A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403862 | ||||||
| chr11:43403959
|
C | T | 1 | a0002c0003t0002g0051 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1333-39C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403959 | ||||||
| chr11:43403977
|
AC | A | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.1333-20delC | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403977 | ||||||
| chr11:43403988
|
C | A | 1 | a0001c0002t0001g0196 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1333-10C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 10/23 | chr11 | 43403988 | ||||||
| chr11:43404305
|
A | G | 26 | a0001c0001t0001g0052a0001c0002t0001g0050a0001c0002t0001g0186others(23): Show | 26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1479+161A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43404305 | ||||||
| chr11:43404419
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1479+275C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43404419 | ||||||
| chr11:43404641
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1479+497C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43404641 | ||||||
| chr11:43404787
|
ATTTAAGT | A | 25 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(22): Show | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1479+646_1479+652d others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr11 | 43404787 | |||||
| chr11:43404887
|
A | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1480-627A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43404887 | ||||||
| chr11:43404942
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1480-572G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43404942 | ||||||
| chr11:43405094
|
CT | C | 25 | a0001c0001t0001g0046a0001c0001t0001g0139a0001c0001t0001g0295others(22): Show | 25 | HG01243.hp2 HG01256.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1480-403delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr11 | 43405094 | |||||
| chr11:43405164
|
A | G | 13 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0068others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.1480-350A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43405164 | ||||||
| chr11:43405323
|
C | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 14 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1480-191C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43405323 | ||||||
| chr11:43405396
|
T | C | 60 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(57): Show | 60 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1480-118T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43405396 | ||||||
| chr11:43405452
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1480-62T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 11/23 | chr11 | 43405452 | ||||||
| chr11:43405707
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1595+78G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 12/23 | chr11 | 43405707 | ||||||
| chr11:43405718
|
G | A | 3 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0001t0001g0267 | 3 | HG01099.hp2 HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1596-68G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 12/23 | chr11 | 43405718 | ||||||
| chr11:43406115
|
G | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761+164G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406115 | ||||||
| chr11:43406156
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0084 | 2 | NA18945.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1761+205C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406156 | ||||||
| chr11:43406369
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1761+418G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406369 | ||||||
| chr11:43406449
|
T | C | 93 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(90): Show | 93 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1761+498T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406449 | ||||||
| chr11:43406566
|
CTTT | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1762-563_1762-561d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr11 | 43406566 | |||||
| chr11:43406639
|
C | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | HG00639.hp1 HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1762-499C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406639 | ||||||
| chr11:43406823
|
G | T | 1 | a0002c0003t0002g0209 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1762-315G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406823 | ||||||
| chr11:43406969
|
C | G | 2 | a0001c0001t0001g0127a0001c0008t0006g0064 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1762-169C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406969 | ||||||
| chr11:43406971
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1762-167A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | chr11 | 43406971 | ||||||
| chr11:43407051
|
TAAGAA | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1762-82_1762-78del others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr11 | 43407051 | |||||
| chr11:43407299
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1840-54T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 14/23 | chr11 | 43407299 | ||||||
| chr11:43407790
|
GT | G | 8 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 8 | HG01168.hp2 HG01261.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2064+226delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43407790 | |||||
| chr11:43408276
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2064+699A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408276 | ||||||
| chr11:43408523
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2064+946A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408523 | ||||||
| chr11:43408545
|
C | T | 5 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041others(2): Show | 5 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064+968C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408545 | ||||||
| chr11:43408720
|
C | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0160a0001c0001t0001g0163others(2): Show | 5 | HG02129.hp1 NA18945.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.2064+1143C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408720 | ||||||
| chr11:43408909
|
A | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG01255.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2064+1332A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408909 | ||||||
| chr11:43408930
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02083.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.2064+1353A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43408930 | ||||||
| chr11:43409002
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2064+1425A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43409002 | ||||||
| chr11:43409032
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2064+1455C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43409032 | ||||||
| chr11:43409241
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2064+1664A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43409241 | ||||||
| chr11:43409312
|
C | T | 6 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0118others(3): Show | 6 | HG00642.hp2 HG01081.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.2064+1735C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43409312 | ||||||
| chr11:43409761
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+2184G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43409761 | ||||||
| chr11:43410007
|
A | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0128 | 3 | NA18953.hp1 NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2064+2430A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410007 | ||||||
| chr11:43410130
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064+2553G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410130 | ||||||
| chr11:43410462
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2064+2885G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410462 | ||||||
| chr11:43410496
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(107): Show | 110 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.2064+2919A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410496 | ||||||
| chr11:43410543
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2064+2966G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410543 | ||||||
| chr11:43410569
|
G | A | 23 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(20): Show | 23 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.2064+2992G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410569 | ||||||
| chr11:43410730
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2064+3153A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410730 | ||||||
| chr11:43410740
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(11): Show | 15 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.2064+3163C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410740 | ||||||
| chr11:43410756
|
T | C | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.2064+3179T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410756 | ||||||
| chr11:43410875
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.2064+3298G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43410875 | ||||||
| chr11:43411000
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2064+3423G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411000 | ||||||
| chr11:43411072
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2064+3495A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411072 | ||||||
| chr11:43411102
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(107): Show | 110 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.2065-3488T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411102 | ||||||
| chr11:43411296
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2065-3294A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411296 | ||||||
| chr11:43411479
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0229 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2065-3111C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411479 | ||||||
| chr11:43411559
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2065-3031G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411559 | ||||||
| chr11:43411666
|
A | T | 1 | a0002c0003t0002g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2065-2924A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411666 | ||||||
| chr11:43411722
|
CTT | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2065-2866_2065-286 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43411722 | |||||
| chr11:43411798
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(63): Show | 66 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.2065-2792T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411798 | ||||||
| chr11:43411957
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2065-2633A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43411957 | ||||||
| chr11:43412069
|
A | T | 1 | a0001c0002t0001g0196 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2065-2521A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412069 | ||||||
| chr11:43412263
|
C | T | 4 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0158others(1): Show | 4 | HG01928.hp1 HG01952.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-2327C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412263 | ||||||
| chr11:43412343
|
C | T | 16 | a0001c0001t0001g0059a0001c0001t0001g0232a0001c0001t0001g0233others(13): Show | 16 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.2065-2247C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412343 | ||||||
| chr11:43412426
|
C | T | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2065-2164C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412426 | ||||||
| chr11:43412561
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2065-2029A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412561 | ||||||
| chr11:43412700
|
T | G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2065-1890T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412700 | ||||||
| chr11:43412893
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2065-1697A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412893 | ||||||
| chr11:43412926
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2065-1664T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412926 | ||||||
| chr11:43412981
|
G | GAC | 31 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0043others(28): Show | 31 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.2065-1563_2065-156 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
G | GACAC | 10 | a0001c0001t0001g0055a0001c0001t0001g0147a0001c0001t0001g0168others(7): Show | 10 | HG00558.hp2 HG01255.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2065-1565_2065-156 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
G | GACACAC | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0079others(3): Show | 6 | HG01256.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2065-1567_2065-156 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
G | GACACACA others(1): Show |
5 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0159others(2): Show | 5 | HG01891.hp2 HG02886.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2065-1569_2065-156 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
G | GACACACA others(3): Show |
1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2065-1571_2065-156 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
GAC | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(22): Show | 25 | HG00642.hp1 HG01069.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.2065-1563_2065-156 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
GACAC | G | 28 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(25): Show | 28 | HG00738.hp2 HG01243.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.2065-1565_2065-156 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
GACACAC | G | 41 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0044others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.2065-1567_2065-156 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
GACACACA others(1): Show |
G | 54 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2065-1569_2065-156 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
GACACACA others(3): Show |
G | 38 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0251others(35): Show | 38 | HG00609.hp1 HG00741.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2065-1571_2065-156 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
GACACACA others(5): Show |
G | 5 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0026others(2): Show | 5 | HG02300.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2065-1573_2065-156 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
GACACACA others(7): Show |
G | 1 | a0001c0001t0003g0105 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2065-1575_2065-156 others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412981
|
GACACACA others(11): Show |
G | 1 | a0001c0001t0001g0124 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2065-1579_2065-156 others(22): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43412981 | |||||
| chr11:43412985
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2065-1605C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43412985 | ||||||
| chr11:43413017
|
CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2065-1571_2065-156 others(15): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43413017 | |||||
| chr11:43413027
|
C | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 21 | HG01255.hp1 HG01261.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.2065-1563C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43413027 | ||||||
| chr11:43413028
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2065-1562_2065-156 others(15): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43413028 | ||||||
| chr11:43413419
|
C | A | 1 | a0001c0001t0005g0152 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2065-1171C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43413419 | ||||||
| chr11:43413545
|
TAGAC | T | 14 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0068others(11): Show | 14 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.2065-1041_2065-103 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43413545 | |||||
| chr11:43413706
|
G | GA | 8 | a0001c0001t0001g0177a0001c0001t0001g0234a0001c0001t0001g0268others(5): Show | 8 | HG02109.hp2 HG02486.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.2065-872dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr11 | 43413706 | |||||
| chr11:43413848
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2065-742A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43413848 | ||||||
| chr11:43413950
|
G | A | 9 | a0002c0003t0002g0207a0002c0003t0002g0210a0002c0003t0002g0213others(6): Show | 9 | HG01496.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2065-640G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43413950 | ||||||
| chr11:43414396
|
A | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2065-194A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43414396 | ||||||
| chr11:43414452
|
G | C | 1 | a0001c0001t0001g0293 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2065-138G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43414452 | ||||||
| chr11:43414521
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2065-69T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43414521 | ||||||
| chr11:43414528
|
G | A | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2065-62G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 15/23 | chr11 | 43414528 | ||||||
| chr11:43414888
|
C | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0144 | 2 | HG01175.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2251+112C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43414888 | ||||||
| chr11:43415104
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2251+328T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43415104 | ||||||
| chr11:43415439
|
G | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.2251+663G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43415439 | ||||||
| chr11:43415456
|
G | C | 1 | a0001c0001t0003g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2251+680G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43415456 | ||||||
| chr11:43415919
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(42): Show | 45 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2251+1143G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43415919 | ||||||
| chr11:43415980
|
T | C | 1 | a0002c0003t0002g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2251+1204T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43415980 | ||||||
| chr11:43416292
|
A | G | 1 | a0001c0002t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2251+1516A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416292 | ||||||
| chr11:43416299
|
C | T | 93 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(90): Show | 93 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.2251+1523C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416299 | ||||||
| chr11:43416307
|
T | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2251+1531T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416307 | ||||||
| chr11:43416466
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(42): Show | 45 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2251+1690T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416466 | ||||||
| chr11:43416551
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251+1775G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416551 | ||||||
| chr11:43416651
|
G | C | 1 | a0001c0001t0001g0279 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2251+1875G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416651 | ||||||
| chr11:43416660
|
T | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2251+1884T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416660 | ||||||
| chr11:43416690
|
T | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | NA18979.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2251+1914T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416690 | ||||||
| chr11:43416819
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251+2043C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416819 | ||||||
| chr11:43416906
|
C | G | 25 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(22): Show | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.2251+2130C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43416906 | ||||||
| chr11:43417358
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2251+2582G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417358 | ||||||
| chr11:43417493
|
A | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2251+2717A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417493 | ||||||
| chr11:43417562
|
A | G | 1 | a0001c0001t0003g0097 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2251+2786A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417562 | ||||||
| chr11:43417664
|
C | A | 1 | a0001c0002t0001g0249 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2251+2888C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417664 | ||||||
| chr11:43417781
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2251+3005G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417781 | ||||||
| chr11:43417792
|
G | A | 257 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2251+3016G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417792 | ||||||
| chr11:43417813
|
C | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(200): Show | 203 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.2251+3037C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43417813 | ||||||
| chr11:43418275
|
C | T | 2 | a0001c0001t0001g0281a0001c0001t0001g0284 | 2 | HG01346.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2251+3499C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418275 | ||||||
| chr11:43418284
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2251+3508A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418284 | ||||||
| chr11:43418370
|
T | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(15): Show | 18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2251+3594T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418370 | ||||||
| chr11:43418443
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2251+3667G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418443 | ||||||
| chr11:43418458
|
C | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0229 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2251+3682C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418458 | ||||||
| chr11:43418561
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2251+3785G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43418561 | ||||||
| chr11:43418649
|
AAAAACAG others(14): Show |
A | 1 | a0001c0001t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2251+3878_2251+389 others(25): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43418649 | |||||
| chr11:43419050
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2251+4274C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419050 | ||||||
| chr11:43419133
|
T | G | 1 | a0002c0003t0002g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2251+4357T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419133 | ||||||
| chr11:43419381
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2251+4605A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419381 | ||||||
| chr11:43419405
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2251+4629A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419405 | ||||||
| chr11:43419740
|
G | A | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2251+4964G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419740 | ||||||
| chr11:43419848
|
A | C | 1 | a0002c0003t0002g0207 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2251+5072A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419848 | ||||||
| chr11:43419945
|
T | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2251+5169T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43419945 | ||||||
| chr11:43420007
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2251+5231G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420007 | ||||||
| chr11:43420087
|
A | G | 2 | a0001c0001t0001g0281a0001c0001t0001g0284 | 2 | HG01346.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2251+5311A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420087 | ||||||
| chr11:43420404
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0255 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2251+5628G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420404 | ||||||
| chr11:43420671
|
G | C | 1 | a0001c0001t0003g0097 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2251+5895G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420671 | ||||||
| chr11:43420774
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2251+5998T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420774 | ||||||
| chr11:43420853
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2251+6077A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420853 | ||||||
| chr11:43420854
|
G | C | 1 | a0001c0001t0001g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2251+6078G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420854 | ||||||
| chr11:43420998
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0228 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2251+6222A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43420998 | ||||||
| chr11:43421051
|
C | T | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2251+6275C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421051 | ||||||
| chr11:43421158
|
T | A | 23 | a0001c0001t0001g0252a0001c0001t0001g0261a0001c0001t0001g0264others(20): Show | 23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.2251+6382T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421158 | ||||||
| chr11:43421167
|
T | G | 30 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0085others(27): Show | 30 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.2251+6391T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421167 | ||||||
| chr11:43421206
|
G | C | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2251+6430G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421206 | ||||||
| chr11:43421235
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2251+6459A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421235 | ||||||
| chr11:43421609
|
A | C | 1 | a0001c0002t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2251+6833A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421609 | ||||||
| chr11:43421870
|
G | A | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251+7094G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421870 | ||||||
| chr11:43421938
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2251+7162A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43421938 | ||||||
| chr11:43422072
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2251+7296T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422072 | ||||||
| chr11:43422124
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2251+7348G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422124 | ||||||
| chr11:43422127
|
A | G | 1 | a0001c0001t0003g0075 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2251+7351A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422127 | ||||||
| chr11:43422290
|
G | C | 25 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(22): Show | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.2251+7514G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422290 | ||||||
| chr11:43422299
|
A | C | 3 | a0002c0003t0002g0221a0002c0003t0002g0222a0002c0003t0002g0225 | 3 | HG01891.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2251+7523A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422299 | ||||||
| chr11:43422328
|
G | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2251+7552G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422328 | ||||||
| chr11:43422438
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2251+7662G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422438 | ||||||
| chr11:43422461
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2251+7685C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422461 | ||||||
| chr11:43422957
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2251+8181A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43422957 | ||||||
| chr11:43423279
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2251+8503G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43423279 | ||||||
| chr11:43423360
|
CAT | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2251+8585_2251+858 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43423360 | ||||||
| chr11:43423930
|
A | G | 1 | a0001c0001t0003g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2251+9154A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43423930 | ||||||
| chr11:43424006
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2251+9230A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424006 | ||||||
| chr11:43424087
|
C | CT | 11 | a0001c0001t0001g0047a0001c0001t0001g0101a0002c0003t0002g0207others(8): Show | 11 | HG00642.hp2 HG01496.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2251+9326dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43424087 | |||||
| chr11:43424122
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251+9346C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424122 | ||||||
| chr11:43424123
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2251+9347G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424123 | ||||||
| chr11:43424260
|
T | C | 27 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.2251+9484T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424260 | ||||||
| chr11:43424283
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2251+9507G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424283 | ||||||
| chr11:43424290
|
C | T | 5 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0115others(2): Show | 5 | HG00323.hp2 HG00735.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.2251+9514C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424290 | ||||||
| chr11:43424442
|
GA | G | 27 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.2251+9669delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43424442 | |||||
| chr11:43424535
|
C | T | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2251+9759C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424535 | ||||||
| chr11:43424550
|
C | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.2251+9774C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424550 | ||||||
| chr11:43424695
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2251+9919G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424695 | ||||||
| chr11:43424799
|
T | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251+10023T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424799 | ||||||
| chr11:43424867
|
A | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2251+10091A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424867 | ||||||
| chr11:43424935
|
A | G | 23 | a0001c0001t0001g0252a0001c0001t0001g0261a0001c0001t0001g0264others(20): Show | 23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.2251+10159A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43424935 | ||||||
| chr11:43425019
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2251+10243G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425019 | ||||||
| chr11:43425153
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2251+10377C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425153 | ||||||
| chr11:43425286
|
T | G | 27 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.2251+10510T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425286 | ||||||
| chr11:43425333
|
T | A | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2251+10557T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425333 | ||||||
| chr11:43425383
|
G | A | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2251+10607G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425383 | ||||||
| chr11:43425476
|
C | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(15): Show | 18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2251+10700C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425476 | ||||||
| chr11:43425600
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2251+10824C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425600 | ||||||
| chr11:43425882
|
G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2251+11106G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425882 | ||||||
| chr11:43425899
|
A | T | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2251+11123A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43425899 | ||||||
| chr11:43426066
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2251+11290G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426066 | ||||||
| chr11:43426202
|
T | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2251+11426T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426202 | ||||||
| chr11:43426386
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2251+11610C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426386 | ||||||
| chr11:43426481
|
C | T | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2251+11705C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426481 | ||||||
| chr11:43426510
|
G | A | 26 | a0001c0001t0001g0052a0001c0002t0001g0050a0001c0002t0001g0186others(23): Show | 26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.2251+11734G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426510 | ||||||
| chr11:43426583
|
A | T | 1 | a0001c0001t0005g0152 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2251+11807A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426583 | ||||||
| chr11:43426624
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2251+11848A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426624 | ||||||
| chr11:43426632
|
C | T | 1 | a0002c0003t0002g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2251+11856C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426632 | ||||||
| chr11:43426917
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2251+12141A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426917 | ||||||
| chr11:43426931
|
G | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(15): Show | 18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2251+12155G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43426931 | ||||||
| chr11:43427250
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2251+12474A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427250 | ||||||
| chr11:43427293
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2251+12517C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427293 | ||||||
| chr11:43427396
|
C | T | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2251+12620C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427396 | ||||||
| chr11:43427398
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2251+12622G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427398 | ||||||
| chr11:43427520
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2251+12744G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427520 | ||||||
| chr11:43427539
|
A | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02922.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2251+12763A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427539 | ||||||
| chr11:43427555
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2251+12779C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427555 | ||||||
| chr11:43427735
|
T | C | 34 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(31): Show | 34 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.2251+12959T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427735 | ||||||
| chr11:43427823
|
C | G | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2251+13047C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427823 | ||||||
| chr11:43427913
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2251+13137C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43427913 | ||||||
| chr11:43428305
|
TA | T | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2251+13539delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43428305 | |||||
| chr11:43428524
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2251+13748G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43428524 | ||||||
| chr11:43428540
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2251+13764G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43428540 | ||||||
| chr11:43428811
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2251+14035A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43428811 | ||||||
| chr11:43428839
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2251+14063C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43428839 | ||||||
| chr11:43428993
|
A | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(15): Show | 18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2251+14217A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43428993 | ||||||
| chr11:43429038
|
A | G | 13 | a0001c0001t0001g0063a0001c0001t0001g0074a0001c0001t0001g0080others(10): Show | 13 | HG00323.hp2 HG00735.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.2251+14262A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429038 | ||||||
| chr11:43429057
|
C | G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2252-14268C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429057 | ||||||
| chr11:43429314
|
G | T | 18 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(15): Show | 18 | HG00323.hp1 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2252-14011G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429314 | ||||||
| chr11:43429331
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2252-13994T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429331 | ||||||
| chr11:43429377
|
C | T | 42 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(39): Show | 42 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.2252-13948C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429377 | ||||||
| chr11:43429599
|
A | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0172others(1): Show | 4 | NA18962.hp1 NA18970.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2252-13726A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429599 | ||||||
| chr11:43429698
|
GAAAT | G | 30 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0085others(27): Show | 30 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.2252-13626_2252-13 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429698 | ||||||
| chr11:43429740
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2252-13585A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429740 | ||||||
| chr11:43429746
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2252-13579G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429746 | ||||||
| chr11:43429907
|
C | T | 27 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.2252-13418C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429907 | ||||||
| chr11:43429960
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2252-13365A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43429960 | ||||||
| chr11:43430569
|
C | T | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2252-12756C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430569 | ||||||
| chr11:43430607
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2252-12718G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430607 | ||||||
| chr11:43430704
|
T | TACACACA others(11): Show |
1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2252-12617_2252-12 others(24): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430704 | |||||
| chr11:43430709
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2252-12616G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430709 | ||||||
| chr11:43430709
|
G | GCA | 58 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(55): Show | 58 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2252-12577_2252-12 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
G | GCACA | 40 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(37): Show | 40 | HG00609.hp1 HG00639.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2252-12579_2252-12 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
G | GCACACA | 23 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0046others(20): Show | 23 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.2252-12581_2252-12 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
G | GCACACAC others(1): Show |
17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(14): Show | 17 | HG00597.hp2 HG01070.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.2252-12583_2252-12 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
G | GCACACAC others(3): Show |
14 | a0001c0001t0001g0021a0001c0001t0001g0048a0001c0001t0001g0049others(11): Show | 14 | HG00408.hp1 HG02257.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2252-12585_2252-12 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
G | GCACACAC others(5): Show |
11 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0054others(8): Show | 12 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.2252-12587_2252-12 others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
G | GCACACAC others(7): Show |
10 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.2252-12589_2252-12 others(20): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
G | GCGCA | 3 | a0002c0003t0002g0216a0002c0003t0002g0217a0002c0003t0002g0224 | 3 | HG02622.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2252-12615_2252-12 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
G | GCGCACAC others(3): Show |
2 | a0001c0001t0001g0027a0001c0001t0001g0029 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2252-12615_2252-12 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
GCA | G | 39 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(36): Show | 39 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2252-12577_2252-12 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
GCACA | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0052a0001c0001t0001g0055others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2252-12579_2252-12 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
GCACACA | G | 12 | a0001c0001t0001g0124a0001c0002t0001g0050a0001c0002t0001g0186others(9): Show | 12 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.2252-12581_2252-12 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
GCACACAC others(1): Show |
G | 16 | a0001c0001t0001g0159a0001c0001t0004g0004a0001c0002t0001g0195others(13): Show | 16 | HG00558.hp2 HG00738.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2252-12583_2252-12 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
GCACACAC others(3): Show |
G | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2252-12585_2252-12 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430709
|
GCACACAC others(5): Show |
G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2252-12587_2252-12 others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43430709 | |||||
| chr11:43430711
|
A | G | 2 | a0001c0001t0001g0028a0001c0008t0006g0064 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2252-12614A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430711 | ||||||
| chr11:43430749
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2252-12576_2252-12 others(17): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430749 | ||||||
| chr11:43430836
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2252-12489T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43430836 | ||||||
| chr11:43431291
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2252-12034A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43431291 | ||||||
| chr11:43431427
|
A | G | 3 | a0002c0003t0002g0216a0002c0003t0002g0217a0002c0003t0002g0224 | 3 | HG02622.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2252-11898A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43431427 | ||||||
| chr11:43431616
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2252-11709A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43431616 | ||||||
| chr11:43431803
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | NA18979.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2252-11522C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43431803 | ||||||
| chr11:43432057
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2252-11268C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43432057 | ||||||
| chr11:43432235
|
A | AG | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.2252-11089dupG | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432235 | |||||
| chr11:43432454
|
G | A | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2252-10871G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43432454 | ||||||
| chr11:43432678
|
G | A | 25 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(22): Show | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.2252-10647G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43432678 | ||||||
| chr11:43432784
|
C | CT | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 14 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.2252-10534dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432784 | |||||
| chr11:43432845
|
T | A | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2252-10480T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43432845 | ||||||
| chr11:43432919
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2252-10406A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43432919 | ||||||
| chr11:43432989
|
G | GTGTTT | 29 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(26): Show | 29 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.2252-10311_2252-10 others(11): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432989 | |||||
| chr11:43432989
|
G | GTGTTTTG others(3): Show |
14 | a0002c0003t0002g0051a0002c0003t0002g0207a0002c0003t0002g0209others(11): Show | 14 | HG01496.hp2 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2252-10316_2252-10 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432989 | |||||
| chr11:43432989
|
G | GTGTTTTG others(8): Show |
5 | a0002c0003t0002g0003a0002c0003t0002g0217a0002c0003t0002g0221others(2): Show | 5 | HG01891.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2252-10321_2252-10 others(21): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432989 | |||||
| chr11:43432989
|
G | GTGTTTTG others(13): Show |
1 | a0002c0003t0002g0211 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2252-10326_2252-10 others(26): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43432989 | |||||
| chr11:43433075
|
G | A | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.2252-10250G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433075 | ||||||
| chr11:43433225
|
T | C | 25 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(22): Show | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.2252-10100T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433225 | ||||||
| chr11:43433251
|
A | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 164 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2252-10074A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433251 | ||||||
| chr11:43433290
|
C | T | 39 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(36): Show | 39 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2252-10035C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433290 | ||||||
| chr11:43433474
|
C | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-9851C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433474 | ||||||
| chr11:43433501
|
T | C | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.2252-9824T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433501 | ||||||
| chr11:43433634
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2252-9691A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433634 | ||||||
| chr11:43433674
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2252-9651A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433674 | ||||||
| chr11:43433692
|
G | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2252-9633G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433692 | ||||||
| chr11:43433824
|
A | G | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.2252-9501A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43433824 | ||||||
| chr11:43434018
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2252-9307T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434018 | ||||||
| chr11:43434036
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2252-9289C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434036 | ||||||
| chr11:43434122
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02922.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2252-9203C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434122 | ||||||
| chr11:43434128
|
T | G | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2252-9197T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434128 | ||||||
| chr11:43434168
|
G | GAC | 3 | a0001c0001t0001g0016a0001c0001t0001g0079a0001c0001t0001g0136 | 3 | HG02818.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2252-9094_2252-909 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
G | GACACACA others(3): Show |
1 | a0001c0001t0001g0060 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2252-9102_2252-909 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GAC | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0037others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.2252-9094_2252-909 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACAC | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 16 | HG00558.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.2252-9096_2252-909 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACAC | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0066others(17): Show | 20 | HG00099.hp1 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2252-9098_2252-909 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(1): Show |
G | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(8): Show | 11 | HG01433.hp2 HG01515.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.2252-9100_2252-909 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(3): Show |
G | 9 | a0001c0001t0001g0007a0001c0001t0001g0084a0001c0001t0001g0090others(6): Show | 9 | HG01243.hp2 HG01516.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2252-9102_2252-909 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(5): Show |
G | 18 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0040others(15): Show | 18 | HG00438.hp2 HG00639.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.2252-9104_2252-909 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(7): Show |
G | 53 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0056others(50): Show | 53 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.2252-9106_2252-909 others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(9): Show |
G | 28 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0039others(25): Show | 28 | HG00609.hp2 HG01069.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.2252-9108_2252-909 others(20): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(11): Show |
G | 13 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0047others(10): Show | 13 | HG00099.hp2 HG00408.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.2252-9110_2252-909 others(22): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(13): Show |
G | 15 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0041others(12): Show | 15 | HG00323.hp1 HG00609.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.2252-9112_2252-909 others(24): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(15): Show |
G | 39 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(36): Show | 39 | HG00741.hp1 HG01099.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.2252-9114_2252-909 others(26): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(17): Show |
G | 22 | a0001c0001t0001g0252a0001c0001t0001g0264a0001c0001t0001g0280others(19): Show | 22 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.2252-9116_2252-909 others(28): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(19): Show |
G | 5 | a0001c0001t0001g0137a0001c0002t0001g0198a0001c0002t0001g0199others(2): Show | 5 | HG01257.hp1 HG01361.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2252-9118_2252-909 others(30): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(23): Show |
G | 11 | a0001c0001t0001g0036a0001c0001t0001g0052a0001c0002t0001g0250others(8): Show | 11 | HG01496.hp2 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2252-9122_2252-909 others(34): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(25): Show |
G | 2 | a0001c0001t0001g0265a0002c0003t0002g0217 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2252-9124_2252-909 others(36): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434168
|
GACACACA others(27): Show |
G | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2252-9126_2252-909 others(38): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43434168 | |||||
| chr11:43434169
|
ACACACAC others(6): Show |
A | 1 | a0001c0001t0001g0131 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2252-9155_2252-914 others(17): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434169 | ||||||
| chr11:43434169
|
ACACACAC others(16): Show |
A | 1 | a0001c0001t0001g0254 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2252-9155_2252-913 others(27): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434169 | ||||||
| chr11:43434407
|
C | G | 10 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.2252-8918C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434407 | ||||||
| chr11:43434480
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2252-8845A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434480 | ||||||
| chr11:43434541
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2252-8784C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434541 | ||||||
| chr11:43434676
|
T | C | 1 | a0001c0006t0001g0203 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2252-8649T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43434676 | ||||||
| chr11:43435009
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2252-8316A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435009 | ||||||
| chr11:43435031
|
CAT | C | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2252-8293_2252-829 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435031 | ||||||
| chr11:43435070
|
G | C | 1 | a0001c0001t0001g0015 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2252-8255G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435070 | ||||||
| chr11:43435077
|
T | TGATA | 71 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0018others(68): Show | 71 | HG00323.hp1 HG00408.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.2252-8196_2252-819 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | |||||
| chr11:43435077
|
T | TGATAGAT others(1): Show |
30 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0030others(27): Show | 31 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.2252-8200_2252-819 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | |||||
| chr11:43435077
|
T | TGATAGAT others(5): Show |
11 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0027others(8): Show | 11 | HG00609.hp1 HG01943.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.2252-8204_2252-819 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | |||||
| chr11:43435077
|
TGATA | T | 43 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0025others(40): Show | 43 | HG00558.hp2 HG00735.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.2252-8196_2252-819 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | |||||
| chr11:43435077
|
TGATAGAT others(1): Show |
T | 36 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0042others(33): Show | 36 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.2252-8200_2252-819 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | |||||
| chr11:43435077
|
TGATAGAT others(5): Show |
T | 4 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0185others(1): Show | 4 | HG00438.hp1 NA18944.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.2252-8204_2252-819 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | |||||
| chr11:43435077
|
TGATAGAT others(9): Show |
T | 2 | a0001c0001t0003g0146a0001c0001t0003g0153 | 2 | NA18964.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.2252-8208_2252-819 others(20): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435077 | |||||
| chr11:43435089
|
A | T | 1 | a0001c0001t0001g0131 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2252-8236A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435089 | ||||||
| chr11:43435100
|
T | TAGATAGA others(5): Show |
1 | a0001c0001t0001g0234 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2252-8214_2252-821 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43435100 | |||||
| chr11:43435210
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2252-8115A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435210 | ||||||
| chr11:43435772
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(36): Show | 39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.2252-7553A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435772 | ||||||
| chr11:43435779
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2252-7546A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435779 | ||||||
| chr11:43435790
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2252-7535A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435790 | ||||||
| chr11:43435915
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA18747.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2252-7410T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435915 | ||||||
| chr11:43435995
|
C | T | 1 | a0001c0002t0001g0197 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2252-7330C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43435995 | ||||||
| chr11:43436438
|
A | G | 1 | a0002c0003t0002g0216 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2252-6887A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43436438 | ||||||
| chr11:43436583
|
T | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-6742T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43436583 | ||||||
| chr11:43436594
|
A | G | 18 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(15): Show | 18 | HG00323.hp1 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2252-6731A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43436594 | ||||||
| chr11:43436721
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2252-6604A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43436721 | ||||||
| chr11:43436723
|
T | G | 16 | a0001c0001t0001g0059a0001c0001t0001g0232a0001c0001t0001g0233others(13): Show | 16 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.2252-6602T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43436723 | ||||||
| chr11:43437006
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2252-6319A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437006 | ||||||
| chr11:43437035
|
C | T | 1 | a0002c0003t0002g0209 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2252-6290C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437035 | ||||||
| chr11:43437395
|
T | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-5930T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437395 | ||||||
| chr11:43437560
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2252-5765C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437560 | ||||||
| chr11:43437578
|
C | T | 44 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(41): Show | 44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.2252-5747C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437578 | ||||||
| chr11:43437612
|
A | G | 18 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(15): Show | 18 | HG00323.hp1 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2252-5713A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437612 | ||||||
| chr11:43437772
|
C | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-5553C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437772 | ||||||
| chr11:43437870
|
A | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 159 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2252-5455A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437870 | ||||||
| chr11:43437898
|
A | G | 14 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(11): Show | 14 | HG00099.hp2 HG01168.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.2252-5427A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437898 | ||||||
| chr11:43437975
|
A | G | 1 | a0001c0001t0003g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2252-5350A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43437975 | ||||||
| chr11:43438160
|
A | G | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2252-5165A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438160 | ||||||
| chr11:43438440
|
C | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-4885C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438440 | ||||||
| chr11:43438881
|
A | T | 1 | a0001c0001t0001g0133 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2252-4444A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438881 | ||||||
| chr11:43438901
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2252-4424A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438901 | ||||||
| chr11:43438910
|
A | C | 1 | a0001c0001t0001g0133 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2252-4415A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438910 | ||||||
| chr11:43438931
|
C | T | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.2252-4394C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43438931 | ||||||
| chr11:43439059
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2252-4266G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439059 | ||||||
| chr11:43439199
|
A | C | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2252-4126A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439199 | ||||||
| chr11:43439262
|
G | A | 1 | a0001c0001t0003g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2252-4063G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439262 | ||||||
| chr11:43439469
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2252-3856G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439469 | ||||||
| chr11:43439471
|
T | G | 3 | a0001c0001t0003g0105a0001c0001t0005g0104a0001c0001t0005g0119 | 3 | HG00609.hp2 HG02040.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2252-3854T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439471 | ||||||
| chr11:43439488
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2252-3837G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439488 | ||||||
| chr11:43439613
|
T | C | 34 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(31): Show | 34 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.2252-3712T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439613 | ||||||
| chr11:43439631
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2252-3694G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439631 | ||||||
| chr11:43439916
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02922.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2252-3409G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439916 | ||||||
| chr11:43439953
|
C | A | 1 | a0001c0001t0001g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2252-3372C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43439953 | ||||||
| chr11:43440259
|
AC | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.2252-3062delC | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43440259 | |||||
| chr11:43440503
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2252-2822C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43440503 | ||||||
| chr11:43440592
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2252-2733T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43440592 | ||||||
| chr11:43440671
|
G | A | 1 | a0001c0002t0001g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2252-2654G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43440671 | ||||||
| chr11:43440868
|
T | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2252-2457T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43440868 | ||||||
| chr11:43440961
|
TA | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(11): Show | 15 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.2252-2352delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43440961 | |||||
| chr11:43441114
|
C | CAAAAAAA others(329): Show |
1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2252-2193_2252-219 others(340): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | |||||
| chr11:43441114
|
C | CAAAAAAA others(310): Show |
20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2252-2193_2252-219 others(321): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | |||||
| chr11:43441114
|
C | CAAAAAAA others(312): Show |
6 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2252-2193_2252-219 others(323): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | |||||
| chr11:43441114
|
C | CAAAAAAA others(329): Show |
1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2252-2193_2252-219 others(340): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | |||||
| chr11:43441114
|
C | CAAAAAAA others(330): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0056 | 2 | HG02055.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.2252-2193_2252-219 others(341): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | |||||
| chr11:43441114
|
C | CAAAAAAA others(331): Show |
8 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(5): Show | 8 | HG01069.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.2252-2193_2252-219 others(342): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | |||||
| chr11:43441114
|
C | CAAAAAAA others(332): Show |
1 | a0001c0001t0001g0228 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2252-2193_2252-219 others(343): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr11 | 43441114 | |||||
| chr11:43441130
|
G | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2252-2195G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441130 | ||||||
| chr11:43441227
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0229 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2252-2098C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441227 | ||||||
| chr11:43441267
|
C | T | 44 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(41): Show | 44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.2252-2058C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441267 | ||||||
| chr11:43441403
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(63): Show | 66 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.2252-1922C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441403 | ||||||
| chr11:43441432
|
A | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02976.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2252-1893A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441432 | ||||||
| chr11:43441499
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2252-1826G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441499 | ||||||
| chr11:43441606
|
T | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG01074.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2252-1719T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441606 | ||||||
| chr11:43441864
|
A | G | 23 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(20): Show | 23 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.2252-1461A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441864 | ||||||
| chr11:43441983
|
G | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(15): Show | 18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2252-1342G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43441983 | ||||||
| chr11:43442051
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2252-1274C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43442051 | ||||||
| chr11:43442206
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2252-1119A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43442206 | ||||||
| chr11:43442474
|
T | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2252-851T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43442474 | ||||||
| chr11:43442743
|
G | C | 44 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(41): Show | 44 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.2252-582G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43442743 | ||||||
| chr11:43443094
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2252-231C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43443094 | ||||||
| chr11:43443228
|
G | A | 3 | a0002c0003t0002g0209a0002c0003t0002g0219a0002c0003t0002g0220 | 3 | HG02559.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2252-97G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43443228 | ||||||
| chr11:43443289
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2252-36G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 16/23 | chr11 | 43443289 | ||||||
| chr11:43443752
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0144 | 2 | HG01175.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2511+168T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 17/23 | chr11 | 43443752 | ||||||
| chr11:43444015
|
T | A | 2 | a0001c0001t0003g0105a0001c0001t0005g0104 | 2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.2512-41T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 17/23 | chr11 | 43444015 | ||||||
| chr11:43444017
|
A | C | 2 | a0001c0001t0003g0105a0001c0001t0005g0104 | 2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.2512-39A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 17/23 | chr11 | 43444017 | ||||||
| chr11:43444452
|
G | C | 1 | a0002c0003t0002g0211 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2665+243G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43444452 | ||||||
| chr11:43444722
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2665+513T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43444722 | ||||||
| chr11:43444722
|
T | TAC | 111 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(108): Show | 112 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.2665+549_2665+550d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | |||||
| chr11:43444722
|
T | TACAC | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2665+547_2665+550d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | |||||
| chr11:43444722
|
T | TACACAC | 19 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0251others(16): Show | 19 | HG00323.hp1 HG01070.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2665+545_2665+550d others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | |||||
| chr11:43444722
|
T | TACACACA others(1): Show |
6 | a0001c0001t0001g0254a0001c0001t0001g0257a0001c0001t0001g0258others(3): Show | 6 | HG01361.hp1 HG02293.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2665+543_2665+550d others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | |||||
| chr11:43444722
|
TAC | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(16): Show | 19 | HG00741.hp2 HG01243.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.2665+549_2665+550d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | |||||
| chr11:43444722
|
TACACAC | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0228 | 3 | HG01069.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2665+545_2665+550d others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr11 | 43444722 | |||||
| chr11:43444900
|
C | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.2665+691C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43444900 | ||||||
| chr11:43444951
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2665+742A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43444951 | ||||||
| chr11:43445562
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2665+1353C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43445562 | ||||||
| chr11:43445897
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | NA18949.hp2 NA18959.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2665+1688A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43445897 | ||||||
| chr11:43445935
|
A | G | 1 | a0001c0001t0001g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2665+1726A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43445935 | ||||||
| chr11:43446131
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2666-1871C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446131 | ||||||
| chr11:43446194
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2666-1808T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446194 | ||||||
| chr11:43446250
|
T | A | 1 | a0001c0001t0001g0185 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2666-1752T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446250 | ||||||
| chr11:43446345
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2666-1657C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446345 | ||||||
| chr11:43446620
|
C | T | 1 | a0002c0003t0002g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2666-1382C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446620 | ||||||
| chr11:43446708
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2666-1294C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446708 | ||||||
| chr11:43446814
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2666-1188A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446814 | ||||||
| chr11:43446950
|
G | C | 9 | a0002c0003t0002g0207a0002c0003t0002g0210a0002c0003t0002g0213others(6): Show | 9 | HG01496.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2666-1052G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43446950 | ||||||
| chr11:43447038
|
G | A | 1 | a0001c0001t0005g0119 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2666-964G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43447038 | ||||||
| chr11:43447253
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2666-749T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43447253 | ||||||
| chr11:43447293
|
G | A | 2 | a0001c0001t0004g0001a0001c0001t0004g0004 | 3 | HG00639.hp2 HG01106.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2666-709G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43447293 | ||||||
| chr11:43447598
|
C | T | 48 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(45): Show | 48 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2666-404C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43447598 | ||||||
| chr11:43447822
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2666-180A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 18/23 | chr11 | 43447822 | ||||||
| chr11:43448147
|
C | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2786+25C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448147 | ||||||
| chr11:43448208
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2786+86G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448208 | ||||||
| chr11:43448333
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2786+211G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448333 | ||||||
| chr11:43448388
|
C | A | 1 | a0002c0003t0002g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2786+266C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448388 | ||||||
| chr11:43448425
|
G | C | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2786+303G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448425 | ||||||
| chr11:43448705
|
C | A | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2786+583C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448705 | ||||||
| chr11:43448714
|
A | G | 2 | a0001c0001t0001g0239a0002c0003t0001g0226 | 2 | HG02132.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2786+592A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43448714 | ||||||
| chr11:43449058
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2786+936C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43449058 | ||||||
| chr11:43449098
|
T | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02976.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2786+976T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43449098 | ||||||
| chr11:43449884
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0117 | 2 | HG00323.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.2787-198G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 19/23 | chr11 | 43449884 | ||||||
| chr11:43450291
|
G | A | 2 | a0001c0001t0003g0105a0001c0001t0005g0104 | 2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.2946+50G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450291 | ||||||
| chr11:43450298
|
G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2946+57G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450298 | ||||||
| chr11:43450325
|
G | A | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2946+84G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450325 | ||||||
| chr11:43450400
|
T | C | 2 | a0002c0003t0002g0222a0002c0003t0002g0225 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2946+159T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450400 | ||||||
| chr11:43450681
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0021 | 2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2946+440G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450681 | ||||||
| chr11:43450787
|
G | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(36): Show | 39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.2947-395G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43450787 | ||||||
| chr11:43451027
|
G | A | 3 | a0002c0003t0002g0209a0002c0003t0002g0219a0002c0003t0002g0220 | 3 | HG02559.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2947-155G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43451027 | ||||||
| chr11:43451143
|
G | A | 4 | a0001c0002t0001g0198a0001c0002t0001g0199a0001c0002t0001g0250others(1): Show | 4 | HG00738.hp1 HG01257.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2947-39G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 20/23 | chr11 | 43451143 | ||||||
| chr11:43451345
|
G | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.3030+80G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451345 | ||||||
| chr11:43451507
|
C | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3030+242C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451507 | ||||||
| chr11:43451557
|
T | C | 4 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0001t0001g0266others(1): Show | 4 | HG00323.hp1 HG01099.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.3030+292T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451557 | ||||||
| chr11:43451650
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3030+385T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451650 | ||||||
| chr11:43451773
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3030+508G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451773 | ||||||
| chr11:43451781
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3030+516T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451781 | ||||||
| chr11:43451804
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3030+539G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451804 | ||||||
| chr11:43451932
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0231 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3030+667G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451932 | ||||||
| chr11:43451932
|
G | T | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3030+667G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43451932 | ||||||
| chr11:43452217
|
C | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3030+952C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452217 | ||||||
| chr11:43452222
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3030+957G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452222 | ||||||
| chr11:43452356
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3030+1091C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452356 | ||||||
| chr11:43452455
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0084 | 2 | NA18945.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.3030+1190C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452455 | ||||||
| chr11:43452573
|
C | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3030+1308C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452573 | ||||||
| chr11:43452768
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3030+1503C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452768 | ||||||
| chr11:43452871
|
T | C | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.3030+1606T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43452871 | ||||||
| chr11:43453113
|
C | T | 1 | a0002c0003t0002g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3030+1848C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43453113 | ||||||
| chr11:43453180
|
A | AAAAT | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.3030+1916_3030+191 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43453180 | |||||
| chr11:43453469
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(36): Show | 39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3030+2204T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43453469 | ||||||
| chr11:43453695
|
T | G | 1 | a0004c0007t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3030+2430T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43453695 | ||||||
| chr11:43453910
|
T | A | 1 | a0001c0001t0001g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3030+2645T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43453910 | ||||||
| chr11:43453949
|
C | G | 3 | a0001c0001t0001g0171a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | NA18979.hp1 NA19083.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3030+2684C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43453949 | ||||||
| chr11:43454041
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3030+2776G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454041 | ||||||
| chr11:43454092
|
G | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3030+2827G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454092 | ||||||
| chr11:43454268
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.3030+3003A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454268 | ||||||
| chr11:43454378
|
C | G | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3030+3113C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454378 | ||||||
| chr11:43454448
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3030+3183T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454448 | ||||||
| chr11:43454531
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3030+3266A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454531 | ||||||
| chr11:43454862
|
A | G | 1 | a0003c0004t0001g0230 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3030+3597A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43454862 | ||||||
| chr11:43455037
|
C | T | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0008t0006g0064 | 3 | HG02145.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3030+3772C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43455037 | ||||||
| chr11:43455172
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3030+3907G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43455172 | ||||||
| chr11:43455232
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0262 | 2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3030+3967C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43455232 | ||||||
| chr11:43455272
|
G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3030+4007G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43455272 | ||||||
| chr11:43455428
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3030+4163G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43455428 | ||||||
| chr11:43456039
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3030+4774A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456039 | ||||||
| chr11:43456179
|
A | AAC | 40 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0025others(37): Show | 40 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3030+4947_3030+494 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | |||||
| chr11:43456179
|
A | AACAC | 29 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0047others(26): Show | 29 | HG00735.hp2 HG01069.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.3030+4945_3030+494 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | |||||
| chr11:43456179
|
A | AACACAC | 4 | a0001c0001t0001g0002a0001c0001t0001g0080a0001c0001t0001g0117others(1): Show | 4 | HG00323.hp2 HG01346.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.3030+4943_3030+494 others(10): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | |||||
| chr11:43456179
|
AAC | A | 18 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0068others(15): Show | 18 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.3030+4947_3030+494 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | |||||
| chr11:43456179
|
AACAC | A | 29 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(26): Show |
intron_variant | MODIFIER | c.3030+4945_3030+494 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | |||||
| chr11:43456179
|
AACACACA others(1): Show |
A | 25 | a0001c0001t0001g0052a0001c0002t0001g0050a0001c0002t0001g0186others(22): Show | 25 | HG00558.hp2 HG00735.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.3030+4941_3030+494 others(12): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | |||||
| chr11:43456179
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3030+4939_3030+494 others(14): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | |||||
| chr11:43456179
|
AACACACA others(5): Show |
A | 1 | a0001c0001t0001g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3030+4937_3030+494 others(16): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43456179 | |||||
| chr11:43456195
|
C | T | 34 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(31): Show | 34 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.3030+4930C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456195 | ||||||
| chr11:43456574
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3030+5309A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456574 | ||||||
| chr11:43456729
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3030+5464G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456729 | ||||||
| chr11:43456906
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3030+5641G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456906 | ||||||
| chr11:43456951
|
G | A | 1 | a0002c0003t0002g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3030+5686G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43456951 | ||||||
| chr11:43457272
|
A | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3030+6007A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457272 | ||||||
| chr11:43457322
|
C | A | 1 | a0001c0001t0001g0009 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3030+6057C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457322 | ||||||
| chr11:43457609
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3030+6344A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457609 | ||||||
| chr11:43457671
|
G | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 156 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.3030+6406G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457671 | ||||||
| chr11:43457881
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3030+6616G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457881 | ||||||
| chr11:43457897
|
T | G | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3030+6632T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43457897 | ||||||
| chr11:43458156
|
T | C | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3030+6891T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458156 | ||||||
| chr11:43458157
|
T | A | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3030+6892T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458157 | ||||||
| chr11:43458174
|
G | A | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3030+6909G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458174 | ||||||
| chr11:43458206
|
A | C | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.3030+6941A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458206 | ||||||
| chr11:43458246
|
G | T | 16 | a0001c0001t0001g0059a0001c0001t0001g0232a0001c0001t0001g0233others(13): Show | 16 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.3030+6981G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458246 | ||||||
| chr11:43458296
|
G | A | 1 | a0001c0002t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3030+7031G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458296 | ||||||
| chr11:43458354
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3030+7089C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458354 | ||||||
| chr11:43458624
|
G | A | 18 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(15): Show | 18 | HG00323.hp1 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.3030+7359G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458624 | ||||||
| chr11:43458808
|
G | A | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0008t0006g0064 | 3 | HG02145.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3030+7543G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458808 | ||||||
| chr11:43458926
|
T | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0151 | 2 | HG02132.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3030+7661T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458926 | ||||||
| chr11:43458948
|
TAATAGTT others(13): Show |
T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3030+7704_3030+772 others(24): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43458948 | |||||
| chr11:43458963
|
G | A | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3030+7698G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43458963 | ||||||
| chr11:43459031
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(36): Show | 39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3030+7766A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459031 | ||||||
| chr11:43459057
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | NA18949.hp2 NA18959.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.3030+7792C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459057 | ||||||
| chr11:43459339
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3030+8074C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459339 | ||||||
| chr11:43459374
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3030+8109T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459374 | ||||||
| chr11:43459663
|
T | C | 1 | a0004c0007t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3030+8398T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459663 | ||||||
| chr11:43459692
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3030+8427T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459692 | ||||||
| chr11:43459760
|
T | C | 1 | a0001c0001t0004g0001 | 2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.3030+8495T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43459760 | ||||||
| chr11:43460090
|
C | T | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3030+8825C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460090 | ||||||
| chr11:43460105
|
A | AT | 24 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(21): Show | 24 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.3030+8853dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43460105 | |||||
| chr11:43460356
|
A | G | 1 | a0001c0002t0001g0187 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3030+9091A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460356 | ||||||
| chr11:43460399
|
T | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(11): Show | 15 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.3030+9134T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460399 | ||||||
| chr11:43460472
|
C | T | 23 | a0001c0001t0001g0252a0001c0001t0001g0261a0001c0001t0001g0264others(20): Show | 23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.3030+9207C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460472 | ||||||
| chr11:43460494
|
C | G | 3 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033 | 3 | HG01433.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.3030+9229C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460494 | ||||||
| chr11:43460668
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3030+9403G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43460668 | ||||||
| chr11:43461011
|
A | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3030+9746A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461011 | ||||||
| chr11:43461111
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3030+9846G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461111 | ||||||
| chr11:43461133
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3030+9868C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461133 | ||||||
| chr11:43461212
|
G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 14 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.3030+9947G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461212 | ||||||
| chr11:43461213
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.3030+9948C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461213 | ||||||
| chr11:43461241
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0048others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3030+9976G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461241 | ||||||
| chr11:43461311
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3030+10046G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461311 | ||||||
| chr11:43461390
|
C | CA | 57 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(54): Show | 57 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.3030+10151dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43461390 | |||||
| chr11:43461390
|
C | CAA | 47 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0061others(44): Show | 47 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.3030+10150_3030+10 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43461390 | |||||
| chr11:43461390
|
C | CAAA | 6 | a0001c0001t0001g0030a0001c0001t0001g0275a0001c0001t0001g0279others(3): Show | 6 | HG01433.hp1 HG02055.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.3030+10149_3030+10 others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43461390 | |||||
| chr11:43461390
|
CAAAAAAA others(2): Show |
C | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3030+10143_3030+10 others(15): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43461390 | |||||
| chr11:43461390
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3030+10136_3030+10 others(22): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43461390 | |||||
| chr11:43461672
|
T | C | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3030+10407T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461672 | ||||||
| chr11:43461943
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3030+10678C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43461943 | ||||||
| chr11:43462089
|
T | TA | 66 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0026others(63): Show | 66 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.3030+10840dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462089 | |||||
| chr11:43462089
|
T | TAA | 7 | a0001c0001t0001g0232a0001c0001t0001g0234a0001c0002t0001g0190others(4): Show | 7 | HG00642.hp1 HG01175.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.3030+10839_3030+10 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462089 | |||||
| chr11:43462223
|
C | G | 25 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(22): Show | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.3030+10958C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43462223 | ||||||
| chr11:43462567
|
A | G | 27 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.3030+11302A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43462567 | ||||||
| chr11:43462645
|
T | A | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3030+11380T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43462645 | ||||||
| chr11:43462695
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3030+11430G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43462695 | ||||||
| chr11:43462921
|
C | CT | 24 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0060others(21): Show | 24 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.3030+11668dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT | 40 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(37): Show | 40 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.3030+11662_3030+11 others(13): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(4): Show |
14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG00558.hp2 HG01069.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.3030+11658_3030+11 others(17): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3030+11657_3030+11 others(18): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0208a0001c0002t0001g0191 | 2 | HG01943.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(24): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(20): Show |
5 | a0002c0003t0002g0051a0002c0003t0002g0209a0002c0003t0002g0210others(2): Show | 5 | HG01496.hp2 HG02559.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(33): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(21): Show |
5 | a0002c0003t0002g0003a0002c0003t0002g0207a0002c0003t0002g0214others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(34): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(22): Show |
9 | a0002c0003t0002g0212a0002c0003t0002g0216a0002c0003t0002g0217others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(35): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(23): Show |
3 | a0001c0002t0001g0198a0002c0003t0001g0226a0002c0003t0002g0211 | 3 | HG01243.hp2 HG01257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(36): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(24): Show |
6 | a0001c0002t0001g0199a0001c0002t0001g0201a0001c0002t0001g0202others(3): Show | 6 | HG00738.hp1 HG01361.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(37): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(25): Show |
11 | a0001c0001t0001g0030a0001c0002t0001g0188a0001c0002t0001g0189others(8): Show | 11 | HG00642.hp1 HG01070.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(38): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(26): Show |
6 | a0001c0001t0001g0052a0001c0002t0001g0050a0001c0002t0001g0186others(3): Show | 6 | HG01069.hp2 HG01074.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(39): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(27): Show |
1 | a0001c0002t0001g0187 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3030+11668_3030+11 others(40): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(28): Show |
2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3030+11668_3030+11 others(41): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462921
|
C | CTTTTTTT others(29): Show |
1 | a0001c0001t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3030+11668_3030+11 others(42): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462921 | |||||
| chr11:43462990
|
ACTGCAAC | A | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3030+11728_3030+11 others(13): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43462990 | |||||
| chr11:43463104
|
C | T | 23 | a0001c0001t0001g0241a0001c0001t0001g0242a0002c0003t0001g0226others(20): Show | 23 | HG01243.hp2 HG01496.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.3030+11839C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43463104 | ||||||
| chr11:43463204
|
G | A | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.3030+11939G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43463204 | ||||||
| chr11:43463508
|
AT | A | 12 | a0001c0001t0001g0063a0001c0001t0001g0074a0001c0001t0001g0080others(9): Show | 12 | HG00323.hp2 HG00735.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.3030+12253delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43463508 | |||||
| chr11:43463821
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3030+12556A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43463821 | ||||||
| chr11:43463945
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02083.hp1 NA18949.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.3030+12680A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43463945 | ||||||
| chr11:43463983
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3030+12718T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43463983 | ||||||
| chr11:43464114
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3030+12849A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464114 | ||||||
| chr11:43464164
|
C | T | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3030+12899C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464164 | ||||||
| chr11:43464279
|
C | CA | 12 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(9): Show | 12 | HG01261.hp2 HG02055.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.3030+13030dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43464279 | |||||
| chr11:43464316
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0004g0001others(1): Show | 5 | HG00639.hp2 HG01106.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.3030+13051A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464316 | ||||||
| chr11:43464432
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0175 | 2 | HG02129.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.3030+13167T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464432 | ||||||
| chr11:43464493
|
A | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(43): Show | 46 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3030+13228A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464493 | ||||||
| chr11:43464517
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3030+13252C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464517 | ||||||
| chr11:43464518
|
G | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3030+13253G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464518 | ||||||
| chr11:43464561
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3030+13296T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464561 | ||||||
| chr11:43464569
|
A | G | 8 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(5): Show | 8 | HG01070.hp2 HG01081.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.3030+13304A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464569 | ||||||
| chr11:43464599
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3030+13334A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464599 | ||||||
| chr11:43464743
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3030+13478T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43464743 | ||||||
| chr11:43465076
|
C | A | 1 | a0001c0001t0001g0137 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3030+13811C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465076 | ||||||
| chr11:43465134
|
C | T | 62 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(59): Show | 62 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.3030+13869C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465134 | ||||||
| chr11:43465224
|
T | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3030+13959T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465224 | ||||||
| chr11:43465262
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3030+13997G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465262 | ||||||
| chr11:43465415
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0174 | 2 | NA18945.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3030+14150A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465415 | ||||||
| chr11:43465578
|
C | T | 1 | a0005c0010t0001g0113 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3030+14313C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465578 | ||||||
| chr11:43465867
|
C | CA | 39 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(36): Show | 39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3030+14604dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43465867 | |||||
| chr11:43465942
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3030+14677A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43465942 | ||||||
| chr11:43466067
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3030+14802C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466067 | ||||||
| chr11:43466115
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3030+14850A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466115 | ||||||
| chr11:43466223
|
G | A | 1 | a0001c0002t0001g0201 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3030+14958G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466223 | ||||||
| chr11:43466301
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3030+15036T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466301 | ||||||
| chr11:43466366
|
C | A | 1 | a0002c0003t0002g0212 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3030+15101C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466366 | ||||||
| chr11:43466486
|
C | T | 10 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.3030+15221C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466486 | ||||||
| chr11:43466937
|
C | T | 16 | a0001c0001t0001g0059a0001c0001t0001g0232a0001c0001t0001g0233others(13): Show | 16 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.3030+15672C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466937 | ||||||
| chr11:43466938
|
G | A | 1 | a0001c0002t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3030+15673G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466938 | ||||||
| chr11:43466953
|
C | T | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0008t0006g0064 | 3 | HG02145.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3030+15688C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43466953 | ||||||
| chr11:43467026
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3030+15761G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467026 | ||||||
| chr11:43467075
|
CAAA | C | 15 | a0001c0001t0001g0169a0001c0001t0003g0031a0001c0001t0003g0032others(12): Show | 15 | HG00099.hp2 HG01168.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.3030+15817_3030+15 others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43467075 | |||||
| chr11:43467138
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3030+15873G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467138 | ||||||
| chr11:43467403
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3030+16138A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467403 | ||||||
| chr11:43467564
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3030+16299A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467564 | ||||||
| chr11:43467568
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3030+16303G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467568 | ||||||
| chr11:43467656
|
G | A | 62 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(59): Show | 62 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.3030+16391G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467656 | ||||||
| chr11:43467786
|
G | T | 5 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 5 | NA18940.hp1 NA18967.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3030+16521G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467786 | ||||||
| chr11:43467856
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3030+16591G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43467856 | ||||||
| chr11:43467874
|
C | CA | 31 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(28): Show | 31 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.3030+16623dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43467874 | |||||
| chr11:43467960
|
CAG | C | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3030+16697_3030+16 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43467960 | |||||
| chr11:43468041
|
G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3030+16776G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468041 | ||||||
| chr11:43468181
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3030+16916C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468181 | ||||||
| chr11:43468488
|
A | G | 5 | a0001c0001t0001g0092a0001c0001t0001g0102a0001c0001t0001g0154others(2): Show | 5 | HG01978.hp2 NA18949.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.3030+17223A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468488 | ||||||
| chr11:43468494
|
G | T | 4 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0048others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3030+17229G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468494 | ||||||
| chr11:43468734
|
A | G | 8 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(5): Show | 8 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.3030+17469A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468734 | ||||||
| chr11:43468880
|
G | A | 1 | a0001c0002t0001g0198 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3030+17615G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468880 | ||||||
| chr11:43468908
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3030+17643A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468908 | ||||||
| chr11:43468974
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3030+17709G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43468974 | ||||||
| chr11:43469074
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(107): Show | 110 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.3030+17809T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469074 | ||||||
| chr11:43469273
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3030+18008A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469273 | ||||||
| chr11:43469299
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3030+18034A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469299 | ||||||
| chr11:43469391
|
A | G | 1 | a0002c0003t0002g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3030+18126A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469391 | ||||||
| chr11:43469757
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3030+18492G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469757 | ||||||
| chr11:43469853
|
A | T | 1 | a0002c0003t0002g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3030+18588A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469853 | ||||||
| chr11:43469872
|
T | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0076others(1): Show | 4 | HG00408.hp2 HG00438.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.3030+18607T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469872 | ||||||
| chr11:43469940
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0229 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3030+18675C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43469940 | ||||||
| chr11:43470120
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3030+18855A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470120 | ||||||
| chr11:43470175
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0155 | 3 | HG02922.hp2 HG02976.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.3030+18910C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470175 | ||||||
| chr11:43470264
|
A | G | 1 | a0001c0001t0001g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3030+18999A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470264 | ||||||
| chr11:43470290
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3030+19025T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470290 | ||||||
| chr11:43470584
|
C | T | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3030+19319C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470584 | ||||||
| chr11:43470654
|
C | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3030+19389C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470654 | ||||||
| chr11:43470963
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3031-19276C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43470963 | ||||||
| chr11:43471096
|
C | G | 4 | a0001c0001t0001g0030a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3031-19143C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471096 | ||||||
| chr11:43471184
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3031-19055C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471184 | ||||||
| chr11:43471198
|
A | C | 11 | a0001c0001t0001g0063a0001c0001t0001g0074a0001c0001t0001g0080others(8): Show | 11 | HG00323.hp2 HG00735.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.3031-19041A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471198 | ||||||
| chr11:43471236
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-19003A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471236 | ||||||
| chr11:43471276
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3031-18963T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471276 | ||||||
| chr11:43471513
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3031-18726C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471513 | ||||||
| chr11:43471525
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3031-18714G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471525 | ||||||
| chr11:43471590
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(36): Show | 39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3031-18649T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471590 | ||||||
| chr11:43471616
|
G | A | 42 | a0001c0001t0001g0246a0001c0001t0001g0251a0001c0001t0001g0252others(39): Show | 42 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.3031-18623G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471616 | ||||||
| chr11:43471731
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(107): Show | 110 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.3031-18508C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43471731 | ||||||
| chr11:43472391
|
G | A | 5 | a0001c0001t0001g0085a0001c0001t0001g0166a0001c0001t0001g0170others(2): Show | 5 | HG02148.hp2 NA18964.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.3031-17848G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472391 | ||||||
| chr11:43472406
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3031-17833T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472406 | ||||||
| chr11:43472418
|
T | C | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3031-17821T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472418 | ||||||
| chr11:43472674
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3031-17565A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472674 | ||||||
| chr11:43472728
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3031-17511A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472728 | ||||||
| chr11:43472841
|
T | TA | 45 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0001g0069others(42): Show | 45 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.3031-17381dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43472841 | |||||
| chr11:43472841
|
TA | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG01884.hp2 HG01928.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.3031-17381delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43472841 | |||||
| chr11:43472876
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3031-17363G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472876 | ||||||
| chr11:43472903
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3031-17336G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472903 | ||||||
| chr11:43472951
|
G | C | 2 | a0001c0001t0001g0285a0001c0001t0001g0286 | 2 | HG00609.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.3031-17288G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43472951 | ||||||
| chr11:43473046
|
G | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3031-17193G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473046 | ||||||
| chr11:43473183
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3031-17056A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473183 | ||||||
| chr11:43473216
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3031-17023A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473216 | ||||||
| chr11:43473597
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3031-16642G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473597 | ||||||
| chr11:43473624
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3031-16615T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473624 | ||||||
| chr11:43473684
|
G | A | 1 | a0002c0003t0002g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3031-16555G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473684 | ||||||
| chr11:43473825
|
G | T | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3031-16414G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473825 | ||||||
| chr11:43473882
|
C | CA | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG01081.hp2 HG01261.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3031-16340dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43473882 | |||||
| chr11:43473961
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3031-16278A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473961 | ||||||
| chr11:43473979
|
C | T | 1 | a0001c0002t0001g0197 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3031-16260C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43473979 | ||||||
| chr11:43474320
|
T | C | 1 | a0001c0001t0001g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3031-15919T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474320 | ||||||
| chr11:43474401
|
T | A | 1 | a0001c0001t0001g0185 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3031-15838T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474401 | ||||||
| chr11:43474406
|
A | G | 24 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0060others(21): Show | 24 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.3031-15833A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474406 | ||||||
| chr11:43474493
|
C | T | 1 | a0001c0002t0001g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3031-15746C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474493 | ||||||
| chr11:43474580
|
C | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 156 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.3031-15659C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474580 | ||||||
| chr11:43474849
|
TAAG | T | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3031-15387_3031-15 others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43474849 | |||||
| chr11:43474963
|
G | A | 41 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(38): Show | 41 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3031-15276G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474963 | ||||||
| chr11:43474974
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02976.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3031-15265G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43474974 | ||||||
| chr11:43475019
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3031-15220G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475019 | ||||||
| chr11:43475033
|
A | G | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3031-15206A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475033 | ||||||
| chr11:43475057
|
G | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(77): Show | 80 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.3031-15182G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475057 | ||||||
| chr11:43475078
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0021 | 2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3031-15161G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475078 | ||||||
| chr11:43475160
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3031-15079C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475160 | ||||||
| chr11:43475247
|
G | A | 34 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(31): Show | 34 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.3031-14992G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475247 | ||||||
| chr11:43475949
|
C | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(257): Show | 261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.3031-14290C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43475949 | ||||||
| chr11:43476024
|
T | A | 5 | a0001c0002t0001g0200a0001c0002t0001g0201a0001c0002t0001g0202others(2): Show | 5 | HG00558.hp2 HG01256.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.3031-14215T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476024 | ||||||
| chr11:43476026
|
C | T | 27 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.3031-14213C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476026 | ||||||
| chr11:43476057
|
A | G | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-14182A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476057 | ||||||
| chr11:43476319
|
A | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(15): Show | 18 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.3031-13920A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476319 | ||||||
| chr11:43476356
|
A | G | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-13883A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476356 | ||||||
| chr11:43476505
|
G | A | 1 | a0002c0003t0002g0212 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3031-13734G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476505 | ||||||
| chr11:43476676
|
G | A | 25 | a0001c0002t0001g0050a0001c0002t0001g0186a0001c0002t0001g0187others(22): Show | 25 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.3031-13563G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476676 | ||||||
| chr11:43476746
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3031-13493C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476746 | ||||||
| chr11:43476916
|
C | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3031-13323C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43476916 | ||||||
| chr11:43477083
|
T | C | 2 | a0001c0002t0001g0250a0001c0006t0001g0203 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3031-13156T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477083 | ||||||
| chr11:43477268
|
C | T | 5 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041others(2): Show | 5 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3031-12971C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477268 | ||||||
| chr11:43477411
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3031-12828T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477411 | ||||||
| chr11:43477743
|
A | G | 1 | a0004c0007t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3031-12496A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477743 | ||||||
| chr11:43477870
|
G | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0047others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3031-12369G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477870 | ||||||
| chr11:43477902
|
T | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.3031-12337T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43477902 | ||||||
| chr11:43478005
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-12234A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478005 | ||||||
| chr11:43478276
|
C | T | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3031-11963C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478276 | ||||||
| chr11:43478378
|
G | A | 34 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(31): Show | 34 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.3031-11861G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478378 | ||||||
| chr11:43478405
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0111a0001c0001t0001g0140 | 3 | HG00558.hp1 NA18948.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.3031-11834T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478405 | ||||||
| chr11:43478455
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0021 | 2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3031-11784C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478455 | ||||||
| chr11:43478592
|
A | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-11647A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478592 | ||||||
| chr11:43478715
|
C | G | 1 | a0002c0003t0002g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3031-11524C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478715 | ||||||
| chr11:43478721
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3031-11518C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478721 | ||||||
| chr11:43478743
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3031-11496C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478743 | ||||||
| chr11:43478744
|
G | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-11495G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478744 | ||||||
| chr11:43478800
|
A | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(36): Show | 39 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.3031-11439A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478800 | ||||||
| chr11:43478918
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(77): Show | 80 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.3031-11321C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478918 | ||||||
| chr11:43478919
|
G | A | 5 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041others(2): Show | 5 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3031-11320G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478919 | ||||||
| chr11:43478962
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3031-11277C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43478962 | ||||||
| chr11:43479092
|
T | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3031-11147T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479092 | ||||||
| chr11:43479164
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(12): Show | 15 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.3031-11075C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479164 | ||||||
| chr11:43479196
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG01074.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.3031-11043C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479196 | ||||||
| chr11:43479239
|
C | CAAA | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-10995_3031-10 others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43479239 | |||||
| chr11:43479247
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-10992G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479247 | ||||||
| chr11:43479476
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3031-10763A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479476 | ||||||
| chr11:43479784
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3031-10455A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479784 | ||||||
| chr11:43479793
|
T | C | 1 | a0002c0003t0002g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3031-10446T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43479793 | ||||||
| chr11:43480055
|
A | T | 21 | a0002c0003t0001g0226a0002c0003t0002g0003a0002c0003t0002g0051others(18): Show | 21 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3031-10184A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43480055 | ||||||
| chr11:43480168
|
C | A | 26 | a0001c0001t0001g0052a0001c0002t0001g0050a0001c0002t0001g0186others(23): Show | 26 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-10071C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43480168 | ||||||
| chr11:43480436
|
A | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0166a0001c0001t0001g0180 | 3 | NA18964.hp2 NA18972.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3031-9803A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43480436 | ||||||
| chr11:43480632
|
G | A | 3 | a0002c0003t0002g0221a0002c0003t0002g0222a0002c0003t0002g0225 | 3 | HG01891.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3031-9607G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43480632 | ||||||
| chr11:43480887
|
C | CA | 23 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(20): Show | 23 | HG00099.hp1 HG00639.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.3031-9338dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43480887 | |||||
| chr11:43480887
|
CA | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 21 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.3031-9338delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43480887 | |||||
| chr11:43480917
|
G | A | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-9322G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43480917 | ||||||
| chr11:43481057
|
AGGT | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3031-9181_3031-917 others(7): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481057 | ||||||
| chr11:43481058
|
GGTA | G | 289 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.3031-9176_3031-917 others(7): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43481058 | |||||
| chr11:43481146
|
T | A | 1 | a0001c0001t0001g0252 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3031-9093T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481146 | ||||||
| chr11:43481151
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-9088T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481151 | ||||||
| chr11:43481186
|
C | T | 1 | a0002c0003t0002g0225 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3031-9053C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481186 | ||||||
| chr11:43481231
|
AAAAG | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-9002_3031-899 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43481231 | |||||
| chr11:43481269
|
G | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0229 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3031-8970G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481269 | ||||||
| chr11:43481360
|
T | A | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3031-8879T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481360 | ||||||
| chr11:43481445
|
G | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-8794G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481445 | ||||||
| chr11:43481486
|
G | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01243.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3031-8753G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481486 | ||||||
| chr11:43481727
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0132 | 2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3031-8512T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481727 | ||||||
| chr11:43481779
|
G | A | 4 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0158others(1): Show | 4 | HG01928.hp1 HG01952.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.3031-8460G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481779 | ||||||
| chr11:43481920
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3031-8319G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43481920 | ||||||
| chr11:43482258
|
GT | G | 46 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(43): Show | 47 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.3031-7969delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43482258 | |||||
| chr11:43482490
|
C | G | 34 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(31): Show | 34 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.3031-7749C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43482490 | ||||||
| chr11:43482529
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3031-7710T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43482529 | ||||||
| chr11:43482800
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.3031-7439G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43482800 | ||||||
| chr11:43482986
|
T | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01884.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3031-7253T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43482986 | ||||||
| chr11:43483152
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-7087A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43483152 | ||||||
| chr11:43483174
|
TTAAG | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-7062_3031-705 others(8): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43483174 | |||||
| chr11:43483190
|
T | TA | 80 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(77): Show | 80 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.3031-7043dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43483190 | |||||
| chr11:43483383
|
A | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 20 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-6856A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43483383 | ||||||
| chr11:43483667
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3031-6572A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43483667 | ||||||
| chr11:43484112
|
A | G | 34 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(31): Show | 34 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.3031-6127A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43484112 | ||||||
| chr11:43484157
|
T | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(28): Show | 32 | HG00099.hp2 HG00639.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.3031-6082T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43484157 | ||||||
| chr11:43484418
|
T | A | 2 | a0001c0001t0005g0104a0001c0001t0005g0152 | 2 | HG00609.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.3031-5821T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43484418 | ||||||
| chr11:43484607
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3031-5632T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43484607 | ||||||
| chr11:43484897
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 19 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.3031-5342G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43484897 | ||||||
| chr11:43485074
|
T | C | 1 | a0001c0008t0006g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3031-5165T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485074 | ||||||
| chr11:43485245
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3031-4994A>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485245 | ||||||
| chr11:43485392
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3031-4847T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485392 | ||||||
| chr11:43485601
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3031-4638A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485601 | ||||||
| chr11:43485699
|
T | C | 31 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(28): Show | 31 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.3031-4540T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485699 | ||||||
| chr11:43485828
|
G | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3031-4411G>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485828 | ||||||
| chr11:43485851
|
T | A | 1 | a0001c0002t0001g0190 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3031-4388T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43485851 | ||||||
| chr11:43485883
|
G | GT | 10 | a0001c0001t0001g0067a0001c0001t0001g0076a0001c0001t0001g0100others(7): Show | 10 | HG00438.hp1 HG00597.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.3031-4336dupT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43485883 | |||||
| chr11:43485883
|
GT | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(81): Show | 84 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.3031-4336delT | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43485883 | |||||
| chr11:43485883
|
GTT | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 21 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.3031-4337_3031-433 others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43485883 | |||||
| chr11:43486157
|
T | TC | 94 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 95 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.3031-4075dupC | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43486157 | |||||
| chr11:43486426
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3031-3813C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486426 | ||||||
| chr11:43486508
|
T | C | 1 | a0001c0001t0007g0179 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3031-3731T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486508 | ||||||
| chr11:43486606
|
A | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 22 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.3031-3633A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486606 | ||||||
| chr11:43486662
|
G | A | 27 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.3031-3577G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486662 | ||||||
| chr11:43486700
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0229 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3031-3539A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486700 | ||||||
| chr11:43486717
|
A | G | 1 | a0001c0002t0001g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3031-3522A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486717 | ||||||
| chr11:43486768
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3031-3471A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43486768 | ||||||
| chr11:43487131
|
A | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 155 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.3031-3108A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487131 | ||||||
| chr11:43487206
|
C | T | 1 | a0002c0003t0002g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3031-3033C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487206 | ||||||
| chr11:43487292
|
C | A | 1 | a0001c0001t0001g0174 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3031-2947C>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487292 | ||||||
| chr11:43487334
|
C | T | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-2905C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487334 | ||||||
| chr11:43487365
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02886.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3031-2874C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487365 | ||||||
| chr11:43487369
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3031-2870C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487369 | ||||||
| chr11:43487619
|
A | C | 27 | a0001c0001t0001g0052a0001c0001t0001g0208a0001c0002t0001g0050others(24): Show | 27 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.3031-2620A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487619 | ||||||
| chr11:43487808
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3031-2431C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43487808 | ||||||
| chr11:43488031
|
A | G | 1 | a0002c0003t0002g0212 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3031-2208A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43488031 | ||||||
| chr11:43488719
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3031-1520G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43488719 | ||||||
| chr11:43489375
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(1): Show | 4 | HG01255.hp1 HG01943.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.3031-864T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489375 | ||||||
| chr11:43489471
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3031-768C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489471 | ||||||
| chr11:43489536
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3031-703G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489536 | ||||||
| chr11:43489717
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | 25 | HG00408.hp1 HG00639.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.3031-522G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489717 | ||||||
| chr11:43489718
|
A | G | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3031-521A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489718 | ||||||
| chr11:43489757
|
A | AGGAGGGG | 13 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(10): Show | 13 | HG01069.hp1 HG01169.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3031-469_3031-463d others(9): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | 43489757 | |||||
| chr11:43489857
|
A | G | 68 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 69 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.3031-382A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489857 | ||||||
| chr11:43489966
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3031-273G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43489966 | ||||||
| chr11:43490070
|
T | A | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-169T>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43490070 | ||||||
| chr11:43490079
|
G | C | 20 | a0002c0003t0002g0003a0002c0003t0002g0051a0002c0003t0002g0207others(17): Show | 20 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3031-160G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43490079 | ||||||
| chr11:43490181
|
G | C | 1 | a0002c0003t0002g0212 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3031-58G>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43490181 | ||||||
| chr11:43490231
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.3031-8C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 21/23 | chr11 | 43490231 | ||||||
| chr11:43490574
|
G | A | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3150+216G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43490574 | ||||||
| chr11:43490668
|
A | C | 19 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(16): Show | 19 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.3150+310A>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43490668 | ||||||
| chr11:43490854
|
C | CA | 68 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(65): Show | 68 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.3150+524dupA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | |||||
| chr11:43490854
|
C | CAA | 30 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0028others(27): Show | 30 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.3150+523_3150+524d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | |||||
| chr11:43490854
|
C | CAAA | 6 | a0001c0002t0001g0189a0001c0002t0001g0190a0001c0002t0001g0199others(3): Show | 6 | HG00738.hp1 HG01175.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+522_3150+524d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | |||||
| chr11:43490854
|
CA | C | 28 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0040others(25): Show | 28 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.3150+524delA | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | |||||
| chr11:43490854
|
CAA | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0241others(3): Show | 6 | HG01243.hp2 HG01516.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+523_3150+524d others(4): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | |||||
| chr11:43490854
|
CAAA | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 31 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.3150+522_3150+524d others(5): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | |||||
| chr11:43490854
|
CAAAA | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(3): Show | 6 | HG01261.hp1 HG01261.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+521_3150+524d others(6): Show |
TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | 43490854 | |||||
| chr11:43491048
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3150+690G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491048 | ||||||
| chr11:43491230
|
C | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 22 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.3151-790C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491230 | ||||||
| chr11:43491303
|
A | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0046others(11): Show | 14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3151-717A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491303 | ||||||
| chr11:43491421
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3151-599G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491421 | ||||||
| chr11:43491800
|
C | T | 23 | a0001c0001t0001g0252a0001c0001t0001g0261a0001c0001t0001g0264others(20): Show | 23 | HG00609.hp1 HG00741.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.3151-220C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491800 | ||||||
| chr11:43491813
|
C | T | 33 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0071others(30): Show | 33 | HG00741.hp2 HG01255.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.3151-207C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491813 | ||||||
| chr11:43491995
|
C | T | 2 | a0003c0004t0001g0230a0003c0004t0001g0247 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3151-25C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491995 | ||||||
| chr11:43491999
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0174 | 2 | NA18945.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3151-21C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 22/23 | chr11 | 43491999 | ||||||
| chr11:43492385
|
A | G | 26 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(23): Show | 26 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.3294+222A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43492385 | ||||||
| chr11:43492508
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3294+345T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43492508 | ||||||
| chr11:43492630
|
T | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3294+467T>C | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43492630 | ||||||
| chr11:43492731
|
G | A | 1 | a0002c0003t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3294+568G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43492731 | ||||||
| chr11:43492980
|
A | G | 46 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(43): Show | 46 | HG00099.hp2 HG00323.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.3295-793A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43492980 | ||||||
| chr11:43493160
|
T | G | 11 | a0001c0001t0001g0063a0001c0001t0001g0074a0001c0001t0001g0080others(8): Show | 11 | HG00323.hp2 HG00735.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.3295-613T>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43493160 | ||||||
| chr11:43493201
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3295-572A>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43493201 | ||||||
| chr11:43493202
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3295-571C>T | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43493202 | ||||||
| chr11:43493381
|
G | A | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(44): Show | 48 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.3295-392G>A | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43493381 | ||||||
| chr11:43493754
|
C | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(112): Show | 116 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.3295-19C>G | TTC17 | ENSG00000052841.16 | transcript | ENST00000039989.9 | protein_coding | 23/23 | chr11 | 43493754 |